Силами многих людей - наших жертвователей, простых людей, компаний, - каждый день (совершенно незаметно и буднично)
делаются добрые дела.
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string(3106) "Настина мама рассказывает нам о своей дочери.
Что может сказать мать о дочери? Разное, конечно.
Если бы вы видели глаза Настиной мамы, то нам не надо было бы писать, что мама рассказывала о том, какая Настюша хорошая, скромная, как она училась на социального педагога, как участвовала в волонтёрских акциях, как помогала людям, как она, мама, ее любит...
И еще много-много всего - всего, что было «до». Мамина любовь осталась, но вот все остальное ...
Это «до» дало о себе знать в начале этого года, когда настроение и состояние Насти резко изменилось. Настю стали беспокоить частые головные боли, появилась апатия, раздражение.
Мать отвела Настю к врачу. Один врач, второй, одно обследование, второе, третье, диагноз ...
Узнав диагноз дочери (опухоль мозга), мама замолчала. Точнее она молчала, молчала и боялась, очень боялась сказать правду, сделать больно самому дорогому человеку на свете.
Однажды, совсем недавно, мама с дочкой смотрели телевизор. Шла передача про то, как известные люди победили «рак».Неожиданно Настя посмотрела на маму и произнесла:
- Мама, ведь у меня рак, да?
Как же тяжело тогда далось это «да»…
Первый шаг сделан. Второй шаг - поездка в Москву, т.к. на Украине ребёнку помочь не могли.
Третий шаг – необходимость в проведении лучевой и химиотерапии в институте Радиологии. Для иностранных граждан лечение платное, порядка 200 тысяч рублей.
Настя очень надеется, что, как и у известных людей из той передачи, у неё получится победить рак.
Пожалуйста, давайте поможем ей эту надежду не потерять и вместе с Настей продолжать делать шаги на пути к выздоровлению
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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Что может сказать мать о дочери? Разное, конечно.
Если бы вы видели глаза Настиной мамы, то нам не надо было бы писать, что мама рассказывала о том, какая Настюша хорошая, скромная, как она училась на социального педагога, как участвовала в волонтёрских акциях, как помогала людям, как она, мама, ее любит...
И еще много-много всего - всего, что было «до». Мамина любовь осталась, но вот все остальное ...
Это «до» дало о себе знать в начале этого года, когда настроение и состояние Насти резко изменилось. Настю стали беспокоить частые головные боли, появилась апатия, раздражение.
Мать отвела Настю к врачу. Один врач, второй, одно обследование, второе, третье, диагноз ...
Узнав диагноз дочери (опухоль мозга), мама замолчала. Точнее она молчала, молчала и боялась, очень боялась сказать правду, сделать больно самому дорогому человеку на свете.
Однажды, совсем недавно, мама с дочкой смотрели телевизор. Шла передача про то, как известные люди победили «рак».Неожиданно Настя посмотрела на маму и произнесла:
- Мама, ведь у меня рак, да?
Как же тяжело тогда далось это «да»…
Первый шаг сделан. Второй шаг - поездка в Москву, т.к. на Украине ребёнку помочь не могли.
Третий шаг – необходимость в проведении лучевой и химиотерапии в институте Радиологии. Для иностранных граждан лечение платное, порядка 200 тысяч рублей.
Настя очень надеется, что, как и у известных людей из той передачи, у неё получится победить рак.
Пожалуйста, давайте поможем ей эту надежду не потерять и вместе с Настей продолжать делать шаги на пути к выздоровлению
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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Когда я была маленькая, то боялась оставаться дома одна, боялась темноты, боялась, что родители за двойку отругают.
Выросла и снова стала бояться, что в институт не поступлю, что на работе не удержусь.
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- Мама, я что умру?
Это кусочек из письма мамы Саши, с которым она пришла к нам в фонд.
Саша заболел в июле 2008 года, как это часто бывает при таком заболевании, у мальчика очень сильно болела голова.
Обследование выявило опухоль головного мозга.
Началось длительное лечение: операция, 8 курсов химиотерапии, лучевая терапия.
Больше года жизни ушло на борьбу.
За это время Саша очень изменился, повзрослел, стал писать стихи.
И лечение помогло, Саша вылечился, многое для себя понял и переоценил.
Казалось, всё самое страшное уже позади. Но в конце мая 2010 года на плановом обследовании выяснилось, что у мальчика метастаз в спине.
Он всего один и с ним можно справиться, но врачи говорят, что необходим препарат Депоцит, который мало того, что стоит больше 2 тысяч евро за флакон, так ещё и не продаётся в России.
Стоимость курса, необходимого для лечения Саши, превышает 20 тысяч евро.
