Donate to the American Porphyria Foundation Today!

Here’s how we make a difference:

✅ Connecting over 6,000 physicians with patients worldwide
✅ Ensuring access to FDA-approved treatments and financial assistance
✅ Providing FREE DNA testing to help with diagnosis
✅ Offering patient and physician education packets, including the Porphyria-safe drug list
✅ Connecting patients through support groups and social clubs like APF Book Club, research partnerships, and the Porphyria Partners Program
✅ Sharing critical information via our website and our APF podcast RARELY DISCUSSED
✅ Hosting Zoom sessions with Porphyria experts and offering complimentary Porphyria warning cards
✅ Building the future of Porphyria care with our Protect the Future Program and many more

💜 These resources support over 18,000 members worldwide. 💜

If the APF has helped you or someone you love, or you would like to support our mission, we greatly appreciate your contributions. The APF does not receive any government funds for support, so we rely on you to continue our mission of putting PATIENTS FIRST! On behalf of the patients, caregivers, and Healthcare Professionals who have relied on the APF for support for over 42 years and continue to do so, WE THANK YOU FROM THE BOTTOM OF OUR HEARTS ❤️

Your generosity fuels these life-changing programs, ensuring that no one faces Porphyria alone. Together, we can make a lasting impact. Thank you for your support! 💜

#PorphyriaSupport #DonateNow #StrongerTogether