Would you care to elaborate? Perhaps a cross country relocation might ameliorate your symptoms?
Like Greg said, just statistics. Denver has a statistically higher incidence of MS than most cities.
Theories vary about why.
They probably won’t vary someday ... once someone understands the mechanisms of MS...
Then it’ll make sense.
Kinda like nobody fully knows why spinal cord patients often end up ridiculously low in Vitamin D over time, more than a forced indoor lifestyle for some percentage of that population might indicate.
All sorts of weirdnesses with spinal stuff.
I spend way too much time reading papers from the Mayo. Haha. Always been a “boring” reader... love stuff like tech papers and accident reports... so I just added learning medical jargon and reading their papers to my reading list. LOL.
My doc says I have “good questions”.
I think that’s code for “Yeah yeah, I know I know, we already checked that, but you’re correct to ask...”
It was fun to read a Mayo paper from 2014 targeted at teaching docs how to diagnose all these maladies. And also reassuring to see my doc hadn’t skipped any steps including some of the very newest tests.
We see people on our support group all the time who’ve had acute attacks and went to a typical ER and weren’t treated with steroids, weren’t recognized as neuro patients, all sorts of awful misdiagnosis in initial assessments... having something rare happen to you that expresses as very non-specific symptoms can be a huge problem for docs. Also can delay important early treatments.
It’s wild what we see folks share there. Rare disorders are hard for the front lines of an ER. If paralysis results they get a neuro involved and it goes well. If less than paralysis — maybe a neuro, maybe not... with varying results that have more to do with timing of when a neuro gets involved.
Usually it’s at the “oh crap” MRI point in time, like mine was. Up until that point it was thought to be an orthopedic problem.
The ongoing joke in the group is the day you were diagnosed js forever known as your “crapiversary”. LOL. People share their onset story and we all yell virtually, Happy Crapiversary!