by emil.fuerst@lvl-up.ch | Feb 23, 2026 | Association, General
Am heutigen Internationalen Tag der Seltenen Krankheiten erinnert das Rare Disease Action Forum (RDAF) daran, dass über 500’000 Menschen in der Schweiz von einer seltenen Erkrankung betroffen sind, viele von ihnen weiterhin ohne gesicherten Zugang zu Diagnose,... by emil.fuerst@lvl-up.ch | Feb 25, 2025 | Association, General
Am 28. Februar 2025 begehen wir den Internationalen Tag der Seltenen Krankheiten. Dieser Tag macht darauf aufmerksam, dass Millionen von Menschen weltweit – und auch hier in der Schweiz – mit seltenen Krankheiten leben und oft vor grossen Herausforderungen stehen. Das... by emil.fuerst@lvl-up.ch | Dec 4, 2024 | Association, General
On 26 November 2024, representatives from politics, patient organisations, healthcare, research, authorities and industry gathered in Bern for the Swiss Rare Disease Summit. The event developed a common vision and a concrete roadmap for better diagnosis, treatment and... by emil.fuerst@lvl-up.ch | May 3, 2024 | Association, General
The Rare Disease Action Forum (RDAF) will host the Swiss Rare Disease Summit on 26 November 2024 (9.30 – 17.30 CEST). The event will take place in Bern, with the additional option of virtual attendance. The Swiss Rare Disease Summit endeavors to forge a collective... by emil.fuerst@lvl-up.ch | May 3, 2024 | Association, General
We are happy to welcome Förderverein für Kinder mit seltenen Krankheiten (KMSK) as the newest member of the Rare Disease Action Forum (RDAF). With Förderverein für Kinder mit seltenen Krankheiten (KMSK) on board, RDAF’s diverse coalition gains further strength,... by emil.fuerst@lvl-up.ch | Apr 3, 2024 | Association, General
We are very pleased to welcome the Centre for Community-Driven Research (CCDR) as the newest member of the Rare Disease Action Forum. CCDR’s focus on facilitating patient engagement and improving health system navigation will bring valuable new perspectives and...