• Skip to main content
  • Skip to footer
VIEW MENUMENU
  • Pachyonychia Congenita
        • What Is Pachyonychia Congenita?
          • Could I Have PC?
          • Getting Diagnosed
          • Genetics
          • Image Library
          • Glossary
          • Brochures
          • Patient Stories
        • Patient Registry (IPCRR)
          • Patient Registry Data
        • Understanding my Genetic Testing Results
          • K6a-pEDD-PC
          • K6b-pEDD-PC
          • K6c-pEDD-PC
          • K16-pEDD-PC
          • K17-pEDD-PC
          • Non-PC Palmoplantar EDDs
        • Managing and Caring For PC
          • Tips and Tools
          • Living With PC
          • PC & Children
          • Working With Medical Professionals
          • Family & Friends: How To Help
          • Video Library
  • For Professionals
        • For Professionals
          • International PC Consortium
          • Pharmaceutical Partners
          • Refer a Patient
          • Patient Registry (IPCRR)
            • Patient Registry Data
            • Non-PC Palmoplantar EDDs
          • Advocacy Partners
        • PC Research
          • Apply for a Grant
          • Awarded Grants
          • Published Research Articles
          • Clinical Trials
        • Patient Voices
          • Quality of Life
          • Patient Stories
          • Patient-Focused Drug Development Meeting
  • Ways To Give
        • Ways You Can Give
          • Donate
          • Donate Just Giving UK
          • Steady Relief Circle
          • Donor-Advised Fund
          • Giving Stock
          • Legacy Society
        • Raise Awareness
          • How You Can Help
          • Fundraising Ideas
          • Share Your Story
          • PC Advocates
          • Volunteer
        • 2025 Donor Gratitude Wall
  • News & Events
        • News
          • Current Newsletter
          • Newsletter Archives
          • Sign up for our Newsletter
        • Events
          • Patient Support Meetings
          • IPCC Meetings
          • Video Library
  • About Us
        • About PC Project
        • Medical and Scientific Advisory Board
        • Financial & Legal Information
        • Contact Us

Welcoming Five New Leaders to the PC Project Board!

July 2, 2025

We’re thrilled to announce the addition of five exceptional new members to the PC Project Board of Directors. Their diverse backgrounds, passion for rare diseases, and commitment to advancing our mission will bring fresh insight and energy to our work. Please join us in welcoming:


Rutu Patel – Pharma Insight & Communications

Rutu blends deep experience in pharmaceutical communications with firsthand experience as both a spouse and parent to individuals with PC. Her insights and dedication have already benefitted the organization through past collaborations.


Bob Lindfors – Board Attorney & Secretary

Bob recently retired from a successful career in law and brings decades of nonprofit experience to the table. As a longtime advocate for equity and access in healthcare, he will serve as both our Board Attorney and Secretary. Bob is already rolling up his sleeves to strengthen our policies and ensure we have strong governance as we grow.


Nate Schwartz – Finance and Patient Perspective

Nate is the son of Executive Director Jan Schwartz and has had a front-row seat to the evolution of PC Project. Professionally, he brings a strong background in finance and risk assessment, and he’s eager to bring that expertise to our Board’s financial strategy. Nate is also deeply connected to our patient community and passionate about making a difference for families living with PC.


Roseann McGrath – Advocacy and Outreach

Roseann is Patient #1 in our registry—and has been a fierce advocate since day one. Her leadership of our Advocacy Team, support of Giving Tuesday, and dedication to PC Awareness Month have made her a guiding voice in our community. Now, as a Board member, she’ll continue amplifying patient stories and pushing for change.


Dr. John Doux – Dermatology, Pharma, and Financial Insight

A board-certified dermatologist and financial analyst, John brings deep medical and business expertise. He’s served on the boards of companies developing PC treatments and is currently on the board of Kamari Pharma. John is especially interested in helping PC Project build strong relationships with pharma partners and expanding our focus into PPK-related conditions.


Together, these new members bring valuable expertise in pharma, law, finance, research, communications, and patient advocacy—and most importantly, a shared passion for PC Project’s mission to help patients and accelerate a cure.

We’re honored to have them join our leadership and look forward to the impact we’ll make together!

See the complete list of the Board of Trustees on the About PC Project page.

About PC Project

Footer

PC Project logo in white
PACHYONYCHIA CONGENITA PROJECT

P.O. Box 17850
Holladay, UT 84117

info@pachyonychia.org

801-987-8758

EIN 68-0567493

  • Facebook
  • Instagram
  • LinkedIn
  • Twitter
  • YouTube

Sign up for our Newsletter

Loading

Support PC Project

There are many ways you can help improve the lives of those who suffer from Pachyonychia Congenita.

Learn More
  • Contact Us
  • About Us
  • Donate
  • Patient Registry