[fusion_builder_container background_color=”” background_image=”” background_parallax=”none” enable_mobile=”no” parallax_speed=”0.3″ background_repeat=”no-repeat” background_position=”left top” video_url=”” video_aspect_ratio=”16:9″ video_webm=”” video_mp4=”” video_ogv=”” video_preview_image=”” overlay_color=”” overlay_opacity=”0.5″ video_mute=”yes” video_loop=”yes” fade=”no” border_size=”0px” border_color=”” border_style=”” padding_top=”20″ padding_bottom=”20″ padding_left=”0″ padding_right=”0″ hundred_percent=”no” equal_height_columns=”no” hide_on_mobile=”no” menu_anchor=”” class=”” id=””][fusion_builder_row][fusion_builder_column type=”2_5″ last=”no” spacing=”yes” center_content=”no” hide_on_mobile=”no” background_color=”” background_image=”” background_repeat=”no-repeat” background_position=”left top” hover_type=”none” link=”” border_position=”all” border_size=”0px” border_color=”” border_style=”solid” padding=”” margin_top=”” margin_bottom=”” animation_type=”0″ animation_direction=”down” animation_speed=”0.1″ animation_offset=”” class=”” id=””][fusion_imageframe lightbox=”no” lightbox_image=”” style_type=”bottomshadow” hover_type=”none” bordercolor=”#ededed” bordersize=”3px” borderradius=”0″ stylecolor=”” align=”none” link=”” linktarget=”_self” animation_type=”0″ animation_direction=”down” animation_speed=”0.1″ animation_offset=”” hide_on_mobile=”no” class=”” id=””] 
[/fusion_imageframe][/fusion_builder_column][fusion_builder_column type=”3_5″ last=”yes” spacing=”yes” center_content=”no” hide_on_mobile=”no” background_color=”” background_image=”” background_repeat=”no-repeat” background_position=”left top” hover_type=”none” link=”” border_position=”all” border_size=”0px” border_color=”” border_style=”” padding=”” margin_top=”” margin_bottom=”” animation_type=”” animation_direction=”” animation_speed=”0.1″ animation_offset=”” class=”” id=””][fusion_text]In May of 2013, Owen was diagnosed with T-cell Lymphoblastic Lymphoma at just 2 .5 years old. The Orr’s spent years taking care of Owen as a one income family; bringing him from Penn Yan to Rochester for all of his treatments. Owen loved to help with his treatment, vitals and blood work and wants to be a doctor when he grows up. Just recently Owen finished his last clinical chemo treatment! He will check in monthly for the next 6 months, then every 2-3 months, then every 6 months. As remission goes they plan to have his port removed in January. While he still struggles with residual pain and weakness, Owen started all-day kindergarten this year. Mom says “We were really struggling just to buy groceries and gas so I finally filled out the application for IACKids after holding onto it for more than a year. We found customized support for what we really needed and people that really care. We feel blessed that IACkids came into our lives.[/fusion_text][fusion_button link=”/meet-the-iackids” color=”default” size=”” stretch=”default” type=”” shape=”” target=”_self” title=”” gradient_colors=”|” gradient_hover_colors=”|” accent_color=”” accent_hover_color=”” bevel_color=”” border_width=”1px” icon=”” icon_position=”left” icon_divider=”no” modal=”” animation_type=”fade” animation_direction=”up” animation_speed=”1″ animation_offset=”” alignment=”left” class=”” id=””]BACK TO MEET THE IACKIDS[/fusion_button][/fusion_builder_column][/fusion_builder_row][/fusion_builder_container]
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