Hello, everyone!
I am brand new here. I was just diagnosed with MS last week. As of right now, my symptoms are pretty minimal. (eye twitching and a numb spot on my abdomen)
I had a bout of double vision around 5 years ago where I had an MRI that showed a few non specific white spots. My neurologist looked at the images and mentioned MS, but wasn't entirely convinced. He said that we could do further testing or take a wait and see approach. At the time, he seemed really ambivalent about it being MS, so I opted to wait.
Fast forward to now, another MRI with increased lesions that were "classic" MS according to the neurologist. And a spine MRI with a lesion.
Now I'm in the decision making process about medications. I would love some input regarding this. Right now, I'm just trying to wrap my head around all of the information and options.
I am brand new here. I was just diagnosed with MS last week. As of right now, my symptoms are pretty minimal. (eye twitching and a numb spot on my abdomen)
I had a bout of double vision around 5 years ago where I had an MRI that showed a few non specific white spots. My neurologist looked at the images and mentioned MS, but wasn't entirely convinced. He said that we could do further testing or take a wait and see approach. At the time, he seemed really ambivalent about it being MS, so I opted to wait.
Fast forward to now, another MRI with increased lesions that were "classic" MS according to the neurologist. And a spine MRI with a lesion.
Now I'm in the decision making process about medications. I would love some input regarding this. Right now, I'm just trying to wrap my head around all of the information and options.
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