I would be grateful if anyone would like to share their favorite lyme resources with me. Although my personal decision was to approach the lyme through alternative means, and the site reflects that, I would like to share all kinds of info for people so that they can make up their own minds. I am looking for your favorite alternative sites & resources and mainstream approach sites as well.

Please share any links that you feel are particularly good.

One thing people dealing with Lyme and with Lyme patients learn is that no one has the one size answer that fits all and that the world is full of people who want to convince others that they have the
product(s), procedures, machine, protocols, supplement, mineral etc. etc. etc.that will solve the Lyme disease problem if only you will buy it.

Frankly, I'm totally overwhelmed with everything going on in my life right now, but my husband and I took the time to get this info public so others who are misdiagnosed have a chance. Just go away if you are not interested and don't want to help.

OF COURSE no one thing is right for everyone. I say that over and over in my note below, as well as in the article. Did you not read this before you answered me? I'm no doctor and I don't have everyone's solution. I did a ton of work to search out what was right for me and I'm simply sharing it for anyone who wants to look at MY choices. It's just another resource for folks to do their own research, as I say OVER AND OVER in the article and in my first posting.

Do you have any idea what it's like to be sick for 20 years with misdiagnosises and no real idea of what's wrong? Do you know what it's like to try thing after thing and pour your money out, and trust doctor after doctor with no real help? Do you know what it's like to try every alternative approach desperate for help for 20 years? Do you know what it's like when people just assume it's probably all in your head? Well if you do, then you might understand why we took the time to post that info (in the midst of some really tough life circumstances by the way), and why we are trying to reach misdiagnosed people. And if you don't know what it's like, maybe you should hold back on judging my motives.

You said:
(quote)
Do you have any idea what it's like to be sick for 20 years with misdiagnosises and no real idea of what's wrong? Do you know what it's like to try thing after thing and pour your money out, and trust doctor after doctor with no real help? Do you know what it's like to try every alternative approach desperate for help for 20 years? Do you know what it's like when people just assume it's probably all in your head? Well if you do, then you might understand why we took the time to post that info (in the midst of some really tough life circumstances by the way), and why we are trying to reach misdiagnosed people. And if you don't know what it's like, maybe you should hold back on judging my motives. (unquote)

The answer to all your questions is "Yup!"
FYI Here is my website: www.geocities.com/ldbullseye

Click on the little arrows up by Yahoo! to get rid of whatever is there. I don't have
control of that.

"No thanks" is my opinion only.
Ann - OH