Feb 27, 2019
As we continue our Rare Disease Interview Series, I am so excited to welcome Emily Anderson.
Emily is an English major for creative writing at the University of Wisconsin Milwaukee. She recently wrote an article for Milwaukee magazine looking to spread awareness for disability rights because she feels that those rights are abused because of convenience. Disability rights and advocating began when Emily was diagnosed with Friedrichs Ataxia, a neuro muscular degenerative disease, at the age of 13.
Listen in as Emily shares her journey living with Friedrichs Ataxia & her mission to continue spreading awareness for disability rights.