Our Highs are Higher

Carrie Woodcock and her family posing in front of a lovely rural stream

Carrie Woodcock and family

Carrie Woodcock is director of the Maine Parent Federation and a parent of 10-year-old Sami who has Down syndrome.


This summer, I attended a conference alongside doctors, nurses, physician assistants, therapists and other medical professionals, all of whom work with children with special healthcare needs and disabilities. I was there to represent parent voices as the director of the Maine Parent Federation, an OSEP-funded Parent Information Center. I am a big supporter of, and was very excited for, the keynote presenter that day, Dr. Brian Skotko.

Dr. Skotko is a genetic specialist and co-director of the Massachusetts General Hospital Down Syndrome Program. He has also gone on to facilitate the creation of many such clinical programs throughout Massachusetts. I was first introduced to him at the annual Massachusetts Down Syndrome Conference. I was so impressed with our first encounter that now, whenever I attend events at which he’s speaking, I always attend his sessions—regardless of their subject matter—and  always walk away having learned something new.

At the conference we attended this summer, Dr. Skotko discussed the impact of a Down syndrome diagnosis on the immediate family. He and his staff had conducted some of the first surveys of parents, siblings and individuals with Down syndrome. To say that I was thrilled that a physician and sibling of an individual with Down syndrome himself took this opportunity to raise awareness for family engagement, a crucial subject many times overlooked by medical professionals, was an understatement. His data were brought to life by his personal experiences, and were overwhelmingly positive. They indicated that a large majority of surveyed immediate family members love and are proud of their family member with Down syndrome.

During a question and answer period following the presentation, a professional in the front of the room challenged some of the data Dr. Skotko had presented. She brought to his attention that perhaps the data were positively skewed because parents and family members would have guilt associated with speaking negatively about their experiences and, ultimately, their own family member. Well, I am not one to hold my tongue, but I did have to pause to ensure I reigned in my “mommy” emotions and represented the parent voice in an assertive yet positive way.

In that moment, memories from my 10 years of being a mom to my precious gift rushed back. Some of the first feelings to come back to me were those that I have been ashamed to admit as a parent. For example, the diagnosis at my daughter’s birth had me thinking that I would always be a parent to a child living at home. The hours in the hospital enduring her open heart surgeries had brought me emotionally to my knees, wishing my child was healthy. I recalled the times her anxiety caused bathroom accidents in public places, which had me wishing for normalcy. Listening to friends talk about their gifted and talented children had me feeling like an outsider. I remember feeling sad because the birthday party and play date invites were few and far between, if at all. For a second I thought that maybe this woman was right; maybe I do sugar coat my family’s reality because I am too ashamed to admit otherwise.

But in the next moment, I saw Sami’s hand reaching for my mom’s face, days after open heart surgery. This was the first expression of her personality shining through. I remembered my toddler son translating her words and being so proud that he was the only one who could understand her. We celebrated her first everything and then celebrated her first everything all over again when she regained a lost skill. I recalled the way that, no matter where we are, she makes people smile, no matter what kind of day they may be having. And the oh-so-many little things in life I would have completely overlooked were it not for her.

I gathered my thoughts, raised my hand, and explained this concept to the group. In fact, the professional that asked the question was right; the challenges are hard and often. We do have doubts about our ability to parent and yes, horrifyingly enough, we will ask “why me?”

However, we celebrate and appreciate all that is positive. We do this in a way that is bigger than any outsider could know, and we do it time and time again. The impact has been so positive—my family completely changed for the better the moment Sami came into our lives. In addition to the daily joy we experience with her, all of us are dedicated to her cause, and the cause of others. My professional career has shifted from sales and marketing to assisting families with their own special loved ones. My husband, who was and still is a physical education teacher, has brought her spirit to the way he interacts with his students, including those with special needs. Lastly, but perhaps my proudest family accomplishment, is how Sami refers to her 13-year-old brother as her hero. No matter the circumstance, he shows no embarrassment towards her, only love and admiration.

I summed up my comments that afternoon, and I’ll leave the same simple thought for you here. “You see, our lows may be lower at times, but our highs are more often, and they are always so much higher. We wouldn’t dream of trading it for anything!”


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Carrie Woodcock and daughter, Sami.
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Director of the Maine Parent Federation and a parent of 10-year-old Sami who has Down syndrome.

