Angela
I am a Special Education teacher who blogs about my super-powered special needs family. My 3 year old has Prader-Willi Syndrome and my 5 year old has Duchenne Muscular Dystrophy and Sensory Processing Disorder. The odds of these random genetic events occurring at the same time are astronomical. When you add our typically developing one year old baby boy to the mix, you have a very busy household!Our lives have too many appointments, too many school problems, and are generally too busy as we try to live life to the fullest.
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Tag Archives: Early Childhood Development
The Busy, Busy Month of May
Springtime. The month of May. Mothers Day. Victoria Day long weekend. Add teaching a spring session of night school twice a week. Add a dozen or so medical appointments. Plus our regular preschool activities and volunteer commitments. Oh, and tee-ball starts … Continue reading
The Princess Gene
I am convinced there is a DNA sequence for attraction to glitter, tulle, and feather boas. I am convinced there is a unique DNA sequence for those who can pull off wearing all three, at once, with style. That person … Continue reading
Drive Thru Mama
Note to my sponsors: all of yesterday’s meals were brought to you by the DRIVE THRU. When on the road, racing to appointments, & out-numbered by 3 kids who can’t walk (just 1 of me, 3 of them), I SO appreciate … Continue reading
Posted in disABILTY, Duchenne Muscular Dystrophy, Early Childhood Development, Half-Past Normal is who we are, Prader-Willi Syndrome
Tagged Accessibility, appointments, disability, Early Childhood Development, healthcare, motherhood, Ontario Early Years Centre, parenting, Special Needs, thought on 'normal'
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