02/09/2024
𝐈 𝐂𝐀𝐑𝐑𝐄𝐑𝐀 𝐒𝐎𝐋𝐈𝐃𝐀𝐑𝐈𝐀 𝐔𝐍 𝐌𝐀𝐑 𝐃𝐄 𝐀𝐋𝐄𝐆𝐑𝐈𝐀
𝘔𝘢𝘳, 𝘶𝘯𝘢 𝘯𝘪𝘯̃𝘢 𝘥𝘦 𝘯𝘶𝘦𝘴𝘵𝘳𝘰 𝘣𝘢𝘳𝘳𝘪𝘰, 𝘴𝘪𝘦𝘯𝘥𝘰 𝘩𝘦𝘳𝘮𝘢𝘯𝘢 𝘥𝘦 𝘯𝘢𝘤𝘪𝘮𝘪𝘦𝘯𝘵𝘰 𝘫𝘶𝘯𝘵𝘰 𝘢 𝘵𝘰𝘥𝘢 𝘴𝘶 𝘧𝘢𝘮𝘪𝘭𝘪𝘢, 𝘵𝘪𝘦𝘯𝘦 𝘶𝘯𝘢 𝘦𝘯𝘧𝘦𝘳𝘮𝘦𝘥𝘢𝘥 𝘥𝘦𝘯𝘰𝘮𝘪𝘯𝘢𝘥𝘢 “𝘙𝘈𝘙𝘈” 𝘭𝘭𝘢𝘮𝘢𝘥𝘢 𝘚𝘠𝘕𝘎𝘈𝘗1.
𝘋𝘦𝘴𝘥𝘦 𝘭𝘢 𝘏𝘦𝘳𝘮𝘢𝘯𝘥𝘢𝘥, 𝘰𝘴 𝘪𝘯𝘷𝘪𝘵𝘢𝘮𝘰𝘴 𝘢 𝘱𝘢𝘳𝘵𝘪𝘤𝘪𝘱𝘢𝘳 𝘦𝘯 𝘦𝘴𝘵𝘦 𝘦𝘷𝘦𝘯𝘵𝘰 𝘴𝘰𝘭𝘪𝘥𝘢𝘳𝘪𝘰, 𝘦𝘴𝘵𝘦 𝘱𝘳𝘰́𝘹𝘪𝘮𝘰 21 𝘥𝘦 𝘴𝘦𝘱𝘵𝘪𝘦𝘮𝘣𝘳𝘦 𝘢 𝘭𝘢𝘴 10:30𝘩
ʟᴀs ʙᴀsᴇs
https://river2time.es/index.php/producto/i-carrera-solidaria-un-mar-de-alegria/
"ℰ𝓁 28 𝒹ℯ ℯ𝓃ℯ𝓇ℴ 𝒹ℯ 2020 𝓁𝓁ℯℊℴ́ 𝒶 ℯ𝓈𝓉𝒶 𝓋𝒾𝒹𝒶 ℳ𝒜ℛ. ℳ𝒜ℛ, ℯ𝓈 𝓊𝓃𝒶 𝓃𝒾𝓃̃𝒶, 𝓆𝓊ℯ 𝒸ℴ𝓃 𝓉𝒶𝓃 𝓈ℴ𝓁ℴ 𝓂𝒾𝓇𝒶𝓇𝓁𝒶 𝓉ℯ 