Sophie Morgan’s film - Fight to Fly - to come out on Channel 4 July 22 < Back Disability, News, Media New documentary on issues faced by disabled air travellers Sophie Morgan’s film - Fight to Fly - to come out on Channel 4 July 22 MMS Staff 19 Jul 2024 2-min read British TV presenter Sophie Morgan’s documentary on the issues faced by disabled people - particularly those with restricted mobility - when travelling by flights is set to release July 22 at 9 pm BST on Channel 4. The film - chronicling the experiences of multiple disabled travellers - follows Morgan as she campaigns for more awareness and sensitivity toward disabled people using mobility devices such as wheelchairs to travel by air. Morgan’s mission to make air travel equitable for all started early last year when, on a flight back from USA to the UK, her carrier damaged her wheelchair. At the time, her social media posts about the incident went viral , prompting her to start a campaign that is now called Rights On Flights. Asked what kinds of problems disabled people often face on flights, Morgan said: “It starts from the minute you book: sometimes airlines can be really difficult and refuse you travel if your wheelchair is a certain height, or a certain width, or over a certain weight, or if your battery is a certain size. And that's if the website is particularly accessible digitally anyway — this is not just about wheelchair users, there are problems across the board for all types of people, with different types of disabilities.” While the documentary itself chronicles experiences ranging all the way from people having to drag themselves to the aircraft toilet to others having to starve and dehydrate themselves while on board to yet others whose mobility aids have suffered damage. Morgan points out that it’s not even necessarily only the fault of the staff being under-trained - the entire system is, in fact, ableist. India, too, is fighting the good fight against ableism in air travel. Last year, on a flight to Mumbai from Delhi, activist Virali Modi was left behind in an aeroplane for almost 40 minutes after all other passengers had deplaned. The campaign has seen Morgan visit Downing Street as well as the White House, calling for better legislation to ensure a better air travel experience for people with disabilities. As for the documentary, it covers the campaign from the beginning, the reason for its establishment, Morgan’s aims and goals, as well as the harrowing journeys of other wheelchair users, who have gone undercover and filmed their experiences for the purpose of the film. “I'm delighted that (the campaign) was successful, but I'm gutted that it happened — it's quite shocking what we uncover, but in many ways it's not shocking. Every time these stories come out, the non-disabled community kind of go 'oh my gosh, that is shocking, I had no idea' and we're like 'we're trying to tell you! This happens to us all the time!’ Morgan said. Ever since starting the campaign, Morgan adds, some airlines have taken note while others still haven’t. “I hope the airline industry sits up and takes notice, I hope they realise that we aren't going anywhere, that they have to meet the problems head-on. There's a real opportunity here for an airline to lead the way and be better, and I can't wait for that airline to really step up and embrace that.” Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

What soaring temperatures, health issues, and systemic neglect can do to those on the margins < Back Climate, Disability, Health Navigating disability, domestic violence & climate crisis in a Delhi slum What soaring temperatures, health issues, and systemic neglect can do to those on the margins Puneet Singh Singhal 20 Jun 2024 5-min read In the narrow, winding lanes of a Delhi slum, where the sun is relentless and the ground is scorched, a story unfolds — one that many will find hard to grasp let alone endure. I grew up in these sweltering corners, living with dyslexia, dyspraxia, and a stammer, all while being the lifeline for my chronically ill mother. We’ve survived domestic violence, yes, but we’re also survivors of an increasingly hostile world — socially, environmentally, and mentally. When environmental crises devastate lives You may read about the heatwaves or monsoon floods, but do you feel them? Can you feel the sweat trickling down your spine as you desperately search for a drop of water? Can you sense the despair, almost tangible, as you watch your mother’s health deteriorate with each passing minute? Living through a Delhi heatwave, in a fragile home with no escape from the oppressive heat, feels like being trapped in an oven. The sun becomes an unforgiving foe, and the air turns into a suffocating shroud. During one unbearable summer, our neighbourhood faced an acute water crisis. Imagine being parched but having not a single drop to drink. Every breath became a laborious task; each moment felt endless. My mother’s existing health issues worsened terribly. Dehydration ravaged her body, while her chronic ailments flared up with newfound intensity. As for me, the heatwaves weren’t just a weather event; they were a neurological, physiological, and psychological disaster. My dyspraxia symptoms intensified, making everyday tasks — like lifting a glass of water — an exhausting struggle. The constant stress and anxiety from watching my mother suffer and feeling helpless to alleviate her pain took a severe toll on my mental