EmarieBake
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I am 22. I had my first seizure a week ago. My husband witnessed it. He says my eyes rolled back in my head and I fell. I knocked a hole in a bedroom door with my head, locked my jaw and convulsed for 30-45 seconds. When I woke, I thought I'd had a panic attack until I saw the hole in the door.
I went to the ER, had a ct scan (results were normal), and was diagnosed with a urinary tract infection and referred to a neurologist. I followed up with the neuro the next day. He scheduled me an EEG, mra/MRI, and some blood work. He also prescribed me Dilantin that day and antibiotics to replace the ones the ER gave me.
I had a horrible reaction to the Dilantin. I took it the night after the visit to the neurologist. 100 mg capsule 3 x a day was prescribed. I took one dose before bed and (even though I had been kept awake the entire previous night by th ER staff due to the knock on my head) was kept awake all night by my entire body shaking, a headache, the need to move around, and dizzy spells that kept me from getting up. I didn't realize this was a side effect of the drug and thought that it was the after effects of a seizure. I took my 2nd dose the next morning to the same effect and looked up the drug on web md.
I have not taken another dose. When I called the doctor he suggested a lower dosage, but I am scared to death of the SE. I haven't been on anything except antibiotics since. The drugs seem so extreme when they haven't diagnosed me with anything or even given me my test results. I go for those tomorrow.
If something distinctly shows in a test result that says I'm likely to have another sz, I'll feel more comfortable cooperating, but the side effects of that medicine made me have to send my daughter to her dad's house. He was fine helping but I couldn't handle having her gone all of the time. I've always had custody. Besides that, I'm terrified in general right now. I'm afraid that I'll have another one, but I'm also scared that using medicine I don't need will damage me. I have been previously diagnosed with dysthymic disorder and have been living unmedicated successfully for 5 years. I would hate for meds I don't need to throw me back into depression.
Are the side effects normal?
How will they know if I'm really epileptic if I only have one sz and then end up on meds which list seizure as a side effect?
Should I just accept this medication even though I feel like I don't need it?
What is the harm in waiting to see if I have a 2nd seizure before starting what I have been led to believe will be a lifelong treatment?
I went to the ER, had a ct scan (results were normal), and was diagnosed with a urinary tract infection and referred to a neurologist. I followed up with the neuro the next day. He scheduled me an EEG, mra/MRI, and some blood work. He also prescribed me Dilantin that day and antibiotics to replace the ones the ER gave me.
I had a horrible reaction to the Dilantin. I took it the night after the visit to the neurologist. 100 mg capsule 3 x a day was prescribed. I took one dose before bed and (even though I had been kept awake the entire previous night by th ER staff due to the knock on my head) was kept awake all night by my entire body shaking, a headache, the need to move around, and dizzy spells that kept me from getting up. I didn't realize this was a side effect of the drug and thought that it was the after effects of a seizure. I took my 2nd dose the next morning to the same effect and looked up the drug on web md.
I have not taken another dose. When I called the doctor he suggested a lower dosage, but I am scared to death of the SE. I haven't been on anything except antibiotics since. The drugs seem so extreme when they haven't diagnosed me with anything or even given me my test results. I go for those tomorrow.
If something distinctly shows in a test result that says I'm likely to have another sz, I'll feel more comfortable cooperating, but the side effects of that medicine made me have to send my daughter to her dad's house. He was fine helping but I couldn't handle having her gone all of the time. I've always had custody. Besides that, I'm terrified in general right now. I'm afraid that I'll have another one, but I'm also scared that using medicine I don't need will damage me. I have been previously diagnosed with dysthymic disorder and have been living unmedicated successfully for 5 years. I would hate for meds I don't need to throw me back into depression.
Are the side effects normal?
How will they know if I'm really epileptic if I only have one sz and then end up on meds which list seizure as a side effect?
Should I just accept this medication even though I feel like I don't need it?
What is the harm in waiting to see if I have a 2nd seizure before starting what I have been led to believe will be a lifelong treatment?