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ME/CFS Moderate → somewhat betterIll 3 years before improving or writing

ME/CFS too tired to stay awake in class, now somewhat better but unable to work

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill before improving or writing
3 years
Last post
Jun 2025
In their words
  • Condition: ME/CFSI have had CFS for over 20 years In context ↗
  • At worst: ModerateI was so tired that I literally fell asleep in class more than once ... After a few weeks, I went to see the Dean and told him what was happening to me and that I had to leave school. In context ↗
  • Now: Somewhat betterthey gradually got somewhat better and plateaued where I am now functioning at around 30-40% of what I was. I haven't been able to work in years but I am able to engage with my family and kids and help out a little. In context ↗
  • Began after: another virusI believe it was the result of having the flu (the real flu, like 4 or 5 weeks).
Read from 20 of their posts and comments; links to the 11 this page draws on

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Summary

A lawyer who fell ill in law school around 2000, he was too tired to stay awake in class and left his studies. The first two to three years were brutal; after about three years he improved somewhat and plateaued. Over 20 years on he functions at around 30-40% of his former level and cannot work, but helps with his family and manages symptoms with naps and cannabis. He tried every supplement, treatment and doctor without real success.

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What they tried

Their words about each treatment
  • supplements · No changeI tried every supplement, treatment, doctor possible but nothing really worked. In context ↗
  • diet (eating less) · No changeDid it improve my CFS? No. In context ↗
  • intermittent fasting · Not saidI am not sure if it helps relieve any symptoms or give extra clarity but I am able to maintain weight without the need for exercise In context ↗
  • Cannabis · HelpedCannabis has been a gamechanger with the aches and pain for sleeping. In context ↗
  • Wellbutrin · HelpedWellbutrin helped me a lot as well. In context ↗
  • naps · HelpedIf I can't get at least a 2 hour nap, I don't even bother because with any less, I get zero benefit. In context ↗
  • getting in tune with my body and managing my symptoms · HelpedIt's not just pacing. You will figure out how your body reacts to pretty much every situation. In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset5 y10 y15 y20 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
law school, late 1990sfell ill in law school, fell asleep in class and had to leave schoolI was stricken with this affliction back when I was in law school In context ↗Moderate
first 2-3 yearsbrutal, unrelenting symptoms at their worstMy first 2-3 years were brutal. Not only was I probably at my worst symptom wise In context ↗Moderate
about 3 years inimproved somewhat then plateauedAfter about 3 years, I improved somewhat but plateaued. In context ↗Moderate
a few times per year, ongoingsevere episodes lasting up to two weeksa few times per year I get severe episodes that last 2 weeks maximum In context ↗Severe
2024-02-28stable at a plateau, unable to work for yearsplateaued where I am now functioning at around 30-40% of what I was In context ↗Moderate

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI still get really tired if I overdo it In context ↗
  • Sleep problemsI take 2 hour naps regularly. Longer sometimes. In context ↗
  • Pain & fibromyalgiaSome nights I am so sore all over that I can't sleep. In context ↗

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