Description
The Rare Diseases Alliance of Latvia (LRSA) is an independent non-governmental organization founded on October 3, 2014, uniting organizations representing various interests of patients with rare diseases. As an umbrella organization, the Alliance represents the interests of more than 90,000 people with rare diseases in Latvia at the national and international level.
In the run-up for Rare Disease Day, we organize a photoshoot for children and adults with rare diseases. Photos will be published during rare disease day 2023 campaign.
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