Jenn and Chris Hawn have a beautiful little boy named Ryan. Ryan has been diagnosed with Spinal Muscular Atrophy, a disease that is going to take him from his parents way, way too soon. There is currently no treatment from SMA, nor is there a cure.
My heart aches for this family. I can’t imagine the pain they must go through on a single day, let alone that poor, sweet little boy. Please head over to their website and leave a comment. I know they would be glad to hear from you with your words of support.
While you are there, please sign the petition to end SMA. You can find it on the right sidebar on their blog or you can go directly to the petition HERE. I signed it. I wish there was more I could do for the Hawn family because my heart just aches for them.