This site is dedicated to our daughter’s ongoing battle, and future victory, against SMA, and to all the people helping us in that fight. Aleena Hope Miller was diagnosed with type 1 Spinal Muscular Atrophy through genetic testing at 3 months old. Our lives have been a wild ride ever since. Our hope is that this site will keep everyone up to date on what's going on in Aleena's life.
We also hope it will provide people information about SMA, current progress toward a cure, and a chance for others fighting the same battle to share some common experiences.