Thursday, October 27, 2011
Hockey Fights Cancer night at Joe Louis Arena
I had Bekki Nill on my podcast last year. She is the wife of the Assistant General Manager of the Detroit Red Wings. She is also a breast cancer survivor. She invited me to the Hockey Fights Cancer night at the Joe Louis Arena. Every hockey team has a HFC night. It is " a joint initiative founded in December 1998 by the National Hockey League and the National Hockey League Players' Association to raise money and awareness for hockey's most important fight." That is off of NHL.com. Needless to say I am happy that the NHL sees the need for more funding going towards cancer, and if you can catch a hockey game in the process, well then I am all for it.
It was my first professional sports game I had been to since diagnosis, and the first game I had seen in a suite since I moved from California to Michigan.
Watching the teams warm up made me want to get on the ice and skate. I hadn't played since March, and there is just something about the sport of hockey that speaks to me in a way that nothing else does.
Watching the game from the suite was an amazing experience. As I sat there watching the game, the players, I felt good. Better than I had in a long time. I think my friend Ashley (another cancer survivor) and I were the only ones into the game, and I get really into the game.
I honestly and truly appreciate Bekki Nill's invitation to Hockey Fights Cancer night at the Joe. Probably more than she realizes.
The Red Wings helped me fight cancer.
Hockey helped me fight cancer.
And it still helps me now through survivorship.
As I think of that night and look through the goodie bag full of stuff I will always be grateful to the Wings, and especially to Bekki, and her husband John for what they have given me, not the autographed Lidstrom puck or the pink hat with the Winged Wheel.
But for something more.
They keep me skating, and advocating.
Hockey really does fight cancer.
Check out my podcast The Cancer Warrior on Empoweradio.com. Available on demand and also available on Itunes.
Sunday, October 16, 2011
Humor Rocks and Laughter heals
Having cancer isn't funny. Everyone knows that. It's a serious disease that takes so much from so many.
I have been blessed with a wicked sense of humor. I get that from my Dad. I remember when I was meeting with the surgeon to discuss my course of treatment I never thought I was going to die. I thought wait, one year of treatment would mean no hockey! Not usually something you think about when faced with a disease like cancer.
Humor and sports. That's what got me through my treatment and still does through survivorship. I remember someone who hadn't seen me for a while saw me while I was going through treatment and commented on how great I looked. Since I was working out so hard for hockey season the docs said I didn't lose as much weight and went through treatment better than most. I said "Cancer is the best diet I ever had!" Some of those around me were shocked by what I said. But I know that my sense of humor was going to get me through this.
That is why I love Save the Ta-tas and their message. It makes me laugh, it brings awareness, and they donate proceeds to various charitable organizations. Did you know that they have donated $690,0000 to charity to date? This means that your purchase can help others. Find out more on the Save the ta-tas site.
Because of the generosity of Julia Fikse of Save the ta-tas I was able to pick out a shirt and one of my readers will win it. (just post a comment why you like the ta-tas brand) I am hoping that the sense of humor will help you through your survivorship as it did mine.
Imagine a world without cancer.
I can.
Can you?
Check out my podcast The Cancer Warrior on Empoweradio.com Available on demand and also available on Itunes.
Saturday, September 24, 2011
Transformation, turning points and clarity in life.
A guest post from Mr. Wonderful
Well here we are, coming close to the end of September. Have you heard? It's Ovarian Cancer Awareness Month! There's a lot to know about ovarian cancer and cancer awareness in general. But, I would like to share something a little different today. Two stories about how ovarian cancer has change my life: the first, about my wife, Sarah Sadtler Feather (1971-2011); and the second about me – after losing my wife. Both stories are about transformation, turning points and clarity in life.
Sarah – Rock climbing at Estes Park, Colorado with First Descents, September 2010
A year ago, Sarah ventured to Estes Park, Colorado to attend a rock climbing program through First Descents, an outdoor adventure program offered to young adult cancer fighters/survivors that is designed to enable a defiance of cancer, a reclamation of life and a connection with others doing the same.
