Jaydon's Electric Wheelchair

Hey, I'm Demi and I've set up this go fund me page to help raise money for my bestfriends little boy!

We are currently raising money so his mum and dad (Laura and Simon) can buy Jaydon an electric wheelchair, to give him more independence and enjoyment from life. Jaydon is currently using a standard wheelchair which has to be pushed by somebody else.

Just a little bit about his condition - Jaydon has an unknown metaphyseal dysplasia, he's under a specialist at Sheffield childrens hospital and has been since being only a few years old. His specialist has sent jaydons xrays and scans and genetic testing on a medical platform for specialists all over the world to see only for us to be told nobody has ever seen this before. He truly is the definition of 1 in a billion. Jaydon grows extra bone on/in his joints which causes extreme restriction in movement and excruciating pain on a daily basis. He's been on 3 different pain medications daily for years now and yet we still struggles to keep it under control. Unfortunately This is not something that is going to disappear or get any better, the extra bone is growing with him which means it's likely to worsen as time goes on and jaydon will begin to be Completly reliant on a wheelchair.

As you could only imagine it's so hard for a 10year old to accept that one day will come that he may never be able to weight bare and be totally reliant on somebody else in order to move around.

This is jaydons story.. its here to educate people on his condition and raise awareness for those disabilities without a name..

Please if you can spare any small amount his family would be eternally grateful if you can't afford anything that's Completly fine. Just a simple share could help give jaydon a whole new lease of life.

Thank you so much for taking the time to read.