{"id":1980,"date":"2018-06-03T16:24:02","date_gmt":"2018-06-03T21:24:02","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=1980"},"modified":"2018-06-03T16:24:02","modified_gmt":"2018-06-03T21:24:02","slug":"anne","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/de\/individuals-with-lgmd-interviews\/2018\/06\/03\/anne\/","title":{"rendered":"EINZELPERSON MIT LGMD: Anne"},"content":{"rendered":"<p><strong>LGMD \"Spotlight Interview\"<\/strong><\/p>\n<p><strong>Name<\/strong>:  Anne\u00a0 \u00a0<strong>Alter<\/strong>:  56 Jahre alt\u00a0\u00a0<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2018\/06\/LGMD2A-Anne-B.png\"><img decoding=\"async\" class=\"lazyload size-medium wp-image-1981 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\/2018\/06\/LGMD2A-Anne-B-300x169.png\" alt=\"\" width=\"300\" height=\"169\" \/><\/a><\/p>\n<p><strong>Land<\/strong>:  Vereinigte Staaten<\/p>\n<p><strong>LGMD Unter-Typ<\/strong>:  LGMD2A - auch bekannt als Calpainopathie<\/p>\n<p><strong>In welchem Alter wurde bei Ihnen die Diagnose gestellt?<\/strong>:<\/p>\n<p>Bei mir wurde Muskeldystrophie im Alter von etwa 4 Jahren diagnostiziert. Die spezifische 2A-Diagnose wurde erst durch einen DNA-Test im Alter von 46 Jahren gestellt.<\/p>\n<p><strong>Was waren Ihre ersten Symptome?<\/strong>:<\/p>\n<p>Mein erstes Symptom war, dass ich auf Zehenspitzen lief und ein Bauchgef\u00fchl, das meine Mutter hatte, dass etwas nicht stimmte.<\/p>\n<p><strong>Haben Sie andere Familienmitglieder, die LGMD haben?<\/strong><\/p>\n<p>Nein, ich bin die einzige Person in meiner Familie.<\/p>\n<p><strong>Was sind f\u00fcr Sie die gr\u00f6\u00dften Herausforderungen im Leben mit LGMD?<\/strong>:<\/p>\n<p>Ich finde es schwierig, ein Teil der Gesellschaft zu bleiben. Da ich nicht in der Lage bin, in die H\u00e4user anderer Leute zu kommen, ins Auto zu springen und zu fahren oder einfach zu anderen Orten zu fliegen, f\u00fchle ich mich ausgeschlossen. Wenn ich mich m\u00fchsam anziehen muss und dann von all den wunderbaren Dingen h\u00f6re, die meine Freunde und meine Familie tun, ist das entmutigend. Ich m\u00f6chte am Leben der Menschen teilhaben und nicht immer nur am Rande stehen.<\/p>\n<p><strong>Was ist Ihre gr\u00f6\u00dfte Errungenschaft?<\/strong>:<\/p>\n<p>Ich bin stolz darauf, dass ich mein Studium abgeschlossen und eine erfolgreiche Karriere gemacht habe. Sich in der Unternehmenswelt zurechtzufinden und sich um neue Stellen zu bewerben, war schwierig, aber ich habe es geschafft! Obwohl ich nicht mehr arbeiten kann, f\u00fchle ich mich gut, weil ich es geschafft habe, w\u00e4hrend mein K\u00f6rper sich verschlechterte.<\/p>\n<p><strong>Wie hat LGMD Sie zu der Person gemacht, die Sie heute sind?<\/strong><\/p>\n<p>Ich glaube, die LGMD hat mich gelehrt, Priorit\u00e4ten zu setzen. Nicht nur bei den Aufgaben, sondern auch bei den Dingen, die die Lebensqualit\u00e4t betreffen. Ich habe nur begrenzte Energie und habe gelernt, sie f\u00fcr Dinge zu verwenden, die f\u00fcr das gro\u00dfe Ganze sinnvoll sind. Schmutziges Geschirr in der Sp\u00fcle ist nicht so wichtig wie Zeit mit meinem Mann oder einem Freund zu verbringen.<\/p>\n<p>Ich glaube auch, dass meine eigenen Probleme mir geholfen haben, mitf\u00fchlender gegen\u00fcber anderen zu sein, die Probleme haben.<\/p>\n<p><strong>Was m\u00f6chten Sie der Welt \u00fcber LGMD mitteilen?<\/strong>:<\/p>\n<p>Ich m\u00f6chte, dass sie wissen, wie l\u00e4hmend diese Krankheit ist und dass sie geheilt werden kann!  Durch Beitr\u00e4ge zur Forschung k\u00f6nnen andere uns helfen, diese Krankheit zu heilen.<\/p>\n<p><strong>Wenn Ihre LGMD morgen \"geheilt\" werden k\u00f6nnte, was w\u00fcrden Sie als Erstes tun wollen?<\/strong>:<\/p>\n<p>Ich w\u00fcrde zu meinem Mann rennen und ihn in die Arme nehmen!<\/p>\n<p>&nbsp;<\/p>\n<p>*** Bitte LIKE, KOMMENTAR und TEILEN Sie diesen Beitrag, um das Bewusstsein f\u00fcr LGMD zu erh\u00f6hen!<\/p>\n<p>&nbsp;<\/p>\n<p>*** Um weitere \"LGMD Spotlight-Interviews\" zu lesen oder sich f\u00fcr ein kommendes Interview anzumelden, besuchen Sie bitte unsere Website unter <a href=\"https:\/\/www.lgmd-info.org\/de\/spotlight-interviews\/\">https:\/\/www.lgmd-info.org\/spotlight-interviews<\/a><\/p>","protected":false},"excerpt":{"rendered":"<p>LGMD \u201cSpotlight Interview\u201d Name:\u00a0 Anne\u00a0 \u00a0Age:\u00a0 56 yrs. old\u00a0\u00a0 Country:\u00a0 [&hellip;]<\/p>","protected":false},"author":1,"featured_media":1981,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,14],"tags":[70],"class_list":["post-1980","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2a","tag-lgmd2a-calpainopathy-united-states"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - 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