MyLymeData: Patient-Powered Research Project

Last night, Dr. Rawls held a webinar with Dr. Neil Spector entitled "The Lyme + Cancer Connection." Based only the title alone, I opted not to watch it. I already have enough clutter in my mental attic.

Anyway, not long ago, I received an e-mail with a link to the webinar replay. Along with that link was information about a registry for Lyme patients called "MyLymeData."

MyLymeData
https://www.lymedisease.org/mylymedata

From the above website:

"MyLymeData is a patient-powered research project. It was conceived by patients, is run by patients, and addresses the issues that patients care about. It lets Lyme disease patients learn from each other and provides data that can help drive research to improve their lives."

Just FYI, for anyone interested.

Does anyone know what herbs to use for rickettsia or Rocky mountain spotted fever by any chance. I've been told I have rickettsia not Lyme even think western blot is pretty Lyme obvious. Rickettsia herbs are the only ones you can't find any info about online I've never even seen anyone post about rickettsia. All info is appreciated