Linda's Legacy
With our Mom's passing, this site has and will change, as we move forward.

The journey that is laid out on this page covers from January 2018 (initial diagnosis of cancer) through the day she passed away (July 14th, 2018). 

Everything from July 14th forward will be posted at http://linda.thepolzin.com (click the button to the left)
Momma's Journey
Saturday, July 14th, 2018 - 10:40PM - Sunset & Sunrise​​
The sun dips low in the western sky. 
It skims the horizon and begins it's nightly lullaby.
The brightest stars appear first to our eyes.
The moon then begins it's nightly rise.

Darkness mounts an all out invasion…
Devoid of light brings an eerie sensation…
The northern lights begin their show…
These are things of which we know…

But in the deep of the night…
Carries on the struggle and the fight…
Things occur and lives can change…
Some good, some bad, along this range…

The light will come, and restore the day…
Same as always before, it happens this way…
The cycle is unbroken, and carries on…
Though human perception of it is gone...

Into the night we go one way…
Yet differently emerge the next day…
The sun and moon perform their tango…
Oblivious are we to this cosmic flow…

Visions and dreams may visit our heads…
While we lie in slumber in our beds…
Some are happy, some are sad…
Some bring joy, some make us mad…

The sun has set on a beautiful soul…
It rises again to collect it's toll…
God keep you Momma, and all of us too…
Our hearts are breaking because we lost you…


For Linda M. Polzin, my Momma
9/18/56 - 7/14/18

~T

Saturday, July 14th, 2018 - 11:35AM - Heart & Soul​​
I fell to my knees at the side of my bed when I returned home from the hospital this morning. The cycles in my mind are running at an inhuman pace right now. What if I'd just gone to the hospital sooner? What if I hadn't left her there last night? What if we'd never let things go on this long to begin with? What if we never went to this hospital to begin with. These are questions I will never have answered, no matter what. We aren't given do overs in life. Please don't tell me that none of this is my fault or that I can't blame myself. Those aren't comments or responses that will be helpful in any way to me. I'm not invincible or superhuman. I'm not a doctor or shaman, not a medicine man or a miracle worker. I am my mother's son. Her advocate. I'm part of her heart and some of her strength. And, right now I'm very lost.

My heart is shattered into a million pieces. I can't talk yet. I don't express myself well in that way and mostly cannot control the overwhelming emotions at this point. I know I'm surrounded by a sea of people, that's never my concern. For self preservation, it's important that I get time to process, and try to calm the incredible chaos in my mind.


I do stand firm with this… there will be changes and consequences at the hospital my mom was at. I'm genuinely appalled and fiercely furious at the blatant mistakes made and the insane lack of progress at every turn. There is a monstrous disconnect and I promise on the entirety of my being that I will lay every card on center stage of the world's table.


I pray on every breath that I breathe and every tear in my eyes that she is finally at rest, and her mind and soul at peace.


I came home with three bags of my Mom's belongings. I don't know what it is that overtook me, but I was moved with an unrelenting urge to wash all of the clothes and organize all of her things. My mom wasn't rich or extravagant, not flashy or a snob. She had no worldly possessions, only things of immense personal and sentimental value.


The past six months have been some of the most challenging of my life. I can't fathom the words it would take to describe all that my Mom has been through and endured. What I wouldn't give to hug her and hold on, laugh with her, or have just one more adventure. I'll forever hold and carry the light from her eyes and the fire from her soul. Both of which tragically went out in her body this morning.


My beautiful Momma was born September 18th, 1956. She went to God July 14th, 2018. For her, the hard part is over. She fought with more ferocity, tenacity, heart and spirit that you'd think would be allowed or required of any one person. God hold my Momma in your embrace. Keep my family in your divine and omnipresent love, and bless and watch over this world - it is in great need.


I'm incredibly sad that she's not here to hold me as we move into these next days, but I'm in some way comforted that I will never again have to watch her suffer in silence, writhe in pain, breakdown from stress, become weary from the trauma, and at her young 61 years of age, I'll never have to see her do worldly battle again.


For us - her children and grandchildren, her Dad and Llani, her Sister and Ron and family, all of her extended family and friends, and the network of warriors who walked with us, She never fought alone.


Thank you to each of you who has reached out via message, text, email or phone call, I wish I could reply to each of you individually to express gratitude, but am just not in that place. Know that your support and messages are very much received and will serve as comfort when my mind comes back to earth.
We'll let you all know when arrangements have been made. Her wish and the plan forming in the fog was to celebrate her life. And so it shall be.


Love and sincere thanks to you all.


~T

Saturday, July 14th, 2018 - 5:00AM - On Angel's Wings
In the early morning hours, my beautiful Momma left this Earth and went to heaven. She succumbed to the numerous traumas she has endured over the years, most recently her battle with what we now know was gastric cancer.

She did not suffer, and we were able to follow her wishes. Though you cannot always give those you love the things they ask for, we held firm to her wants. No machines keeping her alive, no prolonged suffering, no pain.

She has gone into the waiting arms of God, her Mom who passed away in 2011, and her grandparents. She slipped away peacefully after being removed from the life support. She was not alone.

There are not enough Kleenex in existence to soak up all of these tears that just will not stop coming. My heart has broken into a million pieces, and she carries many of them with her. There do not exist words sufficient enough to describe my mom. She was courageous and generous, kind and creative. She was strong and intelligent, humble and gracious. She was full of heart and humor, light and laughter. And she was so much more. Rest now, my beautiful Momma, be finally at peace.

The streets of heaven are a little more crowded today. I thank the Lord God for taking her peacefully and painlessly into his arms. I will look to the heavens and keep you close at hand, Momma. My soul is shattered and my heart is broken, but I know even from afar you will work to comfort and heal them. I'm sorry that I couldn't fix you or heal you or keep you next to me here in Earth. I'm sorry that I did not know what to do to make this all better.

Aside from being my Momma, you were one of my best friends. From our cross country road trip, to silly shenanigans, from quiet meals, to our inside jokes. I cannot thank you enough for the love and life you gave us, for your sacrifices and unconditional support. For giving of yourself no matter the cost. You were the lioness, fiercely protective of our pack.

With our eternal love and endless adoration, may your journey be swift and the destination magnificent. We love you so much. We love you most


~T

Wednesday, July 11th, 2018 - 11:45PM - Silence Isn't Quiet
The last five days have been intense. It started with some confusing conversations, and snowballed into an emergency room visit, a code called over the hospital P.A. system, phone calls to family, emergency plane tickets, and a weekend that can only be described as chaos.

My mom has been admitted to the hospital five times in the past month. We can second guess, point fingers, get mad, yell, cry, fall apart (all of which probably did happen at one point or another). We have to take each situation as it comes, one day at a time, one breath after another.

There are times when it feels as though we have to tell our story so many times that we become calloused to the people at the center of it all. We become robotic, adrenaline and automatic responses take over. Emotion can rule beyond all reason, and defy logic.

Six months ago, we'd just celebrated Christmas, and were only barely through ringing in a new year. Six months ago, our parents lives we're starting to turn upside down. Six months ago, we had energy, full night's sleeping, appetites, and far fewer cares in the world. Six months ago, we were all living in the same state, literally a matter of single digit minutes apart. Six months ago, the promises of a new year and a united family, good health and prosperity were about to be shattered.

The cliche roller coaster really fits amazingly and ominously well for our lives. The anticipation and excitement build while a tinge of fear resides at the pit of our stomachs. We load into the cars, hopeful and anxious. The ride starts and climbs to a step peak at a slow pace. Everyone takes a communal sigh of relief and then holds their breath. In the next moment the floor seemingly comes out from under your feet as you plummet to a possible impending doom. Then just as you think you'll crack because you can't take anymore of the gravitational forces heaving you ever downward, the ride twists, turns, and rockets all the riders in a new, unknown direction.

I don't like roller coasters and I sure as hell want off this ride. Life doesn't give that option, unfortunately. So, at least I'm lucky to have other riders on this coaster called reality.


Half of a year has come and gone. From sitting in my brother's living room, my dad somber and serious, to him slowly getting out the words. I've never been one to control my facial expressions well, and I wish I could tell you what they did in that moment. We went into planning mode. In that instant, life had issued an immediate and dominant alteration to our course. But, she wasn't anywhere near done. Three weeks later, the cold knock of sober reality landed an upper cut to the rib cage with follow through to the neck and head. A phone call which I barely understood in the moment where, through tear filled words, my mom spilled out the words. Ok, universe, that's enough now. What's that you say? Challenge accepted? Eff.


My sister's landlord sells the house she's renting… time to move. She moves in with brother. Oh, universe, you got more? Of course. My brother's landlord sells the house they're renting. Everyone has to move. Life, you haven't thrown enough into the mix? Oh, well that would just be too simple. California calling? I'm gonna put that on hold, hit the ignore, block, rinse and repeat. Ok, don't worry, I got this. I can be three places at once, right? False. There rambling is getting bad, T, get it together.


Some movement. Progress. Positive news. Maybe this Willie is starting to collapse? Spoke too soon. That was just the first wave. Here comes the next. Ok, everyone grab a hose and form a line. We get the fire beat down to a smoulder with random ongoing flare-ups. Sort of.


Then, we get to July 6th, 2018. We must have gotten overly cocky or something. The universe was unhappy with us. Kharmic retribution for… well, something that's going to happen in the future if my only guess because I cannot possibly imagine what dastardly deeds we must have committed to warrant the ongoing saga we now face.


The emergency room doctor must have gotten a case of diarrhea diagnosis mouth or something.


I know this post has been broken and seemingly devoid of sensical speech. But, this is just a small glimpse into what has become our “norm”.
To elaborate, and explain to anyone reading this: July 6th started out as a fairly quiet and passive day. A Friday, normal work day that would quickly and heinously go south. As has become the usual, I was getting ready for work and called to check on my mom. She sounded a little groggy, but generally “ok” all things considered. No additional fires to put out at 8:00 AM.


My sister texted me about an hour later and said that she'd made multiple attempts to get in touch with Mom. When she finally answered, she was very agitated and upset, apparently, by the ringtone on her phone. My sister was going to give the caregiver and physical therapist a heads up… might be a good day to wear football pads to work. We lightly quipped about this, but were worried and not sure why Mom had gotten so worked up in the short time since I'd spoken to her.


Next was another phone call from me to my mom. This is when it sank in that something was definitely going haywire on the day. She didn't answer so I had to activate the Amazon echo in her house to essentially turn on a speaker that lets me talk to her when phone contact isn't happening. We talked a bit and she told me she was having a hard mental day. She was also anxious and upset because she couldn't find one of her dentures. I must stress that although this is normally where I'd crack a wiseass joke, but it was definitely not a laughing matter. I could hear the distress in her voice and everything was escalating. She also tells me about an appointment with her doctor in the afternoon which I know should've been cancelled as we got it moved up to several days before. I reassured her, calmed her a little, and told her I'd start working on appointments.


A few minutes later my phone rang. Aunt Debbie called because she'd had a bit of an off kilter conversation with Mom. She was confused and it was very difficult to understand Mom. I gathered more info and then told auntie I'd call her back. I confirmed with the doctor that the appointment was cancelled. Also tried to contact one of the specialists to see about a same day appointment. Unfortunately that doctor is on vacation until the end of this month. Time to call Mom back.


I updated her about appointments and for whatever reason a trigger was switched. She still hadn't been able to locate her denture and this was the straw that broke the camel's back. I do what I can to calm her, but call auntie back to fill her in. Auntie decides to go over and help Mom and see if she can't calm her some too. We have some success, at least. Debbie finds mom's denture. She helps calm her some and suggests a couple hours nap. Mom has since reinstated the doctor's appointment and wants to see her primary care doctor. But first, a couple hours of sleep.


When auntie returns to get Mom, she gets her all the way out and into her car. Mom is winded and is complaining of shortness of breath. Cue the aid car. Auntie calls to tell me they will be taking her to Providence hospital. I tell her I'll meet then there. I get in the phone to Jill and let her know. I also call California, I mean, my brother to let him know. I arrive at the hospital a solid fifteen minutes before Aunt Debbie gets there. The aid car is another fifteen to twenty after that.


