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Pseudomyxoma survivor support network

Pseudomyxomasurvivor's picture
Pseudomyxomasurvivor
Posts: 1
Joined: Nov 2011
Nov 20, 2011 - 6:19 am

Hi all I am new to this forum so I hope to get to know some of you better and get to read your stories.

I am posting as I was diagnosed with pseudomyxoma peritonei in 2008 and wrongly given less than 3 months to live.

I would love to hear from anyone touched by this cancer. x
janineramage
Posts: 1
 Joined: Dec 2011
Dec 11, 2011 - 6:34 pm
pmp

I too have been recently diagnosed with PMP on november 28 I am still recovering from surgery. I am at a loss and would greatly love to hear any comments, treatments etc.
Tina Brown's picture
Tina Brown
Posts: 1056
 Joined: Nov 2009
Dec 12, 2011 - 3:58 pm
PMP?

I've not about this cancer. Can you tell me about it?

Thanks Tina xxxx
AussieMaddie's picture
AussieMaddie
Posts: 345
 Joined: May 2011
Dec 14, 2011 - 7:24 am
Lack of knowledge

Hi,

I've not heard of it either. Would it be painful to talk about it?

AussieMaddie
abrub's picture
abrub
Posts: 1429
 Joined: Mar 2010
Dec 17, 2011 - 8:20 am
I'm an Appendix Cancer survivor

tho not PMP. However, there is an excellent closed PMP/Appendix Cancer support group on FB, if either of you are interested.

While I had mucinous adenocarcinoma, I did not have the belly-full of mucin common to PMP, just some small pools. I know that I had the same treatment at Memorial Sloan Kettering as my friend with PMP: debulking fo