Kids with CP have varying degrees of physical disability. Some have only mild impairment, while others are severely affected. This depends on the extent of the damage to the brain. For example, brain damage can be very limited, affecting only the part of the brain that controls walking, or it can be much more extensive, affecting muscle control of the entire body.
The brain damage that causes CP also can affect other brain functions and lead to additional medical issues, such as:
Seizures, speech and communication problems, and intellectual disabilities are more common among kids with CP. Many have problems that can require ongoing therapy and assistive devices such as braces or wheelchairs.
Currently, there's no cure for cerebral palsy. But a variety of resources and therapies can provide help and improve the quality of life for kids with CP.
Different kinds of therapy can help them achieve their maximum potential in growth and development. As soon as CP is diagnosed, a child can begin therapy for movement, and other areas that need help, such as learning, speech, hearing, and social and emotional development.
Also, medicine, surgery, or braces can help improve muscle function. Orthopedic surgery can help repair dislocated hips and scoliosis (curvature of the spine), which are common problems associated with CP. For severe muscle pain or stiffness, kids can take medicine by mouth or given through a pump (the baclofen pump) implanted under the skin.
Kids can improve their bone health by eating diets high in calcium, vitamin D, and phosphorus. These nutrients help keep bones strong. Doctors, nutritionists, and even speech-language therapists can work with families to make sure kids are getting enough of the right nutrients and suggest changes to their diets or mealtime routines, if needed.
A variety of medical specialists might be needed to treat different medical conditions. Even if several medical specialists are needed, it's still important to have a primary care doctor or a CP specialist. This doctor will take care of your child's routine health care and also help you coordinate your child'scare.
A team of professionals will work with you to meet your child's needs. That team may include therapists, psychologists, educators, nurses, and social workers.
Taking care of a child with CP can be overwhelming at times. Not only do kids with CP need a lot of attention at home, they also need to go to many medical appointments and therapies. Dont be afraid to say yes when someone asks, "Can I help?" Your family and friends really do want to be there for you.
To feel less alone and to connect with others who are facing the same challenges, find a local or online support group. You also can get information and support from CP organizations, such as:
Staying strong and healthy is not only good for you, but also for your child and your whole family.
Living with CP is different for every child. To help your child move and learn as much as possible, work closely with your care team to develop a treatment plan. This will let your child explore and experience the world in a way that is just right for him or her.
Date reviewed: August 2015
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