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Thai PM joins Bangkok's Pride parade, highlighting the nation's historic push towards legalizing same-sex marriage < Back LGBTQIA+, Gender, News Thailand celebrates Pride Month amidst same-sex marriage advancements Thai PM joins Bangkok's Pride parade, highlighting the nation's historic push towards legalizing same-sex marriage MMS Staff 2 Jun 2024 4-min read The streets of Bangkok were awash with rainbow flags on Saturday, marking the beginning of Pride Month with a spectacular parade that saw thousands of LGBTQIA+ people coming together in a vibrant display of unity and love. As signs and placards bearing the slogan "Love wins'' adorned the city, the event signified more than just a celebration; it marked a pivotal moment in Thailand's journey towards legalising same-sex marriages. "This year's pride parade can be considered one of the biggest because it coincides with the passing of the same-sex marriage," said Avorawan Ramwan, who joined the parade with her partner. The significance of this year's parade is heightened by the anticipation of a landmark legislative change. Thailand is on the brink of legalizing same-sex marriage, with an equality bill set for its final readings in the Senate later this month. An overhead view of the Bangkok Pride parade, showcasing a massive rainbow flag stretching across the street, carried by a large crowd of participants. People line the sidewalks and an overpass, cheering and taking photos, as the vibrant colors of the flag create a striking visual display. The parade highlights the strong support for LGBTQIA+ rights and the push for same-sex marriage equality in Thailand. In a show of solidarity and support, Thai Prime Minister Srettha Thavisin participated in the parade, donning a rainbow shirt. He took to social media to express his support, stating, "It is a basic right to choose who to love." The Prime Minister’s participation and public endorsement reflect a growing acceptance and recognition of LGBTQIA+ rights in Thailand. The bill, which passed the upper house's first reading in April, is scheduled for its second and third readings this month. "The Senate will likely pass the bill on June 18," said Senator Wallop Tangkananuruk, chairman of the Senate's committee on same-sex marriage. Should the bill pass without amendments from the lower house, it will be sent for royal approval, after which it will become law 120 days post-publication in the Royal Gazette. Thailand's embrace of LGBTQIA+ rights is not only reflected in its legislative progress but also in its cultural and social landscape. Known globally as a haven for the LGBTQIA+ community, Thailand has long been celebrated for its inclusivity and acceptance. The country hosts numerous pride events and has a thriving LGBTQIA+ scene that attracts visitors from around the world. "Pride events are meaningful, and Thailand is known worldwide as a paradise for the LGBT community. Therefore, we must help promote and advocate for it, as well as implement laws to support the LGBT community," said transgender woman Aunchanaporn Pilsauta. Her words emphasise the importance of both societal acceptance and legal recognition in creating a truly inclusive environment. As Thailand moves closer to recognizing same-sex marriages, the enthusiasm and hope among the LGBTQIA+ community are palpable. The potential passing of the same-sex marriage bill not only signifies a major victory for LGBTQIA+ rights in Thailand but also sets a progressive example for other nations in the region and beyond. A participant in the Bangkok Pride parade proudly holds a sign reading 'Mr. Gay World,' while carrying a rainbow flag. He is followed by other participants dressed in colorful outfits, including a person in a Dalmatian costume. The parade path is painted in rainbow colors, and the sides are lined with spectators cheering and taking photos. In the background, a stage and balloons in rainbow colors add to the festive atmosphere, celebrating LGBTQIA+ pride and advocacy in Thailand. Context on Thailand's LGBTQIA+ affirmation Thailand has long been regarded as one of the most LGBTQIA+ friendly countries in Southeast Asia. The country’s rich cultural history, combined with its contemporary embrace of diversity, has positioned it as a leader in LGBTQIA+ rights and acceptance. Cities like Bangkok and Pattaya are well-known for their vibrant LGBTQIA+ communities and events, drawing tourists and locals alike to celebrate and support equality. Despite the progress, the journey towards full legal recognition has been a challenging one. Activists and allies have tirelessly campaigned for years, pushing for equal rights and protections under the law. The upcoming potential legalization of same-sex marriage is a testament to their perseverance and the gradual shift in societal attitudes towards greater inclusivity. A step towards equality The momentum for change is building, and the prospect of legalized same-sex marriage in Thailand is a beacon of hope for many. The celebration during this year's Pride Month, with its unprecedented turnout and official endorsements, highlights the critical intersection of cultural celebration and legal progress. As Thailand inches closer to this historic milestone, the spirit of Pride and the message that "Love wins" continue to resonate powerfully across the nation and beyond. This article incorporates information from a Reuters report on the recent Pride events and legislative developments in Thailand. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

