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Andrea P.
Top HealthBlogger
Blog:
http://www.dancingwiththesandman.blogspot.com/
I am a writer, ex-teacher and sufferer of Myalgic Encephalopathy (ME/CFS). I live with my husband and two adorable cats in a beautiful cottage on the wilds of Dartmoor.
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Reply from DoH (Re: Letter to Paul Burstow of 2nd March)
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
Permission to Repost Our ref: DE00000597428 Dear Ms Pring, Thank you for your further email of 2 March to Paul Burstow about myalgic encephalom ...
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ME/CFS Bloggers Unite
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
Following the success of XMRV Bloggerama Day and PACE isn't for ME, Action Now has created a special blog ring for all ME and CFS bloggers wishing to share their know ...
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ME/CFS Blogger Army: PACE Isn’t For Me
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
PACE Isn't for ME's aim was to launch accurate information on PACE into cyberspace and counteract all the recent 'space junk' produced by vested-interest groups aligned ...
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PACE trial aftermath: ME Association writes to the Science Media Centre
by
Andrea P.
Posted in:
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The following email has been sent today to Fiona Fox (Director) and Helen Jamison (Senior Press Officer) at the Science Media Centre. Posted by Tony Britton on ...
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Science Media Centre and the Death of Free Press
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
This communication is being sent on behalf of Margaret Williams. On the 17th of February, a press conference was held at the Science Media Centre to announce the e-publi ...
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Biological Warfare Weapons Development and Testing
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
1980's: Tests of new disabling disease pathogens somewhere in the U.S. and Canada. At the same time mystery diseases were breaking out as far away as Incline Village, Nevada ...
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Letter to MP Paul Burstow Re: Adjournment Debate on ME
by
Andrea P.
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Permission to Repost Dear Mr. Burstow, Following your recent speech in parliament as part of the ME adjournment debate, we would like to address several issues that ...
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Tears for ME
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
I'm collecting all the tears that are shed for ME; teardrop after tiny teardrop, until they fall to the ground in a puddle; until the puddle becomes a restless stream; unt ...
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Call for Action For M.E. Resignations
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
Without the support of AFME the PACE trial may not have been funded. While AFME expressed their firm support for the funding of PACE, the other main ME charity called f ...
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MRC Responds to Professor Malcolm Hooper
by
Andrea P.
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This communication was sent on behalf of Professor Malcolm Hooper. Medical Research Council Professor Malcolm Hooper, 2 Nursery Close, Su ...
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Professor Malcom Hooper Threatened
by
Andrea P.
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Communication sent on behalf of Professor Malcolm Hooper Because of the serious nature of the criticisms I received in a recent communication, I thought it necessary to ...
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Collective International Professional Response to PACE Required?
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
contact@angliameaction.org.uk to CO-CURE Dear All, I write in response to the just-published results of the UK MRC/DWP-backed PACE Trial on 'CFS/ME' in The Lancet[1]. ...
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National ME/CFS protest action in Brussels 14th of March 201
by
Andrea P.
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Call in the interest of all patients who suffer from ME/CFS and fibromyalgia in Belgium! Because the government policies regarding the above mentioned conditi ...
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ME/CFS Blogger Army: PACE isn't for M.E.
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
Drown out the forthcoming news reports on the flawed PACE Trial by writing your own blog post. This follows on from the recent XMRV Bloggerama Day. If you are unable to writ ...
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Response from Jo Best to UK National Research Ethics Service Apology to Phil Parker
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
You can read the letter from Joan Kirkbride of the NRES with the apology to Phil Parker in the note here 8th February 2011 Dear Joan, I refer to your letter of 4th ...
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XMRV Bloggerama: We've Only Just Begun
by
Andrea P.
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The aim of XMRV Bloggerama Day was to get correct and detailed information on XMRV out into cyberspace and counteract all the recent disinformation. The campaign relied on b ...
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ME/CFS Events and Actions
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
The calendar will be updated regularly. Please feel free to share the page link. If you have any events you think should be included you can contact me at andreapri ...
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Dr. Nancy Klimas & ME/CFS Worldwide Patient Alliance on Issues Surrounding ME/CFS & XMRV
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
In January 2011, Dr. Nancy Klimas from the University of Miami and Tina Tidmore from the ME/CFS Worldwide Patient Alliance (MCWPA) were interviewed on the community radio st ...
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Breaking News from ME Association - MRC Invests £1.5m to Encourage Further CFS/ME Research
by
Andrea P.
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From the ME Association on Facebook Tony Britton, Publicity Manager, ME Association ------------------------------------------- MRC invests £1.5m to encourage furthe ...
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Professor Malcom Hooper's Reply to MRC rejection of PACE Trial complaint
by
Andrea P.
Posted in:
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Chronic Fatigue Syndrome
Permission to repost From Malcolm Hooper Ph.D.,B.Pharm.,C.Chem.,MRIC Emeritus Professor of Medicinal Chemistry University of Sunderland, SUNDERLAND SR2 3SD ...
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