calling everyone from west london with childrens with cp spastic.
Hi Everyone, im new here, my name is nerea, my son is 15 months, he just been diagnosed with spastic quadriplegia, cp.
We ve being referred to a lot of groups but never met anyone in the same situation, so im looking to open a group for parents so we can share experiences, and support each other. Hoping to get a good answer. Thanks!

Hello Nerea. My daughter also spastic CP - based in West London.
Will be happy to share with some information...
Lets keep in touch..