Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

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Old 01-08-2009, 08:05 PM #1
buckwheat
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Mrs. D,

You also brought up regardless of the cause, well the MD's getting to the cause is the PROBLEM. How could they help otherwise???

I had Endocarditis.

Blood work is clear for BARTONELLA but thats what I have. I have been on antibiotics for the last 1 1/2 years, at times the atomic bomb.

A huge problem is they just test for a couple strains when their are hundreds.

What are your thoughts?????

Much Love, Roz
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Old 01-09-2009, 01:31 PM #2
buckwheat
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Up worried
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Old 01-09-2009, 03:46 PM #3
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Wink What antibiotics?

Long term antibiotics are nutrient depleters. I have a book that lists most of them.

If you want privacy PM me the list and I'll look them up and advise you. Nutrient depletion is a huge cause of negative side effects. By managing that you can usually still stay on the treatments. But many drop out, when things could be fixed simply.

So PM me your drug list and I'll look them for you.
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Old 01-09-2009, 08:41 PM #4
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Dear Mrs. D

I do hope these lines find you doing well.

I got RSD and Endocarditis from untreated Lyme & Company (co-infections).

I am very thankful to be alive.

Their is alot of controversy about Lyme, but the co infection Bartonella is what caused the heart damage I have. I only wish I would of gotten antibiotics sooner.

I would be running about now.

I just take tablets now nearly off of them, by the grace of GOD.

My RSD pain is nearly gone and my heart is doing much better.

I am concerned about Rosie. Much Love, Roz
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