Miruvor
Sign up
ME/CFS Somewhat better

ME/CFS with leg pain and poor sleep, somewhat better with ketamine nasal spray

Condition
ME/CFS
At worst
Not stated
Ill before improving or writing
Not stated
Last post
Jul 2021
In their words
  • Condition: ME/CFSI have CFS and do psychedelics daily (ketamine) and others in my recreational time. In context ↗
  • Now: Somewhat betterI’m on ketamine for depression and it’s been helping with my pain and energy as a positive side effect ... I don’t shower every day since the heat and the standing are a lot most days
Read from 14 of their posts and comments; links to the 10 this page draws on

Request to remove this story

Summary

Island 91919 worked as a cook in a kitchen around 25 to 40+ hours a week, crashing after two or three days in a row, with stiff leg muscles, weak grinding knees, pain and interrupted sleep. Ketamine nasal spray, started for treatment-resistant depression, eased pain and sleep so they felt less fatigued, and they took Wellbutrin XL for depression. They kept working, paced chores with rests and took several baths a day to cope with heat and standing.

Ask Miruvor AI

Asking aboutIsland 91919’s story

What they tried

Their words about each treatment
  • physical therapy exercises (calf lifts, quad and calf stretches, resistance band lateral walking) · HelpedIt was all pretty low strain and has helped me keep my very stiff leg muscles well built and able to still go to work. In context ↗
  • Body Armor electrolyte drinks · Not saidI personally enjoy body armors the most for electrolyte drinks. In context ↗
  • resting before and between tasks (pacing) · HelpedIt makes things able to be accomplished and I don’t usually get discouraged or tired if I do things this way. In context ↗
  • Wellbutrin XL · HelpedI had to get prescribed Ketamine with it for it to actually start working properly, but my pain and energy has been a lot better even on the days I don’t take the Ketamine. In context ↗
  • ketamine · HelpedI’m on ketamine for depression and it’s been helping with my pain and energy as a positive side effect. In context ↗
  • cannabis · Not saidI smoke a lot of weed In context ↗
  • hot baths · HelpedI do take multiple baths a day since it helps my joints and fatigue In context ↗

Approaches: Other antidepressants · Other drugs and medicines · Pacing

Their path

Very severeSevereModerateMildNear normalRecovered

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, in the order they describe; they don’t give enough times to place each step. Hover or tap a point. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
—CFS onset, trigger not describedMild
2020-10-04Cooking shifts of about 25 hours a week, crashing after two or three days in a rowI usually always crash by the time I’m working for 2-3 days in a row In context ↗Mild
2021-02-15Ketamine eased pain and sleep, so less fatiguedIt has actually been helping me with my pain and sleep so I am fatigued less In context ↗MildKetamine
2021-07-23Still doing physical work; heat and standing are a lot, takes several baths a dayI don’t shower every day since the heat and the standing are a lot most days, but I do take multiple baths a day since it helps my joints and fatigue In context ↗Mild

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI usually always crash by the time I’m working for 2-3 days in a row In context ↗
  • Sleep problemsgetting more uninterrupted sleep In context ↗
  • Pain & fibromyalgiait’s been helping me with my muscle aches and pains In context ↗
  • Muscle weaknessmy condition gives me very weak and grinding knees In context ↗
  • Anxiety & low moodI’m on ketamine for depression In context ↗
  • Temperature regulationthe heat and the standing are a lot most days In context ↗

Ask Miruvor AI

Asking aboutIsland 91919’s story

Similar stories

  • Bedbound with long COVID over two years, now at 85% after ivabradine and duloxetine

    Near normal Eagle 35616 Long COVID Very severe at worstIll 2.5 years before improving or writing reddit.com Jul 2026

    Eagle 35616 fell ill with COVID in January 2020 and spent over two years bed bound, fainting dozens of times a day and unable to stand without collapsing or to hold a fork. Boosters were the worst thing that had ever happened to them. Ivabradine stopped the…

  • Long COVID crashes and wrecked gut, now near normal on antihistamines and diet

    Near normal Badger 97535 Long COVID Mild at worstIll 5.5 years before improving or writing reddit.com Oct 2026

    Badger 97535 developed long COVID after a covid infection in early 2021. He worked through months of 2-4 hours' sleep early on, a wrecked gut, mast cell reactions and flu-like crashes after exercise. Antihistamines, keto and very-low-calorie diets, PEA,…

  • Long COVID brain fog, fatigue and POTS, now much better with pacing and compression

    Much better Vale 64877 Long COVID Moderate at worstIll 17 months before improving or writing reddit.com Oct 2026

    A retired Northern California woman got long COVID in Italy in October 2024, with brain fog, fatigue, tinnitus and gut trouble; POTS was diagnosed later. Low-dose naltrexone, bupropion, acupuncture, osteopathy, pacing, salt and compression brought slow…

  • Mild ME/CFS while working, pain and brain fog somewhat better on low-dose naltrexone

    Somewhat better Harbor 37871 ME/CFS Mild at worst reddit.com Oct 2026

    Harbor 37871 describes themselves as a mild ME/CFS case who still works, pacing and resting to stay within their energy envelope. They take trazodone, sertraline plus bupropion, and low-dose naltrexone, which they say cut their pain and brain fog by 60-70%…

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