Madison Cay was diagnosed with a relatively unknown genetic neuromuscular disease called Spinal Muscular Atrophy (SMA) on October 2, 2007, two days shy of her 1st birthday.

SMA is a group of inherited diseases that destroy the nerve cells called motor neurons controlling voluntary movements such as crawling, walking, head and neck control and swallowing.

Madison has been reacting positively to her respiratory treatments and all of her Therapy thus far. With all of the obstacles and challenges ahead of her, Madison’s smile never fails. There are many ways you can help us in our fight to keep Madison healthy and here a long time..help us to continue her progress by making a donation for Madison's care.

Once we are able to buy all things needed for Madison, we will donate funds to SMA research for finding treatments and a CURE!  Go to www.fsma.org to donate towards finding a cure or treatment, and raise awareness of SMA!

Please Support us!

Please take just a minute to sign a petition to Congress for funding to find a cure for Spinal Muscular Atrophy at www.petitiontocuresma.com