Melanin Children Matter

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MELANIN CHILDREN MATTER

We are servicing children, healing families and educating society, while enhancing awareness surrounding childhood rare diseases like SPTLC2 (pediatric ALS) and autism. Advocating for the lives of our children, caregivers and providers, while providing resources and outlets to bring together all melanin children and families. You are not alone! Our melanin women and children die in hospitals, like our melanin men die by police, hence why advocating is so important. If I can not save my son, I am praying I save someone else’s child. All funds will be put into bringing awareness and researching rare diseases such as, SPTLC2 gene mutation (under the pediatric als) as we work effortlessly with a promising biotech company to create a treatment and/or cure. All other funds will be put towards small grants for families to gain access to communication devices and whole genome sequence testing to minimize misdiagnosis. Thank you for your time and patience.