​Global SJS Awareness Month: August

August – A Month of Awareness, Advocacy, and Action

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Every August, SJS Canada joins organizations and individuals around the world to recognize Global Stevens-Johnson Syndrome (SJS) Awareness Month.  A time dedicated to shining a light on Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN). These rare but severe reactions, most often triggered by medications, can be life-threatening and leave survivors with long-term physical and emotional impacts.

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Why Awareness Matters

Early recognition of symptoms is critical to improving outcomes. Increased awareness among the public and healthcare professionals can lead to faster diagnosis, better treatment, and fewer preventable cases. By educating others, we can help save lives and reduce suffering.

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Our Goals During Awareness Month

• Educate about the signs, risks, and long-term effects of SJS/TEN

• Empower survivors and families to share their stories and connect with others

• Advocate for safer prescribing practices and stronger patient protections

• Engage communities through events, campaigns, and social media outreach

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How You Can Get Involved

• Join our events – including our annual Virtual SJS/TEN Educational Webinar and Move/Walk/Run happening mid to late summer

• Share your story – Survivor voices bring powerful awareness and connection

• Spread the word on social media using our downloadable graphics and hashtags

• Attend our Canada Day booth at Lion’s Park in Brantford (July 1st) to kick off the conversation early

• Support our Membership Drive – Help us grow and sustain our work year-round

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Together, We Are Stronger

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SJS Awareness Month is not just about information—it’s about community, compassion, and action. Whether you're a survivor, caregiver, healthcare professional, or supporter, your voice

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