{"id":7678,"date":"2021-05-04T09:04:04","date_gmt":"2021-05-04T13:04:04","guid":{"rendered":"https:\/\/www.braintumour.ca\/non-classifiee\/cause-to-celebrate-ethans-story\/"},"modified":"2021-08-18T16:21:32","modified_gmt":"2021-08-18T20:21:32","slug":"ethan","status":"publish","type":"post","link":"https:\/\/www.braintumour.ca\/fr\/temoignages\/ethan\/","title":{"rendered":"Une raison de c\u00e9l\u00e9brer \u2013 L\u2019histoire d\u2019Ethan"},"content":{"rendered":"<h5>Le 25 janvier 2021 fut un grand jour pour Ethan Hayes, huit ans, et sa m\u00e8re Cindi.<\/h5>\n<p>\u00c0 la suite d\u2019une tomodensitom\u00e9trie r\u00e9alis\u00e9e la veille, Cindi et Ethan ont appris que le cancer d\u2019Ethan avait disparu, et ce pr\u00e8s de deux ans jour pour jour, apr\u00e8s avoir re\u00e7u son diagnostic initial et un an apr\u00e8s son dernier traitement.<\/p>\n<p>Le plan initial \u00e9tait d\u2019organiser une grande f\u00eate pour c\u00e9l\u00e9brer le premier anniversaire de la fin du traitement d\u2019Ethan. Cependant, comme la plupart des aspects de la vie quotidienne pendant la pand\u00e9mie, ce projet aura \u00e9t\u00e9 mis en suspens.<\/p>\n<p>Ethan a re\u00e7u un diagnostic de m\u00e9dulloblastome, sous-type3, qui s\u2019\u00e9tait propag\u00e9 de son cerveau \u00e0 sa colonne vert\u00e9brale. Il a subi quatre chirurgies, plusieurs complications sont survenues, puis il s\u2019est rendu aux \u00c9tats-Unis pour un traitement exp\u00e9rimental avant de recevoir les bonnes nouvelles.<\/p>\n<p><strong>Se comporter en champion<\/strong><\/p>\n<p>\u00abIl a&#8230; connu bien des tourments\u00bb, explique maman Cindi.<\/p>\n<p>Apr\u00e8s sa chirurgie, Ethan n\u2019a pas pu marcher pendant cinq semaines. Un des effets secondaires incluait une main qui bougeait continuellement. Et cela, \u00e0 la suite d\u2019une infection par le SARM r\u00e9sultant d\u2019une intervention chirurgicale,et \u00e0 cause de laquelle il n\u2019\u00e9tait pas en mesure de participer \u00e0 de nombreuses activit\u00e9s avec les autres enfants de SickKids.<\/p>\n<p>Il a tout tr\u00e8s bien pris, et Cindi a veill\u00e9 \u00e0 prot\u00e9ger la sant\u00e9 mentale de son fils. M\u00eame lorsque confront\u00e9 \u00e0 ces contretemps qui auraient pu facilement \u00eatre d\u00e9courageants, Ethan s\u2019est comport\u00e9 en champion.<\/p>\n<p>\u00abC\u2019est le gamin le plus serein qui soit\u00bb, dit Cindi. \u00abJe pense qu\u2019Ethan m\u2019a appris la r\u00e9silience.\u00bb<br \/>\n<img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-7212\" src=\"https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-640x799.jpeg\" alt=\"\" width=\"500\" height=\"624\" srcset=\"https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-640x799.jpeg 640w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-240x300.jpeg 240w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-820x1024.jpeg 820w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-768x959.jpeg 768w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-1230x1536.jpeg 1230w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-1024x1279.jpeg 1024w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-1200x1499.jpeg 1200w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-1153x1440.jpeg 1153w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1-865x1080.jpeg 865w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image1.jpeg 1242w\" sizes=\"auto, (max-width: 639px) 98vw, (max-width: 