{"id":42546,"date":"2024-01-17T10:00:00","date_gmt":"2024-01-17T16:00:00","guid":{"rendered":"https:\/\/differentdream.com\/?p=42546"},"modified":"2024-01-17T10:00:00","modified_gmt":"2024-01-17T16:00:00","slug":"ea-tef-update-oliver","status":"publish","type":"post","link":"https:\/\/jolenephilo.com\/staging\/ea-tef-update-oliver\/","title":{"rendered":"An EA\/TEF Update: Oliver\u2019s Story"},"content":{"rendered":"\n[et_pb_section fb_built=&#8221;1&#8243; fullwidth=&#8221;on&#8221; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_fullwidth_post_title featured_image=&#8221;off&#8221; _builder_version=&#8221;4.16&#8243; title_font=&#8221;||||||||&#8221; title_text_color=&#8221;#42313A&#8221; title_font_size=&#8221;40px&#8221; meta_font_size=&#8221;14px&#8221; background_color=&#8221;#B4DBC0&#8243; custom_padding=&#8221;50px||50px||false|false&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_fullwidth_post_title][\/et_pb_section][et_pb_section fb_built=&#8221;1&#8243; specialty=&#8221;on&#8221; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;0px||0px|||&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;3_4&#8243; specialty_columns=&#8221;3&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_row_inner _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_image src=&#8221;@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9mZWF0dXJlZF9pbWFnZSIsInNldHRpbmdzIjp7fX0=@&#8221; align=&#8221;center&#8221; _builder_version=&#8221;4.16&#8243; _dynamic_attributes=&#8221;src&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_image][et_pb_text _builder_version=&#8221;4.22.2&#8243; global_colors_info=&#8221;{}&#8221;]<p><em>An <\/em><a href=\"https:\/\/www.childrenscolorado.org\/conditions-and-advice\/conditions-and-symptoms\/conditions\/esophageal-atresia\/\"><em><span style=\"text-decoration: underline\">EA\/TEF<\/span><\/em><\/a><em> update on families who told their stories in previous EA\/TEF Awareness Months means a lot to our community. Today, busy mom and guest blogger, Kelly Simpson is back with an update on her son Oliver, <\/em><a href=\"https:\/\/differentdream.com\/2023\/01\/life-turns-out-differently\/\"><em><span style=\"text-decoration: underline\">whom readers met during EA\/TEF Awareness Month, 2023<\/span>.<\/em><\/a><em> I hope you enjoy hearing about his progress in the past year as much as I did.<\/em><\/p>\n<p><strong>Oliver\u2019s Story<\/strong><\/p>\n<ul>\n<li>Normal ultrasounds and no issues caught or seen during pregnancy.<\/li>\n<li>Born at 39 weeks.<\/li>\n<li>C-section due to <span style=\"text-decoration: underline\"><a href=\"https:\/\/miraclecord.com\/news\/coning-during-pregnancy\/\">coning<\/a><\/span>.<\/li>\n<li>Born unable to swallow: OBGYN and Oliver\u2019s doctor on call decided to have Oliver transferred to <span style=\"text-decoration: underline\"><a href=\"https:\/\/nortonhealthcare.com\/location\/hospitals\/norton-childrens-hospital\/\">Norton&#8217;s Children&#8217;s Hospital<\/a><\/span> in Kentucky.<\/li>\n<li>Diagnosed with Tracheoesophageal Fistula (EA\/TEF) Type C.<\/li>\n<li>EA\/TEF repair two days after birth.<\/li>\n<li>19-day stay in the NICU.<\/li>\n<\/ul>\n<p><strong>Life after the NICU:<\/strong><\/p>\n<ul>\n<li>At 6 weeks Oliver started to have problems swallowing milk. His pediatrician suggested an Ear, Nose, and Throat doctor. A swallow test confirmed narrowing of the esophagus. Esophageal dilation (stretching of the esophagus) at 6 weeks, 8 weeks, and again at 12 weeks.<\/li>\n<li>At 6 weeks he was also diagnosed with <span style=\"text-decoration: underline\"><a href=\"https:\/\/www.hopkinsmedicine.org\/health\/conditions-and-diseases\/tracheomalacia\">tracheomalacia<\/a><\/span> or floppy trachea, which leads to extra movement with crying, laughing, or coughing. Most kids sound like a goose, and cough is deep sounding like a bark.<\/li>\n<li>At 4 months, he was escorted to Norton\u2019s Children for respiratory distress. He was placed in the ICU for a week with aid from a ventilator.<\/li>\n<li>At 6 months old, he had a second ICU stay for a week for respiratory distress, aid from a ventilator.<\/li>\n<li>At 10 months old, he had a 4-day ICU stay for respiratory distress.<\/li>\n<li>Received an airway clearance vest to help keep his airway clear.<\/li>\n<li>Age 3 included multiple cases of pneumonia<\/li>\n<li>Age 4 saw multiple cases of pneumonia<\/li>\n<\/ul>\n<p><strong>An EA\/TEF update since last year\u2019s story:<\/strong><\/p>\n<ul>\n<li>Oliver is almost 5 years old.