Here's to My 56th Trip Around the Sun

Today is my 56^th birthday. In few days, I will also be three years into my cancer diagnosis. These dates will be forever linked.  I will be forever linked to cancer. It is my hope I’m around to “celebrate” that linkage for years to come. I try to measure my worth on this planet by, among other things, the quality of my friends and the quantity of positive karma I share. Good things do happen to good people. This 56 year old living with cancer is a blessed human with some pretty stellar family and friends who definitively feels the good karma today. Thank you.

Happy Birthday to me.

Be well.
jjb

The Group

Every Wednesday evening since we moved to Fort Lauderdale I’ve found myself in a gorgeous, reclaimed “clubhouse” on the Tarpon River with peacocks strutting in the front yard. Sitting in a room with whomever decided to spend their Wednesday evening with me.  I never know who is going to show. Sometimes there are three of us, sometimes there are 20 of us. “Us”. Folks living with Cancer.  All kinds of cancer.  All kinds of stages. From the newly diagnosed to those whom the medical world has given up on. Old. Young. Women. Men. Gender nonconforming. White. Black. Hispanic. Asian. You get the picture.
 

Every week, each night, the 90 minutes we spend together is driven by what’s on our minds. Questions about treatment, how to ask your doctor questions, fear of re-occurrence, healthcare issues, the power of medical Cannabis.  Anything and everything is on the table. Regardless of whether it’s related to our cancer. We do our best to voice our truths and our lives, however refraining from and politics and religion. But every now and then anger at God, or whatever your higher being may be, and or at the current Administration can creep in. Listen, it is an honest conversation. What is most important, though, is we are free to show our fears, our hopes, and our dreams with others who share them with us as a result of our shared circumstance. Our shared relationship with cancer. No alarming the family and friends. No judging. 

Many times, in group dynamics you have a cast of characters. The person who dominates the discussion. Maybe it’s his first group meeting and has been bottling up stuff for some time. Maybe lives alone (or feels alone) and yearns for companionship of others. Others who “understand”.  But I swear can yammer on and on and on.  I’ve grown to be much more patient with this type of human. Before cancer, I would have told him he was being rude and should allow others to talk. Or I may have left the group altogether never to return instead of speaking out. Not now. Now, I listen. I take a deep breath and clear out the clutter in my head and I listen. I smile when he glances my way to encourage him to keep talking. As an acknowledgement I understand where he is coming from. As it turns out, if I really “listen”, I realize I share his fears, his frustrations, his “but I was never sick before this happened”. We just have different ways of expressing them.

Of course, there’s the curmudgeon. She just doesn’t seem to like people. Hates her circumstance prior to cancer and now, well, she’s just unbearable. Doesn’t have a positive thing to say to anyone or about anything. But for some reason she shows up to group. It seems she stills needs the warmth of human companionship. The comfort of understanding folk who listen to her regardless of her defensive bark. I, too, relate to this person. I am angry. Hell, I’m pissed when I let myself go there. I had a wonderful, blessed, existence before cancer. And yet, I can get right down in the muck in the blink of an eye. If I let myself. I rarely do that though. For me, it’s not a “why me?” thing. I don’t feel badly for myself and don’t want others to feel badly for me. Just want people to support me. Just be there for me. And so, me and the curmudgeon, we are there for each other, we co-exist and relate to each other nicely.

Sadly, he just celebrated his retirement only to find out a month later he has cancer. Or she lost her job just a month prior to receiving her diagnosis. She's had to sell her home to pay for her treatments, and now lives in her car. No health insurance, little hope. Yet she comes to group. We share our resources and our hope. 

