Update with MMS and Lyme and need some advice

[Guest guest]

Hi All,

I don't post often but I am writing to provide an update on MMS and

also get some advice.

I have had Lyme disease since 1999 but started having debilitating

neck symptoms since 2003. In 2004 I realized that what I had was Lyme

so have been treating since then.

I did salt/c for about 18 months but am no longer doing it, having

about 20-30% improvement. I started UT in July of 2007 and then added

MMS to my regimen in late December of 2007. I have modified my MMS

regimen a few times but over the last 2 weeks or so have been doing it

at night only. I am up to 8 drops. I have had continual improvement in

symptoms until 2 days ago.

My right arm, the upper arm and shoulder area, has become very weak

and painful and my range of motion is limited. My back is very sore

also and I am afraid to bend because it feels like I will put in out.

This is very unusual for me. For the past 5 years my symptoms have

pretty well been confined to my neck and jaw and now it seems that it

has spread.

Has anyone gone through something similar with MMS?

Thanks,

Olive