You Get What You Fight For, Not What You Wish For

Art Still

Former NFL Hall of Honor Player for the Kansas City Chief’s is now a foot soldier in the Amyloidosis Army fighting for health awareness and inequity in the Black Amyloidosis V122I community. After a long journey to diagnosis Art as a patient is dedicated to bringing awareness to the ones who need it most and are the most underdiagnosed.

Mike Lane

Foot soldier and patient/advocate after a long journey to diagnosis discovered through his self-education and research into Amyloidosis that there was a huge unmet need to bring awareness to the black community which has the highest rate of affliction and the lowest rate of diagnosis. Dedicated to making the Amyloidosis Army the “MORE” than everyone says needs to be done. Mike is on the Amyloidosis Research Consortium Patient Advisory Committee and on the Rare Disease Legislative Advocates Advisory Committee.

Strengthening Communities.

Patients and Doctors Educating Our Communities

At Amyloidosis Army, we envision a world where no one suffers in silence from amyloidosis. Our mission is to empower individuals in our African American communities through awareness, education, advocacy, and support, ensuring early diagnosis and effective treatment. We strive to transform lives by raising awareness, driving research, and fostering a compassionate, informed community that stands united against this rare disease.