Thanks guys, all in all I feel decentmost of the time and since my neuro doesn't seem to do neuro exams now that I am dxd, I rely on getting them from a physiatrist every year but her clinic doesn't do any blood tests or imaging tests so I am going on her exam last Dec. I didn't even know that I had spasticity until she demonstrated my reflexes and asked me to describe how my limbs felt when they were sore and tight.
I go for the scan on June 17 and I will follow up with my GP to get a copy of the results and see if he has any comments.
Thanks again!
Corrie
Hi Corrie -
I agree with DV that it can be challenging to directly tie symptoms to lesion location. I also agree that while 3T is once, it's not necessary. I was diagnosed 2 1/2 years ago and all of my MRI, brain + c & t-spine, were done on 1.5T machines. All 3 locations showed lesions.
Sorry you're having a tough time,
Kyle
I don't know if there's really a way to predict that, Corrie. Your MRI could come back showing new lesions that may or may not correlate to these symptoms.....or, it might not. Some of these symptoms, eg weakness, and I think maybe some urinary symptoms, can be due to lesions in brain OR spinal cord OR both, which may or may not be detected on MRI. Higher strength machine is nice but not required to show all lesions. All my MRIs have been on 1.5T and my last one in particular showed plenty, much to my dismay.
Whether or not these symptoms are detected by MRI, most would be picked up on a thorough clinical exam which ultimately is more important than a bunch of pictures that may or may not correlate to Howe actually feel and function.
Sorry for the new symptoms.....that is always a bummer to have to deal with.