About Us
We are Sarah and Daphne, two dedicated moms on a mission to make a difference in the lives of individuals affected by TUBB4A mutations. Our journey began with our own daughters, who share this genetic condition, driving us to take action and create a foundation committed to finding a cure. As mothers, there is nothing we won't do to ensure a brighter future not only for our children but for every individual facing the challenges of a TUBB4A mutation. With unwavering determination and a shared passion for making a meaningful impact, we are here to advocate, raise awareness, and drive research efforts forward, because every person affected by TUBB4A deserves hope, support, and the promise of a better tomorrow. Join us as we embark on this journey together, united in our pursuit of a cure.
Our mission is to relentlessly pursue research, collaboration, and advocacy to ensure that no child's journey is defined by limitations, but rather by possibilities for a healthier and brighter future!
Board of Directors
Sarah Marta: Co-Founder & President
Daphne Graskewicz Prado: Co-Founder & Vice President
Ashley Jarrin: Secretary
Kristen Ringler: Director of Finance
Michelle Olson: Director of Patient Engagement
Picture from left to right: Ashley, Daphne, Sarah, Kristen & Michelle
Our mission is to relentlessly pursue research, collaboration, and advocacy to ensure that no child's journey is defined by limitations, but rather by possibilities for a healthier and brighter future!
Board of Directors
Sarah Marta: Co-Founder & President
Daphne Graskewicz Prado: Co-Founder & Vice President
Ashley Jarrin: Secretary
Kristen Ringler: Director of Finance
Michelle Olson: Director of Patient Engagement
Picture from left to right: Ashley, Daphne, Sarah, Kristen, Michelle
Your donation is a vital contribution towards our mission to find a cure for TUBB4A-related disorders. With your support, we can fund groundbreaking research initiatives, advance scientific understanding, and accelerate the development of effective treatments. Every dollar brings us closer to unlocking the mysteries of this rare genetic condition and offering hope to individuals and families affected by TUBB4A mutations. Together, we can make a meaningful difference in the lives of those who need it most. Thank you for joining us in this important journey towards a brighter future