Here's something I know you're going to want to see. Watch this PBS interview presented in Houston last week (Nov 3 2006). It's excellent. Kathleen Zabawa has Lyme and really tells it like it is. She's a brave patient and an advocate for us all. One of her most important points is that Lyme needs publicity. Did you know that there are less than 100 doctors in the U.S. who are even Lyme literate?

https://video.google.com/videoplay?docid=-4726635875489946625

Watch it now and then send it to your family members and friends; it will help them understand you and all the weird symptoms. It's fantastic. I'm off to send a thank you note to this woman and the host of the show. There is hope for understanding and hope for healing! We've just got a lot of work to do.

The only thing that saddens me is that it doesn't look like Kathleen has tried Samento or Cumanda, and I've interviewed Lymies who are symptom-free and healthy again because of these powerful, effective alternatives to antibiotics. I wish I could snap my fingers and get everyone with Lyme to try them. But until their doctors recommend them, people are often reluctant to try anything new. Does that make sense, though, when the doctor knows less about Lyme than you do?