SAVE THE DATE! 17 April. #cologne, 🇩🇪. Join the Avanzanite Bioscience team, biotech executives, investors, public officials, physicians and rare disease advocates at the 2024 KNIGHTS for RARE fundraiser.
We started the tradition of Knights for Rare in 2023 to do something meaningful for the people that truly make a difference in patients’ lives every day. Each year, we select one unicorn, “hidden gem”, patient association in Europe, doing just that for people with #rarediseases. Not as a job but as a mission and a legacy.
I’m proud to announce that our 2024 RARE KNIGHT is NEPHROKIDS, a parent’s association from North Rhine-Westphalia, #germany 🇩🇪 , dedicated to children suffering from #kidney diseases, many rare ones.
Nephrokids supports #children, young people, and their families with kidney disease. What’s amazing and really inspiring is that the association was founded by parents whose own children had chronic kidney diseases. And while their kids have grown into young adults, these founding parents continue their mission to support the next generation of children and their families.
Nephrokids is led by Michaela Peer, a parent herself, who founded Nephrokids in 1990 and continues to chair its Board and manage day to day operations.
Go to www.nephrokids.de to learn more about the inspiring things they do.
The 2024 Knights for Rare fundraiser and walking dinner will take place on 17 April 2024 from 1930–2130 at the beautiful Rheinloft Cologne, 🇩🇪
All proceeds and donations from Knights for Rare will go directly to Nephrokids. Tickets are just €89 and you can buy them and register here:
https://lnkd.in/enmtmm7B
If this resonates, you'd better rush as spaces are limited!
#charity, #orphandrugs, #patientadvocacy, #nephrologist, #paediatric, #nephrologie, #biotech, #community, #kindernephrologie,
President at G80 Consulting
3moGood Luck!