Rock climbing was definitely not in Sarah's standard repertoire. As a matter of fact, she'd never even tried it. She was scared, but intrigued. I know she was also excited for the opportunity to check off a new item on the bucket list.
During her five-day trip, she experienced two incredible personal transformation points. Both would remain a part of her to her last day. One would give her strength. The other would ultimately take her life.
It all started with the elevation. At close to 9,000 feet above sea level, the air's a lot thinner than where we live outside of Boston, MA. Ovarian cancer had raided her body, and Sarah knew her lungs were already getting weaker as metastases were taking hold, ever so slowly. Going to the gym was becoming harder, but she still went three or four times a week. In Colorado, the higher elevation made her feel like someone was sitting on her chest. Fatigue had been a part of her daily existence for more than 4 years, but now it took an even deeper hold. Suddenly the idea of rock climbing, an energy/oxygen-intensive activity, was terrifying.
She called me via Skype every night from her bunkroom. Often in tears, exhausted, frustrated and deeply disappointed, she would say how hard things were. She felt like a failure. I did my best to listen and to be supportive. But I'm sure I also gave too much advice, reminding her of how amazing she was and of her wonderful accomplishments.
But Sarah's struggle at Estes Park is what gave her a new strength. While she had already been through hell and back with numerous major surgeries, an ileostomy, chemotherapy more times than I can count, depression and more, this new challenge was powerful and exciting.
With help from her fellow campers and the amazing staff and volunteers at First Descents, Sarah was able to complete climbs, stand at the top, see the views and embrace her successes. Something about the physical experience of climbing a giant rock face, while others cheered her on, let her find a new strength, a deep vigor that would guide her to meet her goals in Colorado, and, later, would guide her at home as she completed her journey of life.
When she returned home at the end of the week, she was different. She knew something she had not known before: the end was coming. Nothing could stop it. It was simply a matter of time. Her lungs where getting worse. She could feel it and knew it was time to help people understand.
But, she also had this new sense of strength, combined with hope and a deep, profound love for life. She shared this with me, with our boys, our family and friends. As she moved closer to the end, she encouraged me to live my life to the fullest, to keep going, to be strong for myself and our kids, and simply to remember her and her love in the best ways I could. And in her deepest, giving way, she especially wanted me to love again.
I don't think she knew it at the time (maybe not even when she died), but she was to become a shining beacon - one that would teach so many about life, about death, about love, about courage, about living to the fullest extent we are able.
(You can read her Estes Park story in the following three posts: “Catching My Breath”, “Looking for Footholds” and “Storming the Castle”.)
Ed – New experiences - dating in Boston, MA, Summer 2011
I felt good, but nervous. We'd been talking all night about life, people, places and experiences. Few were shared between the two of us, but the many similarities and differences created some wonderful contrasts.
The woman sitting across from me was a natural beauty. She was quite stunning with a gentle, beautiful face and long, flowing hair. If she wore makeup, it was very little, and clearly not needed.
Leaning forward, I asked, "What are you looking for in a partner? What do you want?"
"I want to be known," she said, gazing back across the table. I sensed a deeper meaning, but wasn't sure I fully appreciated the significance of her statement.
"Do you mean you want someone who understands you?" I asked, hesitantly.
Her response was deliberate and pointed. "No, I want to be known." She paused, looked at me and then went on. "Lots of my friends understand me. But none... know me. I want to be known."
"Wow," I thought. This was so conceptual, and so far from what I might have expected a woman to say when describing what she wanted in a man or relationship. Her tone was serious, but there was something else. Perhaps a hint of sadness. Clearly something she had pondered, and perhaps had wanted for a long time.
"That takes a long time." I said. "You can only really, truly know someone by spending a lot of time together."
She gave a slight nod. "Mmm" she said, mouth closed, with a hint of a smile.
That she said "I want to be known" was not as surprising to me as was the depth and importance of her statement. This idea was of a kind that, once implanted, remains active, repeatedly asking for ponderance. I went home that night with my mind hunting for a connection to my own life experience, searching for personal understanding. Of course this raised thoughts of Sarah.
