Sharon's Living Fund
My name is Sharon Ann and I am a 23 year old that has to live with a rare form of Muscular Dystrophy, coupled with Scoleosis as it often is, I also have COPD, congenital heart disease, a tracheostomy, and a stomach tube.
In May I went into cardiac arrest and had to spend a month up in Chapel Hill, getting five surgeries including a tracheostomy and a stomach tube. I am in and out of the hospital often but our local hospital is extremely under funded and only makes me worse before I have to be transferred to Chapel Hill. I am seemingly constantly sick now. The hospital where I need be seen for emergencies and for appointments is about four hours away. I need to be able to get back and forth to see specialists at that hospital and another hospital hours away to try to see a Muscular Dystrophy doctor. We do not have anywhere near the money to make these trips that I need or for any medical supplies that I'll have to pay for out of pocket. We are having such a difficult time with all of this and need help. We are also so behind on bills, our back fence is broken, our kitchen sink is broken, we cannot afford groceries towards the end of the month usually, I can't afford my medication. Things are getting more and more stressful. I keep getting sent to see different doctors that we have to cancel with constantly because we don't have the gas to make it.