Let us know what you think of this episode! We read every comment we receive.Lucy takes you through her top 11 tips for suspecting and managing rare disease in a primary care setting. If you're a GP this episode is for you and after listening you can find all the helpful links and more information in Rare Disease 101.Thank you to Dr Will Evans and Dr Gareth Baynam and the whole rare disease community who have contributed to or inspired this list over the years.Perhaps one day we can get some NICE guidelines or RCGP guidelines for rare disease in general...ReferencesWhelan AJ, Ball S, Best L, Best RG, Echiverri SC, Ganschow P, Hopkin RJ, Mayefsky J, Stallworth J. Genetic red flags: clues to thinking genetically in primary care practice. Prim Care. 2004 Sep;31(3):497-508, viii. doi: 10.1016/j.pop.2004.04.010. PMID: 15331244. Do You hear Me - by Nicola MillerFind Zebra - search engine for rare disease diagnoses Orphanet - high-quality information on rare diseasesRare Disease UKGene PeopleUniqueSWAN UK - support for this with undiagnosed conditionsEuropean Reference Networks for rare disease (ERNs)Views, ideas and opinions expressed in this podcast are personal to the individual and Medics4RareDiseases does not accept responsibility for those expressed by guests.M4RD receives funding from commercial companies which it works independently from. M4RD's Partners and Funders do not accept responsibility for any views expressed in this podcast. M4RD does not endorse any companies or products that it receives sponsorship from. For more information please see the show notes and www.m4rd.org/sponsors #DareToThinkRare

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“What did the council decide on item 42?” — answered with the speaker and the moment.

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