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MASSACHUSETTS
Jan Dooley
- I didn't see the tick or a bull's-eye 5 years ago. I had just
moved to South Carolina and was busy settling in, when I became very
weak and couldn't walk and was confused and lost 10 lbs in a month.
I finally got a blood test for Lyme and it was confirmed
Ehrlichiosis, but after 3 months of the nightmare, I got a 14-day
dose and my life has been hell since. I've spent thousands of $ and
been to over 30 doctors including Mass General with no validation of
Chronic Lyme. My story is the same as everyone else's. I am getting
so much help from the book "Unknown Cure" that I now have hope. I
can't do the antibiotics because it gives me "Leaky Gut" so I get
alternative methods and acupuncture. We will find a cure if we all
fight the ignorance of this mind blowing neglect of the medical
community.
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Darlene Travers
- Bitten June 1996,did not get a diagnosis and treatment until
January 1998. I am neurologically affected with dizziness, ataxia,
neuropathy during the times I am Lyme sick. I am presently on two
antibiotics three times per week.
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In
the interest of making the stories palatable for everyone, please
spell-check your submissions, and substitute a word like "antibiotic(s)"
or abx for drug names. This site is foremost about telling the story of our
disease and problems with diagnosis, treatment, etc.
Please refrain from listing every drug and/or dosage you have been
on. We have all been through a unique experience and that is the
focus of this page. Thanks for your understanding and cooperation.
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