The video celebrates the special moments in the lives of people living with a rare disease. Read about Elisa, who is living with Williams Syndrome, and her family!
Together, if you Join us in making the voice of rare diseases heard, both on Rare Disease Day and throughout the year, we can collaborate to strengthen the Patient Voice around the world.
The video has been translated in 35 languages:
العربية, български català, 中国的, hrvatski, čeština, dansk, nederlands, English, suomalainen, français, ქართული, deutsch, ελληνικά, עברית, magyar, indonesia, italiano, 日本語, 한국어, lietuvių македонски, norsk, فارسی ,polskie, português, român, русский, српски, slovaški, slovenski, español, Türk, Український, tiếng việtIf the video is not yet translated in your language, you can send us the translation at [email protected] and we will embed the text as subtitles in the video for you.