{"id":10,"date":"2017-05-11T14:14:36","date_gmt":"2017-05-11T14:14:36","guid":{"rendered":"https:\/\/live-rawf.pantheonsite.io\/2017\/05\/11\/2017-5-11-local-mom-takes-fight-for-brain-tumor-awareness-to-capitol-hill\/"},"modified":"2023-08-01T19:34:31","modified_gmt":"2023-08-01T19:34:31","slug":"2017-5-11-une-mere-locale-se-bat-pour-la-sensibilisation-aux-tumeurs-cerebrales-sur-la-colline-du-capitole","status":"publish","type":"post","link":"https:\/\/www.rawoodfoundation.org\/fr\/2017\/05\/11\/2017-5-11-local-mom-takes-fight-for-brain-tumor-awareness-to-capitol-hill\/","title":{"rendered":"Le directeur de la RAWF se rend sur la colline"},"content":{"rendered":"<div class=\"sqs-html-content\">\n<p>Washington, D.C. - Amy Wood, directrice de la Fondation Raymond A. Wood, s'est jointe au contingent du Maryland qui s'est rendu mardi sur la Colline avec la National Brain Tumor Society pour plaider en faveur d'une l\u00e9gislation visant \u00e0 financer la recherche sur les tumeurs c\u00e9r\u00e9brales. Amy Wood est la m\u00e8re d'Alex, 6 ans, survivant d'une tumeur c\u00e9r\u00e9brale et \u00e9l\u00e8ve de maternelle \u00e0 l'\u00e9cole primaire d'Ocean City.<\/p>\n<p>Wood a rencontr\u00e9 les s\u00e9nateurs du Maryland Ben Cardin et Chris Van Hollen ainsi que le membre du Congr\u00e8s Andy Harris pour discuter de la loi Childhood Cancer STAR Act de 2017. Si elle est adopt\u00e9e, cette loi contribuerait \u00e0 stimuler une recherche plus efficace sur les tumeurs c\u00e9r\u00e9brales p\u00e9diatriques et conduirait \u00e0 de meilleurs traitements qui prolongeraient la vie et am\u00e9lioreraient la qualit\u00e9 de vie des patients. Le s\u00e9nateur Van Hollen est l'un des coparrains du projet de loi.<\/p>\n<p>\"Alex n'a plus de cancer depuis deux ans, mais nous devons faire face aux cons\u00e9quences de cette tumeur tous les jours\", explique Mme Wood. \"C'est l'occasion pour nous de raconter son histoire dans l'espoir qu'elle aidera un autre enfant qui sera confront\u00e9 \u00e0 un combat similaire.<\/p>\n<p>L'ann\u00e9e derni\u00e8re, les tumeurs c\u00e9r\u00e9brales ont d\u00e9pass\u00e9 la leuc\u00e9mie en tant que principale cause de d\u00e9c\u00e8s par cancer chez les enfants \u00e2g\u00e9s de 0 \u00e0 19 ans. Selon la National Brain Tumor Society, jusqu'\u00e0 deux tiers des enfants ayant surv\u00e9cu \u00e0 un cancer souffrent d'effets tardifs de la maladie ou de son traitement, notamment de cancers secondaires et de l\u00e9sions organiques. La loi STAR permettrait de renforcer la recherche sur ces effets, d'am\u00e9liorer la collaboration entre les prestataires de soins et d'\u00e9tablir un nouveau programme pilote pour commencer \u00e0 explorer des mod\u00e8les innovants de soins pour les enfants ayant surv\u00e9cu \u00e0 un cancer.<\/p>\n<p>La famille Wood, Shawn, Amy et Alex, a cr\u00e9\u00e9 la Raymond A. Wood Foundation (RAWF) fin 2016. RAWF est une 501(c)(3) dont la mission est sp\u00e9cifiquement de fournir un soutien \u00e0 la qualit\u00e9 de vie aux survivants de tumeurs c\u00e9r\u00e9brales p\u00e9diatriques.<\/p>\n<p>\"Nous avons vu les d\u00e9fis auxquels ces jeunes survivants sont confront\u00e9s apr\u00e8s le traitement et il y a tant de travail \u00e0 faire pour les aider \u00e0 s'\u00e9panouir tout au long de leur vie\", a d\u00e9clar\u00e9 Mme Wood. \"Se rendre \u00e0 la Colline aujourd'hui a \u00e9t\u00e9 une exp\u00e9rience extraordinaire et je suis optimiste quant \u00e0 l'avenir du traitement des tumeurs c\u00e9r\u00e9brales p\u00e9diatriques et de leurs r\u00e9sultats.<\/p>\n<p>Pour soutenir le Childhood Cancer STAR Act, faites entendre votre voix et appelez vos repr\u00e9sentants. Pour plus d'informations sur la mani\u00e8re d'aider les survivants des tumeurs c\u00e9r\u00e9brales chez l'enfant, visitez le site rawoodfoundation.org.