Nicola Miller

Co Founder at Teddington Trust (SCIO) and Rare Revolution Magazine

Nicola Miller is the parent of a rare child and co-founder of the rare disease charity Teddington Trust. A passionate Rare advocate Nicola has taken accessible education to new heights with the creation of Little Ted a loveable educator spreading awareness for Xeroderma Pigmentosum. Nicola is also the co-founder and Editor of rare disease publication and rare movement Rare Revolution Magazine.