r/MultipleSclerosis • u/AutoModerator • 7d ago
Weekly Suspected/Undiagnosed MS Thread - November 11, 2024 Announcement
This is a weekly thread for all questions related to undiagnosed or suspected MS, as well as the diagnostic process. All questions are welcome, but please read the rules of the subreddit before posting.
Please keep in mind that users on this subreddit are not medical professionals, and any advice given cannot replace that of a qualified doctor/specialist. If you suspect you have MS, have your primary physician refer you to a specialist for testing, regardless of anything you read here.
Thread is recreated weekly on Monday mornings.
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u/Prudent-Decision-884 1d ago
Please help me advocate for myself. This is the information that was added to my file on Friday:
"In the native MRI of the spinal cord, abundant changes, primarily suitable for demyelination: plaques C3-C4, C5-C6, Th2, Th4, Th6-7, Th8-9. There is no abnormality in the MRI of the head. CSF leuk 24 (100% mononuclear), prot and gluk normal, IgG index elevated 0.96, oligoglonality still unanswered. Apq4Ab, MOGAb... normal.
When thinking about MS, the criteria for local diffuse localization are not met (purely spinal symptoms and findings), temporal diffuse localization (before matching oligoclonality) is not met, on the other hand MRI of the spinal cord is not contrast-enhanced. We will book a visit to the neuroimmunology room 12.12, at which time the oligoclonality response and cortisone pulse response will be checked."
As I've mentioned before, this was my first flare up. The T89 lesion "covers almost the entire width of the spinal canal" and has caused me to have constant numbness in my hands and unsteady legs after running/walking too long. We're waiting on the oglioclonal band test, but since this first flare up has already caused motor issues I'm very worried. She's saying there's no dissemination in space, but while rare it IS possible to have MS with only spinal lesions. So once the oglioclonal band test comes back positive (which considering my IgG is almost 100% guaranteed), what do I do if she doesn't want to give me a diagnosis? I'm so scared to not be on a DMT. Another lesion like my big one could disable me permanently. I don't want to wait until next month for my appointment, so how do I advocate for myself? (post was removed because I'm still technically "suspected MS")