1/10/2024 0 Comments Western blot test lyme diseaseGood news is most insurance companies are good about reimbursing visits - mine have been reimbursed at 100% (which is actually cheaper than my in-network copay, which I've always thought was somewhat odd). Just out of curiosity, was the rash you had a typical bull's eye? That's usually the one red flag that'll at least get an ID doctor to pay a little attention.Īs far as LLMDs, there might be some out there that take insurance - a lot don't though. While I'm sure there are exceptions to the rule, generally infectious disease doctors will tell you it's not lyme, almost robotically. Hi Dani - welcome to the forum! I know it can be tough navigating all of this lyme stuff, but we're here to help however we can. I'm really hoping for a diagnosis, but I feel like I'm stuck where I am. I have also seen a Neurologist, Cardiologist, Chronic Fatigue Specialist, Infectious Disease Dr, Adolescent Medicine Dr, etc. I watched the DVD called "Under Our Skin" That was when I realized I need to advocate for myself and not depend on these doctors that are trying to tell me I have Chronic Fatigue Syndrome. I am very well aware of the controversial matters. I was also considering going through the Igenex Lab in California to get a proper diagnosis.Īre LLMD's covered by insurance? I know it depends on the insurance company in most cases. I'm getting a second opinion from a different infectious disease doctor this Thursday. I'm not being treated unfortuantley, I've gone an infectious disease doctor and he doesn't think I have Lyme. The symptoms have worsened over time, but the headaches started in August.then came along all the others symptoms. You are the first person to agree with me that I'm positive, you don't know how happy I was to read that. I did look over the "New to Lyme- Start Here" thread. Many of us here have gotten well and you will do. I hope we can be of help to you here and you can get proper treatment fast. Do not let anyone convince you that an infectious disease dr. Believe me, it will be so worth it to immediately see an LLMD rather than waste your time, energy, health and money with any other doctor. If you haven't researched lyme, you may not know that there is great controversy involving lyme diagnosis and treatment. I would strongly recommend seeing an LLMD which is a lyme literate medical doctor. Hopefully, you are in the early stages as you say you just started to feel ill in August? Did all of these symptoms start since there? Your symptoms are very common and familiar to those of us with lyme. I had a similar test result but band 39 came up on my IGG which gave me a negative reading, resulting in years of misdiagnosis. I dont' know if you have had a chance, but I would recommend reading the first thread on the forum entitled "New to Lyme - Start Here." It contains an unbelieveable amount of information.Īs you know, you have a positive test. Then it went away, I was feeling good up until this past October. I also had a rash on my back during the summer, in August, when I started to feel ill. I would just like an opinion from someone else, or a similar experience to share I know IGm is current, active exposure & IgG is a past exposure. I have a very vague understanding of the results. This is my most recent one for March & this is what it says. I've had the Western Blot test done many times.
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