Primary Ciliary Dyskinesia

Support Groups

The Dutch PCD support group have their own site with information provided in both Dutch and English

Susanne's German PCD/KS Support Group
Information in several languages including English

The Centre for PCD diagnosis and therapy in Pisa, Italy have an Italian language website about their work.

The P.C.D. Foundation is a support group for P.C.D. patients in the United States

The Brompton Fountain are a network of 'Brompton Families' who you can talk to by phone. As parents of children with cardiac or respiratory conditions, they will be on hand to offer support to others who are experiencing similar emotional and practical difficulties. Their aim is to provide a listening service so no parent feels alone.

 

 

News and Events

Article in Wellcome Trust Magazine 8/1/2010
Postponed PCD Adult Lunch from 10th January to 28th February 8/1/2010
Winter 2009 Newsletter 30/11/2009
Great South Run 24th October 2010 30/11/2009
Fiona's Colourful FM interview 1/10/2009
National Voices Survey 10/9/2009
PCD Article in Daily Express 10/9/2009
Jeans for Genes Campaign 2nd October 2009 10/9/2009
Genetic Counselling Research 8/4/2009
PCD - encouraging children to be active