Shift.ms is better if you're logged in

Hi. Hope you are well, not sure how this works but heard about it online and thought to try it out. I got diagnosed with MS back around 2022. Was a huge shock, I was initially seeing doctors about having back and leg pains. I had a couple of MRI's, eventually saw a neurosurgeon who first suggested possible MS when i told him about symptoms. Not just back and leg pain, but on the odd occasion getting numbness or losing feeling in my legs. After that I had a lumbar puncture test and ot was shortly after that I got diagnosis, then after that RRMS after new lesions were found after another MRI. So since then I have been taking Tecfidera, or Dimethfyl Fumerate, seems to be helping so far, no new lesions appearing yet. I am still discovering what my MS does to me, will post some thoughts on that on another post. But now, here I am, trying to understand more how MS affects not just myself but others as well.