{"id":21,"date":"2021-02-26T00:00:00","date_gmt":"2021-02-26T00:00:00","guid":{"rendered":"https:\/\/cota1.wpengine.com\/cotaforteamemmaa\/2021\/02\/26\/march-is-national-kidney-awareness-month\/"},"modified":"2021-02-26T00:00:00","modified_gmt":"2021-02-26T00:00:00","slug":"march-is-national-kidney-awareness-month","status":"publish","type":"post","link":"https:\/\/cota.org\/cotaforteamemmaa\/2021\/02\/26\/march-is-national-kidney-awareness-month\/","title":{"rendered":"March is National Kidney Awareness Month"},"content":{"rendered":"<p>March is National Kidney Awareness Month!&nbsp;<\/p>\n<p>1 in 3 American adults have kidney disease.&nbsp;<\/p>\n<p>37 million people in America have kidney disease, and most don&#8217;t know it.&nbsp;<\/p>\n<p>100,000 people are on the kidney transplant waiting list.&nbsp;<\/p>\n<p>Treatment for kidney failure is either dialysis or a kidney transplant.&nbsp;<\/p>\n<p>Emma was born in kidney failure with a diagnosis of multi-cystic dysplastic kidney disease.&nbsp; She only formed one kidney in utero and it was full of cysts and non-functional.&nbsp; She was born not urinating and in end stage renal failure (ESRD).&nbsp; She has been on dialysis since she was 5 days old.&nbsp; She is currently preparing for a kidney transplant hopefully this summer, her mother Tabatha is planned to be her living kidney donor.&nbsp;<\/p>\n<p>Kidney disease will be a lifelong disease and journey for Emma.&nbsp; Once transplanted she will be on anti-rejection medications for the rest of her life.&nbsp; A living kidney will not last Emma her entire lifetime, she will most likely need 2 or 3 kidney transplants during her lifetime.&nbsp;&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>March is National Kidney Awareness Month!&nbsp; 1 in 3 American adults have kidney disease.&nbsp; 37 million people in America have kidney disease, and most don&#8217;t know it.&nbsp; 100,000 people are on the kidney transplant waiting list.&nbsp; Treatment for kidney failure is either dialysis or a kidney transplant.&nbsp; Emma was born in kidney failure with a [&hellip;]<\/p>\n","protected":false},"author":0,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-21","post","type-post","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/cota.org\/cotaforteamemmaa\/wp-json\/wp\/v2\/posts\/21","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/cota.org\/cotaforteamemmaa\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/cota.org\/cotaforteamemmaa\/wp-json\/wp\/v2\/types\/post"}],"replies":[{"embeddable":true,"href":"https:\/\/cota.org\/cotaforteamemmaa\/wp-json\/wp\/v2\/comments?post=21"}],"version-history":[{"count":0,"href":"https:\/\/cota.org\/cotaforteamemmaa\/wp-json\/wp\/v2\/posts\/21\/revisions"}],"wp:attachment":[{"href":"https:\/\/cota.org\/cotaforteamemmaa\/wp-json\/wp\/v2\/media?parent=21"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}