Anyhoo, so the neck one was good…it shows no sign of disease progression – that is great news!
so… that means, the brain is clear, the neck is clear and uncharacerstically of me, i’m thinking that the spine is clear too.
MS: My Story with Multiple Sclerosis
Anyhoo, so the neck one was good…it shows no sign of disease progression – that is great news!
so… that means, the brain is clear, the neck is clear and uncharacerstically of me, i’m thinking that the spine is clear too.
Anyhoo, so i was about to go into the tunnel for the MRI and i asked the radiologist if i should settle in for about an hour and she said, “no…it’ll only take about 15 mins”. 15 mins????!!!! She couldn’t be serious. For real???? I’d adjusted my medication time so that i would fall asleep right about the time i was in there…i was skeptical and even wondered if she knew which areas i needed to have done but i didn’t say anything (i should have – if they didn’t get all areas i don’t think that Aetna will pay for another), i mean i was scheduled for a neck and spine MRI so she must know what she was doing. I couldn’t believe it – about 15-20 mins later i was out! i think that it was the best MRI i’d ever had done – even though i think that i dint insert the ear plugs properly because it was extremely loud in there (louder than normal, but then again, this wasn’t a normal MRI experience)!
No results yet; i thought that i would have been able toget them soon after, but i couldn’t. I called this morning and left a message so hopefully someone will call me back soon with the results – fingers/toes/legs/eyes all crossed that there’s been no progression.
Went to the doctor today and the results of the MRI were good.
Well…we are here. I am scheduled for my 1st MRI (happy times – NOT) since being on Tysabri tomorrow morning. Luckily i didn’t have to go thru the last rigamaroll (shenanigans/bullshit) like the last time because this time I’m having it done in house at the MS Center. The other good news is that it’s only going to be of my brain so it won’t last 2.5 hours – i really can think of a million other things i’d rather do on a Saturday morning!
This is how the MS Center tests to see if I’m at risk for the brain infection and maybe I’ll also see if Tysabri is helping at all (diminished/decreased/no additional lesions on my brain)…not sure if it’s too soon to see all that – it’s only been 7 months. I have a follow up with my neuro next Tuesday so we’ll see.
So, have u ever laid(n?) on a flat, hard surface completely still (head immobilized by a hannibal type mask) in a cold room (thank goodness they give u a warmed blanket) for 2 hours???? That’s what i did on Saturday!
What an experience…The good news is that i must have fallen asleep because when i came out of “the tunnel”, i asked the technician how long i was in there and she said 2 hrs…there was no way i would guessed 2 hours…so i must been asleep longer than i thought. I knew that i fell asleep but it must have been for a much longer time period than i thought. Luckily for me, the noisier things get, the more relaxed i get so the more that i can sleep. I mentioned before that the machine is very noisy – they actually give u ear plugs – so it was singing a lullaby for me each time.
At some point my head started hurting and i would shift it ever so slightly but it got to a point where it was hurting so much it was actually burning! I guess they didn’t put enuf padding behind it…i actually remember thinking, “shit! I should never have shaved my head…if i had hair, at least that would have given me some padding back there”. Luckily, they had to inject me with a dye before taking more pictures so she was able to put more padding behind it to make it more comfortable.
MRIs are not physically painful, except when they inject the dye…but i absolutely hate to have to do them because they really can be mentally EXHAUSTING!