Tell me about treatment - medical and devices - 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

Tell me about treatment – medical and devices

Tell me about treatment – medical and devices

Can you give me tips about specific foods?

When do they appear, do they change over time?

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