Stories of Hope

Rubi’s Journey with Lymphatic Filariasis

Rubi’s story is just one example of how self-care, education, and support can restore health and dignity to people affected by NTDs.

At 40 years old, Rubi had been living with the effects of Lymphatic Filariasis (LF) for three years. With limited access to treatment and little awareness of the disease in her community, her condition steadily worsened. Painful swelling and recurring fevers became part of her daily life—until everything changed.

About a year ago, Rubi attended a camp through our ASPIRE program, which aims to equip people affected by neglected tropical diseases (NTDs) with tools for long-term care and recovery. At the camp, she learned essential self-care techniques to manage her symptoms and received specialized footwear to help prevent further complications. Most importantly, she joined a local self-support group, where she connected with others facing similar challenges.

Just three months after the camp, Rubi saw a 30% reduction in swelling thanks to the self-care routine she developed. With the encouragement of her family, community, and ASPIRE staff, Rubi’s health continued to improve—along with her overall well-being.

But Rubi’s transformation didn’t stop there.

Today, Rubi is not only managing her condition—she’s also helping others do the same. Her personal progress has inspired greater awareness of LF in her village. She now acts as an advocate, referring others for help and encouraging them to seek care.

Rubi’s story is just one example of how self-care, education, and support can restore health and dignity to people affected by NTDs.

“With support from my community and ASPIRE, I’ve taken control of my health—and now I help others do the same.” – Rubi

Read more stories of hope in our 2024 Impact Report.

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– K Smith, Ottawa

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