On Rare Disease Day (28th February), AMEND launched its new suite of resources for young people affected by the neuroendocrine tumour syndromes, multiple endocrine neoplasia.  The resources include helpful advice for young people aged 14-25 on a range of aspects that can be a challenge for adolescents living with these rare diseases, such as starting university or work, dealing with diagnosis or surgery, and relationships.  In addition, the resource includes several short films starring some of AMEND’s younger members that complement this free web resource.

Find the new web resources here.