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?!💯
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?!💯
The response from Boston Children's Hospital Trust to see if we can create a direct giving page that is SOLELY for KingNazir Gates to have a research fund for a cure of SPTLC2 Amyotrophic Lateral Sclerosis (ALS)... WAS DENIED!!! All donations to the below links will go directly to improving conditions for King'Nazir.
Your support and contributions will enable me to meet my goals and improve conditions for my son, King'Nazir Gates who is 6 years old and has ALS with the SPTCL2 mutation. He needs our help with funding for doctors appointments, things like travel to appointments, and more. I need a handicap accessible house in a warm climate near the one of the best hospitals in the USA. I need a handicap-accessible van with a wheelchair ramp to make our lives easier. I have just found out about Action TrackChairs and they make them for kids. My son would get so much joy out of the standing features and new abilities to go different places like the beach.
He also really appreciates adventures and toys to play with, he loves animals, and if you want to donate for non-medical reasons like a trip to the zoo or the aquarium, school, clothing, food, etc, we would love that so much. Please use the contact form or email me to specify if you are wanting to donate to a specific purpose for King'Nazir. ALS is called "The Beast" for a reason and my child matters.
With King'Nazir, I stand as his mom and WE FIGHT. Your generous donation will fund my mission
Your contribution will enable us to support King'Nazir Gates and his medical expenses.
We are extremely grateful for your generosity.
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