Heather, I am sorry that you feel like we've jumped on you. We can be a bit agressive. There is a reason for it though. We have seen so many people suffer from bad treatment and actually DIE as a result of that bad treatment. Anytime we get a new member on here who is being mislead, we jump in. the mantra from the other side can be so appealing and we have to act strongly in order to get people's attention. We got yours and I am so glad for that. I sinncerely hope that you are able to get the care that you need and find out what is actually going on with your body. Not know sucks so much and it can be incredibly frustrating. We have all been there and struggled through that. Our purpose here is to support people who have Lyme disease and Post treatment lyme disease syndrome; we also help people who have been misdiagnosed, mislead, and try to steer them to the right doctors so that they can get help and feel better. It is also our sincere hope that not another person ends up on long term treatment for a condition that doesn't exist.
There aren't two schools of thought on this matter. there is one that is proven and backed up by study after study, and another where practitioners directly profit from making their patients sick.