{"id":6643,"date":"2023-06-01T01:12:01","date_gmt":"2023-06-01T05:12:01","guid":{"rendered":"https:\/\/loeysdietzcanada.org\/pour-les-enfants-et-les-adolescents-atteints-de-scoliose\/"},"modified":"2025-05-22T13:40:12","modified_gmt":"2025-05-22T17:40:12","slug":"pour-les-enfants-et-les-adolescents-atteints-de-scoliose","status":"publish","type":"post","link":"https:\/\/loeysdietzcanada.org\/fr\/pour-les-enfants-et-les-adolescents-atteints-de-scoliose\/","title":{"rendered":"Higgy Bears : Pour les enfants et les adolescents atteints de scoliose"},"content":{"rendered":"<p>Par : Lauren<\/p>\n<p>Fondatrice de Higgy Bears<\/p>\n<p>&nbsp;<\/p>\n<p>Bonjour ! Je m&#8217;appelle Lauren et je suis la fondatrice de Higgy Bears, un organisme \u00e0 but non lucratif bas\u00e9 aux \u00c9tats-Unis. Je fabrique des ours en peluche sp\u00e9ciaux pour les enfants et les adolescents atteints de scoliose. Je fabrique \u00e0 la main des mini-appareils orthop\u00e9diques que les ours portent pour les enfants qui ont un appareil orthop\u00e9dique. Je couds \u00e9galement des tiges dans leur dos pour les patients qui, comme moi, ont \u00e9t\u00e9 op\u00e9r\u00e9s pour une scoliose. Ils sont un petit ami l\u00e0 o\u00f9 il n&#8217;y en avait pas pour aider l&#8217;enfant dans son traitement de la scoliose.<\/p>\n<p>&nbsp;<\/p>\n<p>C&#8217;est ma propre exp\u00e9rience de la scoliose qui m&#8217;a incit\u00e9e \u00e0 cr\u00e9er les oursons Higgy. J&#8217;ai \u00e9t\u00e9 diagnostiqu\u00e9e \u00e0 l&#8217;\u00e2ge de 13 ans. Je n&#8217;ai jamais port\u00e9 d&#8217;appareil orthop\u00e9dique, mais j&#8217;avais une bosse dans le dos qui me g\u00eanait beaucoup. Je ne connaissais personne d&#8217;autre comme moi et je me sentais incroyablement isol\u00e9e. J&#8217;avais l&#8217;impression d&#8217;\u00eatre la seule personne au monde \u00e0 \u00eatre atteinte d\u2019une scoliose. Je le cachais \u00e0 mes amis et j&#8217;\u00e9tais terrifi\u00e9e \u00e0 l&#8217;id\u00e9e que quelqu&#8217;un remarque ma bosse. Cela a beaucoup affect\u00e9 mon estime de soi lorsque j&#8217;\u00e9tais enfant.<\/p>\n<p>&nbsp;<\/p>\n<p>\u00c0 l&#8217;\u00e2ge adulte, j&#8217;ai enfin rencontr\u00e9 quelqu&#8217;un d&#8217;autre atteint de scoliose. J&#8217;ai ressenti un \u00e9norme soulagement en sachant que je n&#8217;\u00e9tais plus seule. C&#8217;est ce sentiment que j&#8217;esp\u00e8re partager avec les enfants qui re\u00e7oivent un ourson Higgy.<\/p>\n<p>&nbsp;<\/p>\n<p>Jusqu\u2019\u00e0 pr\u00e9sent, j\u2019ai confectionn\u00e9 plus de 20 000 oursons Higgy qui ont \u00e9t\u00e9 envoy\u00e9s dans 130 pays. J&#8217;ai eu le plaisir de faire la connaissance de milliers d&#8217;enfants atteints de scoliose et de leurs parents, et de les guider tout au long de leur parcours. Un fil conducteur semble exister parmi les personnes \u00e0 qui j&#8217;ai parl\u00e9. Les enfants et les adolescents se sentent toujours isol\u00e9s apr\u00e8s avoir re\u00e7u le diagnostic de scoliose. Leur ourson Higgy les aide, mais les enfants ont encore besoin d\u2019un rapport qui n&#8217;existe souvent pas.<\/p>\n<p>&nbsp;<\/p>\n<p>J&#8217;ai mis sur pied ScoliZooms pour aider les enfants \u00e0 rencontrer d&#8217;autres enfants qui vivent la m\u00eame chose qu&#8217;eux. Des enfants du monde entier se retrouvent toutes les deux semaines sur Zoom. Nous parlons et nous nous soutenons les uns les autres. Nous jouons \u00e9galement \u00e0 des jeux amusants sur le th\u00e8me de la scoliose ! Cela aide vraiment les enfants \u00e0 savoir qu&#8217;ils ne sont pas seuls. Je vous recommande vivement d&#8217;impliquer vos enfants et vos adolescents. Vous pouvez m&#8217;envoyer un courriel \u00e0 <a href=\"mailto:lauren@higgybears.com\">lauren@higgybears.com<\/a> pour vous inscrire. Le programme de mentorat Scolios-us est \u00e9galement un autre programme de soutien que je vous recommande fortement.<\/p>\n<p>&nbsp;<\/p>\n<p>Pour en savoir plus sur Higgy Bears, visitez le <a href=\"http:\/\/www.higgybears.com\/\" target=\"_blank\" rel=\"noopener\">site www.higgybears.com<\/a> et suivez Higgy Bears sur <a href=\"https:\/\/www.facebook.com\/HiggyBears\/\" target=\"_blank\" rel=\"noopener\">Facebook<\/a> et <a href=\"https:\/\/www.instagram.com\/higgybears\/\" target=\"_blank\" rel=\"noopener\">Instagram<\/a>. N&#8217;h\u00e9sitez pas \u00e0 communiquer avec moi si vous avez des questions ou si je peux vous aider. N&#8217;oubliez jamais que nous sommes peut-\u00eatre courb\u00e9s, mais nous ne sommes pas bris\u00e9s !<\/p>\n<p>Bon mois de sensibilisation \u00e0 la scoliose !<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Par : Lauren Fondatrice de Higgy Bears &nbsp; Bonjour ! Je m&#8217;appelle Lauren et je suis la fondatrice de Higgy Bears, un organisme \u00e0 but non lucratif bas\u00e9 aux \u00c9tats-Unis. [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":6642,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"site-sidebar-layout":"default","site-content-layout":"default","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"default","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[46],"tags":[],"class_list":["post-6643","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-temoignages-de-patients-et-soutien"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/posts\/6643","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/comments?post=6643"}],"version-history":[{"count":4,"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/posts\/6643\/revisions"}],"predecessor-version":[{"id":8701,"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/posts\/6643\/revisions\/8701"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/media\/6642"}],"wp:attachment":[{"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/media?parent=6643"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/categories?post=6643"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/loeysdietzcanada.org\/fr\/wp-json\/wp\/v2\/tags?post=6643"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}