𝒶𝓁ℯℊ𝓇𝒶 𝓁𝒶 𝓋𝒾𝒹𝒶, 𝒹ℯ 𝒶𝒽𝒾́ 𝓆𝓊ℯ 𝓈ℯ 𝒸𝓇ℯ𝒶𝓇𝒶 𝓈𝓊 𝒶𝓈ℴ𝒸𝒾𝒶𝒸𝒾ℴ́𝓃 𝒰𝒩 ℳ𝒜ℛ 𝒟ℰ 𝒜ℒℰ𝒢ℛℐ́𝒜. ℰ𝓁 ℯ𝓂𝒷𝒶𝓇𝒶𝓏ℴ 𝒻𝓊ℯ 𝒸ℴ𝓃 𝓉ℴ𝓉𝒶𝓁 𝓃ℴ𝓇𝓂𝒶𝓁𝒾𝒹𝒶𝒹 𝓎 ℯ𝓁 𝓅𝒶𝓇𝓉ℴ ℯ𝓃 𝓃𝒾𝓃ℊ𝓊́𝓃 𝓂ℴ𝓂ℯ𝓃𝓉ℴ 𝓅𝓇ℯ𝓈ℯ𝓃𝓉ℴ́ 𝓇𝒾ℯ𝓈ℊℴ. 𝒫ℯ𝓇ℴ 𝒸ℴ𝓃 ℯ𝓁 𝓅𝒶𝓈ℴ 𝒹ℯ 𝓁ℴ𝓈 𝓂ℯ𝓈ℯ𝓈, 𝓈𝓊𝓈 𝓅𝒶𝒹𝓇ℯ𝓈 ℳ𝒶𝓃𝓊ℯ𝓁 𝓎 𝒫𝒶𝓊𝓁𝒶, 𝓋𝒾ℯ𝓇ℴ𝓃 𝒸ℴ𝓂ℴ 𝓈𝓊 𝓅ℯ𝓆𝓊ℯ𝓃̃𝒶 𝓅𝓇ℯ𝓈ℯ𝓃𝓉𝒶𝒷𝒶 𝓈𝒾́𝓃𝓉ℴ𝓂𝒶𝓈 𝒹𝒾𝓈𝓉𝒾𝓃𝓉ℴ𝓈 𝒶 𝓁ℴ𝓈 𝓆𝓊ℯ 𝓋𝒾𝓋𝒾ℯ𝓇ℴ𝓃 𝒸ℴ𝓃 𝓈𝓊 𝓅𝓇𝒾𝓂ℯ𝓇 𝒽𝒾𝒿ℴ ℒℯℴ. 𝒩ℴ 𝓂ℴ𝓈𝓉𝓇𝒶𝒷𝒶 𝓇ℯ𝓈𝓅𝓊ℯ𝓈𝓉𝒶𝓈 𝒶𝓃𝓉ℯ 𝓈ℴ𝓃𝒾𝒹ℴ𝓈, 𝓃ℴ 𝓉ℯ𝓃𝒾́𝒶 𝓊𝓃 𝓈ℯℊ𝓊𝒾𝓂𝒾ℯ𝓃𝓉ℴ 𝓋𝒾𝓈𝓊𝒶𝓁 𝒶𝓃𝓉ℯ 𝒸𝓊𝒶𝓁𝓆𝓊𝒾ℯ𝓇 ℯ𝓈𝓉𝒾́𝓂𝓊𝓁ℴ, 𝒸𝓊𝒶𝓃𝒹ℴ 𝓁𝓁ℯℊℴ́ ℯ𝓁 𝓂ℴ𝓂ℯ𝓃𝓉ℴ 𝒹ℯ𝓁 ℊ𝒶𝓉ℯℴ 𝓅𝓇ℯ𝓈ℯ𝓃𝓉𝒶𝒷𝒶 𝒹𝒾𝒻𝒾𝒸𝓊𝓁𝓉𝒶𝒹ℯ𝓈 𝒹ℯ ℯ𝓆𝓊𝒾𝓁𝒾𝒷𝓇𝒾ℴ, 𝓁𝒶𝓉ℯ𝓇𝒶𝓁𝒾𝒹𝒶𝒹… 𝒰𝓃 