Englishspeaking readers will find lots of information on EM/SJS/TEN from the american site http://www.sjsupport.org/

In Sweden with its' 9 million inhabitants there are not so many diagnosed with EM/SJS/TEN. We don't yet have information on the great variation in the horrors of EM/SJS/TEN. Would you mind sharing your story on this site? To avoid misdiagnosis and to give so much information as possible for those suffering from EM/SJS/TEN in these nordic countries. I also would like to have your permission to translate your story into swedish. Thank you so much for helping out.


All over the world people are, can and will be affected by EM/SJS/TEN -usually caused by adverse reactions to either a drug, chemical or virus. In severe cases, SJS/TEN attacks the skin and mucous membranes. The result can be blindness or even death.
Physicians are often unfamiliar with the condition, which can lead to an initial misdiagnosis.
EM/SJS/TEN remains relatively unknown also to the public.
 
The best way to spread the word is to share our storys.
Early diagnosis and appropriate management to avoid permanent damage, is one of our aims.
Please, share Your story - email me for publishing.
Make it long, or just a short resume.
Anonymous if you wish.
Maybe these questions can help you getting started?


 
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