We are a nonprofit because children shouldn't have to die of ALS and rare diseases!!! Advocacy for rare childhood diseases to be cured should be top priority!!! What if it was YOUR child?!💯
Hello
Welcome
There's much to see here. So, take your time, look around, and learn all there is to know about Juvenile ALS, King'Nazir Disease, and about us at Melanin Children Matter, Inc.
We hope you enjoy our site and take a moment to drop us a line!
About Us
Lakeia Nard, CEO & Founder
I'm Lakeia Nard. I live in Kentucky, United States of America, & I started Melanin Children Matter LLC with the spirit of helping my son, King'Nazir Gates, who is 5 years old with autism and a rare form of SPTLC2 Juvenile ALS. I firmly believe that we should be helping children and families with autism, and I firmly believe that we CAN CU
I'm Lakeia Nard. I live in Kentucky, United States of America, & I started Melanin Children Matter LLC with the spirit of helping my son, King'Nazir Gates, who is 5 years old with autism and a rare form of SPTLC2 Juvenile ALS. I firmly believe that we should be helping children and families with autism, and I firmly believe that we CAN CURE kids with ALS, and WE SHOULD! It is our duty from God and to the universe.
I study holistic medicine and love learning. I am an expert at medicinal plants. I go above and beyond every day for my son, and hospitals do not seem to want make our lives any easier. I do not want this to happen to you. Being alone as a parent in a hospital, you can be forced into situations that are scary and you need to be informed. I never want you to feel that pain. I never want you to be alone in that situation. My kids are my world, and so are yours. ♥
