Sometimes people with
cerebral palsy have problems trying to eat. Problems
may include:
- Coughing and choking, which can lead to breathing
problems or
pneumonia if food is inhaled into the
lungs.
- Poor jaw control, making it difficult to
chew.
- Difficulty sucking and swallowing.
You can help your child with cerebral palsy eat more easily by:
- Providing appropriate utensils, such as special
plates and large-handled spoons.
- Serving oatmeal, pudding, mashed
potatoes, and other semisolid foods.
- Placing the child in a secure
sitting position for eating. Bring his or her arms toward his or her chest to
prevent the child from getting into a position that will make feeding and
swallowing more difficult (such as arching the back and throwing the head
backward).
- Holding one hand against the child's cheek to help him
or her open and close his or her mouth if jaw control is a problem.
Feeding tubes
A child with severe cerebral palsy may need a feeding tube in order
to eat. If a feeding tube is needed for only a short period of time, it is
inserted into the child's nose and passed into the stomach. For long-term tube
feeding, a tube can be placed directly into the stomach through an opening in
the abdomen (gastrostomy tube).
Recent research showed that introducing a feeding tube to a
severely affected child improved the quality of life for both the child and
family in more than 90% of those studied.1