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 Thu May 23, 2013 1:20 am


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 3 posts ] 
Author Message
PostPosted: Wed May 18, 2011 8:05 am 
Offline
Family Elder
User avatar

Joined: Wed Oct 14, 2009 3:00 pm
Posts: 1686
Image

The Multiple Sclerosis Society of Canada is pleased to announce that $6.6 million has been allocated in new research funding. Recently, the grants review and medical advisory committees of the MS Society of Canada met and designated $2.4 million towards 74 personnel awards such as studentships, fellowships and career development awards, as well as $4.2 million towards 17 operating grants. Funding allocations approved through this process will fund projects for up to three years beginning in 2011.... Read More - http://www.msrc.co.uk/index.cfm/fuseact ... ageid/2479

_________________
The Multiple Sclerosis Resource Centre

Squiffy's House of Fun - Laughter for Multiple Sclerosis


Top
 Profile  
 
 Post subject: wow..
PostPosted: Thu May 19, 2011 9:16 pm 
Offline
Family Elder
User avatar

Joined: Tue Oct 06, 2009 3:00 pm
Posts: 287
wow so they will research even more toxic drug's that do not work? well as long as the money keep's rolling in i suppose our health doesn't really matter!.....impress me oh MS society by doing research into like something natural like...natural fruit's or diet change...oh that's right...how would they make money off of that?????????????????????????????????????????????????????????????????????

_________________
GOD BLESS.... CCSVI treatment Dr. Siskin great doc....symptom's improved for about 3 week's (gait, balance, spasticity) now back to square 1...


Top
 Profile  
 
 Post subject:
PostPosted: Tue Jun 14, 2011 9:46 am 
Offline
Family Elder
User avatar

Joined: Fri Jan 01, 2010 4:00 pm
Posts: 123
Studying diet etc is a great ides, but I hopethey DO study more drugs, and specifically for primary progressive ms. I am tired of not even having the option to try DMDs, being excluded from studies, etc. We are a very under-served minority in the MS population.

_________________
Kathy, 49 with PPMS,full time scooter.
Married to a wonderful man, mother to a darling 9 yr old boy


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. MSS of Canada announces $3.8 million for progressive MS

squiffy2

1

392

Wed Nov 30, 2011 8:27 pm

KateCW View the latest post

There are no new unread posts for this topic. $15 million for MS Research on the line

rainer

2

1236

Mon Mar 24, 2008 7:16 pm

rainer View the latest post

There are no new unread posts for this topic. $5 Million Awarded to New MS Research Program

Artifishual

4

1369

Thu Oct 09, 2008 5:19 pm

BioDocFL View the latest post

There are no new unread posts for this topic. $18 million in new research projects launched to stop MS

squiffy2

6

493

Tue Apr 16, 2013 1:16 pm

HarryZ View the latest post

There are no new unread posts for this topic. EMD Serono launches one million euro research grant for MS

squiffy2

0

213

Fri Oct 12, 2012 7:08 am

squiffy2 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: