We believe in the power of coming together to create positive change, especially for underserved communities. Events serve as platforms for advocacy, education, support, and community building within the rare disease community. With a passionate commitment to making the world a better place for those affected by rare diseases and underserved populations, we host and participate in a variety of impactful gatherings. These events represent a journey of resilience, compassion, and unwavering dedication, aimed at illuminating the lives of rare disease patients and their families, as well as addressing the unique challenges faced by underserved communities.
Explore this page to learn about our upcoming events, offering you the opportunity to be part of a shared mission. Additionally, take a stroll through the memories and achievements of our past events, which continue to inspire our ongoing work. Our event page is your gateway to engaging with our community, supporting our advocacy efforts, and joining a collective force dedicated to hope, change, and creating a more equitable future. Thank you for being a part of our journey; together, we can move mountains, change lives, and make a profound difference for the rare disease community and underserved populations alike.
Washington, Feb 28 - Mar 2, 2024
Washington DC | June 19, 2024
Congo Brazzaville | Jun 28, 2024
Maryland | Aug 23, 2024
Rare Disease Week on Capitol Hill is an annual event that invigorates and inspires advocates from all corners of the country. It's a week-long gathering that holds the potential to leave a lasting impact on rare disease patients for generations to come. Petronille Healthy Society (PHS) proudly participated in the activities that unfolded at Capitol Hill during this momentous week. This extraordinary event, orchestrated by the Rare Disease Legislative Advocates, a program of the EveryLife Foundation for Rare Diseases, serves as a focal point for rare disease advocates nationwide.
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Washington, D.C. – Petronille Healthy Society (PHS) had the distinct honor of being invited to participate in the World Sickle Cell Day event hosted at Children's National Hospital in the heart of Washington, D.C. This prestigious gathering proved to be an enlightening and inspiring celebration, bringing together an array of caregivers, advocates, and healthcare professionals committed to the cause of sickle cell disease.
The event served as a heartwarming convergence of individuals united in their dedication to raising awareness about sickle cell disease, a rare and often misunderstood condition that affects countless lives.
Petronille Healthy Society (PHS) is committed to advancing rare disease research and supporting initiatives that can make a real difference in the lives of those affected by these conditions. As part of our ongoing mission, our representatives had the privilege of attending the FDA OOPD (Office of Orphan Products Development) Grant Opportunities Event. This event, served as a significant opportunity to connect with experts, engage in enlightening discussions, and explore grant opportunities that can further our commitment to rare disease advocacy.
The FDA OOPD plays a pivotal role in supporting the development of orphan products for rare diseases. The agency's grant programs are instrumental in fostering innovation, research, and the development of treatments and therapies for underserved patient communities.
On July 14, 2023, at the prestigious Hotel Africana in Uganda, an extraordinary event unfolded under the theme "Breaking Barriers, Building Hope for Sickle Cell." Petronille Healthy Society (PHS) took its place among the esteemed participants, symbolizing our unwavering dedication to improving the lives of those affected by sickle cell disease.
The Sickle Cell Convention emerged as a shining beacon of hope, bringing together a diverse congregation that included healthcare professionals, patients, advocates, and researchers. It was a resounding testament to the shared commitment to advancing sickle cell care, advocating for transformative change, and nurturing a brighter future for individuals and families grappling with this condition.
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