#Developmentaldisabilities

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#Developmentaldisabilities Reel by @advocacywithabbey - To the little girl who at 8 years old didn't want to live anymore after constant bullying from teachers at her school. The girl whose grade 4 teacher
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@advocacywithabbey
To the little girl who at 8 years old didn’t want to live anymore after constant bullying from teachers at her school. The girl whose grade 4 teacher told her she’d end up in jail. The girl who nearly dropped out of high school for thinking she was “too stupid” to graduate. Who was suspended over and over again from elementary & high school for acting out. Who applied to ten universities because she thought she wouldn’t get accepted anywhere. Who was bullied by her classmates and peers for being “annoying,” “weird,” and “stupid.” To the girl who, up until the age of 17, had truly given up on any hope of a future - we did it. In spite of literally every barrier, somehow, someway, we did it. In the middle of all this excitement, my mind keeps circling back to one person: my grade 10 history teacher, Mr. Witmer - the first teacher to tell me that me I was capable of great things. I remember having received a 50% on a test in his class at the beginning of the semester. After handing the tests back, Mr. Witmer asked me to step into the hallway. I walked into the hallway, prepared to get in trouble for something I’m sure I did. Instead, he held up the test, looked me in the eyes and firmly said, “I know you’re capable of more. You can do better than this.” I will remember those words forever. Mr. Witmer was the first teacher who looked past the disruptive behaviour and lack of effort and saw what was actually there. A kid who was told for so long that she was a failure that she eventually believed it. A kid who was overwhelmed. A kid with serious learning & developmental disabilities who was unsupported. Sometimes the difference between a disabled kid who gives up and a disabled kid who gets into Harvard is an educator who sees them and refuses to let them give up. I was accepted to Harvard - not because I overcame my disabilities. Not because I suddenly became easier to teach. But because someone finally gave me the tools, the belief, and the accommodations to succeed.
#Developmentaldisabilities Reel by @nysa_majority (verified account) - March marks Developmental Disabilities Awareness Month. We honor the contributions of people with developmental disabilities and continue working to e
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@nysa_majority
March marks Developmental Disabilities Awareness Month. We honor the contributions of people with developmental disabilities and continue working to ensure equal opportunity and accessibility.
#Developmentaldisabilities Reel by @nakedheartfoundation (verified account) - «А вдруг я что-то упускаю?» 💬

Этот вопрос хотя бы раз задавал себе почти каждый родитель.  Когда речь заходит о ранних признаках нарушений развития,
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@nakedheartfoundation
«А вдруг я что-то упускаю?» 💬 Этот вопрос хотя бы раз задавал себе почти каждый родитель. Когда речь заходит о ранних признаках нарушений развития, тревога может усиливаться. Хочется быть внимательными к своему ребенку — и при этом не накручивать себя. Во многих странах для оценки риска РАС у детей примерно в возрасте полутора лет используют скрининг M-CHAT-R. Его можно заполнить на платформе «Обнажённые сердца онлайн». Важно помнить: скрининг — это не инструмент для постановки диагноза. Он только помогает понять, есть ли повод обратиться к специалисту. Если вас волнует поведение ребенка, можно начать с опросника, а затем обсудить результаты с педиатром, который знает о ранних проявлениях аутизма. «What if I’m missing something?» 💬 Almost every parent has asked themselves this question at least once. When it comes to early signs of developmental disabilities, anxiety can increase. You want to be attentive to your child — but without overthinking everything. In many countries, the M-CHAT-R screening is used to assess the risk of autism spectrum disorder (ASD) in children around 18 months of age. It can be completed on the Naked Heart Online platform. It’s important to remember: screening is not a diagnostic tool. It only helps indicate whether there is a reason to consult a specialist. If you are concerned about your child’s behavior, you can start with the questionnaire and then discuss the results with a pediatrician familiar with early signs of autism.
#Developmentaldisabilities Reel by @madisontevlin (verified account) - Part 1 of answering this question and thank you so much for asking!👇 

