I have tried the open sided machine. I may have tolerated being in it had the tech not been so pushy and uncompassionate. I am looking for thoughts or pictures or something to "take" with me to my test next Monday.
I haven't had an MRI since 2011 and still debate what to do. They didn't find any new lesions and I haven't had any more flare ups. I have the small every so often type symptoms but never a flare up.
My attitude is what can they tell me that I don't already know. Will finding more lesions really do anything for me? Will they have to find another preventive measure? Any thoughts?
https://www.verywell.com/t2-weighted-lesions-(Phone number can only be seen by MyMSTeam users)
How many of you out there have ms but your MRI did not show anything !?
I'm furious because I have been getting some pretty awfull symptoms and I think I'm having a relapse! I have had ms type symptoms for 2 years now! Recently I have been experiencing vertigo, insomnia, burning sensations over different areas of my body, weakness in left arm and left calf and shakes.
What else should I do ?? What about an MRI with ganglion dye !? What could that show ? Any other tests I should… read more
Every time I have to get a MRI with contrast, it makes me nauseated, has anyone experience this before? If so, how can you reduce the nausea?
How many of you request a copy of your MRI results disc for your own personal MS file?
If so, do you ever look at it?
I can't take it..to be shoved into a tight space or tunnel with no room to move...and having to listen to all those loud machine noises...I won't ever go do one again..NO WAY..
I recently had a mild relapse and an MRI showed no active lesions or inflamation. My nuero says this is because an MRI isnt that sensitive, just wondering if anone else has had the same?