Hi I’m Belinda, often known as Belle. I am turning 67 in 2 weeks (yikes!) and developed PPMS at the age of 48. I am now a permanent wheelchair user with no movement except in my right arm and forearm for which I am daily grateful! I have been an MS Buddy for a few weeks and am enjoying communicating with another MSer. How many of you here have PPMS? We are a fairly rare breed I know but I’m curious to know. Hope you’re having a good day today. Keep safe