{"id":8146,"date":"2022-07-11T10:00:00","date_gmt":"2022-07-11T08:00:00","guid":{"rendered":"https:\/\/alcompasrevista.com\/?p=8146"},"modified":"2022-07-13T13:25:04","modified_gmt":"2022-07-13T11:25:04","slug":"ivan-chaquet-o-com-la-musica-salva-vides","status":"publish","type":"post","link":"https:\/\/alcompasrevista.com\/va\/archivos\/8146","title":{"rendered":"Iv\u00e1n Chaquet, o com la m\u00fasica salva vides"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">\u00c9s el dilluns de la primera gran onada de calor de l\u2019estiu. I no se m\u2019oc\u00f3rre una altra cosa que vindre-me\u2019n a La Llosa de Ranes, en plena comarca de la Costera. Per als qui no sou de la zona, ac\u00ed \u00e9s on es va inventar la calor. S\u00f3n les sis de la vesprada i arribe al Carrer Sant Roc. Un carrer estret i costerut; un dels carrers m\u00e9s representatius d\u2019este poble de poc m\u00e9s de tres mil habitants que t\u00e9 una de les bandes m\u00e9s reconegudes dels voltants. A una d\u2019estes cases viu Iv\u00e1n Chaquet amb son pare, F\u00e9lix Chaquet. M\u2019esperen al sal\u00f3 d\u2019una casa -amb l\u2019aire acondicionat enc\u00e8s, per sort- repleta de discs de m\u00fasica, fotografies d\u2019Iv\u00e1n vestit de m\u00fasic, de la seua germana, de sa mare\u2026 El que seria una casa habitual vaja. Tamb\u00e9 hi ha una habitaci\u00f3 amb una bateria. El que seria una casa habitual d\u2019un percussionista, vaja. El que passa \u00e9s que a esta casa viu un percussionista molt poc habitual.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Iv\u00e1n Chaquet \u00e9s un jove que no arriba als quaranta anys i pateix la malaltia rara del S\u00edndrome de Williams. Segons l\u2019Associaci\u00f3 Valenciana del S\u00edndrome de Williams este trastorn del desenvolupament \u00e9s reconegut per tenir unes caracter\u00edstiques facials molt espec\u00edfiques, problemes al cor i vasos sanguinis, problemes alimenticis, irritabilitat, anomalies dentals, problemes de fetge, h\u00e8rnies, hiperacusies, problemes vasculars i retard evolutiu, aix\u00ed com dificultats per a l\u2019aprenentatge. Entre d\u2019altres s\u00edmptomes\u2026Una combinaci\u00f3 \u201cperfecta\u201d de caracter\u00edstiques cl\u00edniques per a les que, a dia de hui, encara no hi ha cura. Hi ha tractaments que ajuden, s\u00ed. Per\u00f2 no hi ha cura.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">La infantesa d\u2019Iv\u00e1n va ser molt dif\u00edcil. La dels seus pares, tamb\u00e9. Tot i que, per sort, ara el diagn\u00f2stic \u00e9s molt m\u00e9s preco\u00e7 que aleshores, F\u00e9lix -son pare- em conta com de complicats van ser aquells anys inicials. \u201cAn\u00e0vem d\u2019ac\u00ed a all\u00e0, d\u2019hospital a hospital, de consulta a consulta, i ning\u00fa ens sabia dir exactament qu\u00e8 passava. Primer era una cosa, despr\u00e9s una altra\u2026 Fins i tot ens van dir que era cel\u00edac i al forn li f\u00e8iem un pa a prop\u00f2sit per a ell -tenien un forn familiar-, per\u00f2 tampoc. Vam tindre metges que ens van ajudar molt, coneguts de la meua dona, per\u00f2 ning\u00fa podia fer res m\u00e9s concret. Estem parlant de que Iv\u00e1n ahi era molt xicotet\u201d. Els primers anys d\u2019Iv\u00e1n van transc\u00f3rrer entre sales d\u2019espera, bates de color blanc i kil\u00f2metres en cotxe. Els que feia F\u00e9lix per portar-los a ell i la seua dona amunt i avall. De Val\u00e8ncia a X\u00e0tiva i de X\u00e0tiva a La Llosa. Aix\u00f2, clar, mentre treballava. Si quedava alg\u00fan dubte, F\u00e9lix, son pare, ha viscut i es desviu pel seu fill.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Estem asseguts a la tauleta del menjador i, pr\u00e0cticament, no hi ha un moment de silenci perqu\u00e8 les an\u00e8cdotes ens sobrepassen. F\u00e9lix \u00e9s una persona molt sentimental, que estima al seu fill, a la seua filla i a la seua dona que, malauradament, va morir a causa de la COVID-19. D\u2019ahi que Iv\u00e1n li dedicara a sa mare el <em>solo <\/em>que va realitzar al Palau de les Arts de Val\u00e8ncia fa molt poc i que, estic segur, molts dels lectors d\u2019 \u201cAl Comp\u00e0s\u201d vau poder gaudir en directe. Iv\u00e1n \u00e9s percussionista des de fa m\u00e9s de vint anys. Tot va comen\u00e7ar, com no, gr\u00e0cies a la dedicaci\u00f3, entrega i valentia dels seus pares, a un gran esfor\u00e7 del fill i a la generositat d\u2019uns mestres i uns companys que van obrir les portes a que, a dia de hui, Iv\u00e1n siga un percussionista m\u00e9s que reconegut a tota la Comunitat Valenciana. \u201cTu porta al teu fill, encara que no s\u00e0piga <em>solfeo<\/em>, porta\u2019l\u201d, recorda F\u00e9lix que li va dir Francisco S\u00e1nchez Roca. \u201c<em>Per aquell entonces <\/em>em van comprar una caixa sorda per a assajar a casa\u201d, diu orgull\u00f3s Iv\u00e1n.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Els 15 anys van ser una edat clau per a Iv\u00e1n i la seua familia. En un mateix any van oc\u00f3rrer dos de les coses m\u00e9s importants a la seua vida: la primera, a finals d\u2019abril, va ser diagnosticat clarament amb el S\u00edndrome de Williams despr\u00e9s d\u2019un an\u00e0lisi i estudi exhaustiu per part dels seus pares i l\u2019ajuda de persones i sanitaris que F\u00e9lix recorda emocionat. I la segona va ser l\u2019entrada oficial a la banda de la Llosa de Ranes de la que, a dia de hui, continua sent membre actiu i, per descomptat, membre imprescindible. Entre mitges, i des d\u2019all\u00e0 fins ac\u00ed, han passat moltes coses, per\u00f2 una d\u2019elles \u00e9s necessari recordar-la: un campament d\u2019estiu junt amb altres pacients d\u2019Espanya diagnosticats del S\u00edndrome de Williams. All\u00e0, i despr\u00e9s de fer un gran esfor\u00e7 econ\u00f2mic, Iv\u00e1n va descobrir per primera vegada que \u201cno era l\u2019\u00fanic\u201d, diu. Desenes de xiquets, joves i no tant joves, van passar unes dies junts a un campament monitoritzat per experts i per membres de l\u2019associaci\u00f3 espanyola d\u2019esta malaltia. All\u00e0, per primera vegada, es van obrir les portes d\u2019una nova vida: una vida d\u2019acceptaci\u00f3, de coneixement, humilitat&nbsp; de generositat i de brillantor. Perqu\u00e8 Iv\u00e1n \u00e9s brillant, tant en la part personal, com en la part musical. No \u00e9s d\u2019estranyar que fins i tot el mestre Mario Roig Vila li haja dedicat un pasdoble amb el seu nom i que ell mateixa ha dirigit. \u201cI l\u2019he de tornar a dirigir amb altres bandes\u201d, diu conven\u00e7ut Iv\u00e1n.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Despr\u00e9s de m\u00e9s d\u2019una hora de xarrada, \u00e9s moment de recollir trastos i deixar que Iv\u00e1n descanse una miqueta, ja que s\u2019al\u00e7a ben de mat\u00ed per anar a treballar. Perqu\u00e8 s\u00ed, perqu\u00e8 Iv\u00e1n tamb\u00e9 treballa. Tot i que clar, ara ja l\u2019hora qu\u00e8 \u00e9s, o b\u00e9 se n\u2019anir\u00e0 al futbol -tamb\u00e9 \u00e9s part imprescindible del club del poble- o al Musical a vore qui troba per all\u00e0. Per\u00f2 abans li pregunte, tant a ell com a son pare, qu\u00e8 ha significat i qu\u00e8 significa la Societat Musical de la Llosa de Ranes en les seues vides. Son pare m\u2019ho afirma r\u00e0pidament: \u201cal meu fill la m\u00fasica li ha salvat la vida\u201d. I el fill em diu que \u201cla banda \u00e9s passar-s\u2019ho b\u00e9 i sobretot tocar b\u00e9\u2026 ah, i que els meus companys de percussi\u00f3 no tinguen por que el meu pasdoble no \u00e9s complicat. El que passa \u00e9s que el bombo i els plats \u00e9s <em>pum\u2026 xam, pum pum, xam xam\u2026 <\/em>i au\u201d. Companys i companyes de percussi\u00f3 de totes les bandes de la Comunitat Valenciana -entre els quals m\u2019incloc-, no tingau por, que no \u00e9s tan complicat i menys encara si ens dirigeix ell mateix. I directores i directors de la Comunitat Valenciana, demaneu este pasdoble per tocar a les vostres bandes perqu\u00e8 darrere d\u2019eixes notes del mestre Mario Roig Vila, hi ha molta vida viscuda i molta m\u00e9s per viure.<\/p>\n\n\n\n<figure class=\"wp-block-gallery has-nested-images columns-default is-cropped wp-block-gallery-1 is-layout-flex wp-block-gallery-is-layout-flex\">\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"760\" height=\"430\" data-id=\"8141\" src=\"https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-32-1.jpg\" alt=\"\" class=\"wp-image-8141\" srcset=\"https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-32-1.jpg 760w, https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-32-1-300x170.jpg 300w\" sizes=\"auto, (max-width: 760px) 100vw, 760px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"760\" height=\"430\" data-id=\"8135\" src=\"https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-17-1.jpg\" alt=\"\" class=\"wp-image-8135\" srcset=\"https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-17-1.jpg 760w, https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-17-1-300x170.jpg 300w\" sizes=\"auto, (max-width: 760px) 100vw, 760px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"760\" height=\"430\" data-id=\"8133\" src=\"https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-30.jpg\" alt=\"\" class=\"wp-image-8133\" srcset=\"https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-30.jpg 760w, https:\/\/alcompasrevista.com\/wp-content\/uploads\/2022\/07\/Diseno-sin-titulo-30-300x170.jpg 300w\" sizes=\"auto, (max-width: 760px) 100vw, 760px\" \/><\/figure>\n<\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">Si vols col\u00b7laborar perqu\u00e8 el S\u00edndrome de Williams es seguisca investigant i, aix\u00ed, poder-ne buscar tractament, busca <a href=\"https:\/\/sindromewilliams.org\/\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/sindromewilliams.org\/<\/a> per entrar al web de l\u2019Associaci\u00f3 Espanyola del S\u00edndrome de Williams o escriu un mail a <a href=\"mailto:avswvalencia@gmail.com\">avswvalencia@gmail.com<\/a> per posar-te en contacte amb els encarregats de l\u2019Associaci\u00f3 Valenciana del S\u00edndrome de Williams. Nom\u00e9s aix\u00ed podrem seguir contant hist\u00f2ries com la d\u2019Iv\u00e1n Chaquet i la seua familia.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>\u00c9s el dilluns de la primera gran onada de calor de l\u2019estiu. I no se m\u2019oc\u00f3rre una altra cosa que vindre-me\u2019n a La Llosa de Ranes, en plena comarca de [&hellip;]<\/p>\n","protected":false},"author":860007,"featured_media":8129,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[29],"tags":[195,192],"portada":[193,191],"class_list":["post-8146","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-noticies-va","tag-llosa-de-ranes","tag-sindrome-de-williams-2","portada-llosa-de-ranes","portada-sindrome-de-williams"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Iv\u00e1n Chaquet, o com la m\u00fasica salva vides - Revista Al Comp\u00e0s<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/alcompasrevista.com\/archivos\/8234\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Iv\u00e1n Chaquet, o com la m\u00fasica salva vides - Revista Al Comp\u00e0s\" \/>\n<meta property=\"og:description\" content=\"\u00c9s el dilluns de la primera gran onada de calor de l\u2019estiu. 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