Ty’s Story, a Rare Disease Patient
There are 7,000 rare diseases affecting 25 β 30 million Americans, many of which are children just like Ty.
Meet Beth, the Patient
Beth’s story is a case study of what one patient advocate can do!
Meet Cathy, the Patient Advocate
Cathy Teal is the Executive Director of the FAIR Foundation.
Meet Emily, the patient
My name is Emily, and this is my experience with Ankylosing Spondylitis (AS).
Meet Sara and her care team at the Arthritis Center
Sara is infuriated that she can’t get the medicine prescribed to her, when she needs it most, from the doctor she trusts.