This Giving Tuesday help bring hope to those living with Pachyonychia Congenita (PC).
Every step hurts. For people living with Pachyonychia Congenita — a rare, painful genetic skin condition — even the simplest moments in life can feel impossible. Walking, standing, or going to school can mean excruciating pain. And beyond the physical toll, there’s the emotional weight: the shame of feeling different, the stares from strangers, and the isolation of a world that doesn’t understand.
But together, we can change that.
On Giving Tuesday (December 2, 2025), you have the power to make a difference. Your support fuels research, delivers answers, and builds a global community where no one with PC faces their pain — or their shame — alone.
What Your Gift Makes Possible
Your donation directly supports:
- Groundbreaking research that brings us closer to a cure.
- Faster, more accurate diagnoses so families get answers sooner.
- Essential support and connection for patients and caregivers navigating this rare disease.
- Awareness and advocacy to ensure PC families are seen, supported, and never forgotten.
Hear Their Stories
Max, PC Patient:
Every step feels like walking on broken glass — but the hardest part isn’t just the pain. It’s the shame of feeling like no one understands. Your support tells me I’m not alone.
Marie, Donor:
I give because I want to bring relief and hope to those living with pain every day. Together, we can change lives.
Hilary, Parent Advocate:
The hardest part is watching your child suffer and not being able to fix it. PC Project gives us hope.
Dr. Pierre Coulombe, Researcher:
We’re getting there — slowly but steadily. Your support fuels the science that will end this pain.
How You Can Help
- Donate – Every dollar brings us closer to ending the pain and shame of PC.
- Share – Spread the word by sharing this campaign with friends and family.
- Join the Movement – Follow PC Project on social media and stay connected to the progress you’re making possible.
Together, We Can End the Pain
With your support, we can create a future where PC patients are rare but not forgotten — where no one suffers in silence, and where science, compassion, and community come together to end the pain once and for all.
