Video blog about chronic and/or neuro-Lyme
kevingianni asked:
www.therenegadehealthshow.com – In this episode I wanted to address some of your comments on Tuesday’s Lyme disease show… There were over 100 comments and I think it’s important to address some of them in this show, particularly the first issue that I bring up. Since I’ve never been “ill” with anything before, I [...]
LymeOrNot asked:
How to self-check symptoms of Autism/Lyme disease (and other autoimmune diseases)? My experiences in observing my (and my son’s)symptoms of Lyme disease (Autoimmune diseases, Autism, Lupus, MS,…etc)at awakenings and after-showers, according to my melanin theory…Powered by Yahoo Answers
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conniekillbug asked:
How do you know if you are well enough to work, if you have Lyme disease? This video discusses factors to consider if you are thinking about working while ill, and may help you to decide whether you are physically, mentally and emotionally able to do so. For more information on Lyme disease, [...]
conniekillbug asked:
In this video, I describe the various treatment modalities I have used for Lyme disease, and discuss which ones have been most effective. For more information on these healing strategies, visit: www.lymebytes.blogspot.comAnne
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thane17 asked:
I talk about my symptoms and my first Rife Machine treatment. lyme rife disease coil doug machine treatment blog depression fatigue anxiety story pain suffering supplements health herx economy collapse chronic unknown illness cfs cfids me ms als marshall protocol under our skinCam
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heiwalove asked:
babbling, per usual. it’s been awhile. … “lyme disease” “chronic lyme disease” update moving “east coast to west coast” “new york city”Violet
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conniekillbug asked:
This video is related to an excerpt in my book, “The Lyme Disease Survival Guide: Physical, Lifestyle and Emotional Strategies for Healing,”, and is entitled: “They Will Never, Ever Understand: Accepting Friends’ and Family’s Limitations.” It discusses the difficulties that Lyme disease sufferers have with family and friends who don’t understand chronic illness, [...]
LymeActionGroup asked:
Group, a southern-Ontario based advocacy group seeking improved Chronic Lyme Disease public policy in Canada, held a press conference at the Ontario Legislature on 7 November 2008. Participating were Helke Ferrie (Part 1, introduction), patient Janet Mitchell (Part 2), patient Dr. Graham Kucan (Part 3), patient Karin Klouman (Part 4), and Dr. Jozel [...]
fontdog1 asked:
Dr. Joseph J. Burrascano discusses the biotoxin work of Dr. Ritchie ShoemakerClancy
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artsyfart66 asked:
Thought i would ignore the fact that i had chronic Lyme disease for the night and just have some fun for a change. Lo & behold, i had a pretty good time! I had dinner with friends, then off to the chocolate bar for dessert, and dancing at the local dance club. I [...]
Jenna’s Lyme Blog