{"id":573,"date":"2020-07-31T20:06:21","date_gmt":"2020-07-31T20:06:21","guid":{"rendered":"https:\/\/humansofchronicillness.org\/?p=573"},"modified":"2021-03-16T20:53:39","modified_gmt":"2021-03-16T20:53:39","slug":"laura-a","status":"publish","type":"post","link":"https:\/\/humansofchronicillness.org\/2020\/07\/laura-a\/","title":{"rendered":"Laura A."},"content":{"rendered":"<h2 style=\"text-align: center;\">Humans of ME\/CFS<\/h2>\n<p>Doctors aren&#8217;t sure if I have ME\/CFS from glandular fever, but all I know is that it&#8217;s debilitating and life changing.<\/p>\n<p>It&#8217;s hard for people to understand that I&#8217;m in constant pain and I&#8217;m tired. I have no energy. Talk about life changing. I&#8217;ve had to leave my dream job, I can&#8217;t do grocery shopping, or do other things that I used to do. I have been a swimming instructor and lifeguard. I wouldn&#8217;t be able to do any of these activities now. I&#8217;m very limited in what I do, and I&#8217;m mentally and physically exhausted.<br \/>\nI don&#8217;t feel like there is enough support and information on this horrible illness, and I pray doctors find a cure soon.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Humans of ME\/CFS Doctors aren&#8217;t sure if I have ME\/CFS from glandular fever, but all I know is that it&#8217;s debilitating and life changing. It&#8217;s hard for people to understand that I&#8217;m in constant pain and I&#8217;m tired. I have no energy. Talk about life changing. I&#8217;ve had to leave my dream job, I can&#8217;t [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":558,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"spay_email":""},"categories":[1],"tags":[],"jetpack_featured_media_url":"https:\/\/humansofchronicillness.org\/wp-content\/uploads\/2020\/07\/laura_a.png","_links":{"self":[{"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/posts\/573"}],"collection":[{"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/comments?post=573"}],"version-history":[{"count":0,"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/posts\/573\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/media\/558"}],"wp:attachment":[{"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/media?parent=573"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/categories?post=573"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/humansofchronicillness.org\/wp-json\/wp\/v2\/tags?post=573"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}