Rare disease families advocate for change, striving to have more control over their diagnosis and treatment options. Patient advocates work to increase awareness of rare diseases and to find better treatments and cures. Families with rare diseases often find themselves struggling financially, as there is a lack of available resources. Patient registries are important in drug development because rare diseases have small population pools and few clinicians with exposure to them.
Balanced News: Rare Disease Families Advocate For Change

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