#Webinar Patient Guide To Clinical Trials And Drug Development: Phases And Terminology Explained Date posted: February 15, 2023 Speaker: Danielle Quarles, Director of Clinical Operations, Sana Biotechnology Have you read announcements for clinical trials but don’t quite understand what they mean? Do you want to feel comfortable advocating for yourself when discussing clinical trial options with your doctor? Join us to learn about drug development including how…
#Webinar JAK Inhibitor Treatment for Alopecia Areata: Understanding Side Effects and Monitoring Date posted: January 18, 2023 Speaker: Maryanne Senna, MD - Assistant Professor of Dermatology, Harvard Medical School Director, Lahey Hair Loss Center of Excellence and Research Unit, Beth Israel Lahey Health JAK Inhibitor Treatment for Alopecia Areata: Understanding Side Effects and Monitoring Learn more about JAK inhibitors for the treatment of alopecia areata. Dr. Maryanne Senna will explain the warning labels on JAK inhibitors, where they come from, and what is…
#Webinar Hanging With Our Young Alopecians Date posted: December 7, 2022 Speaker: Georgia Van Cuylenberg Alopecians are superheroes and Georgia Van Cuylenburg believes our young Alopecians are the Elite Squad! In this month’s webinar, we invite you to join a panel of young Alopecians in a safe and supportive space where we can talk about…
#Community Voice Kristen Turner Date posted: January 31, 2023 Speaker: Kristen Turner One thing about alopecia areata I wish my friends knew is: I’ll have good days and bad days and sometimes those bad days I don’t want to be around anyone, even when I love them dearly. One thing about alopecia…
#Community Voice Noelle Ariana Date posted: January 31, 2023 One thing about alopecia areata I wish my friends knew is: Hair loss is mentally devastating. ESPECIALLY, sudden and unpredictable hair loss that comes with having Alopecia Areata. Check in with me. A day or night with friends makes me…
#Community Voice Courtney Hays Date posted: January 31, 2023 Speaker: Courtney Hays One thing about alopecia areata I wish my friends knew is: Don’t ignore it, instead acknowledge it. Ask them how their doing, but give them space if the need it. Don’t make judgements. Avoid comparisons. Encourage new hobbies. Listen to…