Skip to main content

WORLD DOWN SYNDROME DAY

 

World Down Syndrome is a special day marked every March 21st to celebrate people with Down syndrome. Down syndrome is a lifelong condition in which a person has an extra chromosome. Chromosomes determine how a baby’s body forms and functions as it grows during the pregnancy and after birth.

Early intervention can help individuals to improve on their physical and intellectual abilities. 

Right now, I am so glad that there is so much inclusion in the world. This is exactly what I was hoping for. We have people with Down syndrome that are being recognized!

This year, Sofia Jirau made history as the first Victoria’s secrets model with down syndrome! She was joined along with 17 other women for the company’s new campaign.

We have other people who have Down syndrome and who are totally amazing. Madeline Stuart is an Australian model who has done so much, walking for the New York Fashion Week, Paris Fashion Week, and London Fashion Week, despite having Down syndrome. Tommy Jessop is the first Down Syndrome actor to star in a Primetime BCC drama and also founded the Blue Apple Theatre Company.

We also have movies on Down Syndrome for you to check out. After Life is a movie made in 2003 about a Scottish journalist is torn between a high-profile career and caring for his younger sister who has Downs Syndrome.

Buddies is about an adventure movie on Three young people with Down syndrome who want to live out their wishes.  

For more movies on Down Syndrome, please visit the link Movies about Down Syndrome - IMDb

Let's appreciate people with Down Syndrome today and also on other days too. Inclusion is super important right now! They deserve all the love and support in order to reach their potential. Don’t restrict them!

 


Comments

Popular posts from this blog

EASTER SUNDAY- THE DAY JESUS ROSE FROM THE DEAD AND THE DAY I THOUGHT OF SUICIDE

I believe in the opinion that everyone has thought of suicide, and you can argue, but you know deep down, something may have happened to you to make you say, “I’m going to end it all.” But let’s talk about something that happened to me. Now, this article is not to scare you, or to make me seem easily influenced by the other voice. It is to remind you of three things. One, bottling emotions is not good.  Two, the role of caregiving for someone with a disability is not something that is your sole responsibility. Three, the devil is a bastard.  Okay, let's get into it. If you’ve been following my space, you probably know that I have a brother with Autism. As much as it is a beautiful experience, it is very scary. Whenever my brother is coming to the house from school, we ‘ Tobi-proof ’ the house, meaning that we have to hide some things, lock some things up, and it is quite a lot.  See also: Choosing Love as a neurotypical sibling Long story short. I had a meltdown on Sunda...

SPECIAL NEEDS PARENTS, BREATHE!

Sometimes, you need to say “ Screw it ” and take that break” As special needs parents and caregivers, we are used to being strong and ever-present. The word “ Break ” doesn’t exist in our vocabulary, except when we see intense moments of distress and realize that we need to rest. At the Exhale Conference 6.0, I had the honor of moderating a session on creating a sustainable future for children with special needs and I was reminded of one thing- Now is the time to start planning for the future.  Not tomorrow, not next week, but now.  But guess what? Your long-term planning for the children won’t be effective if you don't take care of yourself. The future is not just about setting up a trust fund but taking care of ourselves to ensure we can continue this journey with resilience and strength. The Exhale Conference was organized by a powerhouse, Mrs. Bukola Ayinde, a disability advocate and a special needs mother to a child with cerebral palsy. It was the first time meeting Mrs. ...

Why Special Education Can Never End

Are you aware that you’re unique? That there is no one else like you. This is not me trying to butter you up. I believe that everyone is unique and in this case, I’m leaning towards the aspect of learning.  You know what upsets me? When parents and teachers compare students to one another. You’ve probably heard the words,” Does this child have two heads? Why did he do better? How is he learning this faster than you are?” Dear comparison master, everyone just learns differently. One thing that many people forget is that each person has unique strengths, challenges, and learning styles. My brother has Autism and leans towards learning in Audio-visual form. I’ve realized that people who are not on the spectrum or neurodivergent, also learn differently.  This brings me to the important point that a classroom should be able to accommodate people’s learning differences.  See: Ten Things to take away from Your Safe Space NG 2024  Let me give you an example. My brot...

Choosing True Love as a sibling of special needs.

What It’s Like to Date as a Special Needs Sibling? The truth is, I worry about love. Who doesn’t? You’re choosing someone to build your life with, and what happens if you make a bad choice? It’s not just about my happiness. It’s about my future children, my stability, and, in my case, my little brother. The topic of caregiving has been on my mind since I reached a certain age, making me think more about the future; my career, my health, my responsibilities… everything. Love and relationships are a huge part of that. I’ve never doubted that I have the best friends around me…people who understand my role as a neurotypical sibling. But when it comes to love? That’s where the anxiety creeps in. Not sure if you’ve noticed, but the dating pool is a big mess. I’d describe it as “shege” before finding real love” except if you’re God’s favorite and somehow skip the drama. My situation hasn’t been smooth, and I’d like to think that God is saving me for the one. Unashamedly, I love romance, ...