AACC champion partners have a shared mission to educate and empower patients with peer-reviewed clinical lab testing content in order to promote better health outcomes and ensure accuracy of the partners' specialty area as it relates to laboratory testing. Visit Champion Partner News for partner resources and programs.
The Heart Rhythm Society (HRS) is a leading resource on cardiac pacing and electrophysiology. This specialty organization represents medical, allied health, and science professionals from more than 70 countries who specialize in cardiac rhythm disorders.
The Hormone Health Network is the nation's endocrine patient education resource. We are committed to helping patients have more informed discussions with their health care providers about hormone health, disease, and treatment. All of our educational resources are based on the clinical and scientific expertise of The Endocrine Society, the world's largest organization of endocrinologists, representing more than 18,000 physicians and scientists.
Patient Power LLC (www.patientpower.info and www.patientpower.eu) is a patient education organization dedicated to connecting patients and care partners to the knowledge of a community of cancer experts to empower them to live well with cancer. From cutting-edge research and treatment news to coping with cancer in everyday life, the community-based health communities cover the topics most important to patients. Through video interviews, in-person events and online features, Patient Power provides patients with the tools and resources needed to better manage their cancer and live with hope. Patient Power is on the forefront of developing research and brings treatment news as it happens through interviews with the top researchers at medical conferences. Also, patients and family members share their stories, insights and inspirational tips for coping with cancer.
123esaaf.com is an online Arabic medical encyclopedia with the most comprehensive and interactive medical resource available online in Arabic language. It provides credible information, supportive communities, and in-depth reference material about health subjects that matter to all Arab people who search for a certified free source for original and timely health information as well as material from well-known content providers.
The International Waldenstrom's Macroglobulinemia Foundation (IWMF) is a patient-founded and patient-led, nonprofit organization dedicated to a simple but compelling vision: Support everyone affected by Waldenstrom's macroglobulinemia (WM) while advancing the search for a cure.
To accomplish this vision, the IWMF offers six invaluable services:
- Information written in patient-friendly language
- Education to help patients and caregivers learn about WM
- On-going updates about WM and the IWMF on www.iwmf.com, through our quarterly Torch newsletter and NEWS releases
- Peer support
- Information for medical professionals with limited experience with our rare disease
- Research directed to better treatments while we search for a cure