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  #81  
Old 02-14-2010, 08:53 PM
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I don't know, I'm not sure. But I was taking 4 medicines before I got the implant, then my doctor slowly took me off depakote because I was doing okay but that didnt work for me so now I may be going on another different medication.
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  #82  
Old 02-16-2010, 06:07 PM
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So, in other words, you will be on the exact amount of medicine that you were on BEFORE the implant. What do you think would have happened if, instead of your doctor installing the implant, he just took you off the depakote, and changed that first, before you did all this. With my sister, they also had her on all kinds of medicine before the implant, but none of those ever almost killed her. It was the implant that almost took her life. Now that the implant has been removed and her medications have been changed, she's been fine as far as the seizures go. She will just be on disabillity for the rest of her life. THAT is what the implant did for her. Mglyn2, if you ever have any questions, feel free to contact me at any time. I am not a doctor, but I have done some very intense and thorough research on this device and might just be able to help. I'm just trying to save another human being from going through hell. Just remember that, okay? NancyB
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  #83  
Old 02-16-2010, 07:39 PM
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Originally Posted by kimberlymeg View Post:
If you read my info you can see my frustration with medicine. I would honestly like to try just the VNS therapy w/out medication and see if it helped me. The most frequent I have ever had seizures is one every 1-2 months. After getting off medicine a second time at the age of 18, the side effects slowly disappeared and I was no longer having seizures. I started to feel normal again. Until, at the age of 20, I had a seizure which I think was brought on by a lack of sleep. I was up until about 5am studying and went to bed 5-8:30am. Had a seizure after I woke up. I'm extremely hesitant to get back on any kind of medicine because I have tried two that helped the seizures but had me suffer so many side effects.

Has anyone here tried VNS therapy as their only treatment for Epilepsy? If you know anything related to VNS therapy I would love to hear it.
I have and it has worked great. I was only having nocturnal seizures 3 yrs. ago and was on medication for that but then I started having complex partials during the day so I had to stop working. Things got worse and medications stopped working so VNS was my only option and it has worked great. No more seizures. I'm still on medication but it's fine with me. I'm basically a freak because it normally just controls seizures, to stop them completely.
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  #84  
Old 02-17-2010, 03:24 AM
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My sister tried VNS and it nearly cost her her life. If your reason for even considering that device is because you think you don't have to take any more medicine, your wrong. Many people with the vns device srill take meds. When my sister got hers it made her seizures so bad, even with adjusting the device, that she spent almost an entire year in the hospital and is now on permanent disabillity. I stay in contact with a mom who watched her child die from a seizure after getting that implant. I also stay in close contact with another mom who almost lost her child. but was able to get the device out in time. This device is NOT the miracle you are seeking, and it most assuredly could end up being the nightmare you will never forget.
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Old 02-17-2010, 09:01 AM
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A lot of VNS patients report that the VNS helps shorten seizure intensity/duration and post-ictal recovery periods even when it doesn't reduce seizure frequency or reliance on anti-epileptic drugs.
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Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback.

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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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