YOUNGSTER Leyton Wright is nearing his fundraising target after just six months.

Leyton, who turns two on Sunday, was diagnosed with spinal muscular atrophy last year which causes muscle weakness and progressive loss of movement.

MORE TOP STORIES:

His parents, Tammy, 24, and Dominic, 25, launched an appeal to buy their little boy a specialist SnapDragon wheelchair costing £25,000 to enable him to be more independent.

Unlike conventional wheelchairs, it can be lowered to allow him to play at floor level with his friends.

And after ‘overwhelming’ support from the community, £18,000 has been raised so far.

The Avallon Way couple, who are due to get married next month, hope he will be able to hire an electric wheelchair so he can ‘scoot’ down the aisle with them.

Tammy said: “We are completely overwhelmed by everyone’s kindness. Everyone has really helped. He is a much loved little boy. It’s amazing how the community have worked together to try and get Leyton when he needs.”

Leyton was diagnosed when he was 17-months-old. Leyton’s core muscles have already been severely affected which has made him weak and as a result of this he will never be able to walk let alone stand without a form of aid.

In time this condition will affect other muscles in his body meaning simply sitting unaided could become impossible.

Fundraising activities have included raffles, fun days, pub events, sponsored waxes and donations.

The latest cheque was from Queen Elizabeth Nursery School in Blackburn who held a minion day. An incredible £294.23 was raised from the day and a cheque was presented to Tammy and Leyton.

Tammy said: “Just lifting a cup can be hard work for him. We have to keep him supported as much as we can.

“It is upsetting for us seeing other children reach their milestones but it’s something we have to deal with every day and we have to look at the positives with Leyton.”

To donate towards Leyton’s wheelchair visit www.annabellerosefoundation.co.uk/leyton.