Carter: After we started that Onfi in May he stopped having drop attacks all together! So while he still has seizures, a couple each month, they are almost always in his sleep and not affecting his every-day life. Unfortunately the seizures have caused some developmental delays (pretty common in seizure kids) and the hope is that as they are controlled and (hopefully) outgrown he will catch right up to where he should be. So, this last fall he enrolled in the same Special Ed preschool Mikayla went to and we are happy to know the system and the teachers already. He gets overwhelmed sometimes and wishes he could stay home with mommy more but for the most part he loves school. In other news, he loves trains, dinosaurs and robots. And he loves to play ball, doesn't matter the sport, anything with a ball will do.
Mikayla is in a small-group kindergarten so that she can get the personal attention she needs with occupational and physical therapy. She is very good with computers and can lock me out of my phone! Its crazy to me how tech-savvy these kids can be! Mikayla is loving and kind and quite the chatterbox, always talking about the people in her life. People are very important to Mikayla.
The biggest adjustment our family has been undergoing treatment for Rebecca's diagnosis of Hodgkin's Lymphoma. We've had 7 successful treatments of chemotherapy and we are hopeful that after 5 more we will be able to put this whole thing behind us. We have the most amazing family and friends who have been there through every step of this battle and we are both humbled and grateful for every blessing we have enjoyed.
Here's to a new year, (hopefully) good health, and much love!
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