Words of Wisdom

Note: October is Down Syndrome Awareness Month.

Jordon Bills

Jordon Bills

Jordan Bills, M.A., CCC-SLP, is a speech-language pathologist (SLP) at Washington Speech in Fairfax, Virginia. She works with children of all ages with various speech, language, and feeding disorders. She received her bachelor’s degree from the University of Virginia and master’s degree from the George Washington University. You can read more about Jordan’s credentials and accomplishments on the Washington Speech staff page.


Why did you become a speech-language pathologist (SLP)?

In high school, I volunteered at a center for blind and visually impaired children for three summers. I worked side-by-side with the speech pathologists, occupational therapists, and physical therapists at the center. The work they did was incredible and I knew this is what I wanted to do! One child in particular had a large impact on me. He was three years old and unable to respond to his name. By the end of our summer together, he was not only turning toward others when they said his name but also responding to their greeting. I’ll never forget the feeling when I heard him say, “Hi, Jordan!” In that moment, I understood the power of communication. Communication is what connects us to one another. It’s what makes our lives so beautiful! I feel lucky to spend my days helping children communicate more effectively.

Why do you enjoy working with children with Down syndrome?

As a pediatric SLP, I have the privilege of working with children with Down syndrome across their lifespans. This is one of my favorite populations to work with because of the great potential for growth. Every milestone is celebrated, even the small ones, as each child works so hard to develop their speech and language skills. Every child with Down syndrome has unique strengths and interests, which I use to support the development of new skills. I have targeted bilabial sounds /b, p, m/ in functional phrases while playing basketball; used a child’s desire for hugs to teach expanded question forms (Can I have a hug?); and taught subject-verb-object sentences using Disney characters.

With younger children, I spend a lot of time playing on the floor. Children tend to learn best through repeated experiences with real objects and situations. Play is their vehicle for learning. As they enter elementary school, our sessions include more structured tasks focusing on the skills they need to participate fully in the classroom and to interact with friends. My goal for all of my clients with Down syndrome is for them to be able to effectively communicate with friends, family, and professionals across environments. My hope is that improved communication will allow them to experience the joys in life that come from making connections with others.

One of my favorite events is the annual Buddy Walk in Northern Virginia. Attending this event gives me the opportunity to see some of my patients outside of the therapy room. I love watching them with their families and friends participating in a community event. It reminds me of why I love what I do!

What are some tips that you have for families with children with Down syndrome?

Parents and other caregivers are the primary communication partners in a young child’s life. Therefore, parents play a critical role in helping their children develop speech and language skills. Below are some strategies for families to support communication development from birth through early elementary school.

Strategies for Birth to First Word Users

  • Focus on pre-linguistic skills. These are skills a child needs to master before words emerge. They include: joint or shared attention, social referencing (checking parents’ facial expressions to understand how to react appropriately in new situations), turn taking, pointing, sustained engagement and attention, and imitation.
  • Use language stimulation techniques in everyday activities to help your child develop his/her understanding and use of new vocabulary words. Techniques include: self-talk, parallel talk, sentence completions, choices, and communication temptations (actions you can take to set up the environment to tempt your child to communicate with you).
  • Consider a Total Communication This evidence-based approach incorporates speech, manual signs, gestures, pictures, and/or a speech-generating device to help children communicate as effectively as possible while developing verbal speech. This approach can reduce frustration and support long-term vocabulary development.
  • Familiarize yourself with the stages of play. Challenge your child to engage in symbolic and early pretend play.
  • When teaching new words, use real objects or pictures of real objects. Incorporate vocabulary learning into your daily activates.
  • Don’t forget about your child’s oral-motor and feeding skills. Children with Down syndrome are at risk for feeding difficulties. A certified speech-language pathologist can evaluate your child and develop an individualized treatment program to help him/her improve oral-motor skills for feeding.

