• COMMUNITY
  • |
  • MY STUFF
  • |
  • DISCUSSIONS
  • |
  • CHAPTERS
  • |
  • GROUPS
  • |
  • PHOTOS
  • |
  • INVITE
  • |
  • EVENTS
  • |
  • FIND OTHERS
Blog Search
Blog Latest Comments
The Beckett family efforts assisted many, my family being one . My oldest son was born very prematurely and with signif...
by PRC_Bernadette on Monday, May 21, 2012
Sorry to post this here but... I keep getting request for donations but its my family and I that could use the help. I h...
by Joe on Monday, May 21, 2012
Hi, Rob. I watched this new in tv on Wednesday. Here in Brazil, a man made a bionic hand controled using the thoughts. T...
by Selvina on Saturday, May 19, 2012
Thank you!!! I'm knowing the website and I'm liking the CRPF's work. Thank you again. Good night.
by Selvina on Thursday, May 17, 2012
Selvina, your interest is great! You have come to the right place to learn all about paralysis and SCI. Anything I can h...
by JLo on Thursday, May 17, 2012
Page  of  Total Items: 152

firstprevnextlast

This is where the staff of the Reeve Foundation is sharing up-to-the-minute information and putting some context around the news affecting the spinal cord injury and paralysis community. Not to mention insight into what's going on here at the Foundation. Feel free to comment and offer suggestions. We'll respond.
JLo
Bookmark and Share
Countdown to NYC Marathon is on for Team Reeve!
Posted by JLo
Monday, October 24, 2011
Comments (0)
This note came to us from Team Reeve runner Allegra Felter and we just had to share. She is dedicated and ready as ever to cross that finish line of the 2011 ING New York City Marathon on November 6 for Team Reeve! Here's her letter:

On November 6 I will be running the NYC Marathon. I am running in memory of my father, Greg Felter, who died of Amyotrophic Lateral Sclerosis (ALS) on June 23, 2007. ALS, more commonly known as Lou Gherig's Disease, attacks the muscle-controlling nerve cells in the brain and spinal cord that control muscle movement. ALS ultimately affects all voluntary muscles, resulting in paralysis. ALS works quick - the disease usually progresses rapidly with most individuals dying within 3- to 5-years of diagnosis. At this time, the causes of ALS are unknown nor is there a cure.

My family watched my father's once strong and lean frame wither away while his mind remained acutely sharp. Despite the clinical trials, medication, and therapy there was nothing for my dad to do but wait out what he referred to his "death sentence." As the disease progressed, he became utterly dependent on others to fulfill nearly every activity - big and small. We fed my father, bathed and dressed him, wrote and surfed the Internet for him, transported him from wheelchair to bed, rolled him over when he wanted to move, adjusted his pillows, lit his cigarettes; even scratched the itch on his nose.

Dad was a main supporter of my athletic pursuits. Early on, he rigged a T-Ball stand out of an old hose for me and my sister to practice our swing. For my 9th birthday, my dad made me my individual baseball card that remains one of my prized possessions. Dad shuttled me to early morning swim practice and was an enthusiastic timer and supporter at my swim meets. I know that if he were alive, he would be very proud of me and here on November 6, bellowing in his characteristically gravely voice "Hustle Leggy!"

I have partnered with the Christopher & Dana Reeve Foundation and have committed to raising 5,000 dollars for this tremendous organization. After actor Christopher Reeve was paralyzed in an equestrian competition in 1995, the Foundation has been committed to improving the quality of life of those individuals with paralysis. When my dad lost mobility in his legs, he was confined to his wheelchair. Simple activities such as going out on long, country drives or eating out at a restaurant posed several challenges. The Reeve Foundation provides grants to community organizations around the country to modify homes and buildings, provide computer-assistance technologies, improve transportation services for individuals, and offer caregiver support and respite. My family can attest how crucial these services are in caring for a person with paralysis.

So, I have got the running covered- what you need to do is help me raise the $5,000. I know its said all the time - but really, ever dollar counts. The easiest (and preferred) way to donate is to click the link and follow the simple steps. Just so you know, all contributions made to the Christopher & Dana Reeve Foundation are fully tax-deductible. Additionally, many companies have a matching contribution program - does yours?

Simply, thank you. Thanks for helping me with my goal and remembering my father. Keep me in your thoughts November 6 because 26.2 miles is no joke!

Best,
Allegra



Like us on Facebook
 Follow us on Twitter YouTube LinkedIn CarePages Life Rolls On Foursquare Tumblr Digg Blogger Reeve Foundation Community Join our community.
 
Categories:  Team Reeve