Can we cure CS now? - CostelloKids – A UK Registered charity –

MENUMENU

Parent Resources
Families
- - Ace
  - Albie James
  - Alex
  - Ali
  - Arden
  - Brenan
  - Brett
  - Bruno
  - Clay
  - Daniell
  - Dario
  - David
  - Ethan
- - Hanalei
  - Haylie
  - Helaina
  - Isla
  - Ivy
  - Jalasa
  - James
  - Jane
  - Jasper
  - Jaylon
  - Jenna
- - Kati
  - Kelsi
  - Kevin-Austin
  - Kiley
  - Logan
  - Lucy
  - Max
  - Priscilla
  - Rachel
  - Regina
  - Thorin
- - Samson
  - Selin
  - Shane
  - Ulysses
  - Valentina
  - Vera
  - Westin
Conferences
Publications
Stories
FAQs
Contact Us

Can we cure CS now?

Can we cure CS now?

If there is no cure, then how do we treat our children?

Who authored the FAQ?

Donate

Donors & Fundraisers

Social

Facebook

International Costello Syndrome Websites

Costello Syndrome Family Network (USA)
French Costello & CFC syndrome Website
Italian Costello Syndrome Website

International Costello Syndrome websites

Costello Syndrome Family Network (USA)
French Costello & CFC syndrome Website
Italian Costello Syndrome Website

Related syndrome support

CFC International
RASopathies Network
Neurofibromatosis, Inc – USA
Neurofibromatosis, Inc. California – USA
Noonan Syndrome Association – USA
The Children’s Tumor Foundation – USA
The Neuro Foundation – UK
The Noonan Syndrome Association – UK

Support Organisations

Family Blogs

le syndrome de costello
ulysses et moi sucre de pasteque
Life With Bobean! Living with Costello Syndrome
Vera de Zwarte’s website
Igor – Costelinho Do Norte (0n Facebook)
Was this in the plan????
Me and My Son, Joey
Ourprincessnicola
Living in invisible cities
lilyinthepink
westinthomas
zaneleland

Designed by www.creativevideosolutions.co.uk

FAQ