THE family of a Kidderminster boy who has a muscle disorder are organising a fundraiser to help support research into the condition.

Wade Haynes has muscular dystrophy, which causes the muscles in his legs in his legs to deteriorate and also effects his heart.

The seven-year-old Comberton Primary School pupil, who also has autism, is needs to use a wheelchair because of the disorder.

Currently, there is no cure but Wade’s mum Alison and sister Jodie have organised a tombola at Kidderminster College on January 22 to help raise funds for research into trying to find a cure.

And the family are now appealing for donations of prizes to boost the tombola.

Jodie said: “Wade’s legs hurt on a daily basis and this is him starting to lose the use of his legs. He uses a wheelchair day to day.

“It is hard to explain to Wade what is happening as he finds it hard to understand some things with due to his autism.

“There is no cure for muscular dystrophy and this is hard as we can't stop his legs hurting or help in anyway.

“We are holding a tombola to raise money that will go towards research and trying to find a cure. It would be great if people could help by donating prizes for this and help Wade and people like him to get better.”

Anyone who is able to donate prizes or wish to buy tickets for the tombola can contact Jodie on 07492 202205 or Alison on 07766 168503.