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  #61  
Old 12-15-2009, 09:14 PM
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s10 and Janie,

I was a scientist/engineer at NeuroPace for 4 years. It was my first job out of college. In that small group of multi-talented individuals, I learned the meaning of teamwork and poured my heart into the device you're using right now.

To hear how this, the only meaningful work of my adulthood, has directly or indirectly improved your lives hits me somewhere very emotional and very raw. It's like Christmas came early.

I'm sure any current or former NeuroPace employee that runs across this thread would agree.

Thank you so much and Happy Holidays
Erem
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  #62  
Old 10-08-2010, 09:52 AM
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Smile


News on my implant lately has been good. Over the past year I have had massive improvements, the RNS implant helped some, but the doctors also put me back on Gabitril which worked for me in the past and was the med that got me to go seizure free for years. They are working my level up on it and have had good news with it. My epileptologist is actually wondering why in the world my old neurologist ever took me off of it. I have even been able to stop having a bottle of Ativan around for cluster seizures. My seizures have gone from upwards of 5 a day to now 1 every 1-2 weeks.

The only bad thing is that with the decrease in seizure frequency, I have a bad habit of forgetting to interrogate the data and send it to neuropace.

Another couple of things that I think have helped is that I am no longer working due to the company I worked for firing me due to absence caused by my seizures, which has resulted in alot less stress, and I have gotten really into bicycling and weightlifting, biking 10 miles a day 5 days a week and lifting 3 times a day. A recommendation from the epilepsy center, its been great too, lost 30 lbs since March.

We really think that the RNS has helped alot and has definitely helped pinpoint the seizures, realizing that most of them are nocturnal and the ones I have now are always nocturnal. Great news on that end, If I can keep it up I may be able to drive soon.

I can't believe how much the exercise has really helped with everything overall too. I have been getting my confidence back, less depressed, and finally more willing to get out among the public. Definitely worth the cost at a fitness center.

All I can say is yay for neuropace, though the Airport next week is gonna be fun as they won't be able to send me through the metal detector.
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  #63  
Old 10-08-2010, 10:35 AM
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Hi s10,

Well look at it this way, you're gonna find out if the airport security is REALLY paying attention! Glad to see you doing better!
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God heals, and the doctor takes the fee.
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  #64  
Old 10-09-2010, 09:22 AM
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Fantastic that your seizure control has improved so much s10. Sounds like you have a lot of changes for the better happening.
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Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback.

Would you like to help support this forum?

We recently had a bunch of new neurofeedback practitioners agree to offer CWE members discounts for service. See post #12 for the list of all participating practitioners.
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Old 02-03-2011, 06:40 PM
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Well, I have officially started into the long term treatment as the short term clinical trial is over for me as I have started year 3 with the implant. According to the feedback from the system, there has been less activity, meaning that the implant has not had to work as hard with the seizures. However, over the last month my seizure frequency increased a bit.

Not sure what to thing as the info from the machine doesn't always seem to matter, as a seizure is a seizure and no matter what is no fun at all. I am trying to keep positive on it, but still pretty worried.
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  #66  
Old 07-17-2011, 11:32 AM
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Well about 6 months into the long term portion of the clinical trials. I have had word with the doctors as I have been feeling like my seizures have gone way down, and they agreed that they are showing that too. I have still been keeping a diary and all seizures have been nocturnal over this past time, I only seem to be having about 1 a month now and the most recent one was due to a missed dose of medication. The other weird thing I get anymore is this feeling saying I'm going to have a seizure while I am laying in bed, this happens on those nights that I have a seizure.

This has sure been making things hopeful, finally I am able to try to work on other issues in my life with less worry.
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Old 07-18-2011, 11:48 AM
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That's encouraging.
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Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback.

Would you like to help support this forum?

We recently had a bunch of new neurofeedback practitioners agree to offer CWE members discounts for service. See post #12 for the list of all participating practitioners.
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  #68  
Old 01-03-2012, 03:25 PM
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When will neuropace be available


My wife's doctor has mentioned this device several times. I thought the device might become available late 2011. However, I have not seen any recent news regarding the device. Is there any word on the status of the device?

Thanks.
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