{"id":15584,"date":"2021-05-20T18:44:57","date_gmt":"2021-05-20T18:44:57","guid":{"rendered":"https:\/\/lpfch.org\/meet-david-your-summer-scamper-patient-hero\/"},"modified":"2024-07-01T21:46:00","modified_gmt":"2024-07-01T21:46:00","slug":"meet-david-your-summer-scamper-patient-hero","status":"publish","type":"post","link":"http:\/\/lpfch.org\/es\/impact-stories\/meet-david-your-summer-scamper-patient-hero\/","title":{"rendered":"Conoce a David, tu h\u00e9roe paciente de las aventuras de verano."},"content":{"rendered":"<p>&nbsp;<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">\u201cEstar en el hospital no me asusta. Tener un problema nuevo ya no me asusta porque me ha pasado muchas veces. No s\u00e9, supongo que mi sangre no me tiene mucho cari\u00f1o.\u201d<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">A los 15 a\u00f1os, David hab\u00eda estado entrando y saliendo del Hospital Infantil Lucile Packard de Stanford tantas veces que pod\u00eda explicar su enfermedad de c\u00e9lulas falciformes, un trastorno hereditario de los gl\u00f3bulos rojos, mejor que nadie.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">\u201cSe supone que tus gl\u00f3bulos rojos son redondos y contienen ox\u00edgeno. Los m\u00edos tienen forma de media luna, de hoz, por eso se llama anemia falciforme, as\u00ed que no recibo la misma cantidad de ox\u00edgeno\u201d, dijo David en el documental de Netflix de 2019 \u201cHuman Nature\u201d de Adam Bolt.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">\u201cA menudo se la denomina la primera enfermedad molecular. Est\u00e1 causada por un cambio singular en la secuencia de ADN\u201d, explic\u00f3 Matt Porteus, MD, PhD, profesor Sutardja Chuk de Medicina Definitiva y Curativa en la Universidad de Stanford. \u201cEs la letra &#039;A&#039; la que cambia a la letra &#039;T&#039;. Se vuelve muy r\u00edgida y no puede pasar, impidiendo que los gl\u00f3bulos rojos lleguen a los tejidos donde deben transportar ox\u00edgeno. Cuando se bloquea el suministro de ox\u00edgeno a esos tejidos, estos no funcionan correctamente y se da\u00f1an\u201d.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">Actualmente, la esperanza de vida de un paciente con anemia falciforme es de tan solo 42 a 47 a\u00f1os. Son 42 a 47 a\u00f1os llenos de di\u00e1lisis, episodios de dolor intenso y riesgo de accidentes cerebrovasculares e insuficiencia org\u00e1nica. Aun as\u00ed, estos riesgos no han impedido que David disfrute de su infancia. Nada le impide hacer lo que m\u00e1s le gusta: jugar al baloncesto.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">\u201cEs como una pulsaci\u00f3n\u201d, dijo David sobre el dolor. \u201cPuedo tener un peque\u00f1o episodio de dolor que realmente no importa, y luego puedo tener algo muy grave. Pero no voy a dejar de jugar al baloncesto. No se puede simplemente dejar de jugar al baloncesto\u201d.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">Pero ahora hay esperanza para m\u00e1s ni\u00f1os como David. El Dr. Porteus est\u00e1 utilizando CRISPR, una revolucionaria herramienta de edici\u00f3n gen\u00e9tica, para desarrollar una cura para enfermedades como la anemia falciforme.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">\u201cSimplemente no cont\u00e1bamos con las herramientas para realizar ese cambio de una sola letra con precisi\u00f3n, especialmente de una sola letra. Antes de CRISPR, logr\u00e1bamos correcciones de 1 a 21 TP3T. Ahora, hemos alcanzado de 50 a 801 TP3T en las c\u00e9lulas\u201d, dijo el Dr. Porteus con entusiasmo. \u201cEsto realmente podr\u00eda funcionar. Podr\u00eda curar a un paciente. Tenemos la experiencia necesaria para hacerlo todo aqu\u00ed. Contamos con la infraestructura del quinto piso del Hospital Infantil Lucile Packard para tratar a estos pacientes\u201d.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">Recientemente, David sorprendi\u00f3 al Dr. Porteus con una videollamada para ponerse al d\u00eda y agradecerle su trabajo en la b\u00fasqueda de una cura.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">\u201cEl hospital ha sido como mi segundo hogar, y aunque suene raro decirlo, algunas de mis personas favoritas las conoc\u00ed all\u00ed o trabajan all\u00ed\u201d, dijo David. \u201cY ni siquiera necesito conocerlas personalmente; puedo hablar en nombre de todas las personas con anemia falciforme, y pr\u00e1cticamente de cualquier enfermedad. Gracias, Dr. Porteus\u201d.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">\u2014Lo agradezco mucho \u2014respondi\u00f3 el Dr. Porteus\u2014. Pero tambi\u00e9n quiero se\u00f1alar que somos un grupo muy grande los que formamos parte de esto. Este tipo de cosas no las hace una sola persona. Se necesita todo un equipo, y ustedes cuentan con un gran equipo detr\u00e1s, y siempre lo tendr\u00e1n.<\/p>\n<p class=\"\" style=\"white-space: pre-wrap;\">Gracias por formar parte del equipo de David. David sigue recibiendo tratamiento en nuestro hospital (aunque ahora que tiene 18 a\u00f1os, \u00a1pronto se trasladar\u00e1 al Hospital de Stanford!) y se enorgullece de participar en Scamper para apoyar a otros pacientes, a su equipo m\u00e9dico y a investigadores innovadores como el Dr. Porteus. Puede que estemos lejos, pero como dice David: \u00ab\u00a1No puedes dejar de participar en Scamper!\u00bb.<\/p>","protected":false},"excerpt":{"rendered":"<p>&nbsp; \u201cEstar en el hospital no me asusta. Tener un problema nuevo ya no me asusta porque me ha pasado muchas veces. Yo\u2026<\/p>","protected":false},"author":17,"featured_media":17743,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"categories":[23],"class_list":["post-15584","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-summer-scamper-heroes"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.3 (Yoast SEO v27.3) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Meet David, Your Summer Scamper Patient Hero - Lucile Packard Foundation for Children&#039;s Health<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"http:\/\/lpfch.org\/es\/impact-stories\/meet-david-your-summer-scamper-patient-hero\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Meet David, Your Summer Scamper Patient Hero\" \/>\n<meta property=\"og:description\" content=\"&nbsp; \u201cBeing in the hospital isn\u2019t scary to me. 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