So informative and important!
What the n-Lorem foundation is doing for rare disease is a game changer. Hearing from Stan Crooke and the experts and families he interviews is so informative.
Flygirl3663 via Apple Podcasts · United States of America · 08/24/22
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Just as I thought! Great podcast can’t wait for the rest of the series.
katsmith12 via Apple Podcasts · United States of America · 05/25/22
It must have been devastating to have a kid with a genetic disease mutation that is the only the single one in the whole world. I hope the army of team who works behind the scene can help Susanna out. Thanks for reminding me of how meaningful it is to keep doing good science
LouisaLeung via Apple Podcasts · United States of America · 05/26/22
Amazing podcast and so glad that we now have these long awaited episodes! Truly helps me understand emphasize with the nano-rare patient. Looking forward to listening to more episodes in this series!!
Storm1133 via Apple Podcasts · United States of America · 05/25/22
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