[et_pb_section fb_built=\u201d1\u2033 fullwidth=\u201don\u201d deshabilitado_encendido=\u201dapagado|apagado|apagado\u201d _builder_version=\u201d4.16\u2033 border_width_bottom=\u201d55px\u201d border_color_bottom=\u201d#29327a\u201d global_colors_info=\u201d{}\u201d][et_pb_fullwidth_header _builder_version=\u201d4.16\u2033 tama\u00f1o_de_fuente_t\u00edtulo=\u201d55\u2033 color_de_fondo=\u201d#29327a\u201d imagen_de_fondo=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2019\/04\/Acerca-del-encabezado.jpg\u201d posici\u00f3n_de_fondo=\u201dcentro_izquierda\u201d relleno_personalizado=\u201d11.5vw||11.5vw||verdadero\u201d relleno_personalizado_tablet=\u201d\u201d padding_personalizado_tel\u00e9fono=\u201d|56px||\u201d padding_personalizado_\u00faltima_edici\u00f3n=\u201den|escritorio\u201d tama\u00f1o_fuente_t\u00edtulo_tableta=\u201d45px\u201d tama\u00f1o_fuente_t\u00edtulo_tel\u00e9fono=\u201d40px\u201d tama\u00f1o_fuente_t\u00edtulo_\u00faltima_edici\u00f3n=\u201den|tel\u00e9fono\u201d z_index_tableta=\u201d500\u2033 elemento_principal_css_personalizado=\u201dposici\u00f3n_fondo: centro 18% !importante;\u201d informaci\u00f3n_colores_global=\u201d{}\u201d]<\/p>\n
[\/et_pb_fullwidth_header][\/et_pb_section][et_pb_section fb_built=\u201d1\u2033 use_custom_gutter=\u201don\u201d gutter_width=\u201d1\u2033 specialist=\u201don\u201d padding_left_1=\u201d35px\u201d padding_left_2=\u201d35px\u201d padding_2_tablet=\u201d|||0px\u201d padding_2_phone=\u201d|||0px\u201d padding_2_last_edited=\u201don|desktop\u201d module_class_1=\u201dbarra lateral-navegaci\u00f3n-secundaria\u201d module_class=\u201dhuella-de-mano-bg\u201d _builder_version=\u201d4.16\u2033 background_image=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2019\/04\/huella-de-mano-azul-solamente.png\u201d parallax=\u201don\u201d parallax_method=\u201doff\u201d ancho_interior=\u201d100%\u201d ancho_m\u00e1ximo_interior=\u201d100%\u201d relleno_personalizado=\u201d0|0px|54px|0px|falso|falso\u201d z_index_tablet=\u201d500\u2033 ancho_borde_superior=\u201d10px\u201d color_border_superior=\u201d#8fd2ed\u201d uso_ancho_personalizado=\u201dactivado\u201d unidad_ancho=\u201ddesactivado\u201d porcentaje_ancho_personalizado=\u201d100%\u201d informaci\u00f3n_colores_globales=\u201d{}\u201d][et_pb_column tipo=\u201d1_4\u2033 _builder_version=\u201d4.16\u2033 relleno_personalizado=\u201d|||\u201d global_colors_info=\u201d{}\u201d custom_padding__hover=\u201d|||\u201d][et_pb_sidebar area=\u201det_pb_widget_area_17\u2033 deshabilitado_en=\u201dencendido|encendido|apagado\u201d module_class=\u201dsubpage-sidebars\u201d _builder_version=\u201d4.16\u2033 animation_style=\u201dfade\u201d z_index_tablet=\u201d500\u2033 border_width_right=\u201d5px\u201d global_colors_info=\u201d{}\u201d]
\n[\/et_pb_sidebar][\/et_pb_column][et_pb_column tipo=\u201d3_4\u2033 columnas_especializadas=\u201d3\u2033 _versi\u00f3n_constructor=\u201d4.16\u2033 relleno_personalizado=\u201d|||\u201d global_colors_info=\u201d{}\u201d custom_padding__hover=\u201d|||\u201d][et_pb_row_inner custom_padding_last_edited=\u201don|phone\u201d _builder_version=\u201d4.16\u2033 custom_padding=\u201d39.4375px|35px|35px||false|false\u201d custom_padding_tablet=\u201d|35px||35px||true\u201d custom_padding_phone=\u201d\u201d animation_direction=\u201dtop\u201d global_colors_info=\u201d{}\u201d][et_pb_column_inner save_specialty_column_type=\u201d3_4\u2033 _builder_version=\u201d4.16\u2033 custom_padding=\u201d|||\u201d global_colors_info=\u201d{}\u201d custom_padding__hover=\u201d|||\u201d][et_pb_text _builder_version=\u201d4.16\u2033 background_size=\u201dinitial\u201d background_position=\u201dtop_left\u201d background_repeat=\u201drepeat\u201d z_index_tablet=\u201d500\u2033 global_colors_info=\u201d{}\u201d]<\/p>\n
Cuando a Sam, el \u00fanico hijo de los doctores Leslie Gordon y Scott Berns, le diagnosticaron progeria en 1998, inmediatamente comenzaron a recopilar toda la informaci\u00f3n que pudieron sobre la enfermedad. Descubrieron que no hab\u00eda mucha informaci\u00f3n disponible: no hab\u00eda forma de realizar pruebas definitivas para detectar la enfermedad, no hab\u00eda fondos para la investigaci\u00f3n sobre la progeria y no hab\u00eda ninguna organizaci\u00f3n que defendiera a los ni\u00f1os con progeria. Por eso, en 1999, reunieron a familiares, amigos y colegas y crearon la Fundaci\u00f3n para la Investigaci\u00f3n de la Progeria con el fin de encontrar la causa, el tratamiento y la cura de la progeria.<\/p>\n
Desde entonces, cientos de voluntarios dedicados se han unido al equipo de PRF para ayudar a avanzar en el campo de la investigaci\u00f3n de la progeria a un ritmo extraordinario. La Junta Directiva, la Junta de Asesores, los miembros del Comit\u00e9, los funcionarios corporativos, los abogados, los contadores, los dise\u00f1adores gr\u00e1ficos y los representantes de relaciones p\u00fablicas de PRF dedican su tiempo, energ\u00eda y talento a PRF de forma gratuita para garantizar que se gaste menos en costos administrativos y m\u00e1s en generar conciencia y encontrar una cura para la progeria. Haga clic en los enlaces de la izquierda para leer m\u00e1s sobre nuestro grupo central y tambi\u00e9n sobre muchos de nuestros otros h\u00e9roes. Los hacedores de milagros de PRF<\/a>.<\/p>\n [\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][\/et_pb_column][\/et_pb_section][et_pb_section fb_built=\u201d1\u2033 clase_m\u00f3dulo=\u201dpie de p\u00e1gina\u201d _builder_version=\u201d4.21.0\u2033 color_de_fondo=\u201d#29327a\u201d margen_personalizado=\u201d-2px|||||\u201d padding_personalizado=\u201d0|0px|0|0px|falso|falso\u201d z_index_tablet=\u201d500\u2033 border_width_top=\u201d12px\u201d border_color_top=\u201d#00b2e2\u2033 global_module=\u201d133\u2033 bloqueado=\u201ddesactivado\u201d global_colors_info=\u201d{}\u201d][et_pb_row estructura_columna=\u201d1_4,1_4,1_2\u2033 make_equal=\u201dactivado\u201d module_class=\u201det_pb_row_fullwidth\u201d _builder_version=\u201d4.16\u2033 ancho=\u201d89%\u201d ancho_tablet=\u201d80%\u201d ancho_tel\u00e9fono=\u201d\u201d ancho_\u00faltima_edici\u00f3n=\u201dactivado|escritorio\u201d ancho_m\u00e1ximo=\u201d89%\u201d ancho_m\u00e1ximo_tablet=\u201d80%\u201d max_width_phone=\u201d\u201d max_width_last_edited=\u201don|desktop\u201d z_index_tablet=\u201d500\u2033 make_fullwidth=\u201don\u201d width_unit=\u201doff\u201d custom_width_percent=\u201d100%\u201d global_colors_info=\u201d{}\u201d][et_pb_column type=\u201d1_4\u2033 _builder_version=\u201d4.16\u2033 custom_padding=\u201d|||\u201d global_colors_info=\u201d{}\u201d custom_padding__hover=\u201d|||\u201d][et_pb_cta button_url=\u201dhttps:\/\/www.progeriaresearch.org\/newsletter-signup\/\u201d button_text=\u201dReg\u00edstrese ahora\u201d admin_label=\u201dSuscr\u00edbase al bolet\u00edn informativo\u201d module_class=\u201dsign-btn\u201d _builder_version=\u201d4.16\u2033 header_font_size=\u201d25px\u201d background_color=\u201d#29327a\u201d animation_style=\u201dslide\u201d animation_direction=\u201dleft\u201d animation_intensity_slide=\u201d25%\u201d header_font_size_tablet=\u201d\u201d header_font_size_phone=\u201d30px\u201d header_font_size_last_edited=\u201don|desktop\u201d z_index_tablet=\u201d500\u2033 radio_borde=\u201dactivado|25px|25px|25px|25px\u201d informaci\u00f3n_colores_global=\u201d{}\u201d color_bot\u00f3n_fondo__hover_habilitado=\u201dactivado\u201d color_bot\u00f3n_fondo__hover=\u201d#8fd2ed\u201d color_borde_bot\u00f3n__hover_habilitado=\u201dactivado\u201d]<\/p>\n [\/et_pb_cta][\/et_pb_column][et_pb_column type=\u201d1_4\u2033 _builder_version=\u201d4.16\u2033 custom_padding=\u201d|||\u201d global_colors_info=\u201d{}\u201d custom_padding__hover=\u201d|||\u201d][et_pb_cta button_url=\u201dhttps:\/\/progeriaresearch.donorsupport.co\/-\/XZHJVWZR\u201d button_text=\u201dDonar ahora\u201d admin_label=\u201d\u00a1Juntos encontraremos la cura!\u201d module_class=\u201dsign-btn\u201d _builder_version=\u201d4.16\u2033 header_font_size=\u201d25px\u201d background_color=\u201d#29327a\u201d animation_style=\u201dslide\u201d animation_direction=\u201dleft\u201d animation_intensity_slide=\u201d25%\u201d header_font_size_tablet=\u201d\u201d header_font_size_phone=\u201d30px\u201d header_font_size_last_edited=\u201don|desktop\u201d body_font_size_tablet=\u201d\u201d body_font_size_phone=\u201d\u201d body_font_size_last_edited=\u201don|desktop\u201d z_index_tablet=\u201d500\u2033 border_radii=\u201don|25px|25px|25px|25px\u201d global_colors_info=\u201d{}\u201d button_bg_color__hover_enabled=\u201don\u201d bot\u00f3n_bg_color__hover=\u201d#8fd2ed\u201d bot\u00f3n_border_color__hover_enabled=\u201don\u201d]<\/p>\n [\/et_pb_cta][\/et_pb_column][et_pb_column tipo=\u201d1_2\u2033 _builder_version=\u201d4.16\u2033 relleno_personalizado=\u201d|||\u201d global_colors_info=\u201d{}\u201d custom_padding__hover=\u201d|||\u201d][et_pb_image src=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2023\/06\/2023-footer-strip-5.png\u201d title_text=\u201dFranja de pie de p\u00e1gina 2023 5\u2033 _builder_version=\u201d4.21.0\u2033 _module_preset=\u201ddefault\u201d custom_margin=\u201d35px||||false|false\u201d global_colors_info=\u201d{}\u201d][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>","protected":false},"excerpt":{"rendered":" [et_pb_section fb_built=\u201d1\u2033 fullwidth=\u201don\u201d deshabilitado_encendido=\u201dapagado|apagado|apagado\u201d _builder_version=\u201d4.16\u2033 border_width_bottom=\u201d55px\u201d border_color_bottom=\u201d#29327a\u201d global_colors_info=\u201d{}\u201d][et_pb_fullwidth_header _builder_version=\u201d4.16\u2033 tama\u00f1o_de_fuente_t\u00edtulo=\u201d55\u2033 color_de_fondo=\u201d#29327a\u201d imagen_de_fondo=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2019\/04\/Acerca-del-encabezado.jpg\u201d posici\u00f3n_de_fondo=\u201dcentro_izquierda\u201d relleno_personalizado=\u201d11.5vw||11.5vw||verdadero\u201d relleno_personalizado_tablet=\u201d\u201d padding_tel\u00e9fono personalizado=\u201d|56px||\u201d padding_\u00faltima_edici\u00f3n=\u201den|escritorio\u201d tama\u00f1o_fuente_t\u00edtulo_tableta=\u201d45px\u201d tama\u00f1o_fuente_t\u00edtulo_tel\u00e9fono=\u201d40px\u201d tama\u00f1o_fuente_\u00faltima_edici\u00f3n=\u201den|tel\u00e9fono\u201d z_index_tableta=\u201d500\u2033 elemento_principal_css_personalizado=\u201dposici\u00f3n-de-fondo: centro 18% !importante;\u201d global_colors_info=\u201d{}\u201d] Nuestra gente [\/et_pb_fullwidth_header][\/et_pb_section][et_pb_section fb_built=\u201d1\u2033 use_custom_gutter=\u201don\u201d gutter_width=\u201d1\u2033 specialist=\u201don\u201d padding_left_1=\u201d35px\u201d padding_left_2=\u201d35px\u201d padding_2_tablet=\u201d|||0px\u201d padding_2_phone=\u201d|||0px\u201d padding_2_last_edited=\u201don|desktop\u201d module_class_1=\u201dbarra lateral-navegaci\u00f3n-secundaria\u201d module_class=\u201dhuella-de-mano-bg\u201d _builder_version=\u201d4.16\u2033 background_image=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2019\/04\/huella-de-mano-azul-solamente.png\u201d paralaje=\u201dactivado\u201d m\u00e9todo_paralaje=\u201ddesactivado\u201d ancho_interior=\u201d100%\u201d ancho_m\u00e1ximo_interior=\u201d100%\u201d relleno_personalizado=\u201d0|0px|54px|0px|falso|falso\u201d z_index_tablet=\u201d500\u2033 ancho_borde_superior=\u201d10px\u201d color_border_superior=\u201d#8fd2ed\u201d uso_ancho_personalizado=\u201dactivado\u201d unidad_ancho=\u201ddesactivado\u201d porcentaje_ancho_personalizado=\u201d100%\u201d informaci\u00f3n_colores_global=\u201d{}\u201d][et_pb_column tipo=\u201d1_4\u2033 [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"[vc_row][vc_column][vc_custom_heading text=\"Our People\" font_container=\"tag:h1|text_align:center\" use_theme_fonts=\"yes\"][vc_separator][vc_column_text]When Drs. Leslie Gordon and Scott Berns\u2019 only child Sam was diagnosed with Progeria in 1998, they immediately began to collect as much information as they could find on the disease. They discovered that there wasn\u2019t much available: there was no way to definitively test for the disease, no funding for Progeria research, and no organization advocating for children with Progeria. So in 1999, they gathered family, friends and colleagues and established The Progeria Research Foundation to find the cause, treatment and cure for Progeria.\r\n\r\nSince then, hundreds of dedicated volunteers have joined the PRF team to help advance the field of Progeria research at an extraordinary rate. PRF\u2019s Board of Directors, Board of Advisors, Committee members, Corporate Officers, lawyers, accountants, graphic designers and public relations representatives all devote their time, energy and talents to PRF for free to ensure less is spent on administrative costs and more on raising awareness and finding a cure for Progeria.Click on the links to the left to read more about our core group, and also read about many of our other heroes, PRF\u2019s Miracle Makers<\/a>.[\/vc_column_text][\/vc_column][\/vc_row]","_et_gb_content_width":"","footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-883","page","type-page","status-publish","hentry"],"yoast_head":"\nInscribirse<\/h2>\n
Para nuestro<\/h2>\n
\u00a1Hoja informativa!<\/h2>\n
Juntos, nosotros<\/h2>\n
VOLUNTAD<\/em><\/h2>\n
\u00a1Encuentra la cura!<\/h2>\n