Maxine-A Davies

My son Kai has Cerebral Palsy, Epilepsy, CVI which means he requires 24 hours care and support. For this he relies solely on me and that can at times become incredibly tiring, mentally and physically draining as well as isolating.
By offering respite care I am able to recooperate and re charge knowing that Kai is happy and well looked after. This allows me not just little luxuries such as uninterrupted sleep, but to perhaps eat out at a restaurant, get on the tube for an outing or even just get housework and shopping completed.
On top of this they offer many other forms of support for my daughter and me via the buddies group and coffee mornings allowing us to break the isolation and meet with people who share similar situations.
This is why I want to say thank you I would be truly lost without them!

Maxine-A Davies