Search Results

How bad media representation of disability fuels stereotypes and excludes disabled voices < Back News, Disability Ableist magazine covers: A look through time How bad media representation of disability fuels stereotypes and excludes disabled voices MMS Staff 6 Jul 2024 4-min read That ableism - a term whose literal meaning is discrimination against people with disabilities - is deeply embedded in our society is no unknown fact. But when it rears its ugly head through mass media, and in the form of magazine covers no less, ableist attitudes are further perpetuated, making life even more difficult for those with disabilities and illnesses. Over the years, many magazines have carried brazenly ableist covers, enraging and prompting pushback by disability activists. This article is a collection of instances when our media has been supremely (and shamelessly) ableist. Instances of ableist magazine and newspaper covers through history Time Magazine (2003): Time Magazine ran a cover titled “Overcoming Dyslexia,” spreading gross misinformation about learning disabilities. The term “overcoming” implies that dyslexia is something to be conquered, rather than a difference to be understood and accommodated. This is especially wrong considering affirming language is crucial in shaping perceptions and attitudes towards disabilities and neurodivergent conditions. Interview Magazine (2015): In 2015, supermodel-entrepreneur Kylie Jenner was criticised for a photoshoot in Interview Magazine where she posed in a wheelchair. Disabled individuals and advocates found this use of a wheelchair as a fashion prop deeply offensive. Beth Grossman, Head of Policy at the disability charity Scope, remarked, “Having a non-disabled person in a wheelchair, as a provocative fashion prop, will offend many disabled people. It’s rare that we see aspirational and authentic reflections of disabled people in advertising and the media.” The Economist (2016): The Economist's April 2016 cover titled “Beautiful Minds, Wasted” was another egregious instance of blatant ableism perpetuated by mass media. Not only did the headline suggest autistic minds are wasted, the inappropriate puzzle piece depiction insinuated that autistic people are 'broken', need 'fixing', or complex beings who can't be 'figured out'. Patronising autistic people by using the ableist phrase "Beautiful Minds, Wasted" shows how even big, global publications don't make the effort to understand autism from a neurodiversity-affirming perspective. The failure to consult with autistic people and include their perspectives in the story was a significant oversight. The New Yorker (2023): The New Yorker stirred controversy with a cover featuring US political leaders using walkers. The cartoon depicted Donald Trump, Mitch McConnell, Nancy Pelosi, and Joe Biden as frail and elderly, using mobility aids they do not actually need. This portrayal was criticised for its ageist and ableist implications, suggesting that age and the use of mobility aids diminish one’s capabilities. The Economist (2024): And the Economist, astonishingly, did it once again with their July 4 cover attacking President Joe Biden, depicting him as a “befuddled old man” using a zimmer frame branded with the presidential seal. This imagery sparked widespread outrage for its ableist undertones, suggesting that mobility aid use equates to unfitness for leadership. Catarina Rivera, a prominent disability advocate, expressed her dismay on LinkedIn: “This week's The Economist cover is ableist, disgraceful, and deeply offensive. It suggests that someone who uses a walker as a mobility aid is unfit to run the country. Disabled people are very capable of leadership — period (not 'despite' our disabilities, just exactly as we are). Using a mobility aid isn't something that's shameful or that makes someone unfit for leadership.” Heather Thompson, another advocate, shared her personal struggle with internalised ableism: “I used to hate my walker; I struggled with my own internalised ableism every time I needed to use the walker in public. What would people think? Your magazine cover validates my fears by normalising these false beliefs. A walker does not represent decline, nor is it synonymous with intellectual weakness.” Julia M, an able-bodied elder, condemned the cover for its harmful implications: “This is the most insulting, discriminatory, ableist cover for a major publication that I can remember. As an able-bodied elder, I condemn this harmful, ageist, and slanderous artwork. This is trash.” These voices highlight the broader impact of such representations, which extend beyond the individual to affect the entire disabled community. The harm of ableist depictions Ableist depictions in the media do undeniable harm. Ableist behaviours, notions and attitudes encourage stereotypes, reinforce bias, and marginalise disabled individuals. When disability is used as an insult or a symbol of incompetence, it results in a culture of exclusion and discrimination. Ableist representations of disability and neurodivergence also contribute to internalised ableism among individuals with these lived experiences, resulting in shame and self-stigma due to negative societal attitudes. Disability advocates emphasise the importance of accurate, respectful representations in the media. As Catarina Rivera pointed out, “Let's not forget that FDR (Franklin D Roosevelt) was a disabled president and a wheelchair user. The impact of this cover extends beyond The Economist itself.” Ongoing instances of ableist behaviours in various institutions and the media highlights the need for continuous advocacy and education. As Heather Thompson said, “Some of the greatest courage I’ve witnessed has come from those stepping into a walker and taking their fierce first steps.” Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

On the occasion of Helen Keller Day & Deafblind Awareness week, Shrutilata Singh shares her ongoing struggle for inclusion < Back Disability, Gender, Health My mental health as a woman with progressive Deafblindness in India On the occasion of Helen Keller Day & Deafblind Awareness week, Shrutilata Singh shares her ongoing struggle for inclusion Shrutilata Singh 27 Jun 2024 4-min read My name is Shrutilata Singh. I am a woman with progressive deafblindness. Here, the word “progressive” means I am slowly losing both vision and hearing day by day. I completed my Bachelor's degree in English and also earned a diploma in Physiotherapy from an association for the blind. I worked as a paediatric physiotherapist for three years, and for the last two-and-a-half years, I have been working with Sense India, advocating for the rights of people with deafblindness in India. Although deafblindness has been recognized in the Rights for Persons with Disabilities Act of 2016 due to sustained advocacy by Sense India , there is still very little awareness about it. Deafblindness is a unique disability in which two vital senses are affected to varying degrees. In my case, I was able to hear and see much better in my early days, but I have slowly lost most of my vision and hearing. My gender, being a girl, adds to my challenges. I live in a developing country where we hear about various crimes committed against women every day. In school, due to my hearing impairment, I was unable to socialise and faced a lot of discrimination from my classmates as well as educators. They would make me sit separately from others. All these behaviors added to the mental stress that I felt. I felt inferior compared to others. There was no feeling of self-worth as I was made to believe I was different in a negative way and that whatever happened to me was my own fault. At an age when students enjoy time with school friends, I was depressed, isolated, and left behind. I was unsure of what the future held. I wasn't learning academics in school, or any social skills. Today, I have come a long way and learned social skills. But the challenges remain the same. I attend family functions, get-togethers with friends, and even tours with loved ones, but due to communication issues, I always feel neglected. It is not like they do not talk to me while I am there in the group, but the communication is very limited, and I cannot be a part of every conversation. People keep telling me I am inspirational as I have achieved a lot despite my challenges. They think I am positive all the time. But they do not know that it takes a lot of effort to keep myself positive. Every day, I am reminded of the fact that I have progressive deafblindness, have already lost much of my vision and hearing, and will lose what’s remaining as well. Although I know the importance of preparing myself for the future, I still am unable to accept reality. Earlier I found myself in distress when I realised that I could no longer hear my favourite song or read books like before because my eyes got tired. Each time, I’d have to find something else to stay positive. Recently, I underwent cochlear implant surgery. I’m now able to enjoy music, interact with people, and talk on the phone. My interaction with my family and close friends has increased. The role of community and technology is very important in bringing these changes for deafblind people. As an advocate, I work with groups of deafblind people from all over India. Most of them have more or less the same issues. Those with progressive deafblindness find it toughest as their families also need to adjust to the changes and accept them. Deafblindness is still largely a neglected impairment even within the disability community. Many people do not know about dual sensory loss and think that because of this disability we cannot do tasks like other disabled people. We continue to feel like “misfits” within society, even within the disabled community. There have been quite a few incidents when I attended gatherings or programs related to disability but ended up feeling lonely as I could not understand what was going on around me, and it is not possible for those who know how to communicate with me to be there with me all the time. Every now and then, I have to pick myself up and force myself to focus on the positive side. Years ago, I did try to end my life by taking pills, but thankfully changed my mind after thinking about my parents. Although the feelings remain the same, we just learn to cope better. I am glad I have a lot of work to divert my attention from the feelings that threaten to drag me into depression every time. It is a never-ending struggle to fit in with family, friends, and the community. Hence, the role of society as a whole is critical in ensuring that we become active participants in it. People should be aware of how their behaviour towards us affects our mental health. And good mental health is very important to live a happy life. Shrutilata Singh has progressive deafblindness. Since joining Sense International India in April 2020, Shrutilata has been engaging with stakeholders to advocate for Rights of People with Deafblindness in India. She is involved in rights-based advocacy as well as capacity building for family members and fellow young people with deafblindness. Shruti has presented papers in national and international conferences as a role model in Deafblindness. She has also participated and contributed as a speaker at (Global Disability Summit) GDS 2022, (United Nations Girls Education Initiative) UNGEI, (United Nations Conference of State Parties) UNCOSP with latest at Civil Society 20 (C20) Summit 2023. She is also an Executive member of Commonwealth Children and Youth with Disability Network (UNGEI Representative). Connect with her on LinkedIn . Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

