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Michael Harrison Nichols
Summer Fun, August 2007
March 18, 1999 - February 17, 2008
Welcome to Harrison's page and to our family's journey. Harrison was diagnosed with Stage IV Neuroblastoma, shortly after his 3rd birthday, in May of 2002. In the 5 plus years since diagnosis Harrison had received over 35 cycles of chemotherapy, 4 surgeries to resect the primary tumor and area lymph nodes, radiation to his primary tumor site, left orbit, lymph nodes, spine, brain and liver, 6 cycles of arsenic trioxide, 5 cycles of GM-CSF/3F8 antibody treatment, 2 cycles of dose escalated heat in-activated 3F8 antibody treatments, 4 cycles of radiolabeled 3F8 antibodies along with 5 cycles of Accutane and a peripheral stem cell rescue. Harrison was treated in New York City at Memorial Sloan-Kettering Cancer Center and in North Carolina at Carolinas Medical Center and he attended The Davidson Day School in North Carolina. Harrison was filled with an unbreakable courage and a strong spirit; he taught everyone he met to live with love and not fear. We were honored and proud to be his family and to share his remarkable journey.
Journal
Tuesday, August 19, 2008 1:21 PM CDT What does a snail say when it rides on a turtles back? “WHAHOO!” —my friend Dave
Last week, I was speaking with one of my dad friends from MSKCC, Dave, who also lost his precious son to NB over a year ago. Dave, with so much kindness and love, reminded me that life is always a matter of perspective. He helped me to remember that were it not for our sons, the lives they led and the places it led us we would never have had the wonderful life we had and still have. We recapped our son’s adventures, both medical and recreational; the unbelievable people and other heroes we met along the way; and the privilege it was to stand by our children every moment of every day. He doth profess that we have indeed had a wonderful life…not everyone would see it that way…it’s a matter of perspective. From where the snail sits, atop a turtle, life seems pretty good.
We talked about how amazing our boys were/are and how they are still making a difference. He asked me…”do you know how lucky we were to have spent everyday with our children, everyday of the 5 plus years each of them was in treatment?” He said he did the math and that in the few years we each had (how ever short they seemed) we had more hours that most of our friends will ever spend with their children because of school, work, and the activities that a traditional life brings. He said…”we were lucky, we had a wonderful life and love with our boys.” He’s right…not everyone would see it that way…it’s a matter of perspective. From where the snail sits, atop a turtle, life seems pretty good.
I needed Dave to remind me, usually I can remember but sometimes it’s hard, not to let what you’ve lost out-way what you’ve had. He’s right, we had more than what some will have in a whole lifetime. So often, it just does not seem like enough but it was all I was given.
Last Sunday, it was six months…how did six months go by? Time is one of those incredible elements that can seem to soar past you at an incredibly slow pace. Kind of like a snail before and during his ride on the turtle.
I miss him, and love him, both, in life and in death…
Thank you, Dave for sharing your perspective.
WHAHOO, Gina
p.s. as promised my Fred’s team page is up and running. The training is grueling but my role model is mightier. The donations are going well, but the sky is the limit. The more we raise the better the chances for a cure and the hope that one less child will suffer and one less parent will be left behind. No amount is too small…it all adds up…it’s just a matter of perspective.
Read Journal History
Hospital Information: MSKCC 1275 York Ave New York, NY 10021
Links: http://harrisonnicholsfoundation.org
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