When your child is diagnosed with cerebral palsy (CP), there's a lot to take on. You have to figure out health care, childcare, and the best path forward for your child. It's normal to feel overwhelmed. But many resources and support services are available to help you.
Here’s what to expect as your child grows – and how to plan for it – so that you can give your child the best start.
This 8-step checklist can help you decide which early steps to take.
Kids who have disabilities or delays get extra support to reach developmental milestones (like walking, talking, and self-feeding) through a program called early intervention.
Early intervention offers free therapy services for babies and children up to age 3. Therapy can happen at home or in a daycare setting. Kids can receive:
Each state runs its own early intervention program. Ask your pediatrician for a referral or visit the Early Childhood Technical Assistance Center directory for state-specific contact info.
After your child turns 3, services can continue at home or in preschool. Contact your school district to arrange this when your child is 2½.
Some kids with CP have trouble eating and swallowing, have seizures, or need medicines at set times. Consider having someone come to your home to help with caregiving. Options include:
Even if you have private health insurance, your child might qualify for Medicaid, the federal health insurance program that provides coverage for people with disabilities. Medicaid can cover treatments that are not covered by your private carrier and can help lower out-of-pocket medical costs.
If you’re looking for a childcare provider, be sure that the one you choose has the skills and setting needed to safely handle your child's needs. By law, childcare providers cannot discriminate against children with disabilities or special health care needs.
In many cases, the state agencies that handle early intervention can provide referrals to appropriate childcare providers.
Talk with a lawyer about making legal and financial plans that will protect your child in the future. One who practices special needs law can advise you on the best plan for your family.
Also talk about creating a will that, aside from financial matters, says who would care for your child in the event of your death.
All children benefit from friendships and play. Here’s some ideas:
By age 3, your child may be eligible for educational services through your local school district. Learn more about navigating the grade-school years.
Life with young children can be overwhelming, and even more so when kids have disabilities or special health care needs. So remember to take time for yourself to relax and recharge: take a walk, read a book, exercise, or do a favorite hobby.
Accept help from friends and family members. After a break, you’ll be better able to enjoy time spent with your family.
As your child grows, stay up to date with all medical visits. This ensures that your child gets the right nutrition, vaccinations, and prescriptions.
Care will change as your child gets older. By knowing what to expect, you’ll feel more confident caring for your child.
Note: All information is for educational purposes only. For specific medical advice, diagnoses, and treatment, consult your doctor.
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