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This talk was given at a local TEDxSnoIsleLibraries event and produced independently of the TED Conferences. Shaela Niles, writer and self-described monster slayer, shares how learning about “selective mutism” on Wikipedia changed her life.. Wikipedia provided Shaela with a key that has helped her unlock her life and future. This blogger, college student, and budding novelist recently wrote a story of a young boy with an anxiety disorder who had to find the courage to fight the monsters that only he saw around him. Shaela is passionate about expressing her thoughts through writing, public speaking and the need to raise awareness about the overcoming the things which can hold you prisoner.. This talk was given at a TEDx event using the TED conference format but independently organized by a local community. Learn more at http://ted.com/tedx
�� Личные и онлайн консультации Светланы Григорьевны Нетрусовой, кандидата медицинских наук, доцента, врача психиатра высшей категории, психотерапевта:. ☎ viber +380672365984, skype: luky.62 ▶. WhatsApp +380672365984. Запись на консультацию: https://psyhosoma.com/priyom-psihiatra. �� Facebook: https://www.facebook.com/pg/Psyhosoma. �� Instagram https://www.instagram.com/psyhosoma.svetlana.netrusova/. �� telegram https://t.me/psihosoma. �� https://vk.com/club148166140. �� https://ok.ru/group/53481693380816. Более подробно о шизофрении читайте на сайте \»Психосома\»: https://psyhosoma.com/. Эхо-симптомы встречаются при кататонической форме шизофрении, а также в виде кататонических включений при других формах этого психического заболевания.. К ним относятся: эхолалия, эхопраксия, эхомимия.. При эхолалии человек непроизвольно (неосознанно) повторяет слова или фразы из чужой речи, даже не обращенной непосредственно к нему.. Эхолалия нередко сочетается с эхопраксией (копирование чужих действий) и эхомимией (копирование мимики).. Эхо-симптомы при шизофрении требуют лечения.. Мутизм — симптом кататонической формы шизофрении или может встречаться в виде кататонических включений при этом заболевании. Мутизм также может быть истерическим.. О таких симптомах шизофрении, как эхо-симптомы и мутизм рассказывает Светлана Григорьевна Нетрусова, кандидат медицинских наук, доцент, врач психиатр высшей категории, психотерапевт: https://youtu.be/a8rtRCoazCQ. Приглашаю вас к просмотру! Подписывайтесь на мой канал в YouTube о тайнах человеческой психики «Светлана Нетрусова – Психосома».
#хотимподелиться #коррекция #семья. По следам одной статьи в научном журнале размышляем, возможен ли \»выход из аутизма\». В статье приводится статистика \»выхода\», которая, с одной стороны, даёт надежду, а с другой — заставляет задуматься.. 0:38 свежая статистика о возможности \»выхода из аутизма\». 2:04 мнение Елизаветы Гуриной. 7:12 мнение Екатерины Жестковой. «Некоторые дети могут «выйти» из аутизма, но проблемы часто сохраняются». https://www.sciencedaily.com/releases/2019/03/190312075923.htm. Amazon изъял из продажи все книги, обещающие «излечение от аутизма» и «дезинформацию о вакцинах». https://www.cbsnews.com/news/amazon-removes-books-promoting-autism-cures-and-vaccine-misinformation. Наша страница на Facebook. https://www.facebook.com/annfromthemoon
Сколько стоит ваша консультация и можете ли Вы поставить диагноз онлайн после консультации? Психоз случился резко и впервые. В течении 2 лет обострений не было. Хорошие ли таблетки трифтазин или лучше заменить их на более современные?
Thank you for the video! I had SM all through my childhood, teachers thought I had a learning disability and sent me to a special school for disabled kids and stayed there for 4 years. It also ruined me more then helped me, I thought really lowly about myself and thought something was wrong with me when it said “learning disability” on my report card. This lead to other complications like Eating disorder, depression, panic disorder, and OCD. Today I’m 23, I’m in college doing accounting where I feel comfortable with talking out loud to the teachers and to my peers around me. Still suffer from anxiety and see a therapist often.
hugs Not the extreme you experience, but like you its been like the gears between my brain, tounge, jaw muscles, lungs, diaphragm, et all just refused to do what I really wanted. The more I wanted to speak the worse it would get. Keep rocking at your own beat, the rest will just have to deal!:)
I’m so happy and proud of you. I know exactly how difficult to have a SM in the family because i have a 16 years old kid just like you. I don’t care if my kid will crawl out from this disorder for 10 or 20 more years from today, for as long as she will be like you one day. You really inspire me that there is always hope in life. Thank you for this wonderful video and your speech was very motivational to parents and people with SM.
Great speech! I had selective mutism from kindergarten until 4th grade. I spoke at home but never in school. As I got older, I spoke to a few classmates when in a private area and I had some friends. I had speech therapy all throughout elementary school and that helped a lot in me overcoming sm. Seeing this and some their videos on here has inspired me to share my story.
amazing. I’ve always felt like it was perfectly okay to be silent and a homebody. nobody seems to think that is okay. why not though? I have a loving family and a beautiful life. I don’t need to talk to everyone or leave my home if it isn’t important. it doesn’t make me broken or wrong. we are all different.
