A life-saving treatment is already real. It’s not a distant dream. It exists - just not yet for Pyruvate Carboxylase Deficiency. The science is there. The breakthrough has happened. Now, we need the funding to bring it to Kiana and children like her.
This isn’t about waiting for a cure to be discovered - it’s about taking action to make it available. Every dollar brings us closer to the moment this treatment can save lives.
We can see it. We can reach it. But we can’t do it without you.
Donate today - Help Save Kiana
The Kiana Research Foundation supports research toward an effective treatment and a cure for Pyruvate Carboxylase Deficiency. Pyruvate carboxylase deficiency is a rare condition, with an estimated incidence of 1 in 250,000 births worldwide. Pyruvate carboxylase deficiency is… Read More
Learn MoreWe are honored to announce our partnership with Dr. Miguel Sena-Esteves for the research and investigation of AAV gene-therapy for Pyruvate Carboxylase Deficiency. In the initial pre-clinical phase of our project, we will commence by synthesizing AAV vectors… Read More
Learn MoreOur children are not just rare disease patients. We are loving families. We have hopes and dreams like everyone else Every 30 minutes, a child is born who will develop a mitochondrial disorder by age 10. Due to… Read More
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