Doctor couple from Rajasthan, three kids among victims of Air India AI171 crash that killed dozens < Back News “They never made it to London”: A family’s dream ends in Air India crash Doctor couple from Rajasthan, three kids among victims of Air India AI171 crash that killed dozens MMS Staff 13 Jun 2025 2-min read Dr Koni Vyas had just resigned from her job at a private hospital in Rajasthan. After years of living apart, she was finally joining her husband, Dr Pratik Joshi, a radiologist based in London, to begin a new life with their three children. The visas had come through. The bags were packed. Their children - eight-year-old Miraya and five-year-old twins, Pradyut and Nakul - were set to board their first international flight. On the morning of June 12, their family of five boarded Air India Flight AI171 from Ahmedabad to London. Before takeoff, they took a selfie inside the plane - Pratik and Koni on one side of the aisle, their children smiling from the other. They sent the photo to relatives, full of excitement for the life ahead. Minutes later, the plane crashed. There were no survivors. The cause of the crash is still under investigation. Authorities have confirmed that at least 11 passengers from Rajasthan were on board. For families in Banswara and Udaipur, the grief is unspeakable. Koni, 38, had been living in Udaipur, where the children were studying. She had temporarily moved to Banswara to finalise paperwork and prepare for the relocation. According to relatives, she had been anticipating this move for months. Pratik had flown back from London just three days earlier to bring his family home. “They had waited for years for this day,” said Koni’s cousin Nayan Joshi. “We all came to the airport to send them off. It felt like a beginning.” Now, those same family members are helping identify bodies at the crash site. Pratik, whose father is a well-known radiologist in Rajasthan, had spent the last six years building a life in the UK. Koni, a pathologist, was known for her dedication to her work and her quiet strength as a mother. The couple had been married for over a decade. “This was not just a tragedy,” said a family friend in Udaipur. “It was a story of hope. They were on their way to something better.” Instead, their journey ended in silence. As rescue and recovery efforts continue, officials have issued an urgent appeal for blood donations in Ahmedabad, particularly from those with negative blood types. Hospitals are treating several survivors of ground-level impact and injuries from debris. In the hours since the crash, social media has flooded with condolences and tributes - not only for the Vyas-Joshi family, but for all lives lost. Yet for those who stood on the tarmac waving goodbye, grief is no longer digital. It is physical. It is real. A photo remains. A family frozen in time - smiling, mid-flight, on the edge of a future that never came. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

With no govt support and just ₹400 a month, Faken Shah is building self-reliance in rural India’s women < Back Disability, Gender, News This blind tailor in Bihar has trained 300+ women for free With no govt support and just ₹400 a month, Faken Shah is building self-reliance in rural India’s women MMS Staff 28 May 2025 3-min read In Bihar’s Sitamarhi district, a blind tailor is stitching a quiet revolution, training hundreds of women for free while waiting on a government loan stuck over a missing electricity bill. In Rikhauli, a small village tucked inside Bihar’s Sitamarhi district, the hum of a sewing machine cuts through the afternoon quiet. Sitting cross-legged behind it is 45-year-old Faken Shah - tailor, teacher, and changemaker. Faken is blind. He has trained over 300 women in stitching and tailoring, free of cost, for the last 18 years. What started as a way to rebuild his life after vision loss and personal tragedy has today turned into a powerful, homegrown model of rural empowerment. And yet, Faken’s dreams of scaling his impact are currently stalled — not by lack of will, but by paperwork. The government won’t grant him a loan to expand because he doesn’t have an electricity bill. From losing sight to gaining vision Faken wasn’t born blind. His vision began to fade when he was around 20 years old. After repeated bouts of untreated jaundice and poor access to medical care, he slowly lost his eyesight completely. “At that time, we didn’t have proper hospitals or awareness. What started as a small illness just… stayed. And then one day, I couldn’t see,” he recalls. A few years later, his wife passed away, leaving behind four children. “I had to keep going. Giving up was never an option.” Learning to stitch after vision loss Faken had picked up tailoring skills as a teenager. After losing his vision, he returned to the needle and thread, not just to survive but to stay rooted in something he knew. Stitching, he says, became a new way of seeing. “I measure cloth by feel. The inch tape has tactile cues — button and bead marks. I know how many layers to cut, how much to sew.” His tailoring shop Shri Mahavir Ajuba Garments and Dress Bhandar gradually became more than a workspace. Women from the village began asking if he would teach them too. Faken didn’t hesitate. Today, his centre is a lifeline for women with no income of their own, especially those discouraged from working outside the home. Chandni Kumari, a trainee, says, “He teaches us with so much patience and clarity. No one leaves without learning something useful.” No fees. No government support. Faken earns between ₹300–500 a day, just enough to support his family and buy materials. He receives a ₹400 monthly disability pension from the government. But he has never charged a rupee for training others. For a few years, he even travelled across nearby villages on an e-rickshaw, collecting orders from government schools for uniforms. That, too, came to a halt when his rickshaw broke down. He couldn’t afford repairs. Yet, what frustrates him isn’t just the lack of income, it’s the bureaucratic hurdles blocking his vision for the future. A loan blocked by a missing electricity bill Faken has been trying to get a business loan under the Pradhan Mantri Mudra Yojana to set up a small garment factory and scale up his work. The local District Magistrate even recommended his case. But