{"id":8,"date":"2023-10-03T00:00:00","date_gmt":"2023-10-03T00:00:00","guid":{"rendered":"https:\/\/cota1.wpengine.com\/cotafortheradkidneykid\/2023\/10\/03\/this-is-us\/"},"modified":"2023-10-18T01:49:49","modified_gmt":"2023-10-18T01:49:49","slug":"this-is-us","status":"publish","type":"post","link":"https:\/\/cota.org\/cotafortheradkidneykid\/2023\/10\/03\/this-is-us\/","title":{"rendered":"This is Us"},"content":{"rendered":"<div class=\"adn ads\" data-message-id=\"#msg-a:r-1522882520264162106\" data-legacy-message-id=\"18af683dc56636d1\">\n<div class=\"gs\">\n<div class=\"\">\n<div id=\":sx\" class=\"ii gt\">\n<div id=\":so\" class=\"a3s aiL \">\n<div>Hi Rad Kidney Kid Fam,<\/div>\n<div>&nbsp;<\/div>\n<div>Some of you have been with us since the beginning, but our little dude&rsquo;s following has grown so much over the last year.<\/div>\n<div>&nbsp;<\/div>\n<div>So, for those of you new, this is us.<\/div>\n<div>&nbsp;<\/div>\n<div>Very late in Austyn&rsquo;s pregnancy, it was discovered that Conrad had a condition called LUTO. LUTO is rare, occurring in an estimated 2.2 of every 10,000 births.<\/div>\n<div>&nbsp;<\/div>\n<div>There are several types of lower urinary tract obstructions. Conrad&rsquo;s LUTO was from Posterior urethral valves, where a thin piece of tissue blocks the urethra. That&#8217;s it: one small piece of tissue caused stage 5 kidney failure in utero for our boy.<\/div>\n<div>&nbsp;<\/div>\n<div>Austyn was hospitalized for the last two months of the pregnancy. Conrad started dialysis on day 7 of life. He is among the first few children placed on CARPEDIEM at Texas Children&#8217;s Hospital. A hemodialysis machine that was created specifically for infants.<\/div>\n<div>&nbsp;<\/div>\n<div>Conrad spent over six months in the NICU, where he underwent several surgeries and many setbacks, but he finally came home at six months old.<\/div>\n<div>&nbsp;<\/div>\n<div>Our family spent almost two years in Texas receiving care from a dialysis center capable of caring for infants on dialysis. Being home has not been without its challenges and surgeries. The thing with dialysis is it&#8217;s a temporary lifeline, and there can be A LOT of complications.<\/div>\n<div>&nbsp;<\/div>\n<div>Our main goal has been to get Conrad big enough for a kidney transplant. Amazingly, Conrad is officially listed for transplant with Stanford Children&rsquo;s Hospital. They have some of the best outcomes in the world for pediatric kidney transplants. Words we dreamed of saying for such a long time.<\/div>\n<div>&nbsp;<\/div>\n<div>Unfortunately, after donor workups, we learned that neither of us can donate to Conrad.<\/div>\n<div>&nbsp;<\/div>\n<div>Now, we are searching for a living donor for our little guy. A living donor is Conrad&rsquo;s best option.<\/div>\n<div>&nbsp;<\/div>\n<div>In Conrad&rsquo;s case, a living donor gives the surgeon plenty of time to do a nephrectomy at the same time as his kidney transplant. Our team is trying to preserve his urine production and, therefore, his bladder.<\/div>\n<div>&nbsp;<\/div>\n<div>Fun fact: kidneys from living donors typically last much longer. Since Conrad could require more than one transplant in his lifetime, this is important.<\/div>\n<div>&nbsp;<\/div>\n<div>We are also currently listed on the deceased donor list with a long waiting time. Our team has explained that this option, specifically for Conrad, will have more complications and surgeries, most likely HD and bladder reconstruction.<\/div>\n<div>&nbsp;<\/div>\n<div>Most importantly, though, Conrad has been on HD a couple of times now, and they don&rsquo;t want to lose access because he will need that again in the future. Without access to dialysis or a kidney, there are no other options, and it&rsquo;s a stark reality we constantly juggle.<\/div>\n<div>&nbsp;<\/div>\n<div>So, ultimately, we are trusting our fantastic team and believing that God is placing it in someone&rsquo;s heart to donate a kidney to Conrad.<\/div>\n<div>&nbsp;<\/div>\n<div>Our little dude is such a fighter, and we are amazed every moment by the miracles we&rsquo;ve witnessed. Besides fighting for his life, Conrad is just your typical, wonderful 20-month-old boy. He loves Miss Rachel, being outside, climbing everything, and reading books.<\/div>\n<div>&nbsp;<\/div>\n<div>He also loves the water, rolling around his bed, and anything messy, but unfortunately, we have to restrict a lot of these things on dialysis. We look forward to the days when he has a kidney and can play outside and take his first bath! It will be a whole new life for us all!<\/div>\n<div>&nbsp;<\/div>\n<div>We&rsquo;re so overwhelmed with gratitude and love for such a fantastic community of support.<\/div>\n<div>&nbsp;<\/div>\n<div>This journey has broken and rebuilt us over and over again. We trust that God will continue to use and move others through Conrad&rsquo;s testament. Thank you for joining us and continuing to pray for our little dude&rsquo;s kidney bean!&nbsp;<\/div>\n<div>&nbsp;<\/div>\n<div>&nbsp;If you want to learn more about becoming Conrad&rsquo;s living kidney donor and our MIRACLE, please get in touch with our Kidney Transplant Program Manager- Gerri James, at 650-498-4905. For more information, check out the Rad Kidney Kid Page.<\/div>\n<div>&nbsp;<\/div>\n<div>With Love, The Rad Kidney Kid Fam<\/div>\n<div>&nbsp;<\/div>\n<div class=\"yj6qo\">&nbsp;<\/div>\n<div class=\"adL\">&nbsp;<\/div>\n<\/div>\n<\/div>\n<div class=\"hi\">&nbsp;<\/div>\n<\/div>\n<\/div>\n<div class=\"ajx\">&nbsp;<\/div>\n<\/div>\n<div class=\"gA gt acV\">\n<div class=\"gB xu\">\n<div class=\"ip iq\">\n<div id=\":t2\">&nbsp;<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Hi Rad Kidney Kid Fam, &nbsp; Some of you have been with us since the beginning, but our little dude&rsquo;s following has grown so much over the last year. &nbsp; So, for those of you new, this is us. &nbsp; Very late in Austyn&rsquo;s pregnancy, it was discovered that Conrad had a condition called LUTO. [&hellip;]<\/p>\n","protected":false},"author":0,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-8","post","type-post","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/cota.org\/cotafortheradkidneykid\/wp-json\/wp\/v2\/posts\/8","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/cota.org\/cotafortheradkidneykid\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/cota.org\/cotafortheradkidneykid\/wp-json\/wp\/v2\/types\/post"}],"replies":[{"embeddable":true,"href":"https:\/\/cota.org\/cotafortheradkidneykid\/wp-json\/wp\/v2\/comments?post=8"}],"version-history":[{"count":0,"href":"https:\/\/cota.org\/cotafortheradkidneykid\/wp-json\/wp\/v2\/posts\/8\/revisions"}],"wp:attachment":[{"href":"https:\/\/cota.org\/cotafortheradkidneykid\/wp-json\/wp\/v2\/media?parent=8"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}