understandingsevereme.blogspot.com
UNDERSTANDING SEVERE ME/CFS : Severe ME is not the same as CFS...
http://understandingsevereme.blogspot.com/2015/05/severe-me-is-not-same-as-cfs.html
SEVERE M.E. INFORMATION - ESSENTIAL READING FOR FAMILY and FRIENDS OF PATIENTS. Severe M.E. Information Pack. Understanding Severe M.E. Information Pack'. I do so hope that both help guide you through the hellish maze that is Severe M.E. Email understandingsevereme@hotmail.co.uk for details. Severe ME is not the same as CFS. Loving this differentiation between CFS and ME. http:/ arainbowatnight.com/2015/05/12/chart/. Subscribe to: Post Comments (Atom). Http:/ www.sophiaandme.org.uk.
understandingsevereme.blogspot.com
UNDERSTANDING SEVERE ME/CFS : Severe ME/CFS...Time for a cure not a new name
http://understandingsevereme.blogspot.com/2015/02/severe-mecfstime-for-cure-not-new-name.html
SEVERE M.E. INFORMATION - ESSENTIAL READING FOR FAMILY and FRIENDS OF PATIENTS. Severe M.E. Information Pack. Understanding Severe M.E. Information Pack'. I do so hope that both help guide you through the hellish maze that is Severe M.E. Email understandingsevereme@hotmail.co.uk for details. Severe ME/CFS.Time for a cure not a new name. I can hear the cruel jokes already. Http:/ www.nature.com/news/us-panel-redefines-chronic-fatigue-syndrome-1.16905. Subscribe to: Post Comments (Atom).
understandingsevereme.blogspot.com
UNDERSTANDING SEVERE ME/CFS : Finally a brilliant BBC interview revealing the cruel reality of Severe ME...
http://understandingsevereme.blogspot.com/2015/07/finally-brilliant-bbc-interview.html
SEVERE M.E. INFORMATION - ESSENTIAL READING FOR FAMILY and FRIENDS OF PATIENTS. Severe M.E. Information Pack. Understanding Severe M.E. Information Pack'. I do so hope that both help guide you through the hellish maze that is Severe M.E. Email understandingsevereme@hotmail.co.uk for details. Finally a brilliant BBC interview revealing the cruel reality of Severe ME. Well done BBC Radio Bristol! Http:/ www.bbc.co.uk/programmes/p02w3d9d. Subscribe to: Post Comments (Atom). Http:/ www.25megroup.org.
understandingsevereme.blogspot.com
UNDERSTANDING SEVERE ME/CFS : Severe ME Ignorance Must End...
http://understandingsevereme.blogspot.com/2015/01/severe-me-ignorance-must-end.html
SEVERE M.E. INFORMATION - ESSENTIAL READING FOR FAMILY and FRIENDS OF PATIENTS. Severe M.E. Information Pack. Understanding Severe M.E. Information Pack'. I do so hope that both help guide you through the hellish maze that is Severe M.E. Email understandingsevereme@hotmail.co.uk for details. Severe ME Ignorance Must End. Http:/ www.theguardian.com/commentisfree/2015/jan/16/me-sufferers-simplistic-news-reports-chronic-fatigue-syndrome? Chapter 1: The Different Levels of M.E. 8220; Every illness affects pe...
getwellfromme.com
Get Well From ME - Links
http://www.getwellfromme.com/links
Neuro-immune diseases, ME, toxins and mould. UK biological medical research charity. ME (CFS), mitochondria and more. Dr Shoemaker, Chronic Inflammatory Response Syndrome (CIRS). TYMES The Young ME Sufferers Trust. Support for children with ME. UK information and support. Support for sufferers of severe ME. Severe ME/CFS - A Guide to Living. United advocacy for neuroimmune diseases. The Grace Charity for ME. Hummingbirds' Foundation for ME (HFME). Voices from the Shadows. Sophia Mirza and ME.
sciencevsantiscience.wordpress.com
SEVERE M.E DAY – A COMMEMORATION OF SOPHIA MIRZA 1973-2005 | sciencevsantiscience
https://sciencevsantiscience.wordpress.com/2014/08/08/severe-m-e-day-a-commemoration-of-sophia-mirza-1973-2005
Life through the lens of an ME sufferer struggling to get treatment. SEVERE M.E DAY – A COMMEMORATION OF SOPHIA MIRZA 1973-2005. Today, August 8th, would have been Sophia Mirza’s 40th birthday. To commemorate her I am writing this blog so that her plight may never be forgotten. Sophia Mirza suffered the severest form of M.E. M.E is recognized as a neurological disease by the World Health Organisation and was understood as such until 1988 when a new criteria was born. Sophia Mirza was tragically ill.
katharineandme.blogspot.com
Katharine and M.E.: May 2014
http://katharineandme.blogspot.com/2014_05_01_archive.html
Saturday, 31 May 2014. A look back on M.E. Awareness Month. It's the last day of May (aka M.E. Awareness Month) and, as I've been rather wrapped up in exams and the inevitable-yet-oh-so-horrible payback from said exams, I thought I'd take the opportunity to reflect on all our awareness-raising efforts. Firstly, though, I want to say a huge THANK YOU. To everyone who read my post (if you've not read it, it can be found here. As well as a 'real-life' tea party, everyone got involved online to drink tea and...
brc4mecfs.blogspot.com
Blue Ribbon Campaign for ME/CFS: July 2010
http://brc4mecfs.blogspot.com/2010_07_01_archive.html
Blue Ribbon Campaign for ME/CFS. Informal Report from the FDA's Blood Safety Advisory Committee Meeting. Written and shared with permission of Heidi Dunlap Bauer. It’s All About the Prostate, Folks. 8221; He called for further studies to establish XMRV as the underlying cause of human diseases in infected individuals. Hear, hear! How does it reach the brain? Is one person more at risk than another? Not one HIV patient in either study had XMRV. I’m fine with that if that is true. An HIV pati...I’m n...
