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Thought for the Day
Keeping cool this summer
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The Bacfelcon Pump
Swimming Is the Best Exercise
Vision and MS
Think Positive
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Life as an MS person
Our Unwelcome guest MS
Social Security Disability
Give Yourself A Break Part 2
Stress leads to new lesions
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We do what we can do
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Know how to relax and live
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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 probable problems
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
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MS and Blood brain Barrier
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Diabled travel keep rolling!
travel any where in comfort
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GOD HAS A Plan
His plan maynot be ours
GOD has a Plan
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Inspirational Poems
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Inspirational Poems
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MS crutches users
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Male Sex Problems
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Ms and your Bladder
Bladder dysfunction
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Some web site to amuse you
My Visit to the Factory -6-98
New Update
Clawson Rocker Shoes
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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
We should be getting the most
You might need a power chair
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
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Relationships
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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
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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




The hazards of marriage and having MS
You have any control about aquiring MS but it will affect everything


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In any marriage the threat of crronic sickness,like MS,especially progressive MS
is hazardous to your marriage.
First you will probably loose the sex urge,second your body may not fit the image
society has planted in many unthinking American minds.
The general image projected by the media will usually prevail in the mind.
It affects the male as well as the female.It is everywhere in our society.
The straping ,hunk of a male,and the sexy slim,and active female.
There isn't any room in some people's mind for a crip in their world.Many even have
trouble talking to you if you are "lower than them "in a wheelchair.
The number of times disabled appear on the media is few and when they do it's driping wit sympathy.

Disability isn't a planned even,and in many people's mind something too difficult
to deal with.
What do you do with a spouse in a wheelchair?or one using a cane or walker.What about
an ugly brace? The devotees may be happy to see you but most are glad when you leave.
What can be done? Dancing is no more,neither is going golfing or in may cases camping
is out.
I have noticed on cruises,I'm a clumbsy item for many to talk with.They are afraid
they will hurt your feelings.Spouses see this also.It makes them almost a crip or one
with a crip.If your spouse is not hard shelled then it will get to him or her.The hims
are usually the most effected and most likely to seek fun and excitment when your back is
turned.
The chances of them running from the marriage compact is better than 60%.

Both Eileen and myself have very understanding spouses,other wise we wouldn't attempt
to write this essay.
My wife was the one who first suggested I get a scooter in my early days after
being dx. She is the one who will say I look tired and need rest.She will save me from
situations she thinks I can't handle.She will open the door when we go any where and
listen for the sound of my crutch hitting the door to block it,and then she goes on in,
knowing I will then be able to manage the heavy spring door.
Yes I can handle the door myself if I have to but when she does it ,it's just another
sign of her love coming through.
We still have a very great life together.we have adapted to both of our disabilities.she has her breathing problems and heart problems and I have my walking and gait problems. The marriage is solid and adjusted to new surprises.

Many MS affected persons have been able to save their marriage.They have done so by
being very frank with each other.It can be worked out.

WHAT MY WIFE AND I HAVE DONE! It works!
She has become quite a card player and goes to tournments to compete.Some of these
tournments are several days in length. She also plays much in our town during the week.
We have two days a week we try to do something together.The rest of the time we are much
appart and doing our own thing.I'm on the computer much of the time,as it's one of the
few activies my body can take for hours. I also paint and try to get out and about in town
once a day.I usuallly go swimming and exaust myself doing my 1/4 mile swim almost daily.
If you are not in each other's hair all day it helps.
My wife is tolerent of my disability,if not down right supportive,as she always has been.
I'm supportive of her disabilities and her desire to play cards nearly all the time.
It works out nicely.
She is well aware of my progressive Ms and where it might go in the future.
I too know of her disability in her heart and know where it could lead in the future.
So for us it's till death do us part.

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

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