Rare Disease Day

  • Category: events
  • Published: Thursday, 20 August 2026 14:20
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Rare Disease DayThe Ivan and Joan Foundation is dedicated to advocating for the well-being of people living with rare diseases, including Fanconi Anemia. As part of this mission, we were honored to participate as patient advocates in the Rare Disease Symposium held at Muhimbili University of Health and Allied Sciences (MUHAS). The symposium was conducted under the theme: "Rare Diseases: More Than You Can Imagine."

Establishment of a rare disease database

- Establishment of a specialized treatment centre for rare disease patients (a Centre of Excellence) that would provide diagnostic tools, orphan drugs, and psychosocial support services.

- ⁠Insurance policies to include exceptional provisions for rare diseases so that they can at least cover about 50% of the treatment costs.

- Establishment of a special rare disease department within the Ministry of Health

- Incorporate rare diseases in national health strategic plans

We support children with rare diseases through awareness, advocacy, and Psychosocial care turning pain into purpose. We are working to establish Tanzania's first FANCONI ANEMIA diagnostic center to ensure timely, accurate identification of rare conditions and better access to treatment.

+255 (0) 754 302 613    This email address is being protected from spambots. You need JavaScript enabled to view it.


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