熱門Ptt文章

[爆卦]odd診斷是什麼？優點缺點精華區懶人包

雖然這篇odd診斷鄉民發文沒有被收入到精華區：在odd診斷這個話題中，我們另外找到其它相關的精選爆讚文章

在 odd診斷產品中有5篇Facebook貼文，粉絲數超過3萬的網紅蔡百祥臨床心理師，也在其Facebook貼文中提到， Hello，我是蔡心。 . 我最早開始學習臨床心理學時，曾學過一套完整的遊戲治療架構，這套遊戲治療最原始的目的，是開發用來處理兒童有「對立反抗症」（ODD）。什麼是對立反抗呢？ . 簡單來說，就是為反對而反對，特別看不順眼權威，喜歡跟長輩（家長或老師）對著幹（疑...怎麼有點在形容我呢？）...

「odd診斷」的推薦目錄
  • 蔡百祥臨床心理師

    odd診斷 在 蔡百祥臨床心理師 Facebook 的最讚貼文

    2019-12-17 11:15:30
    有 256 人按讚


    Hello，我是蔡心。
    .
    我最早開始學習臨床心理學時，曾學過一套完整的遊戲治療架構，這套遊戲治療最原始的目的，是開發用來處理兒童有「對立反抗症」（ODD）。什麼是對立反抗呢？
    .
    簡單來說，就是為反對而反對，特別看不順眼權威，喜歡跟長輩（家長或老師）對著幹（疑...怎麼有點在形容我呢？）對立反抗症特別容易發生在ADHD（過動）或ASD（自閉症或亞斯兒）的身上，因為環境多半對特殊兒童不會很友善，故特殊兒童可能會反彈的更強烈。
    .
    為了說明對立反抗的特徵，我做了簡單的圖文，這是根據DSM-5（精神科疾病診斷與統計手冊第五版）所描述的症狀所做的。但是，請不要隨意給孩子診斷或標籤，還是要經過醫師（與臨床心理師）的專業判斷喔！
    .
    回到第一段所述的，那我會怎麼處理「對立反抗症」（ODD）呢？根據我整理了非常多遊戲治療的學派的觀點，就是要先看懂與理解對立反抗的孩子有顆傷透的心，第一步先透過遊戲修復家長與孩子、還有孩子對孩子自己的良善感受，才能開始透過遊戲對他進行社會規範、命令要求唷！
    .
    若孩子有對立反抗的特質，強烈建議在小學二年級以前搞定。因為小學三年級後，孩子可能會開始有些青春期的味道，反彈、報復或攻擊的手段也會更激烈，也更容易脫離孩子主觀認定不愛他的家庭，若沒妥善處理，大家就等著一起爆炸吧！實在是辛苦家長與老師囉，為人師長，真是天底下最難的事。
    .
    蔡心官方line@
    https://line.me/R/ti/p/%40doi8333v
    蔡心情緒line貼圖
    https://reurl.cc/rl93rN
    蔡心每週三晚上18:45有直播：http://bit.ly/2MX4GFB

  • 蔡百祥臨床心理師

    odd診斷 在 蔡百祥臨床心理師 Facebook 的最佳解答

    2019-12-17 11:15:30
    有 259 人按讚

    Hello，我是蔡心。
    .
    我最早開始學習臨床心理學時，曾學過一套完整的遊戲治療架構，這套遊戲治療最原始的目的，是開發用來處理兒童有「對立反抗症」（ODD）。什麼是對立反抗呢？
    .
    簡單來說，就是為反對而反對，特別看不順眼權威，喜歡跟長輩（家長或老師）對著幹（疑...怎麼有點在形容我呢？）對立反抗症特別容易發生在ADHD（過動）或ASD（自閉症或亞斯兒）的身上，因為環境多半對特殊兒童不會很友善，故特殊兒童可能會反彈的更強烈。
    .
    為了說明對立反抗的特徵，我做了簡單的圖文，這是根據DSM-5（精神科疾病診斷與統計手冊第五版）所描述的症狀所做的。但是，請不要隨意給孩子診斷或標籤，還是要經過醫師（與臨床心理師）的專業判斷喔！
    .
    回到第一段所述的，那我會怎麼處理「對立反抗症」（ODD）呢？根據我整理了非常多遊戲治療的學派的觀點，就是要先看懂與理解對立反抗的孩子有顆傷透的心，第一步先透過遊戲修復家長與孩子、還有孩子對孩子自己的良善感受，才能開始透過遊戲對他進行社會規範、命令要求唷！
    .
    若孩子有對立反抗的特質，強烈建議在小學二年級以前搞定。因為小學三年級後，孩子可能會開始有些青春期的味道，反彈、報復或攻擊的手段也會更激烈，也更容易脫離孩子主觀認定不愛他的家庭，若沒妥善處理，大家就等著一起爆炸吧！實在是辛苦家長與老師囉，為人師長，真是天底下最難的事。
    .
    蔡心官方line@
    https://line.me/R/ti/p/%40doi8333v
    蔡心情緒line貼圖
    https://reurl.cc/rl93rN
    蔡心每週三晚上18:45有直播：http://bit.ly/2MX4GFB

