Anyone currently using the Cal EAP protocol? In the USA?

Tell us what you are using to treat your MS-- and how you are doing.

Postby newlywed4ever » Mon Apr 21, 2008 5:16 am

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.
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Postby CureOrBust » Sat Aug 02, 2008 1:05 am

A little more on Calcium EAP for those who are interested. (by the man himself)
http://www.explorepub.com/articles/neiper2.html
Mineral Research
Treatment of Multiple Sclerosis

©Copyright 1998 by Hans A. Nieper, M.D. Germany
(Explore Issue: Volume 8, Number 6)

I cringed when I saw the reference to "Orgone" energy.
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Re:

Postby drcpr » Mon Nov 28, 2011 10:53 am

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
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Re: Anyone currently using the Cal EAP protocol? In the USA

Postby TeresaL » Thu Nov 21, 2013 4:36 pm

I use the Cal EAP suppositories from College pharm. in Boulder CO. 400 mg. my veins are terrible This works well for me
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Tried EAP IVs in TX. Did help but hard to stick with

Postby TeresaL » Fri Mar 06, 2015 5:53 pm

I used th cal EAP IVs for several yrs, it did help then I. Lost my port a cath and relapsed. One is suppose to do IVs for 7yrs then abLE to switch to oral EAP to continue for life. Mr friend, who saw Dr N in Germany. Did IVs EAP for over 7yrs, had two port a cath put in over the yrs. She has been on a wheelchair for over 10 yrs. The EAP IVs helped her,and I when we were able to stick w it. But it is very hard to stick w with tricky veins.
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
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Re: Anyone currently using the Cal EAP protocol? In the USA

Postby TeresaL » Wed Sep 14, 2016 1:33 pm

It helped me, lost port, had to stop for several yrs. it did work but veins are tricky, tried EAP supportories but didn't work, now tyin high dose D...Dr Ciscero Brazil
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Re: Anyone currently using the Cal EAP protocol? In the USA

Postby TeresaL » Wed Sep 14, 2016 2:18 pm

Helped me but couldn't stick w it, tried EAP suppositories but didn't work. Worse now
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