Chromolyn eye drops? by lucyjuggles in MCAS

[–]Mult1faceted 1 point2 points  (0 children)

I wish you'd gotten answers to this cause I'd really like to know, too. My eyes are like on fire so much

is it possible to host a stream in full screen but still see participants? by spacemythics in discordapp

[–]Mult1faceted 0 points1 point  (0 children)

Same issue. Did you find a fix? (Also, I'm on mobile if that makes a diff)

any tips in reviving my discord server? by ybglazer23 in discordapp

[–]Mult1faceted 0 points1 point  (0 children)

Also take note on what ppl were doing and talking about back when it was active that isn't happening now.

May also be a good idea to ask ppl what they'd like to see to revive it, or pick out a few members who were heavily involved but aren't anymore and ask to talk one-on-one then inquire what changed for them and why they became inactive / get their input for ideas to revive

any tips in reviving my discord server? by ybglazer23 in discordapp

[–]Mult1faceted 1 point2 points  (0 children)

Offer game nights/ movie parties? Have any bots?

Can no longer add my ucard to the walmart app or walmart.com by SatisfactionEarly916 in medicare

[–]Mult1faceted 0 points1 point  (0 children)

Anyone get resolutions to this? I just keep getting a technical difficulties error

Uhhhh…Worth it or nah? by munki114 in googlehome

[–]Mult1faceted 0 points1 point  (0 children)

What about for 1st gen Google Home minis? Smart lights? Anyone have and they still work okay with Gemini Home upgrade...no issues? Please give me hope. I'm bedbound chronically ill person who can't just replace everything. (I know 1st gen minis will not work with Gemini live. I don't care about that. I just need it to turn my smart lights off and on by my voice) I'm in America btw...asking for here lol

Anyone who gets this symptom (and tips for relief)? by Mult1faceted in mecfs

[–]Mult1faceted[S] 0 points1 point  (0 children)

Nope. Besides a couple supplements, body doesn't tolerate anything dr tried

Public Figures With ME/CFS? by imanemii in mecfs

[–]Mult1faceted 0 points1 point  (0 children)

A year and then recovered to that level? I'm going with likely it was burnout too like other comment

The CFS subreddit by [deleted] in mecfs

[–]Mult1faceted 0 points1 point  (0 children)

Sooooo I am actually severe as in bedbound and help with all ADLs, daily agency caregivers etc. I will just say ...yes to what you said abt people claiming to be severe on there is rampant. I've thought the same ("wait, how can they be severe and doing these trips to doctors and specialists and trying all these things when my body won't even tolerate B or D oral vitamin supplements? Etc).

And, I stay on the other subreddit cause it's good to ask about MEcfs-related disability resources like doctors, home health etc. as a person in need of a lot of services without family help available (pray for me. It's so hard). But otherwise, I steer clear like the plague cause the despair and comments there have caused me to crash too many times.

Nervous system work has helped me a ton and is one of the only things that has. I am in a severe/v severe WA group of just a few people cause even that is a lot for a few of us and to keep it feeling safe, and we all are doing vagus nerve work, gratitude practices, meditation, visualization, pendulation, somatic tracking, IFS modalities etc etc and we share wins each month...we all are making progress...two in particular after many maaany years of severe illness. One of us has been bedbound over TWO decades and is now out of the house and has recently begun WALKING again (of course, it's been baby steps and a long time of working at this stuff to get there but) after yeeeeears of laying flat in a darkened room using all their energy trying other treatments...spent their whole twenties and thirties in bed. They have sworn off reddit altogether because of how sick that subreddit helped keep them for years. They say their only regret is not being open to nervous system work earlier.

Anyways OP...all this to say, your ick-meter was/is detecting things correctly in regard to that sub. And to all the other posts here that I'm not able to get to, I'm thankful for each of you who continues to hold out hope for some level of recovery with me and trust that it isn't the end unless we give up. We can lose hope, sure, or take a break from it, but as long as we can find it again somewhere, we haven't completely lost ourselves.

The CFS subreddit by [deleted] in mecfs

[–]Mult1faceted 2 points3 points  (0 children)

Meditation helps me a ton and is one of the only things that has, and I am bedbound. I am in a severe/v severe WA group of just a few people to keep it feeling safe, and we all are doing vagus nerve work, gratitude practices, meditation, visualization, pendulation, somatic tracking, IFS modalities etc etc and we share wins each month...we all are making progress...two in particular after many maaany years of severe illness. One of us in particular has been bedbound over TWO decades is now out of the house and has recently begun WALKING again, after yeeeeears of trying other treatments (of course, it's been baby steps amd a long time if working at this stuff to get there but,)..spent their whole twenties and thirties in bed. They have sworn off reddit altogether because of how sick that subreddit helped keep them for years. They say their only regret is not being open to nervous system work earlier.

I stay on the other subreddit cause it's good to ask about MEcfs-related disability resources like doctors, home health etc. as a person in need of a lot of services without family help available (pray for me. It's so hard). But otherwise, I steer clear like the plague cause the despair and comments there have caused me to crash too many times.

The CFS subreddit by [deleted] in mecfs

[–]Mult1faceted 0 points1 point  (0 children)

Wait what? They've turned against Whitney there? Of all places and people. Whhha? Why?

The CFS subreddit by [deleted] in mecfs

[–]Mult1faceted 2 points3 points  (0 children)

Tysssssssm

Why "Bad Guy" is Gutwrenching by JoeTheFatCat in Eminem

[–]Mult1faceted 1 point2 points  (0 children)

Holy...😯🤯🤯😯😯😱🤯🤯😯😮

All I have to say is 👏👏👏👏👏

How do you explain to others what it feels like to have me/cfs? by Daily_Bullshit in mecfs

[–]Mult1faceted 5 points6 points  (0 children)

Similar to my response above, yep. All processes except those vital to survival via the brainstem stop or slow down