Skin Disease for Clinicians

About this session:

Victoria Werth, M.D., will discuss the identification and treatment of skin manifestations associated with dermatomyositis, including diagnostic criteria, various skin manifestations, and the latest treatment approaches and insights into the complexities of managing dermatomyositis, aiming to improve patient outcomes and quality of life.

About Dr. Werth:

Dr. Werth is a Professor of Dermatology and Medicine at the University of Pennsylvania School of Medicine and Chief of the Division of Dermatology at the Philadelphia Veterans Administration Hospital. Dr. Werth earned her medical degree from Johns Hopkins University School of Medicine in Baltimore, Maryland. Her professional achievements include being recognized for her groundbreaking research in autoimmune skin diseases, particularly in the areas of lupus and dermatomyositis. She has also published extensively in top-tier medical journals, presented her work at major scientific conferences, and received numerous awards and honors for her contributions to dermatology and autoimmune diseases.

Clinician's September Summit 2024

Cure JM September 2024 – Virtual Summit

We are pleased to invite all juvenile dermatomyositis healthcare professionals to join us virtually for the latest presentations, sharing clinical best practices to help providers diagnose, treat, and care for juvenile myositis patients.

Early Promising Data Presented in Car-T for Myositis

Cabaletta Bio Presents Promising Early Data on CAR-T Therapy for Myositis

We expected to hear promising news about the potential for CAR-T therapy to treat myositis at the Global Conference on Myositis (GCOM).

What we heard was more than promising—it was astounding.

What if I told you that there was a therapy that would “reset” the immune system—virtually eliminating the autoimmune response in myositis that causes inflammation, pain, muscle weakness, and other JM conditions of which we are all too familiar.

Join Cure JM

Membership is free and we’ll connect you with a network of support, encouragement, and resources.

Cure JM supports families, patients, and the juvenile myositis research community.

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