My 16 year old daughter's path of being a teenager with Crohn's disease and hypermobility syndrome from her mother's perspective. Crohn's disease is a chronic inflammatory disorder of the gastrointestinal system, and this blog may not always be pretty. We'll probably talk about poop, pain, disgusting tests and disturbing treatments, so don't read if you're squeamish.
Sunday, December 4, 2016
After 3 nights
Three nights have gone by with her new seizure med. Today she was very tired. Tomorrow we will increase the med to twice a day. Dose is still very low. She reported not being able to think clearly enough to do her schoolwork on Friday. I think she may have had another seizure this morning. I am not sure but she seemed a little postictal. It may have just been the brain fog. I'm not looking forward to her taking the med during the day. I have told her to just do what she can with her school work. Already her appetite is gone but not reporting nausea. I'm getting two partial meals in her a day. This is not too different from her norm... Have I mentioned that I hate seizure meds?
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