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September 2006
Keeping Care Complete: Caregivers' Perspectives on Mental Illness &
Wellness
Caregivers from Australia, Canada, Germany, France, Italy, Spain,
the United Kingdom and the United States participated in the survey,
which was developed by the World Federation for Mental Health and
Eli Lilly and Company. The combined findings across countries
reflected in the percentages below represent answers across all
countries and a total number of respondents (982), unless noted
otherwise.
Independent market research companies Ipsos-Insight and All Global
Ltd., conducted the survey of 982 caregivers of individuals with
bipolar disorder, schizophrenia, or schizo-affective disorder or
Australia, Canada, Germany, France, Italy, Spain, the United
Kingdom, and the United States between November 2005 and June 2006.
Data was collected via 30-minute telephone interviews, which
included a set of close-ended questions focusing on topics such as
treatment discontinuation, relapse, caregiver burden, information
exchange between families and treatment teams and long-term
wellness. In addition, the survey included several country-specific
questions.
Caregivers viewed medication management a top treatment priority:
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91% of caregivers say that efficacy is their primary concern when
considering treatment options for their family member.
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90% of caregivers say that an effective medication is needed to
control the symptoms of the family member's condition, before
their overall well-being (physical and mental health) can be
properly tackled
Finding the right medication can be difficult and lengthy, and
many people try different medications for years before they find
the one that works. Of the 756 caregivers who say that their
relative is satisfied with their current medication:
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56% say it took two years or more for their relative to find a
medication that worked
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85% say that their relative tried more than two different
medications before finding the one that worked and 36% say their
relative had to try more than five medications.
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In addition, 82% of all caregivers said that initial experiences
with a treatment influence overall perceptions of the treatment

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