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《HOPE English 希平方》服務條款關於個人資料收集與使用之規定

隱私權政策
上次更新日期:2014-12-30

希平方 為一英文學習平台,我們每天固定上傳優質且豐富的影片內容,讓您不但能以有趣的方式學習英文,還能增加內涵,豐富知識。我們非常注重您的隱私,以下說明為當您使用我們平台時,我們如何收集、使用、揭露、轉移及儲存你的資料。請您花一些時間熟讀我們的隱私權做法,我們歡迎您的任何疑問或意見,提供我們將產品、服務、內容、廣告做得更好。

本政策涵蓋的內容包括:希平方學英文 如何處理蒐集或收到的個人資料。
本隱私權保護政策只適用於: 希平方學英文 平台,不適用於非 希平方學英文 平台所有或控制的公司,也不適用於非 希平方學英文 僱用或管理之人。

個人資料的收集與使用
當您註冊 希平方學英文 平台時,我們會詢問您姓名、電子郵件、出生日期、職位、行業及個人興趣等資料。在您註冊完 希平方學英文 帳號並登入我們的服務後,我們就能辨認您的身分,讓您使用更完整的服務,或參加相關宣傳、優惠及贈獎活動。希平方學英文 也可能從商業夥伴或其他公司處取得您的個人資料,並將這些資料與 希平方學英文 所擁有的您的個人資料相結合。

我們所收集的個人資料, 將用於通知您有關 希平方學英文 最新產品公告、軟體更新,以及即將發生的事件,也可用以協助改進我們的服務。

我們也可能使用個人資料為內部用途。例如:稽核、資料分析、研究等,以改進 希平方公司 產品、服務及客戶溝通。

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希平方學英文 自動接收並記錄您電腦和瀏覽器上的資料,包括 IP 位址、希平方學英文 cookie 中的資料、軟體和硬體屬性以及您瀏覽的網頁紀錄。

隱私權政策修訂
我們會不定時修正與變更《隱私權政策》,不會在未經您明確同意的情況下,縮減本《隱私權政策》賦予您的權利。隱私權政策變更時一律會在本頁發佈;如果屬於重大變更,我們會提供更明顯的通知 (包括某些服務會以電子郵件通知隱私權政策的變更)。我們還會將本《隱私權政策》的舊版加以封存,方便您回顧。

服務條款
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上次更新日期:2013-09-09

歡迎您加入看 ”希平方學英文”
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兒童及青少年之保護 兒童及青少年上網已經成為無可避免之趨勢,使用網際網路獲取知識更可以培養子女的成熟度與競爭能力。然而網路上的確存有不適宜兒童及青少年接受的訊息,例如色情與暴力的訊息,兒童及青少年有可能因此受到心靈與肉體上的傷害。因此,為確保兒童及青少年使用網路的安全,並避免隱私權受到侵犯,家長(或監護人)應先檢閱各該網站是否有保護個人資料的「隱私權政策」,再決定是否同意提出相關的個人資料;並應持續叮嚀兒童及青少年不可洩漏自己或家人的任何資料(包括姓名、地址、電話、電子郵件信箱、照片、信用卡號等)給任何人。

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您承諾絕不為任何非法目的或以任何非法方式使用本服務,並承諾遵守中華民國相關法規及一切使用網際網路之國際慣例。您若係中華民國以外之使用者,並同意遵守所屬國家或地域之法令。您同意並保證不得利用本服務從事侵害他人權益或違法之行為,包括但不限於:
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服務中斷或暫停
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版權宣告
上次更新日期:2013-09-16

希平方學英文 內所有資料之著作權、所有權與智慧財產權,包括翻譯內容、程式與軟體均為 希平方學英文 所有,須經希平方學英文同意合法才得以使用。
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「Scott Williams:非正式照顧者在健康照護體系中扮演的隱藏角色」- The Hidden Role Informal Caregivers Play in Health Care

觀看次數:1737  • 

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Let's put the care back into health care. I've been working in the healthcare sector for the last 15 years, and one of the things that drew me to this sector was my interest in the care component of our healthcare systems—more specifically, to the invaluable role played by carers.

Now, how many of you in this room consider yourself a carer? By this, I mean how many of you have cared for someone suffering from an illness, injury or disability? Can you raise your hand if this is the case? About half of the room. I want to thank all of you who raised your hands for the time that you've spent as a carer. What you do is extremely precious.

I am a former cared-for patient myself. When I was a teenager, I suffered from Lyme disease and underwent 18 months of antibiotic treatment. I was repeatedly misdiagnosed: bacterial meningitis, fibromyalgia, you name it. They couldn't figure it out. And if I'm standing here in front of you today, it's because I owe my life to the stubbornness and commitment of one carer. He did everything he could for me—driving long distances from one treatment center to another, searching for the best option, and above all, never giving up, despite the difficulties he encountered, including from a work and quality-of-life perspective. That was my father. I recovered, and this is largely thanks to his dedication.

