{"id":5,"date":"2018-06-01T00:00:00","date_gmt":"2018-06-01T00:00:00","guid":{"rendered":"https:\/\/cota1.wpengine.com\/cotaforarabella\/our-story\/"},"modified":"2023-11-29T16:49:31","modified_gmt":"2023-11-29T16:49:31","slug":"our-story","status":"publish","type":"page","link":"https:\/\/cota.org\/cotaforarabella\/our-story\/","title":{"rendered":"Our Story"},"content":{"rendered":"<p>Arabella, now 14, went to her 11-year-old well care exam expecting to get sports forms completed for school and routine vaccinations.&nbsp; Instead, she was quickly referred to a local nephrologist after blood and urine tests were abnormal.&nbsp; A biopsy revealed that Arabella has collapsing variant FSGS, a rare kidney disease with no cure.&nbsp; From August 2016 through June 2017, doctors tried to achieve remission of her disease.&nbsp; Unfortunately, she experienced a rapid (and again unexpected) decline in her kidney function and in June 2017, her family transferred her care to Cincinnati Children&rsquo;s Hospital Medical Center.&nbsp; Within two weeks, she had a peritoneal dialysis catheter placed and by the end of July, she was on dialysis.&nbsp; Arabella remained on dialysis in her home for 10 hours each night until December 2018, when she received a kidney transplant, donated to her by her mom. &nbsp;She will be on medication and will be closely followed for the rest of her life for her kidney disease and to maximize the life of her transplant.&nbsp;&nbsp;<\/p>\n<p>Arabella&rsquo;s family has chosen to work with the Children&#8217;s Organ Transplant Association (COTA), which helps children and young adults who need a life-saving transplant by providing fundraising assistance and family support. COTA is the nation&rsquo;s only fundraising organization solely dedicated to raising life-saving dollars in honor of transplant-needy children and young adults. Because of Arabella&#8217;s COTA campaign, she will have much needed assistance available to her for the remainder of her life.<\/p>\n<p>How can you help?<\/p>\n<p>Please make a donation to COTA today. 100% of each contribution made to COTA in Arabella&rsquo;s honor helps assist with transplant-related expenses. Gifts to COTA are tax deductible to the fullest extent of the law.<\/p>\n<p>Check to see if your employer provides a matching gift, which is often accomplished by you submitting a short form. Matching gifts are an excellent way to increase the power of each individual gift. Click on &#8220;see if your company will match your gift&#8221; under the GIVE NOW button to learn more.<\/p>\n<p>Please help spread the word. There is an exponential level of power in friends telling friends and each one contributing even a small amount to COTA in Arabella&#8217;s honor.<\/p>\n<p>Join &ldquo;Arabella&rsquo;s Army&rdquo;&mdash;a select group of individuals who will work with our volunteers to reach the goal. To learn more, contact us on Facebook at <a href=\"https:\/\/www.facebook.com\/ArabellasArmy\/\">https:\/\/www.facebook.com\/ArabellasArmy\/<\/a>.&nbsp;<\/p>\n<p>As the volunteer group dedicated to this cause, we will be posting upcoming events to help raise funds as well as posting specific updates on Arabella&rsquo;s progress toward a transplant. Check back for updates!<\/p>\n<p>For more updates on Arabella&rsquo;s progress, follow and share on&nbsp;<a href=\"https:\/\/www.facebook.com\/ArabellasArmy\/\">https:\/\/www.facebook.com\/ArabellasArmy\/<\/a>.&nbsp;Thank you from Arabella and her family and friends!<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Arabella, now 14, went to her 11-year-old well care exam expecting to get sports forms completed for school and routine vaccinations.&nbsp; Instead, she was quickly referred to a local nephrologist after blood and urine tests were abnormal.&nbsp; A biopsy revealed that Arabella has collapsing variant FSGS, a rare kidney disease with no cure.&nbsp; From August [&hellip;]<\/p>\n","protected":false},"author":0,"featured_media":60,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-5","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/cota.org\/cotaforarabella\/wp-json\/wp\/v2\/pages\/5","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/cota.org\/cotaforarabella\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/cota.org\/cotaforarabella\/wp-json\/wp\/v2\/types\/page"}],"replies":[{"embeddable":true,"href":"https:\/\/cota.org\/cotaforarabella\/wp-json\/wp\/v2\/comments?post=5"}],"version-history":[{"count":0,"href":"https:\/\/cota.org\/cotaforarabella\/wp-json\/wp\/v2\/pages\/5\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/cota.org\/cotaforarabella\/wp-json\/wp\/v2\/media\/60"}],"wp:attachment":[{"href":"https:\/\/cota.org\/cotaforarabella\/wp-json\/wp\/v2\/media?parent=5"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}