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Meghan Garcia

Parent of DRESS Syndrome survivor

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Meghan lives in Phoenix, Arizona, where she is a mother and a Certified Forensic Peer Support Specialist. She is the devoted mom of two boys — Jacob (17) and Imperial (7), a pediatric DRESS Syndrome survivor.

 

In 2024, Imperial developed DRESS after taking sulfasalazine, and Meghan now cares for him full time, guiding his ongoing recovery and medical care. As part of the DRESS Patient Panel, Meghan shares her family’s experience to help raise awareness and improve understanding of this complex condition.

 

Passionate about community support, she reminds parents and patients that their voices matter — that awareness and education, especially among prescribing doctors, can save lives. Meghan also advocates for broader recognition of how DRESS can present across different skin tones, ensuring that all patients are accurately diagnosed and represented in medical education.

 

In her spare time, Meghan enjoys entertaining for family, gardening, and arts and crafts. She hopes her story helps other families feel seen, heard, and empowered to speak up.

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

 

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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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