The
Multiple Sclerosis Society of Canada provides the most accurate
and up-to-date information, in addition to making referrals
to community support resources for the MS community.
Providing
information is a core activity of the Society. The Society collects
and maintains an extensive storehouse of the most accurate and
current information on MS.
The most frequent request that the Society receives from people
diagnosed with MS, is for information about the disease. People
affected by MS look to the Society to provide them with credible
and reliable information about a MS diagnosis, symptoms, treatments,
research, programs and other information about related topics
such as employment, insurance and family issues. By obtaining
the most accurate and up-to-date information about the disease,
people affected by MS can become more knowledgeable about MS,
more aware of resources and better able to make informed decisions
and take control of an unpredictable and complicated disease.
Publications
The
MS Society produces a number of publications that address specific
topics about multiple sclerosis. These publications cover subjects
such as basic facts about MS, specific symptoms, nutrition,
and family issues to name just a few. The Society also produces
children's resources for those who have a parent or loved one
living with MS. These publications can help individuals learn
more about this disease and suggest strategies in coping with
its effects. MS Society publications are available upon request.
The MS Society has compiled a recommended reading list for persons
with multiple sclerosis and others interested in the various
aspects of this chronic neurological disease. The books on this
listing present personal opinions, experiences and information,
which are not necessarily those endorsed by the Multiple Sclerosis
Society of Canada. The books from this listing can be obtained
from your local library, bookstore and from some division and
chapter offices.
The Multiple Sclerosis Society of Canada, Ontario Division
is pleased to offer a wide range of information in booklets and pamphlets.
In
addition, divisions and chapters develop their own resource
centres and lending libraries that supplement the available
Society publications and increase the availability of topical
materials to members.
In
addition to providing information on MS and related issues,
the Society provides referral services and connects people with
MS and their care partners to vital community support resources.
Depending on the community, people with MS may have access to
a wide range of programs and services such as exercise classes,
transportation assistance homecare and many others. On a community-by-community
basis, the Multiple Sclerosis Society of Canada maintains a
database of appropriate resources that can help people manage
and cope with MS in their daily lives.
There is no charge to obtain information or referral services.
However, information is distributed with the understanding that
people use it for their own use and not for reproduction or
profit. The Multiple Sclerosis Society of Canada is a licensee
of CANCOPY and abides by Canadian and international copyright
law.
Information distributed by the Information Resource Centre,
divisions and chapters, does not necessarily represent the views
of the Multiple Sclerosis Society of Canada and is not intended
as medical advice or endorsement. For specific opinion and advice
on personal care and medical treatment, consult your physician.
