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#1
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Results after Neurologist visit.Well I went to see my Neurologist on Wednesday (yesterday). After I told him hold the Lyrica was treating me (weight gain, bloating, swelling of feet & neck), he agreed to take me off it. Starting this morning on only on Trileptal (900MG x 2). The visit was going pretty good until I inquired!! First explained how I my life was doing without my Gall Bladder. I told him that I was trying the G.A.R.D. diet to help with my stomach problems. He started to squirm in his chair a bit. When I said I read that the G.A.R.D. diet also helps with seizures, he squirmed more. But then it happened!!! I told my Neurologist that I wanted to give Neurofeedback a try, and I found a woman that does it in the area. To be fair I asked if Neurofeedback was offered at the hospital. Wow, did he go nuts!! For over 30-40 minutes he went on and on about Neurofeedback not going to work for me. To throw more fuel to the fire, I asked if I could get another round of Video EEG monitoring to update my records. He calmed down a bit. When I asked if my condition could have changed since the last Video EEG session (4 years ago), he when crazy. He went on and on about my condition not changing since I'm still having seizures. I asked if the activity localization could have gotten larger he went ballistic. He did calm down enough to confirm to me that my seizures frequency is just gotten worse since I have seizures at night. As for the G.A.R.D. diet, he didn't say much about it because I said it was to help with my stomach problems. Well that was quite a visit. A family member that went with me noticed something was off with my Neurologist, besides his rocker!. Since my prior visit (6 months ago) he must have been in an accident or something. He was always a big wired, but not like this. I hope he's back to semi-normal for my next visit.
__________________ Member of the Epilepsy Foundation. Undiagnosed sufferer of Dysgraphia. Sufferer of Severe Stress. My RFD LEGO Site & My RFD Store |
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#2
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| Hee-hee-hee ROCKED his little world, didn't you Bigman! Guess you're living up to your name.Don't you just love the open mindedness of physicians? If man-made chemicals won't stop seizures, who's to say a change in eating habits won't either. What makes him so SURE this is doomed to fail?
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#3
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| Quote :
I told him that I read about Neurofeedback and how it has been help seizure patients. But according to him it won't work for "my" seizures. It wasn't an issue that he dismissed the use of Neurofeedback, it was how he did it. When I explained that I have read several reports of some surgery patients dying afterwards. He got all Arnold on me (Whatcha talkin bout Willis?). I knew that would hit a nerve. But like I told him, before I jump into surgery I want to see what other options I might have. He told me that he's glad I'm reading, and wanting to be an informed patient. But he questions what I'm reading. To answer that I told him that I was reading up on Epilepsy Foundation Reports, medical journals, hospital reports, etc. I knew that if I mentioned a few medical forms like here and NeuroTalk, it would cause problems. Just by his reactions to the idea of Neurofeedback, I could tell he would say that these sites are just planting the wrong information in my head. To be honest my previous Neurologist (who IMHO is the best around) got me into learning more about my condition. I know for a fact that if my appointment was with him, he would have been supportive. He would have explained why (why not) alternative treatments work. If I could still go to him I would, but he moved too far away. I don't drive, and I can't get anyone to drive me 100-200 miles just for a doctors appointment.
__________________ Member of the Epilepsy Foundation. Undiagnosed sufferer of Dysgraphia. Sufferer of Severe Stress. My RFD LEGO Site & My RFD Store Last edited by BIGMAN131307; 10-25-2007 at 08:47 AM. |
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#4
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| Sorry to hear that you have a doctor not willing to listen. A great blog article by a doctor: Quote :
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#5
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| Hey Bigman, most doctors are going to react that way when their patients start talking about complementary or alternative approaches - especially if they don't really know anything about them (and most don't IMO). I remember when I was attending a seminar for the VNS a few years ago. There was a nurse practitioner there from from Texas Baylor College of Medicine & Texas Children's Hospital. I spoke with her briefly and asked her what she knew about EEG neurofeedback. She told me quite honestly that she didn't know anything about it. A couple of things that are important to note about EEG neurofeedback:
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback |
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#6
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| Bigman when I lived in Montreal, Canada , the nueros went crazy their because I used vitamins and saw an acupuncturist. I am so use to their negativity , they can't deal with being shown up , their chemicals are always better ,even as it kills you. What feels great is when your choice of altertanative treatment shows them up!!!!!!!! Be patient and do what you believe and trust!!!!!!!!!! Good Luck Riva
__________________ Riva's Memorial |
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#7
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#8
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| Speber your the best !!!!!!!!! Riva
__________________ Riva's Memorial |
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#9
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Sorry to hear that you have a doctor not willing to listen. A great blog article by a doctor: http://www.ultrametabolism.com/blog/...ence_of_t.html |
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#10
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| Well that was quite a visit. A family member that went with me noticed something was off with my Neurologist, besides his rocker!. Since my prior visit (6 months ago) he must have been in an accident or something. He was always a big wired, but not like this. I hope he's back to semi-normal for my next visit. |
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#11
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| Zoe, I don't think the Othmers are affiliated with EEG Spectrum anymore. You can find them at EEG Info or the Brian Othmer Foundation. Links to all these places are on the CWE Resources Page
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback |
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#12
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![]() Nice Show! Let us know how the SQUEAL goes!
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