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Has anyone been denied medication based on the doctor's bias? The first time my neurologist was discussing my options for medications I could take for my epilepsy, the conversation roughly went like this: Medication 1 - most effective but it is known to cause birth defects etc. Medication 2 - not as effective but safer Medication 3 - (I don't remember honestly). I asked for the 1st medication because it's most effective, and I don't want children anyways. BUT SHE DIDN'T WANT TO GIVE IT TO ME. She kept looking to my mom, going over the possible side effects, that were PRIMARILY about birth and pregnancy, and I'm here like, "but it's most effective and that's what *I* want." Then I ended up with Medication 2. Surprise, it didn't work for me at all, all the way to the highest dosage and ended up with my first choice anyways. Has something like this happened to anyone else?
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Epilepsy
Generalized convulsive epilepsy
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Quite the opposite for me. My first neurologist was very short with me. Never asked any questions and seemed to dismiss any opinions I had – just put me on the most effective one he knew despite the potential side effects. And when it wasn't working, he kept upping the dose to borderline unsafe.
@epiclepsy that's kind of how my new neurologist is. He does listen however, but you can tell he wants the appointment to be as short as possible, so it is still short answers. I do feel like I got better help, he actually found out about my second form of epilepsy, which is crazy to think about how the first one missed it. But it does feel rushed 90% of the time
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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