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#2
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| Hi Irene, welcome to the forum. ![]() I hope her vision improves as she recovers from surgery.
__________________ 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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#3
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Welcome to CWE, I hope that you find the information you need to support your relative. |
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#4
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| Ive had this sugery. It was just over ten years ago. I wouldnt change anything that Ive experined in my life time because, its all led me to where I am now. The surgery didnt work for me but, thats still not the end of the road because I was forced to keep searching untill I found what did work for me. If you learn everything you can about epilepsy you will be able to make the best choices concerning your epilepsy and how to control it. |
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#5
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| Welcome to our house Irene. The great thing about this site is you can almost always find someone who has had a similar experience (referring to Mike's comment). Sit down and have a cup of coffee. It sounds like you have had an emotional month. |
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#6
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Irene!Welcome to CWE! Here's wishing a well recovery from the neurosurgery! Feel free to browse around and make yourself a home! |
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#7
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I had a Cavernoma removed from my Right Temporal Lobe in Sept 2000, and I'm pleased to be able to say that I went for 5 years without even an aura let alone a seizure, I think my odds of a complete cure were 50/50, unfortunately, my seizures started again in July 2005, no one really seems to know why, there was no real trigger, no stress, I'd passed my driving test, got a new job, bought a lovely new house with my partner so it just didn't add up. After my surgery, I must say I didn't have any problems with my eyes, I was very badly swollen though and I was told to expect that, I just think we are all so very different, that it must be difficult for the doctors to predict the outcome of brain surgery. I'm waiting to go back into hospital in London, to have my right Hippocampus removed, this is the part of the brain in the Temporal Lobe that looks after the production of new memories, emotions, an spatial awareness, that's why I can't read a map and have no sense of direction, according to my partner. I know the initial scar was caused by my being a forceps delivery, but I would love to know why I have sclerosis of the right Hippocampus. I just think you have to try and learn as much as you can about your condition, I'm also studying it with Leeds University, the human brain has always fascinated me. I hope you relative makes a full recovery, and stays seizure free, all the best, and I hope you find this website as interesting and as helpful as I have. Welcome to the house! Cheers Elaine xx Last edited by Bernard; 04-12-2008 at 09:36 AM. Reason: add whitespace between paragraphs |
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#8
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| I was faced with the decesion of having more surgery after my R.T.L surgery. The next most common Epilepsy Surgery is frontal Lobe surgery after the Temprol Lobe surgery if its unseccessfull. I desided to start Nerofeedback instead. In about six months I stopped seizing for five years untill, heart problems and a heart attack through me into statis epileptsis. I started Nerofeedback again and am happy to say that Im 646 days free today. |
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#9
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I didn't actually have surgery, but my forehead hit a windshield and I had plastic surgery. My eyes were swollen for a while. I recovered from swollen eyes within one month of the accident. I wasn't driving in this accident, by the way. My college roommate's car was totaled. Last edited by alivenwell; 04-12-2008 at 11:51 PM. Reason: Added plastic surgery paragraph |
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| brain surgery |
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