🖤 A nonprofit elevating the voices of rare disease patients, empowering them to advocate for themselves. Promoting allyships between rare disease stakeholders; patients, caregivers, healthcare providers, healthcare systems, pharma/biotech, payors, through provider and patient facing education Developing content for roundtables, discussions, demonstrations and lectures bringing stakeholders together for positive health outcomes and patient interaction. https://www.instagram.com/pathwaystotrust/ Currently expanding programs in Pediatric Pain/ Sickle Cell Disease and Ehlers Danlos Syndrome.