Why Peer-to-Peer Healthcare?
Patient Advocacy – Online Workshops
Learn your rights as a patient, how to stand up for yourself, and find out where to get help. Share your experience and knowledge with others, and ask questions during the Q&A session in our online Zoom workshops.
Our Shared Patient Information Health Survey helps us understand conditions most in need of research. To date, we have collected health data on Migraine and Lupus. We are currently working on adding mental health and immune conditions. Our data includes all types of medicines.
The Learning Academy is designed for anyone interested in becoming an empowered patient, empowered caregiver or those seeking to understand patient engagement and patient-centered care.
Our Impact Peer to Peer Program
When facing a difficult health situation, we need information, education, and support. We need accurate, unbiased, user-friendly information to best deal with our health issues. We need access to education to be able to better understand and manage our conditions and how our healthcare system works (locally). We need support when we are vulnerable, to be shown the way, to be heard and to know our rights and all our treatment options.
HHP IMPACT will solve the problem by providing information, education and support. Information is provided through our Shared Patient Information (SPI) Program. Education is provided through our Patient Education program and support is provided through HHP’s Patient Advocacy. The combination of these elements empowers individuals to best understand and manage their health conditions.
Empower others to change their lives and change your own in the process
More People. More Information. Better Health.
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