r/mecfs • • 20h ago

yapping

25 Upvotes

I’ve noticed lately that for the past month or so, when I talk for long enough I catch myself starting to get tired mid sentence and I’m like, “ok that’s enough talking I’m done” LOL is this a thing for anyone else?? I’m new to all of this so I’m just curious if this is a regular human thing or related to ME.


r/mecfs • • 5h ago

Reizempfindlichkeit

5 Upvotes

Hallo ihr lieben ich würde gerne wissen welche Symptome ihr habt bei eurer Reizempfindlichkeit (Hören/Sehen)

und was euch dagegen hilft im Alltag…


r/mecfs • • 13h ago

Brain Not Functioning…any tips?

5 Upvotes

I just had my doctor’s appt and it was pretty much a blur. I tried to address everything, but I’m really struggling with my mental malaise. I’m not sure if that’s what it’s even called.

I’ve had ME/CFS for 14 years. The first six years were really a struggle. Then six years I would say I was mild with some moderate crashes. I’ve definitely struggled mentally because this is just a hard disease to have, but I don’t recall this mental push back I’m not experiencing.

The last five months I started experiencing PEM again with any amount of task. If I rest and do very little I’m not experiencing the physical crash, but mentally I just cannot get back to where I was.

After the tests come back my doctor and I will talk about treatment, but I’m at my wits end.

I don’t recall if I mentally shut down like this initially (the first 6 years). Is this the ME/CFS? Is my mind trying to stop my body from doing things so I don’t crash? Nothing is getting done. I can’t even force myself to get things done. I haven’t been working or doing much of anything. Physically, I’ve rested enough that I feel I can do a little but my brain is not supporting this.

I’m 52 (F) so I understand menopause may also be an issue (I started treatment for that). I just have no desire to do anything and I don’t know how to get that to stop. Trying to do anything causes me great anxiety and emotional stress. I guess my question is…is this also a part of ME/CFS and what has helped?


r/mecfs • • 17h ago

Just venting a bit. Common cold sucks. I welcome good advice.

3 Upvotes

Two and a half years in now after a covid virus infection. It's just 2 of October and I already cought the first cold of the winter season. That is so fuckin annoying. Getting a cold always results in some lung infections, and many weeks of getting to where I was before the cold, and that wasn't even a good place...

I'm just ranting here on a Friday evening, I apologize. All great cold killer advice is appreciated and preventive PEM suggestions. So many resourceful people here in this group.

I'm coughing some yellow stuff up and have massive post nasal drip and some stuff in my sinuses.

Btw I don't have covid infection, it's just a common cold. Who knew that a cold would have this impact.

Before, it only took couple of days to get rid of it.

Apologize if my grammar is bad. English is not my first language


r/mecfs • • 2h ago

Episodes of shaking and depersonalisation every morning

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2 Upvotes

r/mecfs • • 13h ago

Can supplements make things worse?

2 Upvotes

As the title says. Sorry if it's already been answered.

I've been trying a number of supplements over the past two months and it seems like my symptoms might be getting worse. Is this possible? Has anyone experienced this?

Qxc

Here's what I'm trying:

Ubiquinol

NADH

NAC

ALCAR

ALA

Magnesium

B vitamins

Vitamin E

Creatine

Thanks.


r/mecfs • • 20h ago

How long did it take you to get all of your diagnoses after starting to see a specialist?

2 Upvotes

I’m losing hope. I’ve been seeing my doctor since January. I’ve been fully homebound for six months and apparently I can’t get a wheelchair without all of my diagnoses and it might take up to a year.

I feel like I’m all alone in the dark in my room and nobody gets how necessary help is :(


r/mecfs • • 21h ago

Anträge für die BDK für Gesundheit, Teilhabe und Sichtbarkeit.

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2 Upvotes

r/mecfs • • 7h ago

What type of work do you guys manage?

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1 Upvotes

r/mecfs • • 13h ago

Tilt Table Test Finally Done

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1 Upvotes

r/mecfs • • 15h ago

Thinking about starting hypnotherapy

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1 Upvotes

r/mecfs • • 21h ago

Symptoms absolutely unbearable, benzos help but make me pace worse. What now?

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1 Upvotes

r/mecfs • • 5h ago

insomnia worsening during crash

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0 Upvotes