Hi all - I know this is a little off topic, but know this is an active group, and I want to reach out to folks who won't be looking for this info. We just updated our site with a new article, and I'm trying to reach folks who were misdiagnosed like me.
For over 20 years I was misdiagnosed. I was told Chronic fatigue syndrome, fibromyalgia, and a host of other diagnoses. Because of my symptoms I was checked for lupus, MS, and tons of other diseases. I had tons of tests, went to countless doctors. I was tested over and over for lyme as I knew I was bit by a tick 20 years ago (NOW THEY ARE SAYING LYME CAN BE PASSED BY MOSQUITOS). My tests came back negative every time.
There are new and MUCH more reliable tests out now, and I found a doctor to order the blood test. I came out positive for lyme and babesia which is in the family of malaria. At least I know what it is now and how to target it.
After a great deal of research I created my own strategy which I share on the site, as well as some resources for the newest tests, great links, chat groups, other resources.
I really want people to know about this lyme problem. It is said to be an EPIDEMIC now, and is found all over the country and the world. It can mimic the symptoms of over 300 diseases. If I were someone dealing with a debilitating disease I would be tested for lyme to rule it out.