And there’s ALWAYS someone who has had their road with cancer way bumpier and twisted than anything you’re driving on. She was diagnosed with lymphoma at 22, thrived and had an awesome family  - an awesome husband she is still married to and a wonderful, caring son who is an addict and fearful of relapsing without his mother. And her biggest fear is he will relapse when she dies. Later in life, she was diagnosed with breast cancer that has since spread to her lungs, her liver, her bones. The medical community gave up on her years ago. Yet, she’s still here. Thriving the only way she knows how. Smiling, smoking, selling everything “unimportant” and traveling the world with her husband, eating whatever she wants. She’s made her peace with her God. She has picked out her burial plot (including a seating bench for visitors) under a majestic tree she noticed while driving by. And yet she’s scared to die. At the end of every meeting I make a point to hug her and to tell her she’s wonderful. Every meeting, I worry may be her last. I want her to know I appreciate her and her contribution to my healing every Wednesday evening. Sadly, I have not seen her in weeks.....

This group of somewhat dysfunctional, wide ranging individuals has become my blanket.  They “get me” in my new normal. They have taught me patience with the human condition. While giving me a mirror to what may lie ahead of me, they bring me focus on the here and now. From the frighten, confused faces of those recently diagnosed to the exhausted faces of those staring down end-of-life circumstances. I hope I give as much as I get from these folks. Giving and receiving compassion and empathy from total strangers - there's much power in that. 

My family and friends want desperately for things to be as they were BC (before cancer). I’d like that too. However, after having examined close up just how fragile life is coupled with having your body fail you in such a tragic way changes you. Forever. In this group, I can confide my fears, worries, share my coping skills and pain to total strangers who may know me better in some ways than do most folks in my life.

Outside the group, I try and focus on the positive changes cancer has brought me. How much sharper the sunrises are, how beautiful the sound of birds in the morning stillness, how the smell of a flower brings such delight. My grandma Arlene lived this kind of life. She lived to be 94, and she understood how to live for the moment. I’ve since learned this joy through cancer.

I hope to live to be 94.

If I can from time to time wrap myself in the caring and fellowship of others fighting this disease, I  am convinced my remaining years will be brighter, clearer, and more compassionate and meaningful than my first 55.
(a birthday wish. happy birthday to me.)
 #KeepRooting4Me #FuckCancer

My Recliner

As I sit here in a recliner meant for clinical trial patients, in a room meant for those grasping at anything to make it just one more week, one more month, I think back on my last two years.

I was told in January of 2017 I had cancer. I spent the next 12 months surrounded by hospitals, oncologists, nurses, IV bags full of chemo, plastic surgeons, oncology surgeons, pills for nausea, pills for pain, pills to reduce the side effects of pills. I slept thru 2017 and my wife did everything else. This past year – 2018 – spent outside of the “chemo bubble” has been full of anxiety, pain, apprehensiveness, anger, and yet pure joy.

Today, I’ve completed “phase seven” of my 3-year clinical trial. And with it, I again must break free of a routine that has become comforting and comfortable. I know the nurses. They know me. I can find myself around the Sylvester Cancer Center, housed on the campus of the University of Miami Hospital, with my eyes closed (not really but it is impressive). I found a sense of peace knowing I’d return every 28 days to give blood, pee in a cup, see my oncologist, be deemed “healthy”, and receive my trial vaccine. I felt as if I were moving forward with each visit. I felt I just might be ok after all.

Beginning with the eighth phase and for the next two and a half years, my 28-day routine in this trial extends to once every six months.Three months before I see my oncologist for a "routine" visit. 

I again feel lost and anxious. Of the unknown. What is going to happen to me? Will I be OK in six months? Will I be too sick to walk these halls on my own the next time I visit? Oh, how I hate that this has happened to me.

 
I sit in the recliner, my feet up and under a warm blanket waiting for my vaccine. I past the time laughing with the nurses, smile knowingly at the others sitting in their own recliners fighting this horrid disease, hold my head high and breathe deeply.  I’m a proud survivor. Yet I’m scared, doubtful and terrified. And so it is. My life. Moving onward. But never to be as it was.

#KeepRooting4Me #FuckCancer