Thank you for the links. I see a “caregiver’s corner” [1] over at PMP awareness. Can you give any other recommendations for the friends of families of those with PMP?

Thank you.

[1] http://www.pmpawareness.org/caregiver.htm

There is a PMP network called PMP pals. [1]

This is a group of people who have or had PMP in the past. It is a very rare and scary cancer. So hopefully people have it can stick together and help each other at least.

[1] http://www.pmppals.org/

Gao

Here’s some sources for PMP info. [1,2]

A good group site is at [3]

There are a number of people on the PMPBellybuttons site that have PMP or caregivers of those with PMP. We’re very friendly and answer any and all questions.

My husband had PMP. He had surgery with Dr Sardi and after a complete cytoreductive surgery plus heated intraperitoneal chemotherapy (HIPC) and a few round of follow up chemo (Folfox), he is approaching 2 yrs of being PMP-free. It’s such a rare cancer, you can’t say cured, but disease free. About 1 in 1 million people get PMP, which is about 300 Americans a year.

[1] http://www.pmpawareness.org/index.htm
[2] http://www.surgicaloncology.com/
[3] http://health.groups.yahoo.com/group/pmpbellybuttons/