Inspiring EDS Community Nationwide
I started EDS Education and Empowerment Endeavors to provide support and understanding for those living with Ehlers-Danlos Syndrome. My goal is to create a space where you feel seen and connected—where resources, compassion, and education help you navigate EDS.
By sharing my journey—from mobility loss to recovery through regenerative therapies—I hope to inspire you and remind you that you’re not alone. I’m here to offer support, encouragement, and a listening ear. Feel free to reach out anytime at [email protected]. I’m here with you every step of the way.
Researching EDS Treatment Therapies
I am deeply committed to providing you with the latest information on treatments for Ehlers-Danlos Syndrome (EDS), focusing on regenerative therapies like prolotherapy, PRP, and stem cells. These innovative approaches can improve mobility and enhance your quality of life.
I also believe that targeted and EDS aware physical therapy is essential for our functioning, and not all physical therapists understand EDS, and, in fact, many patients can be injured by traditional physical therapy as they are instructed to do motions that stretch ligaments to far and may go faster than our body can work up to as the gradual approach is essential. Muscles are the secondary stabilizers of the body, and since our ligaments, the primary stabilizers, are not doing their job, strengthing the muscles, gently and gradually, is essential for regaining stability.
I believe in the power of knowledge and the importance of staying informed about the latest research. My goal is to empower you with the information needed to make confident, informed decisions about your health. I encourage you to explore these treatment options as part of your health strategy, taking each step toward a brighter, healthier future.
Transforming EDS Understanding Together
With a deep commitment to supporting those affected by Ehlers-Danlos Syndrome, I focus on making complex information easier to understand and navigate. Traditional medical paths often leave gaps, so I aim to bridge those by offering accessible resources and clarity.
By simplifying medical jargon and addressing every aspect of EDS—from advocacy to regenerative treatments—I create a comprehensive resource. My goal is to build connections and offer guidance to those seeking a better understanding of EDS and how to manage it effectively.
My Mission
My mission is to educate, empower, and advocate for individuals with EDS by providing comprehensive educational resources, sharing personal experiences, and promoting research into new and emerging treatments. I strive to facilitate access to regenerative therapies, such as prolotherapy, PRP, and stem cells to enhance mobility, quality of life, and foster a supportive community.
Tina Sias - Founder
I’m Tina Sias, founder of EDS Education and Empowerment Endeavors. My journey has fueled my dedication to supporting and empowering the EDS community through education and advocacy. I’m committed to providing resources and promoting solutions that make a real difference in people’s lives.