mamapineappleblog.wordpress.com
Information and resources page revamp | The Misadventures of Mama Pineapple
https://mamapineappleblog.wordpress.com/2016/12/16/information-and-resources-page-revamp
The Misadventures of Mama Pineapple. Social awkwardness, flights of fancy, uncontrollable urges to dance…the life and times of one adult-diagnosed autistic woman. Identity-first language, and why it’s important. Resources by and for #ActuallyAutistic people. Getting assessed (a personal perspective). Information and resources page revamp. December 16, 2016. I like to respond to individual messages (and these days I get quite a few, which I’m happy to receive! Also added is a new section on the specifics ...
swanarchie07.wordpress.com
Dear Social Services | half a decade old
https://swanarchie07.wordpress.com/2013/08/06/dear-social-services
Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. August 6, 2013. Do you know how hard I found it to pick up the phone and ring your team asking for help with my disabled son? Do you know how guilty I felt calling you to arrange a ‘child in need assessment’ on my child because i’m not coping with him anymore? Do you know how desperate I am for you to help my family? 1,212 more words. Brian Lamb’s Top 10 Tips for Engaging Parents. Leave a Reply Cancel reply.
swanarchie07.wordpress.com
April | 2015 | half a decade old
https://swanarchie07.wordpress.com/2015/04
Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. Monthly Archives: April 2015. Things we take for granted. April 2, 2015. What’s the point of a parent carer’s needs assessment? April 2, 2015. In all the excitement of Care Act Day, it is important not to lose sight of the fact that important provisions of the Children and Families Act 2014 for parent carers of disabled children and young carers also come into force today (1 April 2015). 1,245 more words.
swanarchie07.wordpress.com
How a year can change things. | half a decade old
https://swanarchie07.wordpress.com/2015/10/14/how-a-year-can-change-things
Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. How a year can change things. October 14, 2015. So I decided to brush the cob webs off and try write today,. I started this blog when Archie turned 5 to talk about what it was like bringing a child up like him and the journey us special needs parents go on, for a while it helped but eventually I felt like I was always ranting about what the local authority wouldn’t do to support us. Enter your comment here.
claireyr123.wordpress.com
May | 2016 | The life of a colourful autism family
https://claireyr123.wordpress.com/2016/05
The life of a colourful autism family. Monthly Archives: May 2016. Go on, be honest….we’ve all said these but have you considered what these instructions mean in real life to children? I mean what are we asking of them? To switch their emotion off? To push the emotion deep down inside so it doesn’t spoil the flow of the day? Or do we really believe that children are able to recognise, understand and modulate their emotion in such a way that they can self talk themselves into a better emotional state?
swanarchie07.wordpress.com
“Life is a rollacoaster you just after ride it” | half a decade old
https://swanarchie07.wordpress.com/2014/04/25/life-is-a-rollacoaster-you-just-after-ride-it
Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. 8220;Life is a rollacoaster you just after ride it”. April 25, 2014. So I am dusting of the cob webs and writing my post today for undiagnosed children’s day and you can check out what’s going on everywhere else today too #. An Alternative Social Care Dictionary ». 2 thoughts on “ “Life is a rollacoaster you just after ride it”. April 27, 2014 at 7:47 am. Wow Patsy, that was an amazing blog, you managed to ...
swanarchie07.wordpress.com
Things we take for granted | half a decade old
https://swanarchie07.wordpress.com/2015/04/02/things-we-take-for-granted
Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. Things we take for granted. April 2, 2015. What’s the point of a parent carer’s needs assessment? How a year can change things. ». Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. It Must Be Mum.
mamapineappleblog.wordpress.com
General information | The Misadventures of Mama Pineapple
https://mamapineappleblog.wordpress.com/information-and-resources/general-information
The Misadventures of Mama Pineapple. Social awkwardness, flights of fancy, uncontrollable urges to dance…the life and times of one adult-diagnosed autistic woman. Identity-first language, and why it’s important. Resources by and for #ActuallyAutistic people. Getting assessed (a personal perspective). This page is a short list of very basic stuff. You might want to use as a starting point. So most of this is copied over from a pinned post on my Facebook page. Firstly, a great little comic strip. A great (...
lovepda.wordpress.com
What is PDA? – lovepda
https://lovepda.wordpress.com/2016/12/01/what-is-pda
Empowering parents of children with pathological demand avoidance syndrome, an autistic spectrum disorder. December 1, 2016. February 1, 2017. PATHOLOGICAL DEMAND AVOIDANCE SYNDROME. Facts and Myth Busters. PDA is not an illness its a difference of mind. PDA is not curable nor does it need to be cured. PDA is a subtype of Autism. People with PDA can be high functioning or low functioning. PDA has very strong criteria and all people with PDA have the following traits. PDA people have amazing ability to se...
lovepda.wordpress.com
About – lovepda
https://lovepda.wordpress.com/about
Empowering parents of children with pathological demand avoidance syndrome, an autistic spectrum disorder. 8217; before I ask the question ‘What should I do? It Must Be Mum. MAKING RAINBOWS WITH PDA. Say It How It Is. Riko's blog: PDA and more. Blog at WordPress.com. It Must Be Mum. A Site for Resources and Reflections That May Help Those Navigating Aspects of the World of 'Special Education Needs'. MAKING RAINBOWS WITH PDA. One mums mission to turn breakdown into breakthrough. Say It How It Is.
SOCIAL ENGAGEMENT