Scoliosis is a personal passion of mine. Some have asked what drew me to this cause and I respond by saying “I didn’t choose Scoliosis, Scoliosis chose me” and I really wouldn’t want it any other way. I have been dealing with my Scoliosis for many years now, since roughly 1999. Now 11 yearslater I have been through three spine braces, seven spine surgeries, a hip surgery and multiple physical therapies all while going through school and trying to be a normal girl.

 

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About Alana

Learn more about founder Alana Hartmann and her personal Scoliosis Awareness Mission since being diagnosed with Juvenile Idiopathic Scoliosis and Kyphosis at age 11.