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To Parents of Children With Cerebral Palsy, From an Adult With CP

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Dear parents of kids with cerebral palsy,

Thirty-something years ago, my parents were where you are now — raising me, their daughter with spastic quadriplegia cerebral palsy. I was blessed with loving parents, who fought for me to have equal opportunities in school and in life, and told me that I could accomplish anything I set my mind to doing. They also made some mistakes, mostly out of fear and their own internal struggles to accept my disability. But through it all, they only wanted what they saw as the best for me.

I grew up to be a relatively healthy and well-adjusted adult, and have lived independently, with the help of personal care assistants, for over 20 years. Although it’s not always easy, I live life on my own terms, and I wouldn’t trade that for anything.

I do my best to be a good example, and help young people with disabilities and their parents to see what is possible. Here are eight ideas and suggestions, based on my own experiences, for how to raise a happy and healthy child with cerebral palsy and give them the best possible opportunities in life.

1. Don’t believe everything the doctors say.

When I was diagnosed with cerebral palsy at 6 months old, the doctor told my mother I would never walk, speak, or feed myself, and I would probably have severe intellectual delays. He suggested that she place me in an institution. She refused to accept that, and instead devoted her life to helping me reach my full potential. You should do the same. Cerebral palsy is different in each person, but if you’ve been given a doom-and-gloom scenario, don’t believe it. Give your child a chance.

Karin at music therapy, age 3.

Karin at music therapy, age 3.

2. Let go of grief and see the possibilities.

I understand that you may be going through a grieving process surrounding your child’s condition. You are mourning what might have been, and I don’t want to discount your feelings. However, if you let that grief drive your decisions, you’ll only be doing a disservice to yourself and your child. It’s important to realize that our perceptions of what human abilities should be are often based on societal expectations. We expect humans to move, behave, and think in certain ways, and when they don’t, we label it as “other.” We see it as negative. We shouldn’t. It’s just different, and different isn’t necessarily bad.

Your child will have many abilities. Your child will do many of the same things other kids do, just in a different way. Your child could become a Paralympic athlete, or the President, or the next Steve Jobs. Or not. Many kids with cerebral palsy grow up to be ordinary adults with ordinary jobs and lives, just like kids without cerebral palsy. Don’t give up on your dreams for your child just because of cerebral palsy.

Karin horseback riding.

Karin horseback riding.

3. Don’t try to “fix” your child with cerebral palsy.

When we humans are faced with disability, our first thought is often, “How can I fix it?” We don’t want others to “suffer,” and some conditions can be painful or perceived as limiting. However, if we look at disability from a social standpoint, many of the problems it causes are actually due to lack of societal acceptance, such as buildings that are poorly designed for people who don’t walk, and inadequate funding for services and technology. Cerebral palsy cannot be fixed, but these problems can be.

While physical and occupational therapies are great in moderation, too much focus on them can be harmful to a child’s psyche. For me, the best therapies involved fun activities that naturally develop the body, such as horseback riding, dancing, and sports. Let your child do the same things that other kids do, and they’ll gain new skills and abilities.

From a child’s perspective, cerebral palsy is not inherently bad. Nothing is “wrong” with them until someone else tells them so. Don’t go chasing after every surgery or therapy or experimental treatment in the hope that it will make your child “normal.” The only thing that will accomplish is making the child feel bad for not being good enough. Your child is good enough as he or she is!

4. Foster your child’s intellectual development.

Karin as a student at Stanford University.

Karin as a student at Stanford University.

My mom put a lot of time and energy into making sure I got a great education, long before I started school. She read to me every night, and as a result I could read on my own before I was 3. Learning to read so early set me up for success in life — I attended Stanford University, and now have a Master’s degree. We can develop our minds at a time when children with typical abilities are focused on developing their bodies. Don’t miss this opportunity.

I was mainstreamed into a regular classroom beginning in preschool. I believe that inclusion is essential for children with cerebral palsy to develop academically and socially. Be an active part of your child’s education. Talk to their teachers regularly, and volunteer in the classroom. Fight to change classes or schools if your child is being segregated or not receiving the appropriate services.

Technology is key to help your child prepare for the jobs of the future. Dictation and communication are just an app download away — much easier than when I was growing up!

5. Make your home and vehicle accessible.

I often see children who are limited in their ability to experience the world because their home and/or their parents’ vehicle is not built for accessibility. For the sake of your child and yourself, make accessibility a priority when buying or renting your home. Choose a one-story home with a large bathroom, and install the proper equipment to help your child learn to care for him or herself as much as possible. If your child uses a wheelchair, buy an accessible vehicle with a ramp so your child can get in and out of the vehicle independently (you’ll spare yourself the lifting, too.) Brand-new accessible vehicles can be very expensive, but there are many used ones available at a more affordable price.

Karin in Washington, DC at age 17.

Karin in Washington, DC at age 17.

6. Embrace the idea of a power wheelchair; one may be key to your child’s independence.

I wasn’t allowed to get a power wheelchair for years, because my mother was afraid I would get less exercise and lose mobility. However, using a manual wheelchair severely limited my life because I wasn’t strong enough to push myself well. It made me socially isolated and frustrated by all the things I couldn’t do. When I finally got a power chair at age 15, my life was transformed. I could go places by myself and cross streets quickly and safely. Even if your child can walk short distances or at home, using a power wheelchair out in the world can give them the freedom to keep up with their able-bodied peers, go to college, and succeed in the workplace.

7. Travel with your child.

My parents passed their love of travel on to me. I was raised to believe that having a disability should not stop you from seeing the world. Growing up, we went camping and visited amazing places all over the country. Traveling helped me believe I could be independent and live in a place of my choosing. Traveling opens your mind to new people and experiences. It can be an opportunity to meet other people with disabilities, at conventions or other gatherings, and find positive role models for your child.

Karin in San Diego, 2014.

Karin in San Diego, 2014.

8. Prepare your child for independence.

Like most young adults, people with cerebral palsy have a desire to build an independent life. Pursuing higher education, finding housing, obtaining employment, and hiring caregivers can all be scary for parents and adult children, and they are not without risk, but the benefits far outweigh the risks.

The best way to ensure your child’s safety after you are gone is to develop a support system for them while you are still healthy. If you are able to provide for them financially, create a special needs trust or ABLE account so the income and resources do not impact benefit eligibility. I encourage you to sign your child up for all available social programs, such as SSI or SSDI, and Medicaid. All of these programs have provisions that allow a person to work and retain benefits; this will ensure that your child can be employed but also get state funding for expensive medical equipment and caregivers.

I hope this list has been helpful to you as a parent. The most important thing you can do is to listen to your child, and empower them to make their own age-appropriate choices in life, just as you would for a child without a disability. With your support, your child will grow up to be the best person he or she can be. Stay strong!

— Karin

Follow this journey on Free Wheelin’.

Originally published: October 5, 2016
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