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Kaleb’s therapist recommended a gait knee immobilizer to work on his Physical Therapy exercises, and with this pandemic, things are so difficult to attain quickly or even easily.

The cost for one is around $60USD but luckily Peyton’s mum Nirala reached out to us to donate this item to KB.


When you look at my son, there are no physical signs of a lifelong challenge that requires intensive adaptive capabilities. He is articulate, highly intelligent and can be described as funny, interesting, confident, sweet and polite.
Ethan is 12 years old and has a diagnosis of Sensory Processing Disorder (SPD), Attention Deficit Hyperactive Disorder (ADHD) and Dyspraxia. Ethan can better function and thrive despite his challenges with intervention but these are all costly.


In May 2019 I was blessed with the most amazing daughter anyone could want and I was filled with joy but after finding out that she was diagnosed with a rare, gene-linked brain malformation called Lissencephaly my heart sank.
Being a single parent of two kids is a lot of work normally but now there are challenges I face daily that I never expected.


It is with a lot of emotion, mainly gratitude, that I feel compelled to write this post. Once again Peyton’s Light Foundation and NiralaLackhan have shown tremendous generosity and compassion towards my son Lucian.
In April of this year, Peyton’s Light Foundation donated the necessary funds for his much-needed blood tests. Based on the results of the said tests Lucian required a few supplements which are quite costly.

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For more info contact:
Nirala Lackhan-Alfonso: 868-775-0531
Lisa Mac Lean: 868-299-9725
Shivani Maynard: 868-731-4645