Hi again,
The twitching and buzzing are likely stemming from the muscles but I'm really not sure. The wooziness is slightly better but I'm by no means cured yet. For 3 months, I've been taking an oral antibiotic but last week I also started intravenous antibiotic treatment. My LLMD (Lyme Literate Medical Doctor) advised this once she saw that there was some abnormality in my white matter (revealed in the SPECT test I had done).
Your symptoms sound similar to mine. I also have ringing in my ears (but I've had that for 5 years so I doubt it's due to Lyme). If you've exhausted other possibilities, I'd definitely look into Lyme. Most doctors don't really know anything about it. I was misdiagnosed by several and as a result, have now had Lyme in my body for at least 2 years. My story is very very common. I tested negative for Lyme twice. But then I started to read how so many people go misdiagnosed because their blood tests come back negative. Those regular blood tests are very unreliable for detecting Lyme. Once I had felt that I had eliminated other possibilities, I got in touch with an LLMD, who ordered more accurate tests (Igenex Lab, MRI, SPECT) and confirmed that I had Lyme. So perhaps it would be a good idea for you to get in touch with a LLMD yourself.
Best of luck, Amiel
The twitching and buzzing are likely stemming from the muscles but I'm really not sure. The wooziness is slightly better but I'm by no means cured yet. For 3 months, I've been taking an oral antibiotic but last week I also started intravenous antibiotic treatment. My LLMD (Lyme Literate Medical Doctor) advised this once she saw that there was some abnormality in my white matter (revealed in the SPECT test I had done).
Your symptoms sound similar to mine. I also have ringing in my ears (but I've had that for 5 years so I doubt it's due to Lyme). If you've exhausted other possibilities, I'd definitely look into Lyme. Most doctors don't really know anything about it. I was misdiagnosed by several and as a result, have now had Lyme in my body for at least 2 years. My story is very very common. I tested negative for Lyme twice. But then I started to read how so many people go misdiagnosed because their blood tests come back negative. Those regular blood tests are very unreliable for detecting Lyme. Once I had felt that I had eliminated other possibilities, I got in touch with an LLMD, who ordered more accurate tests (Igenex Lab, MRI, SPECT) and confirmed that I had Lyme. So perhaps it would be a good idea for you to get in touch with a LLMD yourself.
Best of luck, Amiel