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DRESS Syndrome Foundation welcomes patients, their families and loved ones. We are a committed community of patients, providers and supporters.

You are not alone in your fight. 

Whether you are new to DRESS Syndrome or have been struggling with long-term complications, we believe a strong community and access to education about your condition can make a world of difference. We continue to forge relationships with experienced physicians and researchers in effort to keep you connected those who may help the most. 

Resources

           

  • Our patient community bravely shares their stories and struggles with  DRESS syndrome. Meet them here. >

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DRESS Syndrome Foundation is a 501(c)(3) nonprofit organization founded in 2020. 

Tax ID # (EIN): 84-3088907

Copyright 2023

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Legal: This website is for information purposes only and is not intended to diagnose or treat DRESS or any other type of disease. Every patient’s situation is unique. We are a patient advocacy organization and are not medically trained. Never disregard professional medical advice or delay seeking it because of something you’ve read on this site. In the hope of creating better awareness, we encourage you to share what you learn here with your medical team and others. If you think you may have a medical emergency, call your doctor or 911 immediately.  

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