\nResidence:<\/strong> Mozyr, Belarus
\nDiagnosis:<\/strong> SMA (spinal muscular atrophy) type 2
\nNeeds:<\/strong>a surgery in USA
\nFunds to raise:<\/strong> 1,650,500<\/p>\n
<\/p>\n","protected":false},"excerpt":{"rendered":" We have helped to pay for the reabilitation Age: 3 y. o. Residence: Mozyr, Belarus Diagnosis: SMA (spinal muscular atrophy) type 2 Needs:a surgery in USA Funds to raise: 1,650,500 A year ago, little Elizaveta was diagnosed with SMA. This is a disease when the muscles gradually break down, get atrophied. A child begins to lose the motor skills already acquired, and slowly, one after another, the body functions begin…Keep Reading<\/span><\/a><\/p>\n","protected":false},"author":12,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[114],"tags":[],"class_list":["post-20695","post","type-post","status-publish","format-standard","hentry","category-former-kids-en"],"_links":{"self":[{"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/posts\/20695","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/users\/12"}],"replies":[{"embeddable":true,"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/comments?post=20695"}],"version-history":[{"count":4,"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/posts\/20695\/revisions"}],"predecessor-version":[{"id":21643,"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/posts\/20695\/revisions\/21643"}],"wp:attachment":[{"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/media?parent=20695"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/categories?post=20695"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.orthodiakonia.de\/en\/wp-json\/wp\/v2\/tags?post=20695"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}![\"\"](\"https:\/\/www.orthodiakonia.de\/wp-content\/uploads\/2023\/07\/ElizavetaT.jpg\")
<\/a> A year ago, little Elizaveta was diagnosed with SMA. This is a disease when the muscles gradually break down, get atrophied. A child begins to lose the motor skills already acquired, and slowly, one after another, the body functions begin to fail. There is a way to stop this disease: an injection of the drug Zolgensma. It delivers to a body a working copy of the broken gene. This injection has to be done once in a lifetime, but it is necessary to do this until the child reaches the weight of 21 kg. The cost of this injection is huge: EUR 1,650,500.<\/p>\n