  • 赤米 Nereus

    odd診斷 在 赤米 Nereus Facebook 的最佳貼文

    2018-11-23 09:51:53
    有 4 人按讚


    希望大家可以幫吓可仁啦😢 我希望個個小朋友都可以健康快樂咁成長，可以一齊去公園玩

    【最新消息：募捐行動已於2018年12月3日結束】中大校友慈善基金感謝各界慷慨支持，募捐行動已結束。所得善款將支持張可仁及患上相類疾病需免疫治療的其他6位病童。

    詳情請參閱中大校友慈善基金網頁：https://www.facebook.com/cuhkacf.org/posts/589827338133781

    -------------------------------------------------------------------------------------
    (2018/11/22)

    中大醫學院向大家作出緊急呼籲，支持我們2000年的醫科畢業生張俊傑醫生，拯救他只有17個月大的兒子張可仁的性命。

    可仁早於出生第4天時已被診斷罹患一種罕有心臟病「主動脈狹窄」(Coarctation of Aorta)，需要接受緊急手術。極之不幸的是，可仁最近再被確診患上「第四期神經母腫瘤」(Stage IV Neuroblastoma)，目前可仁的頭骨至腰椎和盆骨均受到癌細胞擴散，脊髓神經線受到癌細胞壓住，痛楚非常，並有癱瘓的危機，癌細胞更正轉移至骨髓。

    可仁現時正住在威爾斯親王醫院兒童癌症中心隔離病房，極容易受到感染。他已開始接受化療，而治療方案將包括化療、手術、放射治療、骨髓移植、免疫治療，治療時間約一年至一年半。他完成化療、手術和放射治療後，會進行骨髓移植，之後需要免疫療法，這可大大提高存活率，由20%升至50%。

    然而，免疫治療需要病人自費，所需費用高達港幣200萬元。張醫生另一兒子患有自閉症，太太辭掉小學主任一職，全職照顧兩位小朋友，並要照顧父母親，經濟上未能承擔高昂的醫療費用。

    中大醫學院2000年畢業同學會發起是次籌款，目的包括：
    1. 為可仁進行骨髓移植後的免疫治療；
    2. 引發社會人士及政府對兒童罕有癌症治療的關注。

    查詢：
    香港中文大學校友慈善基金
    電郵：info@cuhkacf.org
    電話：2180 4316

    -------------------------------------------------------------------------------------

    【Fundraising Campaign Completed on 3 December 2018】According to CUHK Alumni Charity Foundation, the fundraising campaign for Mark CHEUNG Ho Yan has completed. The fund raised will be used to support the immunotherapy of Mark and 6 other patients who are suffered from the same disease. Thank you for all your kind-hearted support and generosity.

    -------------------------------------------------------------------------------------

    (2018/11/22)

    This is an urgent appeal for your generosity to save the life of the 17-month-old son of Dr. CHEUNG Chun Kit, our medical alumnus of Class 2000.

    Dr. Cheung Chun Kit is a CUHK medical graduate of Year 2000. His younger son, Cheung Ho Yan Mark, has recently been diagnosed to have Stage IV Neuroblastoma in November 2018, and is in an emergency need of donation to provide the necessary funding to support the life-saving yet expensive immunotherapy.

    Mark was presented to his paediatrician for fever and cough in late October 2018. His cough resolved with treatment but his fever never completely went away. Two days prior to his diagnosis, Mark was more clingy than usual and did not like to walk. On a video clip, Mark was noted to have foot drop, a very significant red flag which may indicate a compression on the spinal cord. Emergency scans were immediately performed that night, and Mark was found to have a large tumour on the left side of his abdomen. The aggressive tumour had already spread silently to the back of his skull, his spine, his hips and had compressed his nerves which control his lower limbs, resulting in pain on standing and difficulty in walking. Mark is facing an imminent risk of paralysis.

    Mark is diagnosed to have a rare childhood cancer which is called Stage IV neuroblastoma, a cancer which typically presents at late stage because it arises deep in the abdomen. To cure his aggressive cancer, Mark needs to survive through rounds of intensive chemotherapy, radiotherapy, surgery, bone marrow transplant, and finally, immunotherapy. The whole treatment duration lasts 1.5 to 2 years. To completely eradicate all cancer cells, immunotherapy will be needed to boost Mark’s survival from 20% to 50%. However, immunotherapy is a self-financed treatment in the public hospital and the treatment costs could be up to 2 million.

    Such close encounter with death is not the first time for Mark. At the first week of life, Mark was diagnosed to have a rare heart problem called “Coarctation of Aorta”. Mark had received life-saving surgery to reestablish the blood flow across his aorta, the major blood vessel that allows blood to go from the heart to the brain and the rest of the body. In a report published in 2002, only 67 cases with dual heart condition and neuroblastoma were reported, giving an odd of 1 in 100 million for a child to be hit by these two rare diseases. Scientists have not yet completely understood the mechanisms that may cause the two conditions to appear in a single child.

    It never rains but pours that Mark’s elder brother, now 5 years old, was diagnosed to have autism at around age 2. To enable the elder brother to have intensive training to improve his outcome and development, Mark’s mommy quit her job as a primary school teacher since the diagnosis of autism was made for his elder brother. Dr. Cheung, who is a medical doctor for the elderly, became the sole bread-winner of his family.

    CUHK Medical Graduates of Year 2000 have initiated a fund-raising campaign for Mark and his family with the following two objectives:

    1. To appeal for donation to support the costs of immunotherapy for Mark
    2. To increase the public awareness on the grave needs of children with cancers

    Enquiries:
    CUHK Alumni Charity Foundation Limited
    Email: info@cuhkacf.org
    Telephone: 2180 4316

你可能也想看看

搜尋相關網站