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15 month old focal seizure

Sat, 08/18/2007 - 05:00
First time here! One of my 15 month old twins had her first seizure 2 months ago and her second this week. (Maybe has had more at night, we are not sure) Abnormal EEG, normal MRI. Doc said it was "some sort of genetic disorder" Neither my husband or I know of anyone in our family with a seizure history. Started on Trileptal 2 days ago. I just don't really know about this; hoping someone else has/is going through similar situation. I feel bad about putting her on meds. I hate that I may not know if she is seizing since her seizures are fairly subtle eye movements, head twitching and just acting a little off. I would appreciate any advice!

Comments

Re: 15 month old focal seizure

Submitted by xohion on Mon, 2009-09-07 - 17:44

My daughter (now 8) has been diagnosed with focal seizures as well.  Her first seizure (we didn't know it was one) occurred in April 2007.  She was not officially diagnosed until April 2008 when I took her to the hospital with symptoms that were similar to an adult having a stroke.  She was drooling, couldn't speak, etc.  She was able to walk, write, etc.  Her EEG last October showed that during the test she was seizing most of the time, her CT scans came back normal as did her MRI.  She was initially put on Depakote, but the seizures continued.  Her neurologist then added trileptal to her medicine regime.  Seizures occur about every three months with the same presentation....wakes up from sleep, extreme drooling, inability to speak, but is aware of all that is going on.  From the time she comes to get us to the time she is fully recovered (talking without slurring or drooling) is usually about 15 minutes or so.  She recently had Keppra added because her last seizure was inconsistent with past seizures (lost muscle control and lasted longer).  Keppra changed her personality dramatically.  After one month on the meds, I "pleaded" with the doctor to remove her from it.  Thankfully, we have not had anothe seizure, however, if we continue on our pattern, she will be due for another one in October. 

 She is currently taking 750 mg of depakote at night and 9 ml of trileptal morning and night. 

My daughter (now 8) has been diagnosed with focal seizures as well.  Her first seizure (we didn't know it was one) occurred in April 2007.  She was not officially diagnosed until April 2008 when I took her to the hospital with symptoms that were similar to an adult having a stroke.  She was drooling, couldn't speak, etc.  She was able to walk, write, etc.  Her EEG last October showed that during the test she was seizing most of the time, her CT scans came back normal as did her MRI.  She was initially put on Depakote, but the seizures continued.  Her neurologist then added trileptal to her medicine regime.  Seizures occur about every three months with the same presentation....wakes up from sleep, extreme drooling, inability to speak, but is aware of all that is going on.  From the time she comes to get us to the time she is fully recovered (talking without slurring or drooling) is usually about 15 minutes or so.  She recently had Keppra added because her last seizure was inconsistent with past seizures (lost muscle control and lasted longer).  Keppra changed her personality dramatically.  After one month on the meds, I "pleaded" with the doctor to remove her from it.  Thankfully, we have not had anothe seizure, however, if we continue on our pattern, she will be due for another one in October. 

 She is currently taking 750 mg of depakote at night and 9 ml of trileptal morning and night. 

