{"id":8596,"date":"2019-02-08T12:36:18","date_gmt":"2019-02-08T17:36:18","guid":{"rendered":"http:\/\/www.myface.org\/?page_id=8596"},"modified":"2019-02-11T09:59:11","modified_gmt":"2019-02-11T14:59:11","slug":"anibel","status":"publish","type":"page","link":"https:\/\/www.myface.org\/es\/anibel\/","title":{"rendered":"Send Anibel Valentine’s Wishes"},"content":{"rendered":"
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Send Anibel a Valentine's Day Wish<\/h2><\/div>
Please give in Anibel\u2019s honor and send her an encouraging note as she recovers. We\u2019ll add your message to our Valentine\u2019s card for her; it will bring a smile to her face and yours.<\/div><\/div><\/div><\/div><\/div>
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\"Anibel\"<\/td>\nAnibel was born with a condition called Nager\u2019s Syndrome<\/strong>, a very rare syndrome related to Treacher Collins Syndrome. Nager\u2019s Syndrome is characterized by underdeveloped cheek bones and a very small lower jaw. Because of this, Anibel has had a tracheostomy to help her breathe her whole life and uses a feeding tube to get most of her nutrients. She\u2019s had 28 surgeries, and she\u2019s only 14 years old.<\/p>\n

You\u2019d never know how much she\u2019s been through when you meet Anibel. She has a bright personality that brings warmth to everyone she meets. You can\u2019t help but love her.<\/p>\n

Anibel is currently undergoing a painful treatment to expand the room in her face, in the hopes that she will be able to breathe without a tracheostomy. This process will likely take months, but if she\u2019s able to breathe without her trach, she\u2019ll be able to go swimming, build a snowman, and have the snowball fight she\u2019s always wanted.<\/strong><\/h3>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n\t\t<\/div>\n\t<\/div>\n<\/div><\/div><\/div><\/div><\/div><\/div>
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\"Anibel\"<\/p>\n

Anibel was born with a condition called Nager\u2019s Syndrome<\/strong>, a very rare syndrome related to Treacher Collins Syndrome. Nager\u2019s Syndrome is characterized by underdeveloped cheek bones and a very small lower jaw. Because of this, Anibel has had a tracheostomy to help her breathe her whole life and uses a feeding tube to get most of her nutrients. She\u2019s had 28 surgeries, and she\u2019s only 14 years old.<\/p>\n

You\u2019d never know how much she\u2019s been through when you meet Anibel. She has a bright personality that brings warmth to everyone she meets. You can\u2019t help but love her.<\/p>\n

Anibel is currently undergoing a painful treatment to expand the room in her face, in the hopes that she will be able to breathe without a tracheostomy. This process will likely take months, but if she\u2019s able to breathe without her trach, she\u2019ll be able to go swimming, build a snowman, and have the snowball fight she\u2019s always wanted.<\/strong><\/h3>\n\n\t\t<\/div>\n\t<\/div>\n<\/div><\/div><\/div><\/div>
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