Model Gigi Robinson encourages those who suffer from chronic illness

Gigi Robinson Wanting to wake up every morning and take a bite out of life. “My emotions in life change honestly, from making people feel their best, to content shooting, to travel, I try my best to live life to the fullest and enjoy every moment. Every day I start my day with shortness of breath. It’s something that really gave me a place to escape, a place to reflect and focus on one thing, my breath. I also love to move my body in a way that makes me feel good, such as walking and water aerobics. ” From learning to pose to understanding how the camera works, I have always focused on giving people the best feeling when they are in front or behind the camera. I also love creating photos that tell stories and empower people that way. When I focus on building and building a business, I also find ways to tap into my brand policy in my content; I mean I really like the way people feel a certain way when they use content. Another thing I like about getting DM from people is how my content has inspired or helped them in their journey of self-discovery. ”

His career spread across the stratosphere when he was noticed by legends Sports illustrated Editor, MJ Day. “It was iconic and legitimate to have a conversation with such an inspiring person. MJ is someone who changes lives; He provides a platform for people to share and express themselves in ways that sometimes words cannot describe. It’s great that I’ve found a way to get MJ’s attention through a professional platform like LinkedIn. Advocacy and modeling is a profession and sharing it on LinkedIn was the beginning of global brand support, e.g. And. As an advocate for mental and chronic illness, I found it very special to be a part of this experience. For all sorts of people, including me, to fight an invisible disease, it seems unrealistic to have a place in such a world-famous magazine. It is an honor to be a public representative that I will cherish forever! ” Gigi loved to learn about the other finalists, and they were all humbled by the realization that they were agents of charge. “Being a swim search finalist is an incredible feeling, again it seems surreal that I could be a part of it. Meeting other women who chose to be part of the swimming quest was one of my favorite parts because everyone has their own story of empowerment. It was also incredible to meet the team moving and changing through the vibrating art and swimwear; How cool is that? Being part of something like this has really helped me to be clear about the need to represent disability and chronic illness in the modeling industry and in the eyes of the public. “

Gigi’s own journey was not easy. At age 11, he developed Ehlers-Danlos Syndrome, a connective tissue disorder. “I was diagnosed at such a young age that I didn’t really understand or understand what was going on in my body. I had 504 disability accommodations to help me manage my condition as well as constant physical therapy and doctor’s appointments to manage my growing pains. It took me up to my college year to fully understand how this situation would affect my life and how I would do it. During my college years, I had so much trouble managing my health that it led me to a really tough burnout time where I was finally inspired to share my journey with EDS publicly. ” I can explain my life experience with EDS, which is different from how a doctor can describe EDS. From my knowledge and diagnosis, EDS is a connective tissue disorder that affects all patients differently. I experience chronic pain and fatigue, simple wounds and bruises. However, as always, I recommend gathering information from medical platforms when explaining what EDS is, although patient experience is just as important! ” In her case, the effects are unpredictable and difficult for others to understand. “EDS gives me a lot of pain. It’s uncontrollable and sometimes indescribable. It is very difficult for me to explain this to my friends and teachers when it comes to my qualifications. That is why I am so adamant about self-advocacy for chronic illness; Determined to be a source of the necessary visibility and comfort in the context: “I grew up feeling lonely. As part of a digital-first generation, I grew up with people who should leave out in real life what they should and shouldn’t share on social media. Over the past decade, conversations about health and wellness have shifted from how physically fit you are to how mentally fit you are. For me, invisible I didn’t have anyone to talk to me about this illness online and in person and I thought to myself, ‘What if I grow up to be that person to other people and deal with it now?’ That’s the decent thing to do, and it should end there. “

We all need to remember that chronic illness never shows a certain way and we must respect the right of everyone to communicate their feelings and needs on a daily basis. “As I said many times before, you can feel like shit and still look sexy. Ever since I was a kid, people have always told me that I was too young to be sick or too beautiful to be sick and that it was a narrow view of what it was like to be a person. Again, as a teenager, I didn’t know how to deal with this kind of comment. I just kind of nodded and shrugged my shoulders. Chronic illness looks different for everyone and can be very dynamic. One day I could attend a ceremony wearing heels, the next day I could be stuck in bed with chronic pain. Today, however, I make sure that I am clear about my boundaries with people and share what is happening with anyone, especially since I share it publicly. You never know how your body is going to react, so it’s really important to respect them when they can feel the pain. ” The DMs have inspired me to continue. It makes me incredibly proud to know that being vocal about my situation has inspired other people to have conversations with their friends and family about what they are doing, helping students find the space they need and helping other people. It’s been a long time coming, and I’m glad I did. ” When we are brave enough to open up about ourselves, you never know what you can do to help open a door for other people.

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Model Gigi Robinson encourages those who suffer from chronic illness. Photo Credit: Sophie Sahara.