50/50

I was home one day and decided to see if I could find a movie on Netflix. It seemed to be a better choice than watching CNN or any of the twenty four hour news networks. Unless I know ahead of time just what I want to watch.  It can take up to an hour to find something that I feel can hold my interest for more than it’s entirety. Within a matter of seconds, I found a Seth Rogen film I had not seen or even heard of. It was even under the ‘Critically Acclaimed’ category. So, how can I refuse? Now don’t get me wrong, Seth is pretty one dimensional in his work. Throughout his career, he’s pretty much cornered the market as far as lovable losers are concerned. Still, I love his work,  and in many ways, identify with his characters.

Going in, there were two other factors that drew me to the movie. One; It’s filmed in my then current city of Seattle and much like my years as a New Yorker, where I would be able to name most of the streets and locations featured in the various franchises of Law & Order. I easily recognized many of the Seattle streets where the film was created. What I did not expect and did not bargain for was the reaction I had to Jordan-Gordon-Levitt’s character Adam being diagnosed and struggling with cancer. As someone who watched a beautiful soul succumb to leukemia and die when I was only eight and was told I had month to live due to a brain tumor when I was twelve, it fucking wrecked me.

I was seven or eight years old when my Father started dating Angie. She was like no other person I had met before and maybe until I met the woman who would eventually become my wife. Angie was born in Taiwan and lived with her very strict, traditional and educated family in Queens. I’m not sure how the two met, but with Angie being was a teller at a local bank and my father still driving a bus for the city. The chances of them crossing paths was pretty high. On the nights we’d pick her up from the apartment where she lived with her parents. I’d have to hide in the back seat until they emerged and I got the signal that the coast was clear. She, along with her family had immigrated looking for a better life and like many, the chance to work towards the American dream. A recently divorced bus driver with a son was more of a nightmare than a dream.

Angie and my dad were polar opposites in almost every way. While my father stood 6’4 with a booming voice. Angie was tiny in comparison, always speaking softly in what often seemed like whispers. Her jet black hair often hung down below her knees. Often causing her peers to ask how she kept it looking so manageable and beautiful. Though my Dad was always a heavy drinker and an occasional drug user. Unlike my Father, Angie never acquired a taste for alcohol, drugs, or gambling. Such distractions or deviances never interested her. 

Her generosity and penchant for spoiling me were undeniable. However, introducing me to New York City’s Chinatown and adventures on Mott Street would impact and influence me the most. She would read the Chinese comic books I’d buy each time, teaching me a new word, phrase, or Chinese slang term. As a kid who hated the Wringling Brothers, Barnum & Bailey Circus, my Uncle Ray and Aunt Mary would take me to each year. Angie’s taking me to the Taiwanese Circus left my mouth gaping in amazement and adoration. The experience blew my mind.

By the age of seven, I had already witnessed a friend fall to his death and been to a funeral, but seeing Angie fall to Leukemia was the hardest thing I’d witnessed  before or since. Seeing her lay in a hospital bed connected to tubes. Experiencing the process of her flowing black hair become stubble, only compared to what I saw in war movies depicting prison or concentration camps. The treatment, drastic, yet unsuccessful only seemed to make things worse. Eventually, after often brutal chemotherapy treatment that only seemed to worsen her condition, she would come home with my Dad , but it was short lived, as she would soon return to the hospital where she would pass.

Even now, when I bring her up in conversation, my Dad easily recalls detailed memories of her kindness, their time together, and what it was like sitting by her bedside at the hospital. As I write this, I try to focus on all the good and kindness that she brought us. The positive imprint she left in her twenty seven years on this planet. Maybe, writing about the suffering will help me heal enough to focus on the good things.

As for her family. I didn’t meet any of them until the day of the funeral. Like I said, they would have never let their daughter date a man who was divorced with a kid. When I think back to those days; and I often do. I didn’t like it, but I kind of understood. Looking back, I can’t help but think, that experience had a lot to do with my drive in volunteering on so many cancer related fundraisers. To think that something good came out of that tragedy is as rewarding as it is hard to believe. In the end, Angie may have been the greatest, most positive influence on my early childhood. Her presence and overall impact certainly influenced me as an adult and effected the way I’ll always want to treat people. I will always love her and appreciate the short, yet impactful life she lived. Till this day. I still have the Chinatown shirt she bought me on a trip to Mott Street. I had to be eight at the time. Though it hasn’t fit in more than forty years, I keep it as a token of her kindness and the last physical item representing our time together. Thanks Angie, you will always hold a place in my heart.

The Strength Within

A few years back during a visit to my gastroenterologist,  he told me that he was just sharing with his secretary how inspired he was by me and my ability to bounce back from each medical setback, emerging stronger and a bit more wiser. Being that I had been seeing him for an entirely different set of challenges for close tot fifteen years, he had seen me move from one health setback to another. While I was taken aside and visibly humbled by  his words, all I could come up with was some gibberish about how, after all these years of fighting, I was tired and I wasn’t to sure I wanted to fight anymore. Note that this was a few years prior to my latest discovery of another brain tumor and being diagnosed with a neurological disorder that has no cure or known treatment.

Rooftop-1

Still, to this day, I find myself fighting and adjusting to meet new challenges. Truth is, we’re all a lot stronger than we’ll ever give don’t give ourselves credit for. No matter what a person, or doctor tells you. It can’t override your desire, strength or determination to make the most out of what you have.To be happy with what you do have or can do and not to be preoccupied with the things you don’t.

Opening Up

For close to a year now, my doctors, therapists and my wife have urged me to open up about my health issues and the issues that accompany them. Knowing full well that trying to protect myself and loved ones from worrying about me and or thwarting their insistence on helping me, has only hurt me. Hasn’t helped in any way, form or matter. My attempts to hide symptoms and an overall fucked up long term outlook have only made me angrier and wasted much of the time I could have better invested elsewhere.

The hardest part by far has been trying to keep my parents at a safe distance.  When I first arrived in Seattle. I had already been experiencing symptoms that my primary doctor of close to ten years had pretty much reduced my mounting issues as post brain tumor, post stroke relate issues. While numerous blood tests were ordered and performed over the years. Little more was ever suggested or done. It wasn’t until I went out on my own and booked an appointment with a nearby neurologist that my issues were properly addressed and tested, that I found out I had a meninigioma brain tumor. Not a threat to my life, but something else to worry about and keep track of.I was angry at my doctor for his lack of action and insight, but I also couldn’t help but blame myself for trusting him for so long.

Fast forward a few months, my symptoms worsened. I made connections with the right doctors and hoped that removing the new brain tumor would right the course. Further tests were including an MRI and CAT-Scan followed. The results were nothing I ever expected or be prepared for. I was told that alarming amounts of calcium had massed on my brain and I had a rare neurological  syndrome/disease I had never heard of. One that had no cure and no known treatment. One that was progressively erodes your motor skills while wrecking havoc on your speech.

Alki-1

I was given a referrals to speech, a physical therapist and a social worker, My requests for a drano cocktail and a handgun were turned down and taken as a sign that I might be a suicide risk. (Note. New York humor and Washington State humor are very different.)

Since that October meeting. I found a great physical therapist just a few blocks from me. My social worker (One I really appreciated having.) moved back to her home town of Minnesota. I’m on my second walker, one which I need to get around with and one that keeps me from falling down and injuring myself. And while I’m being mentally prepared for a future in a wheel chair. I am doing everything in my power to remain active and positive. I’m boxing, lifting weights, going to the gym, writing  and traveling as much as possible.

In the end, the hardest part has been opening up and struggling not to internalize my feelings or blame myself. I know what my friends and family went through during other life threatening episodes in my life. Because of that, I’ve tried to do everything in my power to shield and protect them from any pain, worry or complicate things any more than possible.  I’m already feeling an immense pressure trying to keep my family at bay, while keeping them as informed and updated as possible. Opening up gives me the chance to breath again and say “I’m alright.” “Just give me the space and time I need to deal with things. I’m not writing this to worry anyone or look for sympathy. I won’t be starting any “Go fund me” bullshit. I’m just hoping for some acceptance and understanding. Below are some links that I thought would be helpful.

Fahr’s Syndrome

Web MD Brain Tumors

Virginia Mason Hospital

Renew Physical Therapy

Suicide Prevention

 

 

No More Crying

NMCIIIt began with the best intentions. The days and weeks since my Neurology follow up had me feeling angry, lost and somewhat hopeless. I had mistakenly opened up to my doctor, therapist and wife that I had briefly thought of suicide, or commented on how I wished the original death notice I received when I was twelve would have ended me instead of prolonging my suffering through related issues. Falling down and not having the control you once had on your life it not easy to get used to. With that said and fully expressed, I had felt a positive shift in recent days that mad me feel as if I had turned a corner. I had all but stopped worrying about what I couldn’t do any more and started thinking about what I could. My intention was to share with my wife that the fear and negativity were behind me. That, whatever it took, I was going to be open minded and more constructive.

As I began to speak to her, I made a point to use the word “Positive”. This exchange was going to let her know that I was leaving behind the negativity and look at all the positives and embrace whatever changes might come. Before I even knew what was happening. Before she even had a chance to reply. She buried her head in my chest and began crying uncontrollably. I did my best to make her laugh and smile “Hey, there’s nothing to cry about. This is all about looking at things with a positive mindset.” “Come on, there’s no crying,” “I’m not crying.” She sniffled, as she reached for the nearby box of tissues. All I wanted to do was tell her how lucky I was to have two parents that loved me and a wife who, despite all my obvious faults, adored me. Still, she kept her head buried in my chest. Unconvincingly trying to conceal the fact that she had become overwhelmed with tears. “I have to pee.” She announced as she quickly made her way to the bathroom. Concerned for what she was feeling, I followed. More than anything, I wanted to comfort her. To let her know that it was okay to cry. Even with the door closed. I could hear her blowing her nose and washing the tears from her eyes. I entered and hugged her. Assuring her that, maybe for the first time since that hospital visit. That everything was going to be okay. That she could cry all she wanted to as long as she didn’t feel the need to hide it from me. “I was trying to tell you that I turned a corner and how I was feeling more positive about things.” “Why are you crying?” Still red in the face and filled with tears. She said something I never thought I’d ever hear. “Because it’s not your fault.” “You didn’t do anything wrong.” I have to say, it was humbling.

NMC

Throughout our entire marriage and even when we were dating. She was always the strong one. The rock, the ying to my yang, or whatever you call it. Being on the other side of the coin. The one to say “Don’t worry. No matter what happens, everything is going to be alright.” It was hard, but I feel it was long overdue. Whatever may come, I hope I can always be there for her when she needs it. Considering how much she’s done for me in reinforcing my health and assuring my happiness. I’ve got my work cut out for me.

Below are a couple of helpful links.

Zen Habits

American Meditation Society