{"id":47909,"date":"2014-03-28T16:12:21","date_gmt":"2014-03-28T20:12:21","guid":{"rendered":"\/news\/?p=47909"},"modified":"2014-03-28T10:31:42","modified_gmt":"2014-03-28T14:31:42","slug":"flowers-we-never-knew-existed-the-contribution-of-down-syndrome-to-society","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/flowers-we-never-knew-existed-the-contribution-of-down-syndrome-to-society\/","title":{"rendered":"&#8220;Flowers we never knew existed:&#8221; the contribution of Down syndrome to society"},"content":{"rendered":"<div style=\"margin-top: 0px; margin-bottom: 0px;\" class=\"sharethis-inline-share-buttons\" ><\/div><div id=\"attachment_47953\" style=\"width: 360px\" class=\"wp-caption aligncenter\"><img aria-describedby=\"caption-attachment-47953\" decoding=\"async\" loading=\"lazy\" class=\"size-full wp-image-47953\" alt=\"a-little-moxie\" src=\"\/news\/wp-content\/uploads\/2014\/03\/a-little-moxie.jpg\" width=\"350\" height=\"347\" srcset=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2014\/03\/a-little-moxie.jpg 350w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2014\/03\/a-little-moxie-150x150.jpg 150w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2014\/03\/a-little-moxie-300x297.jpg 300w\" sizes=\"(max-width: 350px) 100vw, 350px\" \/><p id=\"caption-attachment-47953\" class=\"wp-caption-text\">Via A Little Moxie Instragram.<\/p><\/div>\n<p style=\"text-align: left;\">Meriah Nichols, the mother of a three-year-old girl who has Down syndrome and blogger at <a style=\"line-height: 1.5em;\" href=\"http:\/\/www.withalittlemoxie.com\/\">A Little Moxie<\/a><span style=\"line-height: 1.5em;\">, has written an <\/span><a style=\"line-height: 1.5em;\" href=\"http:\/\/www.news.com.au\/lifestyle\/parenting\/meriah-nichols-on-the-biggest-problem-facing-people-with-down-syndrome\/story-fnet08ui-1226861119511\">op-ed<\/a> explaining what her fast-paced life with her daughter, Moxie, is like. Meriah shares how her heart bursts when, from the background, she watches her daughter sign her way through books, or utilize her art supplies, or play on the beach:<\/p>\n<blockquote><p>&#8230;she knows her own mind so well, she is clear about what she wants and the path she desires. Her \u201cyes\u201d\u2019s and \u201cno\u201ds are firm.<\/p><\/blockquote>\n<p>Meriah, who is deaf, knows what life with a disability is like. However, she challenges the perception that a mental or physical disability is a <em>disadvantage<\/em>:<\/p>\n<blockquote><p>Moxie has Down syndrome. She has an extra chromosome, she has an intellectual disability.<\/p>\n<p>There are so many cards that are stacked against her, I don\u2019t even know where to begin. The biggest one though, the most glaring one to me is this idea that we have as a culture that there is something wrong with her, that she\u2019s broken or something.<\/p>\n<p>\u201cPeople with disabilities are broken\u201d<\/p>\n<p>There is this idea that she needs to be moulded into some kind of mainstream form. That she needs to do as all do, that instead of looking to her to see what she offer and trying to move with her flow, we staunch her flow and divert her stream.<\/p><\/blockquote>\n<p><!--more--><\/p>\n<p>Meriah hits on something deeper than the idea that individuals with disabilities should be <em>accepted;\u00a0<\/em>she suggests, rather, that the core integrity of who they are as individuals be approached with an eye to learning <em>from<\/em> them, seeing what they can teach us, rather than molding them into something more like ourselves.<\/p>\n<p>Meriah has learned lessons about life and love from her daughter that a person without Down syndrome couldn&#8217;t have taught her in the same way. She stresses the importance of cultivating the unique individual that is her daughter. She vehemently opposes the idea that the ideal for Moxie would be to grow into a &#8220;normal&#8221; person, rather than into the unique individual with Down syndrome that she is (emphasis added):<\/p>\n<blockquote><p>If we don\u2019t let them be who they are, if we don\u2019t encourage every aspect of who they are to flourish <strong>so that flowers that we never even knew existed would have the wherewithal to emerge, sprout and bloom<\/strong>.<\/p>\n<p>And that\u2019s part of the key here to me \u2014 \u2018flowers that we never even knew existed\u2018 \u2014 because we know very little about Down syndrome in particular and intellectual disabilities in general. We have been so busy for so long in not listening.<\/p><\/blockquote>\n<p>While Meriah says that Moxie causes her to approach every day with a faster pace, she knows that her awe for her daughter wouldn&#8217;t be any less if Moxie were slower, because the privilege is in traveling through life at Moxie&#8217;s pace, whatever that pace may be.<\/p>\n<blockquote><p>If Moxie was not quick, if she was not so sure of herself, there would be something else.<\/p>\n<p>Three years into raising this child and I\u2019m sure at this point that that something else would shine so brightly that I\u2019d forget about how much I admire whatever it is that I laud now. I\u2019d be singing about that something else.<\/p><\/blockquote>\n","protected":false},"excerpt":{"rendered":"<p>Meriah Nichols, the mother of a three-year-old girl who has Down syndrome and blogger at A Little Moxie, has written an op-ed explaining what her fast-paced life with her daughter, Moxie, is like. Meriah shares how her heart bursts when, from the background, she watches her daughter sign her way through books, or utilize her [&hellip;]<\/p>\n","protected":false},"author":152,"featured_media":47953,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[4],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>&quot;Flowers we never knew existed:&quot; the contribution of Down syndrome to society - Live Action News<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/archive.liveaction.org\/news\/flowers-we-never-knew-existed-the-contribution-of-down-syndrome-to-society\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"&quot;Flowers we never knew existed:&quot; the contribution of Down syndrome to society - Live Action News\" \/>\n<meta property=\"og:description\" content=\"Meriah Nichols, the mother of a three-year-old girl who has Down syndrome and blogger at A Little Moxie, has written an op-ed explaining what her fast-paced life with her daughter, Moxie, is like. 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