Hi everyone,
Just amazed each day how many people battle Alagilles Syndrome. This video really puts a smile on my face to see how positive people can be and are going through similar situation as myself. Here is a video of a loyal fan of the Ellen Show who has a son battling Alagilles as well. This was to good not to share. :-)
About Me
- Milaniya's Brief Bio
- I'm currently 3 years old and reside in Northern California. I was born with a rare genetic liver disorder called Alagilles Syndrome that occurs in 1 in 100,000 live births. Although life may be tough sometimes I'm a very happy little girl who enjoys the company of family, my pets - Mia and Joey, and all the cool toys/gadgets I have to play with. Please stop by my site for the latest update on my life!
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