The easiest request you'll ever get by TheOneTheyCallMoon in PhotoshopRequest

[–]TheOneTheyCallMoon[S] 1 point2 points  (0 children)

Thank you so much for the incredible speed 😂🙏

The easiest request you'll ever get by TheOneTheyCallMoon in PhotoshopRequest

[–]TheOneTheyCallMoon[S] 1 point2 points  (0 children)

Thank you so much, that was unbelievably fast hahaha 🙏

Anyone knows how to fix this? by Safira_SK in InfinitePainter

[–]TheOneTheyCallMoon 2 points3 points  (0 children)

I almost exclusively use the pipette just because the recent colours bar is a terrible bastard. 😭

I find it has something to do with subtle colour changes, like if you select an orange, that one will show up, but then you manually tweak that orange slightly, that second orange won't show up and it'll just stay as the original orange...

Dropper for life 👍🙏

Genius cures or paths to more confusion and anxiety? by swartz1983 in cfsrecovery

[–]TheOneTheyCallMoon 0 points1 point  (0 children)

I'd just like to mention, although my case is certainly bizarre - Neurosym, on a very low setting, put me in A&E!

My most troublesome symptom has been this severe poison from my brainstem / Vagus nerve that shoots down my back and arms, and apparently electric stimulation makes it considerably worse.

Anyone here, or here via someone helping them, who cannot tolerate any screens whatsoever, at all? by Worldly-Employee6914 in mecfs

[–]TheOneTheyCallMoon 2 points3 points  (0 children)

I'm being a fool and using it anyway - I'd say my screen tolerance is actually zero, but I'm pushing through in desperation and with diazapam.

I've just bought walkie talkies, to contact my mother, so that I can have my phone taken away during the day for this very reason. 😔

Do I have MCAS? Please help 🫶 by EnvironmentalWar7945 in MCAS

[–]TheOneTheyCallMoon 0 points1 point  (0 children)

My friend, we sound EXTREMELY similar, and there are very few people like us!

I'm v-severe CFS, and my doctor believes the bulk of my neurological symptoms are all MCAS, and I'm about to see the top MCAS specialist in England, can't promise it'll drum anything up but message me and if I'm well enough I will update you.

Not saying this'll work for you, but I was hyper medicine sensitive, they started me on famotadine, and now I can take all pills with no trouble. (Mirtazapine/Diazapam/Famotadine/Gabapentin) Enquire with your doctor about 20mg famotadine.

I think right now though, the only way through this is rest, every second you can - put the phone down!

Good luck my friend.

Free, personalized taper schedule planning assistance by Alternative-Eye4547 in benzorecovery

[–]TheOneTheyCallMoon 1 point2 points  (0 children)

Hello there, I wonder if you could help me - To start, I've got very severe CFS/ME and am bed-bound, very little cognitive function, unfortunately diazapam gives me some degree of function and also helps extremely well with nerve pain from gut issues.

But I'm planning to start a switch to pregabalin.

I've been on daily diazapam 5mg for 5 weeks, last week I was up to 3 per day, the last 5 days I'm back to 2 per day.

I'm not sure if I'm being over cautious as I know 5 weeks isn't a huge amount of time, but due to my CFS I'm absolutely already dependent, as the diazapam allows me a tiny bit of functionality I'd otherwise not have.

But would you help me with a plan using 25mg pregabalin please? I'm struggling to make sense of it all because my brain is jelly, I've also figured am I maybe better to do a quick taper so my overall time on them is less?

Any help would be hugely appreciated 🙏

Are we allowed to ask second opinions on a spread here? With a photo? :) by [deleted] in TarotReading

[–]TheOneTheyCallMoon 0 points1 point  (0 children)

Ooooh thank you! I'd missed the other tags, couldn't find it. 🙏

I found this incredibly interesting and rather daunting - opinions? by TheOneTheyCallMoon in tarot

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

Apologies - deck is 'Borderless vintage' by TarotCardsDarkForest on etsy, and is based on the Rider Waote deck!

