SJS Awareness Month Challenges | This is how you can join the fight.
During August, we have some challenges you can join to support us in our fight. Check it out. August 3rd Sunglasses Day Challenge:...
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hiep725
Jan 291 min read
Memorial Video 2: In Loving Memory
https://youtu.be/rocX38HOUjE
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sjsandtensgroupcan
Oct 13, 20211 min read
Supportive Counselling & Education for survivors, families and friends.
Attention SJS survivors & care supporters Coming winter 2024 : to secure your spot Email: info@sjscanada.org Our FREE four weeks...
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sjsandtensgroupcan
Sep 20, 20211 min read
Julie’s story
Meet Julie who miraculously survived SJS/TEN, not once but twice. With the help of her supportive mother Jean, Julie now uses her story...
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sjsandtensgroupcan
Aug 1, 20212 min read
YC’s story
I was a completely healthy individual until I got the flu vaccine in October 2019. I was tired and a little achy the next couple of days...
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sjsandtensgroupcan
Aug 1, 20212 min read
Jeremy’s story
I had a bacterial infection in 2005. After 13 days of taking antibiotics, I developed a lot of bumps on my body, my face swelled up, my...
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sjsandtensgroupcan
Mar 16, 20214 min read
Kathleen’s story
My name is Kathleen, and I am from Washington, USA, just north of Portland, Oregon. I had my first reaction to Steven Johnson Syndrome...
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sjsandtensgroupcan
Mar 16, 20213 min read
Anastasia’s Story
I was diagnosed with TEN in early 2016 when I was 28 years old. I was 5th grade teacher at the time, I loved hiking and bike riding, and...
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sjsandtensgroupcan
Feb 12, 20211 min read
SJS Canada founder Featured on Toronto’s The Scoop
SJS Founder, Sonia Whyte-Croasdaile was featured on Toronto’s news and entertainment show, The Scoop. Sonia took the liberty to help...
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sjsandtensgroupcan
Aug 17, 20205 min read
Jane’s story
IT’S TROUBLING TIMES WHEN THE SOLUTION BECOMES THE PROBLEM………. My name is Jane Grady and I’m an SJS/TEN survivor. I was prescribed a...
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sjsandtensgroupcan
Aug 12, 20201 min read
AUGUST is Stevens-Johnson Syndrome Awareness month
The month of August is Stevens Johnson Syndrome Awareness Month in the USA. We wish to join our allies and combine our voices to spread...
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sjsandtensgroupcan
Aug 4, 20205 min read
Jennifer’s Story
My name is Jennifer Lane. I have just turned 48, and this is my SJS/Ten story. It all started on August 1, 2017. I was in Clear Lane, MB...
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sjsandtensgroupcan
May 31, 20201 min read
STUDIES ON GENETICS
A Research titled: – STUDIES ON GENETICS is currently been conducted by: Dr. Bruce Carleton Chair, Division of Translational...
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sjsandtensgroupcan
Feb 25, 20202 min read
Bruce’s Story
Late February 2005, I developed symptoms of fever, headache, and nasal congestion. To alleviate my symptoms, I decided to take different...
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sjsandtensgroupcan
Feb 24, 20191 min read
SJS Annual General Meeting
Thank you to everyone who joined us for our AGM in May Below are some images from the event! Photos of our 2018 Annual General Meeting
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sjsandtensgroupcan
Feb 23, 20192 min read
Kim’s Story
The impact of Stevens Johnson Syndrome affects each victim differently depending on the severity and duration of the illness. Here’s one...
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sjsandtensgroupcan
Mar 2, 20181 min read
The Lonely Path To Recovery
Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) represent different degrees of a severe, acute, life-threatening...
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