
define('DISABLE_WP_CRON', true);{"id":4305,"date":"2012-06-08T13:19:15","date_gmt":"2012-06-08T03:19:15","guid":{"rendered":"http:\/\/sh1ft.org\/blog\/?p=4305"},"modified":"2012-06-11T16:44:15","modified_gmt":"2012-06-11T06:44:15","slug":"the-next-chapter","status":"publish","type":"post","link":"http:\/\/sh1ft.org\/blog\/4305\/","title":{"rendered":"The Next Chapter."},"content":{"rendered":"<p>The call I received on Tuesday evening was expected, but early. 6 weeks early. <em>We&#8217;ve made an appointment for you to come in and see the team at the kids hospital on Thursday morning, is this a good time for you? <\/em><\/p>\n<p>I had pushed the thought of getting the results of Jovie&#8217;s last DNA test all the way to the back of my head, they weren&#8217;t due until the end of July and there was no point in worrying about it when it was still weeks away. Regan and I both suspected Rett Syndrome some 13 months ago, it was on the first referral from our pediatrician but I had not let myself self diagnose and go down that road unnecessarily. <\/p>\n<p>Walking into the observation room at the kid&#8217;s hospital yesterday, we&#8217;re met with familiar faces and some new ones. All friendly, all with knowing eyes. There&#8217;s Jovie&#8217;s file on the table and it&#8217;s got some weight to it, I think. They ask how Jovie&#8217;s been going (<em>Oh, I&#8217;ve been keeping an eye on her stair work and book flipping because she seems to be regressing again. No, she hasn&#8217;t had any seizures<\/em>) and what we&#8217;ve been up to in the 6 weeks since we last saw each other. <\/p>\n<p>We don&#8217;t fluff around much more when the Dr slowly asks me whether I remember what the last DNA test was for &#8211; as if I could of ever forgotten. She nods her head slowly and confirms our instincts were right &#8211; <strong>Jovie has Rett Syndrome<\/strong>. <\/p>\n<p><img loading=\"lazy\" decoding=\"async\" src=\"http:\/\/sh1ft.org\/blog\/wp-content\/uploads\/2012\/06\/jovie080612b.jpg\" alt=\"\" title=\"jovie080612b\" width=\"480\" height=\"480\" class=\"aligncenter size-full wp-image-4310\" srcset=\"http:\/\/sh1ft.org\/blog\/wp-content\/uploads\/2012\/06\/jovie080612b.jpg 480w, http:\/\/sh1ft.org\/blog\/wp-content\/uploads\/2012\/06\/jovie080612b-150x150.jpg 150w, http:\/\/sh1ft.org\/blog\/wp-content\/uploads\/2012\/06\/jovie080612b-300x300.jpg 300w\" sizes=\"auto, (max-width: 480px) 100vw, 480px\" \/><\/p>\n<p>I know alot of people have never heard of Rett Syndrome before &#8211; so here is a brief brief amateur summary from someone with approximately 24 hours experience (hello). Rett Syndrome is neurodevelopmental genetic disorder that is almost exclusive to girls. Every year in Australia, around 1 in 9,000 babies are born with Rett Syndrome. (In comparison to Autism with 1 in 88 children and Down Syndrome with 1 in 660). It causes issues with speech, fine motor, gross motor and growth, aswell as a myriad of other issues (e.g. scoliosis, seizures, hyperventilation, teeth grinding, difficulty swallowing). <\/p>\n<p>In our case, Jovie is able to walk but alot of girls are in wheelchairs. In some cases, they can speak a little but Jovie is unable to currently. 80% will experience seizures. They used to classify it as a degenerative disorder which can result in a shorten typical lifespan, however this is not the case. Yes, some do pass away but some do live long lives with Rett Syndrome.  <\/p>\n<p>One of the traits of Rett Syndrome is Autism, so at the moment we still believe she is Autistic but her diagnosis is Rett Syndrome. We&#8217;ll most likely assess for this again over the years. <\/p>\n<p>It is a random occurrence, not passed down through the family. No one could of detected it unless we were specifically looking for it. There is no current cure. <\/p>\n<p>The Dr is explaining that they found the spelling mistake within Jovie&#8217;s genetics and all eyes are on me, trying to process all this information and the reality of a new stage of our lives, of Jovie&#8217;s life. I&#8217;m all kinds of things in the next 45 minutes &#8211; relieved, sad, tired, happy to have the diagnosis, terrified, optimistic, brave, a wreck. I don&#8217;t cry, I leave that for later that night when I&#8217;m on my own and reality truly sets in, and the team of professionals offer their support as we leave the unit. <\/p>\n<p>Knowing what I know about Rett Syndrome so far, I&#8217;m a bit devastated, if I&#8217;m honest. I would be lying outright if I wasn&#8217;t sad about the diagnosis, I&#8217;m only human. Everyone has to find a pocket for their grief &#8211; whether it&#8217;s the loss of someone you loved, or your child getting a lifelong disorder diagnosed. There is value to that sadness, and you cannot move forward if you&#8217;re pushing that part of your heart away. <\/p>\n<p>However, knowing what I know about Jovie and about myself and our family, we&#8217;re going to be okay. It&#8217;s just going to be a process and always will be.<\/p>\n<p>So what next? Our appointment to the Rett Clinic at the kid&#8217;s hospital is in about a month. We continue to go to therapy and watch our for seizures and regression. Getting quotes to buy Jovie a wheelchair\/stroller. I&#8217;m embarking on a 100-day challenge to sort my own issues out before I burn out. And we continue to love and cherish our family. Now with added Rett&#8217;s. <\/p>\n","protected":false},"excerpt":{"rendered":"<p>The call I received on Tuesday evening was expected, but early. 6 weeks early. We&#8217;ve made an appointment for you to come in and see the team at the kids hospital on Thursday morning, is this a good time for you? I had pushed the thought of getting the results of Jovie&#8217;s last DNA test [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[17,30],"tags":[],"class_list":["post-4305","post","type-post","status-publish","format-standard","hentry","category-jovie","category-rett-syndrome"],"_links":{"self":[{"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/posts\/4305","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/comments?post=4305"}],"version-history":[{"count":24,"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/posts\/4305\/revisions"}],"predecessor-version":[{"id":4332,"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/posts\/4305\/revisions\/4332"}],"wp:attachment":[{"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/media?parent=4305"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/categories?post=4305"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/sh1ft.org\/blog\/wp-json\/wp\/v2\/tags?post=4305"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}