MEETUP.ORG.UK
homeA simple site, with advice for people new to ME/CFS, and a map with links to support groups.
http://meetup.org.uk/
A simple site, with advice for people new to ME/CFS, and a map with links to support groups.
http://meetup.org.uk/
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home | meetup.org.uk Reviews
https://meetup.org.uk
A simple site, with advice for people new to ME/CFS, and a map with links to support groups.
meetup.org.uk
associations
http://meetup.org.uk/associations.html
Looking for advice and help? The big two associations. Are Action for ME. And the ME Association. For children or students. With ME, I recommend Tymes Trust. Run by Jane Colby who has ME herself, was previously a head teacher, conducted a survey in schools with Dr Betty Dowsett on school absence and ME, and works tirelessly to support children with ME. Finally, for those who are more severely affected. There is The 25% Group, formed in 1995. A friendly, all-round support group.
otherpeople
http://meetup.org.uk/newtome/otherpeople.html
Are you new to ME? Many, many people are going to ask you about ME. Even those closest to you will have difficulty in understanding it. I know I found it hard to understand what my son really meant by a foggy brain, even though I could see its effect: or how he could wear a coat to keep warm when others were in shirtsleeves. Now that I have ME myself, I know. If the person asking is genuine, never use the word tired. Yes Remove one teaspoon from your hand and lay it down, then ask And got dressed? By (sa...
youngsters
http://meetup.org.uk/newtome/youngsters.html
Does your child have ME? Young People with ME. First of all, it is important to realise that when we first go down with ME, our bodies pour everything they have into fighting this illness. It doesn't leave much. The number one priority is to ensure that your son or daughter has enough rest. A good diet, and time for the immune system to do its work. This is a really serious long-term illness: do not underestimate it. They can visit when you feel it is possible. The reason that youngsters with ME beco...
socialmedia
http://meetup.org.uk/socialmedia.html
For those of you who are not familiar with forums, they are websites where you can type out a message or opinion and post. It onto one of their webpages, or threads. There are two main types of forum. Are where anybody can see what you have posted, so be very carefull telling everyone that you have gone off on a cruise for a month and your home at 2 Foolish Drive, Little Snoring will be empty. Is a small, friendly site and is more like an online coffee house. Is really just another forum, but is vast and...
Google Maps Multiple Markers
http://meetup.org.uk/map.html
Find support groups near you. Map of support groups. ME and Fibro support groups in the UK. For an ME group. For an FM group. For a general group.
TOTAL PAGES IN THIS WEBSITE
9
North London M.E. Network
http://nlmenetwork.org.uk//links.php
NATIONAL M.E. ORGANISATIONS. Action for M.E. Association of Young People with M.E. For the under 25s). The Young M.E Sufferer s Trust. Also known as Tymes Trust for children/young people and their families). ME Research U.K. Just Four Quid Campaign. Money saving tips website which encourages you to donate your savings to M.E research). Crossroads Caring for Carers. Meditation site, aimed at people with M.E/C.F.S). Online directory of counsellors and psychotherapists). Department of Work and Pensions.
TOTAL LINKS TO THIS WEBSITE
1
Meetup
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home
Welcome to the Meetup Site. Myalgic Encephalomyelitis / Chronic Fatigue Syndrome. What is this site? This site is designed to be an easy way. To start finding out about ME, to find local support groups, and to introduce you to some of the online forums and organisations, It also has links for people with Fibromyalgia. There are very many ME sites out there, and an enormous amount of information to absorb. I hope that this website will help you to make a start. I have tried to keep it simple. Have many us...
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