Agreeing with LMC mom about
how heartbreaking it can be when you are willing to reach out to people. I talk with kids that still live at home frequently, and even though they believe their parents are "on board" with them getting the needed treatments, usually they see only an ID doc and the parents won't take it any further for any reason. This terrifies me because I grew up with these infections and know exactly what that's like!
But that doesn't stop me from sharing all the information I can any time I can!! I was just asked about
it all yesterday - at a party for hubby's Aunt! Some of his cousins are finally curious as to what I went through. I was actually a little surprised when hubby was bragging about
Anyway, Chapelle, I'm not sure how you can use your profession to help people with Lyme, other than being ready to talk to them when they come in with questions - but as a 'regular' person, there are tons of ways!!! What level do you wish to be involved in? In the 'face-to-face' with patients? Getting laws passed and do you wish to be working on the state or federal level? Or do you wish to help online?
Herb only treatment for Lyme & Bart ended 12/11 - no active symptoms for 2 yrs -Herb only treatment for Babesia ended 12/12www.healingwell.com/community/default.aspx?f=30&m=2977364
Had Lyme, Bart, Babs, RMSF, Ehrlichia, Myco, Anaplasmosis, EBV
Back in treatment for new Lyme case 8/2014
*I can usually post a link to any info that I post. Wish to see a link? Please just ask!