The Network provides services to help ensure transplant and end stage renal disease (ESRD) patients are receiving the best care possible. We do this by:
- Working with dialysis and transplant facilities to improve the quality of care
- Investigating patient grievances
- Providing patient and provider education
- And more!
We encourage you and your family to learn more about ESRD and ways that you can become involved in your treatment by looking at topics on this website. Equally important, we urge you to talk to your care team (physicians, nurses, social workers, dietitians, and technicians) and get involved in the decision-making process so that you will find your own best approach to treatment.
The National Coordinating Center (NCC) created a video of a member of the Network's Patient Advisory Council (PAC) that features their ESRD journey, where they garner strength from, their work with the Network, and their hope for other patients.
Do you have a goal you would like to achieve? The Getting Back to Me: A Goal-Setting Journey is a workbook that can assist you with identifying personal goals and setting a plan to achieve them. This resource was developed by kidney patients and family members and designed to help restore a sense of dignity and increase self-esteem through goal-setting.
This flyer includes patient educational resources available from the ESRD National Coordinating Center including New Patient Education and The Kidney Hub, a mobile web tool.
We recommend all new dialysis patients review the resources available on this extensive educational webpage.
Advance Care Planning
Caring Info is a program of the National Hospice and Palliative Care Organization that provides free resources to help people make decisions about end of life care and services.
The Coalition for Supportive Care of Kidney Patients (CSCKP) brings together like-minded people who care deeply about the quality of compassionate, supportive care for kidney patients. The coalition offers professionals from many disciplines and laypersons who are working for true patient-centered care that values quality of life.
End of Life Care
The Coalition for Supportive Care of Kidney Patients brings together like-minded people who care deeply about the quality of compassionate and supportive care for kidney patients.
Every competent adult has the right to make decisions concerning his or her own health, including the right to choose or refuse medical treatment. This website contains health care advance directives education, information, and forms.
ESRD and Health Education
This poster helps to dispel myths about the depression that can accompany a chronic disease such as end stage renal disease (ESRD).
Patients with chronic kidney disease are at increased risk of pneumococcus infection. Read this fact sheet to learn more about the pneumococcal vaccine.
The Social Security Administration wants you to understand what Social Security can mean to you and your family’s financial future. This publication, Understanding The Benefits, explains the basics of the Social Security retirement, disability, and survivors
Kidney failure treatment - hemodialysis, peritoneal dialysis, and kidney transplantation - is costly and most people need financial help. Find out about your options for assistance.
Find and Compare Facilities
Dialysis Facility Compare (DFC) is a service of the Centers for Medicare & Medicaid Services (CMS), an agency of the U.S. Department of Health and Human Services (DHHS). DFC helps you find detailed information about Medicare-certified facilities, compare the services and the quality of care that facilities provide, get other resources for patients and family members who want to learn more about chronic kidney disease and dialysis, and get links to learn more about how Medicare covers people with ESRD.
This site helps you find and compare Medicare-certified dialysis facilities. You can see how each facility compares to others based on star ratings, services offered, and quality of care. This tool is especially helpful if you need to find a temporary facility.
Going Back to Work or School
This is a resource from Life Options, a program to help people live long and live well with kidney disease. This booklet is divided into three parts: Paying for treatment of kidney disease, living productively with kidney disease, and resources for individuals with kidney disease.
This guide helps people with disabilities plan for attending college.
The Little Book About Kidneys by Victoria Hanson and illustrated by Jenny Tulip, will help you talk to young children about your kidneys and the treatments you may experience. It is intended to support you in explaining your kidney failure to children.
This website provides information and resources about how to stop smoking.
This flyer provides recommended immunizations for people on dialysis.
Patients who undergo dialysis treatment have an increased risk of infection. They are at a high risk for infection because the process of hemodialysis requires frequent use of dialysis catheters or the insertion of needles to access the bloodstream. Additionally, hemodialysis patients commonly have...
The official U.S. government site for people with Medicare, family members, and caregivers. Includes the latest information on Medicare enrollment, benefits, and other helpful tools.
