Melissa Blake suffers from Freeman-Sheldon Syndrome, a genetic bone condition. She had always wanted to be a model, but due to her impairment, it was said that her dream would never come true. She got to model at New York Fashion Week years later.
Journalist Melissa Blake focuses on pop culture, relationships, pop culture, and people with disabilities. Blake was born with the inherited bone and muscle condition known as Freeman-Sheldon Syndrome.
The journalist’s spine, hands, hips, and knees have all undergone roughly 26 surgery. Blake always wanted to be a model, despite the difficulties posed by her illness. She claimed that although she grew up reading all of the well-known glossy publications, she never saw somebody who resembled her.
But when Blake was a teenager, someone crushed her hopes, telling her that her disability would prevent her from ever being a model. She carried the hurtful comments with her for a long time.
Discouragement served as more than just a means of stifling her dreams. It was also terrible because it supported the condescending notion that individuals with disabilities have no place in the fashion and beauty industries.
Blake had no idea that she would soon be among those contributing to the shift in the perception of disabled individuals in the fashion business. The 42-year-old watched her fantasy come true 20 years later.
She modeled the new adaptable apparel line for Zappos and walked the runway during New York Fashion Week. As Blake was modeling at the height of the COVID-19 pandemic, she had the opportunity to see a significant global shift.
The journalist noted that a reformation of beauty standards was long overdue, even if she acknowledged that the epidemic was a vulnerable moment for disabled people, leaving them with restricted access to health care and other essentials. She was so honored to be among the icons of this revolution in the fashion industry.
She went on to say that the epidemic had a revolutionary effect on how individuals expressed themselves via apparel in addition to altering lifestyles.
Blake’s home was the setting for the filming of her runway walk. Each of the 25 models had a unique film that combined shots of their stylish ensembles with intimate narratives about their experiences as disabled persons and what it meant to them to be involved in the creation of spaces for the disabled.
The journalist was ecstatic to be seeing this moment and the fashion industry’s shift toward inclusivity. Recalling the days when beauty magazines exclusively featured a particular kind of woman, she was happy to see nonprofits like Mindy Scheier’s Runway of Dreams.
Muscular dystrophy was present in Scheier’s newborn son. As he grew older, he tried dressing like other people his own age, but he found that he had trouble with the zippers and buttons.
It became evident that disabled persons were not well-dressed in both fashionable and functional apparel. Thus, Scheier’s company promotes inclusive clothes through occasions such as New York Fashion Week. Blake writes about her experiences finding love as a person with a disability on her blog, “So About What I Said,” even though she looks up to people like Scheier.
She has contributed her knowledge to reliable websites such as Psychology Today. The title also refers to the freedom for people to retract or clarify statements that were made inadvertently or at the incorrect moment.
Blake consistently confronts cyberbullies head-on. The blogger uploaded three images in 2019. She responded to the critical comments with a caption that read, “During the last round of trollgate, people said that I should be banned from posting photos of myself because I’m too ugly.”
Three years after her tweet went viral, Blake recapped it with a clap of his own: “Because of you, I blossomed instead of withering, took up space instead of hiding.” She wrote, “I’m still standing and rolling.
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