health, leading to heightened levels of stress and anxiety. Dealing with a broken healthcare system When you’re fighting to save a loved one’s life while also grappling with disabilities, every second feels like an eternity. The journey to the hospital was a nightmare. Public hospitals were our only hope, but they were dreadful. Doctors and nurses did their best but were woefully under-equipped to handle the flood of patients. Can you fathom the helplessness I felt when I stammered while trying to explain my mother’s rapidly worsening condition? Time and again, I was met with impatient stares or pitying glances, neither of which helped our dire situation. The agony of being trapped in that atmosphere — where you’re just a number, a statistic — is indescribable. The urgent need for climate-resilient, inclusive healthcare Here’s the gut-wrenching truth: if healthcare infrastructure continues to ignore the heightened vulnerabilities of people with disabilities, we’re not just failing as a society; we’re perpetuating suffering and loss. Our healthcare systems need to be fortified with climate-resilient policies and infrastructures. Wheelchair ramps and Braille signage aren’t luxuries; they’re necessities. Doctors need training to understand the unique challenges that environmental disasters pose to individuals with disabilities. It’s not just about ramps and signs; it’s about creating a space where the most vulnerable can feel safe, especially when the world outside is falling apart. Statistics highlighting the impact According to a 2021 climate report heat waves will last 25 times longer 2036 through 2065 in India if emissions push towards a global temperature rise of 4°C under business-as-usual global emission scenarios. The Lancet Countdown on Health and Climate Change reports that annual heat-related mortality of people older than 65 years is projected to increase by 370% above 1995 – 2014 levels by 2041 – 60 under a scenario compatible with limiting global temperature rise to 2°C, and by 433% under a scenario in which no further mitigation occurs, assuming no further adaptation. By 2081 – 2100, these mortality levels are projected to increase by 683% and 1537% for the two scenarios, respectively. According to this Indian Express article, in Delhi, the world is most likely to temporarily breach the 1.5 degree Celsius limit in the next five years. Each year between 2024 and 2028 is predicted to be between 1.1 degree Celsius and 1.9 degree Celsius higher than the pre-industrial average. Specific healthcare system gaps The public healthcare system in Delhi, and much of India, is severely underfunded. Hospitals often lack essential medical supplies and have insufficient staff to handle patient inflows. For people with disabilities, the challenges are even more pronounced. There are limited provisions for accessible healthcare facilities, and medical staff often lack training in disability-inclusive practices. For instance, during our hospital visits, we encountered long waiting times and inadequate attention to my mother's specific health needs. The lack of air conditioning in many public hospitals exacerbates heat stress for patients and staff alike. Moreover, the absence of accessible communication tools, such as sign language interpreters or text-to-speech devices, creates additional barriers for people with disabilities. Concrete steps for addressing healthcare gaps Investment in infrastructure: Increase funding for public healthcare to improve infrastructure, ensuring hospitals are equipped to handle extreme weather conditions. This includes air conditioning, adequate water supply, and accessible facilities. Training for healthcare professionals: Implement comprehensive training programs for healthcare workers on disability-inclusive practices and climate resilience. Accessible communication: Develop and deploy accessible communication tools in hospitals, such as sign language interpreters and text-to-speech devices, to aid patients with disabilities. Community outreach: Establish community health programs to educate residents about coping mechanisms during extreme weather events and to provide first-response medical aid. Potential measures for climate action Urban planning: Develop urban areas with better heat mitigation strategies, such as green spaces, reflective roofing, and improved water management systems. Early warning systems: Enhance early warning systems for heatwaves and floods to give vulnerable communities ample time to prepare and evacuate if necessary. Sustainable practices: Promote sustainable agricultural and industrial practices to reduce the urban heat island effect and ensure a stable water supply. Policy advocacy: Advocate for policies that prioritise climate resilience in healthcare planning and funding. More than just numbers Statistics can be cold and detached, but stories like mine are filled with raw emotion. The vulnerability, the desperation, the feeling of being caught in an unending cycle of despair — they bring a certain urgency that numbers alone cannot. So here it is, a candid snapshot of what it’s like to live at the devastating intersection of disability and climate-induced healthcare challenges. It’s a cry from the depths of my soul and from the hearts of countless others, who, like my mother and me, are battling more than just social and economic disparities. As we desperately seek solutions for climate change, let’s remember that the first step towards true climate justice is acknowledging and acting upon the exacerbated healthcare challenges faced by the disabled and vulnerable. Let’s strive to build healthcare ecosystems where no one is left to suffer, simply because of who they are or where they come from. The battles we fight today go beyond us; they’re a plea to humanity to wake up, take notice, and act — before it’s too late. Puneet Singh is a disability inclusion advocate and an accessibility professional. He is a person with dyslexia, dyspraxia and stammering. He is the co-founder of Billion Strong, curator of Green Disability and a Bevisioneers fellow. Connect with him on LinkedIn . Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

Top NGOs supporting Autistic children and their families in India < Back List of NGOs that work with Autistic children in India Top NGOs supporting Autistic children and their families in India Ummeed Child Development Center Location: Mumbai Website: https://ummeed.org/ Ummeed Child Development Center is a premier organization dedicated to supporting children with developmental disabilities, including autism. With a holistic approach, Ummeed offers comprehensive care through a multidisciplinary team of medical professionals, therapists, and educators. Their services include developmental assessments, medical consultations, therapy sessions, and educational support tailored to each child’s unique needs. Ummeed is committed to empowering families and building capacity within communities by providing training programs for parents, caregivers, and professionals. Their goal is to ensure that every child reaches their full potential in an inclusive and supportive environment. Latika Location: Dehradun Website: https://latikaroy.org/ The Latika Roy Foundation is a renowned organization based in Dehradun, dedicated to serving children with developmental and intellectual disabilities, including autism. With a holistic and compassionate approach, the foundation offers a wide array of services such as early intervention, special education, vocational training, and therapeutic support. Their inclusive programs are designed to empower children and their families, helping them navigate challenges and achieve meaningful progress. The foundation also focuses on community outreach and advocacy, working to raise awareness and foster acceptance of disabilities within society. Through training workshops and support networks, the Latika Roy Foundation equips parents, caregivers, and educators with essential skills and knowledge, ensuring that every child receives the support they need to thrive in an inclusive environment. Nayi Disha Location: Hyderabad Website: https://nayi-disha.org/ Nayi Disha Resource Centre is a dynamic organization based in Hyderabad, dedicated to providing comprehensive support for families of individuals with developmental disabilities, including autism. Nayi Disha offers an extensive range of resources, including detailed information on education, therapy, and community services, to help families make informed decisions. Their platform is designed to connect parents and caregivers with expert advice, peer support, and practical tools tailored to their unique needs. Nayi Disha is committed to fostering a supportive community through workshops, support groups, and awareness campaigns, ensuring that every family has access to the guidance and assistance they need. By bridging the information gap and advocating for inclusive practices, Nayi Disha empowers families to provide the best possible care for their loved ones. Action for Autism Location: Delhi Website: https://www.facebook.com/actionforautism.nationalcentreforautism/ Action for Autism (AFA) is a pioneering organization in India dedicated to advocating for and supporting individuals with autism and their families. Established to create a more inclusive society, AFA provides a wide range of services including early intervention, special education, vocational training, and family support. Their comprehensive programs are designed to address the unique needs of autistic individuals, helping them to achieve their fullest potential. AFA also focuses on awareness and advocacy, working tirelessly to destigmatize autism and promote acceptance within the community. Through training and outreach initiatives, AFA empowers parents, caregivers, and professionals with the knowledge and skills needed to support autistic individuals effectively. Forum for Autism Location: Mumbai Website: https://www.forumforautism.org/ Forum for Autism is a dedicated organization based in Mumbai, committed to improving the lives of individuals with autism and their families. As a robust support network, the Forum provides a wide range of services including advocacy, educational support, and therapeutic interventions tailored to the unique needs of autistic individuals. The organization actively works to raise awareness about autism through community outreach programs and campaigns, aiming to foster greater acceptance and understanding within society. By organizing workshops, training sessions, and support groups, Forum for Autism empowers parents, caregivers, and educators with the knowledge and skills necessary to support and nurture autistic individuals effectively. Their mission is to create an inclusive environment where individuals with autism can thrive and reach their full potential. Sethu Location: Goa Website: https://sethu.in/ Sethu Child Development and Family Guidance Centre, located in Goa, is a distinguished organization dedicated to supporting children with developmental and learning challenges, including autism. Sethu offers a comprehensive range of services such as early intervention, special education, psychological assessments, and therapeutic interventions designed to cater to each child's unique needs. The centre is committed to fostering an inclusive environment where children can develop their abilities and achieve their potential. Sethu also places a strong emphasis on empowering families through guidance and support, providing them with the tools and knowledge needed to advocate for their children. By conducting workshops, training programs, and community outreach initiatives, Sethu aims to raise awareness and promote understanding of developmental disabilities within the broader community. Their holistic approach ensures that every child and family receives personalized care and support, contributing to a more inclusive society. Sangath Location: Goa, Bhopal Website: https://sangath.in/ Sangath is a highly respected non-profit organization based in Goa, dedicated to improving mental health and well-being across India, with a particular focus on developmental disabilities, including autism. Sangath provides a wide spectrum of services encompassing early intervention, special education, mental health care, and family support. Their innovative programs are grounded in evidence-based practices and are designed to be accessible and effective for diverse communities. Sangath is renowned for its research-driven approach, contributing significantly to the field of mental health through cutting-edge studies and publications. The organization also emphasizes capacity building, offering extensive training for healthcare professionals, educators, and caregivers to enhance their skills and knowledge. By fostering collaborations with local, national, and international partners, Sangath aims to create sustainable and scalable models of care. Their commitment to community engagement and advocacy helps to raise awareness, reduce stigma, and promote inclusive practices, ensuring that individuals with autism and other developmental challenges receive the support they need to lead fulfilling lives. Jai Vakeel Location: Mumbai Website: https://jaivakeel.org/ Jai Vakeel Foundation is a distinguished organization in Mumbai dedicated to supporting individuals with intellectual and developmental disabilities, including autism. Established with a vision to empower and uplift, the foundation offers a comprehensive range of services such as early intervention, special education, vocational training, and therapeutic support. Jai Vakeel Foundation is committed to creating an inclusive environment where individuals can thrive and reach their fullest potential. The foundation also focuses on family support and advocacy, providing parents and caregivers with essential resources and training to better support their loved ones. Through community outreach programs, awareness campaigns, and strategic partnerships, Jai Vakeel Foundation aims to foster greater acceptance and understanding of disabilities in society. Their holistic approach ensures that each individual receives personalized care and support, promoting a more inclusive and compassionate community. WhatsApp Facebook X (Twitter) LinkedIn Copy link Much much relate? Share it now! < Back SHORTS

Another year, another budget, another disappointment for India’s 80+ million disabled folx < Back Disability, News The heartbreaking reality of budget allocation for disability in India Another year, another budget, another disappointment for India’s 80+ million disabled folx MMS Staff 2 Feb 2025 3-min read Despite making up 7 - 8% of the population, disabled individuals have once again been pushed to the margins of India’s financial priorities. While the Union Budget 2025 boasts record-high spending, disability allocations remain shockingly low — a mere 0.025% of the total budget. Even more concerning? The little that is allocated isn’t even fully used. When numbers speak louder than words India’s total budget grew from ₹30 lakh crore in 2020-21 to ₹50 lakh crore in 2025-26 — a massive 66% increase. Yet, instead of rising with it, the budget for the Department of Empowerment of Persons with Disabilities (DEPwD) has actually dropped from ₹1,325 crore to ₹1,275 crore. T he Scheme for Implementation of the PwD Act (SIPDA) — which funds accessibility projects across the country — has been slashed to ₹115 crore, even after a Supreme Court ruling in November 2024 (Rajive Raturi judgement) mandated that public spaces and services be made accessible. The numbers paint a grim picture of chronic underfunding: In 2022-23, SIPDA received ₹240.39 crore In 2023-24, it was cut to ₹135.33 crore In 2025-26, it has been further reduced to ₹115 crore This isn’t just a funding cut — it’s a systematic failure to enforce disability rights. Underutilization: The Silent Crisis Even more infuriating is the fact that the budgeted money is not even being fully used. Government records show a shocking underutilization of funds over the past four years: 64% of funds were left unused in 2020-21 86% were unused in 2021-22 79% were unused in 2022-23 93% were unused in 2023-24 What this means: Even the meagre amount allocated for disability support is not being spent. In practical terms, this results in schools, public transport, workplaces, and