We need rosacea sufferers to join our non profit organization and post in our member forum. If you have rosacea that would, of course, be helpful since you would be more empathetic to those who suffer from rosacea and would be able to post meaningful subjects. If you do not have rosacea you may be at least sympathetic and post some relevant subjects on rosacea in our member forum. If you would like to volunteer to post on rosacea subjects, that is what we need you to do.
The Rosacea Research & Development Institute [RRDi] is the first non-profit organization made by rosaceans for rosaceans that will collect donations for rosacea research to be performed by physicians and biomedical research scientists and includes these specific goals: Goal # 1: To be the first non profit organization for rosacea patient advocacy. Goal # 2: To have a majority of rosaceans the right to vote who sits on the board of directors. You can read the full statement at https://irosacea.org/mission/
The Rosacea Research & Development Institute [RRDi] is the first 501 (c) (3) non profit corporation established June 7, 2004 in the State of Hawaii, USA for the purpose of researching rosacea established by rosaceans for rosaceans. The Charter of the Corporation states the purpose and clearly outlines the goals of the corporation.
The RRDi is a member driven organization and invites rosaceans to become involved. Volunteering is the force that drives the organization and is an integral spirit of the RRDi philosophy. The RRDi warmly invites rosacean participation. Please join.
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