Necrotising Fasciitis Awareness For Nick

In June of 2022, I lost my dad to a rare disease called necrotising fasciitis. I had never heard of the disease until after it was too late and he passed from it. After years of research and creating an understanding of the disease I have decided I want to spread awareness and honour my dad by creating a fundraiser to raise money for: THE LEE SPARK NF FOUNDATION SEVERE STREPTOCOCCAL INFECTIONS AND NECROTISING FASCIITIS SUPPORT. This foundation has supported me throughout my grief and provided me with unforgettable support so I want to not only honour my dad but the amazing foundation. In order to do this I will be running another 10k on december 24th 2025. Any donations will go straight to the foundation and are greatly appreciated!! This disease had changed my life and it means a lot to me to be able to support it. This disease is very rare and is diagnosed to between 700-1,200 people a year- this is another reason I wish to spread awareness. This disease can happen to anyone despite age or health.