SMA MEDICAL SUPPLY

My name is Dana Craven and my first born child was diagnosed with spinal muscular atrophy (SMA) at the age of 6 months. Her doctors told us that she would quickly lose her ability to move, swallow, and breathe, and that she would never live to see her second birthday. But now that she's a teenager, I can say with certainty that the doctors had that piece of it wrong. Although she did lose her ability to swallow, move, and breathe on her own, she's never lost her interest in the world, her sense of humor, or the ability to brighten the lives of everyone who knows her!... I began SMA Medical Supply in the summer of 2007 in order to serve the needs of SMA families. It's almost impossible to believe I've been doing this over a decade! The motivation for starting my little company was simple: frustration with the medical supply industry! As if the day-to-day physical, emotional, and financial strains of having a severely disabled child were not enough, we had a terrible time finding a DME..