the bank asked him for a current electricity bill, something he doesn’t have. His family has electricity at home, but no bills have ever been issued. Without that one piece of paper, the bank says it can’t move forward. When contacted, officials from the electricity department promised to “look into the matter” and issue a bill as per rules. But Faken is still waiting. The bigger picture: Disability and rural entrepreneurship Faken’s story isn’t an isolated one. Across India, thousands of disabled entrepreneurs — especially in rural areas — struggle to access financial services, mobility, and infrastructure, despite the existence of government schemes. The challenges are layered: digital illiteracy, inaccessible documentation processes, lack of local advocacy, and the slow-moving machinery of rural administration. Disability isn’t the barrier — systemic neglect is. If the government truly wants to promote self-reliance and skill-building in rural India, it must begin by removing these structural hurdles for disabled individuals trying to do meaningful work. Faken Shah is asking for a working loan, a printed bill, and the chance to keep building what he’s already been doing for almost two decades. “I just want to open a factory,” he says, adjusting his sewing tape between calloused fingers. “I want the women in my village to stand on their feet. That’s all.” Source: ETV Bharat Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

The Paris Summer Olympics plans to reduce CO2 emissions by about 50 percent. But is that possible? < Back Climate, News Will Paris Olympics 2024 be most eco friendly ever The Paris Summer Olympics plans to reduce CO2 emissions by about 50 percent. But is that possible? MMS Staff 12 Jul 2024 3-min read In about a fortnight, athletes, authorities, staff, and huge congregations of sports enthusiasts from around the world will throng to Paris for the Summer Olympics. In this year’s games, over 10,000 athletes will participate across 800+ events, with 45,000 volunteers and 13 million meals served. Alongside being one of the biggest sporting spectacles ever, Paris 2024 also aims to be the greenest and most eco-friendly edition of the Olympics in history. If you’re wondering how it’s possible to make an event of such a big scale easy on the environment, that’s a 100 percent valid question. It’s enormously difficult. After all, we’re looking at a ton of travel, huge amounts of food & drink, and kilowatts upon kilowatts of energy consumption. But the organisers have a plan, it seems. According to this story on the World Economic Forum website, Paris has pledged to reduce the event’s carbon footprint by close to 50 percent. In exact figures, that comes up to about 1.75 million tonnes of carbon dioxide versus the 3.75 million tonnes that some of the previous editions averaged out to. Additionally, 95 percent of the events will be hosted in existing buildings and venues, which means Paris 2024 also plans to be cutting down on creating new venues from the ground up, something that’s very common for events such as the Olympics. 95 percent of the events will take place in existing venues at the Paris Olympics 2024 Paris 2024’s Athletes' Village will be powered by renewable energy and the athletes will use mattresses made from recycled fishing nets. As part of their offsetting initiatives, Paris 2024 will also invest in environmental and social projects around the world, and, within the city, plant around 2,00,000 trees. The city also plans to add 1,000 km of new lanes for cycling, making it easier for people to get around, cutting CO2 transport emissions. And finally, the games plan to move towards more plant-based meals and cut down on single-use plastics. Picture credit: Paris 2024 While this is all definitely a move in the right direction, sceptics aren’t entirely convinced that these changes will prove effective enough to have the desired impact. In this article, Seth Warren Rose of the Eneref Institute, an advocacy and research group focused on sustainable development, says that close to 50 percent is not enough, and that Paris 2024 must bring it down actually to 50 percent. “Maybe things like the Olympics have to be reconsidered… Having millions of people congregate in a single area is a very intensive thing,” he said. Picture credit: International Olympic Committee Whether or not Paris 2024 manages to hit the 50 percent carbon emission reduction mark is something that remains to be seen, but it’s important - and now more than ever - to be having these conversations, especially around mega events the size of the Olympics. The Global Risks Report 2024 says that vegetarian diets and other low-carbon life choices, including adapting transportation means that are low on CO2 emissions and reducing the consumption of single-use plastic, can, on a large scale, make a significant difference. But how much of a change can individual efforts really bring about when companies - including those sponsoring these kinds of events - aren’t entirely dedicating themselves to incorporating the same eco-friendly practices in their operations? At least organisers are quick to admit not everything is perfect. “We say that sustainability is a collective sport,” Georgina Grenon, director of environmental excellence for the Paris Games said to AP . “Will everything be perfect? No, right? We cannot say that. We’re still working very, very hard to go as far as we can.” Picture credit: Global Risks Report 2024 Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

