Hammilton
Bluelighter
- Joined
- Sep 2, 2008
- Messages
- 3,435
I was diagnosed with 2nd Stage Lyme's (I'm pretty sure she said second and not third, but I was bitten about 2 months ago, and have had quite bad lethargy and joint pain for about 3-4 weeks now) and the doc ordered a Western Blot, CBC, and the usuals. I don't believe she ordered an ELISA, though.
I've been doing some reading, and basically I've found that neither a Western Blot or ELISA are that effective at detecting Lyme's Disease, and that diagnosis is based almost entirely on symptomology, especially since I remember the bite and had the bulls-eye rash. I also saw that ELISA should be done first, and a Western Blot second if ELISA is positive.
So that leads me to the following questions: Why did she only order a Western Blot? And if neither of them are that effective, why order them at all?
I was told that since I'm getting tested outside of the 3-6 week window (after the bite) and in the 8-10 week range, the effectiveness drops off rapidly. That's where I'm at now, so I'm a little confused. Then again, I've read that antibodies might not even be detected until I'm outside of the 2 month window.
What's correct? Surely they can't both be.
Is there anyone else here with Lyme's? I know surprisingly little about it despite my brother and father having had it. They both sought treatment right after being bitten and finding the rash. I guess I knew it could cause symptoms, but I never really thought about it. I thought it was something that lots of people got but almost no one ever had symptoms from. I live in an area with endemic Lyme's disease (central Wisconsin).
The only other person I know of that had symptoms from Lymes was an uncle. He said that he never even had a blood test done, and was diagnosed in the secondary stage.
I know that he still has joint pain today, even though he was treated years ago.
Will the joint pain go away? Will the lethargy?
I've been on doxicycline for about 3 days, and I'm not as tired as I was, but my knees and "bad" elbow are awfully sore. Ibuprofen definitely helps, but it's not a cure-all.
My "doctor" (I think she may have actually been a Nurse practitioner) didn't seem to know much about it, she was more worried about my heart than anything else. Are there any doctors who specialize in Lyme's treatment?
I've been doing some reading, and basically I've found that neither a Western Blot or ELISA are that effective at detecting Lyme's Disease, and that diagnosis is based almost entirely on symptomology, especially since I remember the bite and had the bulls-eye rash. I also saw that ELISA should be done first, and a Western Blot second if ELISA is positive.
So that leads me to the following questions: Why did she only order a Western Blot? And if neither of them are that effective, why order them at all?
I was told that since I'm getting tested outside of the 3-6 week window (after the bite) and in the 8-10 week range, the effectiveness drops off rapidly. That's where I'm at now, so I'm a little confused. Then again, I've read that antibodies might not even be detected until I'm outside of the 2 month window.
What's correct? Surely they can't both be.
Is there anyone else here with Lyme's? I know surprisingly little about it despite my brother and father having had it. They both sought treatment right after being bitten and finding the rash. I guess I knew it could cause symptoms, but I never really thought about it. I thought it was something that lots of people got but almost no one ever had symptoms from. I live in an area with endemic Lyme's disease (central Wisconsin).
The only other person I know of that had symptoms from Lymes was an uncle. He said that he never even had a blood test done, and was diagnosed in the secondary stage.
I know that he still has joint pain today, even though he was treated years ago.
Will the joint pain go away? Will the lethargy?
I've been on doxicycline for about 3 days, and I'm not as tired as I was, but my knees and "bad" elbow are awfully sore. Ibuprofen definitely helps, but it's not a cure-all.
My "doctor" (I think she may have actually been a Nurse practitioner) didn't seem to know much about it, she was more worried about my heart than anything else. Are there any doctors who specialize in Lyme's treatment?