Winston posted this on The Federal Review today. It is a series of clips from The Center for Epilepsy & Seizure Education in British Columbia.
This is a blog about epilepsy. I have lived with seizures for 25 years now and I want to share my experiences to allow others with epilepsy a chance to compare their experiences to mine and to allow those without epilepsy to understand further the condition and how it effects one. I had the VNS device implanted 4 years ago and have posted on that extensively. Please feel free to comment and I will try to respond.
Tuesday, May 15, 2007
Monday, May 14, 2007
Update.... Feeling Better
Just wanted to send a quick update to let everyone know that Scott is recovering from his latest seizure. He is still tired but seems to be feeling better. His only injury is a stubbed toe - which is a nice shade of red and black. Thank you all for your calls and concern.
Christa
Christa
Saturday, May 12, 2007
Yet Another Dreadful Tonic Clonic Seizure
That's right... Scott had another tonic clonic seizure this evening around 9:40 pm while cooking in the kitchen. Our son, Ryan, and I were able to get the kitchen gadgets out of his hands and help him keep from hurting himself too much. Luckily, I was wearing my bracelet which holds a VNS magnet and was able to swipe it early on. Scott did stop breathing for a few minutes but came out of the seizure much more quickly than usual. He is resting now and has only complained of stubbed toes, a sore neck and fatigue. I will try to post more tomorrow to let everyone know how Scott is doing.
Christa
Christa
Thursday, May 10, 2007
No Seizures... since the last one...
I haven't had any more seizures since the one on April 13. So nearly a month now. My goal is that I won't have any more ever again. Wish me luck!
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