The next hour is a bit of a noxious blur in memory. I recall the hospital p.a. system announcing a code sepsis across the loud speakers. No one has told the patient or anyone else in the room if this, thus far. The next time the nurse is in, we ask and she tells us it's a new thing. That's nice. (Not really). Then in quick succession we're told that something is very wrong. It's believed likely that the cancer has spread to Mom's brain and because of her other medical conditions and current medical state, there isn't anything they can do. They then throw in that she has pneumonia. As the very atmosphere and oxygen is completely sucked from my lungs and the room, we start contacting family. Get here. Now.


Emergency plane tickets from California and Michigan for my brother and Grandpa and Llani. And then the flood of emotion and tears in which words literally will not come out of my mouth. I open it to speak and say things, but there is only silence. It is the loudest, most deafeningly brutal silence I've ever known.


Fast forward to Sunday. Two days later. Mom isn't in good shape. We haven't been in contact with a doctor other than the ER doc. Steve was here and we were battening down the hatches, attempting to navigate this storm. We finally corner the treating doctor, literally, and back him into a corner. He's not the ER doctor. Mom has gone through a CT, an MRI, an ultrasound, xrays, and had multiple rounds of lab work / blood tests done. So… what is the news? She isn't and wasn't septic. She didn't and doesn't have pneumonia. The cancer has not spread to her brain. She has some kind of infection, decreased kidney function, decreased liver function, and her body is not expelling the waste at a normal level like it should. Her stomach and legs are quite swollen and painful.


Again, literally not letting the doctor leave the room until we have every answer we need and a plan of action and direction… we ask, “What are you DOING about this!?”


Now we're here, three days later, it's Wednesday. Mom has been in the hospital since Friday for this particular stay. This makes the fifth admit in the last four week span. The contrast given for the CT has essentially hardened and crystalized instead of being expelled normally. This has backed up everything and caused the swelling and severe abdomen pain. They are getting slow but sure movements, getting some of the body's waste out. Kidney function has definitely improved but still has more to go. This is an unfortunate waiting game. Mom was very dehydrated and isn't getting all the nutrients and nutrition she needs because there simply is no room in the abdomen/stomach for food or liquids until the backlog is cleared. It's a scary time. We have having to leave with her still in the hospital for even one minute, but we cannot possibly be there 100% of the time.


My heart has mostly returned to a normal rhythm, but I'd swear that I've aged ten years in these past six months. The important piece is that my brother and Grandpa and Llani were/are here when Mom and we needed them. Her story isn't over. There are many more pages to be written. It's a miserable and uncomfortable situation for Mom, but we shall get through this too. Mom - keep up the fight. We know your energy is low and your spirit is broken. You must understand and hopefully recognize that we're here for you through the good and the bad. You'll have bad days, you'll have great days.. regardless, we'll be there.


There's more to come… but for this post… the only thing more to come is sleep. These words have been garbled, jumbled, confused and clarified. They're here now for you to read. These words are my own.


Until next time…


~T

Friday, July 6th, 2018 - 11:48PM
As many of you already know Mom was hospitalized again today. It has been an awful emotional roller coaster of news, and revised news, tears, phone calls, more tears, different news, a turkey sandwich, a cup of jello and a nap for us. I unfortunately don't have the energy or inner fortitude to update you properly but please Prayer Warriors, send up your loudest most goodest sincerest prayers for Mama and stay tuned for updates.

I'm going to lay down for a few hours. 

~Jill
Friday, July 6th into Saturday, July 7th, 2018 - Matters of the heart
Friends and family, we're back in the hospital with my mom. It's been a whirlwind day and I'm honestly not sure what all has transpired. The day started for her with a lack of sleep and has continued to spiral downhill. She's not been feeling well and the waiting game on the oncology front is taking some swift jabs at us.

I don't know that I can even begin to get my head wrapped around all that has happened over the past six months. Here in the trenches, in the thick of it, we're side by side with each of our parents as these battles wage on. We have not and will not leave their sides. The toll is immense on the circle of warriors, I can't even begin to imagine or pretend to fathom the incredible struggle my parents themselves undergo.

When each and every last card is down, all hands on the table, I would not trade five seconds of this, not for anything in the world. This is time with my parents. A valuable, precious, irreplaceable commodity. There is no currency, possession, or extravagance that rivals the value of presence and time. It is also fleeting, in that the cosmic balance doesn't allow us to bank unused time, there are no rollover minutes.

The people around us say, “Live your life.” I know that this comes from a good and caring place when it is said. I understand the intent. But, to that, I say, “This is my life. Without my parents, I would not have it. Birth and life is a debt created that cannot be repaid and will never be considered owed.” Hearts may break into a thousand pieces. Enough tears may fall to fill an ocean. We will lose sleep and appetites. Our internal and external coping mechanisms will kick in. Minds will battle feeling and emotion in a never-ending duel, where everyone comes out a loser.

I write to let the waters out from behind the floodgates. The words circle in my mind, but cannot find the outlet through verbal means from my mouth. I find this to be very odd happenstance. With my type A personality, and typically loud and and direct communication style, being at a loss for words isn't something I'm accustomed to or really know how to handle. It seems that when it comes to matters of the heart, for me, verbal words just aren't meant to come. I wield a mighty sword in this electronic “pen.” My fear is that my armor may be weakened against the coming battle.


Both of my parents, in the last half-year span have asked, “Am I going to die?” The answer is impossible is many ways. We are all going to die, at some point. There's no sugar coated or outright lie. Death is the only absolute certainty in life. It seems almost a cruel joke that we are rarely destined to know the cause and hour of our death.


I ask all of you… no matter what your beliefs, which (if any) religion you practice, your level of spirituality, whether or not you believe in God or in Gods or a higher power of any kind, no matter your race, creed, the color of your skin, your sexual orientation, gender identity, whether young or old, rich or poor, healthy, sick, fighting, prospering, tired or energized… if you're a human, say a prayer, think positive thoughts, send healing vibes, light a candle, or even toss a coin in a pond or skip a rock across the waters of a lake or ocean in support of my family.


My mom has pneumonia. This we know. There are many other possibilities and factors for which we do yet not have answers. My mom is one of the strongest people I've ever been privileged to encounter. I don't say strongest woman because she's got strength that transcends any gender. I cannot even imagine the war that she wages internally. Would that more of us could be so lucky to have been endowed with the strength, courage and heart she possesses. Fight, Mom. Dig down to the place within yourself where the warrior beats a drum in a rhythm of staunch concentration and fierce preservation. Fight, because we will. Fight, for you, because it's who you are and what you are made of.


My eyes may be as heavy as my heart, tonight. Then I remind myself that my tiredness is nothing in comparison to the exhaustion my parents must face on a regular basis. Through radiation, and chemotherapy, medications, emotions, hospital stays, doctor appointments, strong personalities, worry, anxiety, despair, confusion, disorientation, and countless people giving their opinions, it's not just the weight of the world seemingly pressing down hard on them. It's the weight of the solar system, galaxy, perhaps the entirety of the universe and the heavens applying brute force.


Tomorrow, hopefully, shall bring new light and new perspective. If only my body could understand and keep up with the triathlon my mind is enduring. As I've continued to write this and rewrite this, it is, by the clock, already tomorrow. I fall down to my knees, lift my eyes and heart to heaven and talk to God.
Whether or not I understand the outcome, I know he hears me. It is not sleep that I seek, nor do I expect it, but I hope for rest and some renewed energy.

For my mom - May you receive restful sleep, healing unto your body, rejuvenation as the sun rises, and relaxation and serenity for your mind.


To all of you, reading this and any of my other messages… dry the tears in your eyes. May you also be given the grace, light, and be refreshed by the dawn of a new day. A new chance to change those things which you can, the peace and solace to let go of those you cannot, and the wisdom to know the difference.


The words that have come before and the ones that follow flowed from the gates within my being. Though they may have been said aloud, I offer them to you. Their purpose is the same, may it be bountiful and plentiful and so too are matters of the heart.


Until the next time….
~T


Sunday, July 1st, 2018 - 11:15PM - Memories of the way we were
I take a deep breath. Inhale and hold. A pause, a moment to gather myself and my thoughts. My heart may have skipped a beat. As the rush comes back, I realize I still haven't exhaled. Hold on just a moment longer, don't let go of the waking dream. The memories, the times before. The days of who we used to be.

Halfway through this year that makes me want to use every swear word from every language and add in more that are slang or yet to be spoken. July first. Start of the second half of the year. Where's my silver lining? Sometimes, I feel as though it may be at the bottom of a box of wine, a bottle of beer, a shot of Southern Comfort, or a pounder of Rum and Coke. But alas, none of us really drinks anymore... So nothing to be found in those places. My silver lining may have presented itself in time... We've made it halfway through this &#$@ year. Maybe that means we're on the downhill portion of this cross country endurance test? Regardless. The battles appear to be creeping up on us again, the war far from over.

I know you're not all reading this for my diatribe… but rather want the updates on my parents. Well, maybe some of you are here for the diatribe too. Oh, alright, let's get into it.

Dad updates:
I'm happy to finally claim victory of sorts. Our ongoing sparring with the bullying, backward, bumbling, bulbous, bureaucracy that is Boeing is seemingly appearing to approach an end. The magic day of reckoning is July 19th. Then, Dad can move forward from his work life perspective.
With regards to the medical side: He's nearing the end of his chemotherapy cycle. His lab results have been so positive that the dosage he is infused with has twice been lowered! We proceed with optimism and caution. There is no cure for cancer, but we're well on our way to remission. His PSA (which should be under a 4, and was well into the hundreds), is now registering as a 0.01, which is referred to as undetectable. We're still facing challenges with regards to the extensive dental work that needs to happen, and the financial aspects are a work in progress, but much positive news otherwise! The move forward plan from here is to continue in the clinical trial and follow through his final chemo infusion (also on July 19th). Then in the months following the completion of this chemo cycle imaging will be repeated to determine progress and effectiveness of treatments this far.


We continue to struggle with and cope with what's known as chemo brain. It's causing short term memory loss, fatigue, confusion, and some increased emotional responses. For all intensive purposes, we get to take a collective sigh of relief in Dad's line of care.


Mom updates:
I take another deep breath here. We're in a holding pattern. A bit of hurry up and wait. Just as at the beginning of these journeys, were up against a holiday which causes some additional delay. Over the past three weeks my mom has been admitted and discharged four times from the hospital. Some of the situations are related to each other. Some are related to the cancer. Some are caused by the cancer. One of them, obviously, was the discovery of the cancer. Some things are related to the hospital care and down time. Some issues are mental aspects. There are so many moving parts and pieces in motion and opinions in play that chaos is only the tip of this iceberg.


Her consecutive hospital admissions were so close together that the discharge orders were often unable to be carried out. There was overlap and inconsistency. There was lack of follow through and communication breakdowns. It took quite a bit of maneuvering, but I'm pleased to report, I believe, we're, slowly but surely, moving in the direction we're supposed to be. Then begins the waiting game.


As a recap: Mom broke both bones in both legs two years ago and had multiple resulting surgeries. During the third surgery on her left leg which hadn't healed, a tissue sample was taken. Following the surgery, the pathology of the tissue sample revealed cancer cells. And so began the search for the origin of her cancer. Fast forward through a PET scan, radiation, endoscopy, ENT and GI visits, a mammogram, and countless lab tests to the middle of June. Mom has increasing and severe abdominal pain. It finally gets to the point where she pushes her Life alert button (which doesn't connect…) and then calls 911. The ambulance transports her to the hospital to begin the round robin that spans 4 admits in three weeks. It's determined that fluid has pooled near the top of the remnant stomach left after gastric bypass of 14 years ago. They investigate further through xrays and ultrasounds and discover a perforation in the remnant. The hole leads to the discovery that there is a mass inside the sectioned off piece of the stomach. A biopsy is performed and it is deemed cancerous. While this finally answered the question as to the origin of mom's cancer, it opened a can of worms the size of Mount Everest. Now, let me preface this piece by stating that EVERY patient, reaction, treatment, interaction and process is different when it comes to treating cancer. Gastric cancer is typically aggressive. However, in the gauntlet my mom has already maneuvered, no other cancer has been discovered. So from many points of view, she's a more rare case. At this point, the holding pattern takes over for progression. Mom has another PET scan on July 9th, and really the results will determine the available options and most suggested path. In the meantime, were getting set up with in home health services since we're not able to be by her side 24/7. I don't want to introduce any presumptions or opinions at this stage. I will say that in discussions with the oncologist, there are options ranging from chemotherapy to immunotherapy to surgery and combinations in between. Time will tell this tale. I will also contribute that we have much work to do on this front. It's going to take time and extraordinary effort to coordinate and maintain mom's care from this point forward. Tempers will run high, emotions will be intense, the struggles will be real and very challenging. This is the time where we need to dig deep and bring the fierce fight to the forefront.