1199px) 64vw, 500px\" \/><\/p>\n<p>Il n\u2019y a rien de plus effrayant pour un parent que d\u2019apprendre que son enfant est atteint d\u2019un cancer, mais Cindi \u00e9tait d\u00e9termin\u00e9e \u00e0 ne pas se laisser abattre par la peur. Cindi r\u00e9v\u00e8le qu\u2019apr\u00e8s avoir appris le diagnostic d\u2019Ethan, elle a d\u00fb faire un choix : rester positive et se battre ou c\u00e9der \u00e0 la peur et \u00e0 l\u2019isolement. Cindi a choisi la premi\u00e8re option, \u00eatre pr\u00eate \u00e0 tous les possibles d\u00e9fis \u00e0 venir, et y faire face en restant positive et ouverte d\u2019esprit.<\/p>\n<p><strong>Une occasion s\u2019est pr\u00e9sent\u00e9e<\/strong><\/p>\n<p>Par chance, Ethan a \u00e9t\u00e9 accept\u00e9e pour un essai clinique aux \u00c9tats-Unis, recherche \u00e0 laquelle Cindi attribue le r\u00e9tablissement de son fils.<\/p>\n<p>Ethan s\u2019est rendu \u00e0 l\u2019h\u00f4pital St Jude de Memphis, au Tennessee o\u00f9 il a re\u00e7u 30traitements de protonth\u00e9rapie et sept mois de chimioth\u00e9rapie \u00e0 forte dose.L\u2019essai clinique lui a litt\u00e9ralement sauv\u00e9 la vie.<\/p>\n<p>Maintenant, lorsqu\u2019il est soumis \u00e0 des injections ou des IV, il met en pratique des techniques de respiration profonde pour se d\u00e9tendre. Et, dit Cindi, il a pass\u00e9 une telle quantit\u00e9 de tests de COVID qu\u2019\u00e0 ce stade il les g\u00e8re comme un pro.<\/p>\n<p>Il suit actuellement une kin\u00e9sith\u00e9rapie et une ergoth\u00e9rapie et il ne cesse de faire des progr\u00e8s. On ne se r\u00e9tablit pas du jour au lendemain, mais chaque progr\u00e8s est cause de c\u00e9l\u00e9bration.<\/p>\n<p>Pendant son s\u00e9jour \u00e0 St Jude au Tennessee, Ethan s\u2019est fait de bons amis, avec qui il reste toujours en contact. Une fois par semaine, Ethan rencontre un copain en ligne pour une partie de Super Smash Bros.<\/p>\n<p><strong><img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-7210\" src=\"https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-640x756.jpeg\" alt=\"\" width=\"500\" height=\"591\" srcset=\"https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-640x756.jpeg 640w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-254x300.jpeg 254w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-867x1024.jpeg 867w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-768x907.jpeg 768w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-1024x1210.jpeg 1024w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-1200x1417.jpeg 1200w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-1219x1440.jpeg 1219w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0-914x1080.jpeg 914w, https:\/\/www.braintumour.ca\/wp-content\/uploads\/2021\/05\/image0.jpeg 1242w\" sizes=\"auto, (max-width: 639px) 98vw, (max-width: 1199px) 64vw, 500px\" \/>Sagesse acquise<\/strong><\/p>\n<p>Bien qu\u2019il ressemble \u00e0 un enfant heureux comme les autres, Ethan a acquis une sagesse et une s\u00e9r\u00e9nit\u00e9 d\u00e9passant son \u00e2ge. Son calme naturel a, non seulement, aid\u00e9 Ethan \u00e0 survivre \u00e0 son traitement et \u00e0 son r\u00e9tablissement, mais cela a \u00e9galement eu un effet apaisant sur Cindi.<\/p>\n<p>Elle se souvient d\u2019un jour en particulier o\u00f9 Ethan est venu la voir et lui a dit:<\/p>\n<p>\u00abMaman, tu sais que je n\u2019ai plus le cancer, je vais bien\u00bb.<\/p>\n<p>\u00abIl est en harmonie avec lui-m\u00eame\u00bb, dit Cindi. \u00abIl n\u2019a que huit ans, mais il comprend.\u00bb<\/p>\n<p>Aujourd\u2019hui, Cindi est d\u00e9termin\u00e9e \u00e0 redonner \u00e0 la communaut\u00e9 qui les a soutenus et \u00e0 sensibiliser les gens aux tumeurs c\u00e9r\u00e9brales dans l\u2019espoir que de meilleurs traitements pour les enfants seront d\u00e9couverts au Canada. Et cela ne se limite pas uniquement au cancer, dit-elle. Le stress associ\u00e9 aux tumeurs malignes et non malignes est le m\u00eame, tout comme le manque de connaissances et d\u2019options.<\/p>\n<p>\u00abLes gens doivent \u00eatre conscients de ce fait\u00bb, d\u00e9clare Cindi. Les tumeurs c\u00e9r\u00e9brales, et en particulier les tumeurs c\u00e9r\u00e9brales p\u00e9diatriques, sont consid\u00e9r\u00e9es comme rares et ne retiennent par cons\u00e9quent pas autant l\u2019attention que les autres maladies.<\/p>\n<p>Cependant, lorsque vous \u00eates plong\u00e9s dans ce monde, il est difficile de croire que les tumeurs et les cancers infantiles sont tout sauf courants. \u00abLes gens disent que c\u2019est vraiment rare\u00bb, dit-elle. \u00abOn ne pense pas que c\u2019est si rare lorsque l\u2019on en est entour\u00e9.\u00bb<\/p>\n<p><strong>Soins auto administr\u00e9s pour les parents<\/strong><\/p>\n<p>Il est important pour tout parent qui se retrouve soudainement m\u00e8re ou p\u00e8re d\u2019un enfant canc\u00e9reux de prendre soin de soi, explique Cindi. Parlez aux gens qui vous entourent, qu\u2019il s\u2019agisse du personnel de soutien ou des personnes se trouvant \u00e0 l\u2019ext\u00e9rieur de la bulle m\u00e9dicale. C\u2019est dur, mais il y a de l\u2019espoir.<\/p>\n<p>\u00abIl faut passer par le feu, mais on y arrive\u00bb, dit-elle.<\/p>\n<p>Ethan passe maintenant des tomodensitom\u00e9tries tous les trois mois afin de v\u00e9rifier que le cancer n\u2019est pas revenu. Pendant ce temps, la famille vit dans le pr\u00e9sent et c\u00e9l\u00e8bre ce qu\u2019elle a plut\u00f4t que de s\u2019inqui\u00e9ter de l\u2019avenir. \u00abNous vivons notre vie par trimestre\u00bb, dit-elle. \u00abNous recevons de bonnes nouvelles au sujet de la tomodensitom\u00e9trie et vivons notre vie pendant les trois mois suivants sans trop nous concentrer dessus.\u00bb<\/p>\n<p>Les nouvelles obtenues le 25 janvier ont marqu\u00e9 le d\u00e9but d\u2019un nouveau chapitre pour Ethan et sa famille, et ce n\u2019est que le dernier d\u2019une s\u00e9rie de bonnes nouvelles. \u00ab\u00c0 partir d\u2019aujourd\u2019hui, il ne s\u2019agit plus que de vivre une vie heureuse\u00bb, explique Cindi. \u00abNous allons f\u00eater cinq ans, puis dix ans. C\u2019est ainsi que nous avan\u00e7ons.\u00bb<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Le 25 janvier 2021 fut un grand jour pour Ethan Hayes, huit ans, et sa m\u00e8re Cindi. \u00c0 la suite [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":7209,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[148,164],"tags":[217,378,505],"user_type":[],"locations":[161,198],"class_list":["post-7678","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-temoignages","category-pediatrique","tag-fondation-canadienne-des-tumeurs-cerebrales","tag-marche-des-tumeurs-cerebrales","tag-medulloblastome","locations-canada-wide-fr","locations-toronto-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>Une raison de c\u00e9l\u00e9brer \u2013 L\u2019histoire d\u2019Ethan - 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