#me

My life with It does not discriminate It was sudden It was virally induced It steals EVERYTHING you held precious But if it strikes its up to you then to provide Β£s for biomedical research & to educate medical professionals & to fight the stigma for 20yrs&7mths &counting

πš‚πš–πš’πš•πšŽ πš‹πš’πš πšŠπš—πš πš•πšŠπšžπšπš‘ πš˜πšπšπšŽπš—βœ¨ . . .

Just your hot witchy mom, telling you to drink more water.. ❀️

Gratitude to this whole community. When I first got ill 28 years ago, there was no social media and no sense of community, it was lonely and frightening. Thanks to patients, researchers, carers, Drs, families-everyone who cares about us.

Interested to know, how many with M.E. are completely shielding, isolating at home, working from home etc?

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