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If you are a caregiver, you know that caring for a head-injured person with dementia can be very difficult. It affects every aspect of your life, including family relationships, work, financial situation, social life, and physical and mental health. You may feel unable to cope with the demands of caring for a dependent, difficult relative. Besides the sadness of seeing your loved one’s condition, you may feel frustrated, overwhelmed, resentful, and angry. These feelings may in turn leave you feeling guilty, ashamed, and anxious. Depression is not uncommon.

Different caregivers have different thresholds for tolerating these challenges. For many caregivers, just “venting” or talking about the frustrations of caregiving can be enormously helpful. Others need more help, but may feel uneasy about asking for it. One thing is certain, though: if the caregiver is given no relief, he or she can burn out, develop his or her own mental and physical problems, and become unable to care for the person with dementia.

This is why support groups were invented. Support groups are groups of people who have lived through the same difficult experiences and want to help themselves and others by sharing coping strategies. Mental health professionals strongly recommend that family caregivers take part in support groups. Support groups serve a number of different purposes for a person living with the extreme stress of being a caregiver for a head-injured person with dementia:

• The group allows the person to express his or her true feelings in an accepting, nonjudgmental atmosphere.
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• The group’s shared experiences allow the caregiver to feel less alone and isolated.
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• The group can offer fresh ideas for coping with specific problems.
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• The group can introduce the caregiver to resources that may be able to provide some relief.
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• The group can give the caregiver the strength he or she needs to ask for help.

Support groups meet in person, on the telephone, or on the Internet. To find a support group that works for you, contact the following organizations. You can also ask your health care provider or behavior therapist, or go on the Internet. If you do not have access to the Internet, go to the public library.

For more information about support groups, contact these agencies:

• Brain Injury Association of America - (800) 444-6443
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• Family Caregiver Alliance, National Center on Caregiving - (800) 445-8106
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• Supportpath
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• National Alliance for Caregiving

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