I just spoke with HR about increasing my FMLA due to new worsening of some symptoms. Mind you this is a RN in HR ... She asked if it's this a lifelong illness? Then same conversation "I have a friend with MS that does the infusions too and he's doing very well". .... If she could have seen the look on my face through the phone 🤣. And please please don't compare anyone with MS to someone else you know with MS! We are like snowflakes... No two alike with our problems and what does and doesn't work. We might have similarities and be able to help each other but we don't have a one fits all solution.