Kindergarten - 8th grade was a little harder for me in school. I was the only
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@madisontevlin
Part 1 of answering this question and thank you so much for asking!👇 Kindergarten - 8th grade was a little harder for me in school. I was the only person with Down syndrome and I didn’t have that extra support of special education classes. I struggled a lot because I felt like people didn’t fully understand me or how I learned. Once I got to high school everything changed for me! My mom and dad found a school that we fell in love with. The principal and teachers were amazing, and they had classes that were a lot more specialized for people with different learning styles. I loved having my Multiple Exceptionalities/Developmental Disabilities (MEDD) classes while having the option to integrate into typical classes as well. Having the support of teachers that really took the time to understand me really helped me be the best student I could be. And having a mixture of friends with and without disabilities was so much fun! We’re all different at the end of the day and it’s important to have the opportunity to create a learning environment that works best for our unique needs. Whether we choose MEDD classes or we prefer to be integrated primarily in typical classes, I don’t think there’s a right or wrong way. All that really matters is that we’re included! That we have options, and that we have support, no matter where or how we choose to learn. ❤️ #specialeducation #specialeducationteacher #inclusiveeducation #inclusionmatters #educationforall
#Developmentaldisabilities Reel by @follow_trend11 - This viral X post features a 21-second video of hands manipulating a blue cylindrical fidget toy with colorful sliding beads through segmented slots,
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@follow_trend11
This viral X post features a 21-second video of hands manipulating a blue cylindrical fidget toy with colorful sliding beads through segmented slots, captioned “Reducer stress ...” to promote relaxation, amassing 27,000 likes and 8.7 million views since November 14, 2025. The toy aligns with fidget gadgets designed for tactile stimulation, where preliminary research in journals like Research in Developmental Disabilities suggests such tools can lower physiological stress markers like heart rate in anxious individuals, though large-scale evidence is limited. Post engagement sparked promotional replies with Amazon affiliate links to similar products, illustrating how short-form ASMR-style videos fuel impulse buys for novelty stress-relief items amid rising mental health awareness.
#Developmentaldisabilities Reel by @_walshshane (verified account) - Join @bestbuddies and @specialolympics today on spread the word day to promote respect, inclusion, and belonging for people with intellectual and deve
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@_walshshane
Join @bestbuddies and @specialolympics today on spread the word day to promote respect, inclusion, and belonging for people with intellectual and developmental disabilities. With your help, the R-word can continue to be eliminated from individual’s vocabularies. Sign the pledge here!⬇️ https://www.bestbuddies.org/spread-the-word/ #bestbuddies #specialolympics #inclusion #spreadtheword🗣
#Developmentaldisabilities Reel by @moon.learning_center - "Speech doesn't start with words…"
"This simple touch can improve speech."

Cheek massage is an important oral-motor technique used in speech therapy
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@moon.learning_center
“Speech doesn’t start with words…” “This simple touch can improve speech.” Cheek massage is an important oral-motor technique used in speech therapy to strengthen the muscles needed for clear speech and feeding. This gentle stimulation helps improve: ✔️ Oral muscle strength ✔️ Lip and jaw coordination ✔️ Speech clarity and articulation ✔️ Chewing and mouth control ✔️ Sensory awareness around the mouth For children with speech delay, autism, or oral-motor weakness, regular cheek massage builds the foundation for better communication. Small exercises today lead to big communication milestones tomorrow. 💙 🌱 Sensory Benefits ✔️ tactile stimulation से sensory awareness बढ़ती है ✔️ hypersensitivity कम करने में मदद ✔️ बच्चा touch को tolerate करना सीखता है Cheeks Massage एक effective oral–motor exercise है जो speech delay, autism और oral weakness वाले बच्चों के लिए बहुत फायदेमंद होती है। इस massage से गालों की मांसपेशियाँ activate होती हैं, जिससे lips, jaw और tongue को सही support मिलता है। Regular therapy से बच्चे की speech clarity, feeding skills और mouth control में noticeable improvement देखने को मिलती है। 🌙 Moon Learning Centre: Trusted Autism Center in Delhi ncr We provide both Home Sessions and Online Sessions to make learning more flexible and convenient for you. Faiz sir special educator(intellectual developmental disabilities) RCI registered Contact number 9958692967
#Developmentaldisabilities Reel by @specialolympics (verified account) - This #ThrowbackThursday, we are reminded that #WordsMatter.

The R-word has a long history of being used to demean, insult, and discriminate against p
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@specialolympics
This #ThrowbackThursday, we are reminded that #WordsMatter. The R-word has a long history of being used to demean, insult, and discriminate against people with intellectual and developmental disabilities (IDD). Learn more and join the movement to #ChooseToInclude at the link in #SpecialOlympics bio.
#Developmentaldisabilities Reel by @moon.learning_center - ✨ From Silence to First Words ✨

