PRP Alliance

PRP Alliance

June 2017

What are the SIX “types” of PRP?

The initial five classifications of pityriasis rubra pilaris, were presented to the British Association of Dermatologists in 2003 by Dr. Andrew Griffith, a well-respected London-based dermatologist. His classifications reflected 35 years of diagnosing, treating and researching PRP and have been universally accepted by dermatologists worldwide. According to Griffiths, the PRP patient population can be divided into two categories based on the […]

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PRP and Stress

From the Editor… The National Psoriasis Foundation offers information on stress that may be applicable to pityriasis rubra pilaris. Here are some takeways: ✽  Stress is a common trigger for a psoriasis flare. At the same time, a psoriasis flare can cause stress. ✽  Woman, in particular, seem particularly vulnerable to stress due to psoriasis.According

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Terms of Use

Welcome to the PRP (Pityriasis Rubra Pilaris) website. By continuing to browse this website you are agreeing to comply with and be bound by the following terms and conditions of use. These terms, along with our privacy policy, govern the relationship between the PRP Alliance and users of this website. The term “PRP Alliance” or

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Copyright Notice

All rights reserved © 2013, 2014, 2015, 2016, 2017 by PRP Alliance, Inc., Plano, Texas. The contents of this website cannot be reproduced or copied in any manner other than electronically, and only to the extent necessary to read it on the World Wide Web. The information presented at the PRP Alliance website may not

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General The PRP (Pityriasis Rubra Pilaris) Alliance website is designed for educational purposes only and not for the purpose of rendering medical advice. It is not the intention of the PRP Alliance website to provide specific medical advice, but rather to provide users with information to better understand their disease and treatment options. Because each

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Privacy Statement

SCOPE The PRP Alliance (PRPA) is a nonprofit 501(c)(3) tax-exempt organization devoted to assisting individuals diagnosed  with the pityriasis rubra pilaris (PRP) and their caregivers. PRPA provides information and education to both the lay and the professional communities, advocates on behalf of its members in the political and healthcare arenas, and serves as a “bridge”

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Clothing — Delasco

From the Editor… On January 26, 2017, Jan T (Ringwood, NJ), posted a message to members of the PRP Facebook Support Group regarding clothing.  The feedback she received is well worth including in the PRP Survival Guide. I have attended three annual meetings of the American Academy of Dermatology (Denver, San Francisco and Orlando). Delasco always has

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