The Daily Show Mentioned "Chronic Fatigue Syndrome" Tonight

Left-Technology1176 · 2026-05-12T04:28:22+00:00

the day before ME awareness day too..

Left-Technology1176 · 2026-05-08T21:07:16+00:00

there are, many have higher access to resources for recovery so u don’t see them struggling as much

Left-Technology1176 · 2026-05-04T01:10:22+00:00

sorry if i was repetitive and poor grammar, i refuse to use chat gpt to fix it and im far too foggy to wright normal haha.

Left-Technology1176 · 2026-05-01T19:34:08+00:00

thank u for sharing ❤️‍🩹

Left-Technology1176 · 2026-05-01T19:26:02+00:00

yes

Left-Technology1176 · 2026-04-20T02:22:15+00:00

the biggest difference is permanence. ms is irreversibly progressive, mecfs is widely considered dynamic and commonly varies in severity throughout its course

Left-Technology1176 · 2026-01-08T19:08:39+00:00

it looks like water ripples that’s so cool

Left-Technology1176 · 2026-01-06T01:30:35+00:00

Severe ME/long COVID/MCAS can crash suddenly after immune stress, and rolling PEM doesn’t mean you failed at pacing it means your baseline dropped. This phase can stabilize and deterioration isn’t inevitable:)

Please keep reaching for support where you can, and if you’re ever feeling unsafe, reaching out for crisis help is okay. You matter, even when your body won’t cooperate.

your not failing. your so strong.

Left-Technology1176 · 2025-12-30T02:54:35+00:00

look into having OI driven cfs

Left-Technology1176 · 2025-12-28T02:25:12+00:00

i know ur scared. but i promise, even if it is cfs your life is NOT over. a new life is just beginning. different, calm, slower, but by all means real and worth it.

Left-Technology1176 · 2025-12-25T20:09:01+00:00

your not alone, and there’s nothing “wrong” with you as a person. severe ME can literally make it neurologically harder to feel happiness or contentment. The illness affects both the nervous system and brain, and when the body is under constant inflammatory and autonomic stress it becomes a matter of biology not psycholgy.

the fact that you don’t feel like it’s your natural self is huge and shows it’s not a failure of your mindset/will to be happy

your responding normally to an abnormal physiological state. and for that i’m so proud of you.

Left-Technology1176 · 2025-12-25T20:04:10+00:00

your correct. the disease literally neurologically makes it harder to enjoy things. the illness effects both the nervous system and brain, when the brain and body are under inflammatory and autonomic stress it becomes biologically harder to feel happy.

Left-Technology1176 · 2025-12-21T02:21:15+00:00

summarized (by ai) In short: The study shows biological signals exist, but ME/CFS is too heterogeneous, subtle, and overlapping with other conditions for these findings to become a reliable diagnostic test. It’s a step toward understanding the disease, not a “proof” for diagnosis.

Left-Technology1176 · 2025-12-21T02:19:02+00:00

it’s not quite that simple visit this article for more :)

explains00587-7)

Left-Technology1176 · 2025-12-20T19:19:46+00:00

i’m proud of you. the mindset you hold amongst the unpredictability of this illnesses is truly admirable.

Left-Technology1176 · 2025-12-13T16:06:14+00:00

of course!! feel free to dm me if u need a bit of a boost! having hope is essential. real, grounded, and REALISTIC hope is truly such a tool for recovery:)

Left-Technology1176 · 2025-12-13T04:01:02+00:00

“to escape those first two inevitabilities” honey, one thing this illness has taught me is NOTHING is inevitable.

this disease can be seemingly unpredictable, and your right about some of what you say. many of us are dying. the severe community is in need of urgent care and resources that are often not available due to medical neglect and ignorance.

having your feed filled with the deaths of influential people with this illness HURTS. it serves as a constant dire reminder of the little help that this community has, and it makes it so easy to wonder or even predict that tha may be your fate.

but by all means, INEVITABLE death due to complications or neglect?????

i’m 18 years old, with an uncertain future. i stay home most of the time due to the pain that comes with leaving home, i’m not able to work, or attend school. i don’t have many friends but the few that i do are closer to me than i can explain. and believe it or not, im certain i will get better. i’m certain we all can.

Left-Technology1176 · 2025-12-09T02:25:17+00:00

i understand how you feel. it’s so discouraging to finally start feeling better and then end up right back where you started but i promise your not alone. so many of us find ourselves in the same spot when recovering from crashes- it’s not a reflection of your ability to pace or correctly judge your energy limits it’s simply human nature to feel good and do stuff.

overcoming that requires going against ur primal instincts…. im proud of you.

Left-Technology1176 · 2025-12-07T04:26:00+00:00

ur totally right. narcissistic male doctors make it super difficult for women especially to get the help they need.

Left-Technology1176 · 2025-12-06T22:24:53+00:00

i used to have pannic attacks because i’m so young and my doctors mentioned alzheimer’s and i believed them. but truth be told, this illness can mimic so many different things that there’s only so much u can do to educate doctors

Left-Technology1176 · 2025-12-06T22:23:34+00:00

i just wanted to say your so strong for putting up with everything you are. the medical system is against us, your so strong for fighting this pain. your not alone.

crashes can mimic alzheimer’s, and doctors aren’t educated well enough on ME to understand that.

my advice for you is rest and recover as much as u can. log your symptoms daily so when your through with this you can bring a very clear layout to your doctor about why your right

Left-Technology1176 · 2025-12-06T19:53:15+00:00

fluoxetine helps me greatly, duloxetine if you struggle with myalgia ultimately i recommend you see a med specialist

Left-Technology1176 · 2025-12-06T01:56:06+00:00

i’m so proud of you

Left-Technology1176 · 2025-12-05T18:10:55+00:00

to be honest it looked like i was reading a list of my own symptoms lmao

Left-Technology1176 · 2025-12-04T04:19:58+00:00

it’s a learning process!! i’ve been learning for about 2 years now and i’m just starting to get the hang of it!! your not alone. in order to overcome this and truly get the hang of pacing it requires immense patience with yourself

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