Wow. It seems like everything they do to diagnose it is crap. Fine.. if you happen to fit in the definition. But, like with the brain shrinkage.. I was told they can tell if your brain is shrinking just by looking at the mri and finding space where there shouldn't be space. But obviously that's not true if they had to see yours side by side to see the difference. It's hard to have faith in this diagnostic system. So many of the tests seem to rely on someone's subjective opinion. It's amazing anyone ever gets a proper diagnosis this way. How long did it take you from onset to diagnosis to have them finally figure it out? I know that you were getting tests back in 2007.. but when did the problems start?
I think it's really great that your son is buying a house for both of you!
Well, poo. just lost the note I wrote! I am so sorry to hear that it's PPMS. I'm glad that you have a DX though. Just the validation alone.. and knowing. You can plan and get disability.. finally. Can't they use any of the new MS drugs to help slow it down?
I'm ok.. started lyrica which has helped tremendously. Just went through another set of MRIs, a neuropscy exam, and am waiting on the VEP and a lyme specialist appt. Tired of hearing how i'm passing all of the tests. I mean.. yay, I guess.. ? But I've been doing a lot better this year overall which makes it hard to stick with it.
How are you doing with your DX?
Hey, it replaced my note! That's what I get for clicking on a snazzy cute picture. ..
What I *was* saying.. is that I hope you're doing ok.. I've been thinking about you. Hope you are finding what joy you can.
Jen