Stevens Johnson Syndrome

Stevens Johnson Syndrome Non profit organization dedicated to promoting Stevens - Johnson Syndrome awareness and research
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Do you know the signs of Stevens-Johnson Syndrome?Early recognition can save lives.Fact sheet:https://sjsupport.org/wp-c...
05/13/2026

Do you know the signs of Stevens-Johnson Syndrome?

Early recognition can save lives.

Fact sheet:
https://sjsupport.org/wp-content/uploads/2023/08/SJS-Fact-Sheet-2023.pdf

Hope. Healing. A future worth fighting for.

Right now, families facing Stevens-Johnson Syndrome are going through some of the hardest days of their lives. This is a serious, life-threatening condition that can change everything very quickly. But with awareness, support, and research, no one has to go through it alone.

Your support helps make a real difference by providing:
• Support for patients and families
• Funding for important research
• Education that can help save lives

Every dollar truly matters.

If you’ve ever wondered how to help, this is one way.

Be the light. Be the hope. Be the reason someone keeps going.

Donate here:
https://bit.ly/SJS-Foundation-Donation

Learn more & get support:
https://sjsupport.org
https://sjskidsupport.org

Together, we can turn pain into strength and hope into healing.

💙 Hope. Healing. A Future Worth Fighting For. 💙Right now, families facing Stevens-Johnson Syndrome are navigating some o...
05/01/2026

💙 Hope. Healing. A Future Worth Fighting For. 💙

Right now, families facing Stevens-Johnson Syndrome are navigating some of the hardest days of their lives. This devastating condition can change everything in an instant, but with your help, they don’t have to face it alone.

Your donation provides:
✨ Support for patients and families
🔬 Funding for critical research
📣 Life-saving awareness and education

Every single dollar makes a real difference.

If you’ve ever wondered how you can help, this is it.
Be the light. Be the hope. Be the reason someone keeps going.

❤️ Donate today: https://bit.ly/SJS-Foundation-Donation ❤️

Together, we can turn pain into strength and hope into healing.

The Stevens-Johnson Syndrome Foundation is facing a critical lack of funding, and we urgently need donations to keep goi...
04/28/2026

The Stevens-Johnson Syndrome Foundation is facing a critical lack of funding, and we urgently need donations to keep going. This foundation provides vital support, education, and awareness for this life-threatening condition that impacts so many families.

Without funding, these resources, and the hope they bring, are at risk.

Please consider donating today: https://bit.ly/SJS-Foundation-Donation

Every dollar makes a difference and helps us continue spreading awareness, supporting those affected, and saving lives.

Together, we can keep this mission alive. ❤️

Due to limited funding, the Stevens-Johnson Syndrome Foundation has had to make the difficult decision to close our post...
04/16/2026

Due to limited funding, the Stevens-Johnson Syndrome Foundation has had to make the difficult decision to close our post office box. This was not an easy choice, as we deeply value every connection and piece of correspondence we receive from our community. At this time, mail sent to our previous P.O. box is unfortunately being returned to sender.

We kindly ask for your support in updating your records and sending all future correspondence to our physical mailing address:

Stevens-Johnson Syndrome Foundation
3713 W 85th Avenue
Westminster, CO 80031

Your continued support, connection, and care mean so much to us and to the individuals and families we serve. Thank you for being an important part of our community.

03/28/2026

Stevens-Johnson Syndrome (SJS) is often misdiagnosed and can quickly become life-threatening. The Stevens-Johnson Syndrome Foundation works to raise awareness, support patients and families, and fund education so earlier diagnosis can save lives.

Your donation helps provide resources, advocacy, and hope to those affected by SJS and Toxic Epidermal Necrolysis. Every dollar helps spread awareness and support survivors.

Please consider donating and helping us make a difference.

For the past 30 years, our mission has remained clear: to educate, support, and advocate for individuals and families af...
03/02/2026

For the past 30 years, our mission has remained clear: to educate, support, and advocate for individuals and families affected by Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN).

What started in 1994, when 11-month-old Julie was diagnosed with Stevens-Johnson Syndrome, became the beginning of something much greater. Her mother, Jean, was told she would likely never meet another person affected by SJS. But Jean was determined to change that. She was determined to connect families and ensure that no one would ever have to go through SJS alone.

What began with one family and a mother’s unwavering determination has grown into a global mission — a community of survivors, caregivers, medical professionals, and advocates standing together in support and awareness.

