BLOGS of ME Sufferers and Carers

This page contains details of Blogs set up by people with ME or their carers/parents.

Blogs are now a daily part of many people's lives. There are some useful and interesting topics and experiences on some blogs. So we thought we would devote a page to ME blogs (i.e. a Blog set up by/for a pwme or carer/parent)

The contents of these Blogs are not monitored by IiME and we take no responsibility for either their content or their accuracy.

If you wish to send us details of your Blog to appear here then please contact us.


UK and Ireland

Antoinette Christie
ME has brought many things into my world as a carer.. PAIN, FUSTRATION,ANGER, HOPELESSNESS, AND BELIEVE IT ARE NOT FRIENDSHIP!!!
 

Lizzie Fison
BSc Govt student at the LSE, Conservative activist, juggling life and M.E./CFS since 1998.
 


Jas
I live in the West Country of England and am determined that ME, Fibromyalgia, Rheumatoid Arthritis and now Lyme Disease will not rule my life. I am equally determined to help fight for proper recognition, bio-medical research and treatment for ME.

 

 

International

My name is not important, but what is however is the fact that i have been diagnosed with something called Myalgic Encephalomyelitis (ME for short) and intend to write about it. It hasn't been an easy 7 or so years of misery that ME has brought me and i intend to tell you my story, right here, right now. It has to be written. No longer will i stay silent. No longer. Like the title refers to - being sick in ME/CFS and the like with todays healthcare is a world between tables.


THE NICEGUIDELINES BLOG

Doctor Speedy and ME in search of medical honesty