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Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are severe skin conditions that can be life-altering and challenging. However, amidst these challenges, there are countless stories of hope, resilience, and survival that inspire and provide support to others facing similar battles. The SJS Awareness UK aims to spread awareness and share resources on treatment for SJS , helping individuals and families navigate this difficult journey. Understanding SJS/TEN SJ

In this video, our goal is to improve the publics understanding of how an individuals genetic makeup affects their risk of harm from side effects of medication and how the Yellow Card Biobank Projects aims to research this matter, especially regarding the medication Allopurinol.

In this heartfelt video, Nadia Lawson, the founder of SJS Awareness UK, shares her personal journey with Stevens-Johnson Syndrome (SJS), a journey that has not only tested her strength but also inspired her to advocate for others affected by this serious condition. From the initial diagnosis and the challenging treatment process to her ongoing recovery and advocacy work, Nadia offers a deeply personal look at the realities of living with SJS. Her story is one of resilience an