Today I learned about a little girl named Avery, who has spinal muscular atrophy. She was diagnosed with this when she was five months old. Her parents have created a blog called Avery’s Bucket List to share her adventures and her life with her family.
The blog is written from Avery’s perspective; her parents have created a bucket list of things they want Avery to experience in the 18 months she is expected to live. One of the things Avery’s mom and dad want to do is to educate others about SMA. Take time to visit Avery’s Bucket List. Avery’s Bucket List can also be found on Facebook and Twitter.