Help Emiliano Fight for His Life

Dear friends, family, and kind strangers, we are Lyzanni and Emil Flores - parents to Emiliano.

We’re reaching out with hopeful hearts to ask for your support for our beautiful son, Emiliano. At just 6 months old, Emiliano has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1—a rare and life-threatening genetic condition that affects the ability to move, swallow, and breathe.

Though the diagnosis shook our world, we are determined to fight for Emiliano’s future. There is a once in a lifetime treatment—Zolgensma—that offers hope, but the cost is staggering at 2 million dollars. We are doing everything in our power to secure access to this therapy and the specialized care Emiliano needs. That’s why we’re asking for your help. Time is against us as every day that passes, his muscles get weaker.

Every contribution, no matter the size, brings us one step closer to giving Emiliano a chance at a brighter, healthier life. The funds will be used to secure this once in a lifetime treatment. Your generosity means the world to us. Please share our campaign with your family, friends and social networks. Please helps us give our son a chance to live a long, healthy life with us. Thank you for being a part of our journey and this miracle.

We will be forever grateful and we know that God will bless your act of kindness.

https://youtu.be/Po8oO3ndslA?si=UF2p7fjZdoYtn1Zh