cavecrawlerstory blogspot.com

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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Dancing To The Rythm Of A Ticking Clock

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. 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. Tuesday, January 31, 2012. Micki, the big sis. Tuesday, January 24, 2012.

A PMP survivor!!

My health problems but to offer hope. The small things in life are really the BIG things! You beat cancer by how you live, why you live and the manner in which you live! .

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.

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My Story-My Battle with Pseudomyxoma Peritonei PMP

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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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This web page cavecrawlerstory.blogspot.com states the following, "My Story-My Battle with Pseudomyxoma Peritonei PMP." We saw that the webpage said " Sunday, 25 February 2018." It also said " A New Year brings new adventures! I have also been back underground and taken a colleague of mine on his first caving trip! Its a small, short cave and is a favourite for beginners so was perfect for Piotrs 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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