"Supporting sufferers and their families"
*Please see our updated meetings news on our meetings page during the Coronavirus crisis.
the Sundance award winning documentary about ME
'Jennifer Brea is about to marry the love of her life
when she’s struck down by a fever that leaves her
bedridden. When doctors tell her “it’s all in her head,”
she turns her camera on herself and her community
as she looks for answers and fights for a cure'.
Like to talk to someone?
Phone or text Jenny: 07434 184 095
or Email: firstname.lastname@example.org
Open Facebook: https://www.facebook.com/ssbmesg
*We also have a closed Facebook page for members only see our 'About our group' page
Thank you for visiting our website!
We hope that our information is useful to you and that having contact with other sufferers and carers will be helpful.
OUR MISSION STATEMENT
Our mission is to offer friendship and support to people in our area who are suffering from
Myalgic Encephalomyelitis (ME), their families and carers, and to provide information and raise awareness
of ME, including biomedical research and all other related issues
- to provide a network of mutual support for those suffering from ME, their families and carers
- to facilitate meetings between members
- to disseminate information between members and others
- to maintain links with similar groups
- to raise awareness of ME
The Solihull & South Birmingham Support Group (SSBMESG) Committee monitor
and continually review the services provided by our group.
Our latest QA Survey 2010/ 2011
Our Code of Conduct
Our Equality & Inclusion Statement 2014
Solihull & South Birmingham ME Support Group does not endorse or recommend any treatment/therapies/practitioners but merely reports on discussions or information received.
The reader should always make their own enquiries before acting on any information contained in this website.
Solihull & South Birmingham ME Support Group are not responsible for the content of other websites.