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 9:59 am


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 3 posts ] 
Author Message
 Post subject: The situation in the UK
PostPosted: Wed Apr 20, 2011 5:57 am 
Offline
Family Elder
User avatar

Joined: Sun Feb 12, 2006 4:00 pm
Posts: 345
Location: Sussex UK
Here is what is going on in the UK at the moment. We have made a video commentary on a recently aired programme on the BBC. Steep learning curve in the technical skills area.
http://www.youtube.com/watch?v=QMYu_-ejOvE
Michele

_________________
Michele,  warrior4MS, mother and champion for Ella, the MSer. The solution is out there we just have to ask the right questions.


Top
 Profile  
 
 Post subject:
PostPosted: Wed Apr 20, 2011 6:26 am 
Offline
Family Elder

Joined: Thu Jun 17, 2004 3:00 pm
Posts: 2012
Location: Bedfordshire UK
Michèle, how is Ella doing now? You haven't posted about her for a long while.......................Sarah

_________________
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.


Top
 Profile  
 
 Post subject: Cause of MS is unknown
PostPosted: Fri Apr 22, 2011 2:41 pm 
Offline
Family Elder
User avatar

Joined: Thu Oct 19, 2006 3:00 pm
Posts: 1052
Location: Oxfordshire, England
Everyone who studies MS etiology learns that the cause of MS is unknown. Even neuros accept this before they talk of auto-immunity.
So why Michelle do you present vascular factors as being the cause of MS ?? I listened to your critique and mainly remembered the word 'liberation' as the most repeated one, why ?

The simple message for the UK is:
- CCSVI is a syndrome defined by Prof Zamboni.....
- If pwMS are treated using balloon venoplasty their MS progression slows and in many cases reversal of MS symptoms occurs.
- CCSVI treatment should be available privately to pwMS who cannot be offered drug therapy.

A simple focussed message is best.

MarkW

_________________
Mark Walker - Oxfordshire, England. Registered Pharmacist (UK). 10 years of study around MS.
Mark's CCSVI Report 7-Mar-11:
http://www.telegraph.co.uk/health/8359854/MS-experts-in-Britain-have-to-open-their-minds.html


Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 3 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. Best of a bad situation

Gordon

10

1521

Mon Nov 29, 2010 3:36 pm

Gordon View the latest post

There are no new unread posts for this topic. Situation in Italy...your views?

Zeureka

6

1311

Sat Mar 06, 2010 1:18 pm

Zeureka 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: