MPN Alliance Australia
The Myeloproliferative Neoplasms Alliance Australia (MPN AA) was formed in 2015 by a small group of motivated MPN patients.
The patient-led advocacy group has a goal of achieving better outcomes for Australian MPN patients.
The Myeloproliferative Neoplasms Alliance Australia (MPN AA) was formed in 2015 by a small group of motivated MPN patients.
The patient-led advocacy group has a goal of achieving better outcomes for Australian MPN patients.
The MPN Research Foundation has a single goal: to stimulate original research in pursuit of new treatments — and eventually a cure — for polycythemia vera, essential thrombocythemia and myelofibrosis, known collectively as myeloproliferative neoplasms (MPN).
MPN Cancer Connection (MPN-CC) was founded to serve patients, care partners, physicians, and your healthcare team. They help empower patients to be proactive and to be your own health advocate by asking questions from your healthcare team.
With members throughout the UK as well as many other countries, MPN Voice’s mission is to provide clear and accurate information and emotional support to everyone who has been diagnosed with a myeloproliferative neoplasm (MPN) and their families/friends.
Myeloma Patients Europe (MPE) is an umbrella organization of myeloma and AL amyloidosis patient groups and associations from across Europe. They aim to provide a voice for myeloma patients and improve effectiveness of care.
MISSION
Empowering Health Equity Through Cancer Screening and Early DetectionOatmeal Health is an AI-enabled, value-based lung cancer screening platform. We are fundamentally changing the lives of underserved patients through early identification, engagement, and comprehensive high-touch virtual care for FQHCs, health plans, and employers.
PALTOWN builds disease-specific communities with a mission of empowering patients and caregivers by creating disease-specific communities to address information needs and social isolation through training, technology, and developing purpose-driven community leadership.
The Pancreatic Cancer Action Network (PanCAN) is a non-profit organization dedicated to improving the lives of everyone impacted by pancreatic cancer by advancing scientific research, building community, sharing knowledge, and advocating for patients. PanCAN provides access to critical biomarker testing, personalized clinical trial searches as well as bilingual, comprehensive education for loved ones, caregivers, and patients through Patient Services.
Global physicians and healthcare professionals have been participating in PeerVoice digital activities for over 15 years to acquire new clinical skills, test their knowledge, and improve their practice of medicine.
From innovative omni-channel digital content to live events, our Independent Medical Education (IME) and Continuing Medical Education (CME) activities are carefully designed to deliver meaningful and measurable change in healthcare professional behaviour and improve patient outcomes.
All activities are delivered in multiple formats and multiple languages. They can be consumed quickly, at any time, from any place, and on any device, on a proven platform which professionals trust.
Through our extensive network, our independent medical education activities reach millions of actively-practicing clinicians around the world. We thoroughly measure and analyze each educational activity, ensuring that we are improving patient care and identifying knowledge gaps to be bridged with future learning opportunities.