Sarah and I were together for 18 years. She was my wife, my best friend, my love, the mother of my kids, my muse. I was hers. In our shared experience we touched the depths of each other’s souls. We knew each other so profoundly, so completely that our love felt infinite. Our trust was implicit and complete right up to her very last breath of life.
I held Sarah in my arms as she died. Ovarian cancer had won. As she slipped away and fell limp in my arms I felt my soul shudder. Our love and trust and knowledge had been so complete. Now they were shattered. She was gone.
I do believe the knowledge we shared will remain in me for the remainder of my days. I will always remember our love, our friendship and all she did for me. She wanted me to move on and be able to live a full life, and she encouraged me to love again.
So now, as I think of my date's statement: "I want to be known." I think I may fully understand her meaning. And, I agree. I also want to be known... again.
Cancer awareness. Every month. Every year.
I have some strong thoughts on this subject and have posted them at Carcinista.com. Cancer awareness is important. What is even more important, and could have saved the life of my dear Sarah, is to go see your doctor if you are not feeling well. Don't shrug it off. Get it checked out. Be specific. Make sure they know how you feel. Make sure to get a second opinion if you don't feel like they are taking you seriously. YOU are the only one who truly knows your body.
Be well.
Mr. Wonderful
Tuesday, September 20, 2011
Enforcer
Hockey teams are like family. We protect each other on and off the ice. Many people think hockey is nothing but a boxing match on ice. To those people I say lace em up and see why you are wrong.
This has been a sad year for hockey. Not only with the tragic loss of KHL Locomotiv team from a devastating plane crash, but two hockey players (Wade Belak and Richard Rypien) took their own lives because of (assumingly) their battle with depression.
I subscribe to Sports Illustrated. No surprise there to anyone I am sure.
Reading Brian Cazenueve's article about the deaths of 3 NHL players, in a few months, and the fact that they were all enforcers, it made me sad. The fact that Mr. Cazenueve said that "A third untimely death may spur the NHL to take another look at 'place in the game"
Fighting.
Hmm.
Fighting has its place in hockey. I am not one to disagree with that. I do however disagree that the NHL should look at fighting as the root cause of these players tragic demise.
I battle depression. I hate the word suffer, but yeah sometimes I do. Mental illness still has a stigma attached to it.
Now imagine you are a tough guy in the NHL. Would it be easy to tell someone that you are depressed?
I can tell you it wasn't for me, and I consider myself to be a strong person.
Not as physically strong as a professional hockey player, but strong nonetheless.
I kicked cancers ass, and continue to do so in this blog, and on my podcast.
But the hardest battles are the ones that others can't see.
My friend said to me recently:
Sometimes the scariest place is inside your own head
Maybe the NHL should focus on helping players from the inside out, not worry about players dropping the gloves.
Hockey teams are like a family, and even though I am not in the NHL, or even close to being anywhere near a professional player, I am ok at best, I will drop the gloves for anyone battling depression or any other mental illness.
Even you.
Wanna go?
Mel is the producer/co~host of The Vic McCarty Show. Listen Live Monday~Friday 9am-noon eastern time on wmktthetalkstation.com
Check out my podcast The Cancer Warrior on Empoweradio.com Available on demand and also available on Itunes.
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Saturday, September 3, 2011
Celebration???
September 18th I will celebrate 4 years of being cancer free.
Most people go by the date they were diagnosed.
I always get more introspective closer to the date of my diagnosis. I read old blog posts of mine, sometimes not believing how far I have come, and yet still how far I have to go.
Does anyone else find it strange that we celebrate a day that changed everything?
Don't get me wrong. I am grateful for early detection. For my doctors. For the planets aligning for everything to have gone well so far. I am grateful to God.
But celebrate a day that started out great and ended in a way I could not imagine. In a way that changed my life forever? In some good ways, in some bad.
