Plugging a great MECFS youtube channel (SPD)
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Very severe and gastroparesis
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Anyone know any good cannabis oil for pain?
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Me every day.
Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
Severe and bedridden. Looking for games like Unpacking
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
I HATE toxic work culture, especially about illness
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
I HATE toxic work culture, especially about illness
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Wishing you all if not a happy new year, at least a less difficult one 🤞
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Switch issue - I keep autoselecting everything
Dig, fight, explore, build! Nothing is impossible in this action-packed adventure game. The world is your canvas and the ground itself is your paint.
I miss coffee
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Love jess.a.creates. This one in particular spoke to me, and we all deserve a good meltdown (although blasted PEM prevents us!!!) 🫶
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Quebec government last week informed my doctor they will no longer allow them to give us telephone appointments, by next year.
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Fantasy MECFS/LC/Lyme etc Specialized Centre
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
I hope I’m not posting here too often, I don’t want to hog the space here. Here’s some Arrested Development commissions I did before I became severe
A place for people living with ME/CFS to share any art and creations. It doesn't have to be related to ME/CFS!
Just a lil lighthearted one for any ATLA fans here ♥️
Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
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Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
LC/MECFS be like
Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
Hard not to feel like this lately
Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
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Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
2020 onwards: completely black
Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
I approve of this
Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch
✨Spooky season art 🎃👻🦇 A few I made from previous years ✨
A place for people living with ME/CFS to share any art and creations. It doesn't have to be related to ME/CFS!
For any artists here: a subreddit created where you can share your art 🎨
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
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Support group disguised as a comedy club, run by someone whose autonomic nervous system forgot how to work a light switch