Patients & Caregivers
If you or your loved one is living with a genetically defined disease, you may wish to visit the following resources for more information about treatment, research, clinical trials and other tools:
Pyruvate Kinase Deficiency
MyAgios Patient Support Program (U.S. residents only)
Introducing a patient support program for people living with PK deficiency and their caregivers. We will listen to understand the difficulties of living with a rare disease and are here to help provide disease education. Enroll in the program to be connected with a dedicated Patient Support Manager.
Know PK Deficiency Site
Whether you’ve recently been diagnosed, or you’ve been living with PK deficiency for years, learning as much as you can is important. This website is a good place to start.
Understanding PK Deficiency Brochure
This brochure provides an overview of PK deficiency as well as tools to help you work closely with your doctor to proactively manage your condition.
View Brochure (U.S. residents only)
View Brochure (EU & UK residents only)
Information for Caregivers Brochure
If you are a parent or caregiver of someone with PK deficiency, this brochure can help you understand the condition and the impact living with it can have on someone’s life.
PK Deficiency through the Decade
Understand more about PK deficiency and read summaries of key research papers published over the past decade. The list of publications and information you gather can also be used to build more proactive discussions with your doctor.
View Article (U.S. residents only)
View Article (EU & UK residents only)