Вы себе представляете, что такое 20 тысяч евро для безмерно любящей своего ребёнка матери из Ростовской области?
Когда её зарплата 7 тысяч рублей, а родное предприятие оказало материальную помощь на лечение ребёнка в размере 5 тысяч рублей.
Для мамы это настоящий тупик.
Волонтёры фонда готовы найти и купить это лекарство за границей, вся проблема в деньгах, которых нет даже на 1 флакон, а их нужно 10.
Именно от этих денег сейчас зависит ответ на вопрос Саши…
Можно помочь, отправив деньги на сберкнижку маме. Мы готовы связать Вас с родителями.
Пожалуйста, сообщайте и нам о перечислениях по телефону (499)903-82-81 или (495)506-79-70.
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Когда я была маленькая, то боялась оставаться дома одна, боялась темноты, боялась, что родители за двойку отругают.
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Казалось, что это происходит не со мной. Мой мальчик. Такой жизнерадостный и любознательный…нет сил смотреть в глаза сыну, а он спрашивает:
- Мама, я что умру?
Это кусочек из письма мамы Саши, с которым она пришла к нам в фонд.
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Обследование выявило опухоль головного мозга.
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И лечение помогло, Саша вылечился, многое для себя понял и переоценил.
Казалось, всё самое страшное уже позади. Но в конце мая 2010 года на плановом обследовании выяснилось, что у мальчика метастаз в спине.
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Стоимость курса, необходимого для лечения Саши, превышает 20 тысяч евро.
Вы себе представляете, что такое 20 тысяч евро для безмерно любящей своего ребёнка матери из Ростовской области?
Когда её зарплата 7 тысяч рублей, а родное предприятие оказало материальную помощь на лечение ребёнка в размере 5 тысяч рублей.
Для мамы это настоящий тупик.
Волонтёры фонда готовы найти и купить это лекарство за границей, вся проблема в деньгах, которых нет даже на 1 флакон, а их нужно 10.
Именно от этих денег сейчас зависит ответ на вопрос Саши…
Можно помочь, отправив деньги на сберкнижку маме. Мы готовы связать Вас с родителями.
Пожалуйста, сообщайте и нам о перечислениях по телефону (499)903-82-81 или (495)506-79-70.
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С 5 -и месяцев родители обратили внимание, что их малышка стала плохо кушать, отставать в весе. Обследовались, врачи нашли множество болезней (врождённая липодистрофия, поливалентная пищевая аллергия и другие).
По большому счету ничего страшного. Со всем этим можно было жить.
С 7 лет у девочки появились признаки преждевременного полового созревания, высокий уровень гормонов, увеличение костного возраста.
В ходе обследования была выполнена МРТ головного мозга, которая выявила опухоль. Это было в 2003 году.
Опухоль оказалась доброкачественной и доктора на первых этапах рекомендовали за ней просто наблюдать, следить за динамикой, так как операция могла иметь и негативные последствия.
В феврале 2010 года состояние Сашеньки резко ухудшилось. 27 февраля 2010 года её госпитализировали в коматозном состоянии в Морозовскую больницу, где сделали срочную операцию по удалению внутренней гидроцефалии.
Саму опухоль сейчас удалить уже невозможно, она очень большая…
Единственным вариантом лечения для Саши сейчас является протонное облучение.
Стоимость этого лечения 250 тысяч рублей.
Несколько строк из письма мамы:
"…только это лечение может спасти моего ребёнка, но стоимость его слишком велика, чтобы я могла его оплатить. Я обращаюсь к вам за помощью!
Здоровье моей дочери для меня важнее всего на свете"
Доктор, которая ведёт Сашу, сказала нам, что при проведённом лечении, прогнозы очень хорошие, с такими опухолями (она доброкачественная) пациенты живут вполне нормальной жизнью много лет.
Без лечения всего этого не может быть.
Пожалуйста, давайте поможем!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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С 5 -и месяцев родители обратили внимание, что их малышка стала плохо кушать, отставать в весе. Обследовались, врачи нашли множество болезней (врождённая липодистрофия, поливалентная пищевая аллергия и другие).
По большому счету ничего страшного. Со всем этим можно было жить.
С 7 лет у девочки появились признаки преждевременного полового созревания, высокий уровень гормонов, увеличение костного возраста.
В ходе обследования была выполнена МРТ головного мозга, которая выявила опухоль. Это было в 2003 году.
Опухоль оказалась доброкачественной и доктора на первых этапах рекомендовали за ней просто наблюдать, следить за динамикой, так как операция могла иметь и негативные последствия.
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Саму опухоль сейчас удалить уже невозможно, она очень большая…
Единственным вариантом лечения для Саши сейчас является протонное облучение.
Стоимость этого лечения 250 тысяч рублей.
Несколько строк из письма мамы:
"…только это лечение может спасти моего ребёнка, но стоимость его слишком велика, чтобы я могла его оплатить. Я обращаюсь к вам за помощью!
Здоровье моей дочери для меня важнее всего на свете"
Доктор, которая ведёт Сашу, сказала нам, что при проведённом лечении, прогнозы очень хорошие, с такими опухолями (она доброкачественная) пациенты живут вполне нормальной жизнью много лет.
Без лечения всего этого не может быть.
Пожалуйста, давайте поможем!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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string(3727) "У нас в отделении есть девочка Лиза с глазками "вишенками".
Она - очень особенный ребёнок.
Лиза родилась 22 марта 2008 года.
Она поздний, единственный и очень долгожданный ребёнок.
Роды были непростые.
Из-за врачебной халатности во время родов у малышки развилась острая гипоксия, маме Лизы сделали экстренное кесарево сечение.
Достали ребёнка, который к тому времени уже семь минут как не дышал. Реанимация. Лиза девять дней находилась между жизнью и смертью.
Она справилась, но результатом таких родов стал диагноз ДЦП (высокий тонус рук и ног, задержка психического развития).
Полтора года родители Лизы бились за свою малышку. Различные занятия, массажи, гимнастика. И долгожданный результат: Лиза стала брать в руки игрушки, появился шаговый рефлекс, она могла произносить несколько слов.
Мама и папа были полны надежд, что их девочка сможет полноценно жить.
Но случилось то, чего никто не ожидал.
На плановом осмотре у Лизы обнаружили опухоль печени, которая, как выяснилось потом, оказалась злокачественной. Рак…
Родители не могли поверить в случившееся. Лечение ДЦП пришлось прекратить, т.к. эти болезни лечить параллельно нельзя.
Всё, чего добились за полтора года лечения ДЦП, потеряно.
Сейчас речь о другом - выжить.
Лиза с мамой проходит лечение в отделении онкологии РДКБ.
Малышке делают химиотерапию, в дальнейшем необходима операция.
Лечение ребёнок переносит крайне тяжело.
Ножки и ручки у Лизоньки в постоянном тонусе, они напряжены так, что мама с трудом меняет памперс.
На фоне проводимой химиотерапии тонус конечностей стал ещё сильнее.
На малышку больно смотреть…
Семья находится в сложном материальном положении.
Им очень нужна помощь!
Реквизиты сберкнижки мамы:
Получатель платежа: Казакова Нина Валентиновна
N счета: 42307810538118154192
в Донском отделении Сбербанка
№ 7813 / 01545 г.Москва
Р/с 30301810938006003811
к/с 30101810400000000225
БИК 044525225
ИНН 7707083893
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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Она - очень особенный ребёнок.
Лиза родилась 22 марта 2008 года.
Она поздний, единственный и очень долгожданный ребёнок.
Роды были непростые.
Из-за врачебной халатности во время родов у малышки развилась острая гипоксия, маме Лизы сделали экстренное кесарево сечение.
Достали ребёнка, который к тому времени уже семь минут как не дышал. Реанимация. Лиза девять дней находилась между жизнью и смертью.
Она справилась, но результатом таких родов стал диагноз ДЦП (высокий тонус рук и ног, задержка психического развития).
Полтора года родители Лизы бились за свою малышку. Различные занятия, массажи, гимнастика. И долгожданный результат: Лиза стала брать в руки игрушки, появился шаговый рефлекс, она могла произносить несколько слов.
Мама и папа были полны надежд, что их девочка сможет полноценно жить.
Но случилось то, чего никто не ожидал.
На плановом осмотре у Лизы обнаружили опухоль печени, которая, как выяснилось потом, оказалась злокачественной. Рак…
Родители не могли поверить в случившееся. Лечение ДЦП пришлось прекратить, т.к. эти болезни лечить параллельно нельзя.
Всё, чего добились за полтора года лечения ДЦП, потеряно.
Сейчас речь о другом - выжить.
Лиза с мамой проходит лечение в отделении онкологии РДКБ.
Малышке делают химиотерапию, в дальнейшем необходима операция.
Лечение ребёнок переносит крайне тяжело.
Ножки и ручки у Лизоньки в постоянном тонусе, они напряжены так, что мама с трудом меняет памперс.
На фоне проводимой химиотерапии тонус конечностей стал ещё сильнее.
На малышку больно смотреть…
Семья находится в сложном материальном положении.
Им очень нужна помощь!
