Help that arrives!
Rare diseases caused by genetic mutations in NALCN cause severe neurodevelopmental delays and, in the worst cases, are life-threatening. Many children and young adults with NALCN-related conditions are unable to walk or talk and suffer severe apnea or seizures. But this doesn’t have to be your story.
Genetic research is changing the landscape of rare diseases by providing critical insights into their underlying causes and offering new opportunities for diagnosis, treatment, and ultimately improving the quality of life of those affected. It is important to support and fund genetic research to fully realize the potential of these advances and provide hope to those living with NALCN-related conditions.
All donations are tax deductible and go directly to science & research, as well as education and support for patients and families.