The Grant Pienaar Foundation was established in 2022 to assist and help others with Motor Neurone Disease & people with mobility challenges. This foundation was started by Grant Pienaar shortly after he was diagnosed with Motor Neurone Disease on the 23 Septermber 2021. The disease itself is a neurodegenerative disease and unfortunately has no current cure. Someone is diagnosed every 90 minutes. Grant will be uploading blogs about his own personal experience and doing everything he can to help educate others facing this terrible journey.

Grant’s Vision is to create a platform that will ultimately create awareness & the need to assist South Africans facing these challenges through all social media channels. Grant’s foundation relies on the generousity of others so please join him in making a difference.