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| Hi Raghaven - Welcome to CWE. It has been my understanding that monotherapy is the best route to take, when looking for an anti-epileptic drug to control seizures (at least at first). Quote :
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#4
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| Hi Raghavan, welcome to the forum. ![]() I don't know about the "best" treatment(s) for it, but you might find this interesting: Human Herpesvirus-6B with Mesial Temporal Lobe Epilepsy
__________________ 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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#5
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| Welcome Raghavan!
__________________ "Watch your words, for they become actions. Watch your actions, for they become habits. Watch your habits, for they become character. Watch your character, for it will become your destiny." Epilepsy 101 |
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#6
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| Welcome Raghavan You'll find plenty of comparisons of medication and how some people react.
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#7
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| Hello Raghaven and Welcome! I'm not a Dr., but I sure have gone through it. My best suggestion to you is to keep a journal / log of EVERYTHING you do for about 4-6 weeks. When I say everything, I mean every action from the time you get up to the time you go to bed. Example.... 4/28/02 6AM - Wake up, pills, feel ok (dizzy, etc), 6:15 - wake kids up, Go to restroom (what it looked like....), yoga 6:45 - get kids to bus 7:00 - breakfast.... eggs, muffin, read paper, Dilantin100mg, feeling GREAT (or not) 8-00 - laundry etc..... This is very tedious, however, it really helps create a pattern for your seizures, which you will be able to discuss with your Dr. and even find root causes that weren't there before...or that you didn't think of. The Dr's are all very smart, and they don't always realize there are alternate causes as well as treatments. With this journal, you will be able to show them what is happening in your life. Good luck. |
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#8
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Thank you everybody for the overwhelming response and support. Thank you everybody for the overwhelming response and support. The reason why I asked about Levetiracetam was it acts differently from older anti-epileptic drug as many of you here will know. It acts on a protein in the Synaptic vescicle (I don't remember the name of the protein) and it has no action on the sodium pathway. So it is supposed to be a good adjunct therapy for refractory epilepsy. But unfortunately I am not able to get much material on Levetiracetam's effectiveness in controlling mesial temporal lobe epilepsy. So all of you who are taking medicines for MTLE can please list the medicines that you find effective for MTLE I will get a better idea. But I will never do self medication. You don't have to worry about that. I discuss a lot of technical issues about epilepsy medicines and their mode of action with my neurologist who belongs to the modern era and I interact with him regularly through email as well as personal consultation. Anyway thanks for the overwhelming support. I really appreciate that. Please keep posting your experiences on the treatments that you are taking and the medications in this thread. Thanks again. Regards Raghavan |
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#9
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Levetiracetam / Keppra Raghaven!Welcome to CWE! Levetiracetam is known here as Keppra, and unfortunately Keppra does not agree with me at all, I had to be taken off of it and I wasn't on that drug very long at all! HOWEVER - this drug is considered a wonder drug to half of the population and a nightmare to the other half of the population. It can work FOR you or it can work AGAINST you. I hope it all works FOR YOU! Feel free to browse around the CWE! |
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#10
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Thanks Thanks Brain, I also heard about what you said. It either completely controls or aggravates. Maybe that is the reason my neurologist has not prescribed it in my case. But my friend and school mate who is a neurologist in a hospital in Manchester said in UK they use Levetiracetam as the first line drug for a wide range of epilepsies and that they don't prescribe Oxcarbazepine much. |
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#11
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| Are alternatives ever suggested to you? Or is it only drug centered therapies? I should have included in my above post: Quote :
Preferred was the word ... not best. Last edited by RobinN; 02-26-2008 at 12:11 AM. |
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#12
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| Hi Robin, No alternatives have been suggested to me. What are they ? The link you gave was very useful. Thanks |
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#13
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| Check out my signature for information on alternatives.
__________________ 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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#14
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Welcome from the USA Welcome to our group. It seems to me that the majority of members are from the USA, but there are also members from Australia and Europe. Please stay and be a part of our group. Epilepsy impacts all of us no matter what man made categories we use to define the world. Have a cup of coffee on me. |
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| GENERIC NEURONTIN FROM INDIA ??? | angelll | The Lounge | 9 | 07-23-2007 03:14 PM |