Links to other websites
| Site title | Description | |
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| 25% M.E. Group | The 25% M.E. Group exists to support all who have the severe form of M.E. and those who care for them. This includes people who are housebound, bedbound and wheelchair users. | |
| BRAME Blue Ribbon for the Awareness of ME | The primary aim of BRAME, both in the UK and worldwide, is to create an increased awareness and understanding that ME/CFS is a very real and debilitating illness, and the consequences of living with ME/CFS, for the sufferer, carer and the whole family unit. BRAME also offers support and understanding to those affected by ME/CFS. By donating excess funds BRAME is also supporting much needed research into ME/CFS. | |
| CFIDS Association of America | The CFIDS Association of America is the nation's leading charitable organization dedicated to conquering chronic fatigue and immune dysfunction syndrome (CFIDS), also known as chronic fatigue syndrome (CFS). The Association works to accelerate the pace of CFIDS research, achieve public policy victories for people with CFIDS, and focus mainstream attention on this serious public health concern. | |
| David Axford | In depth issues and information on ME This site has medical information written by Dr Ellen Goudsmit as well as research updates and a good links page. |
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| Dr Myhill | This website gives access to this information and to diagnostic tests (blood tests, tests for infection, nutritional tests, hormonal tests, toxicology etc.) to allow people to diagnose and manage their own medical problems. In addition it allows people to contact me directly. | |
| DReMER | DReMER is a campaign to persuade people with influence that M.E. is a real illness. It seeks to promte bio medical research- asking for more funding, pointing out the urgent need for research and demanding a co-ordinated research programme. |
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| Have a Cuppa for ME |  is up and running The idea is a simple one groups and individuals around the UK (but there's no reason why this couldn't happen world-wide) host a coffee morning on October 14th to raise awareness of and money for research into, ME. Details will be updated on the Invest In ME website www.investinme.org and we have posters available to download. Money raised can be donated directly to your nominated research team but I would ask that you specify the money came from a Have a Cuppa for ME event. I would also like to keep a total of money raised from this initiative so could you feedback the information directly to me? |
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| Hereford M.E. | Herefordshire ME group aim to offer mutual support,share information and to campaign for proper levels of health care with in the NHS-- Support the DReMER Campaign |
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| Invest in ME |  |
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| LocalME | LocalME is a friendly e-mail list, for those involved at local group level, to share news, views, information, hopes and concerns with each other. This members only group has no affiliation to any of the national charities. Please contact: connie.nelson@ntlworld.com or subscribe via LocalME-subscribe@yahoogroups.com giving your full name and details of your local group. |
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| M.E. Association National ME/CFS patient support organisation | The ME Association provides information and support to people with ME through literature, a quarterly magazine, and our telephone helpline ME Connect. We are also involved in campaigning on issues such as benefits, research and the importance of early diagnosis. The MEA also funds research into the underlying physical causes of ME through a designated research fund.? | |
| M.E. support | M.E. Support is an extensive Website founded by M.E. sufferer Louise Sargent. The site covers many aspects of M.E. (also known as PVFS/ CFS / CFIDS) & other chronic fatiguing illnesses. M.E. Support has articles, references & resources on a vast array of subjects. The Website also offers numerous services including: Chat Room, Friendship List, Mailing List & Message Forum |
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| M.E. SUPPORT - NORFOLK | Local support group for Norfolk area | |
| ME Associations blogspot | The MEA is going 'blogging' as a way of keeping people up to date with our news while we recruit a new team of volunteers to run our existing main website, and prepare for the launch of a new MEA website later this year. You can view the blog here and use it to pass immediate comment to us on any items. |
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| ME Research UK | ME Research UK is a national UK charity funding biomedical research into Myalgic Encephalomyelitis (also known as ME/CFS) and related illnesses. | |
| MEA Research | Since 1990, The ME Association's research fund has helped finance a considerable number of major research studies and also supported research-orientated conferences. Future research funded by The Association will concentrate on the topics selected via our new research intiative, which is explained at our research website. |
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| MEActionUK | This website exists to raise awareness of all the issues relating to ME and in turn I hope that the information here gives support for those who are severely ill and disabled by M.E.. Overall my aim with this site is to keep people well informed. | |
| Merge | ME Research UK is a national UK charity funding biomedical research into Myalgic Encephalomyelitis (also known as ME/CFS) and related illnesses. Our principal aim is to commission and fund high-quality scientific (biomedical) investigation into the causes, consequences and treatment of ME, but we also have a mission to Energise ME Research | |
| RiME | RIME Campaigning for research in to M.E. |
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| Sheffield M.E. Group | Sheffield ME Group runs a variety of services, such as information line, regular and special meetings, library and newsletter, listening ear, and social meetings. | |
| The CFS Research Foundation | The CFS Research Foundation was officially launched in 1993 to bring together the best minds to meet the challenge presented by chronic fatigue syndrome, encouraging basic research into the body mechanisms that lead to and continue the illness. | |
| The HHV-6 Foundation | The HHV-6 Foundation sponsors research on the role of HHV-6 in chronic fatigue syndrome, multiple sclerosis, HIV, epilepsy and other conditions. The Foundation has a Scientific Advisory Board that includes the world's top experts in HHV-6 and is funding basic research in this field. The Foundation is supported through private donations. |
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| The National CFIDS Foundation | The Foundation's objective is to fund research to find a cause, expedite treatments and eventually a cure, as well as providing information, education, and support to people who have CFIDS (chronic fatigue and immune dysfunction syndrome also known as chronic fatigue syndrome (CFS), myalgic encephalomyelitis (ME) and many other names). | |
| The School of Molecular Biosciences | YOUR SUPPORT IS NEEDED FOR RESEARCH ON THE NITRIC OXIDE/PEROXYNITRITE THEORY OF CHRONIC FATIGUE SYNDROME, MULTIPLE CHEMICAL SENSITIVITY AND FIBROMYALGIA |
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| Tymes Trust for children and young people with M.E. | Tymes Trust PO Box 4347 Stock Ingatestone CM4 9TE Tymes Trust is the longest established national UK service for children and young people with ME and their families. It is a respected national charity whose entire professional team give their time free of charge. |
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| Why this is a 'Hummingbirds' guide to M.E.... | Because hummingbirds are tough little things with a lot more strength, bravery and determination than most people ever give them credit for - a lot like many of the people who have severe Myalgic Encephalomyelitis (ME/ICD-CFS*) | |