On International Music Day, Swara shares how music shaped her life & inspired her mission to heal others < Back Neurodiversity, Gender The power of music - my path to self-discovery and healing On International Music Day, Swara shares how music shaped her life & inspired her mission to heal others Swara Swami 1 Oct 2024 3-min read I come from a family deeply rooted in music. Even before I could talk, I was singing. My family would often record me as a baby, capturing my little voice on cassette tapes. Music became my solace, my constant companion through the ups and downs of life. During my school years, I was bullied relentlessly, and music became my refuge. It helped me heal. Over the years, I trained in various styles — Hindustani, film music, Western, contemporary — and even dabbled in Carnatic music, though it never quite resonated with me. When I lived in Shanghai, singing and acting became my source of confidence. Even though my peers thought I was different, they noticed my talent in the arts. I was part of a group called ‘Sur Shanghai,’ where we performed regularly, and I began to see how the arts could empower others just like they had for me. That’s when I first considered a career in music. My journey took me to KM Music Conservatory in Chennai, but I quickly realised Western Classical wasn’t for me. I also didn’t feel supported there, and during the holidays, I would help my mother — an accomplished singer herself who worked with disabled children. That’s when I discovered my love for working with children with disabilities. Around the same time, Berklee College of Music visited my school, and I was drawn to their Music Therapy program. I knew that was where I wanted to be. To pursue this dream, I moved to Malaysia to attend the International College of Music (ICOM), which offered a transfer program to Berklee. However, it wasn’t an easy path. I struggled with anxiety and often felt like I wasn’t good enough. I failed semesters due to a lack of accommodations and support, and I couldn’t secure a scholarship, despite getting admitted to Berklee twice. But once I finally made it to Berklee, everything changed. I became part of the Berklee Indian Ensemble, recorded an EP that was nominated for a Grammy, and performed alongside artists like Vijay Prakash and Shreya Ghoshal. I also joined The Lotus Sound, a circle singing group, and we recorded an EP and performed at the International Acapella Festival in Moscow. Despite these successes, I faced setbacks too. I didn’t pass my Music Therapy major on my first try but succeeded the second time. While I was finding my footing academically, I lost my mother to cancer, and my mental health took a hit. A discouraging comment from a professor further eroded my confidence. For five years, I couldn’t pass my Music Therapy exam, which prevented me from securing a job as a Music Therapist in the U.S. In 2020, when the pandemic hit, I returned to India and started my own Music Therapy program at a trust in Nashik, Maharashtra. It was a step forward, but I wasn’t done learning. In 2022, I began a Master’s in Clinical Mental Health Counseling: Expressive Arts Therapy at Lesley University. This hybrid program allowed me to explore all forms of art, not just music. It also helped me rediscover my confidence. I acted in a play, sang at open mics — things I never imagined I could do. Now, I dream of building my own private practice, where the arts are a core part of the healing process for others, just as they have been for me. Music has been a constant in my life, and I hope it continues to be a source of strength and healing for those who need it most. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

No coaching. No resources. A state scheme and Collector backed Yogeshwari Selvam's IIT dream < Back Disability, Education, News From rural TN to IIT-B: Disabled girl to study aerospace engineering No coaching. No resources. A state scheme and Collector backed Yogeshwari Selvam's IIT dream MMS Staff 20 Jun 2025 3-min read When 17-year-old Yogeshwari Selvam from rural Tamil Nadu secured a seat in Aerospace Engineering at IIT Bombay, it was a revolutionary moment for India’s public education system. A disabled girl from a Tamil-medium government school, with no access to private coaching, cracking one of the country’s toughest entrance exams in her first attempt? In a landscape where structural disadvantage is often treated as personal failure, Yogeshwari’s story is one of what’s possible not when you “defy the odds,” but when the system starts to work. A spark in a small village Yogeshwari hails from Padanthal village in Virudhunagar district. Her father works in a tea stall, and her mother is employed in a fireworks factory, both part of Tamil Nadu’s working-class backbone that quietly sustains the state’s economy. Education was always a priority in the Selvam household. Her two older brothers made it through college, and Yogeshwari was determined to follow but with a dream that seemed impossibly distant: to study aerospace engineering. The spark came early. “I developed an interest in space during Class 7,” she says. “I didn’t even know what aerospace engineering meant exactly but I knew I wanted to study it.” It wasn’t until Class 12 that she even heard of the Joint Entrance Examination (JEE), the national-level entrance test required to enter the prestigious Indian Institutes of Technology (IITs). “I got to know about JEE through the Kalloori Kanavu program,” she says, referring to a career awareness initiative under the Tamil Nadu government’s Naan Mudhalvan scheme, which introduces government school students to competitive exams, college streams, and career options. For Yogeshwari, it was a turning point. State support and 40 days of opportunity She was among the 230 students from government schools selected for specialised crash coaching funded by the Virudhunagar District Collector’s office. The classes were held in Erode, over a 40-day period after her plus-two exams. Until then, Yogeshwari had studied in Tamil medium and had never attended English-language instruction. “The training was in English. It was difficult in the beginning,” she admits. “But I picked it up little by little just by staying focused.” She secured the 75th rank under the Differently-Abled (OBC non-creamy layer) category in JEE (Advanced) and with it, a seat at IIT Bombay. Representation, not resilience Yogeshwari’s story is often framed as one of resilience. And it is. But it is also about representation of