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Finding Support Groups and Doctors

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By Bruce Campbell

Looking for a CFS or fibromyalgia support group or a doctor who treats people with CFS and FM? Here are some ideas to aid your search.

Support Groups

Support groups can be a crucial coping resource when you have a serious illness. Contact with fellow patients counteracts isolation and provides an experience of being acknowledged and supported. Such contact can be a way to feel understood, comforted and inspired. Also, groups can provide information, such as names of local doctors who treat CFS and fibromyalgia. Groups offer a way to be helpful, thus counteracting the loss of self-esteem that often results from serious illness. And, finally, they can offer models of successful coping, thus dispelling fear. Similar experiences are available now on the Internet, at online chat rooms and message boards.

A word of warning: While support groups may be very helpful, not all provide a positive experience. Some groups are negative in tone, reinforcing a sense of victimhood. Some groups are dominated by one or a few people. Others focus on responding positively to illness and insure participation from all members who wish to speak. We suggest you evaluate support groups based on the effects they have on you. Contact with fellow patients, especially in a group, can be very powerful. When such contact is negative, it can reinforce isolation and a sense of victimhood. But in a supportive atmosphere, it can be helpful and even healing. Contact with other patients may leave you feeling upset at times, but the discomfort should be followed by a new perspective on your situation, and increased confidence about your ability to manage the illness.

A good group is one in which you feel a sense of belonging, which gives you something positive to take home, either inspiration or practical tips, and which offers models of living successfully with illness.

The CFIDS Association of America maintains a state-by-state list of CFS support groups in the United States. They will mail a list of groups in your state at no cost. (You can contact them at 704/365-2343, email your request to or send a self-addressed, stamped envelope to The CFIDS Association of America, Attn: Support Group Info, PO Box 220398, Charlotte, NC 28222-0398.)

For lists of FM support groups, see the website of the National Fibromyalgia Association ( and also the Immune Support website (, which also has listings for CFS groups. If you are looking for ideas on how to manage your illness more effectively, you might consider self-help classes for people with CFS and fibromyalgia, which include our Internet course.

Another kind of support is the professional help offered by counselors and psychotherapists. A sympathetic professional can offer encouragement, provide an outsider's view of your situation and give you continuity. If you're interested, you might look for one who specializes in working with people who have chronic illness. A local support group is often a good source of leads. Therapy can also be helpful for couples. It can offer a place in which the strains created by living with long-term illness can be explored.

Finding a CFS or FM Doctor

How do you find a doctor who is knowledgeable about your illness and whom you trust? One good starting point is referrals from fellow patients. Support groups are often a good way to meet other patients. As mentioned above, the CFIDS Association of America maintains a state-by-state list of CFS support groups in the United States. (Contact them at 704/365-2343 or through their website: Some local chapters of the Arthritis Foundation ( provide physician referral lists for FM. For lists of FM support groups, see the previous section.

Other resources for finding doctors include the "Good Doctors" list at Co-Cure (, the FMS Community website ( and Devin Starlanyl's site ( ).