Many resources exist for young persons with CFIDS (YPWCs) and their families. Following is a list of some resources we're aware of outside of this webpage. If you know of a resource that should be listed here, please write to webmaster@cfids.org.

The CFIDS Association of America claims no responsibility for information on websites that are not part of the Association's website. This information is provided as a public service.

• Support Groups and Pen Pals
• Websites of Interest
• Education Resources
• Books, Newsletters and Articles

Support Groups and Pen Pals

• Sleepy Teenzzz is a CFS site designed by teenz with CFS for teenz with CFS. Offers opportunities for support.
• About.com CFS Chat Room has scheduled and unscheduled chat's for PWCs of various ages, including a special chat for teens with CFIDS.
• CFS-P offers support to parents of children and teenagers with chronic fatigue syndrome and related conditions.
• CFIDS Support Network
• Starting a Support Group for YPWCs and Parents

Websites of Interest

• About.com Guide to CFS is an excellent resource for information about CFIDS, including original articles, chat and news.
• Alison Hunter Memorial Foundation is an Australian foundation with the goal of reducing the impact in the community of the disease myalgic encephalopathy / chronic fatigue syndrome
• AYME (Association of Youth with ME is a UK-based independent registered charity dedicated to giving help, support and vital contact to children and young people with myalgic encephalomyelitis (M.E.)/CFIDS/CFS.
• The Pediatric Network for chronic fatigue syndrome, fibromyalgia and orthostatic intolerance.

Education Resources

• Action for ME if you are affected by M.E. (Myalgic Encephalomyelitis/ Encephalopathy), CFS (Chronic Fatigue Syndrome) or PVFS (Post Viral Fatigue Syndrome)? This site is for you.
• Chronic Illness Initiative DePaul University. Students with chronic illnesses such as chronic fatigue syndrome, lupus, fibromyalgia, among others, may take advantage of the services of the SNL’s Chronic Illness Initiative. This program was designed to help students who have had difficulty attending traditional programs because of relapses or unpredictable symptom flare ups. Scholarships are available.
• The Pediatric Network for Chronic Fatigue Syndrome, Fibromyalgia and Orthostatic Intolerance has articles on medical, educational, parenting, transition planning, and advocacy topics
• The National Information Center for Children and Youth with Disabilities is a national information and referral center that provides information on disabilities and disability-related issues for families, educators and other professionals.
• Individuals with Disabilities Education Act Homepage (IDEA), provides information on the federal law which mandates a "free and equal education" for children with disabilities.
• The PACER Center expands opportunities and enhances the quality of life of children and young adults with disabilities and their families, based on the concept of parents helping parents.
• HEATH Resource Center is a national clearinghouse on postsecondary education for individuals with disabilities.
• Office of Special Education and Rehabilitative Services (OSERS) of the U.S. Department of Education.

Books, Newsletters & Articles

• "Back in the Swing" with Jill Griffin.
• The CFIDS Chronicle is published by The CFIDS Association of America, Inc. and provides information about CFIDS in people of all ages.
• A Parent's Guide To CFIDS: How to Be an Advocate for Your Child with Chronic Fatigue Immune Dysfunction Syndromeby David S. Bell, Mary Z. Robinson, Jean Pollard, Tom Robinson, Bonnie Floyd.