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STEVENS-JOHNSON SYNDROME CANADA VIRTUAL “MOVE-A-THON” 

Walk, run, or bicycle!

We are moving our bodies in support of Stevens-Johnson Syndrome Canada (SJSC) from August 17-19 2023.

Join SJS Canada from ANYWHERE as part of our Virtual “Move-a-Thon.” 

SJS Canada is a non-profit organization that connects and supports survivors of Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) – rare, but life-threatening skin conditions.

 

Our founder and president Sonia W. Croasdaile, unfortunately was stricken with Stevens Johnson Syndrome and Toxic Epidermal Necrolysis (SJS/TEN) in 2011.

 

Her miraculous survival inspired her to create a well needed outlet to spread awareness about this life-threatening medical illness, that burns the body from inside out.

Here more about Sonia's story at PatientVoice.io
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