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    # WorkForALS

    案例简介:为什么这项工作与媒体有关? “为ALS工作” 运动是对变革的要求,我们针对的是比利时的工作人员和首席执行官。为此,我们使用了多种媒体,以便在世界ALS日的一周内,ALS患者作为求职者无处不在。为了广播我们的信息,我们甚至必须接管国家彩票和天气预报一晚。 背景 肌萎缩性侧索硬化症是一种无法治愈的神经肌肉疾病,使一块肌肉瘫痪,使患者无法移动。在不可避免的终点附近,只有头脑和眼睛保持完整。ALS患者逐渐不得不放弃一切,他们的工作,他们的爱好,最后,他们的生活。绝症患者及其家人永远不会放弃的一件事是希望有一天他们的疾病可以治愈。 要找到治疗方法,我们首先需要钱。不幸的是,罕见的疾病不会得到很多钱。这对制药行业没有意义,人们倾向于不向不影响自己生活的事业捐款。 这项运动的目的是提高人们对ALS的认识 (使公众了解这种疾病,以便对ALS患者产生同情心),并收集捐款以资助ALS治疗的研究。 描述创意/见解 (投票30%) 如果您无法获得任何资金或捐款,您如何获得金钱?你为它工作。如果你身体里剩下的功能就是你的眼睛,那就不容易了。 ALS患者正在寻找一份工作,以资助治愈,因为没有其他人会这样做。搬家不能成为工作描述的一部分的工作。ALS患者直接与首席执行官联系,要求工作并捐赠薪水。人们被鼓励在电视和广播中为ALS工作一天,直到每个人都开始谈论它。 我们一起为ALS工作,所以总有一天会有治愈的。 描述策略 (投票20%) 世界ALS日是揭示患者面临的许多问题的好时机。但是为了找到治疗方法,我们需要行动。首先,我们必须提高对ALS患者仍然无法治愈的事实的认识。然后,我们需要人们感到他们可以很容易地提供帮助。 我们需要完美的组合来显示问题的破坏性影响,但仍然激励人们去做一些事情。 目标是比利时的首席执行官和劳动人民。我们呼吁比利时首席执行官聘请ALS患者从事他们仍然可以做的少数工作。 在第二阶段,患者要求比利时人口也为ALS工作。 描述执行情况 (投票20%) ALS活动的工作针对比利时的首席执行官和员工。首先,直接与首席执行官联系,从6月21日开始,通过直接邮寄,twitter提及,LinkedIn帖子,甚至是全国电视广告,以我们的ALS患者寻找工作为特色。 在第二阶段,从6月25日开始,一段视频介绍了为ALS工作的患者,呼吁比利时人加入他们的行列,并每天努力寻找治疗ALS的方法。患者要求通过国家电视,广播,Facebook和Twitter上的在线视频为ALS工作。 在《7月的3d》上,我们通过使用社交网站上的影响者来提醒人们捐出一天的薪水,从而推动了这项运动。更多的提醒来自我们为国家彩票和天气预报工作的患者,他们在电视上直播,要求人们也为ALS工作一天。 列出结果 (投票30%) 人们提高了对像ALS这样的罕见疾病的资金问题的认识,产生了数千个工作日,并帮助资助了寻找治愈方法的研究。每个工作日都让我们更接近ALS可以治愈的 “一天”。 120公司通过社交媒体进行了宣传。 我们在电视新闻和新闻文章中看到,并在Stubru和RTBF广播电台上出现。 超过6位主要首席执行官雇用了ALS患者,而可口可乐BeLux在现实生活中没有雇用患者,但实际上: 他们已经为这项研究提供了一周的薪水。 ALS患者曾担任博物馆gard,监视代理,考试主管,绘图模型,彩票演示者和天气预报演示者。 + 254% 捐赠: ALS患者不能移动,但他们能够移动整个国家。

    # WorkForALS

    案例简介:Why is this work relevant for Media? The work for ALS campaign was a demand for change in which we targeted the working people and CEOs of Belgium. For that we used a great mixture of media in order for ALS patients as job applicants to be everywhere during the week of World ALS day. We've even got to take over the national lottery and the weather forecast for one night in order to broadcast our message. Background ALS, Amyotrophic Lateral Sclerosis, is an incurable neuromuscular disease that paralyses one muscle after the other, leaving patients unable to move. Near the inevitable end, only the mind and eyes remain intact. ALS sufferers gradually have to give up on everything, their jobs, their hobbies, and in the end, their lives. One thing terminal ill patients and their families never give up on is the hope that one day their disease will be curable. To find a cure we need money first. Unfortunately, rare diseases don't get a lot of money. It's of no interest to the pharmaceutical industry and people tend to not donate to causes that don't affect their own lives. The objectives of this campaign are to create awareness around ALS (make the public understand the disease, in order to feel empathy for ALS patients) and to gather donations to finance research for ALS treatment. Describe the creative idea/insights (30% of vote) How do you get money if you can't get any fundings or donations? You work for it. Not easy if all that remains to function in your body are your eyes. ALS patients were looking for a job in order to fund a cure, as no one else will. A job where moving can't be part of the job description. CEOs were directly contacted by ALS patients asking for a job, and the salary to be donated. People were encouraged to also work a day for ALS on television and radio until everyone started talking about it. Together we worked for ALS so one day there will be a cure. Describe the strategy (20% of vote) World ALS day is a good moment to shine a light on the many problems patients are faced with. But in order to find a cure, we need action. First we had to raise awareness of the fact that for ALS patients there still is no cure in sight. Then we needed people to feel that there is something they can quite easily do to help. We needed perfect mix of showing devastating effects of a problem, yet still activating people to do something about it. The targets were the CEOs and working people of Belgium. We called upon Belgian CEOs to hire an ALS patient for the few jobs they still can do. In a second phase the patients asked the Belgian population also to work for ALS. Describe the execution (20% of vote) The work for ALS campaign targeted both Belgian CEOs and employees. First, CEOs were directly contacted, starting 21st of June via direct mailings, twitter mentions, LinkedIn posts and even national TV commercials featuring our ALS patients looking for a job. In the second phase, starting from 25th of June, a video featuring patients working for ALS calling on Belgians to join them and also work a day to find a cure for ALS. Patients were asking to work for ALS via national TV, radio, online video on Facebook and Twitter. On 3d of July we boosted the campaign by using influencers on social who reminded people to donate a day of their salary. More reminders came from our patients who were working for the national lottery and the weather forecast, live on television, asking people to also work a day for ALS. List the results (30% of vote) Awareness was raised for the funding problem rare diseases like ALS face, thousands of work days were generated and helped to fund the research to find a cure. Every workday bringing us closer to that 'one day' where ALS will be curable. 120 companies were reached out via social media. We were seen in the news on TV and in news articles and present on radio stations Stubru and RTBF. More than 6 major CEOs hired ALS patients and Coca-Cola BeLux hasn’t hired a patient in real life, but virtually: they’ve given the salary of one week to the research. ALS patients worked as a museum gard, a monitoring agent, exam supervisor, a drawing model, a lottery presenter and a presenter of the weather forecast. +254% donations : ALS patients can’t move, but they were able to move a whole country.

    #WorkForALS

    案例简介:为什么这项工作与媒体有关? “为ALS工作” 运动是对变革的要求,我们针对的是比利时的工作人员和首席执行官。为此,我们使用了多种媒体,以便在世界ALS日的一周内,ALS患者作为求职者无处不在。为了广播我们的信息,我们甚至必须接管国家彩票和天气预报一晚。 背景 肌萎缩性侧索硬化症是一种无法治愈的神经肌肉疾病,使一块肌肉瘫痪,使患者无法移动。在不可避免的终点附近,只有头脑和眼睛保持完整。ALS患者逐渐不得不放弃一切,他们的工作,他们的爱好,最后,他们的生活。绝症患者及其家人永远不会放弃的一件事是希望有一天他们的疾病可以治愈。 要找到治疗方法,我们首先需要钱。不幸的是,罕见的疾病不会得到很多钱。这对制药行业没有意义,人们倾向于不向不影响自己生活的事业捐款。 这项运动的目的是提高人们对ALS的认识 (使公众了解这种疾病,以便对ALS患者产生同情心),并收集捐款以资助ALS治疗的研究。 描述创意/见解 (投票30%) 如果您无法获得任何资金或捐款,您如何获得金钱?你为它工作。如果你身体里剩下的功能就是你的眼睛,那就不容易了。 ALS患者正在寻找一份工作,以资助治愈,因为没有其他人会这样做。搬家不能成为工作描述的一部分的工作。ALS患者直接与首席执行官联系,要求工作并捐赠薪水。人们被鼓励在电视和广播中为ALS工作一天,直到每个人都开始谈论它。 我们一起为ALS工作,所以总有一天会有治愈的。 描述策略 (投票20%) 世界ALS日是揭示患者面临的许多问题的好时机。但是为了找到治疗方法,我们需要行动。首先,我们必须提高对ALS患者仍然无法治愈的事实的认识。然后,我们需要人们感到他们可以很容易地提供帮助。 我们需要完美的组合来显示问题的破坏性影响,但仍然激励人们去做一些事情。 目标是比利时的首席执行官和劳动人民。我们呼吁比利时首席执行官聘请ALS患者从事他们仍然可以做的少数工作。 在第二阶段,患者要求比利时人口也为ALS工作。 描述执行情况 (投票20%) ALS活动的工作针对比利时的首席执行官和员工。首先,直接与首席执行官联系,从6月21日开始,通过直接邮寄,twitter提及,LinkedIn帖子,甚至是全国电视广告,以我们的ALS患者寻找工作为特色。 在第二阶段,从6月25日开始,一段视频介绍了为ALS工作的患者,呼吁比利时人加入他们的行列,并每天努力寻找治疗ALS的方法。患者要求通过国家电视,广播,Facebook和Twitter上的在线视频为ALS工作。 在《7月的3d》上,我们通过使用社交网站上的影响者来提醒人们捐出一天的薪水,从而推动了这项运动。更多的提醒来自我们为国家彩票和天气预报工作的患者,他们在电视上直播,要求人们也为ALS工作一天。 列出结果 (投票30%) 人们提高了对像ALS这样的罕见疾病的资金问题的认识,产生了数千个工作日,并帮助资助了寻找治愈方法的研究。每个工作日都让我们更接近ALS可以治愈的 “一天”。 120公司通过社交媒体进行了宣传。 我们在电视新闻和新闻文章中看到,并在Stubru和RTBF广播电台上出现。 超过6位主要首席执行官雇用了ALS患者,而可口可乐BeLux在现实生活中没有雇用患者,但实际上: 他们已经为这项研究提供了一周的薪水。 ALS患者曾担任博物馆gard,监视代理,考试主管,绘图模型,彩票演示者和天气预报演示者。 + 254% 捐赠: ALS患者不能移动,但他们能够移动整个国家。

