The Mo Experience Foundation, empowers individuals and communities through transformative' programs and experiences that foster personal growth, resilience, and social connection. After being diagnosed with Scleroderma, the founder, Monika Hilton transformed pain into passion by creating cookbooks, seasonings, and sauces to help others get "The Mo Experience" in their very own kitchens, even when cooking became difficult, quitting was not an option.
I’m Monika Hilton, in 2017 I was diagnosed with a rare autoimmune disease called Scleroderma, which translates to "hardening of the skin." This connective tissue disorder leads to an overproduction of collagen, resulting in chronic pain, skin tightening, joint stiffness, fatigue, intestinal complications, and potentially organ failure.
For over 20 years, I thrived as a competitive chef and cake artist, showcasing my skills on Food Network's "Cake Wars" and Netflix's "Sugar Rush," while building a significant clientele in the Southeast, as well as within the entertainment industry.
Unfortunately, due to the loss of mobility in my hands, I can no longer cook, bake, or decorate cakes.
Just when I thought my creative journey had ended, I swapped my spatula for a paintbrush, and wow, look at God! 🎨✨ Scleroderma has profoundly impacted my life, but I am now on a mission to raise awareness about this condition through my artwork. Since there is no cure, early detection is vital in slowing its progression which is why my passion for spreading awareness is so important.
My paintings are vibrant reflections of my journey and resilience, and I would love to share them with you. You can view and purchase some of my artwork directly on my website: www.TheMoExperience.org.
I would appreciate the opportunity to schedule an interview with you to discuss Scleroderma, my experiences, and how others can support this cause. By sharing my story, I hope to raise awareness and inspire hope for those facing similar challenges.
If you’re interested in having a conversation and helping to spread the word about Scleroderma, please reach out to me at 404-857-7675 or visit my website to schedule an interview. Together, we can make a difference and bring much-needed attention to this often-overlooked disease. Your support can truly help. Your reach is enormous and im convinced your influence can help me bring awareness to many people on various platforms.
Scleroderma Advocate,
Monika Hilton
Welcome to the Monika Hilton Art Gallery—a celebration of resilience, transformation, and boundless creativity. Diagnosed with scleroderma seven years ago, I believed my journey as a competitive chef and cake artist had come to an end. However, life had a beautiful surprise in store for me. Trading my spatula for a paintbrush, I've embarked on a new artistic adventure, and I invite you to explore this vibrant world with me. Wow, look at God! 🎨✨
At the Monika Hilton Art Gallery, you will find an inspiring collection of my works that blend passion, perseverance, and profound joy. Each piece is a testament to the power of faith and the human spirit's ability to adapt and flourish even in the face of adversity.
Hi, I’m Celebrity Chef Monika Hilton. Just a few years ago, I was a competitive chef and a well known cake artist, once competed on Food Network's, Cake Wars and Netflix's, Sugar Rush, with a huge clientele in the southeast area as well as the entertainment industry and I now experience great difficulties when baking and decorating cakes due to the loss of mobility in my hands and not being able to lift, bend, or stand for extended periods of time.
Scleroderma is a chronic autoimmune disease that affects the connective tissues in the body, causing hardening and thickening of the skin and various internal organs. It is a complex condition with no known cure yet, but ongoing research is essential to better understand its causes, develop more effective treatments, and ultimately find a cure.
By donating a portion of the proceeds to the Scleroderma Foundation, we aim to contribute to the funding of research projects focused on advancing our knowledge of scleroderma and finding ways to improve the lives of those affected by the disease. The donated funds may support studies exploring potential treatments, investigating genetic factors, identifying biomarkers for early diagnosis, or developing strategies to manage symptoms and complications.
This donation not only helps to support the important work of the Scleroderma Foundation but also enables individuals and organizations to contribute towards finding a cure for this debilitating disease. By participating in the event or purchasing the product associated with this initiative, you are not only benefiting yourself but also making a positive impact on the lives of those affected by scleroderma.
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