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My Story-My Battle with Pseudomyxoma Peritonei (PMP)

This blog is the story of my battle with a very rare cancer called Pseudomyxoma Peritonei (PMP). Its an on-going story in a diarised form which I am updating regularly. Only two or three people in every million will develop this rare condition. There are few support groups and many people have never heard of the condition. Hopefully my blog will help fellow sufferers understand that they are not alone as I share my thoughts and feelings.

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My Story-My Battle with Pseudomyxoma Peritonei (PMP) | cavecrawlerstory.blogspot.com Reviews

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This blog is the story of my battle with a very rare cancer called Pseudomyxoma Peritonei (PMP). Its an on-going story in a diarised form which I am updating regularly. Only two or three people in every million will develop this rare condition. There are few support groups and many people have never heard of the condition. Hopefully my blog will help fellow sufferers understand that they are not alone as I share my thoughts and feelings.

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My Story-My Battle with Pseudomyxoma Peritonei (PMP) | cavecrawlerstory.blogspot.com Reviews

https://cavecrawlerstory.blogspot.com

This blog is the story of my battle with a very rare cancer called Pseudomyxoma Peritonei (PMP). Its an on-going story in a diarised form which I am updating regularly. Only two or three people in every million will develop this rare condition. There are few support groups and many people have never heard of the condition. Hopefully my blog will help fellow sufferers understand that they are not alone as I share my thoughts and feelings.

INTERNAL PAGES

cavecrawlerstory.blogspot.com

1

My Story-My Battle with Pseudomyxoma Peritonei (PMP): December 2009

http://cavecrawlerstory.blogspot.com/2009_12_01_archive.html

My Story-My Battle with Pseudomyxoma Peritonei (PMP). Thursday, 24 December 2009. Its Christmas Eve 2009. I'm currently sat in work waiting to go home. The family have all gathered at home and are waiting for me. The girls have stayed at Mum's the last few days and been to the Theatre Royal in Bath to see Sleeping beauty. Its been snowing and the country pretty much brought to a standstill. Things are starting to melt now and the frecast is for a warmer day tommorow. Saturday, 19 December 2009. The drive...

2

My Story-My Battle with Pseudomyxoma Peritonei (PMP): Feb 14th 2010-First Annual Scan.

http://cavecrawlerstory.blogspot.com/2011/02/feb-14th-2010-first-annual-scan.html

My Story-My Battle with Pseudomyxoma Peritonei (PMP). Wednesday, 16 February 2011. Feb 14th 2010-First Annual Scan. So it was that we found ourselves on the now familiar road from Bristol to Basingstoke. My appointment was at 10:45am so we had an early start. I had not been allowed to eat or drink for four hours before the appointment and made a special effort to get up early enough to allow me to have a light breakfast as I can’t start the day without food! It’s not unpleasant just very strange an...

3

My Story-My Battle with Pseudomyxoma Peritonei (PMP): The First Bombshell

http://cavecrawlerstory.blogspot.com/2009/11/first-bombshell.html

My Story-My Battle with Pseudomyxoma Peritonei (PMP). Friday, 13 November 2009. I left work early on the day of my appointment at Southmead Hospital. I was meeting the consultant Miss Burt and the specialist nurse Lesley Atkin. It was a hot day in June and the waiting room was not air conditioned and stuffy. As usual they were running a good hour behind. Cancer, I heard. The CT would give them more of an idea of the problem along with the colonoscopy and enable them to put a care plan together. I was...

4

My Story-My Battle with Pseudomyxoma Peritonei (PMP): Basingstoke-THe Big Day arrives

http://cavecrawlerstory.blogspot.com/2010/02/basingstoke-big-day-arrives.html

My Story-My Battle with Pseudomyxoma Peritonei (PMP). Thursday, 18 February 2010. Basingstoke-THe Big Day arrives. Finally the day we had dreaded arrived. We were all packed and ready to go. Mum and Dad arrived at 09:00 to pick us up. We wanted to get on the road early and ensure we had plenty of time to get to the hospital. It also meant we got our goodbyes to the family out of the way quickly and did not have time to dwell on it. I tore myslef away and we got into the car. We were soon on our way.

