{"id":987495433,"date":"2024-04-03T19:29:48","date_gmt":"2024-04-03T19:29:48","guid":{"rendered":"https:\/\/nwdproduction.com\/ats\/?p=987495433"},"modified":"2024-04-10T20:02:29","modified_gmt":"2024-04-10T20:02:29","slug":"patrick-foster","status":"publish","type":"post","link":"https:\/\/nwdproduction.com\/ats\/2024\/04\/03\/patrick-foster\/","title":{"rendered":"Patrick Foster"},"content":{"rendered":"\n[et_pb_section fb_built=&#8221;1&#8243; theme_builder_area=&#8221;post_content&#8221; _builder_version=&#8221;4.24.2&#8243; _module_preset=&#8221;default&#8221; custom_padding=&#8221;1px|||||&#8221;][et_pb_row _builder_version=&#8221;4.24.2&#8243; _module_preset=&#8221;default&#8221; theme_builder_area=&#8221;post_content&#8221;][et_pb_column _builder_version=&#8221;4.24.2&#8243; _module_preset=&#8221;default&#8221; type=&#8221;4_4&#8243; theme_builder_area=&#8221;post_content&#8221;][et_pb_image src=&#8221;https:\/\/nwdproduction.com\/ats\/wp-content\/uploads\/2024\/04\/patrick-foster.jpg&#8221; _builder_version=&#8221;4.24.2&#8243; _module_preset=&#8221;default&#8221; theme_builder_area=&#8221;post_content&#8221; alt=&#8221;patrick foster&#8221; title_text=&#8221;patrick-foster&#8221; hover_enabled=&#8221;0&#8243; sticky_enabled=&#8221;0&#8243;][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=&#8221;4.24.2&#8243; _module_preset=&#8221;default&#8221; theme_builder_area=&#8221;post_content&#8221;][et_pb_column _builder_version=&#8221;4.24.2&#8243; _module_preset=&#8221;default&#8221; type=&#8221;4_4&#8243; theme_builder_area=&#8221;post_content&#8221;][et_pb_text _builder_version=&#8221;4.24.2&#8243; _module_preset=&#8221;default&#8221; theme_builder_area=&#8221;post_content&#8221; hover_enabled=&#8221;0&#8243; sticky_enabled=&#8221;0&#8243;]<p>When Cathi Foster was six months pregnant, she learned her baby would be born with a congenital heart defect. Three days after her son Patrick arrived, surgery patched a hole between two chambers of his heart and widened two sections of his pulmonary artery.<\/p>\n<p>There was more stressful news 15 months later: Patrick suffered from Diamond Blackfan Anemia, a rare bone marrow disorder Cathi unknowingly carried. The years that followed were punctuated by blood transfusions and steroid treatments. Still, the outlook was bleak.<\/p>\n<p>\u201cWe were told he wouldn\u2019t get past six years old, he would be short in stature and mentally handicapped,\u201d Cathi recalls. But Patrick surprised them all.<\/p>\n<p>At 16, Patrick stands 5-feet-eight inches tall and is looking ahead to college.<\/p>\n<p>A turning point came in 2015 when he received a donated heart valve to further repair and strengthen his cardiac function. Six months after the surgery, his health improved, and he grew six inches. \u201cHe is doing phenomenal,\u201d Cathi says. \u201cHe\u2019s healthier than some of his peers.\u201d<\/p>\n<p>Cathi says she was astonished the heart valve Patrick received was human, not artificial. She thought about the donor, the donor family and the generous gift her son had received. She wondered if additional information was possible and whether they could meet the donor family.<\/p>\n<p>The donor family preferred not to meet, instead sending a letter to the Fosters. It read, in part, \u201cWe are grateful that we had 45 years with [our son]. He was very loving and generous. He had many friends and family members who remember him that way. It makes us happy to know that Patrick and his family can live a more normal life with one part of [our son] working for him.\u201d<\/p>\n<p>The Fosters are thankful for the donor family\u2019s strength and courage in consenting to donation and hope one day to meet the family whose son gave Patrick the gift of life through donation.<\/p>\n<p>Although Patrick can\u2019t tell them in person, \u201cI want them to understand I deeply, deeply appreciate it,\u201d he says. \u201cI\u2019m glad they were willing to say \u2018yes\u2019 and do that for me. I can\u2019t imagine how hard that had to be.\u201d<\/p>\n<p>In addition to preparing for Kuyper College in Michigan\u2014with plans to become a youth minister\u2014Patrick has been living life to the fullest. He visited Vietnam for 10 days as part of a church group, helping Vietnamese youth with English and honing their soccer skills. He also has raised $20,000 on behalf of the Children\u2019s Miracle Network and advocates for donation whenever he can.<\/p>\n<p>\u201cI want to give hope to other people,\u201d he says. \u201cI\u2019m super grateful for donation. It has kept me going.\u201d<\/p>\n<p>For more information on Patrick\u2019s journey, take a look at \u201c<a href=\"https:\/\/www.facebook.com\/Patricks-Fight-with-DBA-311488185546798\/\">Patrick\u2019s Fight With DBA<\/a>,\u201d his special blog on Facebook.<\/p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]\n","protected":false},"excerpt":{"rendered":"<p>When Cathi Foster was six months pregnant, she learned her baby would be born with a congenital heart defect. Three days after her son Patrick arrived, surgery patched a hole between two chambers of his heart and widened two sections of his pulmonary artery. There was more stressful news 15 months later: Patrick suffered from [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":987495436,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"categories":[11],"tags":[],"class_list":["post-987495433","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-donors"],"_links":{"self":[{"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/posts\/987495433","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/comments?post=987495433"}],"version-history":[{"count":4,"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/posts\/987495433\/revisions"}],"predecessor-version":[{"id":987495668,"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/posts\/987495433\/revisions\/987495668"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/media\/987495436"}],"wp:attachment":[{"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/media?parent=987495433"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/categories?post=987495433"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nwdproduction.com\/ats\/wp-json\/wp\/v2\/tags?post=987495433"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}