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Our member forum is open to guests for free rosacea information, however, only members can POST. Because of the spammers and trolls we have securely quarantined our website not only from such nefarious individuals, but also especially for our registered subscribed private members who are seeking to deep dive into rosacea research and development. Our non profit grassroots patient advocacy organization is not sponsored by the skin industry (unlike other rosacea non profit organizations) and relies totally on whether members donate two dollars a month (or $1/month for three or more months if you subscribe) to keep this website and non profit organization going. If you care to donate and deep dive into our member forum which has 95% of our rosacea data, please subscribe. Spammers and trolls, please read our rules and go somewhere else. If you have rosacea you are a rosacean and have found the only grassroots patient advocacy non profit organization for rosacea sufferers. Guest sub-forums are found below: Guests or Feedback • We need 100 Active Subscribers! This would keep our non profit organization going keeping the lights on. Running a non profit organization does indeed cost money and we rely on our members, not the skin industry.
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Welcome to the RRDi. Tell us about your rosacea please with a post.· 0 replies
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Welcome to the RRDi. Are you a registered nurse and have rosacea? Are you willing to volunteer for our non profit?· 0 replies
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Hey Fraziertown, welcome to the RRDi. Can you post something about what concerns you with your rosacea? We are here to help.· 0 replies
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