{"id":26259,"date":"2024-03-14T14:58:07","date_gmt":"2024-03-14T18:58:07","guid":{"rendered":"https:\/\/nephcure.org\/?post_type=patient-story&p=26259"},"modified":"2024-04-29T19:29:32","modified_gmt":"2024-04-29T23:29:32","slug":"jen-m","status":"publish","type":"patient-story","link":"https:\/\/nephcure.org\/es\/patient-story\/jen-m\/","title":{"rendered":"Jen M."},"content":{"rendered":"

Despu\u00e9s de notar que sus tobillos eran del tama\u00f1o de toronjas, a Jen le diagnosticaron GEFS a los 17 a\u00f1os. Los medicamentos de mantenimiento la sustentaron durante cinco semestres en la universidad, despu\u00e9s de lo cual su madre, Judy, le don\u00f3 su ri\u00f1\u00f3n a Jen en 1999. Siete d\u00edas despu\u00e9s, el donado Se determin\u00f3 que el ri\u00f1\u00f3n era inviable y se extirp\u00f3. Esto llev\u00f3 a seis meses de hemodi\u00e1lisis y luego seis meses de di\u00e1lisis peritoneal antes de que Jen recibiera su segundo ri\u00f1\u00f3n de su padre, Jim.<\/p>\n\n\n

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El trasplante se produjo apenas dos semanas despu\u00e9s de graduarse de su licenciatura. El ri\u00f1\u00f3n de su padre le impidi\u00f3 la di\u00e1lisis durante seis a\u00f1os y medio. Durante este tiempo, Jen pudo viajar por el mundo, regres\u00f3 a la universidad para obtener su maestr\u00eda en ense\u00f1anza y se convirti\u00f3 en maestra de escuela primaria. Luego, Jen volvi\u00f3 a someterse a di\u00e1lisis peritoneal durante unos tres a\u00f1os mientras continuaba la b\u00fasqueda de otro ri\u00f1\u00f3n compatible.<\/p>\n\n\n

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\u00a1Jen y Dave celebrar\u00e1n su \u201cTransplantaversario\u201d de 15 a\u00f1os el pr\u00f3ximo mes de junio! Aunque hay recurrencia de la GEFS en el ri\u00f1\u00f3n trasplantado, Jen se enorgullece de estar en remisi\u00f3n parcial con una creatinina inicial de 1,7.<\/h2>\n<\/blockquote>\n\n<\/div>\n\n
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Sin embargo, no necesit\u00f3 buscar demasiado ni demasiado lejos, ya que su t\u00edo Dave era compatible y le dio a Jen un tercer ri\u00f1\u00f3n en 2008, que cari\u00f1osamente ha sido llamado "UDK" (Ri\u00f1\u00f3n del t\u00edo Dave). \u00a1Jen y Dave celebrar\u00e1n su \u201cTransplantaversario\u201d de 15 a\u00f1os el pr\u00f3ximo mes de junio! Aunque hay recurrencia de la GEFS en el ri\u00f1\u00f3n trasplantado, Jen se enorgullece de estar en remisi\u00f3n parcial con una creatinina inicial de 1,7.<\/p>\n\n\n\n

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FSGS no ha frenado a Jen, ya que obtuvo otra maestr\u00eda en 2019 y contin\u00faa experimentando muchos recuerdos incre\u00edbles con familiares y amigos.<\/p>","protected":false},"excerpt":{"rendered":"

Despu\u00e9s de notar que sus tobillos eran del tama\u00f1o de pomelos, a Jen le diagnosticaron GEFS a los 17 a\u00f1os. Medicamentos de mantenimiento...<\/p>","protected":false},"featured_media":26260,"template":"","age-group":[278],"disease-category":[253],"class_list":["post-26259","patient-story","type-patient-story","status-publish","has-post-thumbnail","hentry","age-group-adults","disease-category-focal-segmental-glomerulosclerosis-fsgs"],"acf":[],"yoast_head":"\nJen M. - NephCure<\/title>\n<meta name=\"description\" content=\"After noticing her ankles were the size of grapefruits, Jen was diagnosed with FSGS at age 17. 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