Anyone currently using the Cal EAP protocol? In the USA?
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- Family Elder
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- Family Elder
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http://www.explorepub.com/articles/neiper2.html
I cringed when I saw the reference to "Orgone" energy.Mineral Research
Treatment of Multiple Sclerosis
©Copyright 1998 by Hans A. Nieper, M.D. Germany
(Explore Issue: Volume 8, Number 6)
Re:
newlywed4ever wrote:Hi folks - I've been doing the Cal-EAP drip and supplements for 6 years. I have PPMS and, although this hasn't been a miracle cure and there has been progression, I have to say that I think the progression is slower than it would've been without Cal-EAP. I would highly recommend it - especially since there's not much else out there for those who don't have RRMS. I started treatment in Germany and have a friend who started with Dr Moore in IN - she, too, is happy with this treatment. The other posts regarding Brewer Science Library, etc. are good resources.
Hi I am new here - our daughter just returned from the clinic in Hanover after seeing Dr Wolf & 2 weeks of treatment. Because we do not want to deal with the Flora pharmacy there, I am searching for a source of injectable CA EAP in US - tried contacting Dr Gary Moore. Message says phone is temporarily disconnected. Any current numbers or info on him?
Thanks much
Candy Rotering
Re: Anyone currently using the Cal EAP protocol? In the USA
Tried EAP IVs in TX. Did help but hard to stick with
I have been using EAP suppostories from a compounding pharm in TX. I don't think the suppostories work as well as the IVs
I was able to get the IV EAP from a pharmacy in Germany ."they would mail me the order. I have gotten the order form from TX lupus patient who saw dr N in Germany.
Both myself and my friend tried SCT last summer but we didn't see any improvements. So save your money
Re: Anyone currently using the Cal EAP protocol? In the USA
Re: Anyone currently using the Cal EAP protocol? In the USA
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