Duchenne muscular dystrophy Help save my son and others plz

This is absolutely killing me to write this out and I can only dread to think what it must be like for others but I have a five-year-old son named Archie who was diagnosed with Duchenne muscular dystrophy a month ago after two years of pushing doctors private healthcare people , And hospital workers due to knowing there was something not quite right with my son after being prodded and poked and having a different blood tests. He was finally due to have an operation to have his tonsils and adenoids out a day before the operation the two hospitals collided with each other and gave us an emergency phone call , to not go ahead with the operation and we were demanded the next day to go to the evalina Hospital in st Thomas hospital London. Upon arrival we sat in the reception not knowing what was going on , I mean we always had an idea that there was something not right but never in our minds would we think that we would be diagnosed with this? This is an un curable , untreatable unable defect wrong with our son. After being told that he would be in a wheelchair by the age of 10 and we needed to start looking for specialist wheelchair for him to help his posture. And then to be told that there are many types of muscular dystrophy, but our son has the worst type. This is a horrible thing that takes the lives of people often before their early teens. So I have decided to do a 24 hour charity event one to help praise enough money to get my son a specialist wheelchair and 2 to go towards the hospital to help research into a way to help save my boy. So I think you all right now for any donation whether it be 50p or £50. All I can do is say thank you from the bottom of our hearts.

me and a friend will be live streaming a Facebook live 24 hour pool event in order to raise money for awareness not only for my son but others too. This will be on the 9th of August starting at 7 pm at night.

Zoe and Duane