{"id":1112,"date":"2016-01-18T11:30:03","date_gmt":"2016-01-18T17:30:03","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=1112"},"modified":"2016-01-18T11:30:03","modified_gmt":"2016-01-18T17:30:03","slug":"laurence","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2016\/01\/18\/laurence\/","title":{"rendered":"INDIVIDUELLE AVEC LGMD : Laurence"},"content":{"rendered":"<p><strong>\"ENTRETIEN AVEC LE LGMD\" <\/strong>&#8211; <em>01\/18\/2016<\/em><\/p>\n<p><strong>Nom<\/strong>:  Laurence \u00a0\u00a0\u00a0<strong>L'\u00e2ge<\/strong>: 49<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2016\/01\/LGMD2A-Laurence.png\" rel=\"attachment wp-att-1114\"><img decoding=\"async\" class=\"lazyload size-medium wp-image-1114 alignright\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27169%27%20viewBox%3D%270%200%20300%20169%27%3E%3Crect%20width%3D%27300%27%20height%3D%27169%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2016\/01\/LGMD2A-Laurence-300x169.png\" alt=\"LGMD2A - Laurence\" width=\"300\" height=\"169\" \/><\/a><\/p>\n<p><strong>Pays<\/strong>: France<\/p>\n<p><strong>LGMD Sous-type<\/strong>: LGMD2A \/ Calpa\u00efnopathie<\/p>\n<p>&nbsp;<\/p>\n<p><strong>\u00c0 quel \u00e2ge avez-vous \u00e9t\u00e9 diagnostiqu\u00e9 ?<\/strong>:<\/p>\n<p>J'ai \u00e9t\u00e9 diagnostiqu\u00e9e \u00e0 l'\u00e2ge de 42 ans.<\/p>\n<p><strong>Quels ont \u00e9t\u00e9 vos premiers sympt\u00f4mes ?<\/strong>:<\/p>\n<p>Les sympt\u00f4mes que j'ai ressentis sont les suivants : grande fatigue, difficult\u00e9s \u00e0 monter les escaliers, chutes en marchant sur un sol irr\u00e9gulier et difficult\u00e9s \u00e0 se lever d'une position assise.<\/p>\n<p><strong>Avez-vous d'autres membres de votre famille atteints de LGMD ? <\/strong><\/p>\n<p>Non, je suis le seul membre de ma famille \u00e0 \u00eatre atteint de LGMD2A.<strong>.<\/strong><\/p>\n<p><strong>Quels sont, selon vous, les plus grands d\u00e9fis \u00e0 relever pour vivre avec le LGMD ?<\/strong>:<\/p>\n<p>L'\u00e9volution est assez lente mais je dois faire attention \u00e0 avoir une vie r\u00e9guli\u00e8re sinon c'est pire et l'\u00e9volution est alors plus rapide quand je suis fatigu\u00e9e et que l'atrophie est plus forte.  Il est difficile de la concilier avec des activit\u00e9s priv\u00e9es ou professionnelles.<\/p>\n<p><strong>Quelle est votre plus grande r\u00e9ussite ?<\/strong>:<\/p>\n<p>J'essaie de continuer \u00e0 travailler, ce qui est important, de ne pas trop penser \u00e0 la maladie et de continuer \u00e0 avancer.<\/p>\n<p><strong>Comment le LGMD vous a-t-il influenc\u00e9 pour que vous deveniez la personne que vous \u00eates aujourd'hui ? <\/strong><\/p>\n<p>En luttant contre les douleurs et les difficult\u00e9s physiques, la maladie m'apprend \u00e0 \u00e9tablir des priorit\u00e9s, mais aussi \u00e0 \u00eatre consciente qu'il y a toujours des choses \u00e0 faire.<strong>\u00a0 <\/strong>des personnes qui sont plus malades que vous, de sorte que vous devez \u00eatre optimiste.<\/p>\n<p><strong>Que voulez-vous que le monde sache sur le LGMD ?<\/strong>:<\/p>\n<p>Je veux que le monde sache que la LGMD fait partie des maladies orphelines et qu'il est donc difficile de collecter les fonds n\u00e9cessaires pour trouver un traitement efficace.  Il est important de parler de la LGMD autour de nous, mais surtout \u00e0 la communaut\u00e9 m\u00e9dicale et aux m\u00e9decins g\u00e9n\u00e9ralistes qui peuvent aider leurs patients \u00e0 se rendre dans les centres m\u00e9dicaux appropri\u00e9s. J'ai un exemple tr\u00e8s personnel pour illustrer ce point - avant d'\u00eatre diagnostiqu\u00e9, mon m\u00e9decin g\u00e9n\u00e9raliste m'a dit que mes sympt\u00f4mes \u00e9taient dus \u00e0 une d\u00e9pression nerveuse !<\/p>\n<p><strong>Si votre LGMD pouvait \u00eatre \"gu\u00e9rie\" demain, quelle serait la premi\u00e8re chose que vous souhaiteriez faire ?<\/strong>:<\/p>\n<p>J'aimerais marcher naturellement sans b\u00e2ton et visiter le monde entier, pouvoir aller \u00e0 l'\u00e9tranger avec ma famille, me sentir libre !<\/p>\n<p>Pour lire d'autres \"LGMD Spotlight Interviews\" ou pour vous porter volontaire pour une prochaine interview, veuillez consulter notre site web \u00e0 l'adresse suivante : https:\/\/www.lgmd-info.org\/spotlight-interviews.<\/p>","protected":false},"excerpt":{"rendered":"<p>\u201cLGMD SPOTLIGHT INTERVIEW\u201d &#8211; 01\/18\/2016 Name:\u00a0 Laurence \u00a0\u00a0\u00a0Age: 49 Country: [&hellip;]<\/p>","protected":false},"author":1,"featured_media":1114,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,14],"tags":[12,18,15],"class_list":["post-1112","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2a","tag-calpainopathy","tag-france","tag-lgmd2a"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - 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