government school students, disabled students, rural girls, and Tamil-medium learners in elite Indian institutions that have historically excluded them. Yogeshwari credits District Collector VP Jeyaseelan for helping her realise this path was possible. Through the Coffee with Collector initiative, she and other students had the rare chance to meet a government official who treated their dreams with seriousness. “The Collector told us the State would take care of our education,” she says. “That made my parents more confident.” She also thanks Tamil Nadu Chief Minister MK Stalin for launching schemes like Naan Mudhalvan, calling them a “boon for children from poor families.” But her journey is also a reflection of how much invisible labour students like her must still do, navigating caste, class, disability, and language barriers just to be seen as deserving of the same shot at excellence. Disability, not inability It’s worth noting that Yogeshwari is disabled, though most media coverage around her barely addresses this beyond a category label. In a system where disabled children are routinely segregated or written off, Yogeshwari’s admission into IIT is not a “miracle”. It’s a sign that when disabled students are included in mainstream education with proper support, they thrive. Disability-inclusive coaching, accessible content, and sensitivity training are still missing from many such interventions, a gap that Tamil Nadu’s education policy must now begin to address if it wants more Yogeshwaris to succeed. Looking to the skies What lies ahead for Yogeshwari? She speaks with confidence. “I want to work at ISRO one day,” she says. “Sunita Williams and Kalpana Chawla are my role models. If they can do it, so can I.” But she’s not chasing glory, she’s chasing possibility. And in doing so, she’s also become one: for millions of young girls across India who are told their dreams are too big for their village, their gender, their disability, or their mother tongue. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

Based on a book by an autistic author and featuring an autistic actor, the show is a must watch < Back Neurodiversity, Media Geek Girl: Autistic representation reviewed by Aditi Gangrade Based on a book by an autistic author and featuring an autistic actor, the show is a must watch Aditi Gangrade 26 Jul 2024 3-min read As an autistic filmmaker, watching a show that features an autistic actor playing an autistic character, written by an autistic author, is pure joy. I'm talking about Geek Girl , a Netflix series based on the book series of the same name by Holly Smale. Autistic people are often labelled as weird, rude, lazy, or in this case, “geeks.” Geek Girl follows the story of Harriet Manners, a slightly awkward, not-so-popular, undiagnosed autistic teenager who gets scouted to be a model, along with all her struggles and shenanigans. Btw, this is not a show review. It's a representation review. What makes this show so relatable is how it portrays an undiscovered autistic girl navigating her difficult school life and the overnight fame she receives from the modelling world. While autism isn't explicitly mentioned in the show because the author, Holly Smale, didn't know she was autistic when she wrote it, the book is based on her personal experiences. Many neurodivergent people have lived somewhat similar lives - not knowing why we're different, feeling lost in a world that doesn't understand us. I really hope they mention autism and neurodivergence in upcoming seasons because just imagine the amount of realisations there will be among undiscovered folks. Ex-model turned successful teen author Holly Smale says, “The Geek Girl series is a story about being yourself, no matter what.” And that, in a nutshell, is unmasking! Harriet’s internal monologue throughout the show distinguishes her inner world from the outer world, something I deeply relate to. It was almost healing to listen to her internal monologue. While her peers are eager to get discovered by the fashion world, all Harriet can think about is where to hide at the fashion event she finds herself in. And despite this, she gets discovered by one of the top agents in the fashion industry. Being different often means being bullied. Harriet endures bullying and online trolling simply for being a “geek.” However, the fashion world embraces her with open arms. Amid the flashy lights and overwhelming sets, her modelling career begins to flourish as she establishes her support systems. She finds a friend and mentor in Nick, a supermodel, and her agent Wilbur is shown as one of the most affirming people. Seriously, if you want a guide to being a good manager or boss, look up Wilbur. Wilbur asks Harriet if she needs time or if things are too much for her. He even pushes her to claim her strengths. The label “geek” becomes an important part of her identity that she starts accepting and even celebrating with the help of her village comprising her dad (also very autistic-coded), stepmom, agent, friends, teachers, and even the fashion designers who surround her. Though in the beginning of the show, I didn't like it when Harriet’s dads says, “I don't want any labels on her,” and I think that’s just a wrong way of looking at things. Parents don’t want the neurodivergent label on their kids, but that just doesn't help. Still, throughout the show there are some heartwarming instances where they show Harriet being accommodated, her differences being understood by those around her, and her going out to claim her autistic identity. If you look at the details, you’ll see Harriet and another neurodivergent character, Toby, stimming. The thing I love about the autistic representation in Geek Girl is that it’s not stereotypical. And they haven't used the “geek” label as a stereotype either. Many neurodivergent people have gone undiscovered for years because, among other things, we’ve just never had real, honest, truthful representation. All people knew about autism was the savant-boys-and-men stereotype . Geek Girl has become one of the best autistic representations I've seen. And it is a lesson for all filmmakers, producers, and OTTs: Hire autistic actors, autistic writers, directors, producers, and filmmakers. There are so many of us who are good at what we do and have spent so much time unlearning ableism and learning about the right and affirming ways to address neurodiversity, and reframing the narrative. So if there’s one takeaway you should have, it’s definitely: “Nothing about us, without us.” Watch the #RepUp : Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

