On Rare Disease Day 2024, Be Inspired to Have One Leg Up With Your Rarities 2-28-24
While I was born with VATER Syndrome, that rare disease has not taken me down thanks to the love and support of so many, first and foremost my parents and the NICU doctors! I am here today, so why not share this message for Rare Disease Day 2024!
Resources here: https://rarediseases.org/rare-diseases/vacterl-association/
Become a supporter of this podcast: https://www.spreaker.com/podcast/onelegupalex-media--1101162/support.
The skinny
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