I imagine you all get the emails with the articles, but I'm trying to get caught up with all those and saw this one. I'm sure you all know what this is like, the beginning of each year. This article puts it so much better than I ever could. Last year I went for weeks without meds and ended up in the hospital. This year I knew better and parked myself in the neuro's office, waiting for samples to be brought out!
Boy does this ring true!: I imagine you... - My MSAA Community
Boy does this ring true!
I think most of us have had to deal with this problem. When out insurance changed in January, I had to jump through all the hoops all over again - many times! It's exhausting. I make detailed notes about each call with the name of the person I spoke with, time, what was said, etc. I do have some memory issues at times, so the notes really help. I still have to make numerous calls to numerous places to get things done. It is frustrating.
I'll say it again I know the NHS here in England has lots of faults but the meds and treatment is free from the moment of birth thank goodness! I can only say how hard it must be for u all on insurance xxxx 🤔🤔🤔🤔
Mrsmike9buffering, it's Fancy1959. The article you just shared had very common and valid areas of complaints for the entire MS family and any other long-term health problem. Thanks for sharing.