{"id":443,"date":"2020-12-01T17:00:37","date_gmt":"2020-12-01T17:00:37","guid":{"rendered":"https:\/\/test.deborafoundation.org\/?p=443"},"modified":"2026-01-28T11:55:32","modified_gmt":"2026-01-28T11:55:32","slug":"a-living-for-love-the-story-of-beminet-and-his-mother-asegedech","status":"publish","type":"post","link":"https:\/\/deborafoundation.org\/en\/2020\/12\/01\/a-living-for-love-the-story-of-beminet-and-his-mother-asegedech\/","title":{"rendered":"A Mother\u2019s Love"},"content":{"rendered":"\n
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Asegedech and Beminet\u2019s Story of Hope and Inclusion<\/h3> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n
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When Asegedech Mebre gave birth to her son Beminet, the journey ahead was filled with uncertainty, but never lacking in love. From the very beginning, Beminet battled heart complications. For years, he underwent monthly checkups at Bruck Hospital, until finally, at the age of five, doctors confirmed what had long been suspected: Beminet had Down syndrome and a serious heart condition.<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\u201cI was shocked, \u201d Asegedech recalls. \u201cBut I knew it wasn\u2019t a curse from God. It was just a different path. I used to be very active, but now, I live for him. He needs me, and I will always be there. \u201d<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n

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Today, at nine years old, Beminet is a joyful, social, and deeply loved child. \u201cHe\u2019s so friendly, \u201d his mother says. \u201cThe whole neighborhood adores him. He has many friends, and our community supports us in so many ways. \u201d<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n

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She also expresses gratitude for the free medical treatment Beminet receives at Black Lion Hospital and the knowledge she\u2019s gained to care for him. But one major challenge remains, school.<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\u201cThere are no schools designed for children with Down syndrome, \u201d she says. \u201cWhen I try to enroll him, some parents complain. They don\u2019t want their children in the same classroom as him. It breaks my heart. Every time I send him, I wonder if he\u2019ll be accepted. \u201d<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n

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Still, Asegedech believes in her son and in the power of inclusion. Her message is clear: \u201cDon\u2019t hide your children. Let them be seen. Send them to school. That\u2019s how they learn to communicate, to build confidence, and to grow. \u201d<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n

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Beminet is not defined by his diagnosis, he is defined by his kindness, his joy, and the dreams he holds. All he needs is a world willing to meet him halfway<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n

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Let\u2019s stand together to ensure that children like Beminet are not left behind. With your support, we can create inclusive schools, informed communities, and a future where every child has a chance to shine!<\/p> <\/div>\n<\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n","protected":false},"excerpt":{"rendered":"

Asegedech and Beminet\u2019s Story of Hope and Inclusion<\/p>\n","protected":false},"author":1,"featured_media":880,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"pagelayer_contact_templates":[],"_pagelayer_content":"","footnotes":""},"categories":[27],"tags":[],"class_list":["post-443","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-stories","has-post-title","has-post-date","has-post-category","has-post-tag","has-post-comment","has-post-author",""],"builder_content":"

Asegedech and Beminet\u2019s Story of Hope and Inclusion<\/h3>\n

When Asegedech Mebre gave birth to her son Beminet, the journey ahead was filled with uncertainty, but never lacking in love. From the very beginning, Beminet battled heart complications. For years, he underwent monthly checkups at Bruck Hospital, until finally, at the age of five, doctors confirmed what had long been suspected: Beminet had Down syndrome and a serious heart condition.<\/p>\n

\u201cI was shocked, \u201d Asegedech recalls. \u201cBut I knew it wasn\u2019t a curse from God. It was just a different path. I used to be very active, but now, I live for him. He needs me, and I will always be there. \u201d<\/p>\n

Today, at nine years old, Beminet is a joyful, social, and deeply loved child. \u201cHe\u2019s so friendly, \u201d his mother says. \u201cThe whole neighborhood adores him. He has many friends, and our community supports us in so many ways. \u201d<\/p>\n

She also expresses gratitude for the free medical treatment Beminet receives at Black Lion Hospital and the knowledge she\u2019s gained to care for him. But one major challenge remains, school.<\/p>\n

\u201cThere are no schools designed for children with Down syndrome, \u201d she says. \u201cWhen I try to enroll him, some parents complain. They don\u2019t want their children in the same classroom as him. It breaks my heart. Every time I send him, I wonder if he\u2019ll be accepted. \u201d<\/p>\n

Still, Asegedech believes in her son and in the power of inclusion. Her message is clear: \u201cDon\u2019t hide your children. Let them be seen. Send them to school. That\u2019s how they learn to communicate, to build confidence, and to grow. \u201d<\/p>\n

Beminet is not defined by his diagnosis, he is defined by his kindness, his joy, and the dreams he holds. All he needs is a world willing to meet him halfway<\/p>\n

Let\u2019s stand together to ensure that children like Beminet are not left behind. With your support, we can create inclusive schools, informed communities, and a future where every child has a chance to shine!<\/p>","_links":{"self":[{"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/posts\/443","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/comments?post=443"}],"version-history":[{"count":15,"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/posts\/443\/revisions"}],"predecessor-version":[{"id":938,"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/posts\/443\/revisions\/938"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/media\/880"}],"wp:attachment":[{"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/media?parent=443"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/categories?post=443"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/deborafoundation.org\/en\/wp-json\/wp\/v2\/tags?post=443"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}