Doc: “Great news, tests are back and you are completely healthy!” Me: ⬇️10mo ⋅ DarkSpartan267 ⋅ r/cfs
I’m mostly housebound and bedbound, but on Monday I managed to get to the spray park for about 40 minutes!!!1yr ⋅ bewarethes0ckm0nster ⋅ r/cfs
I made pie to cheer myself up but slept through the timer for 2 hours. Can’t not laugh at my burnt sacrifice1yr ⋅ velvetarian ⋅ r/cfs
From my family's donation, $10,000 is going to the Open Medicine Foundation for ME/CFS research!!!1yr ⋅ Leopard149 ⋅ r/cfs
I (barely) managed to walk through a whole Ikea to get something I've been wanting for years! I doubt I'll be able to do much of anything for a week, but it's worth it for me.1yr ⋅ The_Meats ⋅ r/cfs
Saw this image on a completely unrelated meme and couldn't help but see it as the bill my body hands me every day.1yr ⋅ RabbleRynn ⋅ r/cfs
I made this meme six years ago and posted it on the sub. To quote Gossip Girl, “The more things change the more they stay the same”3mo ⋅ premier-cat-arena ⋅ r/cfs
photo regarding to my last post :) shaved off my hair, makes cfs easier :)1yr ⋅ wonderland2211 ⋅ r/cfs
Went through some documents for a disability application ... and found remnants of my past. I miss my life as a researcher 😥1yr ⋅ m_seitz ⋅ r/cfs
SO BASICALLY TONS OF MAINSTREAM DISEASES LIKE ALZHEIMER’S HAVE POORLY UNDERSTOOD PATHOPHYSIOLOGIES BUT WE DON’T CALL THEM ‘MEDICAL MYSTERIES’ THAT’S ONLY FOR CONDITIONS WE SUBTLY DELEGITIMIZE TO AVOID FUNDING BIOMEDICAL RESEARCH EVEN REMOTELY COMMENSURATE WITH DISEASE BURDEN1yr ⋅ snap793 ⋅ r/cfs
It definitely helps to have a very cute dog resting on your lap while you have to stay in bed all day! I hope this brightens your day!1yr ⋅ Leopard149 ⋅ r/cfs
Internet person advises Whitney to try genetic testing. Whitney is the son of Dr. Ron Davis, a leader of the Human Genome Project (r/dontyouknowwhoiam)1yr ⋅ snap793 ⋅ r/cfs
here’s a meme i made and also i found a more accessible way to listen to music if you’re severe in the post!11mo ⋅ premier-cat-arena ⋅ r/cfs
Fans holding up signs for ME/CFS at a FC Nuremberg football game. This is a good idea for advocacy!1yr ⋅ Aggressive-Toe9807 ⋅ r/cfs
Sometimes my friends share memes like this to be silly. If only they knew this is how it literally feels for us.3yr ⋅ Nime_Chow ⋅ r/cfs
“This Doctor’s Message to Other Doctors - Chronic Fatigue Syndrome is Real!”3yr ⋅ Thesaltpacket ⋅ r/cfs
Why are some people so much in denial they attack people for accepting they are sick?1wk ⋅ YolkyBoii ⋅ r/cfs
when non sick people start telling you how they think you can get better1yr ⋅ Nervous_Media_388 ⋅ r/cfs
Gonna use my carefully allocated energy to try and keep people from getting as sick as I am2yr ⋅ Thesaltpacket ⋅ r/cfs
I am finally making some small progress. I’ve been mostly bedridden/entirely housebound the past 6 months, but the last few days I’ve been attempting some small walks. Small progress, but it’s something1yr ⋅ DarkSpartan267 ⋅ r/cfs
A drawing I did for May 12th/ME Awareness Day. I figured I'd share it here as well, I hope you like it! :) The anemone/windflower is a symbol for illness in some cultures.3yr ⋅ elisesalen ⋅ r/cfs
I normalize so many things; esp after becoming severe over the summer. Too tired to grieve5mo ⋅ EmptyHome2222 ⋅ r/cfs
Neurologist recommended graded aerobic exercise. It’s 2022 ffs, I thought we were past this...1yr ⋅ superboreduniverse ⋅ r/cfs
Amazing new pilot study from Cornell finds ENORMOUS change in how controls and patients respond to exercise1yr ⋅ TomasTTEngin ⋅ r/cfs
18 y. o. with very severe ME abused in a UK hospital. Please share & sign the petition 2mo ⋅ divine_theminine ⋅ r/cfs
Got a tattoo of a bed because of my CFS cause if you don’t laugh about it you cry about it1mo ⋅ Serendipic_Epiphany ⋅ r/cfs
Making CFS visible. To all the people who are tired too. This is my calendar year with CFS. And I'm a mild case.4yr ⋅ last_of_the_lemons ⋅ r/cfs
Self-Promotion Day: I made a graphic novel about coping with ME/CFS4mo ⋅ crankycartoonistclub ⋅ r/cfs
In honor of the new Mean Girls movie, raise your hand if you’ve been personally victimized by ME/CFS4mo ⋅ premier-cat-arena ⋅ r/cfs
Living with an invisible illness is a constant negotiation between what you want to do and what your body will allow.8mo ⋅ glennchan ⋅ r/cfs
Sajid Javid, UK Health Secretary, commits to becoming world leader in the treatment & care for people with ME/CFS. His niece reportedly suffers from the condition...2yr ⋅ snap793 ⋅ r/cfs
😑 was thinking of meeting up w this dude at a bar tomorrow night (sorry we're irish lol his response translates to basically 'you have it so easy'. i try to save mentioning my CPTSD for in person.) how tf do u even navigate dating w this illness....1yr ⋅ newtongeiszler ⋅ r/cfs
The Resident Care Manager decorated the window next to my electric recliner for me today!1yr ⋅ MySockIsMissing ⋅ r/cfs
Having my first CFS flare in about 6 months so here's a photo of my hamster go brighten your day2yr ⋅ Little_Mog ⋅ r/cfs
