Spinal Muscular Atrophy UK (SMA) is a national charity, founded in 1985, providing support via our Support Service team, and information about SMA to all those living with the condition and their families. We also advocate on improving access treatment and issues surround the complexities that living with a rare condition brings. All our health information is accredited by the Patient Information Forum (PIF) and is available via our website in the form of webinars, podcasts and information sheets. We host virtual and in person events that connect the SMA Community together offering a space to share information and offer peer support. Where we can make a difference, we will.