Love my Angel!! My daughter MaKenzie has Angelman Syndrome. She is the happiest sweetest lil girl you could ever meet! As she can not talk she communicates in her own way, she can not walk but is fast getting around her own way and is sneaky about it too. We deal with Epilepsy daily, lists of meds and hardships are a daily occurrence. I would not trade her for the world! I love her with everything I am!
In an effort to combat the alarming misdiagnosis rates of Angelman syndrome, the Angelman Syndrome Foundation has partnered with the Angel Wings Foundation, the Canadian Angelman Syndrome Society and others to launch www.findtheangels.org, an educational campaign to generate greater awareness and understanding of this rare disease.