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reg-is-try [rej-uh-stree] 1. a place where data, records, or laboratory samples are kept and usually are made available for research or comparative study registry. (n.d.). Merriam-Webster's Medical Dictionary. Retrieved January 11, 2010, from Dictionary.com website
The more data we can collect, the better the information we can give to researchers, the sooner they can find better treatements, earlier diagnosis, and one day -- A CURE!! The Pemphigus-Pemphigoid Registry is designed to help the medical and research community understand illness trends, treatment outcomes, disease burden, and some important demographic information about patient(s) age and gender. With this vital information from large numbers of participants we can better advocate for resources to improve patient support and doctor education, and accelerate research discovery. ParticipatingIt takes about 15 minutes of your time to answer some simple treatment, medication, and lifestyle questions. That's it! Your information is collected, stored, and ready when researchers need data on pemphigus and pemphigoid patients. If you have not received your personal, email invitation and link from the IPPF, you have two choices: contact us and we'll send it out to you, or simply go ahead and enter your information in the registry. Stuff you'll needYou will want to get a few things ready before you begin.
Some Additional Things to Consider
QuestionsIf you have any questions, click the Ask a Question link and make sure to select REGISTRY for the Reason. We'll be happy to assist you and get you started right away! Want more information?NDRI Facilitates Major Medical Breakthrough ... in "A Rare Insight" July 2009 Registry Advocacy by Dr. Ani Sinha Tools in Cystic Fibrosis Fight: A Registry by Milt Freudenheim (NY Times)
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