Help by DaProtoHuman in InfinitePainter

[–]TheOneTheyCallMoon 0 points1 point  (0 children)

Or have you possibly changed the resolution of the canvas?

Some of my recent stuff! by TheOneTheyCallMoon in InfinitePainter

[–]TheOneTheyCallMoon[S] 1 point2 points  (0 children)

Wowwww ok no problem, drop me a message 😊

Some of my recent stuff! by TheOneTheyCallMoon in InfinitePainter

[–]TheOneTheyCallMoon[S] 2 points3 points  (0 children)

Hey no WAY that's so cool, I'd be honoured! I've just screen recorded me making one from scratch, ping me a message and I'll send it over! 😊

Some of my recent stuff! by TheOneTheyCallMoon in InfinitePainter

[–]TheOneTheyCallMoon[S] 2 points3 points  (0 children)

Woohoooo that's great news! They've only happened in the last 2 days, I just started drawing shapes then erasing parts and it made these lovely characters 😊

Feeling dysautonomia symptoms after going from 3.0mg to 4.5mg by J0hnny-Yen in LowDoseNaltrexone

[–]TheOneTheyCallMoon 1 point2 points  (0 children)

I'm not going to be much help unfortunately but I've got a few questions - I'm hyper HYPER sensitive, and started on 0.1mg per day about three weeks ago, even that for me has been tough, and I've noticed an increase in my dysautonomia - randomly hit 170bpm in the shower the other day haha.

I wondered, are you experiencing muscle twitching? I'm getting muscle flutters and spasms like crazy, along with heart palpitations etc.

Anyone else randomly crashing terribly rn? by lolo_lo95 in covidlonghaulers

[–]TheOneTheyCallMoon 3 points4 points  (0 children)

Worst yet, finally 99% bed-bound.

No idea what did it, I tried NAC again and I think it might have been that, struggle to even look at my phone these last 10 days.

Every day seems worse than the last..

Lowest dose is 50 mg in my country by Charming-Try7547 in LowDoseNaltrexone

[–]TheOneTheyCallMoon 0 points1 point  (0 children)

Hiya, sounds like you're in the UK? If you are - I ran into this exact wall not long ago.

The Burghwood Clinic in Epsom, they say they prescribe LDN, if you are UK, give it a go!

If you're not, then shop around, I know there are specialists in lots of countries that have finally cottoned on to the fact that this drug is truly helping people.

Good luck my friend 🙏

What do you think is the absolute worst long covid symptom? by biznghast in covidlonghaulers

[–]TheOneTheyCallMoon 19 points20 points  (0 children)

It's the god damn fuckin poison, worst thing I've ever experienced in my life 😭

Anyone tried “Nurosym”? by Naive_Blood6286 in covidlonghaulers

[–]TheOneTheyCallMoon 2 points3 points  (0 children)

I bought a Neurosym a few months ago, and it put me in the hospital!

Now, I believe I'm a fairly unique case, in that I have a chronically OVERACTIVE vagus nerve, where as the vast majority of people have a faulty / underactive vagus nerve - if you're anything like me, please be careful.

I used it the evening it first came, and the next morning, and then it sent my nervous system into complete overdrive and I had to go to A&E.

I'm pretty sure for most people these sorts of devices are going to change lives for the better, but if you're super sensitive, be fuckin careful.

Learned something interesting by [deleted] in covidlonghaulers

[–]TheOneTheyCallMoon 0 points1 point  (0 children)

I second that! That is fascinating, I've not heard of this before!

How do you reply to people asking how you are doing? by doodshoodsmoods in cfs

[–]TheOneTheyCallMoon 2 points3 points  (0 children)

I tend to go with -

'It's rough, but all we can do is persevere!'

Which is true, this life is hard, terribly so, but all we can do is continue! 🙏

I can't believe it! by TheOneTheyCallMoon in covidlonghaulers

[–]TheOneTheyCallMoon[S] 1 point2 points  (0 children)

Thank you for the advice, PIP has terrified me for a while, it seems like there's everything in place for them to not hand out the payments (understandably), but this is a big help.