She loves to play softball, swim, fish, to dance and go to concerts, spend time with her family and go on road trips. Madison Smith was born on October 4, 2006, and was sent home from the hospital with a clean bill of health. Just two days short of her first birthday she was diagnosed with Spinal Muscular Atrophy (SMA) Type 2, which is the second worst stage. Madison is an amazing little girl who doesn’t let her disease get in the way of living life to the fullest. She loves to swim, fish, and swim with the dolphins. She likes to dance and go to concerts, spend time with her family and go on road trips. She also enjoys cooking, baking, painting, hitting baseballs, and most outdoor activities.
Become One of Madison’s Guardian Angels…..help Madison fight her battle against Spinal Muscular Atrophy type 2. This neuromuscular disease causes deterioration of muscles. Madison has never walked or crawled and started using her power wheelchair at age 2. Volunteer with us! We raise awareness for SMA and hold fundraising events to help offset Madison’s medical bills, wheelchair repairs, medical equipment, supplements, caregiver costs, adapted vehicle repair and all things needed to help her live a healthy and accessible life.
Visit https://www.facebook.com/groups/MadisonsWish to follow her adaptive life. Thank you and I hope you enjoy watching her live life to the fullest!