Coming up on four years cancer free. I am grateful I am here, and fighting the fight.
I am not celebrating the fact I had cancer.
I am celebrating the fact I found it in time, and that I am here, and that my doctors are, in my eyes, rockstars.
So if you see me with a sly grin you will know why.
Suck on that cancer.
Mel is the producer/co~host of The Vic McCarty Show. Listen Live Monday~Friday 10am-noon eastern time on wmktthetalkstation.com
Check out my podcast The Cancer Warrior on Empoweradio.com Available on demand and also available on Itunes.
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Monday, August 22, 2011
Merrells
Its funny how certain things can remind you of events. Smells, taste, clothing. I remember when my fiance Doug was in the hospital and I was wearing this original 6 hockey shirt, it had the team logos on it. He seemed ok then he started staring at it and then he had a seizure. (That is what he was in the hospital for)
It took me a year to wear that shirt again. I almost tossed it out, but me being a hockey fan, well, of course it stayed in my wardrobe.
I have this pair of Merrell sandals. They are my favorite shoes. Not only because they signal the advent of spring/summer, they are just so damn comfortable. I wear them whenever I can. Biking, at work, everywhere. I almost wore them to the Warrior dash, but I knew they would get ruined.
I bought them in the bargain basement of a local store. I am not sure what year, but I know it was before I was diagnosed in Sept of 2007.
Now I don't remember what I was wearing when I heard my doc say "It's cancer" but I do remember I had to get my physical the next day. It was already scheduled for Sept 19th. I remember sitting on the exam table waiting for the doc to come in, staring down at my Merrells wondering what the hell was happening to me.
That was almost 4 years ago. As you can see from the photo, they are well worn, and they are loved, and yeah they helped me get through treatment.
So you may look at them and wonder why don't I get a new pair?
Now you know why.
Mel is the producer/co~host of The Vic McCarty Show. Listen Live Monday~Friday 10am-noon eastern time on wmktthetalkstation.com
Check out my podcast The Cancer Warrior on Empoweradio.com Available on demand and also available on Itunes.
Sunday, August 14, 2011
The art of language
Everything has its own language. For example, if you were to sit down next to me and I started talking about hockey and you had no idea what a shot on goal, PIM, one timer was, you would think, what the hell is she talking about.
Language, words. Everybody has a hobby or a job that has its own language or terminology. My friend owns a pilates studio. Before I started taking pilates you told me well today we are getting on the cadillac and doing the one hundred, then we will do the tree and the elephant. I would think wait, we are getting in a car and what going to the zoo. ( I haven't done pilates in a while but I know you cant do the elephant on the cadillac, or at least I am pretty sure)
Another friend of mine chemobabe is a math professor. That has its own language too. If someone came up to me and started talking about word problems, fractions or pi my eyes would start to glaze over and I wouldn't understand what they are talking about. (Did I tell you I totally sucked at math in high school?)
Language.
There is a language I have learned that I wish I didn't know. The language of cancer. The medical terminology that comes with being a cancer patient/survivor. I can talk at lengths about zofran, chemobrain, side effects of herceptin, adrymicin. Tell you how good Biafine felt after radiation. Talk about muga scans, ct scans, insomnia, constipation. Tell you how it sucks when I get depressed. Language.
I hate knowing that language. I wish I was blissfully ignorant of terms like chemo fatigue, neuropathy & left ventricle ejection fraction.
But I know them.
As cancer survivors we all know them. Unfortunately it is not like a foreign language where you get a semester to learn what everything means. You are essentially tossed off the boat into the ocean, where you have to swim and figure this shit out either on your own, or with the help of friends, family and the internet.
Fortunately there are enough of us out there to help if you find yourself stuck in that ocean. The sea of words.
I'll be around to toss you a life preserver and help you out.
Mel is the producer/co~host of The Vic McCarty Show. Listen Live Monday~Friday 10am-noon eastern time on wmktthetalkstation.com
Check out my podcast The Cancer Warrior on Empoweradio.com Available on demand and also available on Itunes.
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