I’ve been reading a few of the forums over the last few weeks and you seem like a lovely helpful bunch so I’m looking for some advice.
I’m diagnosed with M.E.
I’m in the process of investigation for MS after admission to A&E which resulted in an optic neuritis diagnosis.
They asked a neurologist to come take a look at me as I also had some weird sensations - crawling sensations on my skin ,patchy numbness with itching etc .
I’ve received the neurologist report but it’s very confusing . Can anyone help me understand what it means please:
“her significant fatigue over the last few years may possibly be part of another neurological problem” (I think this means rather than M.E)
“visual acuity is 6/12”
“gait was normal with encouragement “ (I was in pain with something else but didn’t mention this to the doctor)
“a little caution on some of the power testing but it was normal”
“patchy sensory loss over the left arm and leg
brisk reflexes with 4 beats of clonus in left ankle
I’ve been referred for an MRI of my spine and brain in a couple of weeks time.
I wouldn’t get too stressed about what the neurologist is actually saying. What’s important is that s/he is arranging for brain and spine MRI. I’ve never been too bothered about what all the different test results: ‘brisk reflexes’, ‘clonus’, ‘visual acuity’, ‘power testing’ (maybe this relates to super powers), etc mean. Ultimately, it’s all a bit meaningless without either talking to the neurologist or having test results.
I hope you don’t have a long wait for your MRI, nor for the results of the MRI thereafter. I think you’ll get a fuller picture after that. And in the meantime, try not to worry too much about it.
Come back to us and let us know what happens next.
Hi, Thanks for posting I’m not worried about the report . I was really just wondering if anyone had any ideas about clonus / brisk reflexes etc . Are these considered normal ?
I assume that the report was sent to your GP, copied to you? If so, you could ask your GP for a translation into English - she/he should be able to have a go at that.
Not speaking neurological, I can’t help with the technicalities, I’m afraid. Quite honestly, I think you might as well wait until the scan results are available and see what that tells them - and you. That’s the big show in town, I think.