<\/li>\n<li>He is healthy and in the 98<span style=\"font-size: x-small\"><sup>th<\/sup><\/span> percentile for both weight and height. What a blessing!<\/li>\n<li>He has not needed an esophageal dilation since he was 12 weeks old.<\/li>\n<li>Eats and drinks normally with no restrictions.<\/li>\n<li>Does require a little extra water with meals just in case.<\/li>\n<li>Loves to run!<\/li>\n<li>Starts Kindergarten in the Fall!<\/li>\n<\/ul>\n<p>What a wonderful EA\/TEF update!<\/p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; background_color=&#8221;#b4dbc0&#8243; custom_padding=&#8221;20px|20px|20px|20px|false|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_blurb title=&#8221;@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9hdXRob3IiLCJzZXR0aW5ncyI6eyJiZWZvcmUiOiJCeSAiLCJhZnRlciI6IiIsIm5hbWVfZm9ybWF0IjoiZGlzcGxheV9uYW1lIiwibGluayI6Im9uIiwibGlua19kZXN0aW5hdGlvbiI6ImF1dGhvcl9hcmNoaXZlIn19@&#8221; image=&#8221;https:\/\/differentdream.com\/wp-content\/uploads\/2023\/01\/kelly-simpson.jpg&#8221; icon_placement=&#8221;left&#8221; image_icon_width=&#8221;100px&#8221; content_max_width=&#8221;800px&#8221; _builder_version=&#8221;4.22.2&#8243; _dynamic_attributes=&#8221;title&#8221; header_font=&#8221;Rubik|500|||||||&#8221; header_text_color=&#8221;#44465f&#8221; header_font_size=&#8221;14px&#8221; header_line_height=&#8221;32px&#8221; body_font=&#8221;Rubik||||||||&#8221; body_text_color=&#8221;rgba(0,6,69,0.6)&#8221; body_link_text_color=&#8221;#ffffff&#8221; custom_css_main_element=&#8221;font-weight: 400;&#8221; border_radii_image=&#8221;on|100px|100px|100px|100px&#8221; border_color_all_image=&#8221;#ffffff&#8221; box_shadow_style_image=&#8221;preset1&#8243; box_shadow_vertical_image=&#8221;20px&#8221; box_shadow_blur_image=&#8221;40px&#8221; box_shadow_color_image=&#8221;rgba(68,70,95,0.27)&#8221; image_max_width=&#8221;100px&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<p>Kelly has lived her whole life in Kentucky. She and her husband, Jeremy, have a four-year-old son, who, born during a deployment, was diagnosed with tracheoesophageal fistula. She has always felt a calling to serve others and is living the dream as an Army wife, middle school teacher, and now, as an encourager to those who are living a dream different than they had planned.<\/p>[\/et_pb_blurb][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_comments _builder_version=&#8221;4.16&#8243; custom_button=&#8221;on&#8221; button_text_color=&#8221;#42313A&#8221; button_bg_color=&#8221;#EBDCB2&#8243; global_colors_info=&#8221;{}&#8221;][\/et_pb_comments][\/et_pb_column_inner][\/et_pb_row_inner][\/et_pb_column][et_pb_column type=&#8221;1_4&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_sidebar _builder_version=&#8221;4.16&#8243; 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type=&#8221;1_2&#8243; module_class=&#8221;horizontal_optin_column_1&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_text_align=&#8221;right&#8221; header_text_color=&#8221;#45107a&#8221; header_3_font=&#8221;Dancing Script|700|||||||&#8221; header_3_text_align=&#8221;center&#8221; header_3_text_color=&#8221;#B4DBC0&#8243; header_3_font_size=&#8221;45px&#8221; custom_margin=&#8221;10px||||false|false&#8221; custom_padding=&#8221;||||false|false&#8221; global_colors_info=&#8221;{}&#8221;]<h3>Subscribe for Updates from Jolene<\/h3>[\/et_pb_text][\/et_pb_column][et_pb_column type=&#8221;1_2&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_signup mailchimp_list=&#8221;JolenePhilo|89f719a52b&#8221; layout=&#8221;bottom_top&#8221; first_name_fullwidth=&#8221;off&#8221; last_name_field=&#8221;off&#8221; email_fullwidth=&#8221;off&#8221; 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read_more_text_color=&#8221;#B6452C&#8221; read_more_font_size=&#8221;12px&#8221; pagination_text_color=&#8221;#B6452C&#8221; pagination_font_size=&#8221;20px&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_blog][\/et_pb_column][\/et_pb_row][\/et_pb_section]\n","protected":false},"excerpt":{"rendered":"<p>Kelly Simpson gives an EA\/TEF update for Different Dream readers and other EA\/TEF parents about her son&#8217;s progress.<\/p>\n","protected":false},"author":1,"featured_media":42785,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"2880","footnotes":""},"categories":[3559,3615,3561],"tags":[3826,4207],"class_list":["post-42546","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-different-dream","category-encouragement","category-special-needs-parenting","tag-ea-tef","tag-personal-stories"],"yoast_head":"<!-- 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