anyone have any experience or heard about babies having seizures? My almost 4 month old had 9 seizures in a 5 day period and was admitted to the hospital a week ago. we are home now:) and she's doing well- no seizures. she is on medication and we go meet with the neurologist tomorrow to go over more test results. All the test results we received at the hospital were normal. We do have a history in our family- my other daughter had similar thing happen- 4 months old seizures- on medication but has not had any in 4 years. I guess i am trying to see if anyone out there experienced this too. My 1st daughter had immunizations 2 weeks before. of course Dr said this was not a reason. (yet they held off doing vaccines for awhile since fevers are a side effect which in turn can cause seizure) my baby now had 1 vaccine- DTAP- about 6 weeks prior to her seizures. Just throwing this out there as many believe vaccines are not that safe- I too am wary of them. Any thoughts? otherwise normal, healthy babies no problems in utero. thanks Kelly
I hope you are able to learn more tomorrow. Feel free to give an update.
These were febrile seizures? If that's the case then no I don't think the vaccines had anything to do with them. Hugs to you. That has to be incredibly scary.
Rachelle, mommy to 8 year old boys!
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my dd1 has seizures due to celiac. if she eats gluten, she has a horrific seizure. once we figured this out, we have been slowly weaning her off trileptal (which wasn't doing anything to stop them anyway) what kind of seizures does she have? if she has complex partial seizures, i woul dget them tested for celiac, or take all wheat out of her diet (and yours if you are breastfeeding). blood tests for celiac are very unreliable in young kids.
i have found in my own research, that nuerologists in the states are more concerned with finding drugs to stop the seizures than with trying to figure out the underlying causes. Italy and Iran were the only countries that had any published journal articles on celiac and epilepsy, and though both studies that i read strongly urged docs to test for celiac if there are comlex partial seizures. dd's nuerologists totally had no clue about it. so, if you are able to research stuff, i would start looking outside the U.S. for research.
do your daughters have the same kind of seizures? there are a lot of benign childhood epilepsys that are genetic and if dd1 grew out of them there is a good chance dd2 will as well. what else do you know about her seizures?