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  #1  
Old 03-28-2008, 03:08 PM
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Recent DX Question?


I was recently DX with Epilepsy by a neurologist but she really didn't explain to much to me about it, so I am wondering is my neurologist the one that I will see about my epilepsy or should they be referring me out?
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Old 03-28-2008, 03:34 PM
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Two alternatives that I see.

Alternative #1 - Make an appointment with your neurologist and write up a list of questions. If you are happy with the answers, then it seems like you have a winning relationship. If you don't like the answers then you go onto Alternative #2

Alternative #2 - Ask for a second opinion, which many of us have done. The best choice would be one that has a specialty of Epilepsy.

My daughter is seeing her third neurologist. Is it that I like her better? Is it that she has a better vision of the bigger picture? I am not convinced of that. I am more knowledgable now after my two years of researching this and can have a more intelligent conversation about the subject. I have learned to take studies and medical facts to discuss.

I would be called a rebel by many I guess, for my alternative beliefs. I do not follow blindly the pharmaceutical route. Nor do I believe that the doctor knows best. I have found too many that are completely clueless.

Remember knowledge is important, especially when it comes to your health.
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Old 03-28-2008, 03:42 PM
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That makes alot of sense! I was just thinking about going for another opinion. I just don't know what is going to happen now, I kinda feel like ok, I know what is wrong now, but what is next?

I like my PA and she is the one that I mainly deal with I very rarely even meet with the neurologist. So that really got me thinking.

Robin you can tell that your a mother!(thats a good thing)
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Old 03-28-2008, 04:28 PM
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A change came over me when I watched my daughter have her first seizure. I was the last one to confront a doctor. I always did what I was told. Believed they knew best. I have since learned that isn't always the case. Sure there are some very good doctors working darn hard to make a difference. Unfortunately they are no longer bothered to deal with the headaches the insurance companies put them through.

( I deleted how I really feel about the medical mess we find ourselves in )
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Old 03-28-2008, 11:44 PM
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Originally Posted by RobinN View Post:
Two alternatives that I see.
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Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback
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Old 03-28-2008, 11:58 PM
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Talking and I will 3d that.......


Originally Posted by Bernard View Post:
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Old 03-31-2008, 09:45 AM
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I set up an appointment with my neurologist on Friday, she said that I could come in this Thursday and she would go over everything with me but my son turns 1 one Thursday! So I am going next Monday. She told me to write down questions, she wants me to log every seizure and how long they last and what happened during them. She also wants me to keep a journal of medicines that I am taking and try to put one together of what I have taken in the past. I must say I am finally feeling that we are moving foward! I don't feel stuck and scared.
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Old 03-31-2008, 09:59 AM
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Wonderful... great feeling I am sure. When you have support you can walk a little easier.
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Old 03-31-2008, 10:08 AM
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Isn't that the truth!
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Old 03-31-2008, 10:30 AM
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Happy Birthday to your little one. ENJOY the day!!

I like the response from your neurologist. That sounds very pro-active and many of us here would love to have a doctor that is that responsive.

Not to counter Robin's suggestions, but looking at meds for a temporary control can help buy you the time to figure out which of the alternatives may help you. I have had this for 26 years and am just now looking at alternatives. Meds have me under control right now, but I hope to live another 30-40 years and the alternatives are appealing. I just want to move forward with caution. Robin and Bernard are very knowledgable on the alternatives.

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Old 03-31-2008, 10:40 AM
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Thank You for the Birthday wishes! I am very proud and sad at the same time!

I'm very pleased with my doc so far or rather the PA. She has been very helpful!

They are very helpful!

I'm so glad that I found this forum
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Old 04-01-2008, 02:58 PM
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I agree with everyone's postings below; it takes
time, just be patient! And it helps to keep a diary,
or a journal or a log to keep a monitoring of
everything as well so you know what to gather
and inform to your Neurologist when you see
the Doctor the next time.
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Advocate & Member of


Head Storms - Resource Center

Last edited by brain; 04-01-2008 at 03:00 PM.
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