HEAR FROM THE acute hepatic porphyria (AHP) COMMUNITY
Voices of AHP is a platform filled with real stories from real people about AHP. These stories may help empower those who have been diagnosed, and encourage those who may be undiagnosed to recognize and understand the symptoms of AHP.
NICOLE’S LONG ROAD TO DIAGNOSIS
Nicole talks about her long journey to an AHP diagnosis, alongside Dr. Angelika Erwin, a porphyria expert, who provides an overview of the disease, including symptoms and ways to test for AHP.
MEGAN'S UNPREDICTABLE REALITY
Megan, along with her mother and husband, discuss her struggles with the unpredictable nature of AHP.
Nathan's long road with Hereditary Coproporphyria (HCP)
Nathan discusses how hereditary coproporphyria (HCP) impacted his life since the age of 7 years old.
ANIA’S FAMILY INHERITANCE
Ania discusses how acute intermittent porphyria (AIP) has affected 3 generations of women in her family with severe attacks and agonizing pain.
REVEALING COLIN'S TRUE CONDITION
Colin shares how porphyria hid behind other diagnoses.
THE CRIPPLING PAIN OF AHP
Patients describe the debilitating symptoms they feel between and during attacks.
GLAUCIENE’S LIFE BEYOND ACUTE INTERMITTENT PORPHYRIA (AIP)
Glauciene shares how she won’t let acute intermittent porphyria (AIP) stop her from accomplishing her dreams.