Hi Anthony,
If I where you I would be constantly calling them everyday till you get the results, after a week, call them twice a day till you get it. Tell them you will only call more often till you get a copy of it!!! Don't just ask once or twice and let it go, stay on there case non stop daily till you get it! If you can't get it spend a day calling them non stop over and over till you get it! Don't take any crap from them! Best of luck getting your results!
Steve
--- In epilepsy@yahoogroup
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> That is why I FIRED my last 2 neurologists. I have a really good neuro now. They never would tell me what was going on. I had a 72 hour eeg with my last one and he said that they didn't catch anything, but won't let me or my new neurologist read the actual EEG. He keeps coming up with excuses as does the eeg lab where I had it done, which also happens to be at the hospital work at.
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> --- On Sun, 1/3/10, CorineW <corkiewol@.
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> From: CorineW <corkiewol@.
> Subject: [epilepsy] aura then stiff neck
> To: epilepsy@yahoogroup
> Date: Sunday, January 3, 2010, 2:32 PM
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> Hello. I'm wondering if what I experience is a common thing for a lot of you. I get a warning before my seizures that is a feeling of my stomach coming up. Then my knees kind of press together. The final symptom is the back of my neck tightens. The back of my neck starts tightening at the bottom, then by the time it's at the top of my neck the full thing hits. Does this sound like a general warning some of you get? I go into my hand/arm violently shaking, my legs pull up and my body shakes. I have partial and occasional complex seizures.
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> Also, I'm scheduled to see an epileptologist in February. My family doctor had his nurse called me after reading the EEG results and referred me to a neurologist because she said I was having seizures. The nurse there asked my husband and me what my "spells" were like and if I get a headache after. She told us it was definitely seizures. On my first visit with the neurologist, she sent notes back to my family doctor stating it was anxiety. The next time we saw her, she called it complex partial seizures. After seeing her again, she said she didn't read the EEG - her colegue did. Since then she has been very vague and calling them "spells". So I made an appointment with an epileptologist to get a specialist's opinion. We are very disappointed with the neurologist. Does this sound like a common story to any of you? Corkie
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