Do fight. A lot of people win against dwp. Seek advice eg from benefitsandwork website. With good advice you can get what you deserve
05.03.2025 11:45 โ ๐ 1 ๐ 0 ๐ฌ 1 ๐ 0
"I was saying pro-abortion"
One of themmuns (they/them)
๐ด๓ ง๓ ข๓ ณ๓ ฃ๓ ด๓ ฟ๐ณ๏ธโโง๏ธโพ๏ธbi flag emoji when
Life on hold by severe #MECFS, currently 99% bedbound ๐
Documenting my life like it is now, advocacy through photography ๐ท
๐Finland
https://nikosuvisto.com/
Love crafts, history, stories, natural world & spending time with husband, children, family & friends. When M.E /CFS & POTS doesn't stop me - which is most of the time right now. Usually found in a dressing gown. Devon, UK โฟ๐ฟ๐ณ๏ธโ๐๐ณ๏ธโโง๏ธ๐บ๐ฆ
Emerg doc, #Wikipedian, promoter of free and open access health info, board chair Wiki Project Med www.mdwiki.org
https://en.wikipedia.org/wiki/James_Heilman
Disabled by #MyalgicEncephalomyeltis ยฐ Ambulatory wheelchair user ยฐ Nazi lives don't matter ยฐ Science is real ยฐ #AuDHD ยฐ #Lutruwita
I mostly repost things rather than write Bluestuff because my mind isn't sharp and lively anymore
Queer, humanist, pantheistic Quaker.
Politically non-partisan.
Disabled & chronically ill
#pwME #MyalgicEncephalomyelitis #SevereME
๐ช๐บ๐ฃ๏ธ ๐ด๓ ง๓ ข๓ ฅ๓ ฎ๓ ง๓ ฟ๐ฆ๐น๐ฉ๐ช๐ช๐ธ๐ซ๐ท๐ต๐น
Disability Justice
Living with ME, EDS, POTS, MCAS, vascular compressions, spinal comorbidities & more
Ambulatory wheelchair user
Cozy gamer, lazy gardener, hopeful baker
SFF/middle-grade fiction/satire writer. Strategy/marketing consultant. Bagel the Dog's emotional support human. Dadjoke teller. Sentence-fragment lover. Disabled with #MECFS She/her effieseiberg.com/stories (or @effies@wandering.shop on Mastodon)
Severe ME/CFS going on 2 years, Optimistic ๐๐ , California mom, absurdist , Pokรฉ trainer, old enough to remember Friendster, she/her, ๐ณ๏ธโ๐ ๐ด๐ค
Disability justice. Former medical student before #mecfs she/her
disabled software engineer; pwME; dogs, knitting, making.
Not to scale. Almost always nice to people. Still figuring this place out.
she/her
a.k.a. _ashley_e@twitter intermittent_gimp@InstaGram
A non-profit social enterprise dedicated to people with Long Covid + ME. Shifting the paradigm one step at a time...
๐๐Home to the #pedanticzebra book club.
https://www.longcovidadvoc.com/
๐๏ธ https://longcovidadvoc.shop/
Sport, history, language, law & humour | Living with and writing about #ME #POTS #IST #Asthma #Dysautonomia | #Celtic ๐ | #LifeWriting at
merrydholl.wordpress.com ๐ด๓ ง๓ ข๓ ณ๓ ฃ๓ ด๓ ฟ
Ex philosopher, Ex Singer-songwriter, Ex Healthy person
Long-term severe #MEcfs #hEDS
Expect sarcasm.
#DrsAreDickheads
Disabled. Living with severe M.E. Watching the world from the window while bedbound. Excuse typos etc, sometimes the cognitive bits donโt work. Also posting on endometriosis and a little on mental illness too ๐ด๓ ง๓ ข๓ ณ๓ ฃ๓ ด๓ ฟ
Severe ME/CFS patient and advocate. Writer, photographer, filmmaker. artist, activist, creative. Bedridden since 2013 sick since 2004. Never. Giving. Up. โ
ME. Spouse w LC, ME. Writer, bread baker, daydreamer. Still waiting on fair funding and apology from HHS. Masking like someoneโs life depends on it.
95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness.
With ME/CFS 36 years, severe ME 31 years.
@IrishMECFSAssoc trustee 28 years
26 publications in peer-reviewed journals
Social media: https://me-pedia.org/wiki/Tom_Kindlon
A global network of people empowering one another to fight for equity for myalgic encephalomyelitis. Home of the #MillionsMissing linktr.ee/meactnet
#pwME #MyalgicEncephalomyelitis #LongCovid #MECFS #ChronicIllness #DisabilityJustice
