Hello PMP,

I just want to give you a warm welcome to our forum and say I'm sorry to hear you were diagnosed with Pseudomyxoma Peritonei (PMP) last June.

When reading your post I thought of another member, [@Luckyme]‍  who was diagnosed with Pseudomyxoma Peritonei and hopefully you two will have a chance to chat.

Other than that, stay strong PMP and do come back to let us know how you are getting on.

Best wishes,

Renata, Cancer Chat Moderator

Hi there.

My dad was diagnosed with PMP last year. Went through a massive 13hr ok and it has come back again this year so he has to go back.

I came on here to talk to other who know people going through it or people who have it.

Hey,

Wondering how it is going for you? My dad was diagnosed with it just 6 months ago, but sadly didn’t make it. He passed away last week. I know it’s an extremely rare form of cancer, but I thought it is quite an aggressive type too. So I would love to hear of your experience and how your dads operation worked out. I could only imagine what your family must be going through. I hope his treatment is going well.

I will keep you all in my prayers x

My heart just broke for you!

That's awful.

How old was your dad if you don't mind me asking.?

My dad has had two operations now.  And now he is on regular chemo every 2 weeks. Wont know if it is working until his CT scan. I'm hoping to god it does. I really couldn't bare losing him.

Did your dad have any operations?

That is so young.

My dad has managed to avoid the stoma bag. 

Yes it's very hard waiting to see if it has all worked.

Hoping for good news. 

Thankyou