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Thought for the Day
Keeping cool this summer
Share your Information
The Bacfelcon Pump
Swimming Is the Best Exercise
Vision and MS
Think Positive
Hand controls
The Healing Power of Prayer
Life as an MS person
Our Unwelcome guest MS
Social Security Disability
Give Yourself A Break Part 2
Stress leads to new lesions
Links to Alternate Medicine
We do what we can do
Gardening for the disabled
Know how to relax and live
Nutrition for you
Life after MS sets in
How the Road with MS could Go.
For men only
Attitudes and desires
ART anyone can do
Travel with your wheelchair or scooter
AFOs or ankle foot orthosis
Making it easy for yourself
PPMS and SPMS survey results
How I deal with MS Fatigue
Understanding The Whole Body
Redisign the way you live
Marriage and Your MS
Picture ID you need one
Eyes Skin and nails reflect
The right yardstick for you
WHEN A PARENT HAS MS
MS
Classic beginning three yrs
experiences with AFOs and etc
The best climate to live in
Do you love your braces
MS is no place for wimps
A proactive approch to your MS
The Open Book
Wheelchair living part 2
Full Time Wheelchairing
The Old Ship
Times forgotton and new times
My 20 plus years as a MSer
The practical Crutches
Meeting Maxine
Tips on wearing braces
MS attacks and takes more grou
the lesson of disable bodies
A short story about an MSer
Pick and chose your priorities
Primary Progressive MS
mainly a form equally shared
The things to expect in PPMS
Making a go of it
Primary Progressive MS
living a severely disabled
Living alone in a wheelchair
HELP you can get
Making the best of life
MS is bad but live with it
Lets make the best of our live
Bladder Wars
Bladder Disfunction part ll
Bladers part 3
More on Bladder and MS
Blood brain barrier
Food and suppliments
MS and Blood brain Barrier
Books
magazines
Publications
Diabled travel keep rolling!
travel any where in comfort
MS people are traveling
GOD HAS A Plan
His plan maynot be ours
GOD has a Plan
Getting about better
Clawson Rocker Shoes
Assistive devices and shoes
Inspirational Poems
Sent By Viewers
Inspirational Poems
Little tidbits of info.
Regular revisions weekly
This and That
MS crutches users
Crutch users only
Male Sex Problems
Sex and MS
Ms and your Bladder
Bladder dysfunction
Museums
Some web site to amuse you
My Visit to the Factory -6-98
New Update
Clawson Rocker Shoes
Humor
MS Humor
Just MS
You just found out it's MS
Newly diagnosed MS patients
Its bad for your health
Living alone in a wheelchair
Living alone and disabled
Crutches that are decorative
Broken Beauties
Live your best way
We can win
The greatness of our body
Most will probably not plan
keep in touch with doctor
Planning your future
New research in MS
New Gene Study In MS
story of beauty in deformed
My narled Tree of beauty
cane,crutches or walker
what you choose will depend
Sorting out assistive devices
Using crutches with ease
New Update
Crutches page 2
Useful information
For Your Information
Relationships
MS Or Who Doesn't Have MS
Relationship Between A Person
Stress is one of your enemies
Learn to relax
The Opposite of Stress
You will roll better than walk
Living alone in a wheelchair
boarderline need of wheelchair
Wheelchair users only
Wheelchair Living if it goes that way
etc. ms interests
some Ms related web sites
links to other MS pages
Other MS pages to see
reinvent your life again
Reinvent your self
some of these chips are here
Medical chips you might need
why exercise?
Keep those organs going!
Exercise to keep you up
Braces why you many need them
A brace will actually extend
A functional need for a brace




Life after MS sets in to your life UPGRADE see heading #3
Don't trade your life away just because of MS


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Jan.9,2001------Update.----If you haven't guessed it by this
time ,you will probably have to reprogram your whole life style
to fit your body ability or disabilitys
All of us had to give up styles of life which we had counted
on to more or less continue as we had planned.But some have
reprogramed their lives to become some thing wonderful in this
unerxpected world.Some have tried their hand at
art, music, writing, computer expert,daily fisherman,maker
of fabric wonders,successful business on the internet,photography,
and on goes the list.It is limited only by your imagination.
One woman actually decorates canes as a business.Another I have
met is giving lectures on cruise ships about the places the
ship will stop at.Another one is now playing music on a cruise
ship.One door closes on you while others are opened because
your mind has to work instead of your legs.RET




Update: October 4,2000 One of the first
things you should do after being diagnosed
is to get started on one of the ABC drugs .
Even us who are in the more progressive forms still
take these medication. Eileen is on copaxone
www.copaxone.com
I'm on betaseron www.betaseron.com
It is very important to get started.
My doctor says if I would stop, my progression
would be like a falling rock .RET


Having Multiple Sclerosis is now a fact for
all of reading this article.Now is the time to ease up
on yourself. What we face isn't a bed of roses but
just the thorns removed from them.
Regardless if you have has MS for 20 years or just
diagnosed cut yourself some slack.Don't let the
disease rule you or it will ruin you.
There isn't any thing you did that got you where
you are now.
In other words it's not your fault.
The chances of a cure is in the works.
Until then get a good neurologist who will
talk to you,and he/she will probably have you
on one of the three ABC drugs.

As I said I wouldn't trade my life of the
last 20+years for anything As if I could anyway.
Something "bad happens" to all of us.
Some die early in life,some have debilating accidents
others have domestic problems ,still others develop
diseases much worse than MS.I'm aware how bad some cases
of MS get,but they are fortunately in the minority.
Eventually you settle into a comfortable grove with MS.
You get your assistive devices and get back into the
stream of life as a different person.

If you are now working try to hang in there.
But should it come too early retirement,relax.
Life shouldn't be defined by what you own or drive.
Nor the residence you live in shouldn't whip lash
your mind.
If you are forced to retire and go on disability
you will live on less.

I have known people on low incomes. As long as
they keep their heads level and don't allow TV
and Hollywood's images to inodate their brains,
they remain very happy. It was found in the survey
of PPMS and SPMS that the ones on SS disability
frequently have more difficulty with finances than
the disease.
The media and their tilted image of what life should
be is what makes us unhappy when we have less money that
the majority seems to possess.

Make sure you always have something that
occupies your mind and keeps you using it.
Hobbies abound which will do nicely.
Mine is painting.It can be inexpensive.
My wants being simple and living in a very
small house, we really don't have room for too
much else. Having nothing much to buy we now
concentrate on just the necessities like food.

If you are really long sighted plan for a ramp
to one of your exterior doors. I was thrust into needing
a wheelchair very suddenly. We had to get a contractor
very quickly to install a ramp, and widen three interior
doors.I know you never want to think about such
things but they do come fast.My first need for a ramp
came when being very clumbsy I tripped and broke a
leg.For the first three months my cast was so huge
I was in a wheelchair. I couldn't keep my balance with
crutches.I was house bound until the ramp could be
built,and one door widen.





Eileen Lukeman and Richard Tanner FL. Eileen(Lobosgirl) and Richard (RET1000) both at aol.com

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