Hi Brad,

I use Colosan which is similar to the ones Roger listed. It is a type of 'oxygen bound magnesium'...it really works for me!

Read this article about "Bell's Palsy of the Gut" by Dr. Sherr. It has helped some of us understand how Lyme affects gut motility.

http://www.ilads.org/sherr7.html

To get those funny 'faces' when you post, just click on 'rich text editor' after you click on 'reply'. I think you asked about that! (?)

Blessings,

Avril

--- In lymestrategies@yahoogroups.com, RRM <rmor67@...> wrote:
>
> are you using something to clean the gut ? homozon or mag 07 workes good, or sue massies has good products for this.
> do you have a rife machine?
>
> roger
>
> Brad Clark ontarioguy2334@... wrote:
> Yea Im already doing all of those. The diluted 35 i have been on for 5 months so far. Im doing the diluted drops, snorting it, and using it with my coffee enemas. Im also putting some salt into my coffee enemas.
> The sugars im just going to have to eliminate along with the carbs i think. That im sure is causing alot of my problems. I think also the sugars in combination with the constipation that I have is something that needs to be fixed. I have lost feeling to my abdomin. Its completly numb. Even when I pinch hard to cut the pain of getting ozone injections or IV's i can hardly feel it! For years my bowels would seize up on me after foods. I just want this to go away, its really runing me down. Im doing lots of magnesium too (one lvl teaspoon in the morning then 4 hours later another one).
> The coffee enemas im doing daily but I cant seem to get motivated to do the evening enema. So i just do one in the morning.
> Anymore advice?
> Thanks for taking \the time to help me out Carolyn
>
>