Welcome to CFSN

The Cystinosis Family Support Network (CFSN) vision is to support families affect with Cystinosis.

To support as many families in the UK as possible. To provide family assistance and education to the public, relatives, and medical professionals who have not been in contact with this disease.  CFSN is a non-profit organisation which relies on support from volunteers, family members of children and young adults diagnosed with cystinosis, and a small number of UK companies. 

We currently have over 134 website members, and over 1870 individual supporters, these individuals have sponsored events, purchased balloons, and generally help raise funds.
 

       
Up and Coming Events

We'll be updating you all soon on what events are planned for 2007.

We are hoping to have the following:
 

Read More 13 May 2007 - T he Leeds Half Marathon plus 1.5 mile family fun run.
Read More Gilroyd Working Men's Club, Barnsley
 
 

 

Latest Events

   
Latest News

New Family Story Online:-

The McTear Family

Daniel was born 28th june 2003 was a healthy 8lb baby.....

full story here

 
 
 
 

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CFSN are not responsible or liable for any diagnosis made by a user based on the content of the website. CFSN is not liable for the contents of any external internet sites listed, nor does it endorse any commercial product or service mentioned or advised on any of the sites. Always consult your own GP if you're in any way concerned about your health.

All content within CFSN.co.uk is provided for general information only, and should not be treated as a substitute for the medical advice of your own doctor or any other health care professional.