Hi Rainie, I must have missed your first post to the group. Sorry about that and sorry that you found that you have Lyme Disease. I did read both Peter and Mike's response to you and they were excellent.
The links below will guide you to major Lyme groups on line which will enable you to find your way to much else as well. In these groups you will find support and information directly related to Lyme Disease, your situation, your symptoms and how best to cope and deal with them, private recommendations to LLMD's according to your location (they will not announce this publicly), and answers to any questions you might have. They will help you to understand how Lyme Disease affects one's psychology, body, emotions, and behavior. You will come to learn about supplements, protocols, and symptomology and how to deal with co-infections if they exist, as well as the medical/legal/political aspects of Lyme that the community is plagued with. Most of all you will find a vast amount of friendship and support from those who completely understand all aspects of Lyme Disease and will consider you part of the family and welcome you with open arms. They are very experienced, and in various stages of Lyme, some of whom have had chronic Lyme Disease for well over 30 years. For now, if you care to, join http://health.groups.yahoo com/group/lymestrategies/ and http://health.groups.yahoo com/group/Lyme_and_Rife/ All the best, Sasha -------Original Message------- From: Rainie Cole Date: 1/8/2010 10:31:39 AM To: [email protected] Subject: CS>recommendations for Lyme Disease Thank you for taking the time to write, Mike & Peter. I'm not sure if I'm supposed to repond directly on the list or to you directly so I'll be safe and do both. It strikes me that by posting it, I may generate more remarks. I have done quite a bit of research involving Lyme. I have not found a LLMD yet who takes my insurance. I pay an incrredible amount for health insurance and cannot really afford to see someone "out of network" which is a major problem. I have a friend who took CS after suffering 3 years with Lyme and she got better. Unfortunately, she cannot recall the brand, the dosage or even the doctor. I am gong to read your post with care and follow up on any of the suggestions I have not already tried. I'll keep you "posted". Very gratefully, Rainie
