Vicki and her husband moved to the UK with their children from South Africa over 20 years ago.
Muscular Dystrophy has been part of her life since her son was diagnosed with Duchenne Muscular Dystrophy at 7 years old. Vicki has dedicated her time to become a full-time carer for her son, and the MD Support Centre became a part of her sons regular routine.
Her daughter suggested that she start volunteering at the centre also - something which Vicki has really grown into this role.
Vicki has a background in office environments for over 25 years, and naturally has a huge wealth of experience with MD.