February was a busy month for the rare disease community (a disease/disorder community is considered rare if there are fewer than 200,000 people).
Bonnell Foundation CEO, Laura Bonnell was the keynote speaker at the 2025 Rare Disease Day Gathering: bridging the gaps. Laura shared her CF journey as the mother of Molly and Emily, and as an advocate for the rare and CF community. This is always a fulfilling conference to attend with so many representatives from the rare community, including incredible caregivers and scientists.
Pictured: Dr. Caleb Bupp and Laura Bonnell
