{"id":3255,"date":"2019-12-20T18:53:00","date_gmt":"2019-12-20T23:53:00","guid":{"rendered":"https:\/\/braintumour.ca\/?p=3255"},"modified":"2020-01-07T14:52:04","modified_gmt":"2020-01-07T19:52:04","slug":"lhistoire-de-gabriel-jolin","status":"publish","type":"post","link":"https:\/\/www.braintumour.ca\/fr\/temoignages\/lhistoire-de-gabriel-jolin\/","title":{"rendered":"L&rsquo;histoire de Gabriel Jolin"},"content":{"rendered":"<p>J&rsquo;avais probablement ma tumeur depuis ma naissance, mais elle n&rsquo;a v\u00e9ritablement commenc\u00e9 a me causer du tord qu&rsquo;\u00e0 l&rsquo;\u00e2ge de 18 mois. Je m&rsquo;appelle Gabriel et j&rsquo;ai bient\u00f4t 7 ans. Il y a maintenant 6 ans qu&rsquo;on m&rsquo;a trouv\u00e9 une tumeur c\u00e9r\u00e9brale au\u00a0<a href=\"https:\/\/www.braintumour.ca\/fr-ca\/8142\/gliome-des-voies-optiques\"> niveau des voies optiques<\/a>. Six ans de traitements de chimios, deux r\u00e9missions et deux rechutes. Cette masse log\u00e9e dans ma t\u00eate, je l&rsquo;ai appel\u00e9e \u00ab\u00a0ma bille\u00a0\u00bb. Elle fait partie de moi, de ma vie et de celle de ma famille.<\/p>\n<p style=\"text-align: center;\"><a href=\"https:\/\/braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel4.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-3256 size-full\" src=\"https:\/\/braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel4.jpg\" alt=\"\" width=\"320\" height=\"339\" srcset=\"https:\/\/www.braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel4.jpg 320w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel4-283x300.jpg 283w\" sizes=\"auto, (max-width: 639px) 98vw, (max-width: 1199px) 64vw, 320px\" \/><\/a><\/p>\n<p>\u00c0 17 mois, j&rsquo;ai commenc\u00e9 \u00e0 \u00eatre malade, je vomissais beaucoup. Je n&rsquo;arrivais plus a marcher pendant plus d&rsquo;une minute alors qu&rsquo;auparavant mes parents pensaient que je serais marathonien. Ils ont consult\u00e9 plusieurs fois en vain avant qu&rsquo;on d\u00e9couvre ma colocataire. \u00c0 18 mois, par chance j&rsquo;\u00e9tais d\u00e9j\u00e0 \u00e0 l&rsquo;h\u00f4pital, car ce matin-l\u00e0 je suis mort&#8230; deux fois&#8230; Mais ma maman \u00e9tait l\u00e0 et elle pleurait, alors j&rsquo;ai d\u00e9cid\u00e9 de vivre pour elle, pour mon papa et mon fr\u00e8re. Depuis ce jour, je me bats. Tr\u00e8s fort. Et ce malgr\u00e9 mon \u0153il gauche et la moiti\u00e9 de mon droit qui ont d\u00e9cid\u00e9 de m&rsquo;abandonner. Et malgr\u00e9 les difficult\u00e9s que \u00e7a occasionne, car je suis souvent fatigu\u00e9 compar\u00e9 aux autres enfants de mon \u00e2ge. Je ne cours pas le marathon encore, mais je cours et \u00e7a me fait toujours plaisir.<\/p>\n<p style=\"text-align: center;\"><a href=\"https:\/\/braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel2.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignright size-medium wp-image-3258\" src=\"https:\/\/braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel2-300x225.jpg\" alt=\"\" width=\"300\" height=\"225\" srcset=\"https:\/\/www.braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel2-300x225.jpg 300w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel2-768x576.jpg 768w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel2-640x480.jpg 640w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2019\/12\/gabriel2.jpg 960w\" sizes=\"auto, (max-width: 639px) 98vw, (max-width: 1199px) 64vw, 300px\" \/><\/a><\/p>\n<p>On a essay\u00e9 une fois d&rsquo;enlever ma bille quand j&rsquo;\u00e9tait tout petit, mais la coquine est bien attach\u00e9e \u00e0 moi et refuse de me quitter. Alors, j&rsquo;ai d\u00e9cid\u00e9 de l&rsquo;accepter et de vivre avec elle, m\u00eame si parfois, je l&rsquo;avoue, elle m&#8217;emb\u00eate vraiment beaucoup. J&rsquo;aimerais \u00e7a \u00eatre comme les autres enfants ; avoir mes deux yeux, ne pas devoir manquer l&rsquo;\u00e9cole pour aller \u00e0 l&rsquo;h\u00f4pital, ne pas avoir de vis dans la t\u00eate, me sentir invincible, tomber amoureux et avoir un jour mon permis de conduire. Mais je suis diff\u00e9rent. Je ne sens pourtant pas qu&rsquo;il me manque quelque chose, au contraire, moi j&rsquo;ai un plus\u2026 Un surplus.<\/p>\n<p>Ma famille m&rsquo;aide beaucoup, c&rsquo;est s\u00fbrement gr\u00e2ce \u00e0 eux que je vais si bien. Un jour, j&rsquo;esp\u00e8re vraiment \u00eatre comme mon grand fr\u00e8re. Je me suis aussi fait des amis \u00e0 l&rsquo;h\u00f4pital que j&rsquo;aime voir chaque semaine. Quand l\u2019un d&rsquo;eux quitte, \u00e7a me fait toujours un peu de peine. J&rsquo;ai aussi ma super infirmi\u00e8re et mon docteur qui m&rsquo;aident beaucoup. Ils croient tous en moi et en ma force. Gr\u00e2ce \u00e0 ma famille et au personnel de l&rsquo;h\u00f4pital, vous savez quoi? Moi aussi je crois en moi! Je vais continuer \u00e0 me battre et vaincre. Je m&rsquo;appelle Gabriel, j&rsquo;ai bient\u00f4t 7 ans et un jour, je serai professeur puisque je suis d\u00e9j\u00e0 un super h\u00e9ro&#8230;<\/p>\n<p><em>\u00c9crit par Sophie, la maman de Gabriel<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>J&rsquo;avais probablement ma tumeur depuis ma naissance, mais elle n&rsquo;a v\u00e9ritablement commenc\u00e9 a me causer du tord qu&rsquo;\u00e0 l&rsquo;\u00e2ge de [&hellip;]<\/p>\n","protected":false},"author":6,"featured_media":3256,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[148,164],"tags":[],"user_type":[133],"locations":[],"class_list":["post-3255","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-temoignages","category-pediatrique","user_type-patient-fr"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.0 (Yoast SEO v27.0) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>L&#039;histoire de Gabriel Jolin - Fondation canadienne des tumeurs c\u00e9r\u00e9brales<\/title>\n<meta name=\"description\" content=\"&#039;avais probablement ma tumeur depuis ma naissance, mais elle n&#039;a v\u00e9ritablement commenc\u00e9 a me causer du tord qu&#039;\u00e0 l&#039;\u00e2ge de 18 mois. 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