There is much more to our story, many more updates to come for both of our parents…


Warrior updates:
As you all know, our band of merry men and women recently underwent some changes. Steve and Anitra, Myah and Micah have now relocated to the bay area in California. In some ways this was like taking a swift punch to the kidney, sitting on the seatbelt in a car, or getting the wind knocked clean out of you. In the moments of parting, it was as though all of the air had been sucked out of the room. Words didn't come. Tears took their place.


The new California division of the West Coast Warriors made it safely on their relocation journey. The settling begins. Our genuine hope is to get my Mom to a stable place so that come October or November we can take her for a visit and reunion in California. A beautiful goal to have!


Still there is a void. An empty place where my brother, sister in law, and niece and nephew once stood. We're grateful for technology and the ways it has brought us together, but their lack of physical presence is definitely felt and incomparably missed.


We look forward and count the days until we're all together again.


As the minutes, hours, days, weeks, and months go by…
Our eyes will gaze upon the sky…
The sun and moon and stars are bright…
No matter where we are on Earth, they remain in our sight.


The heart grows fonder despite the space…
Though we miss our loved ones in this place…
Their embrace will reach us near or far…
Though their absence leaves a scar…


Battle on, we all must…
Helped by those we love and trust…
The world is forever changed…
But the love of our family still remains…


Words abound. There are innumerable words. Words for every situation or description or explanation. Words yet to be spoken. Words that have been forgotten. Words that are biting. Words of love and care and comfort. Words beyond words beyond words. Words can teach, and words can heal. Words give direction and purpose. Words can conquer and defeat. Words can torment and tackle. Words can be the foundation, or with intonation, or the summation. For me, for us, words are communication and inspiration. The words I've written here, they're for your information.


Another page in our story… the book continues on…


Until next time,


~T

Friday, June 29th, 2018 (still) - 11:15PM - Hallowed Ground
I'm back home now, had to drive back from the hospital while I still had the muster to do so. I'm exhausted and my heart is so heavy. The doctor came in before I left. Jill holding tight at the hospital still, for the moment.

Mom's kidney function is an issue. It's what is likely related to the heavy fluid retention and resulting issues for that particular problem (the swelling in her legs, her inability to walk and the the muscle weakness). The ER doctor was going to speak with the internal medicine doctor. They will admit her shortly until they can clear up this problem.

Steve Polzin, Anitra F Polzin, Myah Polzin and Micah, thankfully made it for a visit. This day has been looming for some time now. They're off on their new journey. Over the horizon. New experiences and a new world to explore. In that moment of parting, I couldn't even find words. I haven't cried like this in a long time. It is not often I'm left without words. I'm grateful that the roads were quite empty on my drive home, because the tears fell the entire way. I'll go back to the hospital in the morning, but my eyes are heavy and swollen. Thanks Auntie Debbie and Uncle Ron for coming to help me hold onto the little bits of sanity I've (arguably) got left.

I don't even know that sleep will come. It's been an overwhelming and challenging week, and beyond. I feel as though a big part of my heart will be driving south very soon. Another part is in the hospital. Just broken. Ugh and the waterworks! It's so not my thing. Someone make it stop!

My nephew, Micah asked me, "Uncle, are you sad because I didn't come stay the night at your house?" Between my tears, I managed to nod and squeak out a "Yeah, that's why I'm sad." And in true Micah fashion, his pure innocence and genuine heart filled nature, he says, "Don't be sad, Uncle, I'll just come stay overnight at your house next time." So, that problem solved, he proceeded to dance and giggle his way from Mom's hospital room.


Myah reminded me that she'll be taller than me when next we're together (and she practically is now, so that won't be hard to accomplish)...


And my brother and sister (in law) are two people I've become so incredibly accustomed to having and being around. Everything is changing. Hard to keep up. I'm sure it's all for good reason and purpose, but I'm struggling to see it right now.


For now, this will be it for my words... I must need a breather to recover them as they left me when we said our farewells tonight. Maybe they'll return soon.


Until then... I'll attempt some sleep.


Goodnight all...


~T

Friday, June 29th, 2018 - 7:00PM - Deja Vu
And... We're back at the hospital. Mom has some pretty severe swelling and associated pain in her legs. Both legs are quite inflamed. She's also got some lower back pain and her stomach is hard and swollen again. She said the fluid draining from the tube in her abdomen was about three or four times the normal daily output.

Doctor has been in for a cursory/preliminary exam. They took blood for a bunch of lab tests. Chest and stomach x-ray just happened followed immediately by transport for a CT scan. They'll be doing a vascular study using an ultrasound to make sure she doesn't have any blood clots, after that. This makes the fourth time we've been to the hospital in just three weeks. I'm exhausted and going on about three hours of sleep but we HAVE to figure out what the holy H E double hockey sticks is going wrong.

I've already been asked two times if I work in the medical field. I keep explaining that literally we've gone this so many times I can practically predict good portions of what they'll ask or do. That's not a record or information we necessarily should be proud of... Jesus take the wheel!!

I've got more information and updates from this past two weeks of Dad's appointments and developments and the past month of mom's, but just have to focus on the right now. I'm at the end of my patience with medical failures though... So these folks better prepare for typhoon Tim and sort this on the quick and now... Let's get it together!

More soon....

~T
Monday, June 18th, 2018 - 7:15PM - The Words Don't Come
It's not writer's block. It's sheer, raw, unfettered emotion. The depths of our souls are wounded and bruised. The tears start in our core and flow through the very fibers of our beings. They don't stop, and each teardrop carries another piece of our heart as it falls.

When you feel as though you've become a punching bag for life's woes. When you are continuously pummelled by unforeseen attacks. When the weight on your shoulders outweighs the strength in your legs. When you come to the realization that despite giving it all you have, it just isn't enough. When the questions go unanswered and far outnumber the clarity and results. One. Day. At. A. Time. One. Breath. In. This. Moment. Another. In. The. Next.

Family, friends, angels, warriors, and supporters... I write this post on behalf of my siblings and our family. We do not have good news to relay and struggle with the words and the road ahead. The full pathology still hasn't come back on the biopsy done on the mass discovered in the remnant stomach. That is, however, more of a formality at this point. The preliminary results provide that there are malignant cancer cells within that mass.

Connecting the dots… this means that the cancer discovered in her knee tissue following the third surgery on her left leg originated within the stomach that had been sectioned off during the gastric bypass surgery she underwent some 14 years ago. If by some miracle no other cancer was discovered, then it would've been contained to her knee and likely obliterated by the radiation treatments she's already completed.

This new discovery ultimately sends us back to square one with oncology. We'll soon connect with her doctor at the cancer partnership and determine the way forward, the available treatment options, and which path our torrent of a journey will take.

While trying to provide as much information as possible, please also know that we are essentially in the very early stages and just don't have the answers. This really did raise far more questions than it answered. One. Day. At. A. Time.

I want to extend special thanks and gratitude to two of our aunts. This is not to lessen or diminish anyone else's support in any way, but to Debbie Brevig (mom's sister) and Judy Polzin (one of dad's sisters)... I personally can genuinely say we wouldn't have made it this far without you both. Debbie has been available at all hours, has had, sadly, first hand experience from supporting and caring for her mom (our Grandma) through losing her battle to cancer in 2011. She's fought right alongside us every step… from leg breaks to the temporary stint in assisted living to the multiple leg surgeries and oncology from day one. She was one of the very first to join the Facebook support groups and always asks about my dad's care and progression. Judy, despite living thousands of miles away in Guam has had an immeasurable impact. While on “vacation” here in the states, she was at oncology appointments and the January biopsy. When not here physically, she's continued to be a sounding board for all of my dad's progression and inquires regularly about both my mom and dad.

Sometimes you need that extra push or reassurance that we can make it through even the most difficult of days. Knowing that we're surrounded by so many (these two aunts most definitely included), is ultimately the only way we get through some of these days. We appreciate you more than words can express.

The words don't come. This small phrase has carried much meaning. Sometimes the words don't come to explain the emotional, spiritual, and internal side of how we're affected. The words don't come from the doctor with the answers, not because he won't tell us, but because every individual, every cancer, every experience, course of treatment and every outcome is different. The words don't come because even the most skilled of doctors may not be able to provide them, and sometimes, maybe they just don't yet exist. The words don't come for us to express our appreciation, our genuinely soul moving gratitude for this support and the time with our parents. However long it may last, each and every laugh, smile, conversation, interaction, embrace, prayer, stumble and lesson learned, each and every sunrise and sunset, down to each and every star twinkling in the night sky should be cherished and made into memory.

We're not promised tomorrow. No infinite number of days. Some wise people have told and reminded us lately… make sure you take care of yourself while you're taking care of others.

To our parents… thank you. I don't know if we can or have ever said it enough. You have always been enough. You have filled our lives and taught us what it is to live. You have sacrificed so we didn't go without. You've picked us up when we've fallen down. You've shown us the way into adulthood and passed down innumerable lessons in the ways of the world. You've both suffered a bad wrap, and I know there are parts inside is all that are angry and wonder, “why us?” Beyond it all. Outside the white noise of life. Separate from the wars waged internally and physically. In the deep depths of our existence… there is peace and relief, and I wish it for you. It will come, but until that day, all the many days in between, we'll be there. And you'll never fight alone. I must be honest… this particular post has taken me more than four days to write. To my recollection, that is the longest of any yet that I can remember.

Sometimes, the words don't come… they finally have for me… and now I share them here with you.

Please keep the positive and encouraging messages, prayers, hopes, thoughts and whatever you might find that's appropriate coming…
And to my dear friend, Stacie McMillen… the beautiful flowers were most definitely the token that won the day. Mom had to point them out to all the many people who crossed the threshold into her hospital room today. Thank you for your generosity, and kindness and your entire family's kinship to our journey.

Until the next time….

~T
Friday, June 15th, 2018 - 6:00PM - The Other Side
So, shortly after I published my last post.. the hospital powers that be must have perceived it through osmosis.

Transport was called about ten minutes later and was up to take her down for the procedure about half hour later. She was down in the OR for about an hour and a half. She just returned to her room. Finally, she gets to be on a clear liquid diet... Some nourishment at least... Small steps!

She did well, they tell us, and is a little groggy still. She has her nurse Julie on shift tonight, and she's taking great care of her. Starting her next course of maintenance antibiotics.

Results won't come back until Monday.. so unfortunately that means a weekend at Providence... But some movement, at least. The next shift will be arriving shortly... Updates as we have them!

Until then!

~T
Friday, June 15th, 2018 - 3:15PM - The Ides Of June
Here we are, middle of June, nearly five months since 2018 reshaped the direction of our family. I'm here at the hospital, Auntie Debbie nearby, Mom bundled up in the hospital bed. It's been a trying day so far, to say the least, with little end in sight.

I arrived early this morning as we are waiting on the biopsy procedure to determine if there is cancer is the mass discovered in the remnant stomach left after gastric bypass more than a decade ago. The morning seemed to bring some progression, but that quickly came to a screeching halt. Mom was sitting up in the chair near her bed, and then moved back to the hospital bed itself. The dressing around her IV site was soaked all the way through.

We called in the nurse and she cleaned up the area, but because of the number of times Mom has been poked, she didn't want to attempt to place a new IV line, but instead called for the IV therapy nurse to attempt. While the specialist was able to get an IV line started, she wasn't confident it would hold long as Mom has tough veins, and they were collapsing under the trauma. She recommended placing a special IV line (later decided to be a midline IV). The problem was she couldn't receive the maintenance IV antibiotics or pain meds until they could establish a strong IV line. A midline is designed to last up to 29 days and is similar to a PICC line. It runs, like it's name alludes, up from the mid arm. The next issue... No procedure until the line was established. And the next issue... The team of individuals that places midlines was highly backed up and the hospital very busy.

