I was once told that thoughts are energy and words are power. In this blog, I'm putting my story into words. Here, I'll talk about what it's like to grow up with and live with simple partial epilepsy. Hopefully I can give insight to those who don't live with it and can give a sense of camaraderie to those who do.
Tuesday, March 27, 2012
Because You Can
Tonight we all gathered, my mom and her four sisters, me and my younger sister, my dad, my aunts' spouses, childhood friends whose own children have long since left childhood; new friends, old friends, work friends, family friends, life friends. We all gathered in the same dimly-lit back room of the restaurant where my aunt was married four years ago. Tonight was again in celebration: a birthday. Her sixty first birthday. No, it's not a multiple of ten, no particular anniversary or precious metal, but the most special birthday so far. Without a cane, she seemed to glide and float across the room with a smile that spread from ear to ear as she greeted and was greeted by every glowing guest.
In time we joined together in a joyful chorus of Happy Birthday and when she stood to give a short speech, I soaked up every word I could. Be grateful for every morning that you wake up. Choose to live. Choose to fight. Face life head on, don't watch it pass you by as you wait to die a little more each day. Thank God, thank the earth, thank the people who love you, thank yourself for the world around you! Move your body because you can. Live every single day because you can. Above all, never forget how lucky and blessed you are.
Thursday, March 22, 2012
Seize The Tweetosphere!
Tweets: one hundred and forty characters to tell the world what you're thinking. It gives a numerical value to, "So much to say and so little time". Well, technically it's space, not time, but if I think hard enough, I could probably figure something out with a space-time continuum. I really don't actually know what that means, though, which could cause a problem...
Anyway, for Purple Day, we're Seizing The Internet!! Tonight we start seizing the tweetosphere. A hundred and forty character limit makes getting across a point tricky. To help, I've put together some tweet-sized sound bites for you here. Don't forget to use the hashtag #SeizeTheInternet and feel free to spread the love by tagging your other favorite epilepsy bloggers and tweeters :) Check out Living Well With Epilepsy's Directory for more of us!
(Stats courtesy of Talk About It.org)
50 MILLION people around the world live with #epilepsy. #SeizeTheInternet!
If someone is having a #seizure, DO NOT restrain them! #SeizeTheInternet!
Call 911 if it's someone's first #seizure or if it lasts more than 5 minutes - an ambulance is expensive #SeizeTheInternet!
#Epilepsy is NOT contagious! Who came up with that anyway? #SeizeTheInternet!
Nearly 3 million people in the US have #epilepsy. #SeizeTheInternet!
ONE-THIRD of people with #epilepsy live with uncontrollable seizures because no available treatment works for them. #SeizeTheInternet!
BETWEEN 4 AND 10 OUT OF 1,000 people on earth live with active seizures at any one time. #Epilepsy #SeizeTheInternet!
A #seizure is a jolt of electricity through the brain, kind of like a bolt of lightening. #epilepsy #SeizeTheInternet!
For 6 OUT OF 10 people living with #epilepsy, the cause of their #seizures is unknown. #SeizeTheInternet!
50,000 people die from #epilepsy-related causes in the United States every year. #SeizeTheInternet! @SUDEPAware
If someone is having a #seizure, DON'T put anything in their mouth! It's not possible to swallow your tongue. I promise. #SeizeTheInternet!
Wednesday, March 21, 2012
Seize The Internet for Purple Day!
Tuesday, March 20, 2012
Tides
I reached for the alarm on the new purple cell phone that sat on my nightstand, knowing that I'd already used my allotted one snooze for the day. I slid my finger across the screen, silencing it as I sat up and slowly, ungracefully, swung my legs over the edge of the bed. It's been exactly fourteen months since my first surgery, but as my hand lifted to cover the throbbing on the left side of my skull, just above my ear, not so deeply buried under its scar, I remembered that fourteen months really isn't that long.
Wednesday, March 14, 2012
Working Girl
Sunday, March 11, 2012
Never Thought The Day Would Come
That was two nights ago. Earlier in the day, I sat in one of the two chairs opposite a large desk from my neurologist. We talked about me and John moving back to Minneapolis a few days before, my new job as a Business Analyst at Target that I start on Monday, the headaches I still get, though they're becoming less frequent, how much my hair has grown back over the past year, the fact that I'm still seizure-free. I held my breath and crossed my fingers as I asked the question I'd come for: "Dr. So said that if I made it a year without having a seizure, I could wean off of my Vimpat. Do you think I can start that?"
She paused a moment, a thoughtful look on her face as it searched my medical records on her computer screen for any reason I shouldn't. "Okay."
Relief, joy, disbelief flooded me all at once and I couldn't help the smile on my face as I said, "I honestly never in my life thought this day would come."
I won't be completely off of the drug for a month, but every day I get closer, I have more and more energy, the way I did seven months ago when I got off of my Lyrica, but this time it's even more noticeable. I'm still on Lamictal XR every night and probably will be for the rest of my life, but I'm fine with that. I always figured that liver failure was what would eventually take me one day, but now I really feel I can let that go. I'm gonna be okay.