My niece's name is Katelyn Lee. She is 18 months and she is just like any other kid. She loves to play, smile, laugh, and give BIG KISSES. She have Angelman Syndrome (AS). I am trying to raise awareness for AS. It is a rare syndrome that affects 1 out of 15,000 and some doctors do not even know what AS is, but she is a little smarter than them. She is a little genius if you ask me because I know that those very intelligent scientists CURED IT IN A MOUSE. Unfortunately, we came across one BIG problem, money! This syndrome is not common compare to others and is not funded by the government, so I am asking for your help to raise awareness. Scientists know exactly what is wrong and that is because she is missing a tiny piece of chromosome 15. Because of the missing piece, it is delaying her from learning, talking, walking, and balancing to name a few. She is one of many little cute mice that needs your help. No donation is too little.
Thank you for taking the time to read my story. :) #cureangelman #teamkatelynlee