Joined: 24 Feb 2007 Posts: 2 Location: Oldest Town in TN
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Should I Push For An Mri? Posted: 02-24-07 09:02am
Hello everyone,
I'm 34 years old, not sure what to think.
A Dr. at work (I'm a nurse) suggested that
I need to confront my Dr. on the need for
an MRI. He thinks it sounds possible I
might have MS or some other auto-immune
disease.
My symptoms: (these mostly come and go)
Headache (cannot get rid of it at all -
nothing works) - this headache mostly
centers along my forehead, but when I lay
down, I feel it in the back of my head, on
the sides of my head, and occasionally
right down the center. I live on
Ibuprofen and Acetaminophen, Relafen,
Axert (for migranes), Neurontin, and now,
Topamax. Nothing works at all. I have
had this particular headache continually
for almost 3 full weeks now with *no*
relief. Its starting to make me
depressed. Also, along with this constant
nagging headache, I have these almost like
lightening flash headaches that come on
over my right eye, sharp and sudden, last
about 30 seconds to a minute, and are
gone. This is *not* normal for me.
Dizziness. I can stand up from laying
down for work and fall right over. Last
week, I fell over at the gas station. I
tend to get dizzy while I'm walking and
have to take an extra step or two to
correct. This has been going on for
easily a year now.
Blurry Vision: This is recent. I noticed
about a week ago that I couldn't see my
algebra book (i'm back in college) It was
transitory, after a few minutes, it
cleared. It's happened multiple times
since then. At school, I suddenly
couldn't see the board. I feel pain when
I move my eyes. I have in the past seen
spots.
Tremors: Not all the time - just
sometimes - like at work, when I'm trying
to chart, I'll notice my hand holding my
pen just shaking. If I rest it down, it
stops, but when I pick the pen back up, it
starts again. I thought this might be
blood sugar, but my blood sugars have been
great. It's been a little scary.
Confusion: Sometimes, I feel just
bewildered - not sure where I am, what I'm
doing, or how I got there. This isn't
often, but it's a very strange sensation.
Extreme cold: My feet, in particular,
can't get warm, ever. My daughters will
blow a hair dryer on them, they don't get
warm. If I wear socks, I'm just
insulating the cold There is also an area
in the small of my back like that. My
husband says it's just wierd.
Speech: This one I'm not so sure about,
but I've noticed it. When I talk, I will
know what I mean to say, but the words
come out mispronounced, all wrong.
Sometimes I can't think of the word
atall.
Sense of Taste: Ok, this is weird, but
when I drink cola,it all tastes flat to
me. There are other things that just
don't taste good at all.
Limp: I can't say that it hurts, but for
some reason I've developed a limp in my
left leg.
Clumsiness: Lately, I drop everything. I
can't hold anything without dropping it.
There are more, but I worked last night
and I'm about to fall aslep.
Please feel free to email me with any
feedback.
Thanks,
Stacie
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san54
Experienced User , Rather EHEALTHy
Joined: 28 Dec 2003 Posts: 227 Location: Virginia
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Re: Push For Mri Posted: 02-24-07 09:45am
I definitely would push for an MRI, seek
another opinion. You are your own advacate
for your body. Sometimes the MRI is not
enough. You need the right king of doctor.
Good luck and hang in there.
|
velvetwaves
New User, Becoming EHEALTHy
Joined: 04 Aug 2007 Posts: 2
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Mri Posted: 08-04-07 04:28am
You should definately get an MRI, from
living as a dependent of a person with MS
my mother went through all of that before
she was diagnosed with MS. By then she had
already beed through her first stage.
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Quincybug09
New User, Becoming EHEALTHy
Joined: 13 Aug 2007 Posts: 41 Location: Birmingham, AL United States
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Re: Should I Push For An Mri? Posted: 08-25-07 01:36am
I do agree with the others that you should
push for the MRI. When I developed Optic
Neuritis it started as a spot and then
came the pain when I moved my eye. It got
progressively worse. That was what got me
diagnosed finally. I had mysterious
neurological symptoms for almost 10 year
before the Optic Neuritis.
I am a nurse also and finally started
putting the pieces of my puzzle together
when I was in nursing school. Even then,
no one would test me for MS. It was the
O.N. 4 years later that was my body
screaming "I have MS". And the Doctors
listened this time.
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