Beyond First Words: Learning to Combine

  • Research shows children begin to combine words when they reach a single word vocabulary of around 50 words. Ensure your child has a variety of single words (e.g. nouns, verbs, pronouns, social words, adjectives) he or she can use to combine. Keep a record of the words your child uses to monitor vocabulary growth.
  • Continue to build your child’s vocabulary during play and daily routines. Teach 2-3 word combinations and encourage imitation. Children with Down syndrome benefit from repeated experiences with the same activities and vocabulary.
  • Use expansions (adding one word to what your child says) to model phrases. Do this often! It will likely take many repetitions before your child imitates your expanded phrase.
  • Try a pacing board to help your child learn to combine words. Pacing boards provide a visual and tactile cue to remind your child to use two words. They are helpful for children with Down syndrome given their strengths in visual learning. A simple pacing board can be two large dots on a piece of cardboard or thick paper. Point to the first dot and say the first word, then point to the second dot and say the second word.
  • Read often! Try books with repetitive phrases your child can learn and eventually fill in.

Early School Age

  • As your child’s vocabulary and utterance length increases, speech intelligibility often becomes a main concern. Again, a pacing board can be a useful tool. This time, your focus will be on teaching your child to speak slowly and producing each word deliberately while touching one dot on your pacing board. Speaking with a slowed rate can help improve your child’s overall intelligibility.
  • In speech therapy, your child may be working on specific speech sounds or patterns of sounds. Work closely with your child’s speech-language pathologist to continue practice at home. To increase your child’s motivation, incorporate target sounds into highly meaningful words. For example, if your child is working on the /k/ sound, “cookie” and “car” may be very motivating words. Daily practice is key!
  • Use recasts to help your child develop appropriate grammar. Grammatical recasts are when you take your child’s utterance and repeat it using adult grammar. For example, if your child says, “dog eat,” you would say, “Yes, the dog is eating.”
  • Consider AAC (augmentative and alternative communication) to supplement verbal speech. This may increase your child’s ability to be understood, participate in class, and engage socially. It may also decrease frustration.

Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Things People Say

Note: October is Down Syndrome Awareness Month.

Jessica Wilson and her son, Jasper

Jessica Wilson and her son, Jasper

A guest blog by Jessica Wilson. Jessica and her son, Jasper (aka Jaz, Jazzy, the JazMaster, or Dude!), live in a cozy house of fur with two crazy dogs and two lazy cats. Their favorite activities include singing movie hits, dancing in the kitchen, snuggling and traveling the world together. Jessica is Director of Communication and Dissemination for the Center for Parent Information and Resources (CPIR) and Resources for Access, Independence and Self-Employment (RAISE) projects with the Statewide Parent Advocacy Network (SPAN) in New Jersey.


Number One. “Did you know?”

They never complete the thought, as if just looking at him implies what they’re really asking. I ache to play dumb: Know what? That he would almost never cry as a baby and be a champion sleeper? That he would love to swim but hate to play soccer? That I could love him ‘til it hurts and still get so annoyed by some of his antics? As obnoxious as my brain screams for me to be, I simply answer, “No. After losing the first one, I didn’t want to take any chances with this very wanted baby.”

The mention of my previous sorrow precludes them from saying anything directly about those tests, so I leave it at that. I resist ranting about warped concepts of perfection or the technologies the medical community pushes that are incapable of measuring the value of those born “dappled.” If I launch into my diatribe, their eyes glaze over as they nod in the faux agreement children give their parents when they just want the scolding to stop. I can always tell when they’re thinking, “I would have the test.” I couldn’t guess what they would do if it were positive.

Number Two. “My sister’s/cousin’s/brother-in-law’s/landlord’s daughter/nephew/classmate/neighbor is ‘like him’.”

What, rakishly handsome? Lucky them. A consummate flirt? Better watch out! The self-appointed town mayor, greeting every person or animal we see on the streets? Good luck getting anywhere quickly with such a gregarious kid.

I suppose it’s an attempt to connect, a way to say “he’s okay” because they know someone who knows someone who… But sharing an extra chromosome doesn’t make anyone like someone else any more than two people having green eyes does. Don’t tell me these six-degrees individuals are “like” each other. They aren’t.

Number Three. “He’s so high-functioning.”

Yeah, far more than I am at 3:00 a.m. “MOMMY!” “urgh…?” “WHY ARE YOUR EYES CLOSED?!” “I’m sleeping, baby.” “WHY?!” “unnnhhh…” “READ TO ME!!!!” (seriously?)

Number Four. “Funny, you can’t see it.”

What’s there to see? His almond shaped eyes that look through me as the spark of laughter flickering within them sears my soul? His cute little hands with that long crease across his palms holding mine, petting the cat, learning to write his name, wiping away tears when he’s mad? The orthotics helping reshape his desperately flat feet?

