Brianna’s Story

By 7017444915 February 24, 2026
Home looks different for everyone. For Jon, home is now the place he shares with his sister, Shelly. Jon was already living in Shelly’s home when she became one of Hope Haven’s first Host Home providers. What started as a practical next step quickly grew into something far more meaningfu l. As Shelly shared, “Opening our home to Jon was a blessing we didn’t know we needed.” Through Hope Haven’s Host Home program, individuals with disabilities live in the homes of carefully selected providers who offer guidance, companionship, and everyday support. Host Homes are just one of several residential options at Hope Haven, alongside staffed community living homes, because no two individuals require the same level or style of care. What matters most is creating a place where people can live safely, grow their independence, and feel truly included. For Jon, that environment means being part of everyday family life, whether that’s grocery shopping and shared meals or being able to help with Shelly’s in-home daycare. “Living here makes me feel happy,” Jon says. For Shelly’s family, the experience has been transformative. “We’ve all become more patient and understanding,” she shares. “My boys have learned gratitude, acceptance, and what it means to truly welcome someone into your life.” That mutual impact is what makes Host Homes unique. “It doesn’t feel like a job,” Shelly explains. “It’s more of a relationship. You get to help someone feel independent, yet safe.” She was quick to add that the impact goes both ways. As she puts it, “You just might meet your best friend.” Because of supporters like you, individuals like Jon have the opportunity to live in a home where they are supported and valued — not just as clients, but as people. Your generosity makes it possible for Hope Haven to offer a range of residential supports, creating safe, stable, relationship-centered living options for individuals with disabilities right here in our communities. “Be devoted to one another in love. Honor one another above yourselves.” — Romans 12:10 If you wish to contribute, please 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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