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Conditions and Diseases > Multiple Sclerosis Forum > Should I Push For An Mri?
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Q: Should I Push For An Mri?
asked by: licensednursetn on February 24th, 2007
New User
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
replied on February 24th, 2007
Experienced User
Re: Push For Mri
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. Wink
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velvetwaves
replied on August 4th, 2007
New User
Mri
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
replied on August 25th, 2007
New User
Re: Should I Push For An Mri?
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.

Push for the MRI!
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