I had planned to post video of Zane, but things have been
pretty erratic with what Justin and I have dubbed Zeizures (Zane seizures).
After almost-weekly changes to his medications, things have
not improved. At times, the Zeizures seem less extreme; at others more
dramatic. Justin and I witnessed one of Zane’s worst seizures to date a couple
of nights ago.
I talked to one of my friends who has epilepsy, describing
to her what I had observed with Zane: upset, rapid breathing, and (at times)
terror on his sweet face. She thinks that Zane most likely feels the seizures
coming on now and knows what’s going to happen, which causes panic to set in
for him.
I called and left a message for neurology yesterday, but
they didn’t call back (which is not typical of them). I hesitate to call again
because they want to add a second medication to his regimen, and I am still so
in the dark about seizures and the human brain. Will I lose my Zaner to
medication side effects? Will he want to sleep all the time? Or will he be
completely wakeful (like he was all of last night)? I don’t know what to
expect, which makes me feel out of control. And I like control J
I am going to gauge Zane’s seizure activity today before
calling again. It is probably me simply procrastinating, but you never know.
Maybe the Zeizures will improve.
my kids had them too, susan----it was a hit and miss game lots too--i totally sympathize with you---hang in there--they can usually come up with the right meds <3
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