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MS
M. S.
it doesn’t have to be the END
For those of you who have been diagnosed with Multiple Sclerosis the first thought
may have been;
"No, it’s a mistake", "Not me", "Why me".
The reaction may have been one of numbness, shock, and/or denial.
M.S. is a troublesome disease and it can cause some barriers to us in that we will
find it more difficult to do things that we once found easy. The thing that we need
to realise is that we need to grab hold of what we can do and the things we cannot
do we should think about alternatives. Talk to friends, relatives, counsellors, other
people with MS, and read about how to make life more manageable. Join a social
group, contribute to the group, do something that you can participate in. I myself
am involved in helping people with their paper tole pictures and I get together with
friends to do cross-stitch. I have entered some of my work in the local agricultural
shows in the craft sections. The best thing I have found in life is to feel that I have
accomplished something, that I have brought a smile to somebodies face.
Even the most debilitated people have something that they can do. I know of a
lady who was restricted to an iron lung and could not move. She asked her family
to place the photographs of people to pray for where she could see them and she
asked them to make a list of prayer points and put that where she could see it. She
found release from her restriction by finding something worthwhile to do. We can
do the same.
If you are feeling depressed - try putting some quiet music on the CD, on the radio,
or record player, close your eyes and think of everything that you enjoy or are
blessed with. Everything you are thankful for.
Sunset, Sunrise, Nature, The beach, The forest, Rainbows, Flowers, Friends, Family,
Rain, Cool Weather, Snow….anything and everything.
The Multiple Sclerosis Society of the ACT, Canberra,
Australia
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Objectives & Aims
¨ To encourage and provide
opportunities for all people in the ACT to take an active interest in all
aspects of MS.
¨ To promote and maintain
relationships with other organisations actively interested in the furtherance
of the needs and treatment of those with MS.
¨ To promote research into
the causes and treatment of MS.
¨ To encourage and assist
those with MS, their families and friends to cope with their problems, and
to work with established professional and welfare authorities to this end.
¨ To encourage and assist
those with MS to become self-sufficient.
¨ To actively pursue various
methods to inform and educate persons not affected by MS, as well as those
with MS, of the everyday practical difficulties associated with MS.
¨ To establish and maintain
whatever administrative facilities or organisational structure is necessary
to pursue the objectives and aims of the Society. |
New Phone Number: 02 62852999
New Fax Number: 02 62810817
Web Page is :
http://ms.org.au/home.asp
A really excellent web page
Other sites which will give you information about MS.
http://www.jamesshuggins.com/html/oth
1/multiple_sclerosis_faq.htm
http://www.wvhealth.wvu.edu/clinical/neurologica./mssympt.htm
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