What we do
Provides nationwide support and friendship to families and carers and raise awareness of Cri Du Chat syndrome amongst the medical profession, parents, carers and the general public. Cri du Chat Syndrome is caused by a bit missing from one of your child’s chromosomes, and it’s pretty rare, around 1 in 50,000. Most of the time it’s just random – there’s no reason behind it, no root cause.
Services include a support group, online information, events, in person meetings. There's also a Facebook page.
Can anyone use this service?
Anyone can contact us directly