Avery Lynn Canahuati 11/11/11 - 04/30/12

I don't know how many of you have heard or read about baby Avery. If you haven't, you must visit her blog/bucket list.

It is a blog written as her by her parents. 

April 6th she was diagnosed with Spinal Muscular Atrophy.

As I don't know much about it, I highly recommend going to her blog and reading all about it. Anybody with kids or that wants kids should definitely look into this.

The blog is Avery's bucket list and the following below is one of her last. Please look into doing what you can. Even if everyone does $10 that makes a difference! 

"One of Avery's newest Bucket List goals was to help raise the remaining $365,000 (out of $1mil) needed to bring Dr. Kaspar's SMA Gene Therapy program out of the lab and into her SMA friends.  Dr. Kaspar's SMA Gene Therapy could cure Avery's friends or at the very least offer advancements towards a cure for them.

Click here to donate to Dr. Kaspar's SMA Gene Therapy through Sophia's Cure which is a non-profit organization so all donations are tax deductible."