Miruvor
Sign up
ME/CFS Moderate → much betterIll 6 years before improving or writingNeeds ongoing treatment

Mostly housebound and off work with ME/CFS, now much better with venlafaxine and cannabis

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill before improving or writing
6 years
Last post
May 2026
In their words
  • Condition: ME/CFSMy CFS is not as bad as it once was In context ↗
  • At worst: ModerateMy CFS is not as bad as it once was, I'm in the "mild" category now but used to be moderate. In context ↗
  • Now: Much betterI've gone from moderate to mild and I've got some quality of life back. In context ↗
  • Began after: stress or burnoutBut looking back, I think it actually was the stress in work.
Read from 37 of their posts and comments; links to the 17 this page draws on

Request to remove this story

Summary

An Irish teacher fell ill around 2020, becoming mostly housebound and off work for two years. Venlafaxine, mirtazapine and cannabis helped sleep, pain and energy, and she improved slowly to mild, returning to part-time teaching in 2023. Pregnancy in late 2024 undid that progress, leaving her in bed and sleeping badly. By May 2026 she was back to mild with some quality of life.

Ask Miruvor AI

Asking aboutFlint 72371’s story

What they tried

Their words about each treatment
  • venlafaxine · Helped a lotYes, it significantly helped me quickly when I was at my worst. In context ↗
  • mirtazapine · HelpedMirtazapine which usually works so well for me (100% success for sleep) is now not working very well In context ↗
  • weed (cannabis, edibles) · HelpedWeed. It calms any pain, and disguises the fatigue. Also helps me sleep. In context ↗
  • solpadeine · Not saidBut I can't continue to have weed and solpadeine like they're tic-tacs forever. In context ↗
  • massager · Not saidI have a massager, I have weed, and I have solpadeine. In context ↗
  • Lexapro · Not saidI came off it and then I got sick. In context ↗
  • MDMA (molly) · WorseI've had MDMA twice since getting this...still have it. Sorry to burst your bubble :( it won't help. In context ↗
  • CBD · No changeIve had CBD and it didn't do too much. In context ↗
  • amitriptyline · Not saidI have to take amitriptyline to get to sleep. In context ↗
  • diphenhydramine (nytol) · HelpedI've been taking diphenhydramine (nytol, antihistamine) but it isn't working at the moment. It did help for a while, but not pregnant. In context ↗
  • melatonin · Not saidI've tried weed and melatonin. In context ↗

Approaches: SNRIs · Other antidepressants

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y5 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 were
2020fell ill with exhaustion and twitching while still workingWhen I got this almost 3 years ago, the fatigue made me want to jump out of my skin. In context ↗Mild
2020crashed after a 45-minute bike ride, with months of burning armsWhen I got on my bike and cycled 45 mins before (2020), I got a really bad reaction 20 mins after I got off the bike. In context ↗Moderate
2021mostly housebound and out of work, could hardly standCould hardly stand. Felt like passing out all the time. Even lying down didn't feel like rest. In context ↗Moderate
2022could lie in bed and play games or watch TV; condition stabilizedTwo years in I was fatigued, but I could lay in bed and at least play games or watch TV. In context ↗Moderate
August 2022in the mild category, no longer moderateMy CFS is not as bad as it once was, I'm in the "mild" category now but used to be moderate. In context ↗Mild
January 2023returned to part-time teaching after two years unemployedI just got back to work part time 2 months ago after 2 years of being unemployed and that's BIG for me. In context ↗Mild
December 2024pregnancy undid her progress; signed off work and in bed all dayBeing pregnant has taken away any progress I had made. In context ↗Severe
May 2026back to mild with some quality of lifeI've gone from moderate to mild and I've got some quality of life back. In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseif I do something like cut the grass (which I've done 2-3 times in the last year) I feel a sudden increase in fatigue and hour or two later. In context ↗
  • Brain fogSome brain fog sometimes. In context ↗
  • POTS & dysautonomiaI also have POTS so my heart goes skrrrt. In context ↗
  • Sleep problemsMy insomnia is quite bad - I could go two nights without sleep unless I'm on heavy meds. In context ↗
  • Pain & fibromyalgiaTMJ pain (2020-2023) In context ↗
  • Headaches & migrainehead pain - squeezing feeling and strained eye muscles In context ↗
  • Gut problemsI get digestive issues In context ↗
  • Light & noise sensitivityI am sensitive to noise and it tends to make me tireder. In context ↗
  • Heart symptoms & palpitationsmild-moderate chest pain In context ↗
  • Muscle weaknessCould hardly stand. In context ↗
  • Neuropathy & tinglingBurning arms (2020) In context ↗
  • Anxiety & low moodNow I'm in a mind frame where I want to just end it all, but can't. In context ↗
  • Flu-like symptomsI get a sore throat sometimes after work or in the evening. In context ↗

Ask Miruvor AI

Asking aboutFlint 72371’s story

Similar stories

  • ME/CFS: sudden symptoms, pain and brain fog, somewhat better; antidepressants helped mood

    Somewhat better Harbor 54626 ME/CFS Moderate at worstIll 16 years before improving or writing reddit.com Aug 2025

    They became suddenly ill at 19, going from competitive athlete to pausing on the stairs, with pain, brain fog, migraines and orthostatic light-headedness, and dropped out of university. Diagnosed with POTS but not officially with ME/CFS, they spent a decade…

  • ME/CFS mostly housebound then bedridden, somewhat better sleep with trazodone

    Somewhat better Glacier 69001 ME/CFS Severe at worstIll 25 years before improving or writing reddit.com Apr 2024

    She dated her ME/CFS to mono in college in 1999 and stayed mild and working for years, then dropped from mild to moderate overnight in May 2012 with new pain and weakness, becoming mostly housebound. Trazodone gave her refreshing sleep for over a decade, but…

  • Five years out of action with ME/CFS, now somewhat better with paced activity

    Somewhat better Tundra 21518 ME/CFS Moderate at worstIll 9 years before improving or writing reddit.com Dec 2017

    They fell ill with glandular fever in 2006 aged 17, struggled through a Cambridge science degree and ended in a very bad state. Five years out of action followed, then two years of carefully spaced activity, which they credit for small gains, plus…

  • Long COVID with brain fog, insomnia and PEM, somewhat better with time and pacing

    Somewhat better Harbor 98264 Long COVID Moderate at worstIll 2 years before improving or writing reddit.com Oct 2026

    An avid cyclist in his mid-thirties got long COVID in August 2024, leaving him with near-constant brain fog, visual distortion, insomnia, body aches and PEM. He kept working from home, cut his hours to 32 and paced, crediting time and pacing for slow…

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