Miruvor
Sign up
ME/CFS RelapsedIll 1 year before improving or writing

Most days resting in bed or on couch with ME/CFS-like symptoms, slight gains then a relapse

Condition
ME/CFS
At worst
Not stated
Ill before improving or writing
1 year
Last post
Jan 2026
In their words
  • Condition: ME/CFSI have been dealing with symptoms of ME/CFS for the past 3 months that occured after a viral infection In context ↗
  • Now: RelapsedI feel like ive lost all my gains too ... My latest crash that decreased my baseline, has lasted for 3 months.
  • Began after: another virusAbout 8 weeks ago I fell sick with what I believed was the flu In context ↗
Read from 24 of their posts and comments; links to the 17 this page draws on

Request to remove this story

Summary

Tern 92110 fell ill in February 2025 with a flu-like illness, then strep throat and a bladder infection, and developed ME/CFS-like symptoms with PEM, constant pain and sore throat. They spent most days resting in bed or on the couch. They tried LDN at 0.1 mg but it triggered PEM, and reported only slight gains from ubiquinol, D-ribose, electrolytes, PEA, magnesium, pregabalin and diet changes. A later crash cut their baseline.

Ask Miruvor AI

Asking aboutTern 92110’s story

What they tried

Their words about each treatment
  • carbamazepine (Tegretol) · Worsewhen I take my medications in the morning (carbamazepine and sertraline) it all but knocks me out for an hour or so In context ↗
  • sertraline · No changeI already take anti-epilepsy meds (300mg carbamazepine) and anti-anxiety meds (100mg sertraline) unfortunately they dont seam to do much In context ↗
  • antibiotics · HelpedI was still feeling unwell with fatigue but the aches subsided In context ↗
  • walking the dogs and doing more · Much worseAfter a couple of days of this I was walking the dogs one day and I started feeling like sh*t so I immediately came home and went to bed. Since then I have been going down hill slowly. In context ↗
  • vit c · Not saidvitamins (vit c, b12, mega b, turmeric, king krill, magnesium, PEA) In context ↗
  • magnesium · Helpedglicinato de magnesio (dolores musculares y sueño) ... son las únicas cosas que hacen una ligera diferencia In context ↗
  • PEA · HelpedPEA (dolor y PEM) ... son las únicas cosas que hacen una ligera diferencia In context ↗
  • resting on the couch and pacing · HelpedAfter resting for 3 weeks on the couch, no shopping or house work, I was starting to feel like I was improving In context ↗
  • D Ribrose · HelpedHave you tried D Ribrose? It's given me a little extra boost in energy. I have it as a powder in my electrolyte drink daily. In context ↗
  • electrolytes · Helpedelectrolitos ... son las únicas cosas que hacen una ligera diferencia In context ↗
  • samsung Galaxy watch 6 · HelpedI used it for about a month and I found it helpful with tracking my heart rate In context ↗
  • LDN · WorseNext day I decided to take it in the morning and I had PEM. It made my pain so much worse and fatigue was worse as well. In context ↗
  • ibuprofen · HelpedI take as much ibuprofen and panadol allowed during the day but it only slightly takes the sting away from the pain. In context ↗
  • meditation · HelpedI practise meditation for pain daily in bed and it dose help In context ↗
  • baking soda · HelpedI've been having half a teaspoon of baking soda with a glass of water when I feel PEM coming on or before i do something that may trigger PEM and seams to be helping me. In context ↗
  • gluten free, anti inflammatory diet · HelpedI have modified my diet by eating gluten free ... and have seen some improvements in pain and fatigue In context ↗
  • probiotics, yakult and yoghurt · Helpedtaking probiotics/drinking yakult and eating yoghurt daily ... have seen some improvements in pain and fatigue In context ↗
  • pregablin · Helpedpregablin ... son las únicas cosas que hacen una ligera diferencia In context ↗
  • ubiquinol · HelpedUbiquinol ... son las únicas cosas que hacen una ligera diferencia In context ↗
  • batido de proteínas (protein shake) · Helpedbatido de proteínas ... son las únicas cosas que hacen una ligera diferencia In context ↗
  • benagene 500mg oxaloacetate tablets · WorseI've been using benagene 500mg oxaloacetate tablets once a day and its been giving me a bit of a boost in energy but after a few days of use i would get stomach pain and nausea. In context ↗

