ME Association

@meassociation.org.uk

A UK registered charity for people with #MECFS and Long Covid (and Post Covid ME/CFS). We inform, educate, raise awareness, fund medical research and campaign for positive change.

RPs do not necessarily mean endorsement.

https://linktr.ee/meassociation

@meassociation.org.uk

2/2: N.B. Having a positive mental attitude may help some people to deal with the emotional aspect of having ME/CFS, as a chronic long-term illness can be understandably difficult to deal with. However, we are all individuals and what may help one person may not be suitable for another person.

@meassociation.org.uk

ME Connect is our free, confidential support service offering a safe, understanding space where you're truly listened to. Whether you need someone to talk to, emotional support or simply a compassionate ear, we're here for you.

#MEConnect #MECFS

IMAGE DESCRIPTION: Photo of a man in bed, on his phone. Wording reads: "I was so happy to talk to someone who understands the condition." MEA and ME Connect logos.
@meassociation.org.uk

In the interview, Monbiot says of #pwME “They need more advocates. They need people like you … and they need far more journalists and far more other people, far more politicians supporting them.”

@meassociation.org.uk

An article looking at conditions such as "fibromyalgia, long COVID, endometriosis, chronic fatigue syndrome, and autoimmune disorders, [which] put patients at high risk of experiencing “medical gaslighting”"

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