{"id":2735,"date":"2015-04-20T15:18:03","date_gmt":"2015-04-20T19:18:03","guid":{"rendered":"http:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20.jpg"},"modified":"2015-04-20T15:18:03","modified_gmt":"2015-04-20T19:18:03","slug":"201570_por-20","status":"inherit","type":"attachment","link":"https:\/\/pj.rit.edu\/nppa\/201570_por-20\/","title":{"rendered":"201570_POR-20"},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","template":"","meta":[],"class_list":["post-2735","attachment","type-attachment","status-inherit","hentry","no-comments"],"description":{"rendered":"<p class=\"attachment\"><a href='https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20.jpg'><img loading=\"lazy\" decoding=\"async\" width=\"300\" height=\"200\" src=\"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-300x200.jpg\" class=\"attachment-medium size-medium\" alt=\"\" srcset=\"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-300x200.jpg 300w, https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-768x512.jpg 768w, https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-1024x683.jpg 1024w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n"},"caption":{"rendered":"<p>Chaney Roko, 34, is a single mother of two adopted children. Mary, 9, and her sister Kiera, 4, both have Arthrogryposis Multiplex Congenita, a rare neuromuscular disease that bends the body&#8217;s joints at birth. The disease prevents the girls from speaking, walking, breathing and eating on their own.  The only way to correct these issues is through serial casting, which forces the disrupted bone structure back into a normal state.  Growing up, Chaney&#8217;s family adopted a young girl who was also diagnosed with AMC.  To take care of her two daughters, Chaney quit her job in order to be a full-time mother.<\/p>\n<p>Chaney carries Mary playfully through their home on Oct. 19, 2014 on Lincoln St. in East Rochester, N.Y. In the wintertime, it is hard for Chaney to take her daughters outside. For fun, Chaney likes to carry Mary around the house and tell her she is flying.<\/p>\n"},"alt_text":"","media_type":"image","mime_type":"image\/jpeg","media_details":{"width":3000,"height":2000,"file":"2015\/04\/201570_por-20.jpg","sizes":{"thumbnail":{"file":"201570_por-20-150x150.jpg","width":150,"height":150,"mime_type":"image\/jpeg","source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-150x150.jpg"},"medium":{"file":"201570_por-20-300x200.jpg","width":300,"height":200,"mime_type":"image\/jpeg","source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-300x200.jpg"},"medium_large":{"file":"201570_por-20-768x512.jpg","width":768,"height":512,"mime_type":"image\/jpeg","source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-768x512.jpg"},"large":{"file":"201570_por-20-1024x683.jpg","width":1024,"height":683,"mime_type":"image\/jpeg","source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-1024x683.jpg"},"twentyseventeen-featured-image":{"file":"201570_por-20-2000x1200.jpg","width":2000,"height":1200,"mime_type":"image\/jpeg","source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-2000x1200.jpg"},"twentyseventeen-thumbnail-avatar":{"file":"201570_por-20-100x100.jpg","width":100,"height":100,"mime_type":"image\/jpeg","source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20-100x100.jpg"},"full":{"file":"201570_por-20.jpg","width":3000,"height":2000,"mime_type":"image\/jpeg","source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20.jpg"}},"image_meta":{"aperture":"2.8","credit":"Tom Brenner","camera":"Canon EOS 5D Mark III","caption":"Gitner (Adopted Love - 01 - Chaney Roko, 34, is a single mother of two adopted children. Mary, 9, and her sister Kiera, 4, both have Arthrogryposis Multiplex Congenita, a rare neuromuscular disease that bends the body's joints at birth. The disease prevents the girls from speaking, walking, breathing and eating on their own.  The only way to fix this is through serial casting, which forces the disrupted bone structure back into a normal state.  Growing up, Chaney's family adopted a young girl who was also diagnosed with AMC.  To take care of her kids, Chaney had to quit her job in order to be a full time mother. She wants to move out of her two-story home into a ranch in order to accommodate to her kid's needs, however she faces financial issues that prevent that from occurring anytime soon.)\r\rChaney Roko carries her adopted daughter, Mary, 9, playfully through their home on Oct. 19, 2014 on Lincoln St. in East Rochester, N.Y. In the wintertime, it is hard for Chaney to take her kids outside. For fun, Chaney likes to carry Mary around the house and tell her she is flying.","created_timestamp":"1413736232","copyright":"\u00a9Tom Brenner 2014","focal_length":"28","iso":"4000","shutter_speed":"0.04","title":"","orientation":"1","keywords":[]}},"post":null,"source_url":"https:\/\/pj.rit.edu\/nppa\/wp-content\/uploads\/2015\/04\/201570_por-20.jpg","_links":{"self":[{"href":"https:\/\/pj.rit.edu\/nppa\/wp-json\/wp\/v2\/media\/2735","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pj.rit.edu\/nppa\/wp-json\/wp\/v2\/media"}],"about":[{"href":"https:\/\/pj.rit.edu\/nppa\/wp-json\/wp\/v2\/types\/attachment"}],"author":[{"embeddable":true,"href":"https:\/\/pj.rit.edu\/nppa\/wp-json\/wp\/v2\/users\/1"}]}}