Ford’s Friends

There are many children battling Spinal Muscular Atrophy and many of those children’s families have created foundations or organization to raise funds for a cure and awareness of SMA.  Please take a moment to visit some of these sites and see what they are doing and what you can do to help end the #1 Genetic KILLER of infants!

Families of SMA

Getty Owl Foundation


Gwendolyn Strong Foundation

B4SMA Blankets

Sophia’s Cure Foundation

Miracles for Madison and Friends






One thought on “Ford’s Friends

  1. Kayla and Scott just wanted to let you know that you are not alone in this area of having a baby with sma type 1. (sorry I had to find you by the way of the newspaper. that is so sad. Hope that guy is caught and has to pay).
    I/we live in Mt. Chestnut between Prospect and Butler. We had 3 babies (with type 1) born in 1992,1994 and 1996 and first one lived 6 months, second one lived 5 months and 7 months. it was a difficult thing to go thru. Our Faith got us thru. in 2000 we adopted 2 boys that are now in there late teens.
    I’m here for support if you need any, just to have a listening ear..
    I want to read the rest of your story on your site…you have done a great job at documenting everything and have all the information to inform everyone about the gentics of the disease.
    Your family is in my prayers. There has to be a cure somewhere.
    VirLinda and Randy Bieber

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