The Rosacea Research & Development Institute [RRDi] is the first 501 (c) (3) non profit organization approved by the IRS established June 7, 2004 in the State of Hawaii, USA for the purpose of finding a cure for rosacea, researching rosacea, and to form a patient advocacy organization established by volunteer rosaceans for rosacea sufferers. What is the difference between our non profit for rosacea and all the others? We are rosacea sufferers [rosaceans].
All the other rosacea non profits are not run by rosacea sufferers (see Other Non Profit Rosacea Organizations on this page). Check out the other non profit organizations for rosacea, discover for yourself and you will find out who serve on the board of directors (non rosaceans) and then simply follow the money (what does the organization spend its money on the most?). We have no special interest other than finding the cure for rosacea. Our non profit has no salaries, no spending on private contractors, no expenses for member conventions. Follow the money (this is where we spend our money). Notice where most of the money is spent with another rosacea non profit.
Read our Misson Statement and see if you agree? If you suffer from rosacea, this is the rosacea non profit to join. Your membership increases our impact on the medical community. Our goal is to reach 10,000 members. Please join and help us reach our goal.
The Only 501 (c) 3 Non Profit Organization Founded by Rosaceans [rosacea sufferers] for Rosaceans in the State of Hawaii, USA
All the other rosacea non profits are founded and directed by non rosacea sufferers.
The RRDi is registered at GuideStar
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