Communications and Information Review: NI Report for Rare Diseases

Amy Jayne McKnight, Julie McMullan, Rhoda Walker, Christine Collins

Research output: Other contribution

Abstract

Rare diseases are characterised by their relatively low prevalence individually, but cumulatively they are common, affecting one in seventeen persons at some point in their lives. It is estimated that 350 million people globally have a rare disease with approximately 110,000 people affected by a rare disease across Northern Ireland. Being diagnosed with a rare disease can lead to a significantly reduced lifespan and quality of life for patients and their families. Patients, carers, health and social care professionals consistently describe challenges accessing accurate information about individual rare diseases and accessing appropriate services. Individuals living with rare conditions often describe feeling ‘isolated’ and ‘dismissed’ so improved communication strategies are urgently required. Improved provision of information has been embedded in many national plans for rare diseases, including the Northern Ireland Rare Disease Implementation Plan.

While there are many charities with dedicated patient advocacy services, members of the rare disease community often struggle without a dedicated charity for their rare disease. Many rare disease patients (or their family or carers) need to source information and promote best care for themselves, without any training in how to do so. They frequently report healthcare professionals and service providers being unfamiliar with their rare disease or relevant rare disease resources for information and support. This report reflects feedback from people diagnosed with rare disease(s), people still searching for a diagnosis, their families, carers, and support teams.

Beyond the initial communications review envisaged in the NI Rare Disease Implementation Plan, information has been developed for healthcare professionals, patients living with rare diseases (Stronger Together; RARDTAC), and those helping to care for them. However, there is a strong and continued call for a NI Information Hub for Rare Diseases, in the form both of an online guidance tool, and of “a person at the end of a telephone”, to stabilise information provision and provide an element of sustainable coordination for this isolated and fragmented community.

This information and communication report provides evidence for ten priority recommendations and ten recommendations for further consideration.
Original languageEnglish
Media of outputCommissioned report
Publication statusAccepted - 31 Jan 2020

Bibliographical note

This was a commissioned report of which the content is confidential so the uploaded document should not be publicly available at any stage.
DOI 10.17605/OSF.IO/PUH5B

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