The toymaker is becoming a model for inclusive marketing by prioritising accessibility < Back Disability, News Mattel to make games accessible to colour-blind players The toymaker is becoming a model for inclusive marketing by prioritising accessibility MMS Staff 2 Jul 2024 3-min read Toymaker Mattel has taken a step towards inclusivity by announcing plans to make 80 per cent of its games, including popular games like Uno, Tumblin’ Monkeys, and Blokus, colour-blind accessible by the end of 2024. And by the end of 2025, Mattel aims to extend this accessibility to 90 per cent of its games. This initiative also includes updates to the mobile versions of its games through Mattel 163, the company’s online game studio. To achieve this goal, Mattel is developing custom solutions for each game, allowing players to differentiate components through means other than colour. These methods include adding symbols or icons, patterns, and tactile clues. As part of its commitment to the colour-blind community, Mattel will also donate $30,000 worth of accessible games to summer camps. This initiative is particularly helpful given that data shows 1 out of 12 men and 1 out of 200 women are colour-blind. Interestingly, this is not Mattel’s first foray into accessibility. In 2017, the brand partnered with ColorAdd to create the Uno ColorAdd deck, and in 2019, it introduced Uno Braille to ensure that visually impaired players could enjoy the game as well. Universal needs of consumers and the importance of accessibility Mattel’s commitment to accessibility comes from the understanding that children - and, in fact, people of all ages - want to play games without feeling excluded. More brands need to realise that an aspect of one’s identity should not prevent them from participating fully in shared experiences. And more brands need to design keeping differences in mind, being mindful of the diverse identities they serve. Values drive brand decision-making Mattel’s says its purpose is to “empower generations to explore the wonder of childhood and reach their full potential,” while its mission is to “create innovative products and experiences that inspire fans, entertain audiences, and develop children through play.” Revisiting your brand’s mission, vision, and values is essential for any brand that wants to cater to people with different needs. Evaluate whether your mission statement is inherently inclusive of a broad range of people who face barriers that your brand works to solve. Inclusivity doesn’t require an immediate overhaul but rather a steadfast commitment to making gradual strides towards a more inclusive future. Co-creation is core to success And don’t at all shy away from partnering with the right people in making headway on this front. Mattel themselves have partnered with experts in the field of colour deficiency to work on accessible versions of their games, consulting with individuals as well as designers who have colour blindness. This co-creation process was integral to producing products that genuinely meet the needs of the community, as the insights come from people with lived experience. Co-creation is key to making inclusive products. It not only lowers the pressure of getting everything right on your own but also ensures the end products are more authentic and effective. So remember - if you’re on the path to making your products and services more inclusive, start by revisiting your mission and incorporating inclusivity there. Realign your values, and partner with the right people to co-create your offerings. This story was originally published in Forbes . Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

Thought about checking in on your dad’s mental health? We give you a starting point < Back Health, Parenting The best gift idea for Father's Day you wouldn’t wanna miss Thought about checking in on your dad’s mental health? We give you a starting point MMS Staff 15 Jun 2024 5-min read Father's Day is an opportunity to show appreciation and love for the fathers and father figures in our lives. While traditional gifts like ties, grooming kits, or tools are always appreciated, this year consider giving a gift that could have a lasting impact: the gift of health and mental well-being. Mental health challenges are more common than many realise. As per Statista, as of October 2021, 33 percent of men had depression as compared to women with 31 percent during the same time period. Initiating a conversation about mental health with your dad can be one of the most significant gifts you give. Consider starting a dialogue that addresses the stigma and acknowledges common issues like trauma and provides a supportive space. A new Verywell Mind and Parents survey has found that 75% of dads are looking for more mental health support. Here’s why protecting men’s health is so important First, create a non-judgmental environment where your dad feels safe to express his feelings and share his experiences. Listen patiently, respond with empathy, and remind him that his feelings are valid. Let your dad know that it's not just okay but appreciated to talk about and seek help for mental health. To have a meaningful conversation about health and mental health with your dad, approach the topic with sensitivity, understanding, and respect for cultural nuances. Here’s an expanded guide on how to navigate this important dialogue: Understanding cultural context Be mindful of cultural differences: Recognize that in many families, topics like mental health are not commonly discussed openly due to cultural stigma and misconceptions. Before initiating the conversation, consider how your dad has traditionally viewed mental health and prepare to address these views compassionately. Educate yourself: Equip yourself with knowledge about mental health issues, symptoms, and resources. This information will help you provide factual insights and dispel common myths, making the conversation more informative and less opinion-based. Initiating the conversation Choose an appropriate setting: Pick a moment when both of you are relaxed and have some privacy, such as after a meal or during a quiet evening at home. Avoid times when he is stressed or preoccupied with work or other responsibilities. A calm and comfortable setting can make the conversation more productive. Start with a neutral topic: Start with a broader discussion about physical health, which might be less sensitive. You could bring up topics like diet, exercise, or routine check-ups. Here’s a script: “Dad, I’ve been reading about how important regular health check-ups are as we get older. When was the last time you had a check-up?” Make the conversation relatable: Discuss the health or mental health story of a celebrity, public figure, someone else he might be familiar with, or something that recently appeared in the news or media. This can segue into a broader health discussion. Deepening the discussion Share personal observations and experiences: Gently make conversation more personal by sharing your own experiences with health issues, be it physical or mental. This can make the topic feel more relatable and less intimidating. Here’s a script: “I’ve noticed I feel a lot better when I talk about my stresses. It’s not always easy to open up, but it helps me manage my stress. Have you ever felt something similar?” Introduce mental health gradually: Frame mental health as an integral part of overall well-being. Discuss how mental and emotional health impacts physical health and everyday life, drawing parallels to common physical health problems that are more frequently discussed and accepted. Mention stories of public figures or characters from films or TV shows that dealt with health issues, including mental health. This can make the topic more relatable, less intimidating, and also might help break the stigma around certain health conditions. Discuss trauma and generational patterns: Introduce the concept of trauma, including generational trauma, which may not be immediately apparent or discussed within families. Approach this topic gently and with understanding rather than assigning blame. Here’s a script: "I've been learning about how experiences and habits can be passed down through generations, affecting how we handle stress or conflict. It might help us understand some of the challenges we face as a family." Mention specific incidents or symptoms: Carefully bring up any behaviours or symptoms you've noticed that may indicate mental health struggles. Make sure to approach this part of the conversation with sensitivity and without judgement. Here’s a script: “I've noticed sometimes when things get overwhelming, you tend to withdraw and isolate yourself. I read that it can be a sign of anxiety. It’s something that many of us might not even realise we're doing.” Draw connections between actions and emotions: Help your dad make connections between his behaviours and what they might signify about his emotional state. This can provide him with insights into his own feelings and offer him the language to express these emotions: “When we talk about being anxious and how it leads to shutting down or isolating, it’s really about noticing how our bodies and minds react to stress. Understanding this can help us find better ways to cope.” Offer tools for self-reflection: Suggest simple ways in which your dad can reflect on his feelings and behaviours. This might include journaling, mindfulness practices, or even engaging in regular conversations with you or a therapist. Addressing stigma, misconceptions, and toxic masculinity Discuss cultural stigma: Address the cultural stigmas surrounding mental health openly but sensitively. Here’s a script: “I know it’s often not seen as okay to talk about mental health, but I think it’s really important for us to be open about it. It affects so many people and talking can really help.” Provide information and examples: Through examples, discuss the benefits of mental health awareness and care. Give examples of people who sought help and how their lives changed. Discuss the pressure of toxic masculinity: Talk about the societal expectations on men to appear strong and detached, and how this can be a barrier to mental health discussions. Here’s a script: “I’ve noticed that often, our society expects men to not express their feelings openly, considering it a weakness. But I believe being able to share what we feel is actually a sign of strength.” Discussing action and support Encourage your dad to take small, manageable steps towards improving his mental health. This could look like consulting a professional, getting in a workout, meditation, mindfulness, therapy, or even attending a workshop or seminar on mental wellness. Provide information about local health professionals, credible websites that offer information, and support groups. Offer to help him reach out to these resources if he shows interest. Maintaining an ongoing dialogue Reinforce your support throughout the conversation. Here’s a script: “I really appreciate you taking the time to talk about this with me. I’m here for you, and I think it’s great for us to keep this communication open.” Don’t let this conversation be a one-time event. Check in regularly about what was discussed, offer additional support, and share any new information you come across. This ongoing dialogue will help normalise the discussion of health and mental health in your family. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS