Emotional and Family Issues

Many factors influence how a child feels about having congenital (present at birth) heart disease, and how it affects him/her mentally and emotionally, including the following:

• the type of defect
  Different emotions may be experienced with a congenital heart defect that requires one operation to repair versus one that requires many operations and periodic or constant medical care.
  
  
• the age of the child when the heart defect was diagnosed
  A child who was diagnosed at birth and who has grown up with the heart defect may adjust differently than a child who learns of his/her heart disease at an older age, after living a seemingly healthy life.
  
  
• the number of hospitalizations
  Children who require many diagnostic tests and procedures, surgeries, and/or other hospitalizations due to the nature of their illness may feel angry, fearful, resentful, or withdrawn.
  
  
• the age of the child
  Younger children may have difficulty understanding their illness and may misinterpret the reasons for tests and surgical procedures. Whereas, older children can better understand information about their illness and what it will take to make them well.
  
  
• the coping skills and temperament of the child
  Some children can deal with adversity better than others, and some children are more nervous or anxious than others.
  
  
• body image
  Surgical scars, cyanosis (blue coloring of the skin, lips, and nailbeds), or the need for medical therapies such as oxygen or feeding tubes often make a child feel different from others, and can affect self-esteem and body-image.
  
  
• family dynamics
  A child's emotions can be affected by the way his/her family members cope with the illness, as well as other issues including the stress felt by the family. Finances, work, and insurance problems the family may face, or siblings who are jealous of the extra attention the child with the heart defect may receive due to his/her illness, will all affect your child's emotions.

Physicians, nurses, social workers, counselors, and other healthcare team members can provide guidance and recommendations for managing the many emotions that may accompany a chronic disease. They may also recommend community services and local support groups.
 
Local support groups are made up of children with congenital heart disease and their families. Ask about meetings, outings, and parties for children and their families. It often helps to talk to others in your situation, and for your child to experience activities with others that are like him/her. Your child's cardiologist (or the staff at the hospital) can give you more information about a group in your area.
 
Be sure to also ask about special camps that have been created for children with congenital heart disease to help them interact with each other and have fun. Many of the volunteer counselors at these camps are nurses, physicians, respiratory therapists, and other medical professionals who love having fun with the children in a camp setting, but who are also able to give medications and help with special needs of children with congenital heart disease.

The information on this Web page is provided for educational purposes. You understand and agree that this information is not intended to be, and should not be used as, a substitute for medical treatment by a health care professional. You agree that Lucile Salter Packard Children's Hospital is not making a diagnosis of your condition or a recommendation about the course of treatment for your particular circumstances through the use of this Web page. You agree to be solely responsible for your use of this Web page and the information contained on this page. Lucile Salter Packard Children's Hospital, its officers, directors, employees, agents, and information providers shall not be liable for any damages you may suffer or cause through your use of this page even if advised of the possibility of such damages.