Hi.. as most people know my son ralphie was diagnosed with PWS at 5 weeks old, which is a rare genetic condition, he had a rough start to his wonderful life but he’s now 25 months old and is doing absolutely amazing, but still needs help regarding private physio and therapies for him to develop to his full potential. The NHS have discharged him as he’s walking.. but his low tone will always be there and he needs that extra help.

I never thought I’d have to ask for help or donations but with me still being off work to be Ralphie’s full time carer it’s impossible for me not to do this.

The charity PWSA is very close to my heart, the help and support we have received as a family has helped us in so many ways, even down to us just being able to understand Ralphie’s complex needs. They are just a phonecall away for any families affected which means the world. This charity helps with awareness.. and research into new developments regarding PWS which could change our children’s lives.

The money donated will be for Ralphie’s physio and therapy with a donation also to the charity.

Im forever grateful for everyone’s help and support ❤️