Thank you Jennifer!

We’d like to take a moment to express our gratitude to Jennifer Bierling, who is stepping down from our board. She has been a wonderful team member and was instrumental in the launch of our Global Patient Registry last year. Her hard work helped the project get off...

Attention PURA Siblings!

We are so excited to introduce Chrissie Brock as our new Siblings Ambassador. After meeting at our 2023 PURA Conference in the UK, Chrissie reached out to volunteer to help the Foundation to fill the role of our Siblings Ambassador. She has spent the past few months...
Spotlight on PURA Syndrome – February

Spotlight on PURA Syndrome – February

The February Newsletter is out! Please take a moment to read about the following headlines: A Letter from the Foundation Meet our new Board Members New Research Publication Annual Conference Save the Date World Rare Disease Day PURA Meet Ups Click here to read it,...

Stefano’s Rare Disease Day Story

Francesca Greco gave birth to a beautiful baby boy, Stefano, in 2018 in Italy; however, after noticing early delays, Francesca states “the doctors could not explain his condition or identify a reason for the delays, so they proposed we carry out a Whole Exome...
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