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Welcome to Jayden's Special Page
Hello Everyone! Thanks to our friends the Simmer's, Jayden now has his very own special page! As you probably already read Jayden had a really hard night last night. But I am happy to report that he is recovering quite well. He gave us a scare last night when he had a reaction to the Diastat (med I use to stop seiz). But today he was able to drink his bottle and even eat dinner. He is still really loopy but it hasn't affected his smile. Dr. Collins (neurology UCSF) called today and we discussed different options regarding Jayden's meds. For now we are going to start giving his meds 3x's a day instead of 2. And we are also going up on his Keppra. We are both concerned about his reaction to Diastat. Jayden's seizure are getting longer and requiring more diastat. This is a major concern for us becausDiastat is the only way I can stop a seizure, if I didn't have it we would be calling 911 all the time. The only thing we can do now is work on meds and try to control the seizures as best we can. There is always a concern when seizures are as prolonged as Jayden's are. It can be very dangerous. Thank you for your prayers and kind words. Until next time.....Love and prayers, The Correa's
1 comment:
Hi Jayden... you are such a cutie!!! You are getting so big! We hope to get to see you and your mom in SFO in May!
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