I'm excited to announce that I'll be hosting a webcast for the Williams syndrome Association on Tuesday February 18th and 7 p.m. central time. Join me by clicking here and registering! The webcast will be archived on the same webpage after it airs so if you miss it, you can hear it at anytime.
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About this blog
I am a high school human anatomy and physiology teacher by trade and I double as a mother of a little girl with Williams Syndrome. When my daughter was diagnosed, I was thankful that I understood how the body worked so I could navigate through the condition and understand what the doctors had to say. This is my way of sharing my knowledge so other parents can have that same power.
Information contained in this site is strictly for education purpose to better understand the conditions associated with Williams Syndrome. You should in no way use this site for diagnosis, treatment or medical guidance. Always seek medical advice from your doctor.
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