Lyme disease: mild neurological herx from august

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Uploaded by on Aug 25, 2010

I took this video in august to show what the mild end of my twitching/tremors looked like but because I was in the middle of things I didn't feel ready to make the video public. This is what it looks like sometimes. I'm blessed that it's usually not very severe. I was OF COURSE watching youtube videos. The Neurontin has helped this situation a GREAT deal.

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  • You can check out "Our Story" to see someone else's experience and we have recently added a new ending, because now I'm into my 7th month of doing drastically better after 5 years of traumatic sickness and daily intractable pain...

    We must all share our stories, and in doing so, help one another... As much as possible.

    Praying for you...

    Love, Christa

  • That's me. Can anyone help? Doctors are so dismissive. I shake and have seizures and have 2 western blots that are +. My doc prescribes zoloft.

  • Look up this video on youtube and you will know what to do (copy and paste): “HemoPyrrol-Lactam-uria (HPU), Lyme disease and autism presented by Dietritch Klinghardt, MD”! It is a phenomenal lecture given by Dr. Klinghardt!

  • mine is half this bad.

  • i go through herx like that repeatedly. i feel your pain. you're so brave for showing the world what really happens to us when the bactera die and release the harmful toxins. i have to watch more of your videos to see if you have made progress. sure hope so. me, not so much. from oral abx to a port and then got c diff, had to stop abx and presently back on iv abx through a picc and herxing again. hate it!! it's cruel

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