top of page

ree

It is essential to build self-esteem in children with disabilities as they develop, just as we do for other children. Parents, caregivers, teachers and healthcare professionals often make up the community that surrounds them. Here are a few ways everyone can work together to help children feel properly supported and cared for.


1. Let the child speak.


Let the child speak for themself as often as possible even if their language is limited. When appropriate, direct questions to them, not the adult with them. Be patient, look at them and listen attentively. By doing this, you are validating that what they want, say or need is of significance. Plus, you will be demonstrating important skills of mindfulness, listening and interactivity.


2. Treat the child the same.


Treat children with disabilities the same as you would other children. Don't use their disability as an excuse for inappropriate behavior. Children can be very perceptive and take cues from what you say or how you act. Giving in to a child, pitying them or making things easier for them can all backfire later. Siblings and classmates may become resentful for any 'special' treatment that is given to a peer. Or, they may learn by poor example and treat the child differently than they would other friends and acquaintances.


ree

3. Teach the child manners.


Teach the child about manners and forming friendships as early as possible. As soon as your child is able, help them learn how to introduce themself and be able to ask other children, "What's your name?"


While toddlers and young children typically become friends more through physical activities than language interaction, they may be wary of approaching your child to play. Help your child learn how to initiate contact with other children by role modeling and practicing often. By preparing your child, they will become comfortable making new friends and may have more success than if they waited for someone else to initiate contact. This is an important skill that will serve them well throughout their lifetime.


ree


4. Teach the child about their assistive devices.


When your child is able to understand, explain why they need and use the assistive devices they have. Whether it's hearing aids, a wheelchair, an FM listening system, etc., they should be able to describe what it is and what it does in simple language. Schedule a peer in-service the first week of each school year for their class and let the teacher know your child will be helping to lead it. Let them demonstrate the device(s) they use to their classmates. It is important to become comfortable educating others about what is a necessary part of their life. By participating in the demonstration, it removes the elephant in the room and allows them to set the tone for how they expect to be treated.


ree


5. Discover the child's interests and cultivate them.


Introduce your child to a variety of activities and discover which ones they like. Help them develop their interests by signing them up for classes, joining clubs or participating in the activities as frequently as possible. This can be sports, music, dance, writing, photography, art, cooking, etc. Self-confidence soars when children learn a new skill or hobby they enjoy. They need the relaxation and downtime as well and both you and your child will be proud of their accomplishments.


6. Avoid labeling.


Do not use a child's disability as a descriptive term unless it is necessary to the discussion at hand. Remember, the child is a person first and should not be defined by their disability. It is offensive, damaging and can have long-term effects on their feelings of self-worth.


7. Teach the child self-acceptance.


Don't try to hide the cochlear implant, assistive listening device or other technology your child may use. Make these devices a natural part of their daily life. It is important for both their self-esteem as well as for their benefit. Sometimes people think they are protecting their children by covering up things that help them, but instead, children will often think that it is something to be ashamed of. This is not wise. A child who cannot accept their disability will be certain to encounter much more difficult obstacles as life goes on.


ree


8. Acknowledge effort, not someone else's definition of success.


One of the best ways to boost your child's self-confidence is to acknowledge their academic, physical and social efforts no matter how small. By doing so, you are showing them that your love and approval is unconditional and not based on the outcome of their efforts. Motivation to try should not be inspired by the possibility of a reward from the parent or teacher. Offer praise, not money, gifts or special treatment, for both their efforts and their achievements. This way, they will not feel that they deserve praise or love only when they accomplish what they set out to do.


Children with disabilities often face many obstacles growing up. Early development of self-esteem, self-confidence and self-acceptance are instrumental to their success. Use these tips at home and share them with the educators and professionals who are part of your community. Together, you can ensure your child a bright and confident future.


Paula Rosenthal, J.D. (she/her) is deaf and uses cochlear implants to hear. Her husband and one of her three children also use cochlear implants. Paula is an award-winning advocate for people with hearing loss and their families. She blogs at PaulaRosenthal.com and is available for speaking engagements. To contact her, please send an email to thepaularosenthal@gmail.com.


Interested in this article for your publication? It is available for syndication.

Send an email to thepaularosenthal@gmail.com with your request

and put "Syndicated Inquiry" in the subject line.

No reprints without express permission of the author.

(Social shares are always welcome!)