even government buildings remaining inaccessible — despite legal mandates for inclusion. Disability Pensions: Stuck in 2012 While Prices Skyrocket For millions of disabled people, the Indira Gandhi National Disability Pension Scheme (IGNDPS) is their only source of income. Yet, it remains stagnant at ₹290 crore, with the central share still ₹300 per month — an amount unchanged since 2012. The absurdity of this is clear: ₹300 today barely covers a week’s worth of groceries, let alone rent, medical care, or assistive devices. Meanwhile, the pension scheme remains highly exclusionary, covering only 3.8% of disabled people as per the 2011 Census. Mental Health: A Crisis Ignored The Economic Survey has raised concerns about India's growing mental health crisis for two consecutive years. Despite this, the budget for the Telemental Health Programme has been slashed from ₹90 crore to ₹79.60 crore. Given the alarming rise in mental health disorders, suicide rates, and lack of accessible mental healthcare, this cut signals a complete disregard for one of the most pressing public health challenges of our time. No Relief for Disabled Job Seekers Employment remains one of the biggest challenges for disabled people in India. Yet, the budget offers little to address this crisis. The National Rural Employment Guarantee Act (MGNREGA), which provides vital work opportunities, has not seen any increase in funding, making it harder for disabled individuals to find employment. New government schemes, such as the Manufacturing & Skill Development Boost, offer potential — but will they prioritize inclusion? Opportunities (If Done Right) Amidst the disappointments, the Finance Minister announced some key initiatives that could benefit disabled people — if they are implemented with inclusion in mind: ✅ Credit Guarantee for MSMEs – Will disabled entrepreneurs get access to capital and business growth opportunities? ✅ Manufacturing & Skill Development Boost – Will disabled workers be given equal access to training and jobs? ✅ Jan Arogya Yojana for Gig Workers – Will disabled gig workers, who often struggle to get insurance, be included? Disability Rights Activists Call for Action The National Platform for the Rights of the Disabled (NPRD) has strongly condemned the government's continued neglect of India’s disabled population. On February 10, 2025, NPRD will hold a protest in Delhi, demanding: ✔️ A Right to Pension Act ✔️ An increase in disability pensions from ₹300 to ₹5000 per month ✔️ Expansion of pension coverage to include all disabled individuals under the RPD Act Disability is a human rights issue. India cannot become an economic powerhouse while ignoring 80+ million disabled citizens. Inclusion isn’t just about budget allocations; it’s about dignity, accessibility, and economic participation. Yet, year after year, the Union Budget continues to treat disability rights as an afterthought. Until the government matches words with action, accessibility, employment, and financial security will remain a privilege, not a right, for millions of disabled people in India. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

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A series featuring people with different backgrounds discuss important topics through personal experiences and expert opinions. < Back Series Unheard Stories A series featuring people with different backgrounds discuss important topics through personal experiences and expert opinions. https://www.youtube.com/watch?v=5lSvoxPJjh8 To celebrate International Women's Day ‘23 we featured 11 incredible women who shared their honest and unfiltered experiences of ableism, gender bias, microaggressions, and exclusion. From autism and ADHD to disability and caregiving, these women give voice to the discrimination and challenges that women with disabilities encounter every day. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back ORIGINALS

Honouring the legacy of Helen Keller on her birth anniversary < Back Disability Deafblind Awareness Week: Significance, history and advocacy Honouring the legacy of Helen Keller on her birth anniversary MMS Staff 24 Jun 2024 2-min read Deafblind Awareness Week (June 24 - June 30) is a week dedicated to raise awareness about individuals with multi-sensory impairments, also known as deafblindness. This week focuses on learning about the lived experiences of those who are deafblind, challenging misconceptions, celebrating achievements, and finding ways to support and advocate for the deafblind community. It also coincides with Helen Keller ’s birthday on June 27th, honouring her legacy as a pioneering disability advocate. Understanding deafblindness Deafblindness is a disability characterised by the combined loss of sight and hearing, which significantly impacts daily life. Being deafblind does not necessarily mean complete deafness and blindness. Most people who are deafblind have some degree of both sight and hearing. There are two main types of deafblindness: Congenital Deafblindness: When a person is born with both sight and hearing impairments. Acquired Deafblindness: When a person develops sight and hearing impairments later in life, often due to illness, injury, or age-related factors. People with deafblindness can lead fulfilling and successful lives with the right support and resources. Life with Deafblindness People with deafblindness use various methods to communicate and interact with their