This is the story and blog of a beautiful 5 month old little girl named Avery who is suffering from a rare genetic disorder and has maybe 18 months to live. Her Mom and Dad have started a bucket list for Avery and are blogging to keep her memory alive and to make people aware of her life and this horrific disease.
Here is a link to the blog http://averycan.blogspot.com/
If you can read this without tearing up well then you are stronger then I am because I am sitting here crying like a baby. I have a little girl almost the same age, I cannot imagine what these parents are going through. If you can help, please do.
Thank you.
Here is a link to the blog http://averycan.blogspot.com/
If you can read this without tearing up well then you are stronger then I am because I am sitting here crying like a baby. I have a little girl almost the same age, I cannot imagine what these parents are going through. If you can help, please do.
Thank you.