Over the past 30 years, we have:
💙 Provided trusted educational resources
💙 Connected survivors and families worldwide
💙 Raised critical awareness about adverse drug reactions
💙 Supported research and medical outreach

As we celebrate this 30-year milestone, we also recognize a challenging reality. Since the pandemic, funding has been significantly limited. Like many nonprofits, we rely heavily on individual donations to continue our vital work. Every resource we provide, every family we connect, and every awareness effort we lead is made possible through the generosity of our supporters.

To continue spreading awareness, connecting patients and families, and advancing education about SJS and TEN, we need your help.

Please consider supporting our 30th Anniversary Campaign:
https://bit.ly/SJS-Foundation-Donation

Your donation directly sustains our mission and ensures that no one faces Stevens-Johnson Syndrome alone.

Thank you for standing with us, for sharing our mission, and for helping us continue to make a difference.

Awareness Saves Lives.
1996–2026 | 30 Years Strong 💙

For three decades, our mission has remained clear: to educate, support, and advocate for individuals and families affect...
03/01/2026

For three decades, our mission has remained clear: to educate, support, and advocate for individuals and families affected by Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN).

What began as one family’s determination to bring awareness to a devastating condition has grown into a global community of survivors, caregivers, medical professionals, and supporters. Together, we have worked to ensure that no one faces SJS alone.

Over the past 30 years, we have:
💙 Provided trusted educational resources
💙 Connected survivors and families worldwide
💙 Raised critical awareness about adverse drug reactions
💙 Supported research and medical outreach

As we celebrate this 30-year milestone, we also recognize a challenging reality. Since the pandemic, funding has been significantly limited. Like many nonprofits, we rely heavily on individual donations to continue our vital work. Every resource we provide, every family we connect, and every awareness effort we lead is made possible through the generosity of our supporters.

To continue spreading awareness, connecting patients and families, and advancing education about SJS and TEN, we need your help.

Please consider supporting our 30th Anniversary Campaign:
https://bit.ly/SJS-Foundation-Donation

Your donation directly sustains our mission and ensures that no one faces Stevens-Johnson Syndrome alone.

Thank you for standing with us, for sharing our mission, and for helping us continue to make a difference.

Awareness Saves Lives.
1996–2026 | 30 Years Strong 💙

I Am a Warrior, One in a MillionIt’s not just a statistic — it’s a life that is forever impacted, a family, a story. Ste...
02/28/2026

I Am a Warrior, One in a Million

It’s not just a statistic — it’s a life that is forever impacted, a family, a story. Stevens-Johnson Syndrome (SJS) changes lives forever. On Rare Disease Day, we honor the strength of those impacted and continue our mission to educate, support, and advocate. We are lighting the way to hope for every patient and family affected.

Learn more, get involved, and support our work: 💙 Donate here: https://bit.ly/SJS-Foundation-Donation

Someone I Love Is One in a MillionIt’s not just a statistic, it’s someone’s child, parent, spouse, sibling, partner, bes...
02/28/2026

Someone I Love Is One in a Million

It’s not just a statistic, it’s someone’s child, parent, spouse, sibling, partner, best friend. It’s a life filled with strength, courage, and resilience.

On Rare Disease Day, we stand in love and solidarity with those impacted by Stevens-Johnson Syndrome (SJS). We honor their journeys and are deeply thankful for the support of families and friends who walk alongside them. We continue our mission to educate, support, and advocate for awareness and early recognition.

Learn more, get involved, and help us make a difference:
💙 Donate here: https://bit.ly/SJS-Foundation-Donation

One in a Million. Forever in Our Hearts.Behind every SJS/TEN diagnosis is a name, a smile, a family who loves deeply, an...
02/28/2026

One in a Million. Forever in Our Hearts.

Behind every SJS/TEN diagnosis is a name, a smile, a family who loves deeply, and a story that will never be forgotten. Today, we remember and honor the lives touched by Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN).

On Rare Disease Day, we stand in remembrance of those we have lost and in solidarity with the families who continue to carry their legacy forward. Your strength, love, and advocacy matter.

Together, we remain committed to raising awareness, promoting early recognition, and supporting families impacted by SJS/TEN.

Learn more, get involved, and help us continue this important work:
💙 Donate here: https://bit.ly/SJS-Foundation-Donation

Address

3713 W 85th Avenue
Westminster, CO
80031

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