Well everyone things are going well. My seizures aren't any better, BUT I don't seem to care. I am finally living my life thanks to the VNS helping my depression. I am getting my vns turned up again on June 22. We shall see how that goes. I also am working at home for a couple of places and doing Mary Kay[ http://www.marykay.com/kimmarquart ] I am hoping to get some people who want to be reps for mary kay. I do my business ONLINE mostly so it's great if you wanna do it that way!!!
I hope everyone has a great summer....
And don't forget to check back. I am going to write more often as soon as I am not so NUTSO busy LOL
Kim
8 comments:
Thank you for posting about your experience... my husband has just found out he is a candidate for VSN although it has to go through the hopsitals council before he can see a neurosurgen. Right now he is experiencing 2-3 tonic clonic sezures with several different partials a day.
Thank you Again !! Getting more information is always a good thing!!
I am so very glad I could help you with your search. It's the reason I leave my blog up!!!
Kim
i hope all is well. i just found your blog.. its nice to read posts fom someone in the same boat. next tuesday 11/18/08 i'm scheduled for my 4th vns since 1998. this last one (model 102r) only lasted 3 years. i hope it will last longer next time
i don't remember my login for this blog anymore...stupid memory issues.,......blogger isn't helping much either....anyone have any ideas email me.
HEY. Can you give me any idea what the surgery cost?
Hi,
Epilepsy has gone from an obscure mental illness, to a serious illness recognized by state foundations. This remarkable awareness, is because of the great work organizations, such as yourself, has done. We here, at Disease.com, fully support the cause your organization stands for and we are dedicated to aiding in your mission statement. Disease.com is a website which features disease and infection preventions/treatments. If you could, please list us as a resource or host our social book mark button, it would be much appreciated. Lets dedicate our time to the welfare of the 3 million individuals with epilepsy.
If you need more information please email me back with the subject line as your URL.
Thank You,
Sharon Vegoe
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Hi, my name is Mandy. I'm 17 and I have been recently implanted with a VNS. I am blogging about my struggle with Epilepsy and my new VNS experience. Feel free to check me out or follow if you want. It would be cool to share experiences. I have struggled with Epilepsy for 5 years, going through many stages of deep depression and anxiety. Among that, I've tried almost every medication out there. It's tough to go through so I have resorted to blogging. I think it's also great to promote Epilepsy awareness to our communities. So thanks for blogging and I hope you reach success in beating your Epilepsy! God bless.
http://mandykrzywonski.blogspot.com
Sincerely,
Amanda Krzywonski
(My Life as Mandy)
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