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Hi all,
(Sorry in advance for the length of this post.
)
It's been a long time since I've been here. I've had really good seizure control for more than four years and, after switching to a lower dose, I haven't had particularly bad side effects. But last night I had another freakin' seizure :razz2: It was a simple partial motor, but slightly different than previous ones. Unlike most of my sp motors which started with my arm twisting up and behind and my neck turning while my leg draws up and I end up twisted like a pretzel on the ground, this one mostly affected my leg. Fortunately, I felt strange and grabbed hold of a door frame before my leg felt like it was being run through a wringer - it was tingly and numb, but there was also some pain which is new for me. My dogs heard me cry out and were gathered around and I thought they were jumping up on me, clawing my leg, but when I looked down, they weren't jumping on my leg. The clawing feeling was a phantom feeling. Anyway, I couldn't tell where my leg was. It felt like it was on the ground, but it was drawn up. When the seizure started to let up, my leg felt like lead and I couldn't move it.
My seizures all began because of a brain tumor. After surgery and chemo, the tumor was all but gone - my MRI's for the last few years have looked good. So when I had this seizure last night, I admit I panicked. I was afraid the tumor was growing back (which is, in fact, likely at some time in the future) so I let my dad call for an ambulance to take me to the ER. They did a CT which didn't show anything new and blood work was fine. They talked to my PCP and they decided to up my dosage again.
Anyway, finally getting to the point. My dad remembered that the pharmacy had run out of the generic Keppra they had been giving me, so this week I have been taking some from another manufacturer. I had enough left of my old to take one of the old and one of the new for a week to transition, but this week it's been all the new ones. But also, this week has been very stressful. I'm a full-time caregiver for my Dad who has MS and many other problems. I won't go into details, but we finally had to get my dad a hospital bed and I've been figuring out how to do things. It's been a lot more work, but I haven't had to worry about him falling, so I thought there was less stress.
Okay, so finally a question: How much might this break-through seizure be due to the switch in Keppra (I know little changes can make a big difference) and how much due to stress? I know there's no one right answer, I was just wondering if anyone else who thought their seizures were under control then had a break-through ever figured out what caused it. I really thought I was taking meds as a precaution. Guess not.:-(
(Sorry in advance for the length of this post.

It's been a long time since I've been here. I've had really good seizure control for more than four years and, after switching to a lower dose, I haven't had particularly bad side effects. But last night I had another freakin' seizure :razz2: It was a simple partial motor, but slightly different than previous ones. Unlike most of my sp motors which started with my arm twisting up and behind and my neck turning while my leg draws up and I end up twisted like a pretzel on the ground, this one mostly affected my leg. Fortunately, I felt strange and grabbed hold of a door frame before my leg felt like it was being run through a wringer - it was tingly and numb, but there was also some pain which is new for me. My dogs heard me cry out and were gathered around and I thought they were jumping up on me, clawing my leg, but when I looked down, they weren't jumping on my leg. The clawing feeling was a phantom feeling. Anyway, I couldn't tell where my leg was. It felt like it was on the ground, but it was drawn up. When the seizure started to let up, my leg felt like lead and I couldn't move it.
My seizures all began because of a brain tumor. After surgery and chemo, the tumor was all but gone - my MRI's for the last few years have looked good. So when I had this seizure last night, I admit I panicked. I was afraid the tumor was growing back (which is, in fact, likely at some time in the future) so I let my dad call for an ambulance to take me to the ER. They did a CT which didn't show anything new and blood work was fine. They talked to my PCP and they decided to up my dosage again.
Anyway, finally getting to the point. My dad remembered that the pharmacy had run out of the generic Keppra they had been giving me, so this week I have been taking some from another manufacturer. I had enough left of my old to take one of the old and one of the new for a week to transition, but this week it's been all the new ones. But also, this week has been very stressful. I'm a full-time caregiver for my Dad who has MS and many other problems. I won't go into details, but we finally had to get my dad a hospital bed and I've been figuring out how to do things. It's been a lot more work, but I haven't had to worry about him falling, so I thought there was less stress.
Okay, so finally a question: How much might this break-through seizure be due to the switch in Keppra (I know little changes can make a big difference) and how much due to stress? I know there's no one right answer, I was just wondering if anyone else who thought their seizures were under control then had a break-through ever figured out what caused it. I really thought I was taking meds as a precaution. Guess not.:-(