What exactly are you looking for that will legitimize him in your eyes? Maybe I should carry the envelope with the verdict handed down by some anonymous technician. Perhaps the letter from the state when the lab automatically reported his existence to the county health department “for statistical purposes.” What can’t you see? He’s a kid, growing up loved. What else are you looking for?

Number Five. “I’m sorry.”

You should be. You’ll never hear the thoughts he speaks to me with his smiling brown eyes as he tilts his forehead to rest against mine. You’ll never drink in the heat that radiates from his head or taste his soft hair on your lips. You’ll never be awakened (again) at 3:00 a.m. by the hot air from his mouth on your face as he whispers, “Mommy, I want snuggles.” You’ll never know how it feels to celebrate every jump forward in development that other parents take for granted, but when he finally does it, it’s a very, very large molehill.

You should be sorry that you can only see back in time. This is a new era with new opportunities and new ideas about potential and worthiness. I’m only sorry it’s taken this long and that we still have so far to go.

Number Six. “That’s awesome!”

Thanks, Brian—you are the right kind of friend. May everyone with a kid “like mine” know a man like you.

Number Seven. “I don’t know how you do it.”

I’m his mother. Still confused?

Things I Say.

“I’m so proud of you.” “Boy, you’re handsome!” “Why won’t you let me cut your nails?” “TURN THAT DOWN!” “Wanna go bowling?” “Sweetheart, don’t let the dog beg like that.” “Would you please put this stuff away?” “You’re just too good to be true/Can’t take my eyes off of you.” “No, I don’t want to smell your feet.” “I love you, my sweet angel. You’re my heart and soul, my love and my life.” “You know you drive me nuts, right?”

Number One.

“I’ve loved my son since before he was ever born. What else is there to say?”


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

“Voices from the Field” Interview with Nina Brown, Early Childhood Special Educator in Fairfax County, Virginia

Note: October is Down Syndrome Awareness Month.

Nina Brown

Nina Brown

Nina Brown earned her master’s degree in education from George Mason University and is currently a teacher in Fairfax County, VA, where she has spent the majority of her career. Prior to that, she taught in Liberty County, GA. She has dedicated her career to teaching young children with disabilities and partnering with their families to help build a foundation for educational success. She recently graduated from George Washington University with a degree in education leadership and administration in special education, in hopes of continuing to support students and families throughout the county.


How did you begin your career in early learning and special education?

As a child, whenever we went to visit my grandparents, we would always spend time with my aunt in her group home. She had developmental disabilities and medical needs that prevented her from living at home. Even though I was only a child, I recognized the limited access and opportunities available to her within her community. She was an adult, but had never attended school, which seemed incomprehensible to me. From a very young age, I knew I wanted to go into a profession where I could advocate for people with disabilities. I combined that with my love for children and eventually earned my master’s in early childhood special education. After 17 years of teaching, I recently earned an education specialist degree in leadership and administration in the area of special education. With this degree, I hope to have a broader impact on children and their families throughout the school district in which I work.

What recommendations do you have for improving educational experiences of children with Down syndrome?

I believe that high-quality early childhood education is fundamental to long term success for all children, but most critically to students with disabilities. Early childhood special education is often the “gateway” to the education system, and it has been my goal throughout my career to be a positive liaison between schools and families.

Two steps fundamental in facilitating positive educational experiences are

  1. helping families access community services and supports, and
  2. incorporating evidence-based instructional practices into classroom activities.

Children with Down syndrome tend to have strong social skills, so building upon those strengths to increase their learning opportunities in all areas of development is beneficial, regardless of their age. Teachers and parents should always have high expectations of the abilities of children with Down syndrome. Children with Down syndrome often know much more than they are able to communicate. The use of visuals and manipulatives in acquiring new skills builds upon their strengths as visual learners. Providing increased processing time and consistency are also instructional strategies that complement the learning style of many students with Down syndrome.

What suggestions do you have for expanding access to high-quality early learning opportunities for children with Down syndrome?

