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Long COVID Somewhat betterIll 4.5 years before improving or writing

Long COVID with loss of smell and exhaustion, somewhat better with castor oil and therapy

Condition
Long COVID
At worst
Not stated
Ill before improving or writing
4.5 years
Last post
Mar 2026
In their words
  • Condition: Long COVIDI’ve had LC since getting sick in delta wave back in 2021 In context ↗
  • Now: Somewhat betterI went thru 18 months of physical and occupational therapy that helped a bit, but also it may have just been time. In context ↗
  • Began after: COVIDI've had LC since getting sick in delta wave back in 2021 In context ↗
Read from 6 of their posts and comments; links to the 6 this page draws on

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Summary

Lagoon 88204 has had long COVID since a 2021 delta-wave infection, with brain fog, exhaustion, tinnitus and repeated loss of smell. Castor oil drops were credited with restoring smell to 85-90% after a third infection. Low-dose naltrexone did nothing over three months, while Ritalin or modafinil, plus lithium, caused negative mental and emotional effects. Therapy helped a bit; two falls from ladders left them wary of ladders.

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What they tried

Their words about each treatment
  • castor oil · HelpedOverall though the castor oil drops I think did help. In context ↗
  • Ritalin · WorseI was taking either Ritalin or Modafinil for cognition and fatigue issues ... both of those totally caused me all kinds of negative mental and emotional issues In context ↗
  • lithium · WorseI started taking lithium for severe depression and both of those totally caused me all kinds of negative mental and emotional issues. In context ↗
  • low dose naltrexone · No changeMy doctor had me give up after 3 months with no change. In context ↗
  • SSRIs · WorseSSRIs give me cluster headaches and seizures. In context ↗
  • physical and occupational therapy · HelpedI went thru 18 months of physical and occupational therapy that helped a bit, but also it may have just been time. In context ↗

Their path

Very severeSevereModerateMildNear normalRecovered2 y3 y4 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. The chart starts 20 months after onset: the story doesn’t say how ill they were before that. 1 step says too little to place on the scale and is only in the table. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they were
2021COVID-19 during the delta wave; long COVID followedI've had LC since getting sick in delta wave back in 2021 In context ↗Not stated
2023third COVID infection; lost all smell againAfter my third infection and I had lost smell YET AGAIN In context ↗Mild
September 2023smell returned to 85-90% with castor oil drops, some smells still missingI have maybe 85-90% smell back but I still cannot smell certain things ever In context ↗Mild
2024severe depression; Ritalin/modafinil and lithium caused negative mental and emotional effectsI started taking lithium for severe depression and both of those totally caused me all kinds of negative mental and emotional issues In context ↗Mild
2026-03-15after 18 months of physical and occupational therapy, a bit better; still wary of ladders after two fallsI went thru 18 months of physical and occupational therapy that helped a bit In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Loss of smell or tasteI have maybe 85-90% smell back but I still cannot smell certain things ever like vinegar, pepper, cat litter, skunk In context ↗
  • Brain fogsome of the other long covid issues I deal with like tremors, tinnitus, exhaustion, brain fog, etc. In context ↗
  • Anxiety & low moodI started taking lithium for severe depression In context ↗
  • Headaches & migraineSSRIs give me cluster headaches and seizures In context ↗

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