Let us know what you think of this episode! We read every comment we receive.Lucy introduces the newest season of The Rare Disease Podcast 4 Medics with the help of Melissa. We give some teasers about interviews that will be coming to you this season including episodes about supportive care for newborns, mental wellbeing in sickle cell disease, misconceptions in Huntington's disease and a pair of siblings talking about Addison's disease.Thank you to our 2022 Partners: Alexion, Amicus Therapeutics, Biomarin, Bionical Emas, Healx, Kyowa Kirin, Orchard Therapeutics, PTC Therapeutics and Sobi.Medics4RareDiseases is a charity registered in England and Wales (1183996). The charity is financially supported by commercial partners. Some of these companies are pharmaceutical companies. The charity works independently from these companies who have no editorial control over this content or any of the charity's activities. Learn more.The Student Voice Prize is open for submissions! Until 16th November. Check out the three questions now and if you need a patient advocate to speak to make sure you apply to patient group pairing scheme.LinksThe Association of the British Pharmaceutical IndustryThe ABPI Code of PracticeRAREFest 2022 come watch the Rare MonologuesGrace's blog about rare disease and the emergency department Give Blood, Spread Love, EnglandHuntington's in MindViews, 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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