Our Story
Ellavation was created after the birth of our founder and president’s daughter Ella.
In 2018, The Fajardo Family learned the value of support when Ashley’s husband, Joel, became a victim of a violent crime and was shot on his way home from work. That bullet led to multiple surgeries and near-fatal complications, but with the help of their friends and family, the family weathered the storm.
In 2019, the family was excited to find out that they were pregnant with their third child, Ella.
During a routine ultrasound, they learned she had a severe form of Spina Bifida. Her diagnosis brought a new set of challenges, including an in-utero surgery and a premature birth at just 25 weeks. Ella spent her first six months in the hospital.
Though the journey was filled with uncertainty, the family witnessed time and again how God surrounded them with exactly what they needed—through prayer, encouragement, provision, and a strong community. That love was a constant reminder that they were not alone.
After spending nearly $20,000 in out-of-pocket expenses in Ella’s first six months alone, they quickly realized the financial toll of raising a child with complex medical needs. Over the years, the expenses piled up and everyday joys became harder to afford. Through joining support groups, they met other families facing similar struggles—many without the same kind of support. That’s when Ashley felt a deep calling: to be the same kind of community to others that had been for them a lifeline.
Ashley writes, “Having a child with extra medical needs is stressful enough. All families should be able to enjoy basic quality of life things. However, when a family is faced with thousands of dollars in medical bills, equipment needs, and expensive childcare costs, there is rarely anything extra.”
Ellavation was created to help fill that gap. What began in a garage during the peak of the COVID-19 pandemic is now a growing nonprofit with a mission to bless families navigating life with Spina Bifida.
The Fajardos have seen God’s hand at work in their lives, and now, through Ellavation, they hope to be a reflection of that light. Ashley’s prayer is that every individual interaction with an applicant becomes a chance to show the love of Jesus—not only through the gifts given, but through the care extended.
Ellavation has increased its board members and looks forward to growing and helping families in need!
Ellavation gives us all a chance to step in and support families and individuals affected by Spina Bifida. Any donation or act of support can help restore joy and hope to families in need.
To hear more of Ella’s story, follow her on Facebook by searching “Ella’s Life”