Brianna’s Story

Hope Haven Ambassadors: Changing the Narrative

By 7017444915 • June 26, 2026
“Each of you should use whatever gift you have received to serve others…” 1 Peter 4:10 At Hope Haven, we believe every person has God-given gifts to share. That belief is at the heart of the Hope Haven Ambassadors, a group of individuals served through Hope Haven’s My Day program who are learning to use their voices, share their stories, and advocate for themselves and others. The Ambassadors were formed in January 2025 after a community experience sparked a bigger conversation about inclusion, dignity, and the way individuals with disabilities are perceived. Since then, the group has been working to help change that narrative. The Ambassadors have presented to community groups, attended advocacy trainings, traveled to the Capitol, and spoken about issues that matter. Along the way, they are building confidence, developing leadership skills, and helping others understand that every person deserves to be included and respected. For Maggie, being an Ambassador is about helping her community see people with disabilities as equals. “I want individuals with disabilities to be treated as equal to everybody else,” she shared. “I want my community to know it’s okay to be different.” For Lori, the message is simple but powerful. “We are regular people who have different challenges,” she said. “I want to help my community understand that people with disabilities are not less of a person because of their disabilities.” For Octavio, advocacy means using his voice not only for himself, but also for others who may struggle to speak up for what they need. Through his experience with the Ambassadors, he has learned something important: “Our voice matters.” Programs like My Day are about so much more than daily activities. They are about friendship, confidence, purpose, community, and belonging. They create opportunities for people to discover their strengths, build relationships, serve others, and take part in the world around them. Your support helps us continue creating opportunities like the Hope Haven Ambassadors, where individuals can build confidence, share their stories, and discover the power of their voice. Your gift allows us to keep growing alongside those we serve, making an impact that lasts. If you wish to contribute, plea se CLICK HERE to donate today. Thank you for your continued support, prayers, and partnership in Hope Haven’s mission .
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12-year-old Brianna loves coloring painting and music. In the summertime her favorite activity is – without question – playing in the water. She’s even been dubbed ‘the little mermaid’ because of her beloved pastime. Another part of Brianna’s life is her Angelman Syndrome diagnosis. Angelman Syndrome is a rare genetic disorder that affects the nervous system.

 

Brianna was diagnosed at the age of one and was raised at home by her mother Kandice. Around Brianna’s 7 th  Birthday Kandice met with Faith Hope & Charity (FHC – A division of Hope Haven Inc.) in Storm Lake IA to learn more about respite services for Brianna. However when staff heard of the comprehensive care and close watch that Brianna required at home they also provided Kandice with information about residential services available in an intermediate care facility for the intellectually disabled (ICF/ID).  

 

At the time Kandice was a single mom raising three young girls all on her own. When she learned that the ICF/ID at FHC was equipped to provide 24 hour medical services physical and occupational therapy speech and language therapy  among many other services  Kandice evaluated this new option with more thought. Additionally she took into consideration the “home away from home feel” of FHC and the growing level of care and attention her other two young daughters also required. 

 

Still Kandice grappled with the choice. “It was an extremely hard decision the hardest I’ve ever made ” she remarks. After careful deliberation she decided to move forward with the ICF/ID option for Brianna “I know my child  who needs an extreme amount of care – more than just one person can provide – is getting the constant care and monitoring she needs to thrive.”  

 

Brianna made the move to FHC in 2014 and has experienced significant growth over the past five years. With help from staff  she has identified methods and activities that are therapeutic and beneficial for her like sensory engagement. Brianna is non-verbal so she has also learned to use a communication board to share her thoughts. She’s continually working towards increased independence and more social activity.   

 

When she’s not at FHC she delights in time spent with mom dad two sisters and a brother. Her family comments on her playful spirit sense of humor and sweet demeanor. It’s also noted that when she’s away for long periods of time Brianna is eager to return to FHC. “She has made huge progress and now considers FHC her home ” affirms Kandice. 

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