This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
It is currently Sun May 19, 2013 3:07 pm


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 5 posts ] 
Author Message
PostPosted: Sun Nov 11, 2012 9:29 pm 
Offline
Newbie

Joined: Sun Nov 11, 2012 9:08 pm
Posts: 1
Hi this is jason. I was diagnosed with ms nearly 6 years ago.I'm now 38,am married with 1 child. Started on betaferon then switched to copaxone 2 years ago. Both are worse than the disease. I started relapsing remitting, but now think i'm in the next stage. Have got all symptoms plus some unheard of.Saw on the catalyst about the antibiotic treatment for ms with Dr Wheldon and his wife Sarah. If they could please contact us with the details we need to know as our local doctor is willing to prescribe them to me. Our neurologist didn't want to know about them.
cheers jason


Top
 Profile  
 
PostPosted: Tue Nov 13, 2012 3:47 pm 
Offline
Family Elder
User avatar

Joined: Mon May 02, 2011 3:00 pm
Posts: 101
the treatment and everything about the protocol can be found on www.CPn Help.org. It's a long road but it works!


Top
 Profile  
 
PostPosted: Tue Nov 13, 2012 7:09 pm 
Offline
Family Elder

Joined: Sun Apr 02, 2006 3:00 pm
Posts: 545
Location: Naples, FL
Website has no space between cpn and help. It is all one word. The link won't work if you just click on it. You will have to type it in as directed.


Top
 Profile  
 
PostPosted: Wed Nov 14, 2012 3:41 am 
Offline
Family Elder
User avatar

Joined: Sat Jul 15, 2006 3:00 pm
Posts: 607
Location: midwest U.S.
Loriyas wrote:
Website has no space between cpn and help. It is all one word. The link won't work if you just click on it. You will have to type it in as directed.


The links people post on here to http://www.CPn Help.org always work for me and take me straight to the site. Always. Every single time it's posted. And the link in bartman's post takes me straight to the site.

Edited to add that I tried MY link and it also takes me directly to the site.

_________________
Dx'd with MS & HNPP (hereditary peripheral neuropathy) 7/03 but must have had MS for 30 yrs before that. I've never taken meds for MS or MS symptoms except 1 yr experiment on LDN. (I found diet, exercise, sleep, humor, music help me the most.)


Top
 Profile  
 
PostPosted: Fri Nov 16, 2012 10:15 am 
Offline
Family Elder

Joined: Sun Apr 02, 2006 3:00 pm
Posts: 545
Location: Naples, FL
I just tried it from your post and it did not take me to the site.


Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 5 posts ] 

All times are UTC - 8 hours [ DST ]


Related topics
 Topics   Author   Replies   Views   Last post 
There are no new unread posts for this topic. CCSVI, Stents, Treatments

cocochanel

0

769

Mon Apr 19, 2010 9:45 am

cocochanel View the latest post

 


Who is online

Users browsing this forum: No registered users


You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum

Search for:
Jump to: