{"id":412,"date":"2015-01-06T21:59:11","date_gmt":"2015-01-07T03:59:11","guid":{"rendered":"http:\/\/mainstay-bg.com\/wp\/?p=138"},"modified":"2015-01-06T21:59:11","modified_gmt":"2015-01-07T03:59:11","slug":"138","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/01\/06\/138\/","title":{"rendered":"INDIVIDUAL WITH LGMD:  Martijn"},"content":{"rendered":"<p>01\/06\/2015:<\/p>\n<p><span class=\"userContent\"><strong>NOM :<\/strong> Martijn\u00a0<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/01\/LGMD2A-Martijn.png\"><img decoding=\"async\" class=\"lazyload  size-medium wp-image-146 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\/01\/LGMD2A-Martijn-300x169.png\" alt=\"LGMD2A - Martijn\" width=\"300\" height=\"169\" \/><\/a>\u00a0\u00a0\u00a0 <\/span><\/p>\n<p><span class=\"userContent\"><strong>AGE :<\/strong> 23<br \/>\n<\/span><\/p>\n<p><span class=\"userContent\"><strong>PAYS :<\/strong> Les Pays-Bas<br \/>\n<\/span><\/p>\n<p><span class=\"userContent\"><strong>LGMD Sous-type<\/strong>: LGMD 2A \/ Calpainopathy<br \/>\n<\/span><\/p>\n<p><span class=\"userContent\"><span class=\"text_exposed_show\"><strong>\u00c0 QUEL \u00c2GE AVEZ-VOUS \u00c9T\u00c9 DIAGNOSTIQU\u00c9 ?<\/strong>\u00a0 Approximately around my 15th birthday.<\/span><\/span><\/p>\n<p><strong>QUELS ONT \u00c9T\u00c9 VOS PREMIERS SYMPT\u00d4MES :<\/strong><br \/>\nThe first symptoms were visible since I was a baby. I used to creep like a crab and I was physically \u2018different\u2019 from my peers. I was active in a number of different sports, such as: gymnastics, volleyball, judo and tennis. But my performance was declining due to the on-going progression of muscle weakness in my body.<\/p>\n<p><strong>AVEZ-VOUS D'AUTRES MEMBRES DE VOTRE FAMILLE QUI SONT ATTEINTS DE LA LGMD : \u00a0 <\/strong>No.<\/p>\n<p><strong>QUELS SONT, SELON VOUS, LES PLUS GRANDS D\u00c9FIS \u00c0 RELEVER POUR VIVRE AVEC LA LGMD :<\/strong><br \/>\nThe more practical problems are worse to me. For example walking by my own on the street with crooked sidewalk tiles is quite challenging. It requires a lot of attention and I get tired of this. In most cases I decide to use a wheelchair if I have to walk long distances. Also, explaining my muscle disease to strangers is not my favorite hobby. I am a little bit unsure on how much information I should provide. Some of them are asking about the \u2018whole process\u2019 and the more personal things. And some others feel frightened to ask me about any details. Talking about my disease is not a problem for me, but determining how much information to share is the challenge.<\/p>\n<p><strong> QUELLE EST VOTRE PLUS GRANDE R\u00c9ALISATION :<\/strong><br \/>\nDo you have a few seconds? One of my greatest accomplishes are skydiving, studying and doing everything that healthy people consider as \u2018not possible\u2019 for disabled people. I do like to cross the borders in my live. I am always looking for adventures, like traveling with friends (actually we scheduled a trip to Iceland in February 2015) and so on. Besides that, a personal accomplishment to me is a presentation about my muscle disease and the way I am dealing with the disease to about 500 medical students.<\/p>\n<p><strong>COMMENT LA LGMD VOUS A-T-ELLE INFLUENC\u00c9 POUR QUE VOUS DEVENIEZ LA PERSONNE QUE VOUS \u00caTES AUJOURD'HUI :<\/strong><br \/>\nLGMD has influenced my life for sure! It has made me more mature in many ways. The way I handle problems and enjoy my life has significantly changed since my diagnosis.<\/p>\n<p><strong>QUE VOULEZ-VOUS QUE LE MONDE SACHE \u00c0 PROPOS DE LA LGMD :<\/strong><br \/>\nPeople with LGMD or any other muscular disease are not different from healthy people, they just may need a little assistance, at times. Also, do not talk to the person behind the wheelchair, but speak directly to the person in the wheelchair.<\/p>\n<p><strong> SI VOTRE LGMD POUVAIT \u00caTRE \"GU\u00c9RIE\" DEMAIN, QUELLE SERAIT LA PREMI\u00c8RE CHOSE QUE VOUS VOUDRIEZ FAIRE :<\/strong><br \/>\nI would want to go Sky Diving solo!<\/p>","protected":false},"excerpt":{"rendered":"<p>01\/06\/2015: NAME: Martijn\u00a0\u00a0\u00a0\u00a0 AGE: 23 COUNTRY: The Netherlands LGMD Sub-Type: [&hellip;]<\/p>","protected":false},"author":1,"featured_media":146,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,14],"tags":[12,15,17],"class_list":["post-412","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2a","tag-calpainopathy","tag-lgmd2a","tag-netherlands"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - 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