Muy buena información, muy mala lectura

surveillance

Skip to 12:00 , the intro is extremely long

I'm sorry but so much of the language and information used in this presentation is beyond outdated. You really should not be making general biases about autistic people with phrases like "lack empathy and imagination" not only is it dehumanising, it's incorrect. Also doubling down on wanting the name Pathological Demand Avoidance to remain unchanged while most of the PDA community is very vocal about the name being inappropriate and harmful, and a desire to see it changed. I feel like very few individuals actually suffering from PDA were consulted about this presentation, and while I'm sure any parent or partner seeking information about PDA may find this useful, as an actual PDA sufferer myself I felt it lacked any real understanding or empathy for what the condition is truly like to live with, and almost all of the struggles were generalised or glossed over, with very little detail given to how these symptoms manifest in everyday life. Instead of hearing about how it appears to the concerned mothers of America, I would have much rather heard the accounts from someone who actually exists on that spectrum and can speak from their own lived experiences. I do appreciate the intention and effort made to educate people about PDA, just wish the delivery was enacted with a little more due care for the people it will directly effect.

So, so, so, so, helpful! Thank you very much!

One pov that may be controversial. Don't ask an Autistic person what you can do for them. (to an adult) It presumes an inability/disability and infantilise them. Autistic folk, like all adults, can ask (or learn to ask) for what they want, or start a dialogue of adult negotiations.

How has this only got 45 views 😳

Thank you so much for your presentation. I am a 65 year old women who has PDA and I have not been diagnosed. I really recommend Harry Thompson. He explains it so well. When he comes to you he will be really good. His You Tube videos help me. Your talk will help. I grew up undiagnosed and have been married for 37 years and my husband gets exhausted. I have two neurotypical grown up children and my PDA exhausts them. I also have two grandchildren and they don’t understand what is wrong with me. Appreciate you getting talked about PDA in America ❤

I don't believe PDA is autism. It's parallel to the spectrum but has too many distinct differences so general autism diagnosis becomes impossible which comes before a the PDA profile.

I couldn't even get through the first 5 minutes. Not a smooth execution. The topic is great, the execution was terrible. Try adding people talking when talking instead of just a screen of words. Mix it up please.

Logically applied Emotional intelligence . If this then that. If you treat others how you want to be treated, then you can navigate them as a person. If most people think your different, then most people are common If most people are common then common sense is what they follow. If your funny/liked/useful then most people will make exceptions/less demand If the above then slips in apperence/behavior will be the exception that makes the rule. Anxiety is not right. Its something else.

Awesome video:) I have Asperger’s and I am also transgender:) So glad the world is bringing more awareness to this:) I remember the days where some told one you don’t know if you are transgender because you are on the spectrum. It’s like denying who you are. In reality those are 2 beautiful qualities to have. It’s a shame the neurotypical world doesn’t appreciate it very much.

People WITHOUT ID/DD are free to make unhealthy choices, and they often experiences the consequences of such choices such as obesity, diabetes, fatty liver disease, joint damage, sleep apnea, and heart disease. We often have higher expectations for people with ID than for neurotypical people. On the other hand, neurotypical people understand the risks and consequences more fully than people with ID, so their choices are more fully informed. Where does Dignity of Risk enter into this calculus? This needs to be wrestled with in the ID/DD field. Even a simple awareness by PSWs and case managers that their clients are often expected to live by different expectations, creating a life lacking in the richness that we take for granted. This must be explored an addressed by ID academics, support workers, educators, ethicists, legal experts, and guardians in conversation with self-advocates. We cannot expect more of people with ID than the average person expects of themselves.

Mi hija no tomo leche materna... Y tiene 3 años y tiene autismo

Useless info, Medicaid does not pay for custodial care and companionship only for about 3 to 4 hrs of care per day even if you are providing 24/hr care, especially with all night sundowner's syndrome patients. Being available against risk of falls and injuries are not part of personal care services. These days, people who work in a burger joint make more money than a person helping with toileting for dementia patients.

That's a bunch of BS! This is just a study to render people of color retarded, so white people can be more or seem more superior than other people of different races.😡

Wonderful. :)

You subscribe to me and I subscribe me to you

A great video ppresentation!

I made a site

I would like to help how do I get on in mo.

Inspirational words from people of diverse academic backgrounds!