{"id":45,"date":"2014-10-18T10:07:27","date_gmt":"2014-10-18T15:07:27","guid":{"rendered":"http:\/\/www.angieshope.org\/?page_id=45"},"modified":"2020-02-19T18:56:04","modified_gmt":"2020-02-20T00:56:04","slug":"about-sma","status":"publish","type":"page","link":"https:\/\/www.angieshope.org\/?page_id=45","title":{"rendered":"About SMA"},"content":{"rendered":"<p id=\"page-title\" class=\"title\"><span style=\"font-family: arial, helvetica, sans-serif;\">Spinal muscular atrophy (SMA), is an often fatal genetic neuromuscular disease that destroys the nerves controlling voluntary muscle movement, which affects crawling, walking, head and neck control, and even <span style=\"font-family: helvetica, arial, sans-serif;\">swallowing.<\/span><\/span><\/p>\n<div class=\"region region-content\">\n<div id=\"block-system-main\" class=\"block block-system first last odd\">\n<div class=\"content\">\n<div id=\"node-1\" class=\"node node-page view-mode-full clearfix\">\n<div class=\"content\">\n<div class=\"field field-name-body field-type-text-with-summary field-label-hidden\">\n<div class=\"field-items\">\n<div class=\"field-item even\">\n<p><span style=\"font-family: arial, helvetica, sans-serif;\"><span style=\"color: #4868c8;\">WHO IS AFFECTED?<\/span><br \/>\nSMA is one of the most prevalent genetic disorders.<\/span><\/p>\n<p><span style=\"font-family: arial, helvetica, sans-serif;\">One in every 10,000 babies is born with SMA.<br \/>\nSMA can strike anyone regardless of any age, race or gender.<br \/>\nOne in every 40 people carries the gene that causes SMA. <\/span><span style=\"font-family: arial, helvetica, sans-serif;\">The child of two carriers has a one in four chance of developing SMA.<\/span><\/p>\n<p><span style=\"font-family: arial, helvetica, sans-serif;\">7.5 million Americans are carriers.<\/span><\/p>\n<p><span style=\"font-family: arial, helvetica, sans-serif;\"><span style=\"color: #4868c8;\">TYPES OF SMA<\/span><br \/>\nSMA patients are classified into four types based on milestones achieved at onset of SMA. Type I and II are the most prevalent.<\/span><\/p>\n<p><span style=\"font-family: arial, helvetica, sans-serif;\"><strong>Type I<\/strong> is the most severe form of SMA. It strikes infants between birth and six months old. Children affected with Type I cannot sit without support. Most Type I babies pass away before the age of two.<br \/>\n<strong>Type II<\/strong> patients first show symptoms between seven and 18 months old. Type II patients may be able to sit unaided or even stand with support. They are at increased risk for complications from respiratory infections.<br \/>\n<strong>Type III<\/strong> is the least deadly form of childhood-onset SMA. It strikes children as early as the age of 18 months, but can surface as late as adolescence. Type III patients are able to walk, but weakness is prevalent. Most patients eventually need to use a wheelchair.<br \/>\n<strong>Type IV<\/strong> is the adult form of the disease. Symptoms tend to begin after age 35.<\/span><\/p>\n<p><span style=\"font-family: arial, helvetica, sans-serif;\">Please visit <a href=\"http:\/\/curesma.org\" target=\"_blank\" rel=\"noopener noreferrer\">curesma.org <\/a>for more information<b>.<\/b><\/span><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Spinal muscular atrophy (SMA), is an often fatal genetic neuromuscular disease that destroys the nerves controlling voluntary muscle movement, which affects crawling, walking, head and neck control, and even swallowing. WHO IS AFFECTED? SMA is one of the most prevalent genetic disorders. One in every 10,000 babies is born with SMA. SMA can strike anyone &hellip; <a href=\"https:\/\/www.angieshope.org\/?page_id=45\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">About SMA<\/span> <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-45","page","type-page","status-publish","hentry"],"jetpack_shortlink":"https:\/\/wp.me\/P5e08Q-J","jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/www.angieshope.org\/index.php?rest_route=\/wp\/v2\/pages\/45","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.angieshope.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.angieshope.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.angieshope.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.angieshope.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=45"}],"version-history":[{"count":6,"href":"https:\/\/www.angieshope.org\/index.php?rest_route=\/wp\/v2\/pages\/45\/revisions"}],"predecessor-version":[{"id":505,"href":"https:\/\/www.angieshope.org\/index.php?rest_route=\/wp\/v2\/pages\/45\/revisions\/505"}],"wp:attachment":[{"href":"https:\/\/www.angieshope.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=45"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}