I am going through this too!!! I lost a lot in the beginning before I knew what I had. When I was dx by my LLMD he said it was so common in Lyme patients due to low thyroid even though my panels...
this happened to me a lot in the beginning and got better with treatment. However the foot tingling got worse. I just started my last phase (hopefully) Flagyl an Amoxy been on it now about 1 1/2...
Thanks for your response, I am wondering if you do pulse it does it mean you have to stay on it longer??? From what I have read and I want your opionions out there. Do you feel Flagyl is the most...
I am just curious what different LLMD's rx with Oral Flagyl weather you take it a full 7 days a week or like for 4 or 5 days and 2 or 3 off. How long where you on it? I was recently treating the cyst...
Hi, I am from the Lyme Disease Forum and I thought I would come on over and ask a question about pain management since you guys are most likely the experts. I have extreme muscle and joint pain,...
Thanks to those who responded to my email. I am still feeling crappy today and having swelling, I will try the ice today. I am reluctant to go to the ER because they say that steriods can make the...
Did those of you who were dx with Lupus have positive ANA tests, or does the doc dx with syptoms??...
Hi, my name is annie and I have lyme disease, some of the syptoms are similar to Lupus. Mainly right now I have major swelling in my knees with intense pain. I know this happens with Lupus too I was...