Bill McCue

We begin PRP 101 with the basics. Whether you are a newly diagnosed patient or supportive caregiver (spouse, partner, parent, family or friend), or a more “seasoned traveler”, the questions we hear most often fall conveniently into two categories: ❏½ Questions with answers you WANT to know ❏½ Questions with answers you NEED to know

Lorna Roberts, Eugene, Oregon In 2002, I became a member of the PRP Support Group, the, “you got mail” version. Tierney was there, along with, Jean Luc, Richard Greene, Carolyn Brown, Ralph Gilmore and Smitty, and others. I recall Tierney’s children were young. My interaction with Tierney was limited until the PRP Facebook Support Group

Jan Tenant, Ringwood, New Jersey. The first thing I did when I got my official diagnosis was to write a long letter to my family and friends to tell them what I had been going through with this mystery disease, PRP. The second thing was to join the PRP Facebook Support Group. It was Tierney

This section of Tierney’s Memorial is an opportunity for PRP patients and caregivers to expand their remembrances beyond 500 and even 1,000 words. Please use “Leave a Reply” at the end of this webpage to submit your stories via email to: Imagine, if you will, that Tierney’s friends and family assemble in a living room

The Happy Dance for Tierney This section of Tierney’s Memorial provides EVERYONE with the opportunity to tell stories that will make everyone else smile. Either use “Leave a Reply” to share a ‘laughable moment” where Tierney laughed or made you laugh. You may also send your “laughable moment” to [email protected].   Going to let Tierney

Tierney has been part of my PRP journey from the day I was diagnosed with PRP (November 28, 2012), the day I joined the email-based PRP Support Group, became a subscriber to their list serve and began reading “sharings” from her and others. Whatever the question, she always responded with kindness and concern. The moment