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ME/CFS No benefitIll for 14 years

ME/CFS with Hashimoto, no improvement after levothyroxine dose increase

Condition
ME/CFS
At worst
Not stated
Ill for
14 years
Last post
Nov 2023
In their words
  • Condition: ME/CFSIdk if it’s CFS caused by Hashimoto or what anymore. In context ↗
  • Now: No benefitI was diagnosed in 2009 and never felt any better even after increasing Levothyroxine. In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

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Summary

Owl 67763, posting in r/cfs in November 2023, reported being diagnosed with Hashimoto in 2009 and never feeling any better, even after a GP raised the levothyroxine dose and TSH came down to about 3 from 4 or 4.5, and was unsure whether the illness was CFS caused by Hashimoto. Psychedelics always caused anxiety.

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What they tried

Their words about each treatment
  • Levothyroxine · No changeI was diagnosed in 2009 and never felt any better even after increasing Levothyroxine. In context ↗
  • Psychedelics · WorsePsychedelics all make me anxious. Always did. In context ↗

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 happened
2009diagnosed with HashimotoI was diagnosed in 2009 In context ↗
2023-11-22levothyroxine increased, TSH about 3, still no betternever felt any better even after increasing Levothyroxine In context ↗

Symptoms mentioned

Their words about their symptoms
  • Anxiety & low moodPsychedelics all make me anxious. Always did. In context ↗

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