The feeling is bittersweet. I sit here in Infusion Room 918 at Dana Farber, with my computer propped on my lap and feet up on a nurse’s stool, feeling all too comfortable in my surroundings. Like most Monday’s over the last 3 years, we are here – trying to subtlety battle this horrible disease alongside many others on a similar, and all too familiar, path. Greeting the faces of patients who walk by with a head nod acknowledging the fact that there is a commonality between us. Being welcomed by the rotation of nurses and staff with a polite smile even though they know we are here on business, not pleasure. Asking a volunteer strolling the hall with a cart of goodies for another egg salad sandwich and a Sports Illustrated to pass the time as the hanging liquid attached to Mom empties beside her.
I say bittersweet, because this sucks, no other way around it, but I continue to have, and hold, a strong feeling of support, faith and hope. One of my favorite quotes (painted in the Red WIngs locker room at the Joe) is "faith is to believe what you do not yet see; the reward for this faith is to see what you believe." We have to believe in the future. Whether a patient, caregiver, DFCI staff member, friend or family member – we are in this together. Our thoughts moving a mile a minute and our minds being pulled in a variety of directions, wrapped around the powerful question, “what’s next?”
We truly dread coming to this place, but is there anyone else we'd rather trust for treatment? We are strangely confident to simply hand over control of our outcomes to the experts at Dana Farber. We put our fate in their hands to lead us in this fight with a vision, however distant or challenging ... but a vision to believe there is a future of peace, comfort and health ahead.
So, here we are – Mom and I (again). She has just faded off with the magic of Benadryl clearly doing what it’s paid to do and in about 15 minutes, our favorite nurse will come back in and begin a new treatment – Taxol. As most of you know, chemotherapy is not new to us. It’s been nearly 3 years since Mom’s 2nd diagnosis, but it’s now time for an adjustment. A strategic switch in our battleplan to attack the progressing cells and this is the next move. It’s a somewhat expected, but unwanted new plan and although more difficult, consuming, and taxing, we will continue to fight.
If you know us, then you know our story, and you know we will fight – Mom, sons, wives, grandkids, families, and our amazing support team of friends. It’s the hand we’ve been dealt and we do what we have to do.
Ok, why am I writing all this? If anyone was at our wedding or saw the video, speaking about my Mom and conveying what she means to me is not easy, but it’s important for people to understand why I’m doing this. This woman has been through more in the last 10 years than anyone should have to go through during a lifetime – from tragedy to loss to illness. I don’t feel even slightly bad saying, it is not fair.
We received news last week that Mom’s cancer was progressing and it was time to switch it up. My Mom’s immediate concern – everyone else. How can she ask me to be here every week? How could she “force” her friends at home to help her? What will we do with the damn cat? J (love you, Rem) That’s who she is and always has been – even during the hardest battles in life. Everyone else comes first, but for me, for us, her team, she comes first and we fight for Barbara - the strongest person I know.
Perspective is a funny thing. Today should be a typical work day filled with the usual stress of constant emails to my phone, but right now, they don’t matter. We have a sick baby on the mend who spent the last week sleeping only 2-3 hour stints, but we wake up smiling with her. We have all the other life worries that come with this time of year – Xmas gifts, parties, dinners, fantasy football playoffs (the serious shit) – all the things that are great and needed, but not a priority. I feel like I’ve garnered a strong definition of perspective over the last 10 years and it’s made me a stronger person. It’s not that some things don’t matter or should not consume any of my time or energy, it’s just that some things, and people, are far more important. As I sit here right now, the priority is peacefully asleep across from me strapped to tubes coming out of a machine that makes me jump with every beep.
Ok, so really now, why am I writing this? First of all, because it’s my outlet. So, thanks for that. Second of all, because I’m looking for help – people to join our fight. We sit here today, as clinical trials are not an option. We need more options. We need more research, more dollars, and more chances to cure this disease.
What am I doing about that? I’m honored, proud and a bit petrified to announce that I’m going to be running the 2017 Boston Marathon as part of the Dana Farber Marathon team. I’m all in.
You know what I am not? A runner.
I don’t run from challenges or hard times. I don’t run from fear or anxiety. And I certainly don’t run for fun.
That is changing.
Well, the last part.
Not exactly sure how we got to this point between a conversation over drinks (many a drinks) and a couple quick inquiry emails – but we’re here, and ready.
3 years ago, Dr. B told us, "although we may not be able to cure your cancer, we are going to do everything we can to treat it." Hearing these words was … yeah, not a fun moment. However, we found grace in that we were sitting in the office of the best doctor, at the best hospital in the world. He later went on to forcefully give us a timeframe of “2 years” and that was again, nearly 3 years ago. It is thanks to Dana Farber that I can even say that. It is thanks to Dana Farber that I can run with my Mom in the crowd.
On one of our recent trips, Mom and I counted that we’ve probably been to Dana nearly 100 times in the last 3 years. 100 Monday’s, parking on P5, going for labs on the 2nd floor, waiting for scripts, and heading up the 9th floor to meet with Dr. Bunnell or Dr. Bowers and/or to receive treatment. I say I’m here, but it’s not me getting poked and prodded. It’s not me fighting through bone pain or constant nausea. It’s my Mom and I want to do more.
Her disease is "incurable", but the treatment she has received from DFCI has ensured her, and all of us, a quality of life that cannot be matched. She can travel to California to walk Cam and Lex to school or laugh with the twins. She can take a family vacation to Italy and taste wine, eat pasta and walk through the Vatican. She can roll around on the floor with Riley and lift her up every time she greets Nana with a bigger hug and kiss than anyone else gets.
As for me running the marathon, I can safely say I have thought about it before - probably about 15 times in total to be precise. Once every year for the last 15 years. I think about it while cheering on runners and thinking of how amazing a feat it is. Then I wake up on Tuesday, maybe hit the gym for another solid chest and tri day, and it doesn’t cross my mind for 364 days straight. No chance I could run 26.2.
Well, there is chance and we’re going to put it to the test.
I sit here today as women and men, mom’s and dad’s, nana’s and papa’s, surround me going through exactly what we are. I ride the elevator with children without any hair covered with stickers and carrying toys, oblivious to the battle they are fighting. I watch everyone on their phones playing Sudoko or Candy Crush trying to distract their minds and delay more bad news.
I run for them.
I run for all of Dana Farber as a way of saying thank you. Thank you for the opportunity and options the last 3 years have provided and thank you for giving us many more. When I think about taking a right on Hereford and a left on Boylston, I will be thinking of my Mom, of Julie/Polly/Walter, of the Wilders, of Brian Carey, the Mullaneys, Pat and Jess, and everyone else that is impacted by cancer, the marathon or anything else in life that requires inspiration, true dedication and a perseverance to fight.
We have to fight. It seems like we Marshes are always fighting, but we are still standing. I am honored to wear the DFCI colors on April 17th and be able to continue to say thank you for everything they have done for me and our family.
Please help me in that fight: http://www.runDFMC.org/2017/ryanmarsh
Marshy
#MarshyMarathon
#RunDFMC