This official booklet contains the basics of Medicare, how Medicare helps pay for kidney dialysis and kidney transplants and where to get help. The phone number for Medicare billing and coverage issues is: 800.633.4227 (the Medicare Hotline).
Nutrition and Diet
Anemia is very common in kidney patients. If left untreated, it can lead to loss of energy, headaches, trouble sleeping, dizziness, shortness of breath, lack of appetite, and a rapid heart rate. This fact sheet provides valuable information for dialysis patients.
Kidneys are instrumental in removing excess water in the body, so when your kidneys don’t work, it is harder to keep the right fluid balance. The right balance is important, because if you gain too much fluid, you may have: Swelling in your face, hands, and feet Headaches and low...
The American Association of Kidney Patients is recognized as the leader for patient-centered education – continually developing high quality, professionally written, edited and reviewed educational pieces covering every level of kidney disease.
The American Kidney Fund is dedicated to ensuring that every kidney patient has access to health care, and that every person at risk for kidney disease is empowered to prevent it. The site offers patient programs, kidney disease education, and professional education.
Dialysis Facility Compare (DFC) is a Centers for Medicare & Medicaid Services (CMS) website that helps you learn about specific dialysis clinics and the care they provide.
This document defines what a support group is and provides simple steps for starting one, as well as listing links to resources for additional reference.
Some diseases and conditions put children at risk for kidney disease. A urine test is used to check for kidney disease before symptoms appear. Read more to learn about risk factors, the urine test, and treatment for kidney disease.
Share this document, created by the Network 15 Patient Advisory Council (PAC), with your patients who have questions about peer mentors; what they are and what they are not. It addresses:
- What essential values a peer mentor must have
- What Makes a peer mentor valuable
- What the responsibilities of a peer mentor are
- What a peer mentor is not
Prescription Drug Coverage
Each outreach event will also provide many other services that beneficiaries can take advantage of and have included: vaccinations, blood pressure testing, diabetes screening, cholesterol testing, bone density testing, and much more.
Learn about how to get Medicare Part D drug coverage, what drug plans cover, costs for Medicare drug coverage, how Medicare Part D works with other insurance, and the enrollment dates.
Tools for Dealing with Depression
The Forum of End State Renal Disease (ESRD) Network’s Kidney Patient Advisory Council (KPAC) has developed the Dialysis Depression Toolkit to help patients who feel they may be experiencing depression. This toolkit was designed BY patients and FOR patients and with contributions by professional collaborators. the Toolkit helps to explain depression and provides information on how to find help.
This booklet provides information on how to choose the best treatment option for YOU.
The Spanish language version of this booklet provides information on how to choose the best treatment option for YOU.
This is a fact sheet about hepatitis B. It provides what you need to know about it and why you should get vaccinated for it.
This is a fact sheet about hepatitis B. What you need to know and why you should get vaccinated.
If you are on hemodialysis, a vascular access is the site from which blood can be safely removed and returned to your body. There are both temporary and permanent vascular accesses.
This document tells you about how you can help other patients by sharing your experiences with getting, using, and maintaining your permanent access.
- About Us
- Contact Us
For Patients and Families
- Advance Care Planning
- End of Life Care
- ESRD and Health Education
- Financial Assistance
- Find and Compare Facilities
- Going Back to Work or School
- Healthy Living
- ICH CAHPS
- Infection Prevention
- Medicare Coverage
- Network Podcasts
- Nutrition and Diet
- Patient Education & Engagement Representative (PEER) Program
- Patient Organizations
- Patient Services
- Pediatric Information
- Peer Mentoring
- Plan of Care (POC) Meeting
- Prescription Drug Coverage
- Tools for Dealing with Depression
- Treatment Options
- Vascular Access
- For Providers
- ESRD Network 7
- ESRD Network 13
- ESRD Network 15
- ESRD Network 17
- ESRD Network 18
- HSAG ESRD Alerts, Recalls, and Notices
- Behavioral Health
- Continuing Education
- Data Management
- Emergency Preparedness
- Health Equity and CLAS
- Home Dialysis
- Infection Prevention
- Patient and Family Engagement (PFE)
- Readmissions and Hospitalizations