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ME/CFS Severe → much betterIll 8 years before improving or writingNeeds ongoing treatment

Bedridden with ME/CFS after COVID, now much better with an infrared mat

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill before improving or writing
8 years
Last post
Sep 2026
In their words
  • Condition: ME/CFSSo I have apparently had mild cfs for ~8 years which started with a stress induced autoimmune illness. In context ↗
  • At worst: SevereI went from severe (almost completely bedbound) to mild (almost no symptoms anymore). In context ↗
  • Now: Much betterAt the moment I am mild again, I very rarely have brain fog. My ability to read is like it was before cfs. In context ↗
  • Began after: stress or burnoutstarted with a stress induced autoimmune illness
Read from 24 of their posts and comments; links to the 14 this page draws on

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Summary

Jukarii had mild ME/CFS for about eight years after a stress-induced autoimmune illness, then became bedridden with breathing trouble after a second COVID infection in summer 2024. An infrared mat, started in January 2025, brought a large improvement within days: energy to clean and dance without crashing, and normal sleep. Symptoms returned after five or more days without the mat, and thinking stayed somewhat slower than before.

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What they tried

Their words about each treatment
  • therapy · WorseDue to therapy, symptoms got worse In context ↗
  • do sports · WorseI was very surprised when my therapist tried this with my and i just felt like shit. In context ↗
  • sunlamp · No changeHowever, I tried using a sunlamp before but that didn't do anything for me. In context ↗
  • pacing · HelpedAnd pacing of course, which definitely helped, but mostly in not crashing and not really helped improving. In context ↗
  • visible app · HelpedI've only used it for a couple of weeks by now In context ↗
  • infra red mat · Helped a lotI went from severe (almost completely bedbound) to mild (almost no symptoms anymore). In context ↗
  • intervall fasting · Not saidat the moment I am experimenting with infrared light therapy, intervall fasting (maybe actual fasting in the future) and antihistamines In context ↗
  • cetirizine · No changeI tried cetirizine, but other than that it made me incredibly tired (still not able to sleep though) it did nothing :/ In context ↗
  • meditating · HelpedI have started meditating, which works really well for me. In context ↗
  • anti depressants · Much worseI have tried some anti depressants and anti anxietiy meds but for me any kind of meds seem to make the overall symptoms a lot worse :( In context ↗
  • saunas · WorseI react quite badly to saunas and have lots of trouble with dizziness. In context ↗
  • supplements · Not saidI only tried a couple different supplements, antihistaminika and some different antidepressants, which sadly all either did nothing or made it worse. In context ↗

Approaches: Alternative therapies

Their path

Very severeSevereModerateMildNear normalRecoveredonset2 y4 y6 y8 y

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, with time counted from when the illness began. Hover or tap a point. 1 step has no time and sits in story order between the steps around it. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
~8 years before January 2025mild ME/CFS began after a stress-induced autoimmune illnessSo I have apparently had mild cfs for ~8 years which started with a stress induced autoimmune illness. In context ↗Mild
—winters made symptoms moderate-severe; depression therapy with exercise made things worsebecause my symptoms get a lot worse in Winter (was mild in summer/spring and moderate-severe in fall/winter) In context ↗Moderate
summer 2024second COVID infection left them bedridden with trouble breathingAfter my second Covid infection last summer shit really hit the fan and i ended up being bedridden and having trouble breathing. In context ↗Severe
January 2025infrared mat brought energy back, no crash after cleaning and dancing, normal sleepI'm back to mild cfs I think - but going from basically not able to breath to being able to leave the house without crash In context ↗MildRed light, PEMF or microcurrent (unspecified)
2026-09-05still mild, symptoms slowly return after five or more days without the matAt the moment I am mild again, I very rarely have brain fog. In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI also try to find things that I can do without a crash In context ↗
  • Brain fogI very rarely have brain fog In context ↗
  • Sleep problemsIt usually took me 2-3 hours to fall asleep (if I could fall asleep at all) then slept for like 10h and woke up feeling as tired as before. In context ↗
  • Pain & fibromyalgiaI still have quite some pain I think, just a lot less than before. In context ↗
  • Headaches & migrainelike less energy, headache, back pain, not being able to fall asleep and such In context ↗
  • Light & noise sensitivitywhile listening to loud music (something i couldn't stand for a very long time) In context ↗
  • Breathlessnessi ended up being bedridden and having trouble breathing In context ↗
  • Anxiety & low moodI've been loosing hope for so long and thinking about ending it all because life didn't feel like it was worth living anymore In context ↗
  • Hair lossMy hear stopped falling out when I went back from severe to mild In context ↗
  • POTS & dysautonomiaI react quite badly to saunas and have lots of trouble with dizziness. In context ↗
  • Temperature regulationmy symptoms get a lot worse in Winter (was mild in summer/spring and moderate-severe in fall/winter) In context ↗

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