Miruvor
Sign up
ME/CFS Mild → somewhat betterIll 3 years before improving or writingNeeds ongoing treatment

Crashing through most of 2018 with ME/CFS, now somewhat better with pacing

Condition
ME/CFS
At worst
Mild (working or studying, with limits)
Ill before improving or writing
3 years
Last post
Jul 2019
In their words
  • Condition: ME/CFSI have dealt with various degrees of this over the past six months and have recently started seeing a ME/CFS specialist located in Charlotte, NC. In context ↗
  • At worst: MildI was on a pretty bad cycle of crashing most of 2018 because I pushed myself too hard In context ↗
  • Now: Somewhat betterI was on a pretty bad cycle of crashing most of 2018 because I pushed myself too hard ... It wasn’t until I saw a specialist that I was finally able to let myself start healing. In context ↗
Read from 5 of their posts and comments; links to the 5 this page draws on

Request to remove this story

Summary

A Reddit user with ME/CFS spent most of 2018 crashing from pushing too hard. Cymbalta eased their pain for three years until complications forced them off; low-dose naltrexone worked after three to four weeks but cost more via a compounding pharmacy. A specialist's pacing advice, keeping heart rate under 110 bpm and steps around 4,000-5,000, helped them start healing.

Ask Miruvor AI

Asking aboutQuail 76423’s story

What they tried

Their words about each treatment
  • Cymbalta · HelpedI took Cymbalta for about three years and it was effective at cutting down my pain level. In context ↗
  • LDN · HelpedIt took longer (3 to 4 weeks) to kick in than Cymbalta did, but it is working well. In context ↗
  • tracking heart rate and staying under anaerobic threshold · HelpedIt’s been very helpful for me to have data that I can track and actually see a correlation with the way I feel. In context ↗
  • step tracker · HelpedI also track my steps and have been able to trace poor management of my step activity to crashes. In context ↗

Approaches: Pacing

Their path

What they say at each step doesn’t fit the worst point or outcome above on the severity scale, so the steps are listed as they describe them. Dates are when they posted.

WhenWhat happenedAfter
onsetonset of ME/CFS; on Cymbalta for painI took Cymbalta for about three years and it was effective at cutting down my pain level. In context ↗
2018 to early 2019cycle of crashes from pushing too hard; myoclonus and sensory overload, stopped drivingI was on a pretty bad cycle of crashing most of 2018 because I pushed myself too hard mostly due to the psychological effects of this disorder. In context ↗
April 2019LDN working; body stabilized and felt more normalIt took longer (3 to 4 weeks) to kick in than Cymbalta did, but it is working well. In context ↗Low-dose naltrexone
July 2019pacing with heart-rate and step tracking, good around 4k to 5k stepsI’m good somewhere around 4k to 5k. In context ↗Pacing and the energy envelope

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Pain & fibromyalgiait was managing some of my pain quite well In context ↗
  • Post-exertional malaiseIf I do go over it for only several minutes, crash symptoms will set in. In context ↗
  • Light & noise sensitivityThere was a period of time that I didn’t drive because I felt such a sensory overload. In context ↗

Ask Miruvor AI

Asking aboutQuail 76423’s story

Similar stories

  • Severe, housebound ME/CFS, somewhat better with pacing and low-dose naltrexone

    Somewhat better Harbor 19162 ME/CFS Severe at worstIll 8 years before improving or writing reddit.com Oct 2026

    A UK woman ill with ME/CFS for eight years, severe and housebound since 2021 after graded walks left her wheelchair dependent. She credited pacing and low-dose naltrexone with steady gains, and later a low-histamine diet with curing insomnia, migraines,…

  • Long COVID at its worst mostly lying down, now nearly back to normal with Zepbound

    Near normal Alpine 44425 Long COVID Severe at worstIll 2 years before improving or writing reddit.com Oct 2026

    Ill with long COVID from July 2024; at worst sleeping or lying down most of the day, barely functioning, with fatigue, PEM, brain fog, palpitations and POTS. Antihistamines and supplements raised energy within a week, and nattokinase, bromelain and curcumin…

  • Mostly bedbound with ME/CFS, now somewhat better with fludrocortisone and beta blockers

    Somewhat better Kestrel 92313 ME/CFS Severe at worstIll 15 years before improving or writing reddit.com Oct 2026

    Kestrel 92313 had ME/CFS for about 15 years, mild at first and severe/mostly bedbound (90–95% bedbound) by early 2026. Fludrocortisone, beta blockers, salt and fluids for POTS were part of measures giving about 10% improvement, and they remained severe and…

  • Severe ME/CFS, housebound and often bedbound; walking better after physio, then relapsed

    Relapsed Pebble 29054 ME/CFS Very severe at worstIll 10 years before improving or writing reddit.com Oct 2026

    Pebble 29054, in the UK, has suspected ME/CFS and describes a decline from mild to severe after NHS GET/CBT and exercise, now housebound and often bedbound with crashes, sleep disruption, headaches, dizziness, GI/IBS and electrolyte problems. A private…

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