CHARITY STEPS IN TO SAVE SCOTTISH STUDY INTO POSSIBLE GENETIC CURE FOR M.E. The ME Association, one of Britain's largest charities for people with M.E./Chronic...
Permission to Repost CHARITY STEPS IN TO SAVE SCOTTISH STUDY INTO POSSIBLE GENETIC CURE FOR M.E. The ME Association, one of Britain's largest charities for...
I should be pleased if members of this message board would let me know today, whether you received any letter or flyer from the MEA notifying you of the...
May be reposted With reference to Press Releases: MEA parliamentary briefing, 26 June 2005 and MEA announces further funding for Dr Gow's research I'd like to...
Would readers of this list please let me know if you receive notification of the postponement of Tuesday's MEA EGM in this morning's post (Thursday, 30 June). ...
Issued on behalf of the MEA: May Be Reposted The donations they have been receiving for John Gow et al's gene microassay research 2nd phase, has persuaded...
MERGE is delighted to announce the award of a grant to Dr John Gow, University Department of Neurology, University of Glasgow for a project entitled,...
[The second part of this refers to to a child carer whose mum has CFS] http://news.scotsman.com/features.cfm?id=658982005 Brotherly love is strained to...
[ACAMH = The Association for Child and Adolescent Mental Health] "..The key aspect to the graded activity programme appeared to be capturing the young person's...
Submitted by R. Sanderson, Clerk on behalf of the Massachuestts CFIDS/FM Association - - - - - - - - - - - - - June 17, 2005 FOR IMMEDIATE RELEASE CONTACT:...
ME/CFS From a Young Person's Perspective: Interview with Claire Wade Source: CF-Alliance Newsletter, Summer 2005 Issue, Copyright 2005 When did you first...
In recent years, a charity in the UK has run a campaign looking for 1% of the cost of ME to the country (said to be £3.5 billion a year) to be spent by the...
From CF-Alliance <cf_alliance@...>: BOOK REVIEW - _We're Not in Kansas Anymore: CFS & Politics of Disease_ by Rik Carlson, www.monkeyswithwings.com ...
Dear Friends, The summer edition of The National Forum will be mailed out within days. The current issue includes all the regular columns such as "Just Ask," ...
So many of us have sleep problems. A new supplement that apparently helps is mentioned here. Follwing the link will lead to more information. Adrienne From...
ADMIN: Changes to MEinformUK In addition to maintaining the MEinformUK noticeboard I also have a number of other message board commitments and other projects...
ADMIN: Final posting This will be the final posting for the foreseeable future. The archives will now be changed to "Members only access" and no further...
PERMISSION TO REPOST Campaigning for Research into Myalgic Encephalomyelitis RIME July 2005 There is no need for RiME to make a detailed statement re. the...
NOTICE: Statement 6 concerning the Orchard M.E. Centre [UK] In April, Mr Brian Ashworth of the Orchard M.E. Centre* informed a number of existing and former...
NOTICE: Statement 7: Leger ME and Mr Mike Valentine's close links with the Orchard ME Centre* Leger ME website: http://www.mvys03487.pwp.blueyonder.co.uk Leger...
NOTICE: Statement 8 concerning Brian Ashworth, The Orchard Centre*, Bilston, Wolverhampton We are interested in hearing from the following: Former clients or...
Permission to circulate in its entirety NOTICE: Statement 9 concerning Brian Ashworth and The Orchard Centre 30 January 2006 Over the past eighteen months, we...
************************************************************ Permission to circulate to contacts, ME/CFS forums and local ME/CFS/FMS support group committees...
This is a special one-off message from MEinformUK owner, Suzy Chapman "On a Postcard, please" Campaign | Royal Society of Medicine CFS Conference | Monday 28th...
