We presented the 2DD LIVE forum at the 2019 Global Genes RARE Patient Advocacy Summit. We laughed and cried and had an incredible time connecting with the Rare Disease Community about the patient perspective. Listen to this episode for genuine insight and hearty hilarity from our three panelists:

Onno Faber, founder of RDMDTwitter: twitter.com/onnofaberInstagram: instagram.com/onnofaber

Neena Nizar, founder of The Jansen's FoundationTwitter: twitter.com/neenanizarInstagram: instagram.com/thejansensfoundation

Katie Stevens, Executive Director of Team TelomereTwitter: twitter.com/sixnwsteviesInstagram: instagram.com/sixstevies

If you enjoyed this episode, check out: Be Yourself LIVE at Amicus

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