Hi, my name is Melissa and I live in Plantation right outside of Davie. My daighter Jaelie has a very rare neuromuscular genetic disorder called Spinal Muscular Atrophy Type 1. It is the most severe form of SMA. These kids usually don't live past the age of 2 and my daughter is miraculously still here at the age of 2 and a half. She depends on a numerous amount of machines to get her through her every day. We usually get a charitable donation from the milk bank at Austin and they have been experiencing a shortage for 2 months. We have not gotten any shipments and I'm starting to get very nervous because I'm having to give her less and less and she actually has been very very sick these past 2 weeks and I just KNOW it's from the lack of breast milk! I hope that you can find it in your heart to help me and my baby out! Please let me know if we sound like a possible candidate to recieve your precious gift.
Melissa & Jaelie
meljae0409@gmail.com.