In this episode, Cecy discusses and gives insight into what living with a disability looks like for a teenager with dystonia. She explains her diagnosis, how her therapies have helped her, and how she stays positive and wants to impact everyone she meets. She offers tips on how to be an advocate and how to treat others with disabilities.

In this episode, Laura interviews Ally, the grandmother of CRIT patient, Krestalenn, to discuss the car accident that led her granddaughter to CRIT. She explains how Krestalenn pushes herself through therapies and achieves success with her charismatic personality. Ally brings awareness to the effects of drunk driving and how to persevere despite adversity.

In April, we celebrated Counseling Awareness month by interviewing our licensed professional counselor, Leticia Cavazos. She tells us about her journey to becoming a counselor, how she navigates the most recent COVID-19 pandemic, and how to prioritize your mental health.

In this episode, we discuss the TeletonUSA Event and how it supports CRIT's mission, values, and day-to-day operation. Laura and Natalie interviewed Cristina Prieto, TeletonUSA Foundation's Corporate Sponsorship Officer, to learn about all of the preparation, hard work, and magic that goes into putting on this nationally broadcast telethon event. She discusses how the passion of everyone involved makes TeletonUSA a success year after year, and what this year's event will look like on December 11. 

So many organizations rely on volunteers. In this episode, we discuss why our volunteers help make CRIT so special. We interview Alma González, Heroes for CRIT Ambassador, and we discuss how her contributions spread awareness for our patients and families. Alma then explains the importance of giving back to the community without expecting anything in return.

In this episode, Brooke Matula, Director of Recreational Therapy at Morgan's Wonderland, joins us. She dives into the mission of one of the most inclusive theme parks, Morgan's Wonderland. She also discusses what Universal Design is and how we can inspire the San Antonio community to be inclusive.

In September, we celebrated Spinal Cord Injury Awareness Month. Natalie and Laura interviewed Zivanna and Moises, patients from CRIT, who shared their journey with this condition. They talked about their future goals, and how they want to change how people on a wheelchair are viewed.

As we continue to bring awareness to SMA and celebrate Spinal Muscular Atrophy Awareness Month, we interview Rebecca, one of our genetic counselors. Rebecca explains how genetic counselors help people and their families know how genes in family members carry diagnoses. She also describes how she helps families make the most informed decisions when navigating through their diagnoses. She also advocates how working ahead and knowing your gene history can help you and your family in the future.

In August, we celebrate Spinal Muscular Atrophy Awareness Month. We interview the mother of Gabriel, Jenna, who shares their journey through Gabriel’s diagnosis of SMA. She takes us through finding a specialist to diagnose her son, clinical trials, and finding the treatment options for Gabriel and their family. She also mentions how education and advocating through community groups and other families with children with SMA help spread awareness.

In June, we celebrated Father’s day by interviewing super dad Rufus. He will guide us through what he and his wife went through when adopting Adira, making communication and openness a key component in their family relationship. He gives us insight on navigating life with a new daughter who also happens to have a disability. Lastly, he introduces us to his project, a podcast titled “The Imperfect Gift,” where he highlights the ups and downs of parenthood.