Re: on calcium AEP-from kell in aussie again!

[Guest guest]

Hi Kellie,

Thanks for the quick reply.

I am (was) a nurse and I don't know of any "calcium aep" injections here in the US. I think you're right about it not being available here.

I take all the calcium carbonate tablets that my docs advise me to.

Thanks again and thanks for the MS info that you posted on the site.

Lori

[Guest guest]

LORI, I HAVE BEEN ON CALCIUM EAP INJECTIONS SINCE 1999 AND THEY ARE AVAILABLE HERE IN THE US WITH A LETTER STATING YOU ARE USING A CELL MINERAL THERPY THAT HAS NOT BEEN APPROVED IN THIS COUNTRY. SEVERAL DOCTORS ACROSS THE US ARE PRESCRIBING CALCIUM EAP. ONE IS THE FAMOUS ADKINS CLINIC IN NEW YORK. HE STATES IN HIS VITA NUTRIENT SOLUTIONS BOOK "the most underrated nutrient, autoimmune savior.HE GOES ON TO STATE;CONVENTIONAL MEDICINE OFFERS NO EFFECTIVE THERAPY FOR AUTOIMMUNE DISORDERS OTHER THAN PREDNISONELIKE STEWROIDS AND DRUGS THAT SUPPRESS THE IMMUNE SYSTEM AND THEREFORE EXPOSE PEOPLE TO A VARIETY OF HAZARDOUS SIDE EFFECTS. CALCIUM EAP DOES NOT DO THAT. FOR AN AUTOIMMUNE CONDITION LIKE MS, IT ALLOWS FOR REAL NEUROLOGICAL IMPROVEMENTS. AND IT DOES NOT WORK FOR JUST A HANDFULL OF PEOPLE. IT WORKS FOR THE MAJORITY. FOR REASONS UNCLEAR TO ANYONE, THE US HAS LARGELY IGNORED THIS HARMLESS SUBSTANCE AND FREQUENTLY TRIES TO INTERFERE WITH ITS USE IN THE US. PAGES 258-260 IN THE BOOK. IT IS A SHAME YOU ARE A NURSE AND HAVE NEVER HEARD OF THIS BUT IT DOES NOT SURPRISE ME.THE KEITH BREWER SCINCE LIBRARY HAS A LIST OF DOCTORS WHO USE THIS THERAPY. THEIR NUMBER IS 1-608-647-6513. GOD BLESS, KATHY

----- Original Message -----

From: Lori Jensen

low dose naltrexone

Sent: Saturday, April 10, 2004 9:03 PM

Subject: Re: [low dose naltrexone]on calcium AEP-from kell in aussie again!

Hi Kellie,

Thanks for the quick reply.

I am (was) a nurse and I don't know of any "calcium aep" injections here in the US. I think you're right about it not being available here.

I take all the calcium carbonate tablets that my docs advise me to.

Thanks again and thanks for the MS info that you posted on the site.

Lori

[Guest guest]

Hi Kathy,

Thanks for your info. I was a mainstream nurse at s Hopkins. We didn't talk about alternative therapies there (at that time) so a lot of good info passed me by. And my MS has gotten worse and worse. I'm tired of laying down and taking it! The disease makes me angry and so do the docs that don't give a hoot. I ready to start being my own caretaker!

Lori