Recently diagnosed with PMP

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Hi all, 

I just joined this group tonight (6 Feb 2022).

I am 66 years old, retired, married with 2 children a daughter who is a chartered biologist and editor at a pharmaceutical publishing company and a son who was born with Spina Bifida and hydrocephalus who has a few more medical issues on top.

I was diagnosed with PMP on 14th Jan 2022 and am now under one of the Basingstoke specialists.

I had pains in my right side (appendix?) on Sunday 2nd Jan and called my GP surgery where an answerphone told me to call NHS111 during out of hours, so I called 111 and when 111 said it would be about 45 mins till I could speak to someone, I decided to go online to NHS111 and answer the online questions. The results on this indicated I needed to seek medical help so I clicked on the call back feature, this was early afternoon. I got a call at 23:30 hrs from an admin to tell me that a clinical person would call within 12 hours.

Monday 3rd I decided around 10am I would take myself off to my local A&E having not had a call, the clinical call came about 2:30 pm on the Monday after I had seen a few doctors at A&E.

As they couldn’t get the bloods they wanted from me I ended up being sent home having been told I would be called back on Tuesday for further tests and follow up.

About 9:30am I got a call asking me to go in and report to a specific ward for the further tests etc. Where a wonderful young MEA? trained nurse had no issue getting my bloods and then I got sent for a CT with dye. Following this I was admitted for further investigation e.g. key hole surgery for my enlarged appendix, I was told later that Tuesday evening.

Wednesday I had the procedure and I was told Thursday morning that they had not removed my appendix, as was originally suggested/Implied, and they now suspected PMP and that they had taken a biopsy (I later found out of the Omentum) and could only be confirmed after the pathology reports were back which could take 3 weeks. They did show me some photos of what they found which I quickly snapped on my smartphone.

i was on intravenous antibiotics after the key hole surgery. Once my bloods were OK (the markers I have now read about) I was allowed to go home. However prior to discharge they had arranged for me to speak with the specialist cancer nurse team. Rather shocked having heard all this.

i have now seen one of the Basingstoke team, had a colonoscopy at his request at my local hospital and three vaccinations as I am going to need cytoreductive surgery and HIPEC, date TBA, hopefully soon, as I have 4 quadrant PMP.

Just a quick summary of my year to date. LOL.

  • Hi and a very warm welcome to the online community which I hope you'll find is an informative and supportive place to be.

    Thanks very much for taking the time to tell us your story to date as I'm sure others looking for someone with a similar diagnosis will find it very useful.

    I'm not a member of this group, as I had a different type of cancer, but I'm sure the other group members will try to help answer any questions you have and share their experiences with you.

    Wishing you all the best with your upcoming treatment.

    x

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     "Never regret a day in your life, good days give you happiness, bad days give you experience"

  • Hi , you are in great hands with the Basingstoke team. I was diagnosed in 2010 and had surgery in Basingstoke in 2011. Have you heard any more about your surgery?

    Happy to answer any questions you might have. You can place them here or send me a friend request and connect that way.

    Angela


    Angela 
    Pseudomyxoma peritonei survivor
    Trustee
    Pseudomyxoma Survivor