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Re: 'brain fog'/CFIDS

From: anonymous@obgyn.net
Fri, 27 Jul 2001 13:57:01 +0000


Bonnie:

The symptoms you describe are almost a textbook description of Chronic Fatigue Immune Dysfunction Syndrome. You can have your doctor check several things to see if you have this:

1. Check your natural killer cell count. It may be low. 2. Check your liver function. Two enzymes will be high, but your doctor will say "Hmmm....I'm not sure what's going on because everything else is normal and you don't seem to have liver disease." Your doc may try to diagnose you wih "fatty liver." 3. Get a PET scan of your brain if possible. That will show any areas of abnormal brain metabolism. 4. Have neurocognitive testing done to see how bad your "brain fog" is. 5. Go to a doctor who specializes in Chronic Fatigue Syndrome. 6. You may want to check out http://www.immunesupport.com. They have excellent articles about immune system dysfunction, fibromyalgia and CFIDS. 7. Another good reference is http://www.cfids.org

Best wishes to you in your quest for health.

Donna in Utah > Hi there Celeste
>
> I can definitely relate to what your'e talking about. I've had brain
> fog for the past 4yrs. It has basically turned me my life around. I
> don't feel as carefree as I used to, constantly worrying, anxiety
> attacks etc.etc. This brain fog has really gotten to me, it's altered
> my state of mind completely, sometimes feeling like I've lost my mind
> cause everybody else thinks it's all in the head. I sympathise with
> anyone that has had to live with brain fog. It's taken away my ability
> to study, to do things that I once used to do perfectly normal without
> any effort. Accompanied with the brain fog has been chronic fatigue,
> that has improved a bit now and then of course the depression for which
> I was treated ( anti-depressants made it ten times worse), candida
> ..you name it. How did yours all start? Mine started up just before I
> went overseas back in 1997 and have had no luck since. I'm currently
> being treated for an auto immune deficiency by having Ultraviolet Blood
> irradiation therapy, seems to relieve it a little. Hopefully all gets
> well. Would be great to hear from you!
>
> Bonnie
>




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