Fast forward some six hours... The midline is finally in, and we've just now started the morning maintenance dose of antibiotics. This pushes her procedure into the evening hours. She's had no solid foods for one week due to hospital stays and resulting dietary restrictions.

The bright spot in the day was when the therapy dog got to come through and pay her a visit. I'll post pictures soon. I also found an adorable stuffed giraffe in the gift shop. His name is hightops. He'll be with Mom for the duration and go home with her when it's time, of course. Pictures of him soon too.

For now... These are the words. They may not be the ones we wanted, but true they be. More soon... Same bat channel...


Until next time...


~T

Thursday, June 14th, 2018 - 6:30PM - Calling All Angels & Warriors
We just found out that Mom will need to have a biopsy on a mass that was discovered in the remnant stomach left from the gastric bypass surgery she had years ago.

Tomorrow we'll know more, but tonight we're calling on all of our warriors and the angels watching over us in hopes that this can be resolved expeditiously and finally.

Over the past few days, Jill Evaristo Polzin and auntie (Debbie) have manned the front lines and held down the fort. THANK YOU. I understand that mom's caregiver, Mary, has also taken care of the fur baby Molly and gotten mom's house back in order after the second transport via ambulance this past Monday.

A procedure called a fluroscopy was performed yesterday. As there had been fluid and inflammation and suspected infection discovered during previous tests and from the first hospital visit last week when this ordeal began.

A fluoroscopy is where xrays are used to obtain real-time moving images of the interior of an object, in this case, mom's stomach and the remnant stomach. As I understand, quite a large amount of fluid was removed during the procedure and a drain is still in place to continue to drain the excess fluid from an abscess that formed.

There is a perforation in the stomach remnant (a hole in the leftover stomach that remains in the body after a gastric bypass). There was also a mass discovered which now most be biopsied to determine if it's cancerous. From January.. you may remember that the PET scan that was performed after we started on the oncology path showed two areas of note. One sent us to the ENT doctor, who cleared it, but wanted to follow up months later to confirm his findings. The other area was in the upper GI tract which does include the stomach and remnant stomach. This sent us to the GI doctor and called for the endoscopy.


Not to jump ahead or make assumptions, but this MAY be the area that lit up on the PET scan. This is obviously surreal. If it is the origin of mom's cancer, then we've finally found it. That could mean that the question is answered. Although, it could also raise countless more. It can also be maddening that after all these months and the paths we've walked down and the specialists we've seen... They were all off base and unable to determine the origin of her cancer, but weren't quite looking in the right place. At the same time.. the world works in mysterious ways... Maybe the stomach pain and these hospital visits were a message. We might never have gone this route without them. Time will tell this tale.


I'll be manning the Mom post tomorrow. So, more to come. In the meantime, we ask you all, graciously, to keep us in your thoughts and prayers... We look forward to and appreciate the support... If you can, find a way to send a quick note or message (even reply or post here), we'll share with her).


Even the darkest hours only have 60 minutes... And without the dark, we'd never see all the stars shine. The light will always chase the dark away, only to repeat the cycle and signify the day.


Until the next time.....


~T

Tuesday, June 12th, 2018 - 8:45PM 
Talk about bumps in the road! Mom Linda has been finding out how much a gal can take, with two hospital stays in a week due to a new, as yet unidentified source, health issues.

I'm going to spare you all the nittiest grittiest details, but will tell you she has endured innumerable pokes and blood draws, at least 4 medics, more than a few ER staffers, 2 CT scans, an EKG, an EEG, a Fluoroscopy, 4 hospitalists, 12 nurses, a couple PCTs, a pharmacist, half dozen oncological specialists and a Gastric surgeon with MORE TO COME, and still nobody's sure what the cause of these painful episodes is. She will be in the hospital until they figure it out.

I've been by her side for at least eleventy hours, along with her sister Debbieand her caregiver Mary and those Warriors who already knew she was going through stuff, have been a tremendous source of support. She's gotten some calls and texts which brighten her spirit a bit.

But. Y'all. This takes a toll. And none of us has unlimited energy or hours in the day to care for ourselves and families and be there for her (friend/ relative/Mom/Grandma/Auntie/Sister/Daughter) so I feel compelled to ask...will you take 5 seconds to send her a text or a funny meme on Facebook, or give her a call, prepare a casserole, pick a bouquet, or say a prayer? please if you're able, send positive thoughts and vibrations her way.

In appreciation always,

~her daughter Jill
Wednesday, June 6th, 2018 - 10:45PM - The Way We Were
2018 is set to enter our familial history book with a vengeance and we're not even halfway through it. We continue to wage war for both of our parents. The battles seem never-ending. Our stamina is tested. Our resolve is scathed but unbroken. Our spirits are bruised, but continue to endure.

On the dad front we are fighting the bureaucracy that is Boeing. Their feeble attempts to bury us in paperwork, appointments, conference calls, jargon, inane rules, policies, and antiquated systems for managing human resources are chaotic at best. Sadly these processes are also quite expected. He continues on the chemotherapy path. His next infusion is Friday. He now has a PICC line in one arm to alleviate the number of pokes he needs to receive. We are still searching for a solution to the dental circumstances he faces. At this time we have had no luck and the cost is just too great. It's important but Dad be able to start taking the bone-strengthening medication, however, in order to get to a place where that is possible we must resolve all of the dental issues he's experiencing. This means that he will have to have 16 extractions and be healed with no sign of infection before beginning the medicinal regimen.


While this is an important step we are unable to take it and must worry about more urgent matters at hand. Chemotherapy is first and foremost. And dealing with dad's work life and work future is a close second as it dictates the financial aspects which come into play.


We have often discussed the unknown. The unknown is the most difficult challenge. Not having any sense of direction or specific information is like trying to operate a chainsaw in the dark while blindfolded. I mean, maybe you'll get lucky and cut off the branch of the tree, or maybe you end up cutting off your own foot.


In dealing with the bureaucracy and with the medical folk, specifics are often requested but because there's so much testing and evaluation left to be done specifics cannot often be provided. I find that this particular battle is one in which I must charging like a bull in a china shop, deal my blows, and exit in an equally fantastic stampede. Then I must take a short respite to recover my senses and any semblance of patience, and charged yet again.


On the mom front, as many of you may have seen she remains in the hospital with complications from abdominal pain, possible infection, possible inflammation, and no determinable cause, yet.


It's hard for any of us to try to be in two places at the same time. It can be downright painful to be torn between having to choose which parent to physically be with at any given time. You may also have seen the news that my brother, sister-in-law, niece and nephew are moving to California at the end of this month. In many ways that's like a triangle losing one of its three sides. That's not to say that they won't remain staunch West Coast Warriors, they just won't be Washington State west coast Warriors. There's always a sense of loss and some difficulty and losing any part of your immediate physically present support system.


It is concerning that Mom visited the GI doctor only to later end up in the hospital with what appears to be symptoms highly possibly related to the GI. Signs are not pointing to anything life threatening or Surgical, last we had heard, so we'll take that as a small victory.


In the wake of all of these developments, and as a continuation of our ongoing efforts, I'm working on a redesign of the website and more new additions to the awareness store. We are still working to expand from specific cancer types related to my parents to all cancer types in support and awareness. Our hope is that this will broaden our audience and help raise more.


The summer months are upon us. Father's day around the corner. The challenges ahead are many. The days often bring more questions than answers. 2018 is not only writing the history book, it's reinventing how we read.


We move forward from here and keep on trekking. We thank you all for being in our circle and in the front lines with us through all of this. Your support is truly inspirational.


There's more to come... Of that we're sure. For now, these are words we share with you.


Until next time....


~T

Wednesday, June 6th, 2018 - 7:45PM - A New Wrinkle
I wish I could share with you that it was just an upset tummy, but alas, Mom likes the pudding just enough at Providence that she's going to spend another night there. She's FAR MORE coherent and fiesty today than yesterday. And Debbie her sister, as well as Mary her caregiver, visited her today which always brightens her spirits. 

The brothers and I are taking turns caring for sweet Molly, and Mary has graciously offered to help with that too. 

It was a VERY rough rest-less night due to a rather noisy roommate with dementia so mom switched roomsand is now going to try to get some sleep. We are waiting on results of lab work and word from internists about what to do next. Frustratingly we do not have specific causes or resolutions. Only general treatment for suspected inflammation and infection. 

I don't have words like Timothy J L Polzin or a wide reaching network like Steve Polzin but I can speak for all of us when I say thank you for continuing prayers and well wishes. Believe it or not, it keeps us going! And plus it really brightens my mom's day

~Jill
Tuesday, June 5th, 2018 - 9:05PM - A New Wrinkle
Mom is in the ER. She had an appointment with the GI doctor today. After returning home, she began experiencing sharp abdominal pain and actually activated her Life alert button. It sounds as though there was some disruption in the connection.. and the service wasn't working for her. She called 911 and was taken by ambulance.

The hospital called us and we all arrived shortly after each other. As the location where Mom is really isn't a full hospital, there are some limits to the care they provide.

They've run tests and did a CT scan of her abdomen. The lab work shows only slightly elevated white blood cells. Nothing else jumps out at the doctors. Radiologists have reviewed the films and do see some inflammation in the stomach pouch. They've given her antibiotics and some antacid meds to try to calm and alleviate the inflammation, pain, and possible infection.

They're currently looking to find a bed at a hospital to admit her.

More to come.. one of my siblings or I will post updates as we have them.

Not the words I wanted to share, but mine they are!

~T
Monday, May 14th, 2018 - A Message To Mothers
Happy Belated Mother's Day to all the moms out there!

It has been a busy, often chaotic few weeks. Yesterday, however, we were able to take some time out to spend with mom on her day.
Some quick updates - truly, I don't have a lot, as often times I can't tell if I'm coming or going! I will be out of state on a much needed vacation, next week though. I plan to be as disconnected from technology as is possible, so any pertinent or important updates will come from one of my siblings...

Mom had her mammogram and as hoped and expected - nothing of concern was noted! In the next couple weeks, she'll have some follow up labs and a visit with the primary oncologist. We expect and look forward to more of the same - consistent, steady, and nothing surprising.

For mother's day, my Mom, sister, sister-in-law, and 2 each of my nieces and nephews gathered at my apartment. We had a taco bar buffet! Topped off with some strawberry shortcake (first of our spring/summer season!) a Mother's Day movie (no, seriously, it's called Mother's Day....) and some family time together. My brother, unfortunately, had to work and was unable to attend, but his branch of the family tree was well represented.

"A Mother's love for her child is like nothing else in the world. It knows no law, no pity, it dares all things and crushes down remorselessly all that stands in it's path." - Agatha Christie.

After the last nearly 6 months, this Sunday Mother's Day gathering was a much needed reprieve from what has become our hectic norm.
I do want to add another "plug" or "plea" if you will. I have to continue to run the donation campaigns (and in tandem, the awareness store). Please purchase/donate if you can, share if you would, and above all else, keep us in your thoughts and prayers.

The concern on the horizon is the possibility that mom will need to have another surgery on her left leg/knee because of the screws that are being pushed out. This entire ordeal, from mom's perspective, began with a third surgery and the resulting phone call. Opening up and working on the leg/knee for a fourth surgery is definitely not something we look forward to having to experience.

For now, I leave you with these, my words.

~T

Friday, April 13th, 2018 - 2:20 PM - Sunlight Through Clouds
Hi all! Mom had a visit with the ortho doctor this past Monday. (I know, I'm clearly behind on getting updates out....)

We are pleased to report that there does appear to be some healing progression on her left knee (FINALLY!). As is quite common, there is some bad along with the good.

In evaluating her progression, the ortho doctor also discovered that the screw in her knee is pushing out. He'll continue to watch this, but its sounding as though in the next couple months, another surgery will be necessary to remove the screw completely. That in itself may be positive news as it doesn't sound as though there will need to be a replacement put in, but it's still ANOTHER surgery.

The ortho doctor mom goes to is separating from the Everett Clinic. To maintain that relationship and consistency, she'll be going to see the same doctor at his new practice.

Still have on the roadmap a mammogram, and follow ups with the ENT and Oncologist, but definitely some silver linings to celebrate!

