Lyme Disease – Rife Blog December 2008
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 skin
Cam
November 20th, 2009 at 5:39 am
Butch
I suggest you look up ‘Dr Bob Beck Brain Tuner’.
Also ‘Rick Simpson Hemp oil’.
November 23rd, 2009 at 1:03 pm
Samantha
Sounds like junk science. What a waste of money.
November 25th, 2009 at 5:29 pm
Annemarie
Because the symtops you talked about sound just like mine.
November 26th, 2009 at 9:40 am
Christopher
Yes, why do you ask?
November 26th, 2009 at 12:40 pm
Patsy
Did you get tested for Lyme desease?
November 29th, 2009 at 10:39 pm
Cam
Hey guys….PLEASE register at the Oprah Winfrey website and let her know how much you would like to see her do a show on Lyme disease. Dr. Oz thinks the “UNDER OUR SKIN” documentary is wonderful but a show about Lyme won’t be done unless she sees lots of interest. Request that LLMDS and patients be the guests so that we can be heard. Also, Daryl Hall would make a great guest. OPRAH needs to hear about YOUR experience with Lyme disease. WE ARE ALL IN THIS TOGETHER !
God Bless,
Elaine
December 3rd, 2009 at 10:31 am
Samantha
Wow! Cool! Thanks for showing us the rife?coil machine. I really hope that works for you. Definately keep us posted! I know all about being a recluse. My friends call me “hermit” the frog. LOL! I’m due for another rife session myself but will wait a few more days. I’m still feeling shitty from my hospital stay and want to get my body more rested up and healed from that first so i can withstand the herxing.
December 5th, 2009 at 6:49 am
Emery
Hey Thane. Just stopping by to say that I hope that things are going OK with you and that you have a happy holiday. Best to you, pal.
December 5th, 2009 at 11:37 am
Franny
Yeah, I know what you mean about social situations wearing you out. I miss so many people and a bunch of them (like 10) want to get together at my house just before Christmas. I am really looking forward to it, but I also know that it will be a challenge and that it’s gonna completely blast me. I just miss my friends very much, though and seeing them will help more than it will hurt, I hope. Funny, I can still do a lot of stuff like grocery shopping, but it’s “considered” now, not automatic.
December 6th, 2009 at 2:27 pm
Mary
Thanks for doing these videos. I hope the rife machine helps. I’ll keep watching. Sue
December 8th, 2009 at 9:03 pm
Violette
Wow…I can relate. So much of what you are saying is so familiar to me. Almost all of your symptoms I have, too. Lately I feel like I’m running into all these people that talk so much. Maybe part of it is listening just wipes me out. The insomnia is hard, too. I fall asleep between 2-5. So I guess I’m lucky. Dizziness is harsh and so is the tiredness. It’s hard to not have a life, huh?! When you have to recover from every little thing, that healthy people don’t have to even consider.
December 10th, 2009 at 10:26 am
Carlo
Thanks for posting these videos. I find them extremely interesting. I can relate to all of your videos so far, and am in the process of getting tested for lymes as well. You seem like a really well-rounded cool guy.
Can you make a video about the impact all this has had on your social life? How do you explain everything you’re going through and doing to others before you were diagnosed, and now? How do ppl react? What about work,money etc. how do you manage your personal life? Thnx if u do.