Jess has been extremely lethargic again and she is still having more seizures that usual.  Her Paediatrician checked the levels of her medication to ensure that they weren't too high or too low however that came back normal.  We took Jess to her Neurologist and we have been told that Jess has a condition called Lennox Gastaut Syndrome which is characterised by the frequency and different types of seizures.  Reading up on this condition, it is noted that it is difficult to treat and can also contribute to Jess's developmental delay.  The dosage of her meds have been adjusted now to see if we can bring the seizures back under control.  We are going to monitor her for the next few days and refer back to the Neurologist if there is no change.



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