{"id":815,"date":"2018-07-23T14:22:27","date_gmt":"2018-07-23T18:22:27","guid":{"rendered":"http:\/\/www.dysautonomiainternational.org\/blog\/wordpress\/?p=815"},"modified":"2018-07-05T14:23:07","modified_gmt":"2018-07-05T18:23:07","slug":"what-dysautonomia-feels-like","status":"publish","type":"post","link":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/what-dysautonomia-feels-like\/","title":{"rendered":"What dysautonomia feels like."},"content":{"rendered":"<p>Imagine waking up one day, and everything being ripped out from under you.<\/p>\n<p>In a blink of an eye everything changes. Everything you love to do suddenly you can&#8217;t do anymore.<\/p>\n<p>Scared, worried, unheard&#8230; misunderstood. Doctors clueless as to what is wrong.<\/p>\n<p>Anxiety rising high, as that is the only diagnosis I hear. Knowing that this is far from normal, and anxiety would be treatable and better to have but this&#8230; THIS monster is much bigger.<\/p>\n<p>Tears shed as my heart beats faster and faster with every inch my body rises. Why is this happening? Am I crazy?<\/p>\n<p>Dizzy, faint, lightheaded&#8230; my daily life as the people around me think I&#8217;m lazy, but if they only knew the struggle. The struggle to get up, to take a step, a shower even. The things I took for granted.<\/p>\n<p>My children&#8230; asking why mommy cant do the things she used to. The innocence in their eyes, the empathy they try to show. My explanation feels useless, and I&#8217;m hurting because I&#8217;m not the mom I use to be. I&#8217;m sorry.<\/p>\n<p>My family&#8230; being a burden to them is my constant guilt. How I feel is my daily talk. I feel alone. I am alone. No one can understand unless they go through it. Sympathizing just makes me angry, though it shouldn&#8217;t. How could someone without\u00a0POTS even begin to get it?<\/p>\n<p>Friends&#8230; let&#8217;s go out! I sit there and watch them have fun, as I&#8217;m downing water just to avoid\u00a0fainting. I&#8217;m jealous and it&#8217;s wrong of me to be. I would never wish anyone this. I&#8217;m sad because I&#8217;m the one sitting in the corner, wondering what I would be doing if this monster didn&#8217;t get me.<\/p>\n<p>You don&#8217;t look sick&#8230; some things you just can&#8217;t see. You look perfect on the outside, but on the inside, there is a disaster. I&#8217;m in a constant battle with my heart. Every second, every hour, every minute of every day.<\/p>\n<p>A doctor&#8230; a doctor that takes you by the hand and believes you&#8230; a miracle. The words, &#8220;yes, you have POTS.&#8221; The I knew it was more than anxiety, it was more then something simple.<\/p>\n<p>The truth&#8230; there is no cure at this current time. There is medicine to help, but each person is different. The words you may need a wheelchair, a shower chair and medicine for life.<\/p>\n<p>My mind&#8230; why did this happen to me? From pregnancy, Mono and maybe even my car wreck my doctor replied. What about my life? I&#8217;m only 22. POTS doesn&#8217;t discriminate.<\/p>\n<p>My faith&#8230; dear God, what did I do to deserve this? Please take this away, please, I&#8217;m sorry.<br \/>\nA daily prayer to Him, wondering why and how this was in my plan.<\/p>\n<p>A future&#8230; what now? How do I move forward being so sick? Pushing through for my family, for my babies. I&#8217;m their hero. I cant look weak. I have to be strong.<\/p>\n<p>A story&#8230; to be continued.<\/p>\n<p>&nbsp;<\/p>\n<p><em>Guest author Emily J. is 23 years-old and living with\u00a0postural orthostatic tachycardia syndrome and inappropriate sinus tachycardia. She hopes this will let others know they are not alone in feeling this way about living with dysautonomia.<\/em><\/p>\n<p>Remember, you are never alone on this journey. Dysautonomia International offers support groups to help people impacted by dysautonomia\u00a0connect with others who &#8220;get it.&#8221; Visit <a href=\"http:\/\/www.dysautonomiainternational.org\/support\" target=\"_blank\">www.dysautonomiainternational.org\/support<\/a> to find a support group.<\/p>\n<a class=\"synved-social-button synved-social-button-follow synved-social-size-16 synved-social-resolution-single synved-social-provider-facebook nolightbox\" data-provider=\"facebook\" target=\"_blank\" rel=\"nofollow\" title=\"Follow us on Facebook\" href=\"http:\/\/www.facebook.com\/dysautonomiainternational\" style=\"font-size: 0px;width:16px;height:16px;margin:0;margin-bottom:5px;margin-right:5px\"><img loading=\"lazy\" decoding=\"async\" alt=\"Facebook\" title=\"Follow us on Facebook\" class=\"synved-share-image synved-social-image synved-social-image-follow\" width=\"16\" height=\"16\" style=\"display: inline;width:16px;height:16px;margin: 0;padding: 0;border: none;box-shadow: 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In a blink of an eye everything changes. Everything you love to do suddenly you can&#8217;t do anymore. Scared, worried, unheard&#8230; misunderstood. Doctors clueless as to what is wrong. Anxiety rising high, as that is the only diagnosis I hear. Knowing that &hellip; <a href=\"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/what-dysautonomia-feels-like\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">What dysautonomia feels like.<\/span> <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-815","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/posts\/815","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/comments?post=815"}],"version-history":[{"count":4,"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/posts\/815\/revisions"}],"predecessor-version":[{"id":819,"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/posts\/815\/revisions\/819"}],"wp:attachment":[{"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/media?parent=815"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/categories?post=815"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/dysautonomiainternational.org\/blog\/wordpress\/wp-json\/wp\/v2\/tags?post=815"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}