ME/CFS

Sat 11 Dec 2021, 11:17

Oh my word Malcolm Blackmore

I'm worn out reading that! :-)

Thu 9 Dec 2021, 18:10

OMEGA has been mentioned and is worth following up. 

Also worth checking out is Dr Sarah Myhill who has been interested in ME/CFS since the 90s where and when, as a GP for a rural Welsh hill-farming area she got invasions of strong and healthy young men and women collapsing…

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Mon 6 Dec 2021, 19:26 (last edited on Tue 7 Dec 2021, 14:23)

Hi Linda. I'm here. I would very happily chat. This is from a while back (lots I would say differently or with new understanding, now), but in case it's helpful: 

https://www.youtube.com/watch?v=fPj2Wur8P-M

Sun 5 Dec 2021, 19:02

There is a support organisation for ME/CFS in Oxfordshire called OMEGA. Email address is omegaoxon@gmail.com. Website is http:/omegaoxon.org They issue a very informative newsletter and I can forward the latest issue to you if you give me your email address.

Sun 5 Dec 2021, 11:23

I have ME/CFS myself and wondered if there was anyone else near by who would like to chat to someone who understands.

Sun 5 Dec 2021, 10:20

Yes, and daughter has too.

Sun 5 Dec 2021, 00:25

Yes.  The latter.  Why?

Sat 4 Dec 2021, 21:38

Does anyone in Charlbury have ME/CFS or know someone who does?