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Links
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 bodiesA short story about an MSer
Pick and chose your prioritiesPrimary Progressive MS
mainly a form equally sharedThe things to expect in PPMSMaking a go of it
Primary Progressive MSliving a severely disabled
Living alone in a wheelchairHELP you can getMaking the best of life
MS is bad but live with itLets make the best of our liveBladder Wars
Bladder Disfunction part llBladers part 3
More on Bladder and MSBlood brain barrier
Food and supplimentsMS and Blood brain BarrierBooks
magazinesPublicationsDiabled travel keep rolling!
travel any where in comfortMS people are travelingGOD HAS A Plan
His plan maynot be oursGOD has a PlanGetting about better
Clawson Rocker ShoesAssistive devices and shoesInspirational Poems
Sent By ViewersInspirational PoemsLittle tidbits of info.
Regular revisions weeklyThis and ThatMS crutches users
Crutch users onlyMale Sex Problems
Sex and MSMs and your Bladder
Bladder dysfunctionMuseums
Some web site to amuse youMy Visit to the Factory -6-98
New UpdateClawson Rocker ShoesHumor
MS HumorJust MS
You just found out it's MSNewly diagnosed MS patientsIts bad for your health
Living alone in a wheelchairLiving alone and disabledCrutches that are decorative
Broken BeautiesLive your best way
We can winThe greatness of our bodyMost will probably not plan
keep in touch with doctorPlanning your futureNew research in MS
New Gene Study In MSstory of beauty in deformed
My narled Tree of beautycane,crutches or walker
what you choose will dependSorting out assistive devicesUsing crutches with ease
New UpdateCrutches page 2Useful information
For Your InformationRelationships
MS Or Who Doesn't Have MSRelationship Between A PersonStress is one of your enemies
Learn to relaxThe Opposite of StressYou will roll better than walk
Living alone in a wheelchairboarderline need of wheelchairWheelchair users only
Wheelchair Living if it goes that wayetc. ms interests
some Ms related web siteslinks to other MS pages
Other MS pages to seereinvent your life again
Reinvent your selfsome of these chips are here
Medical chips you might needwhy exercise?
Keep those organs going!Exercise to keep you upBraces why you many need them
A brace will actually extendA functional need for a brace|
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| It good to communicate to just one safe person |
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| It good to get it off your chest,We are very private .Its not like posting on a message board. Here you talk with only one person either Eileen or me Eileen's private email is lobosgirl@aol.com Mine is RET1000@aol.com (Richard) Both of us have had MS for a long time.We both have been through a lot of pain,experiences,hospital visits,familar with all sorts of assistive devices such as wheelchairs ,power or manual. I have used crutches now more than 19 yrs and braces the last 13yrs.(RET) Eileen has the experience of a baclofen pump in fact she wrote an article about it on this web site. We both are in the SPMS stage. April 11,2008 I received a e-mail from a person ,a man in his 60s He writes to me that he is finding getting useed to be in his wheelchair all the time.He started using a chair about 7 years ago but usually then in the beginning only part time. Now for the last 8 months it has been full time. I say the transition from walking just a little to no walking at all and being a wheelchair user is probably one of the great challenges an MSer has to make.Its hard I kid you not.RET |
| Eileen Lukeman and Richard Tanner | FL. | Eileen(Lobosgirl) and Richard (RET1000) both at aol.com |
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