For Kids
The Multiple Sclerosis Society of
Canada recognizes that a diagnosis of MS affects all family
members. Children faced with the realities of a parent with
multiple sclerosis react in different ways and need their parents'
support to work through changes that MS brings to their lives.
It is important that children have at least a basic understanding
of the disease and how it specifically affects their parent
to better deal with their situation.
Publications available through the MS Society
of Canada that are helpful to children and teens include:
- Myelin is Getting on my Nerves
- Don't Lose Your Balance
- My Mommy has MS
The MS Society also has a publication to
help parents talk to their children about their diagnosis.
How to Talk about MS with Your Children is a practical guide
to help parents communicate better with their children about
multiple sclerosis. The booklet may also be useful for anyone
who wants to provide help or support young children or teens
who have a parent with multiple sclerosis.
In addition, the MS Society developed a series
of web sites designed specifically for kids, teens or parents
living with MS. These sites provide age-appropriate information
and resources about MS and create an interactive environment
where kids, teens or parents living with MS can share and support
one another.
Let’s Talk MS web sites, available
in English only, were developed and are maintained by the Manitoba
Division.
La colonie SP, available in French only, was developed
and is maintained by the Quebec Division.
In support of children of parents with MS,
the National Client Services Department applied for and received
a grant from Health Canada for a two-year national program
addressing their needs. The project, called Growing
up Strong: Supporting the Children of parents with MS,
was launched in August 2002 and will develop, evaluate and
deliver integrated services and programs nationwide for children
aged 6-18 who have a parent or parents with MS. For more information
on Growing Up Strong please click
here.
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