Miruvor
Sign up
Long COVID Somewhat better

Long COVID facial pain and constant depersonalisation, somewhat better with Lexapro

Condition
Long COVID
At worst
Not stated
Ill before improving or writing
Not stated
Last post
Sep 2026
In their words
  • Now: Somewhat betterIt got to be less frequent and less severe but it’s still there. In context ↗
  • Began after: COVIDsevere what I assumed was migraines and head pain daily for about 6 months straight after I got COVID
Read from 10 of their posts and comments; links to the 7 this page draws on

Request to remove this story

Summary

They have had long COVID since 2021, with daily facial, head and neck pain, neuralgia and migraines and constant depersonalisation for years. Nortriptyline helped the pain for about a year then wore off; gabapentin, pregabalin, steroid injections, chiropractic, acupuncture, massage, physiotherapy and a Mayo clinic did not settle it. Lexapro greatly reduced the DPDR. COVID vaccinations amplify their pain; a Florida holiday eased it.

Ask Miruvor AI

Asking aboutTide 75216’s story

What they tried

Their words about each treatment
  • nortriptyline · HelpedI was on nortriptyline and it worked great for like a year and then started wearing off. In context ↗
  • lyrica · No changeI’m trying out lyrica right now but this is definitely not helping In context ↗
  • Lexapro · HelpedI started anxiety medication (Lexapro) and that actually made it way better for me. In context ↗
  • vacation to Florida · Helped a lotWe went on vacation to Florida and it was the best week of my life pain-wise In context ↗
  • gabapentin · Not saidI have tried medication (gabapentin, pregabalin, nortriptyline) In context ↗
  • chiropractor · Not saidchiropractor, acupuncture, massage, PT, cervical steroid injections In context ↗
  • Mayo Clinics Long Covid Care Clinic · Not saidI went through Mayo Clinics Long Covid Care Clinic In context ↗
  • COVID vaccines/boosters · WorseI get incredibly sick from it every time In context ↗

Approaches: Tricyclic antidepressants

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 were
2021COVID infection, then daily head pain and constant depersonalisationI had severe what I assumed was migraines and head pain daily for about 6 months straight after I got COVID In context ↗Mild
—pain eased for about a year on nortriptyline, then it wore offI was on nortriptyline and it worked great for like a year and then started wearing off In context ↗Mild
—depersonalisation much reduced on LexaproI started anxiety medication (Lexapro) and that actually made it way better for me. In context ↗Mild
2026-09-20still has pain; depersonalisation only now and thenI will get the feeling here and there when I am driving now but it doesn’t last long In context ↗Mild

Adverse events

  • COVID vaccination as treatment“I get incredibly sick from it every time ... Fever, intense body aches, migraines, etc. essentially all the pains I feel daily amped up 10x.” Made symptoms worse

Symptoms mentioned

Their words about their symptoms
  • Headaches & migrainesevere what I assumed was migraines and head pain daily for about 6 months In context ↗
  • Vision problemslike viewing life a degree behind your eyes In context ↗
  • Anxiety & low moodthe DPDR seems like it was triggered by anxiety for me In context ↗

Ask Miruvor AI

Asking aboutTide 75216’s story

Similar stories

  • Bedbound for years with ME/CFS, improved on antivirals then relapsed

    Relapsed Mesa 34322 ME/CFS Very severe at worstIll 16 years before improving or writing reddit.com Oct 2026

    Be fell ill around 2010 with a coxsackie B4 infection and mild meningitis that left them unable to walk. They were bedbound for years, then improved on Dr Chia's antivirals: tenofovir reduced their flu symptoms and let them leave the house in a wheelchair,…

  • Housebound and off work with ME/CFS, now much better with LDN and pacing

    Much better Pond 30780 ME/CFS Moderate at worstIll 3 years before improving or writing reddit.com Oct 2026

    Diagnosed with mild to moderate ME/CFS and POTS in the UK in 2024, after a covid-triggered episode in 2022 and a parasite infection in April 2024. Before starting LDN they had been housebound, used a wheelchair when out and were off work. Low-dose…

  • Bedridden with ME/CFS for a year, now somewhat better but still unwell

    Somewhat better Plover 90634 ME/CFS Severe at worstIll 18.5 years before improving or writing reddit.com Oct 2026

    ME/CFS began in August 2003, in her early forties, probably from a virus plus inborn myopathy; she was bedridden and using a wheelchair for about a year, then improved over years to walking about a mile a day with help, though unable to hold a job. She later…

  • Housebound and mostly in bed with ME/CFS, Abilify helped then relapse

    Relapsed Hare 75846 ME/CFS Severe at worstIll 16 years before improving or writing reddit.com Oct 2026

    A US software engineer who fell ill in 2010 at age 30 went from mild to severe after pushing himself while preparing to change jobs in 2017, ending up housebound and mostly in bed. Low-dose Abilify lifted him from severe to mild within weeks in 2020, but the…

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