This is topic I have Lyme induced Parkinsons in forum Medical Questions at LymeNet Flash.


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Posted by saved10 (Member # 18413) on :
 
Looks like I have Lyme induced Parkinsons. I'm still in treatment for Lyme.

I have a PICC Line, Rocphen 5 days a week, just finished 6 months now working towards nine months.

They are not for sure if they can reverse the damange or not they say it's 50 - 50

I'm bummed, but pressing forward

[ 04-18-2011, 12:34 PM: Message edited by: saved10 ]
 
Posted by payne (Member # 26248) on :
 
parkinsons was discovered by your LLMD or your reg. MD ?
I fear parkinsons...was this a test?
lab?...
saved10 hope you find a path to being stable again...
 
Posted by saved10 (Member # 18413) on :
 
From both LLMD and Nuro. They want to do more test, they say I am a complicated case.

Only time will tell. The rest is in Gods hands
 
Posted by GiGi (Member # 259) on :
 
Dr. K. made it known years ago that all patients that came to him with a Parkinson diagnosis tested positive for Lyme. That said, they also have problems with toxic metals, dental infections, parasites, fungi and mold, chemicals.

The body needs a major cleanup just as it does for any Lyme afflicted. It's never just Lyme, and it is never just Parkinsons as school medicine sees it.

There is no conclusive Parkinson test that I know of and there is no one cause for Parkinsonism.

Take care.
 
Posted by saved10 (Member # 18413) on :
 
As far as I know my nuro is going to seek advice from DR H in CA.
 
Posted by Lymetoo (Member # 743) on :
 
Good luck to you. I hope your treatment works!! [group hug]
 


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