<\/p>\n<p>\u00a0<\/p>\n<p>\u00a0<\/p>\n<\/div>\n<div\n        class=\"image-block-outer-wrapper          layout-caption-below          design-layout-inline\"\n        data-test=\"image-block-inline-outer-wrapper\"\n    ><\/p>\n<figure\n            class=\"sqs-block-image-figure              intrinsic\"\n            style=\"max-width:960px;\"\n        ><\/p>\n<div\n\n\n              class=\"image-block-wrapper\"\n              data-animation-role=\"image\"\n\n  data-animation-override\n\n><\/p>\n<div class=\"sqs-image-shape-container-element              has-aspect-ratio\" style=\"                position: relative;                  padding-bottom:75%;                overflow: hidden;-webkit-mask-image: -webkit-radial-gradient(white, black);              \"\n              ><\/p>\n<p>                  <noscript><img decoding=\"async\" src=\"https:\/\/images.squarespace-cdn.com\/content\/v1\/587bc3d946c3c4be42a60e48\/1494511971753-57305EMLO3419XMIN8WI\/image-asset.jpeg\" alt=\"Les d\u00e9fenseurs de la recherche sur les tumeurs c\u00e9r\u00e9brales de toute la nation ont converg\u00e9 vers la Colline pour soutenir les cr\u00e9dits de recherche m\u00e9dicale et pour s&#039;exprimer en faveur du Childhood Cancer STAR Act (loi sur la recherche sur le cancer chez les enfants). Photo avec l&#039;aimable autorisation de la National Brain Tumor Society.\" \/><\/noscript><img decoding=\"async\" class=\"thumb-image\" src=\"https:\/\/images.squarespace-cdn.com\/content\/v1\/587bc3d946c3c4be42a60e48\/1494511971753-57305EMLO3419XMIN8WI\/image-asset.jpeg\" data-image=\"https:\/\/images.squarespace-cdn.com\/content\/v1\/587bc3d946c3c4be42a60e48\/1494511971753-57305EMLO3419XMIN8WI\/image-asset.jpeg\" data-image-dimensions=\"960x720\" data-image-focal-point=\"0.5,0.5\" alt=\"Les d\u00e9fenseurs de la recherche sur les tumeurs c\u00e9r\u00e9brales de toute la nation ont converg\u00e9 vers la Colline pour soutenir les cr\u00e9dits de recherche m\u00e9dicale et pour s&#039;exprimer en faveur du Childhood Cancer STAR Act (loi sur la recherche sur le cancer chez les enfants). Photo avec l&#039;aimable autorisation de la National Brain Tumor Society.\" data-load=\"false\" data-image-id=\"59147163197aeab3e2485e5b\" data-type=\"image\" \/><\/p><\/div>\n<\/p><\/div><figcaption class=\"image-caption-wrapper\">\n<div class=\"image-caption\">\n<p>Les d\u00e9fenseurs de la recherche sur les tumeurs c\u00e9r\u00e9brales de toute la nation ont converg\u00e9 vers la Colline pour soutenir les cr\u00e9dits de recherche m\u00e9dicale et pour s'exprimer en faveur du Childhood Cancer STAR Act (loi sur la recherche sur le cancer chez les enfants). Photo avec l'aimable autorisation de la National Brain Tumor Society.<\/p>\n<\/div>\n<\/figcaption><\/figure>\n<\/p><\/div>","protected":false},"excerpt":{"rendered":"<p>Washington, D.C. - Amy Wood, directrice de la Fondation Raymond A. Wood, s'est jointe au contingent du Maryland qui s'est rendu mardi sur la Colline avec la National Brain Tumor Society pour plaider en faveur d'une l\u00e9gislation visant \u00e0 financer la recherche sur les tumeurs c\u00e9r\u00e9brales. Amy Wood est la m\u00e8re d'Alex, 6 ans, survivant d'une tumeur c\u00e9r\u00e9brale et \u00e9l\u00e8ve de maternelle \u00e0 l'\u00e9cole primaire d'Ocean City.<\/p>","protected":false},"author":6,"featured_media":5594,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[41,1],"tags":[],"class_list":["post-10","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-uncategorized","generate-columns","tablet-grid-50","mobile-grid-100","grid-parent","grid-33","no-featured-image-padding"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>RAWF Director &quot;Heads to the Hill&quot; - Raymond A. 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