I had selective mutism between 3-10 years old at school and when spending time with certain relatives, nobody ever seems to understand how hard it is (except former/current sufferers) and it’s so incredibly debilitating, it’s not just not talking, it’s eye contact, body language, and generally terrible, terrible anxiety. I went through periods where I was too scared to run in public, blow my nose (I still struggle with this one) and more. Not to mention none of the therapy I received actually worked, it made it so much worse, not only did I have to worry about how I do literally everything all the time, but now extra pressure is added to talk, which makes it even more impossible to talk. People who deny that it’s a real disorder make me so angry, «it’s just because she doesn’t want to talk,» Christ no, believe me I really, really wanted to talk to you, but I just couldn’t, I just couldn’t do it, whenever I tried to my throat would close up, my brain would enter extreme anxiety mode like a car was rushing towards me or something, it wouldn’t let me speak. Even though I was diagnosed at a very young age (luckily) it still wasn’t seen as a viable reason to not speak, my parents threatened to put me up for adoption, my teachers bullied me over it, trying to force me to speak, and I had hardly any friends. Life is so hard when you are experiencing a terrible mental disorder completely alone as a small child (not to mention some problems at home as well, BAD problems, but I don’t think I could write about that)
I had SM and when I told me friends thy didn’t accept it as a real disorder. One of them went through surgery when they were little and said that they had a REAL disorder. How do I respond to that and tell them just because I had a different challenge it doesn’t make my challenges less hard than hers.
I have SM and if I were to speak in front of a crowd, I couldn’t because I wouldn’t know what to say about what I had been through. How does (shaela niles) know what to say? seems unfair for me since I think SM is when people think that individual talks inappropriately all the time. that’s what I thought selective mutism was. I also felt my throat closing up and suddenly couldn’t talk or breathe. But I just thought that was normal so I went on with life.
Сколько стоит ваша консультация и можете ли Вы поставить диагноз онлайн после консультации? Психоз случился резко и впервые. В течении 2 лет обострений не было. Хорошие ли таблетки трифтазин или лучше заменить их на более современные?
Thank you for the video!
I had SM all through my childhood, teachers thought I had a learning disability and sent me to a special school for disabled kids and stayed there for 4 years. It also ruined me more then helped me, I thought really lowly about myself and thought something was wrong with me when it said “learning disability” on my report card.
This lead to other complications like Eating disorder, depression, panic disorder, and OCD.
Today I’m 23, I’m in college doing accounting where I feel comfortable with talking out loud to the teachers and to my peers around me. Still suffer from anxiety and see a therapist often.
hugs Not the extreme you experience, but like you its been like the gears between my brain, tounge, jaw muscles, lungs, diaphragm, et all just refused to do what I really wanted. The more I wanted to speak the worse it would get. Keep rocking at your own beat, the rest will just have to deal!:)
I’m so happy and proud of you. I know exactly how difficult to have a SM in the family because i have a 16 years old kid just like you. I don’t care if my kid will crawl out from this disorder for 10 or 20 more years from today, for as long as she will be like you one day. You really inspire me that there is always hope in life. Thank you for this wonderful video and your speech was very motivational to parents and people with SM.
Great speech! I had selective mutism from kindergarten until 4th grade. I spoke at home but never in school. As I got older, I spoke to a few classmates when in a private area and I had some friends. I had speech therapy all throughout elementary school and that helped a lot in me overcoming sm. Seeing this and some their videos on here has inspired me to share my story.
amazing. I’ve always felt like it was perfectly okay to be silent and a homebody. nobody seems to think that is okay. why not though? I have a loving family and a beautiful life. I don’t need to talk to everyone or leave my home if it isn’t important. it doesn’t make me broken or wrong. we are all different.
I had selective mutism between 3-10 years old at school and when spending time with certain relatives, nobody ever seems to understand how hard it is (except former/current sufferers) and it’s so incredibly debilitating, it’s not just not talking, it’s eye contact, body language, and generally terrible, terrible anxiety. I went through periods where I was too scared to run in public, blow my nose (I still struggle with this one) and more. Not to mention none of the therapy I received actually worked, it made it so much worse, not only did I have to worry about how I do literally everything all the time, but now extra pressure is added to talk, which makes it even more impossible to talk. People who deny that it’s a real disorder make me so angry, «it’s just because she doesn’t want to talk,» Christ no, believe me I really, really wanted to talk to you, but I just couldn’t, I just couldn’t do it, whenever I tried to my throat would close up, my brain would enter extreme anxiety mode like a car was rushing towards me or something, it wouldn’t let me speak. Even though I was diagnosed at a very young age (luckily) it still wasn’t seen as a viable reason to not speak, my parents threatened to put me up for adoption, my teachers bullied me over it, trying to force me to speak, and I had hardly any friends. Life is so hard when you are experiencing a terrible mental disorder completely alone as a small child (not to mention some problems at home as well, BAD problems, but I don’t think I could write about that)
I had SM and when I told me friends thy didn’t accept it as a real disorder. One of them went through surgery when they were little and said that they had a REAL disorder. How do I respond to that and tell them just because I had a different challenge it doesn’t make my challenges less hard than hers.
I have SM and if I were to speak in front of a crowd, I couldn’t because I wouldn’t know what to say about what I had been through. How does (shaela niles) know what to say? seems unfair for me since I think SM is when people think that individual talks inappropriately all the time. that’s what I thought selective mutism was. I also felt my throat closing up and suddenly couldn’t talk or breathe. But I just thought that was normal so I went on with life.