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ME/CFS No benefitIll for 2 yearsNeeds ongoing treatment

ME/CFS brain fog and low blood pressure for two years; no benefit from supplements or B12

Condition
ME/CFS
At worst
Not stated
Ill for
2 years
Last post
Oct 2017
In their words
  • Now: No benefitI suffer most days for it In context ↗
  • Began after: another virusthey found cytomegalo virus (CMV) when I had a serious bronchitis spell
Read from 2 of their posts and comments; links to the 2 this page draws on

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Summary

Birch 32034 has had severe brain fog and low blood pressure spells for about two years, following a serious bronchitis illness when CMV was found. Provigil was the only treatment that helped, but supplies were limited to one dose a day and sometimes unavailable for months. Many supplements and biweekly B12 injections did nothing. No recovery is described.

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What they tried

Also tried

Their words about each treatment
  • Provigil · HelpedThe only thing thats has helped was taking Provigil ... with stocks limited I can only take 1 a day (where I really need 2) In context ↗
  • biweekly B12 injections · No changeeven biweekly B12 injections etc. Nothing helps In context ↗
  • supplement regiments · No changeI've gone through many supplement regiments ... Nothing helps 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
a couple of years agoserious bronchitis; CMV foundthey found cytomegalo virus (CMV) when I had a serious bronchitis spell, it was the sickest I have ever been In context ↗
2017-10-13still has severe brain fog and low blood pressure spells; Provigil helps but supply is limitedI suffer most days for it, severe brain fog coupled with low blood pressure spells In context ↗

Symptoms mentioned

Their words about their symptoms

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