This little child once struggled with speech delay and was unable to say even simple words like "Mummy" or "Papa." Th
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@moon.learning_center
✨ From Silence to First Words ✨ This little child once struggled with speech delay and was unable to say even simple words like “Mummy” or “Papa.” Through consistent speech therapy, structured oral-motor exercises, sound stimulation, and parent involvement, we focused on building communication step by step. Today, hearing this child call out “Mummy” and “Papa” is a proud and emotional milestone. ❤️ This progress reminds us that early intervention, patience, and the right therapy can truly change a child’s world. Every small word is a big victory. Every voice deserves to be heard. 🌈 🌙 Moon Learning Centre: Trusted Autism Center in Delhi ncr We provide both Home Sessions and Online Sessions to make learning more flexible and convenient for you. Faiz Sir special educator(intellectual developmental disabilities) IDD RCI registered Contact number 9958692967 #speechtherapyworks #speechdelay #firstword #autism #mummypapa
#Developmentaldisabilities Reel by @thepastdiary_ - Katherine and Nerissa Bowes-Lyon were first cousins of Queen Elizabeth II because their father, John Herbert Bowes-Lyon, was the brother of the Queen
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@thepastdiary_
Katherine and Nerissa Bowes-Lyon were first cousins of Queen Elizabeth II because their father, John Herbert Bowes-Lyon, was the brother of the Queen Mother, Elizabeth Angela Marguerite Bowes-Lyon. Born with severe developmental disabilities, Katherine (15) and Nerissa (22) were placed in a mental hospital by their parents. At first, the family visited them, but over time, the visits stopped completely. Official records falsely claimed that their deaths had occurred, keeping the public unaware of their true lives. The sisters spent most of their lives at the Royal Earlswood Mental Hospital in Surrey, a facility for individuals with developmental and mental disabilities. Caretakers described them as playful, mischievous, and capable of expressing themselves in small ways, despite being non-verbal. Life at the hospital was largely isolated, but the sisters found moments of joy and connection with those who cared for them. For decades, the sisters’ lives were kept secret to protect the royal family from scrutiny over hereditary illness and public questions about the family’s reputation. When the story finally broke in 1987, it shocked the public: Nerissa had just passed away, and Katherine was still alive. Buckingham Palace issued no comment at the time, fueling speculation that the secrecy was intentional. Their story later inspired documentaries and a storyline in Netflix’s The Crown, showing the human side of royal life hidden from the world. #QueenElizabethCousins​ #HiddenHistory​ #RoyalFamilySecrets​ #ForgottenLives​ #MentalHealthHistory​
#Developmentaldisabilities Reel by @madisontevlin (verified account) - From January 30th to February 1st, you can grab the limited-edition @TimHortons Special Olympics Donut. And the best part? 100% of proceeds goes direc
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@madisontevlin
From January 30th to February 1st, you can grab the limited-edition @TimHortons Special Olympics Donut. And the best part? 100% of proceeds goes directly to supporting inclusive sport programs across Canada! I can’t think of a better way to support an incredible cause. @specialocanada creates spaces where athletes with intellectual and developmental disabilities across Canada are supported, celebrated, and given opportunities to live their best lives, on and off the field. And that means everything to me! I didn’t grow up playing sports myself, but I’ve watched how they can open doors, build confidence, and create a true sense of belonging for so many people. I believe every athlete deserves access to that feeling! I’m incredibly proud to partner with Tim Hortons, a longtime supporter of Special Olympics. This year their partnership is REALLY sweet 🍩😉 So if you’re already stopping for a coffee, add a donut to your order! And help give more athletes opportunities do what they love ❤️#ad #ChooseToInclude
#Developmentaldisabilities Reel by @experiential.life.community - If your child is under 18, save this.
You'll want it sooner than you think.

1️⃣ I applied for services through my state's developmental disabilities
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@experiential.life.community
If your child is under 18, save this. You’ll want it sooner than you think. 1️⃣ I applied for services through my state’s developmental disabilities agency when my son turned 14. Every state has an application process for Home and Community Based Services waivers, and almost every state has a waitlist. You can apply at any time - but in most states, funding and services don’t begin until your child is 21. 2️⃣ I am working with an organization that will help me apply for social security benefits for C. I know the process is long and comes with a lot of paperwork and bureaucratic hoops. I also know I won’t do the paperwork unless someone is literally holding my hand through the process. 3️⃣ I am putting together the medical and financial power of attorney documents and making sure all of his medical providers have them before he turns 18. Everyone talks about “future planning.” Very few people tell you what to do first - or when to start. That’s why I tell families it’s better to learn this early - instead of scrambling to piece it together later. What would you add to the list? If future planning feels overwhelming, we’re talking about it live with a future planning expert on March 12. Comment “onward” and I will DM the details.

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