Miruvor
Sign up
ME/CFS Moderate → somewhat better

Housebound with ME/CFS and unable to work, somewhat better after improved mental health

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill before improving or writing
Not stated
Last post
May 2026
In their words
  • Condition: ME/CFSeven while i was on it my ME/CFS was awful. In context ↗
  • At worst: ModerateI'm on the severe side of moderate, i guess? i'm housebound most days and can't work. In context ↗
  • Now: Somewhat betterI had some improvement in my mental health in the past few months and my symptoms have improved. In context ↗
Read from 6 of their posts and comments; links to the 5 this page draws on

Request to remove this story

Summary

Sequoia 32986 reports ME/CFS with post-exertional malaise, unrefreshing sleep and anxiety, and later notes comorbid POTS. They described being housebound most days and unable to work, needing help to get to the bathroom and days to recover after small tasks. In 2024 they said improved mental health had improved their symptoms, but in 2026 they described their ME/CFS as awful while on spiro. No onset date, duration or recovery is given.

Ask Miruvor AI

Asking aboutSequoia 32986’s story

What they tried

Their words about each treatment
  • managing how much i do in a day · Helpedwhat has helped is managing how much i do in a day In context ↗
  • wheelchair · HelpedHaving a wheelchair means i can go out and do things. In context ↗
  • spiro · No changemy body could NEVER get enough salt on spiro, but even while i was on it my ME/CFS was awful In context ↗

Approaches: Pacing

Their path

They say too little about how ill they were at each step to draw it on the severity scale, so the steps are listed as they describe them. Dates are when they posted.

WhenWhat happenedWhere they were
—ME/CFS symptoms with PEM; onset not datedpanic attacks and anxiety can cause PEM and CFS symptoms In context ↗Not stated
2022-10-24Housebound most days and unable to work; needed help to the bathroomi'm housebound most days and can't work ... i've needed help to get up and go to the bathroomModerate
2024-05-01Improved mental health in past few months; symptoms improvedI had some improvement in my mental health in the past few months and my symptoms have improved. In context ↗Not stated
2026-05-17Still ME/CFS awful while on spiro; comorbid POTSI'm also Comorbid with POTS ... even while i was on it my ME/CFS was awful. In context ↗Not stated

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaisepanic attacks and anxiety can cause PEM and CFS symptoms In context ↗
  • Sleep problemsi sleep 8 hours a night and wake up feeling tired. a lot of days i'll have a nap midday too and that won't help. In context ↗
  • POTS & dysautonomiaI'm also Comorbid with POTS In context ↗
  • Anxiety & low moodI have CPTSD from familial trauma and intense panic attacks. In context ↗

Ask Miruvor AI

Asking aboutSequoia 32986’s story

Similar stories

  • Unable to walk around house with long COVID, much better after pacing and antihistamines

    Much better Falcon 84129 Long COVID Severe at worstIll 3 years before improving or writing reddit.com Oct 2026

    A Canadian man with long COVID for about three years was unable to walk around the house for the first two years, with constant migraines, brain fog and PEM. From year three, pacing, rest, stress reduction, H1/H2 antihistamines, hydroxyzine for sleep,…

  • Mostly bedbound and housebound with ME/CFS, pacing and rest helped before a relapse

    Relapsed Valley 16092 ME/CFS Moderate at worstIll 25 years before improving or writing reddit.com Oct 2026

    Valley 16092 has had ME/CFS and fibromyalgia for about 25 years; stress and lifelong health problems led to a crash from 60-hour workweeks. They never became severe but have been mostly bedbound and housebound, and pacing, rest and comorbidity medication…

  • Mostly housebound with ME/CFS, now a little better on Klonopin and low-dose naltrexone

    Somewhat better Valley 89571 ME/CFS Moderate at worstIll 3 years before improving or writing reddit.com Oct 2026

    Joseph, 47, in Los Angeles, developed ME/CFS in January 2024, about 18 days after a second COVID infection. He declined from mild to the bad end of moderate over six months, becoming mostly housebound. Klonopin, low-dose naltrexone, midodrine and propranolol…

  • Long COVID brain fog, somewhat better with nicotine patch and naltrexone

    Somewhat better Pebble 25278 Long COVID Mild at worst reddit.com Oct 2026

    Pebble 25278 developed long COVID with brain fog, distorted smell, headaches, nerve pain and trouble sleeping. A quarter of a 10 mg nicotine patch restored much of their speech and thinking, and low-dose naltrexone further raised their cognitive and physical…

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