As an aside - we've had a lot of family activity going on these past few months, and things are in a giant state of flux. The house Jill was renting was sold. We also recently learned that the house Steve is renting is going up for sale at the end of June.

The only constant in life - is change. We continue to roll with the punches! Again, please forgive my being remiss and not posting more frequent updates. Sometimes, I need someone to update me so I can update you all!  :)

And, another random aside (it's kind of my thing.... ) today is Friday the 13th, and I don't know about you all - but I'm feeling the weird.

Wishing you all a speedy and productive Friday, and a wonderful weekend!

For now, I leave you with these, my words!

~T
Wednesday, April 4th, 2018 - 11:35 PM - The Turning Tide
Hi everyone! My apologies for the lateness of this post. Life has its way, and life finds a way...

Last week, Mom had a followup / recap visit with her oncologist, Dr. Lukas. In all honesty, the communication caused a mix of emotion for those present, Mom especially. As you might imagine.. It's a lot to take in and absorb.

Following her course of radiation and visits to multiple specialists, an endoscopy, and repetitive series of labs.. The news is positive, although still doesn't provide any sort of closure or finality. Labs revealed nothing of concern. Specialists were unable to discover any other cancer cells or areas of concern. My gut and first reaction is - YAHOO!!!!

We have clearly won the battle. On the flip side, that doesn't certify the end of the war. The best way I can explain this is to say that Mom now goes into what I'd refer to as "maintenance mode." Having no other course of treatment deemed necessary, we quite literally do nothing... And wait... I'm sure everyone realizes how patient I am! In truth, it's wonderful news that there is nothing that doctors can FIND to treat. It's that one word - FIND.

Now, by no means does this allude to Mom being a ticking time bomb. There was always the POSSIBILITY that the cancer either truly originated in the leg and was caught early and soon enough so that radiation effectively obliterated the cancer cells. There was also the remote possibility that IF the cancer had originated elsewhere in her body and moved to the leg, that its move was in total, meaning that no remnants of cancer cells remain in the original location. In short, we simply don't have a definitive answer. I reiterate, that is NOT a bad thing. After looking, and looking, and LOOKING, no other cancer was found!


All of that said.. Where does the path take us now? Maintenance mode. Mom is going to follow up with the orthopedic doctor - appointment is this coming Monday morning. Then, unless something changes, drastically, she'll take respite from the roller coaster. Down the road, it will be prudent for another PET scan. In the near future, she'll need (and want) scans and labs to determine the effects and results of the radiation treatments.


All in all, this is wonderful. Moving towards one of the very best possible outcomes that could be expected. There is light within the darkness. There is always hope. There is power and meaning in the fight. For now, cancer is flying a flag of surrender... And is in retreat.


On behalf of my Mom, and siblings and families, we genuinely thank you for defending the front lines along side us. The clash with the Titan is not over. But today, we should rejoice in celebration. My sincere hope is that I'll be able to continue to deliver positive, progressive news as we move forward. I, for one, am grateful to see some calm in the chaos.


For now, this night, I leave you all with these, my words, and a spirit lifted up. More to come...

~T

Wednesday, March 28th, 2018 - 12:35 AM - Our Lives, With Cancer
I posted yesterday on my own (facebook) wall. I realize you all cannot see that post, nor is it really necessary. As outspoken as I can be, it may surprise many of you to discover that I'm actually a very private person.

Since December, I, personally, have learned some incredible life lessons. I've been given some bold reminders, and made some educational mistakes. I'd like to venture that all of us, touched by this incredible journey, have too, in some way or another.

I'm not a person you'll see cry in public. I often mask hurt and pain inside, choosing to allow release on my own, away from the spotlight. To some of you, that's concerning or disturbing. To me, that's where my inner strength takes over. My inner fire burns brightest in the darkest of times.

I'm sure that my nieces and nephews and even some of my young cousins will tell you I'm the mean one. I'm the rule follower. The one who sees in only in black and white. I caution each and every one of us... Our opinions become words. Words become biting criticism. The sting from the bite becomes a lasting scar. The scar leaves a mark for all time. In many ways, we as individuals are at our simplest point, a mere collection of our scars. Some of us hide them better than others. Some of us are marred and nearly deformed by them, and others bare their scars just beneath the skin. That pain remains constant, but it's rarely visible on the surface.

The earlier post I refer to, although partially conceived in irritation, frustration, and exhaustion, came directly from my core and really embodied many of the lessons I have recently learned, some of which came easier than others. I'm not invincible. I have an effective self-armor, but it is not indestructible. I do have my moments where I find it necessary to close all the doors, turn off all the lights, sit on the floor in the corner, hold a pillow in front of my face and release a wailing scream that would put the banshees to shame. I find emotion and reminiscing take over sometimes. Understanding and realization of the forced metamorphosis within my family are not easy to contend with 100% of the time. And the hits seem to keep coming.

I am protective of myself to a level beyond comprehension. Part of this comes from the society we live in, the generation I was raised with, and the impact of some old school, outdated beliefs. There was a time in my life where I felt I had to carefully conceal a large part of who I am (and was). You take on almost a dual personality.. fearful that if you revealed the truth, you'd be persecuted, abandoned or even physically harmed. Thankfully, that was not my experience for the most part. You can't be everything to everyone. Growing up and living life includes learning to surround yourself with the right kind of people.

There's a term that has been turned into a meme. (I'll help you here... A meme is parody, or humourous image, video or text that is spread throughout the internet realm and often mocks a real life situation or event) The term is xennial. It's used to describe someone who was born and sits on the cusp between Generation X and the Millennials. They're said to have experienced an analogue childhood with a digital adulthood. They possess and exude the cyncism of Generation X and the Millennials optimism and drive. Well... Part of me must lean more towards Generation X because we've long considered the Millennials as the "do nothing" generation. It's more as if they're optimistic if they get to drive (Mom and Dad's car....) I feel as though I can get behind being a Xennial.


In large part, we are today, part of a progressive American society. Because I realize that this post is part of a public forum, I promise to not delve into political discussion. Never before has our country been as forward thinking. We've also never been as dependent on technology for our everyday creature comforts (and yes, I write this on a handheld portable mobile device AKA a cell phone... That irony isn't lost on me.) Can you imagine if the youth of today was drastically and suddenly ripped from the technology age?


A quick side story here - I've been in banking as a career for almost sixteen years. When I first started, bank employees still had to go to the police station for mandatory fingerprinting. We had to be licensed and bonded. We had to prove via testing and on the job demonstration that we could count money and make change without a computer and rarely even with a calculator. I'm still a beast on a ten key! In my sixteen years I've moved through the ranks and have had the distinct honor of being a trainer, supervisor, and manager of new and experienced employees. I remember working in multiple locations and experiencing power outages. The senior staff with long banking experience would nearly explode with sheer joy having been relieved of the technology burden, if only temporarily. The young staff, however, would virtually go into catastrophic shock and anxiety attacks with a virtual near death experience because a customer would ask to deposit $67.00 out of a $100.00 bill. It was an... Interesting time to say the least.


Back to our regularly scheduled programming... And my train of thought... There are numerous cliches and anecdotes I could put out here to emphasize my point... "Walk a mile in someone else's shoes" "when I was a kid... " or "you can lead a horse to water..." ( Which would be silly and pointless... Ride the horse to the water... Good gravy.) Blah blah blah. But... I'm me and that's not necessarily my style... So I'll go with this, instead:


Everyone has their demons. Skeletons in the closet. Vices. Pet peeves. Stressers. Triggers. Addictions. Flaws, faults, quirks, differences and opinions. Some are worn plainly within view. Easily identified, readily acknowledged, and carefully navigated. Others are sub cutaneous scars. Living, thriving, and surviving beneath the surface. Poking at them inflicts pain, but it's unnecessary. As we go through life, we may discover or realize scars we ourselves didn't know we had. As bad as things get, as much as the world hurdles at you, chances are there is someone else who, despite all you think has piled and is working against you, still has it worse than you do.


There isn't a comic tally keeping score on who has the most or worst scars. If we change the mentality and our way of thinking, perspective casts it's own, unique form of light. If we all believe that someone somewhere is worse off than we are, things tend to not look so bad. That's not to diminish the severity or importance of anything... But, suppose my bank tellers in training took those power outages as opportunities to educate themselves on how to reduce reliance on a computer to do the thinking for them? Maybe in life, we need to look harder for a window or the next door because the one behind us has closed. Then again, if you're a millennial... Your GPS watch doesn't provide the location of opportunity or self-improvement as markers on the map.


To my nieces and nephews, young cousins, and the generations that have and will follow mine - self sufficiency, independent thinking, new ideas, outside the box mentality, forward and progressive innovations and ideas about all aspects of life are what will be your legacy, your mission impossible, if you choose to accept. Don't be the "do nothing" generation. Be the generation the unifies BECAUSE of our differences and uses the ever advancing technology to further your cause and plight in this chaotic life. I'm the rule following mean one, but my thinking is in full 4K Ultra 2080p High Def vivid colors.


To my siblings especially and my parents -


This road is rocky. It's not one we chose to take. 
But hand in hand, we shall this journey take.


The turns are sharp, the climbs quite steep.
Our bodies and minds exhausted, they beg us for a sleep.


A warriors job is simply never done. 
So on we fight until the battle's won.


Victory will be our lasting memory.
But the greatest trophy is our warrior family.


Of words I have many... I share them here with you.
Now I'll hit the post button and this message will be through.


Until next time...

~T

Wednesday, March 13th, 2018 - 2:35 PM - Small Triumph
This morning Mom had her endoscopy procedure. The gastroenterologist had ordered the endoscopy to explore and confirm that the area of Mom's stomach which showed as a dull glow in the PET scan was clear.

The great news is that it WAS completely clear - no areas of note or concern. The small grey cloud is that the GI doctor now wants Mom to have a colonoscopy since it's been more than ten years and just to further rule out any lower GI issues.

I'm confident and strongly feel that while colonoscopy is beneficial for overall health and well-being... It will not reveal or find anything either. All results that have been communicated to us have stressed that IF anything were to be of concern from the PET scan, it would be the upper GI tract. While the small intestine is the technical "end" of the upper GI tract, that should have been visible via endoscopy. We were also told that colonoscopy has a relatively low chance of discovering cancer cells in general. The percentage isn't zero, but it's small. This, again, will be a "rule out to be safe rather than sorry" procedure.

The endoscopy was actually quite fast. In total, less than twenty minutes of actual procedure. The pre and post procedure were far longer, however, as a person works through the conscious sedation medication. I'm taking Mom to her radiation appointment in just a little bit, this is number 7 of ten, so the light is at the end of the tunnel for this piece, at least.

For those of you also in my Dad's group - I'm working on a post, and have been for a couple days now. Some new developments to cover there, very soon. I'm continually working and updating the awareness store and will be adding updates to the donation campaigns for both parent's Cancer Care funds. It's an incredible thing for people to give in this day and age and is truly heartwarming and inspiring. After our battles with cancer become a thing of memory into the past, It is my personal goal that the awareness portion of our website stands for a long time in support of all cancer types, all cancer survivors, and as inspiration to all cancer fighters and the warriors who support them.

Donations will be made throughout time as long as I can maintain in the name of cancer support and research for a cure. Maybe, just maybe, a cure will be found within our lifetimes and we'll bare witness to the eradication of the venomous existence of cancer.

Our enduring gratitude and appreciation to each of you that have played a role in our lives, and continue to on the daily.

There is more to come. More fight in the near future, so for now, I leave you with these, my words.

~T
Friday, March 9th, 2018 - 7:45 PM - The Field Of View
Today, although it's been a LONG day, was productive and positive.

We started the morning (far earlier than should be allowed within the human species...) With back to back to back appointments. For any of you that don't know me, or haven't had the pleasure, I'll just explain that I'm the epitome of "Not a morning person". Which is odd, I know, because for the last 16 years I've worked a "day" job where I'm required to be nice to people and provide excellent customer service. I'd just explain that, well, I'm paid to do that, so I don't give it away for free  😂 😂 😂. I'm a pitbull by nature and especially in defense of my family... Add in a requirement to be up before 7am and I'm a rabid Rottweiler on steroids who's not been fed. Just saying...

