Coping with FTD can be scary, frustrating, and embarrassing for the patient and family members. FTD may be taking away my father, but I am gaining a great deal of respect for my mother for keeping her promise to … FTD is the most common cause of dementia in people under the age of 50. Tips for managing aggressive behaviour in FTD . Fronto Temporal Lobe Degeneration - A different kind of dementia, most often called FTD. The archives will be open to all members to read. Further information on FTD can be found at www.theaftd.org If FTD is diagnosed early in the course of the disease, doctors can prescribe medications and help families prepare and cope with symptoms. It is a common misconception that dementia is a condition exclusively of old age. Frontotemporal dementia (FTD) is a group of disorders that result from damage to the frontal and temporal lobes of the brain. Behaviours exhibited by people with FTD can be unpredictable and distressing. Long-Term Care for People with FTD For many caregivers, there comes a point when they can no longer take care of the person with a frontotemporal disorder without help. Families need to care for their own well-being, while making sure that their loved one is treated with dignity and respect. The condition may last from three to 17 years before death, with an average duration of eight years after diagnosis. I hope this blog helps you to understand. So family members shouldn't take their loved one’s behaviors personally. With this blog, I am hoping to offer information and insight into dealing with FTD, whether you have the disease, are a caregiver for someone who does or if you know or love someone who has the disease and want to learn more about it. It is important, however, to understand that the behaviour exhibited by people with FTD is a result of the disease process in the brain as FTD … Depending on the location of the damage, the disorder causes changes in social behavior, personality, and/or loss of language skills. Problem solving, personality and common sense are all affected, along with memory, language comprehension and hearing. And of course there are the articles about the spouses and children that are coping with the disease. The grieving begins long before physical death. Putting One Foot In Front of the Other is author Nancy Carlson’s candid blog post about coping with her husband’s diagnosis of frontotemporal degeneration (FTD). Such groups allow caregivers to learn coping strategies and share feelings with others in the same position. The NY Times recent article here is a pretty good read. 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