The 'good news' about contracting Lyme disease:
1. If you don't get bitten you can't get infected
2. A fairly large percentage of ticks are incapable of conferring Lyme disease even you're bitten.
That's about it for good news.
In the U.S. a good site to go to is:
Lyme Disease Quick Facts.
For Canada, go to:
CanLyme – Canadian Lyme Disease Foundation | The Canadian Lyme Disease Foundation (CanLyme) was formed to promote Lyme education in Canada and raise funds to advance Lyme disease research.
My qualifications for discussing Lyme disease are my years as the leader for Lyme support groups, both physical and on-line in the U.S.
I also had a web site for Lyme information and support which I recently closed.
I've been a patient advocate for Lyme patients for over a decade.
I was also a member of CanLyme and 2 European Lyme forums. I haven't participated in either of those for several years.
Read at those two sites I gave and if you have any questions I'll try to answer them or direct you to valid articles that can help.
It's a jungle out there with all the mis- and disinformation about Lyme disease. The CDC and the NHS have mis-information about Lyme. That's not just my opinion but the opinion of many top tier doctors and thousands of Lyme patients who believed the info on those sites and now have chronic Lyme.
1. If you don't get bitten you can't get infected
2. A fairly large percentage of ticks are incapable of conferring Lyme disease even you're bitten.
That's about it for good news.
In the U.S. a good site to go to is:
Lyme Disease Quick Facts.
For Canada, go to:
CanLyme – Canadian Lyme Disease Foundation | The Canadian Lyme Disease Foundation (CanLyme) was formed to promote Lyme education in Canada and raise funds to advance Lyme disease research.
My qualifications for discussing Lyme disease are my years as the leader for Lyme support groups, both physical and on-line in the U.S.
I also had a web site for Lyme information and support which I recently closed.
I've been a patient advocate for Lyme patients for over a decade.
I was also a member of CanLyme and 2 European Lyme forums. I haven't participated in either of those for several years.
Read at those two sites I gave and if you have any questions I'll try to answer them or direct you to valid articles that can help.
It's a jungle out there with all the mis- and disinformation about Lyme disease. The CDC and the NHS have mis-information about Lyme. That's not just my opinion but the opinion of many top tier doctors and thousands of Lyme patients who believed the info on those sites and now have chronic Lyme.