Tomorrow is one year to the date that I was diagnosed with SPMS - I'm still without a primary care provider so it's been a year of hell going to walk in clinics and not knowing where to go or what to do for advice other than online forums. Where I live in Canada primary care physicians are scarce as hen's teeth and though I did find a wonderful one he was diagnosed with a rapid degenerative kidney condition so he fell off the map quickly. The last GP I tried out responded to me when I explained about going to emergency with MS hug type back spasms that that sort of thing can happen to any of us - so I gave him the heave ho PDQ.
Not the kind of anniversary I ever expected to experience or would ever wish on anyone.