{"id":496,"date":"2015-03-31T08:45:20","date_gmt":"2015-03-31T13:45:20","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=496"},"modified":"2015-03-31T08:45:20","modified_gmt":"2015-03-31T13:45:20","slug":"496","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/tr\/individuals-with-lgmd-interviews\/2015\/03\/31\/496\/","title":{"rendered":"INDIVIDUAL WITH LGMD:  Eva"},"content":{"rendered":"<p>03\/31\/2015<\/p>\n<p>Name:\u00a0 Eva\u00a0\u00a0 \u00a0Age: 33 Yrs. Old<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/03\/Unknown-Eva.png\"><img decoding=\"async\" class=\"lazyload  size-medium wp-image-497 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\/2015\/03\/Unknown-Eva-300x169.png\" alt=\"Unknown - Eva\" width=\"300\" height=\"169\" \/><\/a><\/p>\n<p>Country:\u00a0 Kenya<\/p>\n<p>LGMD Sub-Type :\u00a0 Unknown<\/p>\n<p><strong>KA\u00c7 YA\u015eINDA TE\u015eHIS KONULDU?\u00a0<\/strong><\/p>\n<p>Bana 14 ya\u015f\u0131mda te\u015fhis konuldu.<\/p>\n<p><strong>\u0130LK BELIRTILERINIZ NEYDI?<\/strong>:<\/p>\n<p>I had difficulty running fast and raising my hand up with ease. I was never able also to bend and sweep the floor properly when it came to doing house chores.<\/p>\n<p><strong>LGMD HASTASI OLAN BA\u015eKA AI\u0307LE \u00dcYELERI\u0307NI\u0307Z VAR MI?<\/strong>:<\/p>\n<p>No. I am the only one with muscular dystrophy in our family.<\/p>\n<p><strong>LGMD I\u0307LE YA\u015eARKEN KAR\u015eILA\u015eTI\u011eINIZ EN B\u00dcY\u00dcK ZORLUKLARIN NELER OLDU\u011eUNU D\u00dc\u015e\u00dcN\u00dcYORSUNUZ?<\/strong>:<\/p>\n<p>My muscles are getting weaker by the day and that means my level of dependency is also increasing. It\u2019s hard for me to keep a personal caregiver because most of them do not have the heart, they start complaining just weeks after being employed. I am grateful for the support I get from my husband and relatives who show up to keep my house clean and assist in any way possible.<\/p>\n<p><strong>EN B\u00dcY\u00dcK BA\u015eARINIZ NEDIR<\/strong>:<\/p>\n<p>Getting married and starting a family with my husband, \u00a0Creating awareness about Muscular Dystrophy in Kenya. Many people are now aware of the condition and are glad to have started because I have met more people in the country with the same condition through Muscular Dystrophy Awareness of Kenya and hoping still to do more.<\/p>\n<p><strong>LGMD BUG\u00dcN OLDU\u011eUNUZ KI\u015eI OLMANIZDA SIZI NASIL ETKILEDI?<\/strong><\/p>\n<p>Because of\u00a0 LGMD I think I have to plan my days in advance, I cannot just wake up in the morning and say, today am going out simply because transport has to be arranged, I must have an escort e.t.c. I am also very optimistic of the future and my life is influenced much with my Christian beliefs.<\/p>\n<p><strong>D\u00dcNYANIN LGMD HAKKINDA NE BI\u0307LMESI\u0307NI\u0307 I\u0307STI\u0307YORSUNUZ?<\/strong><\/p>\n<p>A diagnosis of LGMD\u00a0 is not a death sentence, you can live your life to the fullest doing what you can at the time. LGMD weakens your muscles but it shouldn&#8217;t weaken your spirit. People living with LGMD can work and employers should not shy away from employing us. With the research work going on, plus the trials a cure for muscular dystrophy is in the horizon, I hope it gets here sooner.\u00a0<strong>\u00a0<\/strong><\/p>\n<p><strong>LGMD HASTALI\u011eINIZ YARIN \"TEDAVI\u0307\" EDI\u0307LEBI\u0307LECEK OLSA, YAPMAK I\u0307STEYECE\u011eI\u0307NI\u0307Z I\u0307LK \u015eEY NE OLURDU?<\/strong><br \/>\nI would kneel down, raise my hands towards heaven and worship my God.<\/p>","protected":false},"excerpt":{"rendered":"<p>03\/31\/2015 Name:\u00a0 Eva\u00a0\u00a0 \u00a0Age: 33 Yrs. Old Country:\u00a0 Kenya LGMD [&hellip;]<\/p>","protected":false},"author":1,"featured_media":497,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13],"tags":[34,33],"class_list":["post-496","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","tag-kenya","tag-unknown"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>LGMD Spotlight Interview - Eva<\/title>\n<meta name=\"description\" content=\"Eva, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"http:\/\/www.lgmd-info.org\/tr\/individuals-with-lgmd-interviews\/2015\/03\/31\/496\/\" \/>\n<meta property=\"og:locale\" content=\"tr_TR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"LGMD Spotlight Interview - 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