Having hearing loss used to be an obstacle, then it became my superpower.


ree

Mom of 3 kids, law school grad, suburban housewife, serial entrepreneur and oh, yeah, I'm deaf. The one thing that was never really a big deal while growing up, suddenly became a central focus during adulthood. Out of necessity, I used what many would consider a disadvantage and turned it into an asset. Coupled with my "there's always a silver lining" outlook of positivity, my deafness propelled me into a world where I have helped thousands of people deal with issues related to theirs or their child's hearing loss.


I never set out to be a role model but life is funny that way. The universe sent out strong smoke signals that were simply too big for me to ignore.


Read on for the story of how I got there, where I am today and what this means for you.

​

Back in 1992 I graduated from law school, one of only two people admitted with a physical disability my year. The other person was completely blind and I had a profound, bilateral hearing loss. We used to debate who had the "better" disability to have, each claiming our own. I didn't realize it then, but it was a testament to how our families had raised us, to always keep moving forward and not let our disabilities define us or what we could achieve.


Truthfully, growing up had been easy for me. I was talking and reading ahead of my diagnosis at three years old and was immediately fitted with hearing aids. For a long time my powerful hearing aids and expert speech-reading skills kept me afloat and I sailed my way to my first-choice college, far from home, unaware of the troubled waters ahead. While college had a lot of ups and downs, (largely due to my lack of self-advocacy skills) I managed to finish on a high note. I spent a few semesters on the Dean's List, rebooting my self-confidence after a rocky freshman year when I had been placed on academic probation and nearly flunked out of school.

​

While in law school I married Howard, a terrific guy who, like me, was entrepreneurial and just happened to have hearing loss too. Soon after my graduation we moved to Long Island, New York, started a family and began to develop a string of businesses.


Life seemed idyllic but the blissful bubble was about to burst.


The month we had our second child, our firstborn was diagnosed with hearing loss. She was 23 months old and we learned she also had significant speech and language delays as a result of the late diagnosis. Thus began a super stressful chapter in my life that was filled with anxiety, fear and uncertainty - not exactly the way I expected married life or motherhood to go.

​

Navigating the world as a parent of a child with special needs is, in a word, difficult. Researching special education programs, learning about Individualized Education Programs (IEPs), understanding parental rights in the special education process, honing much needed negotiation skills, along with finding qualified medical, therapeutic and educational professionals suddenly occupied most of my time. Coupled with the all too common cycle of grief, anger, guilt and sadness that comes with a diagnosis of a disability, not to mention a newborn baby, it was an incredibly overwhelming period.

​

I resolved to learn everything I could and began participating in a parent support group, attending workshops and joined a global organization supporting parents whom I thought were like me.


At my first convention I came face to face with another parent who expressed utter disbelief that I had graduated from college

despite my hearing loss.


Upon learning that more than 90% of deaf children are born to hearing parents, I realized that I was not quite like most of the other parents. It dawned on me that I was in a unique position where I could help others to better serve their children through awareness and education.


With two young children to care for and newly settled in the Midwest for a school that would help teach my child to listen and speak, I embarked on a brand new journey.


I designed and founded a community website called HearingExchange.


There I hosted live chats and message boards, wrote syndicated articles and newsletters and quickly connected people with valuable resources and services.


HearingExchange led to numerous speaking engagements all over the United States. I have spoken on a variety of topics before parents and hearing loss support groups, educational institutions and non-profit organizations. My child and I were two of four people featured in a public service video about cochlear implants directed by Academy Award nominee, Josh Aaronson of Sound and Fury fame. The video was widely distributed to thousands of people worldwide, shown to hundreds of convention attendees and, for many years, ran in a continuous loop at EPCOT in Disney World.

​

Today, I use cochlear implants to hear, as does one of my children and my husband. We have five cochlear implants among us and are grateful to have a remarkable quality of life. My children are grown and almost flown and I'm back to share more lessons I've learned over the years.


I am committed to empowering families who are facing the challenges of

raising children with disabilities.


You are not alone. Join me and learn how I found the strength to become the parent and advocate that my child needed and how you can too.

​

XoXo,

Paula Rosenthal signature

​

Paula Rosenthal, J.D. (she/her) is deaf and uses cochlear implants to hear. Her husband and one of her three children also use cochlear implants. Paula is an award-winning advocate for people with hearing loss and their families. She blogs at PaulaRosenthal.com and is available for speaking engagements. To contact her, please send an email to thepaularosenthal@gmail.com.

​


bottom of page