environment, such as tactile signing, braille, assistive technology, and support service providers. Celebrating Helen Keller Deafblind Awareness Week marks Helen Keller’s birth anniversary, June 27th. Helen Keller was an influential author, educator, and disability rights advocate. Born in 1880, Keller lost her sight and hearing at 19 months old due to an illness. With the help of her teacher Anne Sullivan, Keller learned to communicate using tactile sign language and braille. She was the first deafblind person to earn a Bachelor of Arts degree. Keller travelled worldwide, delivering lectures, working to improve the lives of individuals with disabilities. Advocating and supporting the Deafblind community Here are some ways you can advocate for and support individuals with deafblindness: Learn about deafblindness and share accurate information to help dispel myths and raise awareness. Advocate for accessible public spaces, transportation, and digital content to ensure inclusivity. Encourage educational institutions and workplaces to implement accommodations and inclusive practices, creating opportunities for individuals with deafblindness. Offer your time and resources to organisations that support the deafblind community. Push for the development and availability of assistive technology that enhances independence and communication for those who are deafblind. Listen to the experiences of the deafblind community and help amplify their voices in public discussions and advocacy efforts. Deafblind Awareness Week is also a time to celebrate the remarkable contributions to society that individuals with deafblindness have made in various fields such as education, arts, advocacy, and technology. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

Love, disability, and representation took center stage at 2025's Creative Arts Emmys < Back Disability, Media, News Disability-led stories win big at the Emmys Love, disability, and representation took center stage at 2025's Creative Arts Emmys MMS Staff 9 Sept 2025 3-min read In a world where disability is often erased, sidelined, or reduced to a side plot, two groundbreaking shows that center disabled lives and love stories just won top honours at the Creative Arts Emmy Awards 2025. Netflix’s Love on the Spectrum and Patrice: The Movie, a powerful Hulu documentary, both walked away with major Emmy wins this weekend. Besides being great TV, these shows are cultural milestones. They’re redefining who gets to be seen, celebrated, and loved on screen. Love on the Spectrum: Dignity, not drama Love on the Spectrum won two Emmys: for Outstanding Unstructured Reality Program and Casting, marking a continued recognition for a show that has already collected five Emmys in past seasons. Created by Cian O’Clery, the series follows autistic adults in the US as they navigate dating and relationships, portraying the full range of human emotion: nervous laughter, awkward silences, budding chemistry - all with radical empathy and zero pity. “From the beginning, our aim has been to create a series that treats our participants with dignity and respect while offering genuine insight into their experiences,” said O’Clery. “These awards celebrate not only our production team’s efforts but also the courage of our participants who have touched millions with their personal journeys and helped reshape the public’s understanding of autism.” The show, a spinoff of the original Australian version, has been renewed for a fourth season. It's a clear sign that audiences want more stories where neurodivergent people are shown as complex, lovable, and worthy of screen time. Patrice: The Movie: Love isn't always a legal right In the same awards ceremony, Patrice: The Movie won the Emmy for Exceptional Merit in Documentary Filmmaking. The Hulu film follows Patrice Jetter, a disabled woman who dreams of marrying her long-time partner. There’s just one catch: if she gets married, she could lose her Medicaid and Social Security benefits, essential lifelines for disabled people in the United States. It’s a chilling reflection of how the system penalises disabled people for daring to pursue intimacy, independence, and joy. The film doesn’t just spotlight this injustice, it humanises it with tenderness and rage in equal measure. A shift in the room where it happens This year’s Emmy ceremony was as much about who won as it was about who was present. Marlee Matlin and Nyle DiMarco, two Deaf icons in entertainment, were among the presenters. DiMarco, also a producer of the AppleTV+ doc Deaf President Now!, has long been an advocate for more authentic disabled representation across media. Their presence signals a broader cultural shift: disability is not a theme to be explored once a year. It’s a community, a culture, a lens through which millions experience the world. And now, finally, Emmy voters seem to be paying attention. Beyond the awards: why the wins matter Representation is not the same as liberation. But it’s a start. For too long, disabled people have only seen themselves on screen as either tragic heroes or magical savants. These Emmy wins mark a move away from outdated tropes, and toward something more honest: the messy, beautiful, deeply human experience of disability. That includes dating. That includes joy. That includes wanting to be seen, and being worthy of love. Not in spite of disability, but alongside it. What we hope comes next Stories like these are not just entertainment. They’re political. They challenge ableist systems. They make visible what society would rather hide. And they remind us that love, agency, and self-expression are basic rights, not luxuries reserved for the non-disabled. As disabled creators, advocates, and storytellers continue to claim space, our hope is that this moment sparks loud applause and even louder action. Because disabled people don’t just deserve to be on stage when it’s time for awards. We deserve to be in the writers’ room, behind the camera, and holding the mic. And when we are, the stories hit different. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

