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I was diagnosed with RRMS over 10 years ago, but only recently started experiencing what seem to be flares and relapses. I’m meeting with a neuroimmunologist tomorrow and would appreciate hearing from others who have been through something similar.
Was anyone initially misdiagnosed or told their MRI findings were unclear? My MRI only shows a few white matter lesions/scars, and I also have a history of Traumatic Brain Injury, which makes it difficult to know which symptoms are coming from MS… read more
You can work while on SSD. You’re allowed to make x amount of dollars. I think it’s over $1,600 a month now. It used to be $988. I applied for SSD myself and got approved my first time trying. That was 20 years ago. I also have a host of other things wrong with me. Best of luck!!!
Thanks so much! Are you able to still work or on disability? I’ve heard the process of applying can be grueling!
But even now I’m having vision, balance, pain, fatigue issues. What medication has helped you the most?
Ms don’t discriminate, hope for as many lesions as possible, and I would definitely utilize and PT therapies and meds if needed early on. All in all, every case of ms different but can be very similar.
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