The MS Society of the ACT is pleased to be able to provide information
about multiple sclerosis. Our comments are based on professional
advice, published experience and expert opinion, but do not represent
or replace therapeutic recommendations or prescriptions. For specific
information and advice, please consult your General Practitioner
or Neurologist.
Frequently Asked Questions
Browse this list of our most frequently asked questions. Includes:
what is MS; who gets MS; how many people have MS, and more.
Fatigue workshop resource kit
Fatigue impacts on up to 80% of people with MS, self-management is the key.
Parenting and MS resource kit
Parenting issues have a major impact on many people with MS.
People with MS
Find out about this support group for people who have multiple
sclerosis.
Mens Stories
Men have a different experience of living with MS. The idea to
write our stories came from within the men's group, largely to
create more community awareness of MS, and particularly to inform
men and others newly diagnosed with MS.
Supporting a person with MS
Information about supporting a friend, relative or loved one who
has multiple sclerosis.
Publications
Information about the bi-monthly newsletter, brochures and booklets
that are available from the Multiple Sclerosis Society of the
ACT.
