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absence seizures memory
Thu, 11/13/2008 - 13:35Comments
Re: absence seizures memory
Submitted by nyjetsnc on Mon, 2009-12-07 - 18:57
Re: absence seizures memory
Submitted by pgd on Thu, 2010-01-07 - 09:33
Regarding short term memory, the very old medicine caffeine may temporarily help a few persons (not everyone) a little (not a cure). For some, caffeine works a little; for others caffeine may appear to be neutral; and for still others, caffeine may lower the seizure threshold/change how a med for epilepsy works. RSNA.org: Coffee Jump-starts Short-term Memory - http://www.rsna.org/rsna/media/pr2005/Coffee.cfm - Best wishes.
Regarding short term memory, the very old medicine caffeine may temporarily help a few persons (not everyone) a little (not a cure). For some, caffeine works a little; for others caffeine may appear to be neutral; and for still others, caffeine may lower the seizure threshold/change how a med for epilepsy works. RSNA.org: Coffee Jump-starts Short-term Memory - http://www.rsna.org/rsna/media/pr2005/Coffee.cfm - Best wishes.
Re: absence seizures memory
Submitted by JT on Tue, 2009-12-01 - 20:51
Hi. I am new to this so please bear with me!
My 13 year old son has recently been diagnosed with absence seizures . We believe he has been having them for years but they were so short that they just seemed like he was "spacing out" as he calls it. He has had a sleep deprived EEG which showed 1 seizure. His MRI was normal. He then had a 24 hr. Digi-trace EEG. He showed 13 episodes, 2 of which were approximately 20-30 seconds. The seizures never seem to occur when he is active, riding his bike, shooting baskets, outside playing, etc. He is a straight A student and never has trouble in school. He is rather shy and sometimes has difficulty getting along with and making friends. He is not athletic and the one thing he takes pride in his is scholastic achievement. He has a twin sister who dances and plays sports and I think that this has always made him try harder at school. We are deciding on meds and after reading up on them we are very concerned that they will interfere with his quality of life and really damage his already low self esteem. His Neuro also can't decide if meds are the right thing for him at this point in his life as he feels there may be some evidence that he is outgrowing the seizures. He has already recommended that we talk to the epilepsy specialist at a larger hospital in Boston.
We have already decided if it is a safety issue then it will have to be the meds. His neuro would like to start him on Zarontin. Anyone out there who has experience with this med please help! Does it take long to see the benefits? If there are side effects how long do they last? Has anyone had a long stretch of absence seizures and then a grand mal? I realize this will be different for each individual child but I am just looking for general answers.
Hi. I am new to this so please bear with me!
My 13 year old son has recently been diagnosed with absence seizures . We believe he has been having them for years but they were so short that they just seemed like he was "spacing out" as he calls it. He has had a sleep deprived EEG which showed 1 seizure. His MRI was normal. He then had a 24 hr. Digi-trace EEG. He showed 13 episodes, 2 of which were approximately 20-30 seconds. The seizures never seem to occur when he is active, riding his bike, shooting baskets, outside playing, etc. He is a straight A student and never has trouble in school. He is rather shy and sometimes has difficulty getting along with and making friends. He is not athletic and the one thing he takes pride in his is scholastic achievement. He has a twin sister who dances and plays sports and I think that this has always made him try harder at school. We are deciding on meds and after reading up on them we are very concerned that they will interfere with his quality of life and really damage his already low self esteem. His Neuro also can't decide if meds are the right thing for him at this point in his life as he feels there may be some evidence that he is outgrowing the seizures. He has already recommended that we talk to the epilepsy specialist at a larger hospital in Boston.
We have already decided if it is a safety issue then it will have to be the meds. His neuro would like to start him on Zarontin. Anyone out there who has experience with this med please help! Does it take long to see the benefits? If there are side effects how long do they last? Has anyone had a long stretch of absence seizures and then a grand mal? I realize this will be different for each individual child but I am just looking for general answers.