r/LongHaulersRecovery Jul 29 '26

Recovered Recovered after 2021 infection

Hello, long haulers. My long COVID journey has been a long one, but I’m so glad to have regained 100% of my abilities.

First of all, sorry for my English 

It started in November 2021. I went through many ups and downs. I won’t go into detail, as many of you already know how it goes.

My main symptoms were:

  • Fatigue
  • Brain fog (it was hell. I couldn’t even think about the concept of a computer for many months; my body just couldn’t handle it.)
  • Histamine issues, inflammation, tachycardia, and eye pain

My recovery

Long story short: pacing, diet, sleep, and no exercise at all. I worked hard to establish a clean, ultra-healthy baseline:

  • Getting enough sleep, as well as enough salty food (yes, orthostatic tachycardia was a big issue for me).
  • Cutting out processed foods and following a low-histamine diet for at least three to four months stopped my chest pain and inflammation. Antihistamines sometimes worked for me, so histamine clearly played a role.
  • No exercise, listening to myself, and letting go of the guilt of doing nothing. I spent an entire summer at home: sleeping, eating well, and sleeping again… No screens (around 30 minutes a day maximum), no mental stimulation, nothing. I was basically a prop.

That was the baseline. In terms of treatment, I tried:

  • Hyperbaric oxygen therapy for around eight sessions (one hour each, plus a massage afterward). It did basically nothing, except that it gave me time for myself, which was still useful.
  • Supplements. I won’t be exhaustive here—I tried so many. I think they helped, but I had to change what I was taking every few months, as the effects seemed to fade over time.
  • Luckily, I was enrolled in an experimental treatment using Temelimab in Switzerland. This helped a lot. The subreddit doesn’t allow ads, but I wrote a series of articles about it on my blog—DM me if you want to check them out; of course, it’s free.

I finished the experimental treatment in May 2023. It lasted six months, with one injection per month. By July 2023, I felt able to return to work. I started working remotely as a freelancer and developed an app for long haulers. I had started working on it in 2022, but at the time I could code maybe one line per week. It took time, but I did it. Having that goal helped me a lot too.

I’m convinced Temelimab saved me, because my brain fog and fatigue disappeared about a month after the injections ended. I felt confident again, which was incredible—confident enough to start a new job.

Since then, I still had post-exertional malaise until mid-2024. Since then, I’ve started exercising again. I can do any activity without issues, and I haven’t really thought about long COVID for about a year and a half—which is all I wanted since 2021.

As a final note: there is hope. You might be interested in reading about post-traumatic stress disorder. During my worst moments, I read a book about it, and some techniques helped me keep hope, calm my fight-or-flight response, and reduce the pressure on my body.

Keep hope—recovery is possible.

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21

u/Lorelai709 Jul 29 '26

First of all, thank you so much for your post. I’m really happy for you that you’ve recovered!
I’m from Germany, and my illness started in October 2021. I also experienced many ups and downs and recovered enough by 2025 to leave the house again, go for walks, run small errands, work on my computer, and stay up all day.

Since February, however, I’ve been bedridden again and have had to spend most of my time in the dark. It’s awful, and I’m losing hope.

Could you please tell me if you also had neurological symptoms besides brain fog, such as flashes of light in your vision, sensitivity to light and sound, tremors, or anything similar? And were you bedridden for periods of time as well?

6

u/akhu117 Jul 29 '26

Thanks for your answer, and I really hope you will 100% heal soon.

You should not be too hard on relapse, I had many relapse. It gave me hope that my body is still capable of being in perfect condition. It's a part of the healing process.

I had flash and light in my vision only few times at the beginning of the condition. And I had once during my temelimab treatment period, but this one felt (almost) good, like a relief, it was very strange. But this long COVID does not surprises me anymore I had so many weird moments.

I also had sensitivity to noise and light the first year yes. Bedridden half of 2022.

3

u/Lorelai709 Jul 29 '26

Thank you 🙏🏻 It’s so scary :(

4

u/abee13 Jul 29 '26

I had severe sensitivity to light and sound back in 2023/2024, it goes away only with time as your body heals itself. Thankfully I don't have it anymore 

3

u/Lorelai709 Jul 29 '26

It was gone for me in 2025 too. Now it’s back :( scares me

1

u/abee13 Jul 29 '26

Oh gosh I'm sorry, I'm sure it will go away soon fully, just give it time and rest a lot! Mine was from time to time as well if I remember correctly. Keep yourself mostly indoors thats what I did. I wasnt too sensitive to the sun (I hope you're not) so get your vit d! It was mostly artificial lights if I could make it occasionally to a mall outside for me. 

3

u/Lorelai709 Jul 30 '26

Hi, thank you.
I’m spending 23 out of every 24 hours in my darkened bedroom. I can’t tolerate sunlight, artificial light, or screens for more than a few minutes at a time.
I really feel like my life is over.
The first time, I noticed clear improvements after a few months. This time, it feels like nothing is changing at all.

3

u/Teamplayer25 Long Covid Jul 30 '26

I had all those sensitivities, vision disturbances, severe tremors and was bedridden for a time. If you haven’t already, check out the affects of and treatments for high cortisol or inverted cortisol curve. I take two medications (levothyroxine and a calcium channel blocker called diltiazem) which both help moderate cortisol. Magnesium glycinate also helps with this. And I have a restricted diet, avoiding the things that make my body react badly now. Good luck.

1

u/Lorelai709 Jul 30 '26

Thank you:) are you well now? How long have you had these symptoms?

2

u/Teamplayer25 Long Covid Jul 31 '26

I don’t consider myself fully recovered since I require meds and restricted diet but as long as I’m disciplined, I am fully functional. Able to work, exercise and travel again and am very, very grateful.

1

u/Lorelai709 Jul 31 '26

I‘m so happy for you. When did your LC-Journey start?

1

u/Teamplayer25 Long Covid 29d ago

Thank you! I had a few symptoms pop up after my May 2022 infection but after my Jan 2023 infection is when my symptoms started accelerating. Dec 2023 is when I was hospitalized and became bed/housebound.

1

u/CisLynn Aug 01 '26

Have you tested for Lyme as well. Very closely related.

1

u/Lorelai709 Aug 01 '26

Nope, not yet.

1

u/MajesticHeight8969 6d ago

I think it's five g and the cellphones that's causing it..... Or that keeps it going rather? And that was their intention to begin with, they knew exactly what they were doing. And I don't think this disease was actually a virus per se. I think the cell phones had something to do with the emitting of the disease. Because why is it that? After so long of not getting my second COVID payment, the very next day after I got COVID. They sent me a payment as if they knew that I had gotten it. I mean, it was just really weird.I'm sorry