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

From unmasking at work to exploring new passions, here's how to navigate your new path < Back Neurodiversity, Work, Education 7 tips for reinventing your career after your neurodivergence discovery From unmasking at work to exploring new passions, here's how to navigate your new path MMS Staff 1 Aug 2024 5-min read So you were young, you fell in love with your idea of a career path or job, you pursued it, got placed at a company. And then it happened - you got an answer to a lot of your life’s questions with a late diagnosis or discovery, finding out you’re neurodivergent: ADHD, dyslexia, dyscalculia, autism... or any of these conditions. And now, you want to unmask. You keep replaying your life thus far in your head, and you feel like you’d much rather do something else, be somewhere else, and be so much better at it too. Most late diagnosed/ discovered folx have been here - thinking their chosen job or career is something they want until the discovery/ diagnosis happens, and then suddenly they’re in the woods. Fortunately, there are some things you might want to consider if you’re in the same boat. Unmask at your current workplace - slowly, safely Let’s get this straight right up front - unmasking is difficult. And totally not recommended if you’re in a place where you might get taken advantage of. With that said, it is also one of the few ways to let your peers and co-workers know about the challenges you’re having. If you think you can speak to your boss about this, and they’ll understand, maybe that’s something to consider? It won’t make the job feel less boring, but accommodations and support can surely go a long way in making things bearable until you’re able to find something more suited to your needs. Shift to a more suitable job within your organisation Picking up where point one left off, if it’s the role you truly despise, and your boss or upper management understands your situation, maybe shifting to a different role within the same organisation might be something to consider. A lot of people, especially those with customer-facing roles find they’re actually not so suited for those roles once they start doing them. Ask to be shifted to a department where the work is more suited to your talents. Upskill A lot of companies, including Google, IBM and Meta, offer online courses that you can take to learn a new skill. Certificate courses can be taken part time at a flexible schedule, which you can figure out based on your current workload, and they’re relatively inexpensive as well. Once you have a certificate in a skill that’s in demand, apply for new jobs. Sure you’ll have to begin as a fresher, but it will be worth it in the long run if you truly have a passion for it. Go back to college If you feel like a simple certificate course won’t cut it, and that you need to learn the fundamentals all over again, it’s never too late to consider going back to college. This is a path a lot of people have taken well into their 50s and 60s, and if it’s something you’re sure about, the plunge will be worth it. The flipside - college is expensive and a lot of people aren’t able to afford it. But there’s always scholarships and grants that you can apply for. Explore flexible work options Figure out what about the job or career doesn’t feel right. If it’s the long hours, see if your workplace is able to offer you a flexible schedule. If it’s the social aspect, figure out if socialising is something you can limit to only certain days or hours a week. If it’s a long commute, explore WFH or hybrid formats of work. It’s important to know which aspect of the job seems cumbersome and unsustainable for you in the long run so you don’t wind up in the same boat over and over again. Experiment with side projects or part-time work If work overall doesn’t feel good, and you can afford some time off, pick up that side project that you always wanted to but never could. See if that could turn into a paid opportunity. With so many businesses relying on the internet and social media, you’ll be surprised what people will pay for. Or, for the time being, while you figure things out, you could take up a part time gig just to pay the bills. The extra headspace always helps put things in perspective! Consider freelancing or entrepreneurship And if working in a corporate or an office environment at your desk for 9 hours a day every day just doesn’t feel so good anymore, you might want to consider a freelance career. Lots of specialists offer their time to companies as a ‘fractional’ consultant, which means they work that same role with multiple companies. While the work might still be hectic, at least you’re your own boss and you'll be able to work by your hours. Another path to consider is entrepreneurship. And while running your own shop might have many downsides (and wayyyy more stress!), if aspects such as innovation, improvisation, and leadership come to you naturally, you’ll excel at it. Whichever of these paths you wind up taking, remember that it’s important to focus on your strengths. You will need to learn to advocate for yourself politely and assertively, and while it may seem like a drag to try and be social, networking within different communities really helps give perspective (and also, who knows, job opportunities in a field you like!). Join WhatsApp and Telegram groups started for neurodivergent folx by neurodivergent folx, and don’t be afraid or shy to ask for help from people there. It’s easy to blame yourself when things aren’t going right, but this is probably when it’s most important to actively practise self-compassion. Keep telling yourself that no time is ‘too late’ to have had a diagnosis or discovery, and that you can still pursue what you really like, what suits you, and pays you well. Finally - use social networks like LinkedIn and Indeed to keep yourself up-to-date on the job market in your field of interest. Follow companies you want to work with, and learn how to build a solid resume that highlights your strengths. And, if through this journey you see your mental health taking a toll, don‘t beat yourself up over it. Instead, consider therapy. Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS

The journey of two siblings navigating the world with mutual respect and a shared perspective < Back Neurodiversity Siblings who "get it": The neurodivergent brother-sister bond The journey of two siblings navigating the world with mutual respect and a shared perspective Aditi Gangrade 17 Aug 2024 4-min read As someone who’s autistic and ADHD, I’ve always felt that the bond I share with my younger brother, who also has ADHD, is different from anything else in my life. Growing up neurodivergent in a world that often doesn’t understand you can be incredibly isolating, but having a sibling who “gets it” changes everything. It took us many years to understand each other as both of us grew up as undiagnosed neurodivergents, only to realise in our adulthood that we’re neurodivergent. After many years of fights, love, and care, our relationship is now built on a deep understanding of each other’s needs, struggles, and joys. Unspoken understanding of sensory needs One of the things my brother and I instinctively understand about each other is our sensory needs. We don’t need to explain to each other why certain lights are too bright or why certain textures are unbearable — we just know. I remember countless times when he’d walk into a room and immediately turn down the volume on the TV because he could tell I was getting overwhelmed. He’d ask my parents to get soft socks for me as the texture of most socks hurt me. These small, unspoken gestures are a huge part of what makes our relationship special. We’ve learned to create a comfortable environment for each other without even thinking about it. Navigating social expectations together Social situations have always been challenging for both of us. I’ve often felt out of place, not understanding social cues or the unwritten rules everyone else seemed to know. But having my brother by my side made these situations easier to handle. We’ve developed our own way of communicating when we’re in public, with little signals that say, “I need a break” or “Let’s get out of here.” It’s like having a partner in a world that sometimes feels like it’s speaking a different language. The comfort of predictability Routine has always been my safe space, and I know my brother feels the same. We both find comfort in the predictable rhythms of our daily lives. Whether it was our morning chai ritual or the way we always had movie afternoons on chill days, where we binge-watched our favourite shows. These routines ground us. They’re our way of creating a world that feels safe and manageable. It’s something we’ve always done for each other, even when the rest of the world feels chaotic. Mutual respect for boundaries Growing up, we both learned the importance of respecting each other’s boundaries. I’ve always needed my alone time to recharge, and so has he. We never took it personally when one of us needed to retreat to our room after a long day — it was just understood. This respect for boundaries has been a cornerstone of our relationship, allowing us to support each other without overwhelming each other. It’s a form of love that’s based on deep understanding and acceptance. Coping mechanisms and strategies Over the years, my brother and I have developed our own set of coping mechanisms to manage our neurodivergence. From stimming to using specific apps that help us stay organised, we’ve always shared what works for us. I remember when he introduced me to a new time management app that completely changed the way I handle my daily tasks. These strategies are more than just tools — they’re a way of saying, “I understand what you’re going through, and I’m here to help.” Handling meltdowns with empathy Meltdowns are a part of our lives, and having a sibling who truly understands what that feels like has been invaluable. When I’m on the brink of a meltdown, my brother knows exactly what to do — whether it’s giving me space or just sitting quietly with me until I’m ready to talk. I do the same for him. There’s no judgement, no impatience — just empathy. We’ve been through it enough times to know that sometimes the best thing you can do is just be there for each other. The joy of special interests One of the most joyful aspects of our relationship is the way we connect over our special interests. Whether it’s long sessions playing our favourite video games or a marathon discussion about a topic like our favourite snacks, these shared passions bring us closer. It’s about celebrating the intensity and enthusiasm that comes with our neurodivergence. In these moments, we see each other’s true selves, and there’s nothing more affirming than that. Experiencing the world differently, together The world can be overwhelming, confusing, and even hostile for neurodivergent people. But my brother and I experience it together, and that makes all the difference. We might perceive things differently from others, but we share that experience with each other. It’s like having someone who speaks your language in a foreign land. We just “get” each other in a way that’s hard to put into words, but it’s something I wouldn’t trade for anything. Being neurodivergent siblings has shaped the way my brother and I relate to each other and the world. For us, it’s not just about being siblings — it’s about being allies, friends, and each other’s greatest champions in a world that doesn’t always understand us. We truly are siblings who get it. 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