One of my responsibilities as an early childhood special education teacher is to transition preschool students into kindergarten, helping to ensure they will be educated in the least restrictive environment, with their peers, in the school closest to home. It has been my experience that acceptance of students with disabilities varies among schools within the same district, even though inclusion benefits all students, with and without disabilities. Schools may look at a label or diagnosis of a student to help in their decision making for programs and services. I believe it is my responsibility, and that of all teachers, to look at the individual child and their abilities first and foremost. In all aspects of my job, I strive to advocate for the needs of students in order to help build a strong educational foundation to make the most positive impact on their future.


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.


Baby G — Spreading Awareness

An OSERS Guest Blog post by Felipe Martinez, a father of a daughter with Down syndrome.


The Martinez family, including Baby G.

The Martinez family, including Baby G.

We started with 32 week old twins. Throughout that struggle, we had no idea what was yet to come. Eighteen months later Baby G was born. Our world was about to be turned upside down…again.

Upon receiving the preliminary diagnosis of Down syndrome, I was in shock. I had no clue about what doctors and nurses were telling me, and I had not even had a chance to speak with my wife, Amy, about the newest addition to our family. Upon receiving the news of possible heart defects, the Down syndrome diagnosis took a back seat. Our next mission was to get Baby G to gain some weight to be able to handle open heart surgery. The services were not available locally, so we had to make arrangements to leave town for two weeks. After the initial confusion and medical procedures, Amy and I finally had a chance to sit down and discuss our future. The twins were well, and Baby G had recovered from her major operation.

Baby G has played a major role in how we are spreading awareness today. She has brought a whole new meaning to celebrating life. She is the happiest human being we have ever met. She is the most loving person on the planet. This comes with a slight price, though. She has learned that her charisma can get her out of tasks that she would rather not do. It has been particularly difficult getting her to focus on school and academics.  Although she started early education when she was two and a half, she has never had an environment with a structured program in place. She is now five years old, and is having a difficult time adjusting to a public school system that offers more structure. After two Admission, Review, and Dismissal (ARD) meetings, we are still struggling to come up with a plan that will help her focus and learn.

Collaborating with school administration, Amy and I continue to establish a routine that comes home with her every day. We try to do the same types of activities and achieve the same goals at home and school. We, as parents, sometimes feel guilty for not implementing these types of strategies earlier in her life; it may have helped her adapt more easily to the new setting. There are no regrets, but through our experience, we can help other families avoid similar situations.

Five years have gone by, and I would not trade them for anything in this world. I am the President of the Down Syndrome Coalition for El Paso. Baby G has pushed me to be her best advocate. She has also taught me to live in the moment. Most importantly, I have learned that there are so many families that share a similar story. Our goal is to raise awareness so that no other family has to worry about its child’s future.


Opinions expressed herein do not necessarily reflect the position of the U.S. Department of Education and such endorsements should not be inferred.

Challenges Not Barriers

An OSERS Guest Blog post by Jadene Sloan Ransdell, who has a son with Down syndrome.


Matt with his mother, Jadene

Matt with his mother, Jadene

I share my life with a son who has Down syndrome. His life has been filled with twists and turns that have helped to make me the person I am today. We’ve been through a lot—Matt and I—from the time we received his diagnosis and were encouraged to place him in a state institution, to residential placement in Germany while my husband served in the U. S. Army, to now—he is over 40.

Matt experienced delays in his development despite my dedication to keeping him stimulated and as active as possible. He took his first steps just before his third birthday and was finally toilet trained when he was nine years old. When Matt was a teen, he had a seizure in the shower. His use of words for communication was inconsistent, as he would gain a vocabulary and then lose it, several times throughout his life. He displayed many characteristics that resemble Autism, although he was not diagnosed until he was an adult. Over the years he has received several mental health diagnoses that now make sense with identification of early onset Alzheimer’s. There is much to share about that discovery, but I want to focus on Matt’s incredible accomplishments, despite the challenges that he has faced!

Matt left public school in 1996. We paid privately for him to attend a community program two days a week, although he wasn’t especially happy there. In late 1997, he received funding through a Medicaid Home and Community Based Waiver to pay for needed services. With that resource, he moved into his own home (with live-in support) and did something that he enjoyed. Of course, when he moved, I missed him terribly, but I knew that he deserved to grow up and lead his own life, just as his brother had.

