Email & Social Media
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The National Rosacea Society is active on social media, where you may also connect with other rosacea patients and people interested in the disorder. Follow us on Facebook, Twitter, Pinterest and YouTube!
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Please take a moment to give us your email address, and you'll be among the first to receive timely news and information on rosacea, as well as access to new educational materials, free product samples, discounts and opportunities to participate in research. You can also become a member and help support the NRS research grants program, receive our quarterly Rosacea Review newsletter, educational materials and more!
196 James St.
Barrington, IL 60010
The National Rosacea Society is a 501(c)(3) nonprofit organization whose mission is to improve the lives of people with rosacea by raising awareness, providing public health information and supporting medical research on this widespread but little-known disorder. The information the Society provides should not be considered medical advice, nor is it intended to replace
consultation with a qualified physician. The Society does not evaluate, endorse or recommend any particular medications, products, equipment or treatments. Rosacea may vary substantially from one patient to another, and treatment must be tailored by a physician for each individual case. For more information, visit About Us.