Cure SMA Walk-n-Roll
Tuscaloosa, Alabama
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On October 11, 2006, Jennifer and Jason Patrick became the proud parents of a precious baby boy, Logan Patrick. His parents thought he was such a happy, healthy baby. When Logan was about four months old, however, they noticed that he was not meeting his milestones such as lifting his head and rolling over. On March 27, 2007, the pediatrician and pediatric neurologist diagnosed Logan with Spinal Muscular Atrophy, type 1. The doctors told his parents that there was no cure and most babies with SMA, type 1 do not live to see their second birthdays, and that baby Logan would require a feeding tube, a bi-pap to help him breathe, an oxygen machine, a suction machine, etc. Unfortunately, the disease has progressed where Logan has all of the aforementioned equipment. But with the prayer, hope and love from our families and friends, we gladly tell you that Logan will turn three on October 11, 2009!!
Please help us celebrate by joining us at the Cure SMA Walk in Tuscaloosa, Alabama.





Learn more about Logan and his progress by visiting his caring bridge site.

View Logan's feature story in The Tuscaloosa News.




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