Miruvor
Sign up
ME/CFS Outcome unclear

ME/CFS with brain fog so bad they could only sit through day; salt and vitamins no help

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill for
Not stated
Last post
Nov 2021
In their words
  • Condition: ME/CFSSo I have small fiber neuropathy and pots along with cfs. In context ↗
  • At worst: ModerateI cannot think or do anything but sit here and battle to get through the day so I can sleep. In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

Request to remove this story

Summary

An Australian Reddit user with CFS, POTS and small fiber neuropathy described mental exhaustion and brain fog so bad they could only sit through the day. Salt, fluids and vitamins B, C, D and magnesium made no difference. Wellbutrin taken for a few days caused dizziness and insomnia, so they stopped, and they noted Adderall is illegal where they live and doctors can only prescribe it for very specific conditions.

Ask Miruvor AI

Asking aboutGrove 60669’s story

What they tried

Also tried

salt and fluids· No changevitamin D· No changestandard supplements (B, C, magnesium)· No changeWellbutrin· Worse
Their words about each treatment
  • salt and fluids · No changeI've tried all the salt and fluids as well as the standard suppliment In context ↗
  • vitamin D · No changethe standard suppliment... B, c, d, magnisum etc... Nothing makes any difference. In context ↗
  • Wellbutrin · WorseI took it for a few days it made me dizzy as hell and wouldn't let me sleep. So I stopped. In context ↗

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Brain fogMy brain fogs and my eyes start to tear up from how sore they are In context ↗
  • POTS & dysautonomiaSo I have small fiber neuropathy and pots along with cfs In context ↗
  • Vision problemsmy eyes from about 10am onwards feel like they haven't closed for days In context ↗

Ask Miruvor AI

Asking aboutGrove 60669’s story

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