SO! First up was the GI (gastroenterologist) doctor. He talked very quickly and typed nearly as fast... That's to his credit. He reviewed history, and even confirmed that he'd read through mom's chart, and was actually aware of what was going on. He did a general exam and then talked about options. In reviewing the PET scan results and including today's appointment which she'd for a history and performing an exam... He concluded that a colonoscopy really wasn't necessary. There aren't any signs or familial history that would point to a high risk or need for the procedure. However, due to the point of interest in Mom's stomach, which isn't at all alarming or urgently concerning to the GI doctor (nor was it to the oncologist), he did schedule an endoscopy simply to rule out any slim/remote possibilities. From his perspective, for all intensive purposes, it's highly unlikely that the cancer cells in Mom's leg are a result of colon cancer or intestinal cancer. IF ANYTHING (and that's A BIG IF) it calls for a second look at her stomach. It's completely feasible and quite likely that the PET scan showed activity in that area from the to gastric bypass surgeries and previous ulcer. But, as a precaution, endoscopy will validate. And should there be any concerns, the area of note is quite small which would mean something early stage or easily removed IF it even got that far.

There was a short span in between the GI and ENT so Mom got some required lab work taken care of, so that was good to get accomplished.


Then the ENT was up. He had seen Mom about a year ago, for unrelated circumstances. Good guy as doctors go (and that's saying a lot coming from me!). He was the first doctor to show us the actual images from the PET scan. That's not to say we hadn't been given the RESULTS just never had opportunity to see the direct images captured. I'll admit I went to my inner nerd. It's fascinating. The image captures work in 3-D but on different plains. First set we saw looked like you'd entered the top of the head and traveled downwards. The human brain has immense activity and appears as a platinum white light source. That means mom's brain works very hard! Then he scrolled through her upper skull area into the cheek bones and jaw. He showed us what area had been noted. The lymph node at the left side of her jaw glowed a dull burgundy. Extremely pale in comparison to the brain. The ENT was also able to use a measuring tool on the screen to determine how big that area was. It was a miniscule 15mm (that's 0.59 inches!). Then there's a pulled back view of Mom's body which when scrolled through made it look like she was a ballerina spinning in a pirouette.


After doing what I can only imagine was an uncomfortable exam with a lighted scope inserted into the nostril and some cursory pressing along mom's face and jaw with his fingertips, the ENT was ready to present. He wants her to come back in three months for a follow-up. Don't hold your breath waiting for the other shoe to drop. THAT'S IT!


Unless the area of her jaw gets bigger, becomes infected or painful or any other significant changes or concerns present themselves, he only feels it's necessary to recheck in three months. During the treatment with the oncologist there has already been discussion and plans for a repeat PET scan somewhere in the 6 month to a year timeframe. The ENT was even okay to wait until that time to decide if any other action was even necessary. While he's happy to go in and cut things out, it's really not something he sees Mom needing to do!!


With that happy news, I headed off to work! Mom had her 4th radiation treatment this afternoon, so it wasn't long before I saw her again! She's home (hopefully) resting now... After all the excitement of the day. Nearly halfway done with radiation, a weekend at hand, and really good news from the two specialists!


I think that's an excellent place to leave things for tonight! I leave you with all of these, my words, and wishes for a restful and wonderful weekend!


~T

Tuesday, March 6th, 2018 - 6:40 PM - The Beat Goes On

Mom started radiation treatments today. We previously had a consultation with the radiation oncologist and then they took a mold of mom's leg and injected some markers into her leg that are visible during the treatments which are given in tandem with a CT scan. This allows the therapist administering the treatment to focus on a particular area and verify that as much as possible, healthy skin and cells aren't being irradiated. The mold is used to ensure that her leg is in the same position for each treatment.​

Today was the first of ten treatments. She'll go in every weekday until her series of ten is complete. No weekend treatments are scheduled. So the final treatment, at this juncture, is scheduled for 3/19.


Friday, March 9th, we begin appointments with some specialists as we look to obtain confirmation that cancer hasn't spread to or from other areas of the body that were noted with the PET scan results. (There were two other areas of note, not major concern, that the doctor discovered from the PET scan. The lymph node at the base of the jaw on her left side below the ear and the right lower stomach where she previously had an ulcer and two gastric bypass surgeries.) Mom has appointments with an ENT and GI doctor both on Friday morning as well as a radiation treatment that afternoon.


All in all, she was saying that today went pretty well. It's nerve racking because going to radiation really brings things to the forefront, makes them more tangible and in your face. She said they were very gentle with her and she didn't experience any pain or discomfort from the treatment itself and it really went very quickly. Though, on the way home, she did mention feeling a bit tired, which is understandable, and a common side effect of treatments is some fatigue.


As always, more to come, probably following the Friday appointments.


In the meantime, our continued thanks for the support through donations, awareness store purchases, cards, notes, letters, Facebook messages and emails. PLEASE keep them coming. Continuing to work towards expanding items offered in the store to include all/more cancer types. The simple, sad truth is that there are just far too many.


For now, these have been my words, and I share them with you all.

~T

Monday, March 5th, 2018 - 6:20 PM - A View Of The Horizon
Please lift up and surround Mom. Keep her in your thoughts and prayers now especially as tomorrow is her first radiation treatment (@ 10:45AM, Pacific time). Hoping for smooth sailing through this part of the process. Friday we begin some follow-ups with specialists, looks to be a busy week indeed!​

Our continued appreciation to you all for your love, support, interactions and participation as fellow warriors in the battles we have and will face.


I'll update the group, likely after I'm off work tomorrow and of course as things progress.


Until then, asking for a flood of yellow and lavender from the butterfly brigade, and all our cancer kicking warriors!


I leave you with these, my words. And my many thanks!


~T

Friday, March 2nd, 2018 - 11:25 PM - Blurred Lines
It has been a bit since I've posted an update. There are many reasons, some excuses, a few soul searches and even the occasional ferocious tirade which I'll "explain" as the cause for the lack of posting.​

This weekend is the two month mark for the biopsy that turned things topsy-turvy in our lives. Mom's discovery would follow just 18 days later. I'll forever remember that moment in time. It was like sitting in the car on a roller coaster that had just completed its steep climb towards the heavens, only to provide a brief respite and false sense of security as it levels out momentarily before the floor seemingly drops out from under you and gravity asserts her maniacal hold pulling you ever more swiftly back towards the rocky earth before changing her bipolar persona and slingshoting you just as quickly back to the sky.


Aside from being a traumatic and emotionally and physically stressful time, having both of our parents battling cancer has been an incredible learning experience. Not just in the book learning sense, either. It's also been an eye opener. You learn what you're made of. You gain understanding and insight about those around you. There is no hiding, all the cards are down. Time is not wasted in determining if the cards are stacked for or against you. Your allies and advocates materialize in crystal clear fashion. The enemies and naysayers fade quickly into the shadowed background.


We are constantly walking a fine line in how we handle any given situation. We have to evaluate and make decisions that truly directly impact life and death. Quality of life isn't really a phrase you hear often in everyday life. But, having spent nearly as many hours at oncologist offices as I have spent sleeping in the last few weeks, it's a phase that becomes ever more relevant and ever more prevalent. It causes the line to be even more difficult to walk.


I know some of you have raised an eyebrow or may be slightly panicked by what I've just written. And if that's the case, I'm glad to have your attention. There are often times where there seems to be a lack of urgency or we are lulled into complacency by the brief steadying of the roller coaster car. I realize that, to say the very least, I'm quite different than what today's society would consider the "normal" everyday Joe. (no pun intended). Individuality is a phenomenal gift, and far too many don't capitalize on it. (my goodness, he's rambling again!)


OK. Cancer is a heartless, feckless thug. It is stealth. It's clinical and cold. Cancer is fierce and unforgiving. Cancer doesn't discriminate nor is it subjective. Cancer is relentless and dauntless. It's consuming and altering. Cancer is soulless and isn't swayed by emotion or brute strength. It is unfortunate, that anymore, we are developing calluses against accepting or even hearing about the vile enigma that is Cancer. Cancer causes pain. Unimaginable pain. Physical pain, emotional pain, anxiety and depression, coping pain, growing pain, harsh reality and mortality checks and scars that remain long after our fight is done.


Yet, we fight. We kick and scream and get furious. We cry our eyes out and curse the existence of the demon called Cancer. We wrap ourselves around our loved ones or wrap ourselves in a cocoon deep inside the visible outer layers. Survival mode is running at full speed and capacity. We speak the horrors into existence. We fall to our knees and pray to the almighty for miracles. We crave solace and understanding. We reminisce and ponder, harkening to the days of wonder. We revert to childhood and the state of mind and sense of being carefree and at the precipice of greatness, the entire cosmos as our oyster.


The line between quality of life and irreparable alterations is acutely presented. How do we navigate the rocky waters and achieve smooth sailing without sacrificing speed and efficiency? How do we keep the wheels running and maintained without wearing out the tread? Where do we stop to rest and regain our strength? What nourishment will satiate the coming tide of hunger? The human equation calls for the x factor. The unknown. Unanswered questions are the drive. The force behind obtaining knowledge and life long learning.


The lines are blurred between physicality and morality. How do we subdue the pain without sacrificing the invaluable and vital immunities and defenses? How do we comfort and reassure our parents without masking the intensity and significance of the truths? These and many other questions are what occupy our time and minds as of late.


While never wishing pain or suffering upon living creatures, we may actually cause harm in our inactions, or by masking or withholding the difficult truths. If there were a mystical button we could press, a magical food you could eat, an enchanted drink you could ingest, or an imbued incantation we could speak, we would move the earth and heaven to make them happen for you. There just isn't. There is hope, and faith, and determination and hard work. Speak positivity into existence. Tunnel vision is an all out attack. We are the light. Open your eyes. Listen with your ears, not your emotions and speak with your heart, not your mouth.


Mom will begin aseries of radiation treatments this coming week. I've been at her most recent appointments with her and to the best of my abilities will continue to do so for both of my parents. My mom has her ups and downs as do we all. Adding cancer to her existing conditions only serves to exacerbate the misery of it all, and for that we are truly saddened. Undeterred, but empathetic and sympathetic to her plight. It's like adding the anti-cherry to the top of the anti-sundae that was delivered by the anti-christ Amazon Logistics driver (sorry, couldn't let the opportunity to deal another glancing blow to the AMZL drivers...)


I cannot personally imagine the full extent of the extraordinary toll that cancer exacts on the human body and soul. And it may be different for each person it encounters. 
The hard truths are these - the body and immune system are repeatedly subjected to harsh chemicals, radiation, traumatic lab tests, repeated evaluating, persistent side effects and unforseen reactions. That's all on a good, low key day.

An inactive body or a traumatized body cannot heal as an active, healthy body will. An unending, vicious vortex forms and sucks us all in. Winning isn't even the goal. At some point, simply surviving takes precedents. As a society, we treat symptoms, not diseases. The box may say "cold medicine" but, it treats runny nose, congestion, cough, sore throat, fever, and minor aches and pains. On the grander scale... We "treat" cancer by targeting radiation to alleviate swelling, pain, and shrinking tumors or lesions which may be impacting muscles, nerves or bones. We use chemo and immuno therapies to treat the division of abnormal cells within the body. We literally teach our cells to attack invading cells in our body. By reducing pain with medications we cause side effects such as fatigue, insomnia, lack of appetite, low blood pressure or swelling and fever. Then, what do we do? We prescribe additional medications to treat those resulting side effects, which are then referred to as "symptoms."


Please don't get me wrong. There is necessity and value in treatments. But the hard truth is, we won't solve or resolve every issue or symptom. Quality of life. It's important. We want the absence of suffering and pain. But we must also balance the good with the bad and find the finite line in which we shall walk single file until the job is done.


Please, continue to surround my parents with your love and support, your wisdom and insights, your experiences and intuitions. No matter how small of an impact you feel you will make - you may not feel like a somebody in the big world, but you are the world to somebody.


For now, I leave you with these, my words, and wishes for a restful weekend.

