I want to let you know that my post for the Epilepsy Blog Relay is uploaded on the Living Well with Epilepsy website now. The topic is "A System of Support." I hope you enjoy reading it.Let me know what you think!
The Living Well with Epilepsy Blog Relay has begun for March 2019. Enjoy reading all the different perspectives about this disease and learn how people cope with it.
I have a byline on the Living Well With Epilepsy website, and will post my story there instead of here as I have in years past.
International
Epilepsy Day falls on the second Monday of February. This year, it was on
February 11, 2019. I happened to come across an article just now about a bridge
in Istanbul, Turkey that was lit in purple to raise awareness about epilepsy.
This kind of symbolic action is meaningful and is a first step in removing the
stigma of epilepsy, especially in those countries with less access to
healthcare and education.
It’s
been almost five years since I’ve lived with the Vagus Nerve Stimulator (VNS). I had it implanted in
late November 2014 and activated at the beginning of December 2014. See my
posts:
On
January 16, 2019, at 8:00 pm Eastern Time, a Facebook Live event for people with
epilepsy will take place. It is a talk with award-winning journalist and New
York Times best-selling author Kurt Eichenwald, about his book A Mind Unraveled, about his life with
epilepsy.
They
will be offering free copies of his book. However, it is first-come, first-serve
and there are a limited number available.
Wishing you all a very Happy, Healthy, and Prosperous New Year!
I hope 2019 brings more advances in epilepsy treatments and seizure freedom (or at least reduced seizures) to those who suffer from the effects of epilepsy.
With our advocacy, I am optimistic that the outlook will improve.