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FAMILIES OF SPINAL MUSCULAR ATROPHY

Dylan's Angels Walk n Roll

Walk for our cousin Dylan - Mike, Phil & Aly

Dear Friends,

As many of you already know, our nephew, Dylan was diagnosed with Spinal Muscular atrophy (SMA), the number one genetic killer of children under the age of two. This condition affects crawling, walking, head and neck control, and even swallowing. One in every 6,000 babies is born with SMA. Of children diagnosed before age two, 50 percent will die before their second birthday.

On Saturday, September 24th, we are going to participate in the First Annual Walk N' Roll to Cure SMA in Long Beach, New York. This walk is to help raise money for research to help SMA children, like Dylan and hopefully find a cure.
We are asking that you sponsor us. Any donation that you may wish to make will be greatly appreciated. Many thanks for your support -- and don't forget to forward this to anyone who you think might want to donate too! Sincerely, Liz and Bob Goldstein

Supporters

Comment Donation
Anonymous our love and much luck to you and to Dylan's family
$50.00
Rose and Bob White To a beautiful family...we love you
$50.00
Maylin Travers We hope and pray for Dylan and all other ALS kids and their families.
$50.00
Liz and Robert Goldstein In honor of our nephew Dylan and all SMA children
$1,500.00
The Jalali Family
$30.00
Anonymous Thinking of you all...........xox
$15.00
Anonymous
$50.00
Anonymous
$50.00
DeBenedetto Family For a wonderful family and an important cause.
$25.00
The Zim Family In Honor of Dylan and in hope for a cure for SMA
$50.00

Donation Summary

Raised Offline
$0
Raised Online
$1,870
Total Raised
$1,870
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