This experience turned me into a patient advocate. The closer I looked, the more I saw carers providing the same kind of support that my father provided to me, and playing a crucial role in the healthcare system. I don't think it's an exaggeration to say that without informal carers like him, our health and social systems would crumble. And yet, they're largely going unrecognized.

I am now a long-distance carer for my mother, who suffers from multiple chronic conditions. I understand, now more than ever, the demands that caregivers face. With aging populations, economic instability, healthcare system stress and increased incidents of long-term chronic care needs, the importance and demands on family caregivers are greater than ever. Carers all over the world are sacrificing their own physical, financial and psychosocial well-being to provide care for their loved ones. Carers have their own limits and needs, and in absence of adequate support, many could be stretched to the breaking point. Once seen as a personal and private matter in family life, unpaid caregiving has formed the invisible backbone of our health and social systems all over the world.

Many of these carers are even in this room, as we have just seen. Who are they, and how many are they? What are the challenges that they are facing? And, above all, how can we make sure that their value to patients, our healthcare system and society is recognized? Anyone can be a carer, really: a 15-year-old girl caring for a parent with multiple sclerosis; a 40-year-old man juggling full-time work while caring for his family who lives far away; a 60-year-old man caring for his wife who has terminal cancer; or an 80-year-old woman caring for her husband who has Alzheimer's disease.

The things carers do for their patients are varied. They provide personal care, like getting someone dressed, feeding them, helping them to the bathroom, helping them move about. They also provide a significant level of medical care, because they often know a lot about their loved one's condition and needs, sometimes better than the patients themselves, who may be paralyzed or confused by their diagnosis. In those situations, carers are also advocates for the patient.

Also of critical importance is the fact that carers also provide emotional support. They organize doctor's appointments, they manage finances, and they also deal with daily household tasks. These challenges are challenges that we can't ignore. There are currently more than 100 million carers providing 80 percent of care across Europe. And even if these numbers are impressive, they're most likely underestimated, given the lack of recognition of carers. As we have just seen, many of you in this room weren't sure if you could be qualified or considered to be a carer. Many of you probably thought I was referring to a nurse or some other healthcare professional.

Also stunning are the benefits that carers bring to our societies. I want to give you just one example from Australia in 2015. The annual value provided by informal carers to those suffering from mental illness was evaluated at 13.2 billion Australian dollars. This is nearly two times what the Australian government spends on mental health services annually. These numbers, among others, demonstrate that if carers were to stop caring tomorrow, our health and social systems would crumble. And while the importance of these millions of silent carers cannot be denied, they've largely been unnoticed by governments, healthcare systems and private entities.

In addition, carers are facing enormous personal challenges. Many carers face higher costs and can face financial difficulties, given the fact that they may not be able to work full time or they may not be able to hold down a job altogether. Many studies have shown that often carers sacrifice their own health and well-being in order to care for their loved ones. Many carers spend so much time caring for their loved ones that often their family and their relationships can suffer. Many carers report that often, their employers don't have adequate policies in place to support them.

There has been improvement, though, in the recognition of carers around the world. Just a few years ago, an umbrella organization called the International Alliance of Carer Organizations, or IACO, was formed to bring together carer groups from all over the world, to provide strategic direction, facilitate information sharing, as well as actively advocate for carers on an international level. Private entities are also starting to recognize the situation of carers. I am proud that my personal engagement and enthusiasm towards this topic of carers found an echo in my own workplace. My company is committed to this cause and has developed an unprecedented framework for its employees and society as a whole. The objective is to empower carers to improve their own health and well-being and bring about a greater balance to their lives.

Nevertheless, much more needs to be done to complement these relatively isolated initiatives. Our societies are facing increased health pressures, including aging populations, increased incidence of cancer and chronic conditions, widespread inequality, amongst many others. To confront these challenges, policymakers must look beyond traditional healthcare pathways and employment policies and recognize that informal care will continue to form the bedrock of care.

Caring for someone should be a choice and should be done without putting one's own well-being in the balance. But to really put the care back into health care, what's needed is a deep, societal, structural change. And this can only happen through a change in mindset. And this can start today. Today, we can plant the seed for a change for millions of carers around the world.

Here's what I want to suggest: when you go home today or to the office tomorrow morning, embrace a carer. Thank them, offer him or her a bit of help, maybe even volunteer as a carer yourself for a couple hours a week. If carers around the world felt better recognized, it would not only improve their own health and well-being and sense of fulfillment, but it would also improve the lives of those that they're caring for.

Let's care more.

Thank you.

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