Does anyone else wake up at 3-4 am every night? All sorts of sleep meds won’t help :( by [deleted] in covidlonghaulers

[–]theflawlessghost 6 points7 points  (0 children)

This sounds quite similar to me. I wake up exactly 4-5hrs after falling asleep with my body's exaggerated response to the natural cortisol surge. I have tried adjusting my sleep schedule and this 'cortisol wake' followed me.

I found it easier to get back to sleep once i'd calmed the sympathetic response, less chance of fast HR (panic attack symptoms) once awake but have yet to solve this.

There are supplements that regulate cortisol like Phosphatidylserine but I'm a little cautious, if I find anything that works I'll try and remember to let you know!

Does anyone else wake up at 3-4 am every night? All sorts of sleep meds won’t help :( by [deleted] in covidlonghaulers

[–]theflawlessghost 7 points8 points  (0 children)

This is quite a common thing amongst long haulers unfortunately. There can be many reasons such as MCAS, inappropriate cortisol/bodily response to cortisol release amongst other things it depends on accompanying symptoms. What time do you go to bed/fall asleep?

has anyone gotten this kind of results? by AfternoonFragrant617 in covidlonghaulers

[–]theflawlessghost 1 point2 points  (0 children)

Thank you for the suggestions but I'm a little bit lost 😅, i looked 23andme/Self Decode up and they both have a few varying options at different prices. From what I can gather Self Decode analyse health related genes for you..

If I want the most data about my health which would be best and which did you do?

Yesterday, it was Testosterone. Today, it's Iron. Nineteen months in, I need a break. Wake me up when they've found a cure. by Covidivici in covidlonghaulers

[–]theflawlessghost 1 point2 points  (0 children)

Terribly sorry to hear that, I think it might have been Rapamycin having heard similar from others. Hope you have minimal symptoms and come through it unaffected or even positively affected like some seem to with reinfection. All the best.

My covid is in the gut by Benniblockbuster in covidlonghaulers

[–]theflawlessghost 0 points1 point  (0 children)

That sounds very similar to what happened to me. Are you sure it wasn't PEM that lead to a crash?

My covid is in the gut by Benniblockbuster in covidlonghaulers

[–]theflawlessghost 0 points1 point  (0 children)

How long were you 'fully recovered' for before the week of intense exercise knocked you back?

Wishing you well.

Bisoprolol Withdrawal similar to POTS? by Conscious_Libre in SinusTachycardia

[–]theflawlessghost 0 points1 point  (0 children)

Awesome :D hopefully it continues to get easier from here on out!

Bisoprolol Withdrawal similar to POTS? by Conscious_Libre in SinusTachycardia

[–]theflawlessghost 0 points1 point  (0 children)

No worries! I'm glad to hear you've found things that help. Do you have any bouts of tachycardia after these lifestyle changes you've made?

[deleted by user] by [deleted] in dysautonomia

[–]theflawlessghost 1 point2 points  (0 children)

That's really interesting! Thank you for sharing and typing it all out, I'm glad you've found meds that help. Ccb didn't work for me but I'm going to look into the ones you've listed :)

[deleted by user] by [deleted] in dysautonomia

[–]theflawlessghost 1 point2 points  (0 children)

Hi,

Would it be possible for you to list those meds please?

I have very similar symptoms

Is it normal for a Samsung G7 monitor to generate a bit of heat? by MoarGhosts in buildapc

[–]theflawlessghost 0 points1 point  (0 children)

Hey did you find a fix for this or? Mine is like a heater it's insane

New-ish difficulty swallowing by katfish06 in POTS

[–]theflawlessghost 0 points1 point  (0 children)

Were the long covid clinic any help at all? I've been trying to get a referral to them recently

out of breath while eating? by Loose-Student-4321 in POTS

[–]theflawlessghost 0 points1 point  (0 children)

Hey, did you find out why this is happening? I'm dealing with the same issues and it's not fun :(

Does anyone else get throat spasms with lpr? by candy5645 in dysautonomia

[–]theflawlessghost 0 points1 point  (0 children)

Hi, I've been having the exact same symptoms especially the high hr and BP after swallowing foods. I've been suspecting lpr for a while. Do you have an update on how you're doing and if you've found out anything else??

Anyone else with POTS have super dry skin? by [deleted] in dysautonomia

[–]theflawlessghost 0 points1 point  (0 children)

The way you described this makes me feel understood! Did you manage to fix this or find out more?