This is a blog of a beautiful little 5 month old girl who was diagnosed with SMA, a rare genetic disease that is incurable. Her parents and family are making the best of the short life she was given and are checking things off of her bucket list. Go to their site and offer your prayers and support. You won't be able to leave the blog without crying, but be happy that this little girl has such an amazing family who is making every moment a memorable one in her life.
Remember to share her website with your friends to help spread the news of her tremendous journey!