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

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

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

From birthmarks to prosthetics, these dolls celebrate what makes each child unique < Back Disability, News This woman makes toys that help kids with disabilities feel less alone From birthmarks to prosthetics, these dolls celebrate what makes each child unique MMS Staff 17 Apr 2025 4-min read When Amy Jandrisevits worked as a social worker in a paediatric oncology unit, she quickly learned how important dolls were for children coping with serious illness. Play therapy was a vital tool but something about it didn’t sit right with her. “The dolls had long eyelashes, full heads of hair, and perfect smiles,” she recalls. “They looked nothing like the kids holding them.” That disconnect planted a seed. Today, Amy is the founder of A Doll Like Me, a nonprofit that handcrafts dolls to reflect the unique physical characteristics of children with disabilities and medical conditions, from limb differences and albinism to surgical scars, burns, and birthmarks. What started as a personal project has now become a global movement centred on one powerful belief: every child deserves to see themselves represented just as they are. Dolls that validate, not "fix" In a world where children with disabilities are often made to feel invisible, Amy’s work offers more than just toys. It offers belonging. Each doll is thoughtfully made to match the child receiving it, not in a caricatured or exaggerated way, but with dignity, detail, and care. “These kids don’t need to be ‘fixed,” Amy says. “They’re already whole. What they need is representation.” The message is clear: children with disabilities are not broken: they are beautiful, and they deserve to be seen. From passion project to nonprofit mission Amy’s first custom doll was made for a young girl who had lost her leg. When the child saw the doll, she whispered, “She’s just like me.” That single sentence ignited what would become A Doll Like Me. Initially, Amy funded the project on her own and charged a fee for each custom doll. But she soon realized that many families couldn’t afford the cost. So, she started a GoFundMe campaign to ensure that no child would miss out on a doll that could change the way they saw themselves. As of now, she’s raised over $23,000 and hopes to reach her $25,000 goal to formally register the project as a nonprofit. Each doll costs around $100 to make. Amy doesn’t cut corners because, as she puts it, “You can’t put a price on self-worth.” A Doll Like Me now works with children's hospitals across the US to identify children who would benefit from receiving a personalised doll. Paediatricians and child life specialists recognise the psychological value of these dolls, not just in building self-esteem, but also in helping children process trauma, grief, and identity. Amy sees it as emotional medicine. “Mental health is health. If a doll can make a child feel less alone, more confident, or simply smile on a hard day, that’s everything.” One doll, one child, one story at a time Each doll Amy makes is different, just like the kids who receive them. She listens to parents’ stories, studies photographs, and pays attention to details that matter: a favourite colour, hairstyle, tiny brace, scar that tells a story. One doll might have a feeding tube. Another might have a birthmark shaped like a heart. The reactions are powerful. Videos on the A Doll Like Me Facebook page capture tearful parents, laughing kids, and quiet moments of awe as children recognise themselves in their new dolls. In a world that often sidelines disability, A Doll Like Me is a soft but powerful revolution. It affirms that representation isn’t just a matter of policy or entertainment, that it starts early. In childhood. In play. In toys that tell the truth. As Amy puts it, “These dolls are a way to say, ‘You are perfect just the way you are.’ And every child deserves to hear that.” Much much relate? Share it now! WhatsApp Facebook X (Twitter) LinkedIn Copy link < Back SHORTS