Реквизиты сберкнижки мамы:
Получатель платежа: Казакова Нина Валентиновна
N счета: 42307810538118154192
в Донском отделении Сбербанка
№ 7813 / 01545 г.Москва
Р/с 30301810938006003811
к/с 30101810400000000225
БИК 044525225
ИНН 7707083893
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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string(2) "s1"
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NULL
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NULL
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string(2) "30"
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}
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NULL
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string(10) "16.09.2014"
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string(1) " "
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bool(false)
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string(1) "/"
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string(3) "500"
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string(8) "children"
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NULL
["~IBLOCK_EXTERNAL_ID"]=>
NULL
["LID"]=>
string(2) "s1"
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string(2) "s1"
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NULL
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array(0) {
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string(4480) "Очень жалко больного ребенка. Особенно, если этот ребенок никому не нужен. В июне 2009 года в отделении онкологии появился Женя. Он приехал из детского дома, сражаться со своей болезнью один на один. Однако в ходе обследования выяснилось, что опухоль у Жени доброкачественная, а "с такими опухолями живут 100 лет".
Мы все очень радовались за Женю - такого жизнерадостного и открытого ребенка, - но от мысли, что теперь ему, не совсем здоровому, придется возвращаться в детский дом, становилось как-то не по себе. Благодаря помощи многих неравнодушных людей мы смогли найти семью, которая приняла Женю как родного.
Из письма мамы Жени: "Женя находится в нашей семье с сентября 2009 года. Усыновляя ребенка, мы с мужем знали о многочисленных заболеваниях, которые врачи обнаружили у ребенка. За то время, что Женя находится в семье, практически все диагнозы сняты, ребенок сделал огромный рывок в своем развитии: научился бегло читать, считает, пишет печатными буквами, поет, очень подрос и поправился. Одним словом, стал совсем домашний мамин-папин мальчик, как он сам себя называет "взрослый парень". А еще у ребенка просто потрясающее чувство юмора, это на редкость открытый и коммуникабельный ребенок! Женя очень хочет заниматься спортом-фехтованием и боксом, он сам так сказал, но есть одно существенное препятствие: моему сыну требуется операция по удалению ганглионевромы (опухоли средостения слева). В связи с тем, что опухоль объемная, расположена в непосредственной близости от левого легкого, а так же примыкает к позвоночнику, есть большая вероятность того, что во время операции и после нее могут возникнуть осложнения.
Я обратилась к проф. Дитриху Фон Швайницу (Мюнхен, Германия), который проводит подобные операции и является специалистом мирового уровня. Я отправила профессору выписку из истории болезни моего сына и результаты МРТ спинного и головного мозга Жени. Профессор согласился провести операцию по удалению опухоли в клинике г. Мюнхена. Однако у меня нет средств на оплату операции и послеоперационной реабилитации".
Чтобы вылечить Женю нужно собрать 6440 евро. После этого лечения Женя станет обыкновенным здоровым ребенком в обыкновенной любящей семье - это именно то, о чем он всегда мечтал! Давайте поможем Жене! Очень жалко больного ребенка. Особенно, если этот ребенок бесконечно важен для своих родителей.
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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string(4376) "Очень жалко больного ребенка. Особенно, если этот ребенок никому не нужен. В июне 2009 года в отделении онкологии появился Женя. Он приехал из детского дома, сражаться со своей болезнью один на один. Однако в ходе обследования выяснилось, что опухоль у Жени доброкачественная, а "с такими опухолями живут 100 лет".
Мы все очень радовались за Женю - такого жизнерадостного и открытого ребенка, - но от мысли, что теперь ему, не совсем здоровому, придется возвращаться в детский дом, становилось как-то не по себе. Благодаря помощи многих неравнодушных людей мы смогли найти семью, которая приняла Женю как родного.
Из письма мамы Жени: "Женя находится в нашей семье с сентября 2009 года. Усыновляя ребенка, мы с мужем знали о многочисленных заболеваниях, которые врачи обнаружили у ребенка. За то время, что Женя находится в семье, практически все диагнозы сняты, ребенок сделал огромный рывок в своем развитии: научился бегло читать, считает, пишет печатными буквами, поет, очень подрос и поправился. Одним словом, стал совсем домашний мамин-папин мальчик, как он сам себя называет "взрослый парень". А еще у ребенка просто потрясающее чувство юмора, это на редкость открытый и коммуникабельный ребенок! Женя очень хочет заниматься спортом-фехтованием и боксом, он сам так сказал, но есть одно существенное препятствие: моему сыну требуется операция по удалению ганглионевромы (опухоли средостения слева). В связи с тем, что опухоль объемная, расположена в непосредственной близости от левого легкого, а так же примыкает к позвоночнику, есть большая вероятность того, что во время операции и после нее могут возникнуть осложнения.
Я обратилась к проф. Дитриху Фон Швайницу (Мюнхен, Германия), который проводит подобные операции и является специалистом мирового уровня. Я отправила профессору выписку из истории болезни моего сына и результаты МРТ спинного и головного мозга Жени. Профессор согласился провести операцию по удалению опухоли в клинике г. Мюнхена. Однако у меня нет средств на оплату операции и послеоперационной реабилитации".
Чтобы вылечить Женю нужно собрать 6440 евро. После этого лечения Женя станет обыкновенным здоровым ребенком в обыкновенной любящей семье - это именно то, о чем он всегда мечтал! Давайте поможем Жене! Очень жалко больного ребенка. Особенно, если этот ребенок бесконечно важен для своих родителей.
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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["DETAIL_TEXT"]=>
string(2639) "Саша уже взрослый и серьёзный человек. Со сложившимися взглядами на жизнь.
С самого раннего детства он мечтал о том, как поступит в Суворовское училище, представлял, как им будут гордиться родители, особенно папа.
После шестого класса мальчик стал проходить медицинскую комиссию для поступления в училище.
Прошел различные анализы, исследования.
Врачей насторожили частые головные боли юноши, они стали искать причину.
Она оказалась очень серьёзной - опухоль головного мозга.
О поступлении в Суворовское училище речи уже не шло.
На повестке дня стоял совершенно другой вопрос - как выжить.
В июне 2009 года мальчику попытались сделать операцию в институте Бурденко.
Именно попытались, т.к. опухоль оказалась неоперабельной (удалить её невозможно).
Радовали только результаты гистологии - опухоль "не очень злая", она является как бы промежуточной между доброкачественными и злокачественными опухолями.
А значит, шансы на выздоровление высоки.
Так как хирургическое лечение невозможно, врачи предложили пройти химиотерапию препаратом "Темодал". На четыре цикла химиотерапии необходимо 8 упаковок Темодала по 100 мг. и 4 упаковки по 20 мг. Общая стоимость лекарств порядка 250 тысяч рублей. Семье Осяниных самим с такой суммой не справиться, а время совсем не ждёт.
Лечение необходимо начинать уже 20 февраля.
В наших силах помочь Саше выжить, а поводы для гордости у родителей найдутся…"
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string(2536) "Саша уже взрослый и серьёзный человек. Со сложившимися взглядами на жизнь.
С самого раннего детства он мечтал о том, как поступит в Суворовское училище, представлял, как им будут гордиться родители, особенно папа.
После шестого класса мальчик стал проходить медицинскую комиссию для поступления в училище.
Прошел различные анализы, исследования.
Врачей насторожили частые головные боли юноши, они стали искать причину.
Она оказалась очень серьёзной - опухоль головного мозга.
О поступлении в Суворовское училище речи уже не шло.
На повестке дня стоял совершенно другой вопрос - как выжить.
В июне 2009 года мальчику попытались сделать операцию в институте Бурденко.
Именно попытались, т.к. опухоль оказалась неоперабельной (удалить её невозможно).
Радовали только результаты гистологии - опухоль "не очень злая", она является как бы промежуточной между доброкачественными и злокачественными опухолями.
А значит, шансы на выздоровление высоки.
Так как хирургическое лечение невозможно, врачи предложили пройти химиотерапию препаратом "Темодал". На четыре цикла химиотерапии необходимо 8 упаковок Темодала по 100 мг. и 4 упаковки по 20 мг. Общая стоимость лекарств порядка 250 тысяч рублей. Семье Осяниных самим с такой суммой не справиться, а время совсем не ждёт.
Лечение необходимо начинать уже 20 февраля.
В наших силах помочь Саше выжить, а поводы для гордости у родителей найдутся…"
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Эффекта данное лечение не имело.
24 апреля 2009 года Джабраил был госпитализирован в отделение онкологии Российской детской клинической больницы в Москве. После биопсии стало понятно, почему не помогало прошлое лечение, ведь рак не вылечить витаминами….
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Но всё не так просто…
Мальчику в качестве поддерживающей терапии назначили препарат "Пегинтрон".
Применять это лекарство необходимо длительно на протяжении 70 недель, если не возникнет индивидуальной непереносимости.
Стоимость лекарства НА НЕДЕЛЮ 12 000 рублей.
Сейчас Джабраил с родителями дома, они пытаются найти деньги на эти лекарства.
И ещё они очень надеются на нашу с вами помощь.
Помочь можно деньгами или самостоятельно купить лекарство и передать семье.
Пожалуйста, если это в наших силах, давайте поможем!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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Эффекта данное лечение не имело.
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Но всё не так просто…
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Применять это лекарство необходимо длительно на протяжении 70 недель, если не возникнет индивидуальной непереносимости.
Стоимость лекарства НА НЕДЕЛЮ 12 000 рублей.
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Пожалуйста, если это в наших силах, давайте поможем!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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NULL
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Костя заболел в июне 2009 года: появились боли в животе, температура.
Обратились в больницу.
При осмотре хирург обнаружил огромную опухоль забрюшинного пространства (15х8 см), она оказалась злокачественной… Так мама с Костей оказались в Москве, в отделении онкологии РДКБ.
Ребёнок очень тяжело переносит лечение, каждая химиотерапия дается "с боем" (рвота, температура, потеря аппетита, падение показателей крови) это лишь некоторые из симптомов, которые переживает шестилетний мальчик.
Костя старается, он борется за свою жизнь, поддерживает маму.
В перерывах между химией он играет в солдатиков, рыцарей, индейцев.
В его играх всегда "хорошие" побеждают "плохих". Всегда!
Семья верит, что и в главной борьбе за жизнь ребёнка они смогут победить.
Но им, как и многим другим семьям, попавшим в такую ситуацию, нужна помощь!
Из письма мамы Кости:
"Основным источником дохода семьи является зарплата мужа, который работает в пожарной части нашего посёлка. Живем мы вместе с моими родителями: бабушка - пенсионерка, дедушка- инвалид 2-й группы (уже 8 лет на костылях, перелом таза и тазобедренного сустава)"
Для продолжения лечения необходимы средства.
Пожалуйста, давайте поможем!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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Костя заболел в июне 2009 года: появились боли в животе, температура.
Обратились в больницу.
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Костя старается, он борется за свою жизнь, поддерживает маму.
В перерывах между химией он играет в солдатиков, рыцарей, индейцев.
В его играх всегда "хорошие" побеждают "плохих". Всегда!
Семья верит, что и в главной борьбе за жизнь ребёнка они смогут победить.
Но им, как и многим другим семьям, попавшим в такую ситуацию, нужна помощь!
Из письма мамы Кости:
"Основным источником дохода семьи является зарплата мужа, который работает в пожарной части нашего посёлка. Живем мы вместе с моими родителями: бабушка - пенсионерка, дедушка- инвалид 2-й группы (уже 8 лет на костылях, перелом таза и тазобедренного сустава)"
Для продолжения лечения необходимы средства.
Пожалуйста, давайте поможем!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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string(3369) "Владику семь лет.
1 сентября он со своими сверстниками пошёл в школу. С огромным букетом цветов, в первый раз, в первый класс.
Первый звонок, всё только начинается, столько всего впереди!
Еще в начале осени Владька внешне был абсолютно здоровым ребёнком, жизнерадостным, ласковым, немного озорным.
В один из дней мама обратила внимание, что у Владика покосился и припух глаз.Обратились в больницу, сделали снимки.
Результаты шокировали всех - опухоль ствола головного мозга.
Такие опухоли не оперирую нигде в мире. Нигде.
Молдавские врачи сразу признали своё бессилие, со словами "ничем помочь не можем, готовьтесь к худшему" отпустили домой. Это страшно…Сидеть дома, видеть как каждый день твоему ребёнку становится хуже, как он теряет возможность ходить, говорить, держать ложку…
Всё это пришлось увидеть маме мальчика.
Ситуация очень тяжёлая.
Единственное, что можно сейчас сделать - это провести курс лучевой терапии.
Именно за этим Владик с мамой и приехали в Москву.
Лечение для иностранных граждан платное, порядка 250 000 рублей.
У мамы Владика, которая одна воспитывает двоих детей, таких денег нет.
Надежда только на нас с вами.
А что потом?
Как сказал доктор "надеяться, что лучевая терапия поможет, что будет ремиссия, а дальше ходить в церковь, ставить свечки и молить Бога о чуде".
Когда мы привезли Владика в Москву, в институт Радиологии, он долго не соглашался выходить из машины, боялся.
Уговорить его удалось, только подарив маленький игрушечный вертолёт, который теперь он не выпускает из рук.
Жизнь этого мальчика такая же хрупкая как вертолетик в его руках. Он летит, но нужно быть очень аккуратным, направлять его, защищать, беречь, любить…
Пожалуйста, давайте поможем Владику!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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string(3231) "Владику семь лет.
1 сентября он со своими сверстниками пошёл в школу. С огромным букетом цветов, в первый раз, в первый класс.
Первый звонок, всё только начинается, столько всего впереди!
Еще в начале осени Владька внешне был абсолютно здоровым ребёнком, жизнерадостным, ласковым, немного озорным.
В один из дней мама обратила внимание, что у Владика покосился и припух глаз.Обратились в больницу, сделали снимки.
Результаты шокировали всех - опухоль ствола головного мозга.
Такие опухоли не оперирую нигде в мире. Нигде.
Молдавские врачи сразу признали своё бессилие, со словами "ничем помочь не можем, готовьтесь к худшему" отпустили домой. Это страшно…Сидеть дома, видеть как каждый день твоему ребёнку становится хуже, как он теряет возможность ходить, говорить, держать ложку…
Всё это пришлось увидеть маме мальчика.
Ситуация очень тяжёлая.
Единственное, что можно сейчас сделать - это провести курс лучевой терапии.
Именно за этим Владик с мамой и приехали в Москву.
Лечение для иностранных граждан платное, порядка 250 000 рублей.
У мамы Владика, которая одна воспитывает двоих детей, таких денег нет.
Надежда только на нас с вами.
А что потом?
Как сказал доктор "надеяться, что лучевая терапия поможет, что будет ремиссия, а дальше ходить в церковь, ставить свечки и молить Бога о чуде".
Когда мы привезли Владика в Москву, в институт Радиологии, он долго не соглашался выходить из машины, боялся.
Уговорить его удалось, только подарив маленький игрушечный вертолёт, который теперь он не выпускает из рук.
Жизнь этого мальчика такая же хрупкая как вертолетик в его руках. Он летит, но нужно быть очень аккуратным, направлять его, защищать, беречь, любить…
Пожалуйста, давайте поможем Владику!
Всю дополнительную информацию можно получить по телефону (495) 506-79-70"
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["LINK_IBLOCK_ID"]=>
string(1) "0"
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string(1) "N"
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string(1) "N"
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string(1) "N"
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string(1) "N"
["VERSION"]=>
string(1) "1"
["USER_TYPE"]=>
NULL
["USER_TYPE_SETTINGS"]=>
NULL
["HINT"]=>
string(0) ""
["PROPERTY_VALUE_ID"]=>
NULL
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string(0) ""
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string(0) ""
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NULL
["VALUE_XML_ID"]=>
NULL
["VALUE_SORT"]=>
NULL
["~VALUE"]=>
string(0) ""
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string(0) ""
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["~DEFAULT_VALUE"]=>
string(1) "0"
}
}
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array(5) {
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array(37) {
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string(2) "20"
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string(2) "15"
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string(10) "Адрес"
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string(1) "Y"
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string(3) "500"
["CODE"]=>
string(7) "ADDRESS"
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string(0) ""
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string(1) "S"
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string(1) "1"
["COL_COUNT"]=>
string(2) "30"
["LIST_TYPE"]=>
string(1) "L"
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string(1) "N"
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NULL
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string(0) ""
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string(1) "5"
["TMP_ID"]=>
NULL
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string(1) "0"
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string(1) "N"
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string(1) "N"
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string(1) "Y"
["IS_REQUIRED"]=>
string(1) "Y"
["VERSION"]=>
string(1) "1"
["USER_TYPE"]=>
NULL
["USER_TYPE_SETTINGS"]=>
NULL
["HINT"]=>
string(0) ""
["PROPERTY_VALUE_ID"]=>
string(4) "3016"
["VALUE"]=>
string(14) "Молдова"
["DESCRIPTION"]=>
string(0) ""
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NULL
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NULL
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NULL
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string(14) "Молдова"
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string(0) ""
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string(10) "Адрес"
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string(0) ""
["DISPLAY_VALUE"]=>
string(14) "Молдова"
}
["AGE"]=>
array(37) {
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string(2) "19"
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string(19) "2014-08-08 12:08:39"
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string(2) "15"
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string(14) "Возраст"
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string(1) "Y"
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string(3) "500"
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string(3) "AGE"
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string(0) ""
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string(1) "S"
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string(1) "1"
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string(2) "30"
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string(1) "L"
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string(1) "N"
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NULL
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string(0) ""
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string(1) "5"
["TMP_ID"]=>
NULL
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string(1) "0"
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string(1) "N"
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string(1) "N"
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string(1) "Y"
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string(1) "Y"
["VERSION"]=>
string(1) "1"
