I don't necessarily have an issue caring for a child with a seizure disorder.
However, i would NOT allow him to return to care until he SEES a neurologist and you have a plan of action from the NEUROLOGIST (not just from mom).
I would also have mom sign a release with the neurologist and for me saying I can call the dr and ask questions if I need to. I would need to know what daily meds are prescribed for prevention. I would also need to be sure mom understands that most of those meds require sometimes twice weekly, weekly, then monthly blood work to determine their levels. If she can't seem to get off of work to take the child to a neurologist then how do I know she is going to take the child for the blood work every week?
I sure hope they educated mom to NOT give that rectal medication unless he has a grand mal lasting more than 3 minutes (some docs say 5 minutes). That medication is a LAST RESORT.
The seizures you are describing are NOT grand mal seizures.
So, to answer your question. I WOULD watch and have watched a child with a seizure disorder. But a lot of things come into play. As in the type, frequency, parent follow up etc before I would even THINK about accepting the child.
If I could NOT (whether that's due to ratio and my inability to watch the child closely enough, maybe I can't allow a child to sleep as much as they want, maybe the child simply requires more care than I can give) continue or agree to watch the child, as long as it's not JUST because of the medical condition... it's NOT DISCRIMINATION.
If I couldn't continue care I would give notice describing that I am unable to adequately provide the care the child needs while STILL providing care to the others in my home. End of Story.
However, i would NOT allow him to return to care until he SEES a neurologist and you have a plan of action from the NEUROLOGIST (not just from mom).
I would also have mom sign a release with the neurologist and for me saying I can call the dr and ask questions if I need to. I would need to know what daily meds are prescribed for prevention. I would also need to be sure mom understands that most of those meds require sometimes twice weekly, weekly, then monthly blood work to determine their levels. If she can't seem to get off of work to take the child to a neurologist then how do I know she is going to take the child for the blood work every week?
I sure hope they educated mom to NOT give that rectal medication unless he has a grand mal lasting more than 3 minutes (some docs say 5 minutes). That medication is a LAST RESORT.
The seizures you are describing are NOT grand mal seizures.
So, to answer your question. I WOULD watch and have watched a child with a seizure disorder. But a lot of things come into play. As in the type, frequency, parent follow up etc before I would even THINK about accepting the child.
If I could NOT (whether that's due to ratio and my inability to watch the child closely enough, maybe I can't allow a child to sleep as much as they want, maybe the child simply requires more care than I can give) continue or agree to watch the child, as long as it's not JUST because of the medical condition... it's NOT DISCRIMINATION.
If I couldn't continue care I would give notice describing that I am unable to adequately provide the care the child needs while STILL providing care to the others in my home. End of Story.
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