PolyPeople

A Support Group
For Patients &
Their Families

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 Gardner’s Syndrome (FAP) plus Peutz Jegher’s Syndrome, Juvenile Polyposis and MYH (Mut Y Homolog) whether patient, family, friend or those with an interest in the Gene.

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!

Would you like to contact us or support us via our membership forum, click here to find out more

As well you can download our membership form which will support us, download now: Membership Registration Form (Version 28/2/11) (111).

Please Note that this site does not offer any medical advice. For this you should contact your consultant or GP. Also no details of contacts or E-mail addresses will be made available to any third party.