Me/cfs

lita

Would someone mind recommending some websites for ME/CFS please?

Thank You


ETA Why has the title change to lower case when I wrote it in upper case???? Strange!

elaina79

Here are 2 for you

http://www.meassociation.org.uk/
http://www.nmec.org.uk/

maytaurus

lita wrote: »

Would someone mind recommending some websites for ME/CFS please?

Thank You


ETA Why has the title change to lower case when I wrote it in upper case???? Strange!

Hi lita :hello:

have a look here #122

prettypeach_2

http://www.ahummingbirdsguide.com/

Loads of information on this site, very good symptom lists, also has quite a lot about the current controversies around the condition, view or lack of view of medical profession, common mistreatment (abuse) of M.E. patients by doctors (many but not all doctors) etc.

Myrtle

I like this one:
http://www.foggyfriends.org/forum/index.php

Brighton_belle

I can really recommend this one:

http://www.cfsrecovery.com/default.asp

In 20 yrs of the condition and having tried most things going, this one has really really helped.
And compared to so many things, it is very affordable (with a 6 month money back guarantee), so very MSE . The chap who has put it together, Ashok Gupta, a former ME sufferer, is totally genuine.
A friend and I started it at the same time and her life/health has been transformed over the last year.

Worth a look. But I am only drawing it to your attention so you can explore his ideas if you want to. Not intending to try and 'convince' anyone to do it: I know how much I have hated that in the past for myself.

babymoo

www.ukfibromyalgia.com is really good xxx

Flaxseed

Try AYME if its for a youngish person

Mojisola

Or Tymes Trust - https://www.tymestrust.org/ - which has just won the Queen's Award for Voluntary Service for pursuing the educational rights and advancing the care of children with ME. Their publications are well worth looking through and some are useful for adults as well as young people.