{"id":4963,"date":"2017-05-26T15:36:44","date_gmt":"2017-05-26T15:36:44","guid":{"rendered":"https:\/\/laforcedmd.com\/?p=4963\/"},"modified":"2022-05-03T18:22:25","modified_gmt":"2022-05-03T18:22:25","slug":"jean-philippe-victor-race-for-dmd","status":"publish","type":"post","link":"https:\/\/laforcedmd.com\/en\/jean-philippe-victor-race-for-dmd\/","title":{"rendered":"Jean-Philippe and Victor race for DMD"},"content":{"rendered":"<p><strong>Learning that your son is suffering from Duchenne muscular dystrophy is watching your child lose his muscular ability month after month. This is Jean-Philippe Morand\u2019s reality: his son Victor is stricken with Duchenne muscular dystrophy. In adversity, some men go beyond their limits, and this is what Jean-Philippe will do this Sunday, May 28, by participating in the Ottawa Marathon in the company of his son Victor.<\/strong><\/p>\n<p>Actually, for the past 4 years, the Morand family has been holding a fundraising event called the \u201c<em>Dystrospin<\/em>\u201d. A portion of the money raised was invested in the purchase of a suitable wheelchair. It\u2019s because of this kind of generosity that Jean-Philippe is able to participate in the Ottawa Marathon with his son. There\u2019s nothing better than a father\u2019s courage to raise awareness about Duchenne muscular dystrophy.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>Hope for treatment<\/strong><\/p>\n<p>Duchenne muscular dystrophy is an incurable and 100% fatal disease. Duchenne muscular dystrophy is a rare genetic disorder that affects mainly boys. The progression of DMD is unforgiving: the body\u2019s muscles gradually weaken, leaving the boys in a wheelchair at the age of 12, with a life expectancy of 20 to 30 years. Today there is hope for DMD, and several new treatments are on the horizon. This hope motivates Jean-Philippe to go beyond his limits for his son; but what he does also benefit all children with DMD.<\/p>\n<p>Every effort to raise awareness about this rare and devastating disease will help us to facilitate access to new treatments.<\/p>\n<p>For this reason, we, from the bottom of our hearts, invite you to share this story of courage.<\/p>\n<p>We at <em>La Force<\/em> are proud to support Jean-Philippe Morand and his family.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>To learn more about:<\/strong><\/p>\n<ul>\n<li><a href=\"https:\/\/www.facebook.com\/dystrospin\/?fref=ts\" target=\"_blank\" rel=\"noopener noreferrer\">Dystrospin<\/a><\/li>\n<li><a href=\"\/?p=4769\" target=\"_blank\" rel=\"noopener noreferrer\">La Force &amp; Dystrospin association\u00a0<\/a><\/li>\n<li><a href=\"http:\/\/www.runottawa.ca\/races-and-events\/tamarack-ottawa-race-weekend\">Run Ottawa<\/a><\/li>\n<li><a href=\"http:\/\/www.teamhoyt.com\/\">Running chair<\/a><\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Learning that your son is suffering from Duchenne muscular dystrophy is watching your child lose his muscular ability month after month. This is Jean-Philippe Morand\u2019s reality: his son Victor is stricken with Duchenne muscular dystrophy. In adversity, some men go beyond their limits, and this is what Jean-Philippe will do this Sunday, May 28, by [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":4975,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[20],"tags":[],"class_list":["post-4963","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-testimonial"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Jean-Philippe and Victor race for DMD<\/title>\n<meta name=\"description\" content=\"Jean-Philippe will be participating Sunday, May 28, at the Ottawa Marathon in the company of his son Victor afflicted with DMD.\" \/>\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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