Ok, for those out there who care and want to know (and even if you don't, too bad! That's my post today! :) ) here's an update on Emma Grace.
So last Thursday was so busy! (as you well remember from my last post) and so I didn't have the time/energy to talk about her appointment with Dr. Milstein in Bellevue. (or the fact I had to drive past the la-dee-dah Porsche and Mercedes dealerships) drool......
ok, so back to reality.
When Dr. Milstein walked in, he looked very grandfatherly. I immediately felt reassured, just by his "look" if that's fair.
So he's really thorough, yea, but it took almost an hour and a half, when all was said and done! What a visit! :) He gave Emma a pretty thorough neurological test, like the "touch my finger, touch your nose" with each hand separately, which she did okay on with her right hand, but failed miserably with her left hand.
He had her walk across the floor on her tip-toes, which she could not do. She flat-footed it across the room. There were a few other tests, but you get the drift. Needless to say, he said that the Mary Bridge docs were wrong in their dyspraxia diagnosis, he said it was more an apraxia.
Then he asked me bunches of questions about family history and seizures and then he told me he's diagnosing her with childhood seizure disorder, and put her on Tegretol and he plans on keeping her on that for 2 years, not adjusting it, and allowing her body to just outgrow the meds as she grows. His hope is that she'll outgrow the seizures and it won't turn into epilepsy and that she'll be fine.
When I went to the pharmacy to get the meds, the pharmacist pulled out her big PDR book and read to me all about the drug and possible side effects. S.C.A.R.E.Y. But necessary for Emma right now. The one thing she urged me to do was to get her involved in some kind of program to help her with the inevitable delays in education. There is where my frustration comes into play. She's been tested through Child Find twice already, once as an exit interview kind of thing when she left the birth to three program,and then again at the beginning of the school year. She was just shy of making it into the program for preschool, but she missed by .02% and the school only tests children every 6 months. So I'm a little frustrated. Should I call the school and tell them about her diagnosis and meds? Do you think that would nudge it better to allow her into the program?
So my dear friends, there we have it. The immediate side effect I notice? Emma is tired all the time, and not just sleepy, but downright groggy, red-eye and all.
So on the one hand I'm grateful she will be on preventative meds for seizures, and on the other hand, it makes me sad to see her so tired all the time. And C.R.A.N.K.Y!!! Whoo, baby, when she's tired like that, she sure is cranky! But then so is everyone, right?
Thanks for listening to my whine. Have a great day!
Holiday Cards Are Easy For Me
11 years ago








