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{"id":503,"date":"2014-12-21T00:05:47","date_gmt":"2014-12-21T00:05:47","guid":{"rendered":"http:\/\/hopeinautism.com\/?p=503"},"modified":"2015-02-03T14:30:54","modified_gmt":"2015-02-03T14:30:54","slug":"remembering-the-christmas-diagnosis","status":"publish","type":"post","link":"https:\/\/hopeinautism.com\/remembering-the-christmas-diagnosis\/","title":{"rendered":"Remembering the Christmas Diagnosis"},"content":{"rendered":"
Seven years ago today, I took Samuel to the Kansas City Regional Center to meet with a psychologist for autism testing “just to rule it out.” Instead, we left with an official diagnosis of moderate\/severe classic autism. He was constantly scripting with no meaningful language, playing “inappropriately” with toys (focused on spinning wheels\u00a0\u00a0 instead of driving, or lining up toys), and had severe meltdowns that involved banging his head repeatedly.<\/p>\n
Today, we spent the day at grandparents’ house for our Maryland family Christmas. We walked in the house to a beautiful array of gifts spread under the tree, and on the fireplace hearth. Sam greeted his grandparents, uncle and girlfriend, then flitted around the tree excitedly flapping his hands. He doesn’t typically flap his hands unless he is REALLY excited. He waited patiently (at least, as patiently as he could) before getting to open presents. He smiled and said “thank you” for his gifts. He conversed with his brothers. He played appropriately with his new Nerf rifle and Star Wars inquisitor light saber. He pretend-played. He ate dinner with us without having a meltdown. He played outside with his brother. He asked for food when he was hungry. He asked to watch a movie, and then watched it with the family together.<\/p>\n