{"id":28912,"date":"2022-02-25T11:21:55","date_gmt":"2022-02-25T11:21:55","guid":{"rendered":"https:\/\/touchneurology.com\/?post_type=media_gallery&p=28912"},"modified":"2022-03-04T12:07:50","modified_gmt":"2022-03-04T12:07:50","slug":"megan-hunter-rare-disease-day-2022-living-with-myasthenia-gravis-a-journey-to-diagnosis","status":"publish","type":"media_gallery","link":"https:\/\/touchneurology.com\/neuromuscular-diseases\/conference-hub\/megan-hunter-rare-disease-day-2022-living-with-myasthenia-gravis-a-journey-to-diagnosis\/","title":{"rendered":"Megan Hunter, Rare Disease Day 2022: Living with myasthenia gravis – A journey to diagnosis"},"content":{"rendered":"
Megan Hunter<\/b> is living with myasthenia gravis (MG) and joins us for Rare Disease Day to discuss her initial symptoms, the journey to diagnosis and the treatment regimen that followed. She also discusses her coping strategies and the impact that treatment and living with MG has had on her life. Megan reminds us that every person\u2019s MG story is unique, which is why it is so important for every patient\u2019s story to be heard.<\/span><\/p>\n Touch Medical Media is supporting Rare Disease Day<\/a> (28 February 2022) to shine a light on healthcare inequalities for people living with rare diseases, focusing on patient quality of life and the difficulty of diagnosing patients early.<\/span><\/p>\n Questions<\/b>:<\/span><\/p>\n Disclosures<\/b>: Megan Hunter has nothing to disclose in relation to this video.<\/span><\/p>\n Support: <\/b>The production of this video was supported by Touch Medical Media.<\/span><\/p>\n Other content available in support of Rare Disease Day includes:<\/strong><\/p>\n Megan Hunter is living with myasthenia gravis (MG) and joins us for Rare Disease Day to discuss her initial symptoms, the journey to diagnosis and the treatment regimen that followed. She also discusses her coping strategies and the impact that treatment and living with MG has had on her life. Megan reminds us that every […]<\/p>\n","protected":false},"featured_media":29144,"template":"","class_list":["post-28912","media_gallery","type-media_gallery","status-publish","has-post-thumbnail","hentry","vocabulary_1-neuromuscular-diseases","vocabulary_1-rare-diseases"],"acf":[],"_links":{"self":[{"href":"https:\/\/touchneurology.com\/wp-json\/wp\/v2\/media_gallery\/28912"}],"collection":[{"href":"https:\/\/touchneurology.com\/wp-json\/wp\/v2\/media_gallery"}],"about":[{"href":"https:\/\/touchneurology.com\/wp-json\/wp\/v2\/types\/media_gallery"}],"version-history":[{"count":9,"href":"https:\/\/touchneurology.com\/wp-json\/wp\/v2\/media_gallery\/28912\/revisions"}],"predecessor-version":[{"id":29146,"href":"https:\/\/touchneurology.com\/wp-json\/wp\/v2\/media_gallery\/28912\/revisions\/29146"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/touchneurology.com\/wp-json\/wp\/v2\/media\/29144"}],"wp:attachment":[{"href":"https:\/\/touchneurology.com\/wp-json\/wp\/v2\/media?parent=28912"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}\n
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