Sally is a semi-retired university lecturer living in South Wales. Since being diagnosed with a neuroendocrine tumour in 2009, Sally has experienced many consultations with different clinicians over the years. Sally believes it is an absolute necessity for all NET patients to have access to a specialist NET service. She also feels patient support is crucial for patients living with NETs and has been involved in patient groups and advocacy for many years. 

Sally Jenkins has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies: