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 Welcome to Pseudomyxoma Survivor, the home of the support network for survivors and carers of Pseudomyxoma Peritonei (PMP).
Our support network offers emotional encouragement and a community where fellow patients and care givers can collaborate online. This allows us to share our stories, enforcing the fact that we are not alone in this fight, as well as further the growing online PMP community. The community has already proven an invaluable source of strength to so many survivors of this rare disease.
We now have an online support network of over 400 people easily contacted through this site and through our online Facebook group, all completely free of charge with no subscriptions. Although this web site is UK-based, we have fellow survivors WORLDWIDE in our support forum. Support is
via email, -
over the
phone,
-
by
joining the Facebook
support group where you will find hundreds of
fellow PMP survivors from all over the world.
This help is offered to anyone fighting this disease, be it as patient or loved ones. Pseudomyxoma Survivor is a registered charity. As such, in addition to offering emotional support and practical advice on living with PMP and its managing symptoms, our aim is to raise more awareness of this disease.
As a survivor and carers group, information here is from our perspective - we are not health care professionals. We are all individuals, everyone is different. We recommend that you take advice from your doctors for specific information.
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