Re: 15 month old focal seizure

Submitted by julieanna30 on Sat, 2009-01-03 - 02:28

HI MY NAME IS JESSICA I HAD MY DAUGHTER JULIEANNA AT 17 ON JAN 30TH 2007 MY DAUGHTER HAD A NORMAL LIVE SHE WAS HAPPY AND EVERYTHING. IN MAY OF 2008 SHE WAS 15 MONTHS OLD SHE HAD LOSS RESPONSE TO ME SO I TOOK HER TO THE E.R AND THE DOCTOR SAID IT WAS A FEBRILE SEIZURE I WAS A RECK I DIDN'T KNOW WHAT TO THINK FOR THE SIMPLY FACT IS MY HUSBAND AND HIS FAMILY HAVE A HISTORY OF SEIZURES. ABOUT TWO WEEKS LATER I WOKE UP AT 7:OO AM AND BABY GIRL WAS TWITCHING ALL OVER HER BODY I PANICED AND CALLED 911 WHEN THEY GOT THEIR THEY SAID SHE DID NOT HAVE A FEVER I MY HEART DROPPED AND I STARTED CRYING HARDER. I JUST THOUGHT SHE IS EPILEPTIC. EVER SENSE THEN MY DAUGHTER HAS A AROUND 45-50 SEIZURES. THEY HAVE DONE 2 EEG, 3 CTSCANS. AND 1 MRI AND THEY HAVE NOT FOUND ANYTHING ABNORMAL SHE IS ON PHENOBARBITAL. IF YOUR CHILD HAS A RELATION TO MY DAUGHTER JULIEANNA PROBLEM AND TESTS RESULTS AND U FOUND THE REASON Y PLEASE LETME KNOW THANK U. 

HI MY NAME IS JESSICA I HAD MY DAUGHTER JULIEANNA AT 17 ON JAN 30TH 2007 MY DAUGHTER HAD A NORMAL LIVE SHE WAS HAPPY AND EVERYTHING. IN MAY OF 2008 SHE WAS 15 MONTHS OLD SHE HAD LOSS RESPONSE TO ME SO I TOOK HER TO THE E.R AND THE DOCTOR SAID IT WAS A FEBRILE SEIZURE I WAS A RECK I DIDN'T KNOW WHAT TO THINK FOR THE SIMPLY FACT IS MY HUSBAND AND HIS FAMILY HAVE A HISTORY OF SEIZURES. ABOUT TWO WEEKS LATER I WOKE UP AT 7:OO AM AND BABY GIRL WAS TWITCHING ALL OVER HER BODY I PANICED AND CALLED 911 WHEN THEY GOT THEIR THEY SAID SHE DID NOT HAVE A FEVER I MY HEART DROPPED AND I STARTED CRYING HARDER. I JUST THOUGHT SHE IS EPILEPTIC. EVER SENSE THEN MY DAUGHTER HAS A AROUND 45-50 SEIZURES. THEY HAVE DONE 2 EEG, 3 CTSCANS. AND 1 MRI AND THEY HAVE NOT FOUND ANYTHING ABNORMAL SHE IS ON PHENOBARBITAL. IF YOUR CHILD HAS A RELATION TO MY DAUGHTER JULIEANNA PROBLEM AND TESTS RESULTS AND U FOUND THE REASON Y PLEASE LETME KNOW THANK U. 

Re: 15 month old focal seizure

Submitted by vickival on Mon, 2009-01-26 - 21:25
I am sorry to hear that your daughter is having seizures.  My daughter is 2 1/2 and starting having complex partial seizures about three months ago.  It is scary to see your child have a seizure and frustrating not knowing what you can do to help her.  My best advice is to seek a second opinion in a level 4 seizure facililty.  It is imperative that you get an accurate diagnosis with a high resolution MRI.  This is the only way that I feel as a parent you can feel like you have done all you can!  Also, research every terminology that the doctors tell you.  When you are dealing with neurologists they are a special breed :).  They use big words and you have to research yourself so that you know what they are talking about and are prepared to ask questions.  Find a doctor that is willing to listen to you and patient/knowledgeable about the fluctuations of medications.  It is our experience that a lot of seizure medicines take time to work in the system and some have delays of a month or more.  So, there is a lot of experimentation with meds to see what work and what does not work.  My daughter was on Trileptal at first but was having uncontrolled clustering seizures.  The neurologist that we first worked with kept telling us to take her to the E.R. if we felt that she was abnormal.  What is normal...when it comes to seizures.  It is very scary at first and it is hard to determine was is normal or appropriate.  Now after two hospitalizations (the last at a level 4 hospital) we are better equipted to handle her diagnosis and treatment.  Good luck to you and God Bless your little girl.  Also, seek out your local seizure disorder or epilepsy support group; they will be a good resource.  Be patient but consistent.  You are your childs best advocate!

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