Miruvor
Sign up
Long COVID Moderate → somewhat betterIll 8 months before improving or writing

Long COVID with fatigue, brain fog, pain and POTS, somewhat better with Ozempic

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
8 months
Last post
Dec 2024
In their words
  • Condition: Long COVIDI have long covid (may 22) In context ↗
  • At worst: Moderateback then it was too exhausting for me to write a lot in text form to have a lot of info In context ↗
  • Now: Somewhat betterI did notice improvement in my energy levels ... still have a lot of LC symptoms
  • Began after: COVIDI have long covid (may 22) In context ↗
Read from 7 of their posts and comments; links to the 6 this page draws on

Request to remove this story

Summary

Long COVID since May 2022 left them with fatigue, brain fog, pain, IBS, anxiety and POTS. Ozempic, begun in September 2022 for PCOS, slowly improved their energy, joint pain, IBS and brain fog. Stopping it for surgery in summer 2024 brought symptoms back; restarting helped tremendously, but they still had many symptoms in December 2024. Zoloft eased mood but worsened dysautonomia, and methotrexate made them more fatigued.

Ask Miruvor AI

Asking aboutStarling 45434’s story

What they tried

Their words about each treatment
  • hydroxychloroquine · Not saidI had a diagnostic of seronegative RA right before long covid, it got worse after my covid infection, I was put on hydroxychloroquine. In context ↗
  • methotrexate · WorseThen, we added methotrexate (subcutaneous) and I swear I didn’t get better 😅 I was more fatigued, nauseous In context ↗
  • symptom journal (ratings out of ten) · Not saidI kept it to numbers out of ten In context ↗
  • ozempic · Helped a lotIt took quite a while (because it takes time to up the dosage) but I did notice improvement in my energy levels In context ↗
  • leflunomide · No changegot switched on leflunomide and still have a lot of LC symptoms In context ↗
  • Zoloft · WorseNow after 8 weeks I am at 100mg ... it is making my dysautonomia symptoms worse for sure In context ↗
  • Concerta · Not saidI get this from my Concerta for the first couple of hours after taking it In context ↗
  • occupational therapist and pacing · HelpedI started seeing an occupational therapist, she helped me a ton on a lot of issues. In context ↗
  • wood blocks under the bedframe to raise the head of the bed · Helpedtwo 5 inches wood blocks under my bedframe so the bed is slightly up at the head, way better than pillows ... It helps me a lot In context ↗

Approaches: GLP-1 drugs · Pacing

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 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. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
May 2022long COVID onsetI have long covid (may 22) In context ↗Moderate
2022-2023energy, joint pain, IBS, anxiety and brain fog improved after Ozempic dose titration; could read a book in her second language againI did notice improvement in my energy levels, joints pain (Rheumatoid arthritis), IBS, anxiety, recurring negative thoughts, brain fog. ... I could read a book in my second language again ! In context ↗MildSemaglutide (Ozempic, Wegovy)
summer 2024stopped Ozempic for surgery; symptoms returned within a monthI had to stop this summer for a surgery and after a month, these symptoms came back slowly but surely. In context ↗Mild
2024-11-05Zoloft worsened dysautonomia symptomsit is making my dysautonomia symptoms worse for sure.. POTS, fatigue, dizziness, tachycardia, dyspepsia and so on came back with vengance. In context ↗Mild
2024-12-01restarted Ozempic, helping tremendously, but still many long COVID symptomsIt is helping tremendously. ... still have a lot of LC symptomsMildSemaglutide (Ozempic, Wegovy)

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI get PEMs from mental activity or stress In context ↗
  • POTS & dysautonomiaPOTS, fatigue, dizziness, tachycardia In context ↗
  • Gut problemsdyspepsia and so on came back with vengance In context ↗
  • Pain & fibromyalgiajoints pain (Rheumatoid arthritis) In context ↗
  • Anxiety & low moodrelief from anxiety/depression it is giving me In context ↗
  • Light & noise sensitivityevery noise makes me cringe by 3pm In context ↗

Ask Miruvor AI

Asking aboutStarling 45434’s story

Similar stories

  • Housebound with ME/CFS and brain fog, now much better with pacing and antihistamines

    Much better Lagoon 80616 ME/CFS Moderate at worstIll 6.5 years before improving or writing reddit.com Oct 2026

    Ill from March 2020, they were housebound with POTS, brain fog and PEM early on, and in May 2023 said treatments had taken them from about 30% to 70% of normal. Blood thinners, guanfacine, antihistamines, continuous progesterone, pacing and other medications…

  • Housebound with ME/CFS, improved on LDN and memantine then relapsed

    Relapsed Nightjar 86870 ME/CFS Moderate at worstIll 9 months before improving or writing reddit.com Oct 2026

    After COVID in August 2024 they were housebound for months with severe GI flares, then fatigue, body and joint pain and brain fog. They credited low-dose naltrexone and memantine for lifting them from housebound to roughly 75–80% recovered, with semaglutide…

  • Housebound and mostly bedbound with ME/CFS, now much better with pacing and support

    Much better Kite 28184 ME/CFS Severe at worstIll 6 years before improving or writing reddit.com Oct 2026

    They fell ill in 2018 at 18 and spent three years housebound and mostly bedbound, unable to bathe or feed themselves, worsening further after graded exercise therapy. After diagnosis, they followed a strict pacing plan with a therapist and family support,…

  • Nearly bedbound with long COVID, now close to normal after ganglion blocks and nicotine

    Near normal Dusk 66875 Long COVID Severe at worstIll 3.5 years before improving or writing reddit.com Oct 2026

    A former daily 5K runner, he caught COVID and was nearly bedbound in the second month with dysautonomia and PEM. Over more than two years he tried many treatments, crediting stellate ganglion blocks and nicotine, and was trying rapamycin. He was not fully…

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