Use these tools and tip sheets to help you along your journey and track your experiences with overt hepatic encephalopathy (HE).
CARE PLAN RESOURCES
- symptom tracker
- he treatment plan checklist English Spanish
- patient health insurance roadmap English Spanish
- CAREGIVER TIP SHEET English Spanish
- HOW TO TALK TO OTHERS ABOUT HE English Spanish
- MANAGING RELATIONSHIPS & HE English Spanish
For more information about chronic liver disease and complications, visit these advocacy or medical groups:
American Liver Foundation (ALF) The ALF makes a measurable difference in the fight against liver disease by providing financial support for medical research; educating patients, families, caregivers and healthcare professionals; advocating for patients and their families; and creating public awareness campaigns about liver wellness and disease prevention. To find a local support group near you, head to liverfoundation.org.
National Organization for Rare Diseases (NORD) NORD is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services. To learn more, visit rarediseases.org.
Global Liver Institute (GLI) The GLI is a patient-centered, non-profit organization focused on improving the lives of patients and loved ones impacted by all liver diseases. The GLI has a wide range of programs and resources dedicated to liver health education, support and advocacy. For more information, check out globalliver.org.