Progressive Supranuclear Palsy (cont.)
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Support Groups and Counseling
PSP is a difficult disease for you and those who care for you. It can be particularly stressful for family caregivers. The condition affects every aspect of life, including family relationships, work, financial status, social life, and physical and mental health. If you are a family caregiver for a person with PSP, you may feel overwhelmed, depressed, frustrated, angry, or resentful. These feelings may in turn leave you feeling guilty, ashamed, and anxious.
While understandable, these feelings do not help the situation and usually make it worse. 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. Support groups serve a number of different purposes for a person living with the stress of being a caregiver for a person with PSP.
Support groups meet in person, on the telephone, or on the Internet. To find a support group that works for you, contact the organizations listed below. 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 the following agencies:
For More Information on Progressive Supranuclear Palsy
Medically reviewed by Joseph Carcione, DO; American board of Psychiatry and Neurology
Medically Reviewed by a Doctor on 12/8/2015
Eric R Eggenberger, DO
Robert A Hauser, MD
Francisco Talavera, PharmD, PhD
Stephen Berman, MD, PhD
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