Meet Sage Aaron
Diagnosed with Spina Bifida before birth, Sage Aaron began life facing significant challenges. Yet through early surgery, consistent therapy, and dedicated family support, he is already showing remarkable progress. His journey is a powerful reminder that early intervention can change the trajectory of a child’s life.
Empowering Parents to Lead Change in Their Own Lives
In 2025, Mukisa Foundation championed a powerful truth: when parents are empowered to own life’s challenges and design their own solutions, entire families grow stronger. Through training, mentorship, and business grants, parent groups transformed ideas into sustainable enterprises — building resilient communities where children with disabilities can thrive.
Tracy Nabagesere: A Story of Strength and Support
At 19, Tracy Nabagesera has faced the challenges of epilepsy and intellectual disability with remarkable courage. Through consistent medical care, vocational training, and family support at Mukisa Foundation, she has grown stronger, more confident, and hopeful about her future — a true story of strength, dignity, and transformation.
Tracy Naggirinya
From early therapy sessions at age three to pursuing a law degree today, Tracy Naggirinya’s journey is a powerful story of resilience, opportunity, and transformation. Through Mukisa Foundation’s holistic, family-centred support, Tracy not only overcame developmental challenges but is now rising as a passionate advocate for the rights of persons with disabiliti
Florence Namaganda, Founding Member/Director
Mukisa is now a thriving 20-year-old—my baby, my blessing. What began as a dream when I was just 19, studying physiotherapy and encountering children with disabilities for the first time, has grown into a national organization supporting thousands of children and families with hope and dignity. From generous donors to dedicated staff, faithful co-founders, and trusting families, every person involved has helped Mukisa flourish. I pray her legacy continues to grow, reaching every child in need across Uganda and beyond
Covid Relief Program
The Covid-19 pandemic hit Uganda hard, with lockdowns and movement restrictions leaving children with disabilities cut off from essential services. Many suffered from hunger, missed medical care, and increased abuse and neglect. In response, Mukisa sought special permission from the Ministry of Health to launch an emergency rescue program—transporting children to hospitals, providing food and medicine, and supporting victims of sexual abuse through justice and care. Joined by other organizations and government bodies, the initiative reached over 9,000 children across multiple districts, offering a lifeline during one of the most challenging times in recent history
Manuella Project
The process of imagining what later became the Manuela Project started as far back as 2016, when our friends Ismael and Maite from Spain met Manuela—a girl in Moyo Babies Home showing evident signs of mental disabilities. Her story was heartbreaking: a mother who vanished, and a father unequipped to cope. What struck the visitors most was how common this situation was. Many families saw disability as a curse, a disgrace, or something shameful. That realization sparked conversations with LDG authorities and revealed a pressing need: a project to support children with special needs and their families.
Florence
At 19, Florence is rebuilding her life after teenage pregnancy and heartbreak. Through Mukisa Foundation’s tailoring course and therapy for her son, she’s found hope, purpose, and the strength to inspire other young mothers.
Zuriel
At just 3 years and 9 months, Zuriel has come a long way. Born with Down syndrome and recovering from heart surgery, she now walks, plays, and communicates with growing confidence. Her progress is a beautiful reflection of resilience and care.
Would you like a shared intro or outro for the blog section that ties all these stories together—perhaps something that highlights Mukisa Foundation’s holistic approach or celebrates the families behind each milestone?
Catherine
Catherine was born with cerebral palsy, facing major physical challenges. With therapy and her mother’s support, she learned to walk and now lives independently—playing, feeding herself, and thriving.