August 14, 2012
I became involved with this foundation through my wife who has epilepsy. Like most people I didn't know much about epilepsy and had very stereo-typical ideas about people with epilepsy. i.e. they look different, they act different, they are constantly having an "episode", they cannot lead a normal life, they are "slow", etc. I know it sounds awful but it's what many people believe. My wife is the very opposite of the above description; she is one of the most physically fit, motivated, disciplined, and intelligent persons I have ever met. She did not tell me about her epilepsy until months after dating and even after getting married I sometimes learn of old adversities that she has had to face due to others prejudices. This foundation has taught me so much about this condition and has encouraged me to give back in both my professional life and personal life. I am a chiropractor and have dedicated a significant portion of my practice to helping those that have epilepsy through spinal and cervical adjustments. It's no cure but the research shows there are benefits. Without this foundation, my wife would still be the incredible person she is today, she's a fighter, but I'm not sure I would be the husband that I am today. Thank-you Epilepsy Services Foundation.
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