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Latest topics Statistics We have 16 registered usersThe newest registered user is nasim marie jafry Our users have posted a total of 242 messages in 101 subjects | Welcome to the M.E. Recovery Group Discussion Forum.
Hi All... I would like to welcome you to what we hope will be a useful place for any M.E./CFS sufferer or their carer to talk, share, offer advice or even have a moan... Although the M.E. Recovery Group charity is based in the Scottish Borders, anyone is welcome to use this facility... All that we ask is that you treat everyone with respect and that you above all gain something from this new service... On the left is the Navigation section which allows you quick links to the whole forum and the website. Also on the left, scroll the last 25 posts for quick viewing. I look forward to "meeting" you...Kind regards... Carole.xxx NOTICEBOARD Urgently needed:Anyone who is willing to take on the role of secretary for the Group would be very gladly welcomed. John Greaves has been covering this role for a while now, but as he is also the nutritional therapist amongst other duties, it would be wonderful if someone could take on the role of secretary. All responsibilities would be explained on application.
Please contact:
J Greaves on 01573430230.
Thank You.
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A Support Group is due to be organised to meet once per month at the Borders General Hospital Chaplaincy Centre. For more information see here.
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The ME Association wants to hear from as many people as possible about their experiences – good or bad – of coping with ME.To do this they have produced a questionnaire which asks about treatments that work, treatments that don't work, and what people want when it comes to GP and hospital based services.
They also want to build up the biggest ever picture of what happens when people are given cognitive behaviour therapy or graded exercise therapy – two controversial forms of treatment that have been recommended in a guideline produced by NICE. They can then go back to the Department of Health with a really comprehensive nationwide picture of this illness, along with recommendations on how diagnosis and services can be improved. To take the survey go here Please leave your thoughts on the survey on this forum and we will pass them on to the M.E. Association.
The survey will be open until 31 August 2008.
If you have ME, or care for someone with ME, please try and fill in the questionnaire. A paper copy will be available later for use by people with ME, and their carers, who do not use the web.
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The ME Association wants to hear from as many people as possible about their experiences – good or bad – of coping with ME.