{"id":9970,"date":"2015-09-22T10:11:06","date_gmt":"2015-09-22T15:11:06","guid":{"rendered":"http:\/\/www.wheelchairmommy.com\/?p=9970"},"modified":"2015-09-22T10:09:56","modified_gmt":"2015-09-22T15:09:56","slug":"september-update-on-nathans-strabismus","status":"publish","type":"post","link":"http:\/\/www.wheelchairmommy.com\/closed\/2015\/september-update-on-nathans-strabismus\/","title":{"rendered":"September update on Nathan&#8217;s strabismus"},"content":{"rendered":"<p>My sweet boy had a follow-up with his eye doctor yesterday. The timing was good because his left eye was frequently bloodshot. She didn&#8217;t seem to think it was a concern.<\/p>\n<p>There is not much else to report. We WILL have to do surgery at some point. His vision seems stable. The glasses don&#8217;t seem to be changing his vision by much, maybe one line. We can patch if we want, which we will because his eye does straighten when we do.<\/p>\n<p>We see her and the retina specialist again in January.<\/p>\n<p><a href=\"http:\/\/www.wheelchairmommy.com\/wp-content\/uploads\/2015\/09\/IMG_4358.jpg\"><img decoding=\"async\" src=\"http:\/\/www.wheelchairmommy.com\/wp-content\/uploads\/2015\/09\/IMG_4358.jpg\" alt=\"\"><\/a>&nbsp;&nbsp;<br \/>\n<a href=\"http:\/\/www.wheelchairmommy.com\/wp-content\/uploads\/2015\/09\/IMG_4350.jpg\"><img decoding=\"async\" src=\"http:\/\/www.wheelchairmommy.com\/wp-content\/uploads\/2015\/09\/IMG_4350.jpg\" alt=\"\"><\/a>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>My sweet boy had a follow-up with his eye doctor yesterday. The timing was good because his left eye was frequently bloodshot. She didn&#8217;t seem to think it was a concern. There is not much else to report. We WILL have to do surgery at some point. His vision seems stable. The glasses don&#8217;t seem [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","jetpack_post_was_ever_published":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[132,355,370],"tags":[],"class_list":{"0":"post-9970","1":"post","2":"type-post","3":"status-publish","4":"format-standard","6":"category-family","7":"category-my-3-sons","8":"category-nf1-neurofibromatosis","9":"entry","10":"has-post-thumbnail"},"jetpack_sharing_enabled":true,"jetpack_featured_media_url":"","jetpack_shortlink":"https:\/\/wp.me\/p5zEve-2AO","_links":{"self":[{"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/posts\/9970","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/comments?post=9970"}],"version-history":[{"count":0,"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/posts\/9970\/revisions"}],"wp:attachment":[{"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/media?parent=9970"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/categories?post=9970"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.wheelchairmommy.com\/closed\/wp-json\/wp\/v2\/tags?post=9970"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}