5

My Story-My Battle with Pseudomyxoma Peritonei (PMP): Results of SeHCAT Scans....

http://cavecrawlerstory.blogspot.com/2015/04/results-of-sehcat-scans.html

My Story-My Battle with Pseudomyxoma Peritonei (PMP). Friday, 3 April 2015. Results of SeHCAT Scans. So it’s official, I am suffering with bile salt malabsorbtion. The results of my recent SeHCAT scans have shown this to be the case. However I am lucky enough not to be suffering from the usual side effects experienced by most people (chronic diarrhoea) and instead it has manifested itself in my low vitamin B12 count. There are three classifications of types of bile salt malabsorbtion-. My mum stumbled up...

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keeshamist-pmp.blogspot.com

A PMP survivor!!

http://keeshamist-pmp.blogspot.com/2010/03/i-just-realised-how-long-it-has-been.html

As I mentioned in the title blurb - I am sharing this blog because I was asked to …. My health problems but to offer hope. SO- If sharing my journey helps even one person to cope with a cancer diagnosis such as PMP/Appendix cancer then I am very happy indeed! Life is such a blessing each and everyday! Treasure each of the small things life brings. And always remember -. The small things in life are really the BIG things! Sunday, March 7, 2010. I just realised how long it has been since my last post .

keeshamist-pmp.blogspot.com

A PMP survivor!! : A follow up on my surgery

http://keeshamist-pmp.blogspot.com/2010/10/follow-up-on-my-surgery.html

As I mentioned in the title blurb - I am sharing this blog because I was asked to …. My health problems but to offer hope. SO- If sharing my journey helps even one person to cope with a cancer diagnosis such as PMP/Appendix cancer then I am very happy indeed! Life is such a blessing each and everyday! Treasure each of the small things life brings. And always remember -. The small things in life are really the BIG things! Sunday, October 24, 2010. A follow up on my surgery. The Prof put a gel called Adept...

keeshamist-pmp.blogspot.com

A PMP survivor!! : My Latest CT Scan

http://keeshamist-pmp.blogspot.com/2008/07/my-latest-ct-scan.html

As I mentioned in the title blurb - I am sharing this blog because I was asked to …. My health problems but to offer hope. SO- If sharing my journey helps even one person to cope with a cancer diagnosis such as PMP/Appendix cancer then I am very happy indeed! Life is such a blessing each and everyday! Treasure each of the small things life brings. And always remember -. The small things in life are really the BIG things! Friday, July 4, 2008. My Latest CT Scan. I am now trying to decipher things like;.

cancer-schmancer.blogspot.com

Dancing To The Rythm Of A Ticking Clock: December 2011

http://cancer-schmancer.blogspot.com/2011_12_01_archive.html

Dancing To The Rythm Of A Ticking Clock. Formerly Cancer Schmancer- subject to change without notice. Wednesday, December 28, 2011. For my Sister (guest blogger - Micki). 169; T. Hutchinson. I wish you sweet sleep, my sister dear. Although there's so much that you've left bare. I hate that you had to endure such pain. On my mind, your saddened eyes have left a stain. I want to know what crossed your mind. Unspoken words you've left behind. Undone things we'll never do. No sharing thoughts you never knew.

cavecrawler-snowdonwalk.blogspot.com

Snowdon Horseshoe Fundraising Walk: October 2010

http://cavecrawler-snowdonwalk.blogspot.com/2010_10_01_archive.html

Snowdon Horseshoe Fundraising Walk. Snowdon Hourseshoe walk in aid of Psuedomyxoma Peritonei reseach. On 21st August 2010 I along with several freinds will be attempting the Snowdon Horseshoe walk to raise funds for Basingstoke and Northampshire Hospital -Pseudomyxoma Peritonei fund. The hospital is one of only two specialist centres in the country and the money will help buy equipment and fund research into this little known form of Cancer. Saturday, 30 October 2010. A Huge Thank You! I would like to ta...

cavecrawler-snowdonwalk.blogspot.com

Snowdon Horseshoe Fundraising Walk: The Snowdon Horseshoe - The big day arrives....

http://cavecrawler-snowdonwalk.blogspot.com/2010/08/snowdon-horseshoe-big-day-arrives.html

Snowdon Horseshoe Fundraising Walk. Snowdon Hourseshoe walk in aid of Psuedomyxoma Peritonei reseach. On 21st August 2010 I along with several freinds will be attempting the Snowdon Horseshoe walk to raise funds for Basingstoke and Northampshire Hospital -Pseudomyxoma Peritonei fund. The hospital is one of only two specialist centres in the country and the money will help buy equipment and fund research into this little known form of Cancer. Wednesday, 25 August 2010. The final team consisted of-. After ...

