Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
The Dr Seuss MS Poem
I love MS it's just so neat
the way it swept me off my feet
I love the pain, I love the numb
and sticking needles in my bum.
I love the way my world's a blur
the way I shake , the words I slur.
I love my chair and walker , too
I love MS ....I do.. I do...
I love my lazy sleepy days
I shake with joy within my haze
I'm just as happy as can be
It makes me pee and pee and pee
I love my legs that will not walk
my twisted tongue that will not talk
I love the way my poop does bind
I do believe I've lost my mind.
(this was sent to me by my sister and was written by Morgan)
I love MS it's just so neat
the way it swept me off my feet
I love the pain, I love the numb
and sticking needles in my bum.
I love the way my world's a blur
the way I shake , the words I slur.
I love my chair and walker , too
I love MS ....I do.. I do...
I love my lazy sleepy days
I shake with joy within my haze
I'm just as happy as can be
It makes me pee and pee and pee
I love my legs that will not walk
my twisted tongue that will not talk
I love the way my poop does bind
I do believe I've lost my mind.
(this was sent to me by my sister and was written by Morgan)
I had to print it and keep it on my desk. It really does explain it all for us. Im very thatnkful I have had few problems, hopefully that will be a continuing thing for me, at least for as long as Id like.
Today I'll smile...all day!
better then me an my sis tryin 2 make a song about havin a day
...that Multiple Sclerosis is the name for what is wrong with me.
...that my memory may not always be what it use to be.
...that if not already,that maybe someday I will use a wheelchair or cane.
...that each day for the rest of my life I will probably feel some form of pain.
I fear...
...Others reactions when they find out what is wrong with me.
...the day i wake up no longer able to go to work and support my family.
...the day that I don't have insurance and can't afford my medicine.
...people not understanding that I'm still me despite what's happening to me.
I reject...
...giving up and feeling sorry for myself.
...succumbing to the depths of depression with this dreaded disease.
...the idea of staying down even after a bad spill.
...those who tell me I can't because I can and will!!!
I hope...
...that people understand most days I feel like crap,although I look just fine.
...that others don't get upset when I need more sleep.
...that friend's can't accept me for me and not run away or show pity.
...and mostly, I hope that science is able to find a cure for what I have.