Approaches: Other drugs and medicines · Pacing · Supplements

Their path

Very severeSevereModerateMildNear normalRecoveredonset3 mo6 mo9 mo

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. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they were
February 2025fell ill with a flu-like illness (fatigue, body aches, dry cough)About 8 weeks ago I fell sick with what I believed was the flu In context ↗Mild
April 2025crashed while walking the dogs and declined from then onI was walking the dogs one day and I started feeling like sh*t so I immediately came home and went to bed. Since then I have been going down hill slowly. In context ↗Moderate
September 2025some improvement in pain and fatigue after diet changes and pregabalinhave seen some improvements in pain and fatigue (but did start some other things during that time like pregablin) so hard to tell In context ↗Moderate
October 2025big crash that lowered her baselineMy latest crash that decreased my baseline, has lasted for 3 months. In context ↗Severe
January 2026a little more energy than during the crash; oxaloacetate gave a small energy boost but upset her stomachThis is the first time since then that I've had a little more energy. In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI've been in the push crash cycle for months In context ↗
  • Pain & fibromyalgiaI am in pain 24/7 with little days of respite inbetween. In context ↗
  • Flu-like symptomsmore pain (aching, muscle soreness, migrating pain), more fatigue and the dreaded tender lymph nodes In context ↗
  • Headaches & migrainemy symptoms are PEM, joint and muscle aches, sore throat, head aches, malaise and extreme fatigue In context ↗
  • Anxiety & low moodI have diagnosed anxiety to which I have been taking 100mg of sertraline for. In context ↗
  • POTS & dysautonomiaIve been having dizziness, veritgo (when watching TV and playing video games) and increased pain and tingling. In context ↗
  • Neuropathy & tinglingincreased pain and tingling In context ↗

Ask Miruvor AI

Asking aboutTern 92110’s story

Similar stories

  • Not enough detail to draw a path

    Bed-bound with ME/CFS as a teen, now much better on a vegan low-carb diet and pregabalin

    Much better Maple 60589 ME/CFS Very severe at worstIll 4 years before improving or writing reddit.com Aug 2024

    Maple 60589 had ME/CFS from age 15, mild at first and severe and bed-bound by 17, with daily crashes, pain, IBS, POTS, neuropathy and seizures. A vegan low-carb, gluten-free diet, pregabalin and supplements were credited as they improved to moderate,…

  • Housebound with long COVID, pacing and CoQ10 helped, then largely housebound again

    Relapsed Oak 19396 Long COVID Severe at worstIll 3.5 years before improving or writing reddit.com Aug 2024

    A UK man caught COVID in late January 2021 and was largely back to normal for a month or so before fatigue began around May 2021, with worsening generalised pain. He was housebound for about two months in 2022, in bed 15-16 hours a day, and was diagnosed…

  • Almost bedridden with ME/CFS, now much better after a specialist regimen and pacing

    Much better Fox 20038 ME/CFS Severe at worstIll 6.5 years before improving or writing reddit.com Oct 2026

    A California woman infected with COVID in March 2020 was sick six months, partly recovered, then relapsed and was almost bedridden by early 2023, unable to drive and sensitive to light and noise. An out-of-pocket ME/CFS specialist regimen of LDN, Abilify,…

  • ME/CFS at rock bottom, now much better but still often in bed with pacing

    Much better Cedar 14930 ME/CFS Severe at worstIll 38 years before improving or writing reddit.com Oct 2026

    Cedar 14930 has had ME/CFS for over 30 years, with a sudden flu-like onset, and deteriorated until hitting rock bottom around 11 years before 2020; since then they have improved but remain far from well, often spending 16–23 hours a day in bed and unable to…

A little hope, every Sunday

New recovery stories and data-driven research on ME/CFS and long COVID. Ideas worth considering, and the evidence behind them.

Free · Unsubscribe anytime