Hi, everyone! I haven't oficially been made a member of the Lyme Club, because I haven't been diagnosed yet, but I have strong "credentials" - I present ALL of the characteristic symptoms of chronic lyme (heart, muscle, joint, neurologic), some of them in severe form. I've received a Lupus diagnostic that never really checked out so, naturally, considering that Westchester, NY has more lyme than a mojito cocktail, I started thinking that I might have lyme disease. After doing a lot of research online, I started saying "Wait a minute. I don't just THINK I have lyme disease, I am actually pretty sure of it!". It seems the internet can teach you everything you need to know about
this crazy disease but it won't point you in the direction of a good doctor. I don't want to visit Westchester Medical Center's Dr. Gary Wormser because I really don't want to hear all that "post-lyme syndrome" BS when I've already found out how hard to to treat this illness can be. Chronic lyme exists, Dr. Wormser! WE know it, MOST doctors know it, and probably YOU know it, too! You just need to start acting like you know it.
Anyway, I am not racing to get diagnosed as quick as possible because there's a very slim chance that I actually don't suffer from this disease. The basic reason I'll have all my blood tests done is to check for co-infections. My aim is to find a good doctor (is it that hard???) that can recommend a long-term protocol. BTW, I suspect I've been infected more than 10 years ago. At first I thought I was a "one in a million" type of case but after doing research I found out that there are a lot of people who have discovered this illness after suffering for many years and probably just as many that have lived all their lives with it and never knew it. This is one crazy disease, that's for sure.
I hope I haven't bothered anyone with my slightly playful way of writing, because, hey, you know they say that you should never lose your sense of humor. I am just trying not to lose mine... I KNOW that this is a serious illness. Trust me. My symptoms made that very clear, guys.
So, if anyone can help me with the name of a lyme doc in my area (Westchester, NY) I'd really appreciate it.
I've sent Ticker an email about a week ago but he hasn't responded yet. Well, I'm still waiting.
Email me at lymelight44@yahoo.com
Hang in there, fellow lyme sufferers! I hope all of us find the strength to live a good life, even if we have to deal with this disease.