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.
newlywed4ever
Family Elder
Posts: 255
Joined: Thu Apr 17, 2008 2:00 pm
Location: Michigan
Contact:

Post by newlywed4ever » Mon Apr 21, 2008 4:16 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.

User avatar
CureOrBust
Family Elder
Posts: 3366
Joined: Wed Jul 27, 2005 2:00 pm
Location: Sydney, Australia

Post by CureOrBust » Sat Aug 02, 2008 12:05 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.

drcpr
Newbie
Posts: 2
Joined: Thu Nov 24, 2011 6:57 am

Re:

Post by drcpr » Mon Nov 28, 2011 9:53 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

TeresaL
Family Member
Posts: 81
Joined: Wed Oct 23, 2013 4:14 pm

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

Post by TeresaL » Thu Nov 21, 2013 3:36 pm

I use the Cal EAP suppositories from College pharm. in Boulder CO. 400 mg. my veins are terrible This works well for me

TeresaL
Family Member
Posts: 81
Joined: Wed Oct 23, 2013 4:14 pm

Tried EAP IVs in TX. Did help but hard to stick with

Post by TeresaL » Fri Mar 06, 2015 4:53 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

TeresaL
Family Member
Posts: 81
Joined: Wed Oct 23, 2013 4:14 pm

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

Post by TeresaL » Wed Sep 14, 2016 12:33 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

TeresaL
Family Member
Posts: 81
Joined: Wed Oct 23, 2013 4:14 pm

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

Post by TeresaL » Wed Sep 14, 2016 1:18 pm

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

Post Reply
  • Similar Topics
    Replies
    Views
    Last post