PKD International 🌷 AIRP 🌷ePAG/ERKNET
(Views are my own, rtw ≠ endorsement) http//pkdinternational.org http//renepolicistico.it 📍Zürich 📍Siena
Come say hi — we’d love to connect, share insights, and talk all things #ADPKD & #ARPKD ! #PatientEngagement
Come say hi — we’d love to connect, share insights, and talk all things #ADPKD & #ARPKD ! #PatientEngagement
🙋 Open to all in the rare disease community
🗓 22–24 May | 📍 Riga, Latvia
👉 go.eurordis.org/EMM25
#PatientVoice #RareDiseases #ARPKD
🙋 Open to all in the rare disease community
🗓 22–24 May | 📍 Riga, Latvia
👉 go.eurordis.org/EMM25
#PatientVoice #RareDiseases #ARPKD
We stand together to raise awareness for Autosomal Recessive Polycystic Kidney #ARPKD a rare genetic condition affecting children from birth.
To all affected: You are not alone. Your strength drives change.
#StrongerTogether @pkdinternational.bsky.social
We stand together to raise awareness for Autosomal Recessive Polycystic Kidney #ARPKD a rare genetic condition affecting children from birth.
To all affected: You are not alone. Your strength drives change.
#StrongerTogether @pkdinternational.bsky.social
Merry Christmas & Happy New Year! 🌟
Merry Christmas & Happy New Year! 🌟
A new chapter begins—stay tuned for the journey ahead! #ADPKD #ARPKD