For Patients
Chronic fatigue syndrome, or CFS, is a complex illness that can be challenging for health care professionals to diagnose and treat—and equally challenging for patients and their families to endure.
Scientists still don’t know what causes CFS, and there isn’t a cure yet. However, significant progress has been made in recent years by researchers and the medical community in unraveling the mysteries of this illness. This progress has led to a greater understanding of how CFS affects the body and of how to treat this illness more effectively. There are treatment options available to help patients improve their quality of life and increase their activities and level of function.
If you think you or a loved one may be suffering from CFS, here you’ll find up-to-date information to assist you in understanding CFS. There are a number of resources available to help you.
Get informed. Get diagnosed. Get help.
Patient Brochures
- Introducing CFS. This newly revised 8-page pamphlet from the CFIDS Association serves as a easy-to-understand primer on the basics of CFS. It also answers many frequently asked questions like, Who gets CFS?, How is CFS treated? and Do patients get better? Click here for a downloadable copy.
- Understanding CFS: A Guide for Patients. This brochure provides a brief overview of how CFS is defined, diagnosed and treated. It was designed for the campaign and will be distributed at sites where "The Faces of CFS" exhibit travels.
Information on Talking to Your Doctor
- Should I Talk to a Health Care Professional about Chronic Fatigue Syndrome?. If you suspect you may have CFS, and you wonder if you should discuss it with your doctor, this resource is for you. It’s an easy, one-page list of questions that will help you identify your symptoms and the impact of those symptoms. The questionnaire can be filled out at home and taken with you to your next appointment.
- Doc Talk. This article from the CFIDS Chronicle includes strategies for improving communication with your health care professionals. It can help you take some of the frustration out of the doctor-patient relationship.
- Choosing a Doctor. This fact sheet can help you find and work effectively with health care professionals to manage CFS.
The CFIDS Chronicle
The CFIDS Chronicle is the premier publication for CFS patients and others who are interested in this illness, filled with articles about treatment options, research advances, tips on winning disability claims, coping strategies, advice on saving money on prescription medications and many other topics. The magazine, which is mailed to Association members four times each year, also features poignant personal stories about patients and family members living with CFS and their struggles and triumphs. You can join the Association and subscribe to this publication online.
Click here for a link to a sample article from the summer 2006 issue, "Matters of the Brain" by researcher Floris de Lange.
The Science & Research of CFS
This 65-page magazine published in 2006 features articles from leading CFS experts around the world. People who are searching for current, accurate and reliable information about CFS will find it here. Click here for a table of contents and links to several sample articles.
CFIDSLink
This monthly newsletter features breaking news related to CFS, keeps you informed about new research discoveries, and profiles patients, clinicians, researchers and CFS advocates. It’s delivered right to your inbox the first Tuesday of each month. You can subscribe online.
Disability Packet
The CFIDS Association of America has numerous resources available for people interested in Social Security disability and CFS:
Member Services
When you join the CFIDS Association of America you enjoy a wide variety of member services and membership benefits, in addition to supporting efforts aimed at ending CFS.
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