Welcome to our exclusive club 😉 hopefully you rebound from this attack. You don’t have much entered into your profile for us to offer suggestions. There are people from all over the world in this forum with a wealth of experience. Ask whatever you want and you can search using the little magnifying glass in the upper left.
I was Dx in 2005 with RRMS that now appears to be transitioning to SPMS so I am a testament that MS is changing all the time as are the treatments and our symptoms. This is a good intro article on MS that will lead to a lot more info- https://www.healthline.com/health/multiple-sclerosis/what-ifs-after-diagnosis?slot_pos=article_2&utm_source=Sailthru%20Email&utm_medium=Email&utm_campaign=multiplesclerosis&utm_content=2019-10-10&apid=29101565#takeaway