cancer-schmancer.blogspot.com

Dancing To The Rythm Of A Ticking Clock: Service & Travel information (guest blogger - Micki George)

http://cancer-schmancer.blogspot.com/2011/12/service-travel-information-guest.html

Dancing To The Rythm Of A Ticking Clock. Formerly Cancer Schmancer- subject to change without notice. Monday, December 12, 2011. Service and Travel information (guest blogger - Micki George). Following is information for friends and family that will be attending the services:. For those flying in from out of state. MOV Regional airport in Parkersburg, WV has numerous direct flights from Cleveland via the Continental carrier. The viewing will be held at Leavitt funeral home, Friday, December. Rooms are av...

cancer-schmancer.blogspot.com

Dancing To The Rythm Of A Ticking Clock: March 22nd - Lynch Syndrome Hereditary Cancer Awareness Day

http://cancer-schmancer.blogspot.com/2012/03/march-22nd-lynch-syndrome-hereditary.html

Dancing To The Rythm Of A Ticking Clock. Formerly Cancer Schmancer- subject to change without notice. Thursday, March 22, 2012. March 22nd - Lynch Syndrome Hereditary Cancer Awareness Day. Guest blogger - Micki. Today is March 22nd Lynch Syndrome Hereditary Cancer Awareness Day. Proclamations signed by Ohio and West Virginia Governors along with several other states. Micki, the big sister. March 24, 2012 at 10:02 PM. March 25, 2012 at 2:17 AM. January 5, 2014 at 11:14 AM. February 27, 2014 at 1:27 AM.

cancer-schmancer.blogspot.com

Dancing To The Rythm Of A Ticking Clock: July 2011

http://cancer-schmancer.blogspot.com/2011_07_01_archive.html

Dancing To The Rythm Of A Ticking Clock. Formerly Cancer Schmancer- subject to change without notice. Thursday, July 21, 2011. Now For The Next Chapter. A lot has happened in the last week or so. Honestly, I'm so cloudy that I have to reference my last post to remember what the heck I was talking about. Now that I've done it, it's kind of a relief that I do remember snapping out of the funk. I even remember the moment- it was during a cheesy song in a yogurt commercial. Hm. Whatever it takes. I didn't re...

cancer-schmancer.blogspot.com

Dancing To The Rythm Of A Ticking Clock: January 2012

http://cancer-schmancer.blogspot.com/2012_01_01_archive.html

Dancing To The Rythm Of A Ticking Clock. Formerly Cancer Schmancer- subject to change without notice. Tuesday, January 31, 2012. Happy Birthday - (guest blogger - Micki). Happy Birthday Rachel, my best friend and little sister. A birth. Micki, the big sis. Rachel's 35th birthday party, January 2011. Tuesday, January 24, 2012. Thank you (Guest blogger - Micki). Subscribe to: Posts (Atom). View my complete profile. There is no such thing as 'No Chance' Henry Ford. Hit counter. Started March 6- 2010. Origin...

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Snowdon Horseshoe Fundraising Walk

Snowdon Horseshoe Fundraising Walk. Snowdon Hourseshoe walk in aid of Psuedomyxoma Peritonei reseach. On 21st August 2010 I along with several freinds will be attempting the Snowdon Horseshoe walk to raise funds for Basingstoke and Northampshire Hospital -Pseudomyxoma Peritonei fund. The hospital is one of only two specialist centres in the country and the money will help buy equipment and fund research into this little known form of Cancer. Wednesday, 21 December 2011. Saturday, 30 October 2010. I would...

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My Story-My Battle with Pseudomyxoma Peritonei (PMP)

My Story-My Battle with Pseudomyxoma Peritonei (PMP). Sunday, 25 February 2018. A New Year brings new adventures! I have also been back underground and taken a colleague of mine on his first caving trip! It’s a small, short cave and is a favourite for beginners so was perfect for Piotr's first trip. The nice big entrance soon gives way to narrow passages and rifts and interestingly named obstacles such as “The coffin lid” and “ The drainpipe”! Ive only managed a few short clips whilst I get the hang of u...

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