Re: OT: KPU Protocol - and H Pylori

[Guest guest]

Just a quick note on HPylori--it releases something, I have my notes somewhere

else--but basically a baking soda effect--reducing stomach acid. I take HCL,

Enzymes, things to help stomach digest and if the ulcer type feelings come back,

I add pinneaple to the beginning of every meal, I read somewhere that it is good

for chronic HPylori and it is soothing to my stomach. Y'all keep going on about

KPU and I feel like I am still at the Lymes Kindergarten level, but oh well!

Take care, Jen

>

>

> From: son <chrisnmarsha2002@ yahoo.com>

> Subject: OT: KPU Protocol - Why is it so difficult?

> To: " Lyme Group " <Lyme_and_Rife@ yahoogroups. com>

> Date: Sunday, February 7, 2010, 11:11 PM

>

>

>  

>

>

>

>

>

> I looked at the KPU protocol and was wondering why someone would have to work

with a doctor while doing it and what makes it so difficult or what problems

does it cause?  Of course, I am getting the test done, but there aren't any

practioners listed anywhere near where I live.  My ND friend said he would

learn, and we both have quite a bit of experience, but wonder if this would be

enough.  And someone mentioned switching to the " core " supplements- --what does

that mean?  Sorry I have SO many ???, but I think this is probably going to be

something I need to address.  I was already thinking about having this test

done last summer, when reading some info about it that was totally unrelated to

lyme.  Thanks for helping me so much.  Blessings!  Marsha

>

[Guest guest]

Hi Jen that is interesting. Also one of the symptoms for KPU is we don't make HCL. Like you, I also take HCL and Enzymes. Hopefully when KPU is working my body will make it on its own. Time will tell. I hear u about feeling ur in lyme kindergarten. Even as long as I have been dealing with it I feel the same,especially since things keep changing. Actually,I was disabled 28 yrs ago and only found out at 23 yrs that I am dealing with lyme and co.I feel I had it way longet than that though. So it actually it has not been that long that I have known. Then 4 1/2 yrs of hellish killing and then finding that I am dealing with KPU. So sort of starting all over again. Healing Blessings JoyceSubject: Re: OT: KPU Protocol - and H PyloriTo: Lyme_and_Rife Date: Wednesday, February 10, 2010, 1:10 PM

Just a quick note on HPylori--it releases something, I have my notes somewhere else--but basically a baking soda effect--reducing stomach acid. I take HCL, Enzymes, things to help stomach digest and if the ulcer type feelings come back, I add pinneaple to the beginning of every meal, I read somewhere that it is good for chronic HPylori and it is soothing to my stomach. Y'all keep going on about KPU and I feel like I am still at the Lymes Kindergarten level, but oh well! Take care, Jen

>

>

> From: son <chrisnmarsha2002@ yahoo.com>

> Subject: OT: KPU Protocol - Why is it so difficult?

> To: "Lyme Group" <Lyme_and_Rife@ yahoogroups. com>

> Date: Sunday, February 7, 2010, 11:11 PM

>

>

> Â

>

>

>

>

>

> I looked at the KPU protocol and was wondering why someone would have to work with a doctor while doing it and what makes it so difficult or what problems does it cause? Of course, I am getting the test done, but there aren't any practioners listed anywhere near where I live. My ND friend said he would learn, and we both have quite a bit of experience, but wonder if this would be enough. And someone mentioned switching to the "core" supplements- --what does that mean? Sorry I have SO many ???, but I think this is probably going to be something I need to address. I was already thinking about having this test done last summer, when reading some info about it that was totally unrelated to lyme. Thanks for helping me so much. Blessings! Marsha

>