“Some people come into our lives, leave footprints on our hearts, and we are never the same.” -Franz Peter Schubert
The medical staff at the Mayo Clinic define “Cerebral palsy” (CP) is a general term for a group of disorders that appear during the first few years of life and affect a child’s ability to coordinate body movements. Cerebral palsy can cause muscles to be weak and floppy, or rigid and stiff.
In the United States, cerebral palsy occurs in about two to four out of every 1,000 births. The disorder is usually caused by brain injuries, including lack of oxygen, also called hypoxia or anoxia. Cerebral palsy isn’t curable. Medical evidence supports theories that infections, birth injuries, and poor oxygen supply to the brain before, during, and immediately after birth result in up to 15% of cases.
Between 35% and 50% of all children with CP will have an accompanying seizure disorder and some level of mental retardation. They also may have learning disabilities and vision, speech, hearing, or language problems. Often parents are overwhelmed when their child is given this diagnosis and rightly so. There are many questions and no clear answers. As a parent of a child with special needs, you may be asking:
- Why did this happen to my child?
- How am I going to pay for what my child needs now and in the future?
Every circumstance is unique, just like very child and every family. If you have questions about that care you received or the birth experience or the care your child received after birth and you think it may be a factor in your child’s condition, you can get answers. We have significant experience handling these types of cases and have many nationally known experts who are willing to review your child’s case and determine what happened. As a parent, and as a patient advocate, I urge you to get answers if you have these questions. You owe it to yourself and your child.