CheckRare

CheckRare was proud to cover the 2024 WMS Meeting in Prague 📹 Check out our website for interviews from the meeting! #CheckRare #RareDiseases #WMS2024

Patty Ketting, Executive Director of the HypoPARAthyroidism Association and a patient with hypoparathyroidism, discusses challenges of hypoparathyroidism. #CheckRare #RareDisease #Hypoparathyroidism https://lnkd.in/essV6svm

Kristina Allikmets, MD, PhD, Senior Vice President, Head of R&D for the Plasma-Derived Therapies Business Unit at Takeda, discusses a breakthrough therapy for the treatment of CIDP. #CheckRare #RareDisease #CIDP https://lnkd.in/eu58Wadm

Michelle Reyes, Associate Director of the HypoPARAthyroidism Association and patient with the disease, discusses living with hypoparathyroidism and how the HypoPARAthyroidism Association can help. #CheckRare #RareDisease #Hypoparathyroidism HypoPARAthyroidism Association https://lnkd.in/e2m6ykER

Aromatic L-amino acid decarboxylase #AADC deficiency is a rare genetic disorder that affects the central nervous systems of young patients Check out our learning page for more information #checkrare Center for Rare Neurological Diseases https://lnkd.in/gnE79Nm

"Tools are keys... With the right key, any complicated lock can be opened." Marshall Thompson, Senior Manager, Digital Marketing, Alnylam Pharmaceuticals, presents a case study to help identify PH-1 patients in his talk: Upgrade your social media marketing campaigns with Generative AI imagery at Reuters' Pharma Customer Engagement USA. #RECustomerUSA #Alynylam

Polyzois Makras, MD, PhD, Endocrinologist with the Hellenic Air Force & VA General Hospital, gives an overview of Langerhans cell histiocytosis #LCH #CheckRare #RareDisease https://lnkd.in/eEw6XD4N

Mohamed Ladha, President and General Manager of Recordati Rare Diseases, discusses the company’s involvement in the rare disease community. #CheckRare #RareDisease #RecordatiRareDiseases https://lnkd.in/d_Ef3DGd

🩺 Early diagnosis and intervention in Fabry disease can be life-changing. By catching this rare disease early, health care providers can better manage symptoms and improve patient outcomes. 💪 Join us in our latest podcast featuring William Burns, MD (Greenwood Genetic Center), Nicola Longo, MD (University of Utah School of Medicine), and patient advocate, Maya Kineen. #FabryDisease #RareDisease #EarlyDiagnosis #CheckRare Canadian Fabry Association Fabry Support & Information Group https://lnkd.in/egiDdMay

NORD CEO Pam Gavin opens up Day 2 of the #NORDSummit with a Fireside Chat: From Drug Approval to Patient Access featuring Robert M. Califf, MD, Commissioner of the US Food and Drug Administration #FDA and Meena Seshamani, MD, PhD, Deputy Administrator and Director of the Center for Medicare at the Centers for Medicare and Medicaid Services #CMS #RareDiseases