About: Landon, born on 12/31/2013, has Spinal Muscular Atrophy (SMA) Type II. Landon will never walk, his ability to move is extremely limited, & he will one day require breathing assistance. Landon has started the first-ever approved treatment that targets the underlying genetics of SMA. The medical field is on the verge of further breakthroughs that will continue to change the course of SMA for everyone affected. Follow Landon’s story on Facebook and to learn more about Spinal Muscular Atrophy, visit www.CureSMA.org
Landon
About: Landon, born on 12/31/2013, has Spinal Muscular Atrophy (SMA) Type II. Landon will never walk, his ability to move is extremely limited, & he will one day require breathing assistance. Landon has started the first-ever approved treatment that targets the underlying genetics of SMA. The medical field is on the verge of further breakthroughs that will continue to change the course of SMA for everyone affected. Follow Landon’s story on Facebook and to learn more about Spinal Muscular Atrophy, visit www.CureSMA.org
Follow his Journey. God Bless!
Landon on FacebookSpecial Treat: Landon is our Sam’s Kid selected for the month of March 2017. As his special treat, Landon requested a shopping trip to Toys R Us.
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