Logan's mother knew something was
amiss that afternoon when he wet his pants while napping beside her on
the couch.
Her bright and active 5-year-old son hadn't done that in
years! She tried to awaken him but couldn't, and he lay limp and
lifeless in her arms for several minutes as she called 911.
He became
sick to his stomach in the ambulance and then remained sleepy and
confused for several more hours. His mother knew that something
significant had happened. The doctors couldn't be sure, but they
suspected Logan had had a seizure.
One month later, Logan had a second episode. At that point, his astute mother knew deep inside that these were seizures, even before the doctor confirmed this with an EEG -- electroencephalogram -- or brain wave test.
Logan is intelligent, creative and imaginative, to the point that he
likes to pretend he is Superman -- and in many ways, he demonstrates the
same courage as his superhero. "We were concerned," his mother says.
"When the doctor told us he needed to take daily medication, we decided
to seek a second opinion." Logan's parents would do anything to protect
their Superman from harm, but the prospect of daily medication made them
uneasy.
After a
detailed discussion of the possible risks and benefits, Logan's family
elected to defer daily treatment. They instead have pre-measured doses
of rescue medicine that may be given rectally to stop a seizure after it
starts. Over a two-year period they used it only twice, both times with
good success.
Logan's experience reminds us that epilepsy should no longer be considered a strange and mysterious illness.
We now know that it is usually an immanently treatable neurological condition.
The key to a successful outcome is a full understanding of the epilepsy
type and underlying cause. A meticulous history and physical
examination, along with an EEG and brain MRI, usually provides a
complete picture of the patient's neurological condition.
Among the many questions asked by families every day, the following two are among the most frequent.
YAHOO NEWS
0 comments:
Post a Comment