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Survey from National Fibromyalgia Association and American Pain Foundation released on reveals impact of fibromyalgia on patients' quality of life.
Survey from National Fibromyalgia Association and American Pain Foundation released on reveals impact of fibromyalgia on patients’ quality of life.
Survey results released by the National Fibromyalgia Association (NFA) and American Pain Foundation (APF) reveal “the debilitating effects of diagnosed or undiagnosed fibromyalgia or other chronic pain conditions on the lives of sufferers.”
A news release from the APF explained that the survey “survey looked at the impact that living with a chronic pain condition, such as fibromyalgia, can have on everyday tasks, parenting, relationships and life decisions.” The online survey was completed by 3,018 people living with diagnosed or undiagnosed fibromyalgia or other chronic pain conditions (including 2,559 people diagnosed with fibromyalgia).
Survey findings include:
Half of survey respondents also reported that “not being able to be there for their partner, spouse, or family” was a primary reason for seeing a health care provider about their pain. On average, patients consulted with four types of physician specialists over the course of three years between first experiencing symptoms and receiving a diagnosis of their condition.