{"id":945,"date":"2015-07-06T10:35:46","date_gmt":"2015-07-06T15:35:46","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=945"},"modified":"2015-07-06T10:35:46","modified_gmt":"2015-07-06T15:35:46","slug":"ramesh","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/pt\/individuals-with-lgmd-interviews\/2015\/07\/06\/ramesh\/","title":{"rendered":"INDIV\u00cdDUO COM LGMD: Ramesh"},"content":{"rendered":"<p><strong>07\/06\/2015:<\/strong><strong>\u00a0<\/strong><\/p>\n<p><strong>NOME<\/strong>: Ramesh \u00a0<strong>IDADE<\/strong>: 28 anos<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/07\/LGMD2B-Ramesh.png\"><img decoding=\"async\" class=\"lazyload  size-medium wp-image-946 alignright\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27169%27%20viewBox%3D%270%200%20300%20169%27%3E%3Crect%20width%3D%27300%27%20height%3D%27169%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/07\/LGMD2B-Ramesh-300x169.png\" alt=\"LGMD2B - Ramesh\" width=\"300\" height=\"169\" \/><\/a><br \/>\n<strong>PA\u00cdS<\/strong>: \u00cdndia<br \/>\n<strong>LGMD Sub-tipo<\/strong>: LGMD2B \/ Disferlinopatia<\/p>\n<p><strong>COM QUE IDADE FOI DIAGNOSTICADO<\/strong>:<br \/>\nComecei a ter sintomas aos 19 anos, mas s\u00f3 me foi diagnosticada por volta dos 22 anos.<\/p>\n<p><strong>QUAIS FORAM OS SEUS PRIMEIROS SINTOMAS<\/strong>:<br \/>\nO meu primeiro sintoma foi que, quando estava a ir para o escrit\u00f3rio, ca\u00ed de repente. Consultei o meu m\u00e9dico e ele sugeriu-me fisioterapia, mas n\u00e3o ajudou muito. Depois disso, ach\u00e1mos que seria melhor consultar um m\u00e9dico em Bangalore (\u00cdndia). Fiz uma biopsia muscular e nervosa e estive engessado durante dois meses em cada perna, uma de cada vez. Ela mandou-me para um neurologista para fazer mais exames.<\/p>\n<p><strong>TEM OUTROS FAMILIARES QUE SOFREM DE LGMD<\/strong>: N\u00e3o<\/p>\n<p><strong>QUAIS S\u00c3O, NA SUA OPINI\u00c3O, OS MAIORES DESAFIOS DE VIVER COM A LGMD?<\/strong>:<br \/>\nConsidero que o maior desafio de viver com a LGMD \u00e9 o facto de as pessoas terem dificuldade em compreend\u00ea-la. N\u00e3o \u00e9 f\u00e1cil descrever a LGMD a algu\u00e9m. Muitas pessoas pensam que estou a exagerar ou mesmo a mentir sobre o facto de ter esta doen\u00e7a.   Para al\u00e9m da doen\u00e7a, considero que a falta de acessibilidade e as atitudes sociais em rela\u00e7\u00e3o \u00e0s pessoas com defici\u00eancia s\u00e3o muito limitadoras. Gostava que as pessoas estivessem mais abertas a aprender sobre estas doen\u00e7as e a compreender como se livrar desta doen\u00e7a.<\/p>\n<p><strong>QUAL \u00c9 A SUA MAIOR REALIZA\u00c7\u00c3O<\/strong>:<br \/>\nA minha maior realiza\u00e7\u00e3o \u00e9 conseguir trabalhar e continuar a trabalhar \u00e0 minha maneira.<\/p>\n<p><strong>COMO \u00c9 QUE A LGMD O INFLUENCIOU A TORNAR-SE A PESSOA QUE \u00c9 HOJE<\/strong>:<br \/>\nAprendi a apreciar as pessoas que me ajudam, a ter paci\u00eancia, a manter a esperan\u00e7a e a evitar a depress\u00e3o, a agradecer por tudo, a compreender as pessoas que n\u00e3o est\u00e3o na mesma situa\u00e7\u00e3o que eu e que est\u00e3o numa situa\u00e7\u00e3o dif\u00edcil, a valorizar o que tenho e a ser poupada, a dar mais amor \u00e0 minha fam\u00edlia todos os dias como se fosse o \u00faltimo... Aprendi a ser paciente e a aceitar o facto de que todos precisam de uma m\u00e3o amiga!<\/p>\n<p><strong>O QUE \u00c9 QUE QUER QUE O MUNDO SAIBA SOBRE A LGMD<\/strong>:<br \/>\nMesmo a maior parte dos profissionais de sa\u00fade n\u00e3o tem conhecimento desta doen\u00e7a, pelo que devem estar conscientes deste facto e ensinar aos doentes como estar seguros e desafiar a vida.<\/p>\n<p><strong>SE A SUA LGMD PUDESSE SER \"CURADA\" AMANH\u00c3, QUAL SERIA A PRIMEIRA COISA QUE GOSTARIA DE FAZER<\/strong>:<br \/>\nAntes de mais, gostaria de felicitar todos os m\u00e9dicos que me ajudaram pessoalmente. O mais importante \u00e9 que gostaria de abrir um blogue sobre esta doen\u00e7a e orientar e apoiar os doentes na supera\u00e7\u00e3o da doen\u00e7a. Eu sei como estou a sofrer com esta doen\u00e7a. N\u00e3o vou dar hip\u00f3tese a que outros sofram novamente.<\/p>","protected":false},"excerpt":{"rendered":"<p>07\/06\/2015:\u00a0 NAME: Ramesh \u00a0AGE: 28 yrs. old COUNTRY: India LGMD [&hellip;]<\/p>","protected":false},"author":1,"featured_media":946,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,22],"tags":[21,30,23],"class_list":["post-945","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2b","tag-dysferlinopathy","tag-india","tag-lgmd2b"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>LGMD Spotlight Interview - Ramesh<\/title>\n<meta name=\"description\" content=\"Ramesh who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares his experience in living with this progressive neuro-muscular disease.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.lgmd-info.org\/pt\/individuals-with-lgmd-interviews\/2015\/07\/06\/ramesh\/\" \/>\n<meta property=\"og:locale\" content=\"pt_PT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"LGMD Spotlight Interview - 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