["USER_TYPE"]=>
NULL
["USER_TYPE_SETTINGS"]=>
NULL
["HINT"]=>
string(0) ""
["PROPERTY_VALUE_ID"]=>
string(4) "3015"
["VALUE"]=>
string(8) "7 лет"
["DESCRIPTION"]=>
string(0) ""
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NULL
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NULL
["VALUE_SORT"]=>
NULL
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string(8) "7 лет"
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string(0) ""
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string(14) "Возраст"
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string(0) ""
["DISPLAY_VALUE"]=>
string(8) "7 лет"
}
["DIAGNOSTIC"]=>
array(37) {
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string(2) "21"
["TIMESTAMP_X"]=>
string(19) "2014-08-08 12:08:39"
["IBLOCK_ID"]=>
string(2) "15"
["NAME"]=>
string(14) "Диагноз"
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string(1) "Y"
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string(3) "500"
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string(10) "DIAGNOSTIC"
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string(0) ""
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string(1) "S"
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string(1) "1"
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string(2) "30"
["LIST_TYPE"]=>
string(1) "L"
["MULTIPLE"]=>
string(1) "N"
["XML_ID"]=>
NULL
["FILE_TYPE"]=>
string(0) ""
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string(1) "5"
["TMP_ID"]=>
NULL
["LINK_IBLOCK_ID"]=>
string(1) "0"
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string(1) "N"
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string(1) "N"
["FILTRABLE"]=>
string(1) "Y"
["IS_REQUIRED"]=>
string(1) "N"
["VERSION"]=>
string(1) "1"
["USER_TYPE"]=>
NULL
["USER_TYPE_SETTINGS"]=>
NULL
["HINT"]=>
string(0) ""
["PROPERTY_VALUE_ID"]=>
string(4) "3017"
["VALUE"]=>
string(57) "опухоль ствола головного мозга"
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string(0) ""
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NULL
["VALUE_XML_ID"]=>
NULL
["VALUE_SORT"]=>
NULL
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string(0) ""
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string(14) "Диагноз"
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string(0) ""
["DISPLAY_VALUE"]=>
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}
["NAME"]=>
array(37) {
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string(2) "18"
["TIMESTAMP_X"]=>
string(19) "2014-08-08 12:08:39"
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string(2) "15"
["NAME"]=>
string(6) "Имя"
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string(1) "Y"
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string(3) "500"
["CODE"]=>
string(4) "NAME"
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string(0) ""
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string(1) "S"
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string(1) "1"
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string(2) "30"
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string(1) "L"
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string(1) "N"
["XML_ID"]=>
NULL
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string(0) ""
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string(1) "5"
["TMP_ID"]=>
NULL
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string(1) "0"
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string(1) "N"
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string(1) "N"
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string(1) "Y"
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string(1) "Y"
["VERSION"]=>
string(1) "1"
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NULL
["USER_TYPE_SETTINGS"]=>
NULL
["HINT"]=>
string(0) ""
["PROPERTY_VALUE_ID"]=>
string(4) "3014"
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string(12) "Владик"
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string(0) ""
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NULL
["VALUE_XML_ID"]=>
NULL
["VALUE_SORT"]=>
NULL
["~VALUE"]=>
string(12) "Владик"
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string(0) ""
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string(6) "Имя"
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string(0) ""
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string(12) "Владик"
}
["SURNAME"]=>
array(37) {
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string(2) "17"
["TIMESTAMP_X"]=>
string(19) "2014-08-08 12:08:39"
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string(2) "15"
["NAME"]=>
string(14) "Фамилия"
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string(1) "Y"
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string(3) "500"
["CODE"]=>
string(7) "SURNAME"
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string(0) ""
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string(1) "S"
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string(1) "1"
["COL_COUNT"]=>
string(2) "30"
["LIST_TYPE"]=>
string(1) "L"
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string(1) "N"
["XML_ID"]=>
NULL
["FILE_TYPE"]=>
string(0) ""
["MULTIPLE_CNT"]=>
string(1) "5"
["TMP_ID"]=>
NULL
["LINK_IBLOCK_ID"]=>
string(1) "0"
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string(1) "N"
["SEARCHABLE"]=>
string(1) "N"
["FILTRABLE"]=>
string(1) "Y"
["IS_REQUIRED"]=>
string(1) "Y"
["VERSION"]=>
string(1) "1"
["USER_TYPE"]=>
NULL
["USER_TYPE_SETTINGS"]=>
NULL
["HINT"]=>
string(0) ""
["PROPERTY_VALUE_ID"]=>
string(4) "3013"
["VALUE"]=>
string(16) "Чеботару"
["DESCRIPTION"]=>
string(0) ""
["VALUE_ENUM"]=>
NULL
["VALUE_XML_ID"]=>
NULL
["VALUE_SORT"]=>
NULL
["~VALUE"]=>
string(16) "Чеботару"
["~DESCRIPTION"]=>
string(0) ""
["~NAME"]=>
string(14) "Фамилия"
["~DEFAULT_VALUE"]=>
string(0) ""
["DISPLAY_VALUE"]=>
string(16) "Чеботару"
}
}
}