Brantley Muscular Dystrophy

My name is Lauran Scherretz. I recently found out that my 5 year old son has Duchenne muscular dystrophy. There is a trial in Florida going on and we are trying to get to be apart of it. This will involve a 8 hour round trip once a week for treatment, weekly local physical therapy, biweekly appointments with his muscular doctor, and appointments with a cardiologist. So, as you can guess, a lot of medical bills. I've never done anything like this before so it's completely out of my comfort zone, but we will need the help.