posted
anyone have been told they have this related to
nuero lyme.? this disease just keeps on
giving. any info please. thank you
Posts: 16 | From RHODE ISLAND | Registered: Jan 2014
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GretaM
Frequent Contributor (1K+ posts)
Member # 40917
posted
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.
Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013
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posted
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.
Posts: 123 | From Pawleys Island SC | Registered: Mar 2013
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