“Any questions?” – INTENS researchers reply to patients’ questions
INTENS has been working with The Short Gut Families Support Group to hear and answer their questions about our research. The support group, which is a global network of support for anyone ‘who knows and loves a child with short gut syndrome or a similar diagnosis’ is run through Facebook and has over 3000 members. Being in dialogue with those affected by short gut syndrome is of the upmost importance to INTENS, in sharing insight and shaping future priorities for…