Not diagnosed but got questions?
Hey everyone 💚 I wanted to reach out to people who have ‘I might have MS’ on their profile. I remember how overwhelming it was to have a million questions. I want to remind you that you're not alone while you’re waiting. If you have any questions or concerns, drop them in the comments below and I'll do my best to answer 👇
I’m wondering if it’s possible to have symptoms, have a normal MRI, but still possibly have Ms or is it a clear as day “not Ms.” If one has symptoms that are from ms is it always going to show on mri?
Having been oscillating between neurologists and physiotherapists for the last 6 years who have said I definitely do have MS to possibly have MS to probably don't have MS I've finally been diagnosed with a Functional Neurological Disorder - symptoms are just like MS, prognosis somewhat better than MS, but only seemingly effective treatment is neurophysiotherapy which doesn't always work (and is less likely to do so the longer it takes to start it after the onset of symptoms). Heigh ho . . .