LymeNet Flash: palsey

This is topic palsey in forum Medical Questions at LymeNet Flash.

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Posted by pollyanna (Member # 43166) on :

anyone have been told they have this related to

nuero lyme.? this disease just keeps on

giving. any info please. thank you

Posted by GretaM (Member # 40917) on :

Yes I had this for the first two months of the worst of my neuro lyme.

I still have some permanent asymmtetry on my face from losing muscle definition during those two months.

And when the brain pain gets bad my face droops again and it's hard to drink eat kiss or chew.

Posted by seibertneurolyme (Member # 6416) on :

Do you mean Bell's Palsy of the facial muscles?

That is what Greta is referring to.

Bea Seibert

Posted by GretaM (Member # 40917) on :

Thank you Bea [Smile]

Haha! I see I forgot to put that part in.

Posted by Lymetoo (Member # 743) on :

Lots of Lyme info here:

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=088555;p=0

Posted by Crawgir1 (Member # 40229) on :

One evening I found my bulleye rash, the very next morning I had Bells Palsy in the left side of my face; it lasted only 3 1/2 weeks.

But five years later, after living under stress for an extended time, I got BP in the right side, which has been with me since, going on six years.

Bells Palsy is one of the #1 Lyme indicators that the CDC uses I believe, buy my stupid MD still didn't get it.