Initial MRI
Not sure if it’s MS or Fibromyalgia but have had weakness, fatigue, eye issues and numbness that lasted about three months. For the last month, the symptoms have subsided and just lingering numbness here and there and fatigue is still there. Had my first MRI and read the report. Not sure what this means: There are a few scattered foci of increased T2 and FLAIR signal in the subcortical white matter which are nonspecific.
I’m waiting for my neurologist to call me but he’s been very dismissive and told me it’s most likely stress and wondering if he looks at this and tells me this means nothing, should I get a second opinion or push for a spinal? Just wondering anyone else’s experience.
I'm truly sorry you're going through this uncertain and challenging time with your health. It sounds incredibly frustrating to be experiencing symptoms without clear answers or support from your neurologist. The uncertainty can be overwhelming, especially when you're left waiting for answers. Your concerns are completely valid, and it's important to advocate for yourself and seek the best possible care. If your neurologist continues to be dismissive or if you're left feeling unsure about their assessment, seeking a second opinion could provide you with much-needed clarity and peace of mind. There are so many in this community who can say that they've gotten second, third or even fourth opinions just to be certain on everything. You wouldn't be alone in seeking a second opinion at all.
While we're not medical professionals and can't give medical advice here, discussing the possibility of a spinal with another healthcare provider might be a good idea to explore further insights into your condition if they agree that it's the appropriate path to take.
Try to remember this while you're seeking your answers: your health and well-being are of the utmost importance, and you deserve to have a healthcare team that listens to your concerns and works with you to find the best path forward. It's not always easy but you deserve that, and so much more!
Please keep us posted on how everything's going and we're always here for you if you need to vent, need an ear, or support, yeah? 🧡 Kayleigh, MultipleSclerosis.net team
