Sorry, I realized I didn't follow up after our appointment with the Plastic Surgeon about the Drooling.
Turns out the surgery to “tie off” the salvation glands is not as simple as the geneticist made it sound plus it is permanent. He also gave us an alternative to inject Botox in the gland to paralyze it for 3-8 months, but he couldn't guaranty the Botox wouldn’t get in her facial muscles and therefore affect her appearance.
I did some research and the conclusion is that you shouldn’t take such dramatic steps until you give the child enough time to get control of swallowing (after the age of 6). The dentist who saw her a few weeks ago agrees that it’s a little dramatic right now. We should give her time to develop mentally. Considering her feeding/swallowing age is around 12-18 months, we should give her till her developmental age to see if she can get control of it on her own. I read that lots of kids still drool up to 2-4 years of age.
Our life, our experience, our history, about my daughter with a rare chromosome disorder. She is missing a small portion of her 8th chromosome, which is called a deletion. She also has a small part of XP added to that. Her karotype or diagnosis is deletion 8p23.3 with extra xp22.2 to the terminal deletion (a new chromosome test summer 2011 changed her karotype to deletion 8p23.2 with extra xp 22.12, essentially meaning more missing chromosome 8 and more added xp). #herrarelife
Time is a Thief
I don't remember the first time I heard the sentiment, "time is a thief." Recently it is heavy on my mind. I haven't post...
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and the flu panic begins... http://www.cloroxclassrooms.com/downloads/teacher_brochure.pdf
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Sadie has been having spasm type clinch arm and mouth type movements that last about 2 seconds randomly starting in June. For the past mont...
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Today I was feeling the need to read other stories about other children with chromosome disorders. I googled blogspot to see if I could find...