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
[info]As well you can sign-up via our membership form which will support us, sign-up now by clicking here.[/info]
[error]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
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