The200forsma - the200forsma.com - The 200 for SMA - Help Us Raise $1,000,000 for SMA in 1 Year!
General Information:
Latest News:
AVA MAE KLOIBER & TEAM AVA MAE – CURE SMA 8 Nov 2012 | 02:41 am
Our daughter, Ava Mae Kloiber, was born on March 23, 2007 and at 3 weeks of age was diagnosed with an incurable genetic disease called SMA (Spinal Muscular Atrophy), Type 1. The doctors told us...
Fight For FORD 2 May 2012 | 05:08 am
Fight for Ford pledges to raise $5000.00 for Spinal Muscular Atrophy Research. Ford Sniezek our son was born a healthy baby and passed all his newborn screening. We were so excited about starting our ...
Avery’s Bucket List.*UPDATE 5/19/12 $321,100.33 has been raised In AVERY’S NAME 2 May 2012 | 04:39 am
A baby named Avery came into the world about 5 months ago, she was born with SMA, please learn about Avery here www.averycan.blogspot.com ..Sadly Avery passed away yesterday, as you can imagine her pa...
Drews Team…helping to Stomp out SMA!!!! 23 Dec 2011 | 03:56 am
Meet Drew’s Team Yes, it takes a village and Drew has the very best! The following list includes 20 of the professionals that care for Drew and keep him healthy and happy. This holiday season we r...
Meet the amazing Craven Family stepping up to make the commitment…. 10 Sep 2011 | 06:57 am
The Sydney Craven Family Sydney was diagnosed with Type I SMA at the age of 6 months and we were assured she would not live to age two. But here I am, trying desperately to think of what to get her ...
Congratulations Sandy Gardner & Family & Friends!!!! 22 Aug 2011 | 04:21 am
I am so happy to have met the 200 Commitment Goal my family made but I would never have made it if it wasn’t for the generous and caring Antonopoulos Family. Tina and her daughter Noel wanted to stay...
Welcome aboard Quinnell Family!!!!! 17 Aug 2011 | 04:57 am
Our little miracle, Kennady, entered this world June 15, 2010, weighing 7 lbs 2.5oz and she was 20.5 inches long. During the pregnancy Kennady was VERY active, and when she was born she was a strong b...
Thank you Sehgal Family……..believing in Dr. Kaspar’s program all the way from India!! 29 Jun 2011 | 03:59 am
We are so grateful to have received a donation of $1,500 in honor of Kavya for Dr. Kaspar’s Gene Therapy Program, her mother Ritesh wrote the following poem : “Our sweet Princess Kavya, So beautiful...
In honor of Sydney Grace Potjer…. 26 Jun 2011 | 11:25 am
Sydney came into this world as a precious gift. A gift of love to her parents, a gift of friendship to all those lucky enough to have known her, a gift of courage and hope to all those that will conti...
Welcome Aboard Unite 4 Peyton….. 25 Jun 2011 | 04:51 am
Peyton was born on April 14, 2008, a healthy baby girl. Her lungs were strong as was her body. Peyton went home from the hospital with a clean bill of health to her mom, dad and big sister. In the fir...
