MMS Vs. Lyme Blog- Day 3
theincrediblejy asked:
One man’s documentation of his experience taking MMS to treat Chronic…
Violette
Jenna’s Lyme Video Blog
Video blog about chronic and/or neuro-Lyme
3 Responses to “MMS Vs. Lyme Blog- Day 3”
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May 30th, 2009 at 1:37 pm
Sandra
Hmmm. Well your vlog is certainly interesting so far. And those pains you describe having, are something that I have as well. They usually occur on the same side of the body in joints.
May 31st, 2009 at 8:28 pm
Janet
I’m so sorry to hear what a struggle you and and your family are enduring. And I truly hope that MMS can help bring that ray of hope that we all so desperately need. In the meantime, are there some immediate needs that I and my friends might be able to help out with? Dealing with this has forced me to become very resourceful, so please let me know if there is anything you and your family may need a hand with. And thanks for the kind support and encouragement.
June 2nd, 2009 at 4:01 pm
William
Thanks for being our guinea pig! Here’s our stats: Whole family of 4 with Lyme, no more career income (can’t work anymore), Social Security Disability failing us, local wellfare failing us, family failing us, house in foreclosure, sicker every day, medicaid failing us…we desperately need to see some light at the end of the tunnel, and we are really pulling for you with this new treatment.