~T

Friday, February 16th, 2018 - 11:40 PM - Course Correction
Sometimes it's necessary to make a course correction. The ship may be sailing along, but not moving fast enough, or the rough seas may warrant a new direction. And there are those times when it's even necessary to replace the captain at the helm. I'm proud of my siblings and parents. This week was... Challenging... To say the least.​

At the risk of being a broken record... I'll say again.. Sometimes we simply go through the motions and do what the doctors instruct. It's OKAY to challenge that which is prescribed or instructed. Each of us should be a staunch advocate for our own health and care (with your warriors covering your back!). We must each be a willing participant in the treatment and healing processes for them to be effective.


This week was also very much a divide and conquer game plan. Between Mom and my dad, there were 10 (at last count) appointments scheduled between Monday and Friday. It becomes a bit chaotic, but somehow the three of us have been able to find time to coordinate, attend most appointments, talk and share notes and keep the momentum. To Jill Evaristo Polzin and Steve Polzin - we did good this week and we must recognize and celebrate those successes as much as any other. There will be bad days, and good, we'll take each in stride.


My updates tonight carry a bit of a different tone. (I apologize if my writing goes a bit haywire... I find, as I'm sure many others do, that there is a tremendous lack of hours in the day compared to tasks needing completion.) I'll again include my disclaimer that I'm not a doctor. I'm good at observing and learning and absorbing information. I'm pretty good at reading people, knowing and articulating their characters and breaking things into smaller pieces while maintaining a view of the big picture.


I promise that I haven't (yet) gone (completely) off the deep end. My point is this. There isn't enough talk, discussion, recognition, or education about the overwhelming toll that cancer imposes. I know some may think (or say) that I may come across cold and unfeeling or lacking in compassion. I concede that outward appearance may suggest that. Emotion can get the best of us all.


We fight battles on multiple fonts. I can't even begin to fathom how anyone would be able to survive a war with cancer without an extended coalition of support. Nor would I ever wish it on anyone. And so long as I have it within my range of free will, I won't allow it to be any other way with my family. This week with Mom brought us direction and clarity, and really positive news from the PET scan results. Unfortunately, the referral to the radiation oncologist and associated assistant ended up feeling like an unexpected rectal exam. (I don't know if I can say that on television {aka this Facebook post}... But, well, I did. And, it should provide insight into the situation and how it got under the skin and may still be irritating it.)


I won't go into the long rambling unimportant details. I'll say that as a family, we made strong and prudent decisions this week. We made "course corrections" with both of our parents' care.


For mom, that meant changing the radiation oncologist provider to another member of that team. After experiencing the consultation with my mom, I was not only extremely taken a back by the behavior of the medical staff, and truly upset for my mom's reaction, but I was also genuinely irritated and frustrated by a medical unit tasked with caring for cancer patients.


I was, however, able to advocate for my mom (after talking with her and my siblings to come to a consensus) without swearing, yelling, or suggesting that objects be inserted into orifices. That's not to say I didn't FEEL as though those things were warranted, I just managed not to say them aloud. I'm confident that I got my message across and feel as though things are again progressing as they should. Not that I'll hesitate in suggesting other and future course corrections if needed, of course!


There is more to come, more to do, things to be said and tasks to be completed. For now, I believe a good hearty rest is in order for us all...


For tonight, I leave you with these words... A collaboration by three siblings.

~S ~J ~T


Tuesday, February 13th, 2018 - 6:30PM - New Direction
Sorry to have kept you all waiting. It's been a bit of a chaotic day. As you know, today was the follow up with Mom's oncologist to find out the results of the PET scan from last week. I promised more clarifying information.​

Tonight, after work, I stopped to pick up a few things at the store (more on that a little later)... But as I walked through the store, a piece of home decor caught my eye. I didn't buy it, but, the phrase on the wooden block read, "You can't create the masterpiece of your life until you master peace in your life." I found it very fitting for the day... And I'm sure I'll incorporate that in some way.


The details from today: First, THANK YOU Auntie (Debbie) and Steve for being there. Regardless of the outcome, that wasn't an appointment any of us should've gone to alone (mom especially) or even just one other person with her.


Mom has what is called adenocarcinoma. This is, a relatively broad term, however. It refers to or classifies as a malignant tumor formed from glandular structures in epithelial tissue. (epi-what?) Think epidermis. The outer layer of skin on our bodies. This doesn't, however give an exacting origin for the cancer found in the tissue sample taken from mom's leg during the most recent surgery.


The oncologist, Dr. Lukas has been great, and works with both of my parents. He's very good about understanding patients and their support systems and answering questions for all involved or in attendance. He's the director of clinical trials at the Cancer Care Partnership. It truly takes the right kind of person not only to be in the medical field, but to have chosen to focus on an area such as oncology. As we have recently learned in our (all too much) exposure to cancer, the world of medicine, the science of medicine, the society of medicine has taken leaps and bounds in advancements. Although I know we have lost countless loved ones to the beast that is cancer, a vast number of cancer strains and diagnoses are now considered very treatable. Adenocarcinoma is one such strain. Please don't let me undercut the importance or severity or reduce the sense of urgency in any way. Cancer is very serious. So while Mom isn't 100% free and clear, all signs tell us she just took a giant leap in that direction.


The PET scan overall looked good. As I mentioned, there were a couple areas of note. On the left she of her face - the lymph node at back of the jaw displayed increased activity on the PET scan (remember - PET is based on metabolism and energy in the body, with the added radioactive material that's injected, and tracked through the scan.) It's enhanced imaging really does provide ultra specific results. The second area of note was an area of the stomach (and we'd interject that it's in roughly the same area that was previously affected by two gastric bypass surgeries and an ulcer). While not dismissive of these two areas, the doctor, again, wasn't raising any red flags. They warrant a double check by experts in those areas of medicine - an ENT, (who is actually an otorhinolaryngologist, or Ear-Nose-Throat doctor) and a GI (gastrointestinal) doctor. I'm going to stick with ENT and GI for convenience sake. ENT will check the lymph node at the back of the jaw and surrounding areas and the GI will get... Well, all up in her business! The doctor recommends both an endoscopy and a colonoscopy because of the area of the stomach that was noted, best to check the surrounding glands from both sides. My brother, Steve Polzin was a trooper and volunteered to have a simultaneous colonoscopy of his own! (KIDDING!!) Adenocarcinoma CAN originate in numerous places in the body, but that doesn't mean it DID.


There are rare cases of the cancer having originated in another part of the body and then having literally transferred to its present location. Think about it like this - say the cancer originated somewhere else. Mom has had a LOT of trauma and surgery on her legs, especially the left leg. The body throws its natural defenses up to focus on and heal the damaged areas. So when your cells are attacking the invading force, they in some instances have relocated cancer to a new home in your body. Happenstance has it that on a whim, the ortho doctor tested tissue samples on the most recent surgery and discovered cancer's current location within Mom's leg. It's also a possibility that a previously unknown tumor in her leg caused or contributed to the weakened bones and only amplified the breaks when they occurred. Again, the PET scan didn't call out or highlight anything to positively identify other areas of cancer. And the additional tests with the ENT and GI are meant to rule out those other lesser possibilities.


All of that said. We STILL have to deal with the existing cancer. But, at this time, radiation oncology will be evaluating her and my guys is that she'll have to have a mapping scan completed (just as Dad did) in order for them to focus the radiation treatments. Just being the way things worked out, the radiation oncology department had an opening tomorrow morning at 8:15, so we're going to knock that piece out sooner than later!


So long as the ENT and GI doctors don't identify any other concerns (and they aren't expected to), the radiation will hopefully zap the adenocarcinoma into oblivion. It would then be regular maintenence checkups to ensure that no other issues have arisen and no other areas of concern have popped up. All in all, positive news. The blood work that looks for additional or other kinds of cancers all came back negative. So the journey still lies ahead, but the destination is on the horizon. We NEED this to get Mom back to full mobility and eliminate or greatly the pain management necessary to function.


That brings this post mostly full circle. Mom's new awareness color will be YELLOW. I stopped to pick up ribbons and will have those items out soon. I also ordered the bracelets and pins and will have them in the next couple days.


For now, I leave you with these, my words... And a giant SIGH of relief.


~T

Tuesday, February 13th, 2018 - 1:45PM - The Answers We Seek
A quick update... I'll give more detail later, but, I can say that today for all intensive purposes was GOOD news. The PET scan didn't reveal any areas of major concern. There are two "active" areas, but neither identified outwardly as cancer. They will require additional tests, and to treat the cancer that exists in her leg, she'll undergo radiation treatment.​

I'll fill in additional details later... But wanted to get this out... We're breathing a heavy sigh of relief.


More to come!


~T

Saturday, February 10th, 2018 - 2:00 PM - The Calm
​As the song goes, "The silence isn't quiet." (Rise up by Andra Day). I don't think that very many of us are good at waiting, myself included. It is in these times, the silence in between, where some of the most amazing things can happen.​

Today, I just wanted to take a moment to say a very special thank you to some of our fellow warriors.


First, Karen Sundin and Kristin Kruiswyk. I can't express how much we appreciate your time and endeavors today. Karen and Kristin (and family!) came into our lives many years ago... Though our family's stories haven't run in tandem for many years, we are extremely grateful that they once again found a way to intersect not too long ago. I know each of us has faced our share of trials and tribulations, it's incredibly impressive that after many years we come full circle.


As some of you may have seen... My mom's fur baby and everyday companion, Molly, was in need of some pampering and TLC. She's a sweet lovey little dog who loves mama just as much as any of her human children. I know that she is acutely aware of when my mom isn't feeling well, or when something isn't quite right. Molly was beside herself when my mom and her were separated for months after mom's original fall in July of 2016. In true family fashion, we took care of Molly (I need to see if I can find the video or pictures from when my nephew Micah was walking her...) During that time, Molly was also introduced to Jill Evaristo Polzin's dog, Bentley, and promptly showed him (a Lab, Husky, Burmese Mountain Dog mix some 10 times her size) who was boss. It can always be stressful for my mom who has to figure out how to get back and forth with Molly to the groomer or the vet, if needed. With everything else Mom has on her plate, she's been a bit down, understandably so. My mom has an intense desire and her immense maternal love always pull her to try to take care of everything for her kids... Human and fur alike.


Kristin & Karen were both bright beacons of light, shattering the invading dark. Kristin selflessly asked if she could take Molly along side her own fur baby to be groomed. She'd be in the area near where mom lives and would take care of all the arrangements and transportation. As an added bonus, Karen would come for a visit! Her friendship and companionship are so very treasured and any opportunity to spend some quality time together brings mountains of joy to my Mom.


I spoke to my mom yesterday on my way home from work. She was near to tears as she said to me, "I'm just incredibly touched. It's so hard to find that kind of good and genuine kindness left in the world."


Aside from taking away the stress and financial aspect of giving Molly the care she needed, making arrangements with the groomer, transportation and the use of your own (as we all know) invaluable commodity {time!} , you also created an incredible opportunity for our Mom to have some time to connect again and enjoy all that encompassed a friendship that began so long ago.


Then, and, not to be overlooked in any way... To the warrior amongst us that arranged and paid for lunch to be delivered... THANK YOU. You are appreciated, and your contribution to the day (and your many others) does not go unnoticed.


All of your affirmation that she doesn't fight alone is crucial and impactful. THANK YOU cannot express the full magnitude of what these things mean to our Mom and in turn, to us.


I leave you with these, my words. Hopefully, I also leave you with some of the incredible spirit and uplifting comfort our fellow warriors have graced us with today!


~T

Wednesday, February 7th, 2018 - 6:00 PM - Mission Accomplished
Mom came through with flying colors... I, on the other hand, may have walked away a little worse for wear!​

After some anxiety, a discussion, some information, a tech who loves his job (and talking way too much), a fainting TJ, an injection, some (albeit short) rest and the scan with a flip in the middle to get head to toe, she emerged!


Technology and all its wonders. For all the jabbering the tech did (and I apologize if he was a doctor, and I keep calling him tech, but I'm fairly certain he isn't...) he really did give us some useful and informative tidbits.


A PET scan will essentially measure energy within the body. Since cancer cells metabolize at a much higher rate than normal cells, the PET allows us to pinpoint where within the body cancer cells are located. He also shared that in the last 20 years.. Cancer treatment as a whole has taken enormous leaps forward. Lymphoma, for example is nearly 100% CURABLE. Not just treatable.. It can be cured. A few decades ago, a cancer diagnosis was... Well... The end of the road. Today, however... There are over 400 options for chemotherapy medications as compared to around 30 just 20 years ago.