Online misogyny is moving from boys’ feeds into classrooms, homes and real-life attitudes < Back Gender, News, Media Manosphere content is teaching young boys to hate women offline Online misogyny is moving from boys’ feeds into classrooms, homes and real-life attitudes MMS Staff 11 Jun 2026 4-min read The manosphere is no longer staying inside boys’ phones. Its language is turning up in classrooms. Its ideas are surfacing at dinner tables. Its contempt for women is being repeated by children who are still young enough to need help understanding the weight of their own words. For years, misogynistic influencers have sold toxic masculinity as confidence, discipline, success and “male self-improvement.” Through short videos, podcasts, gaming spaces and algorithm-driven feeds, Andrew Tate-style content can reach boys long before they are old enough to question what it is teaching them. And it is handing out a script where women are inferior, mothers exist to serve, female teachers can be disrespected and violence against women can be mocked, excused or treated as normal. That is why online misogyny is no longer only an internet safety problem. It is now a parenting problem, a classroom problem and a gender-based violence problem. When online hate leaves the screen Misogyny rarely arrives in a child’s life looking dangerous. It often comes dressed as a joke, a viral clip, a podcast line, a gaming insult, a gym video or a blunt “truth” about women. To a boy scrolling after school, it may look like entertainment. But repetition has power. A phrase becomes funny. A joke becomes familiar. An attitude becomes behaviour. In Australia, teachers have warned that Andrew Tate-style misogyny is already entering classrooms. Some female teachers have said sexist language and behaviour from boys have made them feel unsafe at work. The issue is not simply bad manners or teenage rudeness. It is boys challenging women’s authority, repeating online misogyny and treating female educators as people they do not have to respect. A classroom cannot function if girls are expected to absorb sexism and women teachers are expected to manage misogyny as ordinary misbehaviour. When contempt for women becomes a performance of masculinity, the damage does not stay online. Now, a similar warning is coming from inside Irish homes. The warning from Ireland Sonas, a domestic violence charity in Ireland that supports women and children through refuges and safe homes, has warned that boys as young as eight are repeating degrading views about women. In one reported case, an eight-year-old boy called his mother a “dish pig” and threw objects at her after he disliked his dinner. The phrase is being discussed here as an offensive insult aimed at women and care work. It is not a comment on people who do dishwashing work. The deeper concern is how cooking, cleaning and domestic labour are being turned into tools to humiliate mothers. This points to a worldview being sold to boys online: that care work is women’s duty, that mothers are there to serve and that boys are entitled to punish or degrade women when they do not get what they want. The child’s mother reportedly had parental restrictions on his social media. Yet masculinity influencer content was still accessible. For many parents, that is the most frightening part. They may be checking phones, setting limits and trying to monitor what their children watch. But misogynistic content does not always come from obvious extremist accounts. It can travel through reposted clips, meme pages, reaction videos, gaming communities and accounts that appear harmless at first. Algorithms do not need a child to search for hate. They only need him to pause long enough for the next video to arrive. When survivors hear misogyny at home Sonas has also raised another painful concern. Some women escaping domestic violence are now facing hostility from their own children after leaving abusive homes. In one case, a woman was describing the physical abuse she had experienced from her husband when her teenage son said she “deserved it.” For a survivor trying to rebuild safety, that sentence can be devastating. It can make the violence feel as if it has followed her into another room, in another voice. This is where online misogyny connects to coercive control. Coercive control is not only physical violence; it can include humiliation, intimidation, emotional abuse and the belief that one person has the right to dominate another. A child who repeats misogyny should not be written off as dangerous or evil. But adults cannot ignore what those ideas are teaching him. Boys need guidance, boundaries and support before online hate hardens into a worldview. The responsibility cannot sit with parents alone Sonas is urging Ireland’s media regulator, Coimisiún na Meán, to strengthen online safety