Italiano: [et_pb_section fb_built=\u201d1\u2033 fullwidth=\u201don\u201d disabled_on=\u201doff|off|off\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 title_font_size=\u201d55\u2033 background_color=\u201d#29327a\u201d background_image=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2019\/04\/About-Header.jpg\u201d background_position=\u201dcenter_left\u201d custom_padding=\u201d11.5vw||11.5vw||true\u201d custom_padding_tablet=\u201d\u201d custom_padding_phone=\u201d|56px||\u201d custom_padding_last_edited=\u201don|desktop\u201d title_font_size_tablet=\u201d45px\u201d title_font_size_phone=\u201d40px\u201d title_font_size_last_edited=\u201don|phone\u201d z_index_tablet=\u201d500\u2033 custom_css_main_element=\u201dbackground-position: center 18% !important;\u201d global_colors_info=\u201d{}\u201d]<\/p>\n
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Quando nel 1998 all'unico figlio dei dottori Leslie Gordon e Scott Berns, Sam, fu diagnosticata la Progeria, iniziarono immediatamente a raccogliere quante pi\u00f9 informazioni possibili sulla malattia. Scoprirono che non c'erano molte informazioni disponibili: non c'era modo di effettuare test definitivi per la malattia, nessun finanziamento per la ricerca sulla Progeria e nessuna organizzazione che sostenesse i bambini con Progeria. Cos\u00ec nel 1999, riunirono familiari, amici e colleghi e fondarono la Progeria Research Foundation per trovare la causa, il trattamento e la cura della Progeria.<\/p>\n
Da allora, centinaia di volontari dedicati si sono uniti al team PRF per contribuire a far progredire il campo della ricerca sulla Progeria a un ritmo straordinario. Il consiglio di amministrazione, il consiglio consultivo, i membri del comitato, i dirigenti aziendali, gli avvocati, i contabili, i grafici e i rappresentanti delle pubbliche relazioni di PRF dedicano tutti il loro tempo, la loro energia e il loro talento a PRF gratuitamente per garantire che si spenda meno in costi amministrativi e di pi\u00f9 per aumentare la consapevolezza e trovare una cura per la Progeria. Fai clic sui link a sinistra per leggere di pi\u00f9 sul nostro gruppo principale e anche per leggere di molti altri nostri eroi, I creatori di miracoli della PRF<\/a>.<\/p>\n Italiano: [\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][\/et_pb_column][\/et_pb_section][et_pb_section fb_built=\u201d1\u2033 module_class=\u201dfooter\u201d _builder_version=\u201d4.21.0\u2033 background_color=\u201d#29327a\u201d custom_margin=\u201d-2px|||||\u201d custom_padding=\u201d0|0px|0|0px|false|false\u201d z_index_tablet=\u201d500\u2033 border_width_top=\u201d12px\u201d border_color_top=\u201d#00b2e2\u2033 global_module=\u201d133\u2033 locked=\u201doff\u201d global_colors_info=\u201d{}\u201d][et_pb_row column_structure=\u201d1_4,1_4,1_2\u2033 make_equal=\u201don\u201d module_class=\u201d et_pb_row_fullwidth\u201d _builder_version=\u201d4.16\u2033 width=\u201d89%\u201d width_tablet=\u201d80%\u201d width_phone=\u201d\u201d width_last_edited=\u201don|desktop\u201d max_width=\u201d89%\u201d 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global_colors_info=\u201d{}\u201d][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>","protected":false},"excerpt":{"rendered":" Italiano: [et_pb_section fb_built=\u201d1\u2033 fullwidth=\u201don\u201d disabled_on=\u201doff|off|off\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 title_font_size=\u201d55\u2033 background_color=\u201d#29327a\u201d background_image=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2019\/04\/About-Header.jpg\u201d background_position=\u201dcenter_left\u201d custom_padding=\u201d11.5vw||11.5vw||true\u201d custom_padding_tablet=\u201d\u201d custom_padding_phone=\u201d|56px||\u201d custom_padding_last_edited=\u201don|desktop\u201d title_font_size_tablet=\u201d45px\u201d title_font_size_phone=\u201d40px\u201d title_font_size_last_edited=\u201don|phone\u201d z_index_tablet=\u201d500\u2033 custom_css_main_element=\u201dbackground-position: center 18% !important;\u201d global_colors_info=\u201d{}\u201d] La nostra gente [\/et_pb_fullwidth_header][\/et_pb_section][et_pb_section fb_built=\u201d1\u2033 use_custom_gutter=\u201don\u201d gutter_width=\u201d1\u2033 specialty=\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=\u201dsidebar-secondary-nav\u201d module_class=\u201dhandprint-bg\u201d _builder_version=\u201d4.16\u2033 background_image=\u201dhttps:\/\/www.progeriaresearch.org\/wp-content\/uploads\/2019\/04\/blue-handprint-only.png\u201d parallax=\u201don\u201d parallax_method=\u201doff\u201d inner_width=\u201d100%\u201d inner_max_width=\u201d100%\u201d custom_padding=\u201d0|0px|54px|0px|false|false\u201d z_index_tablet=\u201d500\u2033 border_width_top=\u201d10px\u201d border_color_top=\u201d#8fd2ed\u201d use_custom_width=\u201don\u201d width_unit=\u201doff\u201d custom_width_percent=\u201d100%\u201d global_colors_info=\u201d{}\u201d][et_pb_column type=\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":"\nIscrizione<\/h2>\n
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