Immunotherapy, radiation, technology, chemotherapy, medicine in general are all advancing at rapid pace. He said, almost exactly, that it "doesn't mean you won't have to put on boxing gloves from time to time" .. But.. Cancer is now very treatable if not curable. PET scans bring about 3-d images of the body after glucose is injected that carries a radioactive molecule. The images follow the molecules throughout the body and are able to accurately pinpoint cancer cells throughout. This aids oncologists in focusing and customizing treatment and also provides incredible tracking for warriors being treated. Before, patients would have multiple CT scans and their progress was judged by the lesions or tumors having shrunk since the previous scan. Now, with the PET accuracy, and focused and directed treatment, we can see in just a short turn around time whether or not the current direction is effective or whether adjustments need to be made.


Within an hour the actual images are available to the doctor. They are read by the radiologist team. Then they are sent to a specialist in Seattle who can read both nuclear and radiological images and a final report is sent to the oncologist. The specialist in Seattle has a special license to actually decode the imaging and write the report that is provided to doctors. This normally occurs within just a day or two instead of having to wait almost a week for results with some other imaging processes.


Mom has a followup with the oncologist to get the results and determine next steps on the 13th (for those of you watching my dad's care and progression.. Yes, it's the same day as his initial radiation appointment! In fact they are scheduled about an hour apart...)


In the meantime.. We'll return to the waiting game.. And I'm going to get some rest.


I'll have custom awareness ribbon pins (based on our situations and the logos I've created for these groups) up for sale soon. They're not pricy by any stretch, but I'll be using that same platform for donations as well to hopefully help with some of the ever growing cost of medical treatments for both parents.


Until the next time... I leave you with these.. My words..


~T

Wednesday, February 7th, 2018 - 4:30 PM - Waiting.
Quick update.. We're waiting for mom to complete her PET scan. I'm going to get this out of the way now... I appreciate everyone's concern... It's really not about me. I'll probably not hear the end of this anytime soon, so just going to do this once.​

We were in the room with mom as she went through preprocedure preparation. There was a point where the tech that put in her IV wasn't happy with the vein.. And, there was only a minor amount of blood. I'll be honest.. I've never really had issue with the sight of someone else's blood. Now if it was my own, all bets are off..


Anyways, he explained the scan and talked... A lot.. Then, I started feeling like it was warm in the room. I was going to step out and needed some air anyways. I turned around and in that moment I felt like it was a thousand degrees...i remember leaning forward over the sink in the room... And... That's about it...


Next thing I remember.. I was laying in the hallway... On a gurney... With my feet elevated and my head lowered...and some strange lady (very nice... But previously unknown to me) staring at me...


So yeah.. That happened.. We'll have a mom PET scan update later this evening.


For now.. I'm going to sit and drink more water...


~T

Tuesday, February 6th, 2018 - 11:00PM - The Path Before Us
​​Hi everyone! Time for a flood of good vibes, thoughts, strong prayers, and meaningful wishes. Tomorrow is Mom's PET scan. We need this to give us definite answers and direction. Hoping for the very best possible outcome. Jill and I will be there! 2:00 PM (Pacific time).

Join with us in this flood of positivity!


Thank you all, as always, for being present with us through this journey.


For tonight, I leave you with these, my words...


~T

Saturday, February 3rd, 2018 - 11:30 AM - Inspiration & Motivation
Tomorrow is World Cancer Day. Keep your eyes peeled tomorrow for our story.. That post is a work in progress.
Today, spilling over from yesterday, I've gotten a second wind.. Some new inspiration and motivation.. Thanks, in part, to an unexpected and unintentional donation from Amazon.com (its a long story, but funny...)


You all have probably seen my graphic designs, and there have been multiple inquiries as to how to get the dual ribbon heart shaped logo. Well... I think I've found a way to make it happen  😁. Stay tuned.. I'll publish finished pieces once I determine the best way to get it worked out (that's some TJ OCD and quality assurance that needs to happen!)


Some activity to update you all:
Mom had a follow up at the office of her Ortho doctor on Friday. Unfortunately, not a lot to report here. The doctor that did the actual surgery wasn't present for this appointment.. Which leads to another follow up in the coming weeks...


The P.A. did give some information though. The cancer was discovered in mom's leg with a bit of happenstance. It's not typical that tissue samples are obtained during the surgery to insert metal rods following bone breaks. In this case, because the surgery had been repeated now a third time, and the healing process wasn't producing results, the tissue was taken and sent for pathology. Not necessarily the best news or the way we think this should work.. But, mom was told that in truth, it could have gone undiscovered for an undetermined amount of time otherwise.


The important next step is the PET scan which is scheduled for February 7th at 2:00pm Pacific Time. Keep mom, and all of us close in your thoughts for answers and positive outcomes.


As always, we'll share more as soon as we get information.


On the horizon - the oncologist has now set an appointment for follow up and it should include review of the PET scan results and the lab work. This appointment is set for the week of Feb 12 - 16. I don't have the details of date and time, just yet.


For now, I'll leave you with these, my words..

~T

Monday, January 29th, 2018 - 6:45PM - WCD Rally Cry
This Sunday, February 4th is World Cancer Day. The theme, which has continued from 2016 and 2017 is "We Can. I Can."​

This is the day in which the World declares that everyone – as a collective or as individuals – can do their part to reduce the global burden of cancer. Those diagnosed with cancer are NOT a burden.. It's intention is to reduce the cancer epidemic in all its forms and focus on finding a cure so we can obliterate this vicious disease from existence.


Please take some time this Sunday for reflection. For most of us.. This won't be reflection about ourselves. (With the exception of survivors and those currently affected by cancer) This is about the big picture. Cancer as a world disease.


As the song by Andra Day says - Rise up! Rise unafraid! Rise up! In spite of the aches! Rise up! And we'll do it a thousand times again!

I'm not asking for a moment of silence. I'm asking for us to cry out in one loud unmistakable voice - "They do not fight alone!" We can. They Can!
(I invite you all to share your message in whatever form it may take... This Sunday (2/4/18)... WORLD Cancer Day.


~T

Sunday, January 28th, 2018 - 6:45 PM - Colors of Cancer
It's amazing, and quite sad that cancer has SO many variations that we even have to have such a wide multitude of colors representing different strains of this disease. For my mom, for now, we'll be lavender because that's the color that represents all cancers.​

Part of my focus in the coming weeks will be identifying charities and other organizations that can and will support our cause.

I also wrote to Ellen via The Ellen Degeneres Show website. I'm grateful to have you all to walk alongside us. Whether it's physically, emotionally, or virtually, you are appreciated and recognized.


We may never be able to find a way to recognize all of your contributions, in whatever form they take. It is my hope that even if I'm not the one posting the message, that our appreciation is loud and clear.


I'll be working on some other projects today.. So although I may not have a medical update today... I'll likely be posting more soon!

~T

Friday, January 26th, 2018 - 7:15 PM - Obscurity
Obscurity is the state of unknown.​

It's not our intention to leave anyone is the dark... But in these early stages, please understand we are sitting there together.
The initial interaction with the oncologist is truly about discovery in my Mom's case. There really isn't a known cancer that starts in the leg tissue in the way this was identified. Now, let me also say... If it's going to be something weird... It's going to happen to one of us. (You're welcome, family!) We really are magnets for the weird.


It begins with an all out barrage of lab tests, scans, evaluations, and when it comes down to it, opinions. It's like putting together a puzzle with all the pieces flipped over. You can find some that fit, but can't yet tell if the end result will match the picture on the box.

The lab work today will be combined with the results from a PET scan (that stands for Positron Emission Tomography) it's a medical imaging scan, it doesn't have anything to do with her sweet Molly.  🐕 The scan is used to observe metabolic processes in the body.

The hope is that the total of these results can help determine the origin of the cancer cells. That's like turning on the flood lights over a dark stadium. It should give us some definite answers and provide treatment direction.


From this perspective... We now begin the hurry up and wait phase. I ask that you all keep spirits high. Our purpose is akin to "Footprints In The Sand". When strength wanes, I will bare the burden. When you feel alone and only see one set of footprints in the sand, it is because I carried you. When a runner falls and drops the baton, the next is on their heals, picking it up and taking the next leg of the journey.


Thank you all for coming along with us. Together, we shall piece the puzzle together. We'll be the glue that holds it there. And we'll be the light that obliterates the darkness.


I am often the voice. But, I am only one voice. My cadence is steady, my words are careful, my speech is mindful and my message is clear.

I try to remember, and frequently to say, THANK you. Cancer has far reaching effects. It's imperative that we surrounds ourselves with positivity and focus our combined energies and walk together through the obscurity, so that we are strengthened when we face it on the other side.


Please continue to share your messages, thoughts, prayers, well wishes, wisdom, courage, heart and spirit.


I leave you with these, my words.


~T

Friday, January 26th, 2018 - 6:00 PM - The Journey
Today is surreal. It's like existing in limbo. The space between. Sometimes there are more questions than answers.

I'm going to fill in what I can. Today, my sister warriors were with Mom at the first appointment with the oncologist.


For a moment, we're going to get into a time machine and get caught up.​

July, 2016. My mom tripped on a bathroom rug and fell forward. She broke both legs. At the time, she was unable to get to a phone, and spent the night yelling for help until her upstairs neighbor heard her and called the ambulance. I am sure that I nearly broke the sound barrier when I got the call the next morning. Mom was in the hospital at that point. She would end up having surgery on both legs during which doctors placed steel rods in both legs from the knee to the foot. After days in the hospital she was transferred to a rehabilitation facility.

Although we're visiting the past.. there are parts of this story I can't bring myself to relive. At any rate.. Mom would be in the rehab facility for months. When she finally returned home, it would be with regular in home caregivers and physical therapists.

There would be healing and improvement in her right leg. But, the left leg would continue to be an issue. A second surgery was performed in 2017, in hopes of encouraging the left leg to heal.

Fast forward into October of 2017. My mom stands hand in hand with her kids as we begin to deal with the harsh reality that our Dad (my mom's ex husband nearly 20 years divorced) was facing prostate cancer. Wheels were set in motion. And life for all of us forever changed. We had to get a grasp on what to do. He was undergoing a battery of tests and we didn't have any real answers or direction. Before we knew it, the holidays were upon us.

We struggle in a normal ("normal", such as it is) environment to find time all together, even at the holidays. Things this time around were even more difficult. Thanksgiving passed, and Christmas was knocking at the door. We finally gained some footing and the news wasn't what anyone imagines. Dad did have cancer and it was metastasized. (Meaning it had spread from the point of origin). Plans were set into motion, but in truth at the point, there's nothing you can really DO in that moment.

All of this really goes on in the background for my mom. She's still there, because that's what mom's do for their kids. She's still continually fighting her own battles, including the healing in her left leg. As we get through Christmas and the New Year is a blink away... We learn that my dad will have a biopsy on the 4th of January and my mom finds out that she'll be going in for a third surgery on her leg.

That brings us to 2018. January 18th Mom goes in for the third round of leg harassment. When all is said and done, she actually seems to come out of this surgery better than the previous two. Doctors have her up and walking by the second day. It's extremely painful, but she pushes through, determined that this time will be the last. She's released from the hospital on the third day. Saturday, January 20th.

The weekend passes and we, her kids, return to work. Monday, as I'm driving home, my mom calls me. When I answer the phone, I know that something is wrong, immediately, but I've learned to at least attempt to control my knee jerk reactions.


She explains that the pathologist working with the orthopedic doctor called her. They had taken some tissue samples during her procedure on Thursday to test. They wanted to identify why or what the cause of the lack of healing was in her leg.

As an absolutely unbelievable outcome, she is told that she has cancer present in the tissue samples. The world literally tilted slightly and stopped it's rotation for long moments. You don't absorb that information. Your dad was diagnosed with cancer confirmed by biopsy on the 4th of January. It's just not possible that your mom is told she has cancer on January 22nd. 18 days. A mere 18 days separate their diagnoses.

The amazing resolve and stamina of my immediate family is abundantly evident. We have and will continue to rally around, support, and advocate for both of our parents. This is our journey. She will never fight alone.

That brings us to today, Friday, January 26th and the first appointment with the oncologist. Update coming momentarily!

~T