website

Thanks for sharing Carla. Interesting stuff. Glad I have a doctor who can look into really what's important for me because there is NO way I could determine what's going to potentially help me or hinder me. It's just so much information out there.

Some of them are doing Skype now. So you aren't limited to who is nearby. Perhaps look into this. I think you need at least one central doctor that at least understands enough about the body and lyme that you can partner with and definitely bounce things off of. Some people do not have a llmd, but a doctor who is knowledgeable enough to guide them through these hazy and murky waters.

Not offhand, but perhaps others will know and can contact you via email.