Adults with mild cerebal palsey

The population of adults diagnosed with cerebral palsy CP is increasing along with the survival rate of children born with the disability. Adults with CP need health services for the continued monitoring and management of their condition. Moreover, the development of additional health problems in adulthood increases the need for ongoing access to health services. Adults with CP manifest a higher rate of chronic health conditions and eventual decline in strength and functional reserve, deterioration in physical activity, increased risk of musculoskeletal complications, and gradual changes in swallowing ability. They are also reported to exhibit difficulty engaging socially and have a low health-related quality of life QOL. However, there are a large number of adults with CP who cannot access medical services adequately and are therefore not effectively treated.
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28.03.2021
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Emerging Issues in Cerebral Palsy Associated With Aging: A Physiatrist Perspective

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New NICE guideline on Cerebral palsy in adults

Cerebral palsy in adults is a new guideline which follows on from the previously published NICE guideline on cerebral palsy in children and young people and is also related to the NICE guideline on spasticity for the age group of children and young people up to 19 years. Cerebral palsy is a lifelong condition and there is not yet a cure for the underlying brain disorder. The main aim of the guideline is to help and support health and social care professionals and people with cerebral palsy particularly related to their changing needs with age in making shared decisions about the clinical and social care that is on offer. The guideline makes specific recommendations about regular clinical reviews of people with cerebral palsy.
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New NICE guideline on Cerebral palsy in adults

Did you know that each year, approximately every two to three children out of 1, are born with cerebral palsy in Europe? From the frustrations of limited mobility to the physical pain of a chronic illness, adulthood presents its own hurdles. Yet, with a healthcare system that dedicates most of its efforts to treating children with CP, these problems often go unnoticed.
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