I’ve been using MMS for 7 weeks now. Started with one drop daily, currently at 20 drops. I ran into a little nausea at 8 and 11 drops, dropped down a drop for 3 days, then ramped back up.
These are the benefits I recognize so far from MMS.
I had 3 tiny painful sores on my tongue for about two years now. Nothing I nor my doctor did helped. Trust me, these were very painful. Eating spaghetti sauce became a thing of the past. This past summer, the pain was at its worst. I was sure this was some kind of pathogen, but just couldn’t get rid of it. The pain continued to worsen.
When I started MMS, I decided I would take a sip and hold it in my mouth for a minute or so before swallowing. I no longer have any sores on my tongue. The pain is completely gone. The only change in my treatment protocol was the addition of MMS.
Next and more important, I was dealing with the worst fatigue and brain fog for the past 6 months. Seven weeks of MMS and now my fatigue and brain fog are much better. I can actually do some things again. Walking to the mailbox is now something I can do anytime I wish. Before, most days I couldn’t make that short walk. I’ve been spending some time working out in my yard, something I haven’t done in the past 6 months.
I definitely feel there is a benefit for anyone with Lyme disease using MMS. I am under the care of a few doctors at the Mayo Clinic and just yesterday I had a physical exam of my thyroid. All was normal. I will test for TSH, T4 and T3 at the end of the month. But for what this doctor can tell from all the past TSH tests done there, this too should be considered normal.
