Time
to spread the love. Shout out all your favorite HA’s! Make sure to
share a few sentences explaining just how grateful you are for them
It
is great to see a community of bloggers get together and spread
awareness about their conditions. Why I love blogathons to be honest.
There have been some great posts along the way and some great bloggers.
Dear Dr. What’s-Your-Name…
I think I have in fact met this doctor. He and others like him is why I
don't go to the ER for status migraines. Because they don't care. They
don't treat me. And why when I Didn't go to the ER for a status migraine
I ended up with permanent nerve damage. Hell, it wouldn't have made any
difference had I gone. Even when I went to My doctor at the time about
the nerve damage he said it was likely a form of persistent migraine
aura, even though I told him that tactile persistent migraine auras were
exceptionally rare and this didn't even feel like that.
Dear Yahoo, This may sound silly, but…by Janice Tindle This
one gets extra credit for the rare disease of Visual Snow, which I also
have. Used to be considered part of a persistent migraine aura until
recent research determined it is its own entity, however, 50% of people
with VS actually have migraines as well. Her vision sounds a lot like
mine with VS, migraine with aura and persistent migraine auras. I
suppose mine is a little funky all the time.
Enter Quote, Stage Left… #HAWMC Day 3 This was just one fun post to read.
.jpg)