    #WorkForALS

    案例简介:Why is this work relevant for Media? The work for ALS campaign was a demand for change in which we targeted the working people and CEOs of Belgium. For that we used a great mixture of media in order for ALS patients as job applicants to be everywhere during the week of World ALS day. We've even got to take over the national lottery and the weather forecast for one night in order to broadcast our message. Background ALS, Amyotrophic Lateral Sclerosis, is an incurable neuromuscular disease that paralyses one muscle after the other, leaving patients unable to move. Near the inevitable end, only the mind and eyes remain intact. ALS sufferers gradually have to give up on everything, their jobs, their hobbies, and in the end, their lives. One thing terminal ill patients and their families never give up on is the hope that one day their disease will be curable. To find a cure we need money first. Unfortunately, rare diseases don't get a lot of money. It's of no interest to the pharmaceutical industry and people tend to not donate to causes that don't affect their own lives. The objectives of this campaign are to create awareness around ALS (make the public understand the disease, in order to feel empathy for ALS patients) and to gather donations to finance research for ALS treatment. Describe the creative idea/insights (30% of vote) How do you get money if you can't get any fundings or donations? You work for it. Not easy if all that remains to function in your body are your eyes. ALS patients were looking for a job in order to fund a cure, as no one else will. A job where moving can't be part of the job description. CEOs were directly contacted by ALS patients asking for a job, and the salary to be donated. People were encouraged to also work a day for ALS on television and radio until everyone started talking about it. Together we worked for ALS so one day there will be a cure. Describe the strategy (20% of vote) World ALS day is a good moment to shine a light on the many problems patients are faced with. But in order to find a cure, we need action. First we had to raise awareness of the fact that for ALS patients there still is no cure in sight. Then we needed people to feel that there is something they can quite easily do to help. We needed perfect mix of showing devastating effects of a problem, yet still activating people to do something about it. The targets were the CEOs and working people of Belgium. We called upon Belgian CEOs to hire an ALS patient for the few jobs they still can do. In a second phase the patients asked the Belgian population also to work for ALS. Describe the execution (20% of vote) The work for ALS campaign targeted both Belgian CEOs and employees. First, CEOs were directly contacted, starting 21st of June via direct mailings, twitter mentions, LinkedIn posts and even national TV commercials featuring our ALS patients looking for a job. In the second phase, starting from 25th of June, a video featuring patients working for ALS calling on Belgians to join them and also work a day to find a cure for ALS. Patients were asking to work for ALS via national TV, radio, online video on Facebook and Twitter. On 3d of July we boosted the campaign by using influencers on social who reminded people to donate a day of their salary. More reminders came from our patients who were working for the national lottery and the weather forecast, live on television, asking people to also work a day for ALS. List the results (30% of vote) Awareness was raised for the funding problem rare diseases like ALS face, thousands of work days were generated and helped to fund the research to find a cure. Every workday bringing us closer to that 'one day' where ALS will be curable. 120 companies were reached out via social media. We were seen in the news on TV and in news articles and present on radio stations Stubru and RTBF. More than 6 major CEOs hired ALS patients and Coca-Cola BeLux hasn’t hired a patient in real life, but virtually: they’ve given the salary of one week to the research. ALS patients worked as a museum gard, a monitoring agent, exam supervisor, a drawing model, a lottery presenter and a presenter of the weather forecast. +254% donations : ALS patients can’t move, but they were able to move a whole country.

    # WorkForALS

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    #WorkForALS

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