Self-Advocacy Principle 4
Keep Careful Track of Health InformationPrinciple 4 Editor’s Note — The unveiling of Principle 4 is scheduled for January 26, 2023
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Keep Careful Track of Health InformationPrinciple 4 Editor’s Note — The unveiling of Principle 4 is scheduled for January 26, 2023
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Make the Most Out of Every Office Visit Editor’s Note — The unveiling of Principle 3 is scheduled for January 12, 2022.
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Principle 1Build a Strong Healthcare Team EDITOR, PRP SURVIVAL GUIDE — The authors of “Standing Up for Your Health: Self-advocacy for patients with rare diseases” want patients with a rare disease to THINK TEAM. The consensus among PRP patients and caregivers, however, is that healthcare professionals involved in the treatment of pityriasis rubra pilaris are
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I need your help to continue identifying 100 questions that PRP patients and their caregivers either (a) need to know or (b) want to know. In so doing, 100 Questions will be become the “official” tutorial for and by PRP patients and caregivers. ✓ STEP ONE — Identify the specific questions or general topics ✓ STEP TWO — Organize the questions
Archived — 100 Questions Read More »
There is no excerpt because this is a protected post.
Protected: Tierney: The Global Vigil Continues Read More »
On the passing of Tierney Lynch Ratti Condolences from the Land of Hope were swift and sincere. Tierney had left a mark on the PRP global community. Laura N, Kingston upon Hull, Yorkshire, England Very sad news, thinking of her family and friends. Rest in peace now. Frank B, Kitchener, Ontario, Canada You were such
Rest in Peace Continued Read More »
A personal remembrance of my Tonto by Bill McCue September 22, 2020 Tierney Lynch Ratti has been part of my PRP journey from the day I was diagnosed with PRP (November 28, 2012) and joined the old email-based PRP support group, became a subscriber to their list serve and began reading “sharings” from her and
Bill McCue Testimonial to Tierney Read More »
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Protected: 2020-2021 Rare Skin Referral Initiative Read More »
Caring, Sharing and COUNTING. Tierney was more than just caring and sharing. She wanted PRP patients to “Stand up and be counted”. This section of Tierney’s Memorial asks PRP patients/caregivers to update their patient profiles and identify PRP-savvy dermatologists. Just another way to say “Thank You” to Tierney. LINK TO 2020 PRP GLOBAL CENSUS
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Tierney’s Story (circa 1994) Tierney Ratti did not formally chronicle her PRP journey beyond the following letter. 30 November 1994 Dear Lady and Gentlemen: After being diagnosed with pityriasis rubra pilaris in October, I contacted the National Organization for Rare Disorders, Inc., and was given your names as others with this disease. I have spoken
Tierney’s Story through 1995 Read More »