{"id":5708,"date":"2022-04-05T15:44:07","date_gmt":"2022-04-05T15:44:07","guid":{"rendered":"https:\/\/www.lgmd-info.org\/?p=5708"},"modified":"2024-02-09T14:23:55","modified_gmt":"2024-02-09T14:23:55","slug":"individual-with-lgmd-yasemin","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/de\/individuals-with-lgmd-interviews\/2022\/04\/05\/individual-with-lgmd-yasemin\/","title":{"rendered":"EINZELPERSON MIT LGMD: Yasemin"},"content":{"rendered":"

\n

\"\"<\/p>\n

LGMD: \"Spotlight-Interview\"<\/strong><\/p>\n

Name<\/strong>: Yasemin
<\/strong><\/p>\n

Alter<\/strong>: 4 Jahre alt<\/p>\n

Land<\/strong>: Die Niederlande<\/p>\n

LGMD Unter-Typ<\/strong>: LGMD 2A\/R1 Calpain 3-verwandt<\/p>\n<\/p>\n

In welchem Alter wurde bei Ihnen die Diagnose gestellt?<\/strong>?<\/p>\n

Bei unserer Tochter wurde die Diagnose im Alter von 2 Jahren gestellt.<\/p>\n

Was waren Ihre ersten SYMPTOME?<\/strong><\/p>\n

Sie hat noch keine Symptome. Da sie sehr langsam w\u00e4chst, hat man im Krankenhaus einige Tests durchgef\u00fchrt und festgestellt, dass sie sehr hohe CK-Werte hat. Nach weiteren Tests fand man heraus, dass sie LGMD 2A\/R1 hat.<\/p>\n

Haben Sie andere Familienmitglieder, die an LGMD leiden?<\/strong><\/p>\n

Niemand sonst in unserer Familie hat LGMD.<\/p>\n

Was sind f\u00fcr Sie die gr\u00f6\u00dften Herausforderungen im Leben mit LGMD?<\/strong>?<\/p>\n

Wir (Eltern) hoffen, dass unsere Tochter mit einer positiven Einstellung aufw\u00e4chst. Und dass ein Heilmittel entdeckt wird, bevor die Symptome auftreten.<\/p>\n

Was ist Ihr gr\u00f6\u00dfter ERFOLG?<\/strong><\/p>\n

Als Eltern hoffen wir, dass wir ihr das Gef\u00fchl geben k\u00f6nnen, dass sie alles sein kann. Alles, mit ein paar Einschr\u00e4nkungen.<\/p>\n

Wie hat LGMD Sie zu der Person gemacht, die Sie heute sind?<\/strong><\/p>\n

Sie ist erst 4 Jahre alt. Wir hoffen, dass sie sich zu einer charakterstarken Person entwickelt. Wir hoffen, dass wir alles in unserer Macht Stehende tun k\u00f6nnen, um ihr das praktische Leben zu erleichtern.<\/p>\n

Was m\u00f6chten Sie der Welt \u00fcber LGMD mitteilen?<\/strong>?<\/p>\n

Wir wollen, dass die Welt wei\u00df, dass es diese Krankheit gibt. Und dass ein Mensch mit dieser Diagnose Bed\u00fcrfnisse hat und problemlos an der Gesellschaft teilhaben kann.<\/p>\n

Wenn Ihre LGMD morgen \"geheilt\" werden k\u00f6nnte, was w\u00fcrden Sie als Erstes tun wollen?<\/strong>?<\/p>\n

Als Eltern w\u00fcrden wir feiern und zusehen, wie Yasemin in dem Wissen aufw\u00e4chst, dass sie mit allem fertig werden kann - selbst wenn Mama und Papa eines Tages nicht mehr da sind.<\/p>\n<\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"","protected":false},"author":3,"featured_media":5709,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"image","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,14],"tags":[],"class_list":["post-5708","post","type-post","status-publish","format-image","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2a","post_format-post-format-image"],"acf":[],"yoast_head":"\nINDIVIDUAL WITH LGMD: Yasemin - LGMD Awareness Foundation<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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