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Neil Minkoff; Natasha Mesinkovska, MD; and Brett King, MD, PhD discuss the diagnosis and disease assessment in alopecia areata along with clinical considerations.

Key opinion leaders provide their final thoughts on the current disease state of endometriosis, as well as opportunities forthcoming for treatment management.

The panel shares recommendations for standardization of early education regarding endometriosis.

Dr Lopes requests panelists to share opportunities for improving disease state awareness for endometriosis.

Key opinion leaders discuss barriers regarding endometriosis, as well as opportunities to alleviate these challenges to optimize patient care.

The panel explores common disparities in the medical community impacting care for patients with endometriosis.

Expert panelists navigate patient needs and describe how to achieve successful endometriosis management from a patient perspective.

Dr Lopes leads a discussion surrounding payer considerations with an emphasis on patient-centered care in endometriosis management.

Amber Hagen, NP; Eric Surrey, MD; and Tara Hilton navigate various treatment pathways for endometriosis, including medical and surgical interventions.

Dr Surrey provides perspective regarding guideline-directed treatment options for endometriosis.

Amber Hagen, NP, and Tara Hilton provide insights on the diverse landscape and variability for treatment of endometriosis.

First-line therapies for endometriosis are explored, including drug treatment and surgical options.

A panel of experts illustrate risk factors contributing to endometriosis, as well as associated burdens affecting patients.

Maria Lopes, MD, MS, leads a panel of experts in a discussion surrounding clinical and patient burden associated with endometriosis.

A moderated digital open forum facilitating an interactive discussion among health care professionals, health system executives, health care payers, and health policy influencers about promise and the barriers to the expanded use of biosimilars in ophthalmic applications.

15-year-old Matthew and his parents share personal advice for young patients with alopecia and their caregivers.

Matthew and his parents reflect on challenges they experienced with finding information and positive social support online during the COVID-19 pandemic.

Jamie and Tony share their experiences with supporting a young patient with alopecia and emphasize the importance of emotional support for the whole family.

A patient and his family discuss the emotional, social, and financial burdens associated with treating adolescent-onset alopecia.

Matthew and his parents share insights into the challenges they experienced while trying therapies to treat his alopecia.

15-year-old Matthew and his parents discuss the initial signs of alopecia that they noticed in their son and reflect on the effect his diagnosis has had on the family.

Peyton shares advice for young people with newly diagnosed alopecia areata and urges patients to embrace humor when they can.

Peyton reflects on the changes alopecia areata brought to her morning routine and how she enjoys the diversity it brings her.

14-year-old Peyton, a patient with alopecia areata, comments on the difficulties she’s encountered and how her diagnosis actually improved aspects of her life.

Peyton recalls being diagnosed with alopecia areata at age 8 and her decision to embrace her hair loss instead of pursuing more than 1 therapy.

Ebony explains the importance of a supportive network when living with alopecia areata and shares some advice for the newly diagnosed

Ebony reflects on how living with alopecia areata has affected her personal relationships and how she learned to navigate them.

Ebony describes the lifestyle modifications she made after her alopecia areata diagnosis, including her daily makeup routine.

Ebony explains challenges that significantly affect her day-to-day life such as social discrimination.