{"id":468,"date":"2019-10-13T15:23:25","date_gmt":"2019-10-13T20:23:25","guid":{"rendered":"https:\/\/www.blog.carriewrites.net\/?p=468"},"modified":"2019-10-13T15:25:22","modified_gmt":"2019-10-13T20:25:22","slug":"symbrachydactlyprinted-in-the-republican-october-2019","status":"publish","type":"post","link":"https:\/\/www.blog.carriewrites.net\/?p=468","title":{"rendered":"Symbrachydactly"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">printed in the Republican October 2019<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">This past summer, my mother came in contact <br> with a family whose daughter has the same hand <br> deformity as she does, called symbrachydactly. It is a <br> congenital abnormality characterized by missing <br> limbs, hands or feet. In many cases bones are <br> missing along with fingers or toes. The hand may <br> have small stumps of soft tissue where fingers would <br> be. The cause is unknown, but could be caused by a <br> loss of blood supply in the development of the arm or <br> foot during pregnancy. Generally, children born with <br> symbrachydactly are able to adapt to their physical                          limitations and experience a full life. The limb <br> differences occur in 30,000 to 40,000 births.<br><br> In Michigan, a family formed a nonprofit <br> organization to raise awareness and celebrate <br> children born with symbrachydactly. The Lucky Fin is <br> dedicated to being a parent support network, and <br> provides medical resources and education on limb <br> differences. It also holds events and provides <br> financial support for children to attend specialized <br> camps and provide prosthetics.<br> <br>My mother has always taught me to be <br> independent and not let my disabilities get in the way <br> of what I want in life. She has always not let her own <br> deformity stop her from being successful in her own <\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>printed in the Republican October 2019 This past summer, my mother came in contact with a family whose daughter has the same hand deformity as she does, called symbrachydactly. It is a congenital abnormality characterized by missing limbs, hands or feet. In many cases bones are missing along with fingers or toes. The hand may [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-468","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=\/wp\/v2\/posts\/468","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=468"}],"version-history":[{"count":2,"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=\/wp\/v2\/posts\/468\/revisions"}],"predecessor-version":[{"id":470,"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=\/wp\/v2\/posts\/468\/revisions\/470"}],"wp:attachment":[{"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=468"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=468"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.blog.carriewrites.net\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=468"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}