Matt volunteering at the local VA hospital

Matt volunteering at the local VA hospital

About five years ago, he was given a chance to volunteer at the local VA hospital. It was a life-changing opportunity, as he takes incredible pride in his job. He loves working with his “soldier men” and the patients appreciate seeing him. The medical staff and other volunteers have told us that he is a wonderful asset. In fact, former Congressman C.W. “Bill” Young (deceased) formally thanked Matt for his service to the veterans and that tribute can be found in the May 20, 2013 Congressional Record!

I am proud of Matt and the path that he has walked. Some painted a bleak future for him. The recommendation of a day program and group home placement was not best for him, and I knew it. I worked tirelessly, encouraging people to discover the incredible person that I knew. And Matt worked hard, too. Even though he never spoke more than a few words at a time and had periods of unsettling behaviors, Matt has created a life that is beautiful and very meaningful to him, me, and the world. He has shown me there is always hope for the future!


Opinions expressed herein do not necessarily reflect the position of the U.S. Department of Education and such endorsements should not be inferred.

To The Mother Who Just Learned Her Child Has Down Syndrome

An OSERS Guest Blog post by Eliana Tardio, a mother with two children with Down syndrome. 


Ayelen and Emir holding hands

Ayelen and Emir holding hands

I was five months pregnant and ready to learn my baby’s gender. All I wanted to know was which would be the best color to paint the walls of his or her room. I didn’t want to know anything else, really. I honestly didn’t know there was something else to be learned at that appointment. However, and because life is totally unexpected, his gender was unveiled alongside another big surprise. The doctor said, “He may have a genetic disorder.”

I saw the world breaking apart into small pieces right in front of my eyes. I felt an immense disappointment and a desperate need to blame someone or something. I blamed myself, and then I challenged God by asking him for a proof of his greatness. I wanted my child to be cured, just because at that point of my life, I was so supremely ignorant, that I just didn’t know that Down syndrome is not an illness, but simply a way to exist and to be.

The following months were tough. I remember living on a roller coaster of emotions between denial and surrender to the incredible love growing up inside my womb. As the day finally came, I didn’t feel any physical pain, because all I wanted to see was his face. I wanted to see how he looked. He didn’t cry, and so, I had only a few minutes to hold him in my arms before he was taken to the NICU. In those hundredths of seconds, I looked into his eyes, and that was enough to fall in love. Down syndrome and all, I realized that he was already the most amazing and perfect child, because he was mine, born from me and to me.

Emir and Ayelen together

Emir and Ayelen together

It has been 12 years since Emir was born. Three years after, Ayelen, my second child, was born. This time it was a girl, who was born with Down syndrome as well. To the mother who just learned her child has Down syndrome, I offer this:

  1. You may not believe me now, but even if you never dream of this moment, this may turn into your dream life.
  2. All these painful and confusing feelings you are going through right now are just a path to a total transformation of your soul and your heart. Be patient and don’t blame yourself. These feeling are not out of lack of love or acceptance of your child. They are instead a proof of how much you love him, and how much you have to learn.
  3. Yes, your child is going to be perfectly fine. He’s going to be happy, he’s going to be smart, he’s going to make you cry out of pride, and he’s going to become your reason to believe, your strength to fight, and your most amazing excuse to slow down and enjoy the small things in life.
  4. For sure, there are going to be tough times. Just as you are going to meet amazing people, you are going to be challenged by mean and indifferent individuals as well. They will both teach you something. The first, that everything is possible. The second, that everything can be possible but you have to hold the power to make it happen—and you will.
  5. Your child, as any other child, is going to be the reflection of your love, faith, devotion and hard work as a parent. Being a parent is never easy, but it is definitely worth it!

And in a couple of years, on top of all the things that typical parents do for their children’s well-being, you are going to be proud to be an advocate, a specialist, an expert and the one who defines his future, has the power to change what needs to be changed, and to create what hasn’t been built yet. You are the parent of an inspiring human being who has no comparison: Your child!

Congratulations for that!


Opinions expressed herein do not necessarily reflect the position of the U.S. Department of Education and such endorsements should not be inferred.

Eliana Tardio, a proud mother with two children with Down syndrome, Emir and Ayelen. She works as a Program Director for the Parent Education Network and is well known as a diversity and Latino activist that works through her different online platforms to create awareness. Her English website is www.elianatardio.us.

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A mother with two children with Down syndrome, a Program Director for the Parent Education Network and is well known as a Diversity and Latino Activist.