ℳ𝒶𝓇 𝒹ℯ 𝒶𝓁ℯℊ𝓇𝒾́𝒶 𝒮 𝒴 𝒩 𝒢 𝒜 𝒫 1 𝒮𝓊𝓈 𝓅𝒶𝒹𝓇ℯ𝓈 𝓈ℯ 𝓇ℯ𝒸ℴ𝓇𝓇𝒾ℯ𝓇ℴ𝓃 𝓉ℴ𝒹ℴ𝓈 𝓁ℴ𝓈 𝒽ℴ𝓈𝓅𝒾𝓉𝒶𝓁ℯ𝓈 ℯ𝓍𝒾𝓈𝓉ℯ𝓃𝓉ℯ𝓈, 𝓎 𝒹ℯ𝓈𝓅𝓊ℯ́𝓈 𝒹ℯ 𝓊𝓃𝒶 𝓁𝒶𝓇ℊ𝒶 𝓁𝓊𝒸𝒽𝒶, 𝒹ℯ 𝒸𝒾𝓉𝒶𝓈 𝓂ℯ́𝒹𝒾𝒸𝒶𝓈 𝓆𝓊ℯ 𝓃𝓊𝓃𝒸𝒶 𝓁𝓁ℯℊ𝒶𝒷𝒶𝓃, 𝓊𝓃𝒶 𝓅𝒶𝓃𝒹ℯ𝓂𝒾𝒶, ℯ𝓉𝒸 …𝓅ℴ𝓇 𝒻𝒾𝓃 𝓅𝓊𝒹𝒾ℯ𝓇ℴ𝓃 𝓈𝒶𝒷ℯ𝓇 ℯ𝓁 𝒹𝒾𝒶ℊ𝓃ℴ́𝓈𝓉𝒾𝒸ℴ 𝒹ℯ 𝓈𝓊 𝓅ℯ𝓆𝓊ℯ𝓃̃𝒶. ℳ𝒜ℛ 𝓉ℯ𝓃𝒾́𝒶 𝓊𝓃𝒶 ℯ𝓃𝒻ℯ𝓇𝓂ℯ𝒹𝒶𝒹 𝒹ℯ𝓃ℴ𝓂𝒾𝓃𝒶𝒹𝒶 “ℛ𝒜ℛ𝒜” 𝓁𝓁𝒶𝓂𝒶𝒹𝒶 𝒮𝒴𝒩𝒢𝒜𝒫1. 𝒟ℯ 𝓇ℯ𝒸𝒾ℯ𝓃𝓉ℯ 𝒹ℯ𝓈𝒸𝓊𝒷𝓇𝒾𝓂𝒾ℯ𝓃𝓉ℴ, ℯ𝓁 𝓈𝒾́𝓃𝒹𝓇ℴ𝓂ℯ 𝒹ℯ 𝒮𝒴𝒩𝒢𝒜𝒫 1 ℯ𝓈 𝓊𝓃 𝓉𝓇𝒶𝓈𝓉ℴ𝓇𝓃ℴ ℊℯ𝓃ℯ́𝓉𝒾𝒸ℴ 𝓆𝓊ℯ 𝓅𝓇ℴ𝓋ℴ𝒸𝒶 𝓊𝓃𝒶 𝒹𝒾𝓈𝒸𝒶𝓅𝒶𝒸𝒾𝒹𝒶𝒹 𝒾𝓃𝓉ℯ𝓁ℯ𝒸𝓉𝓊𝒶𝓁 𝒹ℯ 𝒹𝒾𝒻ℯ𝓇ℯ𝓃𝓉ℯ ℊ𝓇𝒶𝒹ℴ 𝓎 𝓊𝓃 𝓇ℯ𝓉𝓇𝒶𝓈ℴ 𝓂𝒶𝒹𝓊𝓇𝒶𝓉𝒾𝓋ℴ ℊℯ𝓃ℯ𝓇𝒶𝓁 𝒹ℯ 𝒹𝒾𝒻ℯ𝓇ℯ𝓃𝓉ℯ 𝒾𝓃𝓉ℯ𝓃𝓈𝒾𝒹𝒶𝒹 ℯ𝓃 𝒸𝒶𝒹𝒶 𝒸𝒶𝓈ℴ. ℰ𝓁 𝓅𝓇𝒾𝓂ℯ𝓇 𝒸𝒶𝓈ℴ 𝒻𝓊ℯ 𝒹𝒾𝒶ℊ𝓃ℴ𝓈𝓉𝒾𝒸𝒶𝒹ℴ ℯ𝓃 2009 𝓎 𝓈ℯ 𝒸𝒶𝓁𝒸𝓊𝓁𝒶 𝓆𝓊ℯ 𝒶 𝓃𝒾𝓋ℯ𝓁 𝓂𝓊𝓃𝒹𝒾𝒶𝓁 𝒽𝒶𝓎 𝒹ℯ 1 𝒶 4 𝒸𝒶𝓈ℴ𝓈 𝓅ℴ𝓇 𝒸𝒶𝒹𝒶 10.000 𝓅ℯ𝓇𝓈ℴ𝓃𝒶𝓈. ℰ𝓃 ℰ𝓈𝓅𝒶𝓃̃𝒶, 𝓈ℯℊ𝓊́𝓃 𝓁𝒶 𝒜𝓈ℴ𝒸𝒾𝒶𝒸𝒾ℴ́𝓃 𝒮𝒴𝒩𝒢𝒜𝒫 1 ℰ𝓈𝓅𝒶𝓃̃𝒶, 𝒶𝒸𝓉𝓊𝒶𝓁𝓂ℯ𝓃𝓉ℯ 𝒽𝒶𝓎 𝒶𝓁𝓇ℯ𝒹ℯ𝒹ℴ𝓇 𝒹ℯ 30 𝓅ℯ𝓇𝓈ℴ𝓃𝒶𝓈 𝒹𝒾𝒶ℊ𝓃ℴ𝓈𝓉𝒾𝒸𝒶𝒹𝒶𝓈 𝒸ℴ𝓃 ℯ𝓁 𝓈𝒾́𝓃𝒹𝓇ℴ𝓂ℯ 𝒮𝒴𝒩𝒢𝒜𝒫 1. 𝒮𝒾𝓃 ℯ𝓂𝒷𝒶𝓇ℊℴ, ℯ𝓈𝓉𝒶 𝒸𝒾𝒻𝓇𝒶 𝓅ℴ𝒹𝓇𝒾́𝒶 𝓈ℯ𝓇 𝓈𝓊𝓅ℯ𝓇𝒾ℴ𝓇, 𝓎𝒶 𝓆𝓊ℯ ℯ𝓁 𝒹𝒾𝒶ℊ𝓃ℴ́𝓈𝓉𝒾𝒸ℴ ℯ𝓈 𝓊𝓃ℴ 𝒹ℯ 𝓈𝓊𝓈 𝓅𝓇𝒾𝓃𝒸𝒾𝓅𝒶𝓁ℯ𝓈 𝓇ℯ𝓉ℴ𝓈 𝓎 ℯ𝓃 𝒶𝓁ℊ𝓊𝓃ℴ𝓈 𝒸𝒶𝓈ℴ𝓈 𝓈ℯ 𝓁𝓁ℯℊ𝒶 𝒶 𝒸ℴ𝓃𝒻𝓊𝓃𝒹𝒾𝓇 𝒸ℴ𝓃 ℴ𝓉𝓇ℴ𝓈 𝓉𝓇𝒶𝓈𝓉ℴ𝓇𝓃ℴ𝓈, 𝒸ℴ𝓂ℴ ℯ𝓁 𝒶𝓊𝓉𝒾𝓈𝓂ℴ. 𝒞ℴ𝓃 ℯ𝓁 ℴ𝒷𝒿ℯ𝓉𝒾𝓋ℴ 𝒹ℯ 𝒻ℴ𝓂ℯ𝓃𝓉𝒶𝓇 𝓈𝓊 𝒸ℴ𝓃ℴ𝒸𝒾𝓂𝒾ℯ𝓃𝓉ℴ 𝓎 𝒸ℴ𝓃𝒸𝒾ℯ𝓃𝒸𝒾𝒶𝒸𝒾ℴ́𝓃, 𝓁𝒶 ℯ𝓃𝓉𝒾𝒹𝒶𝒹 𝒾𝓃𝓉ℯ𝓇𝓃𝒶𝒸𝒾ℴ𝓃𝒶𝓁 𝒮𝓎𝓃ℊ𝒶𝓅 𝒢𝓁ℴ𝒷𝒶𝓁 𝒩ℯ𝓉𝓌ℴ𝓇𝓀 ℴ𝓇ℊ𝒶𝓃𝒾𝓏𝒶, 𝒹ℯ𝓈𝒹ℯ 2020, 𝒸𝒶𝒹𝒶 21 𝒹ℯ 𝒿𝓊𝓃𝒾ℴ ℯ𝓁 𝒟𝒾́𝒶 ℐ𝓃𝓉ℯ𝓇𝓃𝒶𝒸𝒾ℴ𝓃𝒶𝓁 𝒹ℯ 𝒮𝒴𝒩𝒢𝒜𝒫. ℰ𝓁 𝓈𝒾́𝓃𝒹𝓇ℴ𝓂ℯ 𝒹ℯ 𝒮𝒴𝒩𝒢𝒜𝒫 1 𝓎 𝓈𝓊𝓈 𝓇ℯ𝓉ℴ𝓈 ℯ𝓃 ℯ𝓁 𝒹𝒾𝒶ℊ𝓃ℴ́𝓈𝓉𝒾𝒸ℴ ℰ𝓁 𝓈𝒾́𝓃𝒹𝓇ℴ𝓂ℯ 𝒮𝒴𝒩𝒢𝒜𝒫 1 ℯ𝓈𝓉𝒶́ 𝓅𝓇ℴ𝓋ℴ𝒸𝒶𝒹ℴ 𝓅ℴ𝓇 𝓊𝓃𝒶 𝓂𝓊𝓉𝒶𝒸𝒾ℴ́𝓃 ℊℯ𝓃ℯ́𝓉𝒾𝒸𝒶 𝒹ℯ𝓁 ℊℯ𝓃 𝒮𝒴𝒩𝒢𝒜𝒫 1 𝓆𝓊ℯ 𝒾𝓃𝓉ℯ𝓇𝒻𝒾ℯ𝓇ℯ ℯ𝓃 𝓁𝒶 𝓅𝓇ℴ𝒹𝓊𝒸𝒸𝒾ℴ́𝓃 𝒹ℯ 𝓁𝒶 𝓅𝓇ℴ𝓉ℯ𝒾́𝓃𝒶 𝒹ℯ𝓁 𝓂𝒾𝓈𝓂ℴ 𝓃ℴ𝓂𝒷𝓇ℯ, 𝒸𝓁𝒶𝓋ℯ 𝓅𝒶𝓇𝒶 𝓁𝒶 𝒸ℴ𝓂𝓊𝓃𝒾𝒸𝒶𝒸𝒾ℴ́𝓃 ℯ𝒻ℯ𝒸𝓉𝒾𝓋𝒶 𝒹ℯ 𝓁𝒶𝓈 𝓃ℯ𝓊𝓇ℴ𝓃𝒶𝓈. ℰ𝓁 ℊ𝓇𝒶𝓃 𝓇ℯ𝓉ℴ 𝒶𝒸𝓉𝓊𝒶𝓁𝓂ℯ𝓃𝓉ℯ ℯ𝓈 𝓈𝓊 𝒸ℴ𝓂𝓅𝓁𝒾𝒸𝒶𝒹ℴ 𝒹𝒾𝒶ℊ𝓃ℴ́𝓈𝓉𝒾𝒸ℴ. ℰ𝓍𝒾𝓈𝓉ℯ 𝓊𝓃 𝒶𝓂𝓅𝓁𝒾ℴ 𝒶𝒷𝒶𝓃𝒾𝒸ℴ 𝒹ℯ 𝓈𝒾́𝓃𝓉ℴ𝓂𝒶𝓈 𝒶𝓈ℴ𝒸𝒾𝒶𝒹ℴ𝓈 𝒶 ℯ𝓈𝓉𝒶 ℯ𝓃𝒻ℯ𝓇𝓂ℯ𝒹𝒶𝒹 𝓎 𝓃ℴ 𝓉ℴ𝒹ℴ𝓈 ℯ𝓁𝓁ℴ𝓈 ℯ𝓈𝓉𝒶́𝓃 𝓅𝓇ℯ𝓈ℯ𝓃𝓉ℯ𝓈 ℯ𝓃 𝓁𝒶𝓈 𝓅ℯ𝓇𝓈ℴ𝓃𝒶𝓈 𝒶𝒻ℯ𝒸𝓉𝒶𝒹𝒶𝓈 𝓅ℴ𝓇 ℯ𝓈𝓉𝒶 𝓂𝓊𝓉𝒶𝒸𝒾ℴ́𝓃. ℰ𝓈𝓉𝒶 𝓋𝒶𝓇𝒾𝒶𝒷𝒾𝓁𝒾𝒹𝒶𝒹 𝒹ℯ 𝓁𝒶 𝓈𝒾𝓃𝓉ℴ𝓂𝒶𝓉ℴ𝓁ℴℊ𝒾́𝒶, 𝓊𝓃𝒾𝒹ℴ 𝒶 𝓈ℯ𝓇 𝓊𝓃𝒶 𝓅𝒶𝓉ℴ𝓁ℴℊ𝒾́𝒶 𝒹ℯ𝓈𝒸𝓊𝒷𝒾ℯ𝓇𝓉𝒶 𝓇ℯ𝒸𝒾ℯ𝓃𝓉ℯ𝓂ℯ𝓃𝓉ℯ 𝓎 𝓁𝒶 𝒻𝒶𝓁𝓉𝒶 𝒹ℯ 𝒸ℴ𝓃ℴ𝒸𝒾𝓂𝒾ℯ𝓃𝓉ℴ 𝒹ℯ 𝓁𝒶 𝓂𝒾𝓈𝓂𝒶 𝒸ℴ𝓃𝓈𝓉𝒾𝓉𝓊𝓎ℯ𝓃 𝓊𝓃𝒶 𝒹ℯ 𝓁𝒶𝓈 𝓅𝓇𝒾𝓃𝒸𝒾𝓅𝒶𝓁ℯ𝓈 𝒹𝒾𝒻𝒾𝒸𝓊𝓁𝓉𝒶𝒹ℯ𝓈 ℯ𝓃 𝓈𝓊 𝒹𝒾𝒶ℊ𝓃ℴ́𝓈𝓉𝒾𝒸ℴ.𝓏 ℋℴ𝓎 ℯ𝓃 𝒹𝒾́𝒶 ℳ𝒜ℛ 𝒽𝒶 ℯ𝓋ℴ𝓁𝓊𝒸𝒾ℴ𝓃𝒶𝒹ℴ 𝓂𝓊𝒸𝒽ℴ ℊ𝓇𝒶𝒸𝒾𝒶𝓈 𝒶 𝓁𝒶 𝓁𝓊𝒸𝒽𝒶 𝒹𝒾𝒶𝓇𝒾𝒶 𝒹ℯ 𝓈𝓊𝓈 𝓅𝒶𝒹𝓇ℯ𝓈, 𝓈𝓊 𝒽ℯ𝓇𝓂𝒶𝓃ℴ, 𝒻𝒶𝓂𝒾𝓁𝒾𝒶 𝓎 𝒶𝓂𝒾ℊℴ𝓈 𝓆𝓊ℯ 𝒿𝓊𝓃𝓉ℴ𝓈 𝒽𝒶𝓃 𝒸ℴ𝓃𝓈𝓉𝒾𝓉𝓊𝒾𝒹ℴ ℯ𝓈𝓉𝒶 𝒶𝓈ℴ𝒸𝒾𝒶𝒸𝒾ℴ́𝓃 𝓁𝓁𝒶𝓂𝒶𝒹𝒶 𝒰𝒩 ℳ𝒜ℛ 𝒟ℰ 𝒜ℒℰ𝒢ℛℐ́𝒜. ℳ𝒜ℛ 𝓈𝒾ℊ𝓊ℯ 𝓈𝒾ℯ𝓃𝒹ℴ 𝓉ℴ𝓉𝒶𝓁𝓂ℯ𝓃𝓉ℯ 𝒹ℯ𝓅ℯ𝓃𝒹𝒾ℯ𝓃𝓉ℯ, 𝒹𝒾́𝒶 𝓎 𝓃ℴ𝒸𝒽ℯ, 𝓈𝓊𝒻𝓇ℯ 𝒸𝓇𝒾𝓈𝒾𝓈 𝒻ℯ𝒷𝓇𝒾𝓁ℯ𝓈 𝓆𝓊ℯ 𝓁ℯ 𝓁𝓁ℯ𝓋𝒶 𝒶 𝒸𝓇𝒾𝓈𝒾𝓈 ℯ𝓅𝒾𝓁ℯ́𝓅𝓉𝒾𝒸𝒶𝓈 𝓎 ℴ𝓉𝓇𝒶𝓈 𝓅𝒶𝓉ℴ𝓁ℴℊ𝒾́𝒶𝓈 𝓉𝒾́𝓅𝒾𝒸𝒶𝓈 𝒹ℯ ℯ𝓈𝓉𝒶 𝒹𝒾𝓈𝒸𝒶𝓅𝒶𝒸𝒾𝒹𝒶𝒹. 𝒫ℯ𝓇ℴ 𝓃ℴ 𝓅ℯ𝓇𝒹ℯ𝓂ℴ𝓈 𝓁𝒶 𝒻ℯ, 𝓎 𝓈ℯℊ𝓊𝒾𝓇ℯ𝓂ℴ𝓈 𝓁𝓊𝒸𝒽𝒶𝓃𝒹ℴ 𝓅𝒶𝓇𝒶 𝓂ℯ𝒿ℴ𝓇𝒶𝓇 𝓁𝒶 𝒸𝒶𝓁𝒾𝒹𝒶𝒹 𝒹ℯ 𝓋𝒾𝒹𝒶 𝒹ℯ ℳ𝒜ℛ, 𝓁𝓁ℯ𝓋𝒶́𝓃𝒹ℴ𝓁𝒶 𝒶 𝒹𝒾𝓈𝓉𝒾𝓃𝓉𝒶𝓈 𝓉ℯ𝓇𝒶𝓅𝒾𝒶𝓈, ℯ𝓈𝓉𝓊𝒹𝒾ℴ𝓈 𝓎 𝒶𝓈𝒾́ 𝓅ℴ𝒹ℯ𝓇 𝓉𝒶𝓂𝒷𝒾ℯ́𝓃 𝒶𝓎𝓊𝒹𝒶𝓇 𝒶 𝓃𝒾𝓃̃ℴ𝓈 𝓎 𝓃𝒾𝓃̃𝒶𝓈 𝓆𝓊ℯ 𝓃𝒶𝓏𝒸𝒶𝓃 𝒸ℴ𝓃 𝒮𝒴𝒩𝒢𝒜𝒫1. 𝒫𝓊ℯ𝒹ℯ𝓈 𝒸ℴ𝓃𝓉𝒶𝒸𝓉𝒶𝓇 𝒸ℴ𝓃 𝓃ℴ𝓈ℴ𝓉𝓇ℴ𝓈 𝒶 𝓉𝓇𝒶𝓋ℯ́𝓈 𝒹ℯ 𝓃𝓊ℯ𝓈𝓉𝓇ℴ ℐ𝓃𝓈𝓉𝒶ℊ𝓇𝒶𝓂 @𝓈𝓎𝓃ℊ𝒶𝓅1𝒶𝓃𝒹𝒶𝓁𝓊𝒸𝒾𝒶 ℴ 𝓁ℴ𝓈 𝓉ℯ𝓁ℯ́𝒻ℴ𝓃ℴ𝓈 +34 625 20 45 90 ℴ́ +34 667 99 85 13. 𝒢ℛ𝒜𝒞ℐ𝒜𝒮 𝒫𝒪ℛ 𝒮𝒰 𝒜𝒯ℰ𝒩𝒞ℐ𝒪́𝒩"
