Our Story

Who We Are.

green_grass_in_the_park-1024x768A PATIENT SUPPORT GROUP

We are a support group who aim to provide support and information to anyone whose lives are or have been affected by Familial Adenomatous Polyposis and Gardners Syndrome (FAP) plus Peutz Jeghers Syndrome, Juvenile Polyposis and MYH (Mut Y Homolog) whether patient, family, friend or those with an interest in the Gene.

 

PolyPeople is a Patient Support Group dedicated to assisting people suffering from FAP/ Familial adenomatous polyposis. For clinical issues you must seek the advice of a QUALIFIED Healthcare Professional

Support PolyPeople

If you would like to take part in any of the fundraising we do or you want to do your own fundraiser for PolyPeople please get in touch with us, we would love to hear from you!

Contact Us

The Committee

Peter Grainger
CHAIRMAN
Stephanie Green
SECRETARY
Jason Brace
TREASURER/HEAD OF FUNDRAISING
Ruth Pike
Co-Webmaster
Katherine Brace
TEENAGE LIAISON OFFICER
David Harris
Co-Webmaster
Thelma White
GENERAL COMMITTEE
Louise Marr
GENERAL COMMITTEE
Martin Green
GENERAL COMMITTEE
Rachel Ward
GENERAL COMMITTEE
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