Advocates call for progress in rare diseases treatment

Ljubljana, 28 February - Rare diseases associations called on the government to set up a palliative care system for children, provide better assistance to families and expand treatment funding ahead of Rare Disease Day, observed on 28 February.

Brdo pri Kranju
The head of the Association for Rare Diseases, Jo┼że Faganel.
Photo: Bor Slana/STA

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