rules. The charity wants platforms to reduce the algorithmic promotion of misogynistic content, improve age-gating and limit children’s exposure to material that normalises coercive control, violence against women or hatred of women. But regulation alone will not be enough. Parents, teachers and caregivers also need to treat sudden hostility towards women, mothers, girls or female teachers as a warning sign. Jokes about women belonging in the kitchen, contempt for feminism, anger at boundaries or claims that women are inferior should not be brushed off as harmless internet humour. The response does not have to be panic. It has to be attention. Where did you hear that? What do you think it means? Why is that funny? How do you think your mother felt when you said it? These questions are not small. They are the beginning of intervention. Boys deserve better than algorithms that turn insecurity into resentment. They deserve better than influencers who sell domination as strength. They deserve better than a culture that tells them masculinity must come at the cost of women’s safety. The goal is not to fear boys. The goal is to reach them before misogyny does. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

Fans reflect on the lasting impact of Linkin Park's music and Chester's legacy < Back Health, Media, Neurodiversity Remembering Chester Bennington: 7 years later Fans reflect on the lasting impact of Linkin Park's music and Chester's legacy MMS Staff 20 Jul 2024 2-min read July 20 marks seven years since the tragic, sudden death of Chester Bennington, the frontman of rock band Linkin Park. Bennington lived with a history of abuse and addiction, and had on many instances spoken openly about his depression. Many of Linkin Park’s songs were written by him, and allude to depressive thoughts and suicidal ideation. In this article from last year, Linkin Park rapper and Bennington's bandmate Mike Shinoda mentioned they were about his condition but "nobody knew the depths of it." "I've never heard such a crazy upbringing, such a crazy childhood. Like, running wild in the streets and doing hard drugs on the roof of his high school, just like barely staying out of jail. That's what made our dynamic what it was... He was outside because he was scrawny, he was like picked on, he was bullied all the time," Shinoda said. At the time of his death, reports also mentioned he had a hard time dealing with the suicide of his friend Chris Cornell, frontman of the band Soundgarden. Listen to Bennington's heartwarming eulogy to Cornell below: Bennington's difficult childhood experiences growing up, his parents' divorce, followed by rampant bullying in school caused him major emotional distress. He also grappled with substance abuse throughout his early adulthood and into his 20s, until he joined Linkin Park as lead vocalist and the band shot to fame with their 2000 album Hybrid Theory. The rest, as they say, is history. Bennington was found hanging in his CA home this day in 2017, survived by his wife Talinda and six children. A year after his passing, Talinda said in an interview about his depression: “I am now more educated about those signs, but they were definitely there: the hopelessness, the change of behaviour, isolation,” she told CNN during an interview with Anderson Cooper. On his seventh death anniversary, we spoke to some of our readers for whom Linkin Park and Chester’s music have been a constant companion through tough times. Swara Swami: As a kid, I was bullied heavily and it took a huge toll on me. And, listening to Linkin Park would help me channel all my aggression. Just listening to their music, their lyrics was a huge release. Pranav Sethi: I learned that poetry will make sense only when you start living those moments, those words will mean nothing to those who have not experienced any of it. That’s why poetry is so confusing for everyone. People don’t get it, they don’t understand because their experiences won’t allow them to grasp the meaning behind it. For many people around me they will never know the meaning of your songs nor will they understand the trauma I have lived through. I guess I connected with you so closely because I know we share a similar history. This tribute is a few years late but I guess I was figuring out what to say and how to say it. I guess I am breaking the habit tonight. Venkat Baliga: Being always at odds with the world, not understanding the ways of the world as a teen, the sheer rage towards bullies and people who constantly brought me down - 'Numb' made me feel like I wasn't alone. Now, after my autism and ADHD discovery, and understanding my mental health struggles, when I watch the music videos of Linkin Park and when I watch Chester Bennington sing (old videos), and observing the lyrics of most of their songs being so relatable - it all makes so much sense. Farhad Samiwalla: Hybrid Theory got me through some really tough times back when it came out. It was the first album that really hit me at the perfect time and every single song just spoke to where I was at mentally. Chester’s passionate screaming coupled with Mike’s poetic lyricism also blended so perfectly to express some really deep emotions. Allan D'souza: "Your friends all plead for you to stay Sometimes beginnings aren't so simple Sometimes goodbye's the only way" What is your favourite Linkin Park song/ lyric? Tell us in the comments below. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS