[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column width="2/3"][vc_column_text]The Cullere’s lives changed forever when their son Benji, just 15 months old, was diagnosed with MPS1 Hurler Syndrome. This rare genetic...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]Video courtesy of 1440 Film Co.[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_video link="https://player.vimeo.com/video/783045440?badge=0&autopause=0&player_id=0&app_id=58479`` frameborder=``0`` allow=``autoplay; fullscreen; picture-in-picture; clipboard-write; encrypted-media; web-share`` referrerpolicy=``strict-origin-when-cross-origin"][/vc_column][/vc_row]...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]Video courtesy of 1440 Film Co.[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_video link="https://player.vimeo.com/video/1127569121?badge=0&autopause=0&player_id=0&app_id=58479`` frameborder=``0`` allow=``autoplay; fullscreen; picture-in-picture; clipboard-write; encrypted-media; web-share`` referrerpolicy=``strict-origin-when-cross-origin"][/vc_column][/vc_row]...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column width="2/3"][vc_column_text]Luca and his twin brother were born prematurely at 26 weeks. Both boys spent the first four months of their lives in...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]Video courtesy of 1440 Film Co.[/vc_column_text][vc_empty_space][vc_video link="https://vimeo.com/849573581?share=copy"][/vc_column][/vc_row]...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]Video courtesy of 1440 Film Co.[/vc_column_text][vc_empty_space][vc_video link="https://vimeo.com/438272096?share=copy"][/vc_column][/vc_row]...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]Video courtesy of 1440 Film Co.[/vc_column_text][vc_empty_space][vc_video link="https://vimeo.com/783045440?share=copy"][/vc_column][/vc_row]...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]In 2020 when Raymond was just 15 years old, he was diagnosed with Spindle Cell Sarcoma in his leg. Spindle Cell Sarcoma is...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]For the Boulanger family, the Ronald McDonald House of Delaware has been a “home-away-from-home” for over 20 years. Shawna has Osteogenesis Imperfecta, also...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text]Sixteen-year-old Marissa Faust is one of five people in the world with her diagnosis. The unnamed syndrome is connected with a gene, HNRNPR,...