Passing Lyme to kids?

Thanks All.

Gosh that sucks. I'll talk to my husband about it tonight.

Tigerwithlyme - I'd love to hear about your ozone experience tomorrow. I've got a deposit down to try an IV Ozone treatment with a dr in Santa Rosa, CA and will make the appt once my broken shoulder/arm is a little better. I was diagnosed with Parkinson's in Dec 2015 so any articles you can pass on about the relationship between the disease and spirochetes would be great. How long have you been on Cowden and what has your experience been? I'm on day 24.

Dashgirl, what was interesting in the info this dentist had about spirochetes was that it had little to do with Borrellia. Evidently there are 6 or 7 types of spirochetes, one for our disease, one for syphilis and other ones as well. I would hope that those in those studies would team with those that have focused on borrellia spirochetes in all of these diseases. To answer your question about coinfections, little research has been done to know? We know Babesia and other subsets of borrellia are in the blood supply.

I have been on Cowden full time since January. At the same time I have been doing biofeedback therapy. I slowly saw improvement but over the last 60 days I really have improved. My worse symptom is chronic motion sickness. I always feel like I am on a rocking boat when I am out of bed. Like Parkinson's my movements would stop when I am asleep. That part is getting much better. I will post info on Ozone Therapy. Mine will not be by IV but through adding some of my blood to O3 and putting it back in me.

Let me know any more questions you have on Cowden. You can always email me too.