At MediFind, we don't rely on patient ratings and reviews. It's not because we don't like stars - it's because research shows that they don't actually correlate with expertise or quality of care. Instead, we rely on our 21+ years of of continuous learning-by-doing in healthcare analytics and our patented methodology to provide an objective gauge of physician expertise that helps patients find the right care, right away.
Each of the more than 3 million global physicians on MediFind are evaluated for their expertise against thousands of health conditions and procedures, including complex and rare diseases, based on their real-world experience. And it's worked - MediFind is now the #1 place patients go to find a doctor from Google, where the vast majority of healthcare searches begin.
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Mayo Clinic is widely recognized as the leading health system in the US. With locations in Minnesota, Arizona, and Florida, Mayo Clinic is also recognized as a Rare Disease Centers of Excellence by the National Organization for Rare Disorders (NORD).
Penn Medicine is a world-renowned academic medical center, committed to improving the health and well-being of people through research, education, clinical care and community service. Penn Medicine is dedicated to discoveries that advance science, to outstanding patient care throughout the world, and to the education of physicians and scientists who carry on its legacy of excellence.
NORD (National Organization for Rare Disorders) is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD, along with its more than 300 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services.
M Health Fairview is a collaboration among University of Minnesota, University of Minnesota Physicians and Fairview Health Services. M Health Fairview Masonic Children’s Hospital was named one of the 31 Rare Disease Centers of Excellence by the National Organization for Rare Disorders (NORD).
The Myositis Association (TMA) exists to improve the lives of persons affected by myositis, fund innovative research and increase myositis awareness and advocacy.
Alex’s Lemonade Stand Foundation (ALSF) is changing the lives of children with cancer by funding impactful research, raising awareness, supporting families and empowering everyone to help cure childhood cancer.
Rare Patient Voice provides patients and caregivers an opportunity to share their opinions through surveys and interviews to improve medical products and services. The RPV community has over 100,000 patients and caregivers across more than 600 different conditions, both rare and non-rare.
Chive Charities supports veterans, first responders, and rare medical diagnosees with life-changing grants and spreads awareness through sharing the personal stories of grit, courage, and never giving up. Since 2012, Chive Charities has provided grants to over 270 rare medical recipients with more than $10.5M in aid.
Simon’s Heart is a nonprofit organization dedicated to raising awareness about, and preventing deaths from, conditions that cause sudden cardiac arrest in children
The Castleman Disease Collaborative Network (CDCN) is dedicated to accelerating research and treatment for Castleman disease, a disease at the intersection of cancer and autoimmunity, and revolutionizing biomedical research to cure many more diseases.