Archive for the ‘Treatments’ Category

Canada AM & the latest MS Research

 

Please click below to see the clip from Monday, January 14th's Canada AM interview with Dr. Karen Lee, Vice President, research at the MS Society of Canada.

Dr. Karen Lee of the MS Society explains while a cure for multiple sclerosis is still unknown, 2012 brought exciting and promising new research.

   Canada AM… a part of the CTV News Video Network    

 

 

 

 

 

Dr. Karen Lee of the MS Society explains while a cure for multiple sclerosis is still unknown, 2012 brought exciting and promising new research.

Canada AM… a part of the CTV News Video Network

Social Action for MS e-Alert

There are a number of ways you can "TAKE ACTION" for MS. Please read the latest E-Alert from Social Action team at MS Society Canada.

Topics of interest:

Ontario Government Relations

National Government Relations

The Reading Room

Mark Your Calendars

MS Society Canada launches SOMEONELIKEME.CA

Following a research project at the MS Society of Canada in 2009 looking at social innovation and youth, the Society acknowledged and concluded that their traditional service delivery model did not fully capture, engage or support youth in a comprehensive and age-appropriate way.

They set out on a course to change that and in late early 2010 began developing an MS youth strategy to address ways in which they could better support Canadian youth impacted by multiple sclerosis. Since that time, the MS Society has identified a new MS youth ambassador, Aaron Solowoniuk who is the drummer from the band Billy Talent. Aaron is a philanthropist, fundraiser and agent of social change who is passionate about the MS cause.

Diagnosed in 1998 with relapsing remitting multiple sclerosis, Aaron has supported young Canadians living with MS by raising funds and building awareness through his involvement in art shows, golf tournaments and rock concerts around the world.

In addition, the MS Society since recruited and convened a National MS Youth Advisory Group comprised of youth and young adults impacted by MS. The goal of the MS Youth Advisory Group is:

  • to bring the voice of youth and young adults to the organization that provides meaningful opportunities to provide guidance and feedback
  • to create a forum for young Canadians living with MS to work in a youth friendly environment that respects and values their opinions and input
  • to involve young Canadians living with MS in aspects of decision making for youth initiatives developed by the MS Society of Canada that is informational and educational

The MS Society of Canada remains committed to supporting young Canadians whose lives have been impacted by MS through this new on-line community and innovative new resources and activities that will be explored in the coming years.

Visit the site at www.someonelikeme.ca 
 

Multiple Solutions Newsletter June 2011

Durham Regional Chapter's June 2011 issue of Multiple Solutions Newsletter.

No one knows more about what it’s like to have MS than other people living with it

We invite you to join MS Discuss! An online forum for those living with Multiple Sclerosis.

Welcome to the MS Discuss message board, a place where you can connect with other people who have common experiences and concerns! After all, no one knows more about what it’s like to have MS than other people living with it.

TODAY is World MS Day! sign the petition

Why World MS Day?

Multiple sclerosis (MS) is a chronic, often disabling disease. It is one of the most common disabling neurological conditions amongst young adults in the northern hemisphere. Over 2,000,000 people in the world have MS. The aims of world MS day are to raise awareness and mobilise the global movement.

About World MS Day

World MS Day was launched on 27 May 2009 with over 200 events in 67 countries. It’s an opportunity to raise awareness about MS and to strengthen the network of people living with MS across the world

World MS Day in previous years

World MS Day 2009 and 2010 were great successes with activities taking place in more than 60 countries worldwide. These photos represent the highlights from the past two years. To read about the activities why not take a look at the ‘news’ section of the site.

SIGN THE PETITION

Audio copy of the 2011 MS Research Teleconference now available!

On May 11, 2011, the MS Society of Canada hosted the annual MS Research Teleconference. This year, Dr. Paul O’Connor discussed the latest in MS research including CCSVI and took questions from callers.

Download the MP3

During MS Awareness Month support real action on MS in Ontario!

May is MS Awareness Month, and its time for real change that will directly benefit Ontarians living with MS and their families. During May, and in preparation for the 2011 provincial election, the MS Society is pressing Members of Provincial Parliament (MPPs) for commitments on three important issues:
 

  • Funding to find answers on a possible MS treatment for narrowed veins (CCSVI)
  • Work place supports for family caregivers
  • Funding for an Ontario Brain Strategy

 
Early action on these commitments would ensure a clinical trial of a possible new approach to treating narrowed veins proceeds quickly, if and when scientific evidence shows one is warranted. It would also mean that caregivers who must work to support their loved ones can receive the supports they need and that Ontarians with neurological conditions have the services and supports they need to live well.
 
You can help by sending a message to your MPP now. Help us win real action.
 

Your voice will make a difference! 
 

Do you have a question? MS Answers can help

About MS Answers

Learning for Life is a series of client-focused educational initiatives where the key objective is to provide timely, credible and unbiased information to the MS community. The Learning for Life series features an online forum, online educational sessions and e-bulletin series that provide people with MS and their families’ information and tools to enhance their quality of life.

In the spring of 2006, the Multiple Sclerosis Society of Canada launched the Ask the Expert web site, located at www.msanswers.ca. This online forum has allowed people with MS, caregivers and others affected by MS to discuss issues of importance and obtain accurate answers to MS specific questions from subject experts including neurologists, nurses, psychiatrists and other health care professionals totaling over 40 active experts.

Since its launch, the website has received an average 3 questions a day, clearly indicating a need and interest for information that is accurate, up-to-date and targeted to the everyday reader. This website allows people to submit questions electronically in French or English at their convenience. Questions are submitted anonymously and answers are provided by the most appropriate expert based on subject matter. New questions and answer are posted to the Ask the Expert up to website five times a week and are then stored within the website’s library.

Federal Election 2011; Support real action on MS!

Send a message to the candidates in your riding!

You can quickly send a message to candidates in your riding to ask for support on the important issues facing people living with MS.

It’s easy to do. Just fill in the form on the MS Society Canada website including your address and postal code so you can find your candidates. A prepared letter will then be sent to your local cadidates, from you, outlining important issues.

Newsletter
The Durham Regional chapter publishes a newsletter for the local community. Signup today for your free electronic copy.

Multiple Sclerosis Newsletter

MS WALK
MS Walk - Fundraising walk to end Multiple Sclerosis

Multiple Sclerosis Society Canada Durham Chapter

400 Dundas Street West, Whitby, Ontario L1N 2M7