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Brody, Me and GDD – Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility & no primary diagnosis.

Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility & no primary diagnosis.

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Brody, Me and GDD – Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility & no primary diagnosis. | brodymeandgdd.wordpress.com Reviews
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Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility & no primary diagnosis.
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Brody, Me and GDD – Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility & no primary diagnosis. | brodymeandgdd.wordpress.com Reviews

https://brodymeandgdd.wordpress.com

Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility & no primary diagnosis.

INTERNAL PAGES

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1

Acceptance

https://brodymeandgdd.wordpress.com/2016/12/05/acceptance

December 5, 2016. January 22, 2017. Posted in SWAN UK. Every so often, something will happen to highlight how delayed Brody is either cognitively or physically. And every so often it catches my breath or punches my gut. But the dreams I once had at night where we had conversations the ones where I’d wake up and for a brief moment think that he was. Now that Brody is nearly 5, I have finally got used to the fact that Global Development Delay (GDD) doesn’t mean may catch up for us. Exactly who he is. There...

2

Sorry For The Inconvenience. We Are Trying To Change The World…

https://brodymeandgdd.wordpress.com/2016/10/25/sorry-for-the-inconvenience-we-are-trying-to-change-the-world

Sorry For The Inconvenience. We Are Trying To Change The World. October 25, 2016. January 2, 2017. You know that saying (and I’ve used it before. By Martin Luther King. Nothing in the world is more dangerous than sincere ignorance and conscientious stupidity. Well, I just keep being reminded of it. The Mighty recently published my latest article in relation to fully accessible toilets. Or to be more specific Changing Places. And Space to Change. Anyone of us could face this dilemma. A changing table],.

3

Why Isn’t This News Worthy?

https://brodymeandgdd.wordpress.com/2016/10/11/why-isnt-this-news-worthy

Why Isn’t This News Worthy? October 11, 2016. October 14, 2016. Thousands of disabled children and adults in the UK have continence issues and as a result of their disabilities cannot use a toilet at all or require a hoist in order to do so. My son Brody can’t use a toilet and is still in nappies. At 4 years old he is far too big for a baby changing table. But what’s the alternative? And sadly, we share this dilemma with thousands of other families. I really don’t understand why this issue isn’t newswort...

4

What’s In A Word?

https://brodymeandgdd.wordpress.com/2016/10/09/whats-in-a-word

What’s In A Word? October 9, 2016. October 14, 2016. What’s in a word? Words can be powerful. They can bring joy. One word can change someone’s day – life even. But in the same speed in which they can bring happiness, they can also cause hurt and damage – even when mindlessly spoken. It was Martin Luther King who said that. 8220;nothing in the world is more dangerous than sincere ignorance and conscientious stupidity”. He hit the nail on the head with that one. Doesn’t violate their community standards.

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LINKS TO THIS WEBSITE

raisingtherainbows.co.uk raisingtherainbows.co.uk

Raising The Rainbows: October 2016

http://www.raisingtherainbows.co.uk/2016_10_01_archive.html

You can buy this Blogger template in our store. Life on the spectrum is never dull. A to Z of Autism. Friday, 28 October 2016 20:05. Win Some Trolls Goodies. So have you been dragged to the cinema by the kids yet to see the new Trolls movie? Or were you the one doing the dragging? We have yet to see the film as we have been away on holiday and busy, but the kids can't wait to see those iconic Trolls! They are the perfect gifts for any Trolls fan! Open to UK and Ireland residents over 18years. 1. Delivery...

swanarchie07.wordpress.com 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.

community.fireflyfriends.com community.fireflyfriends.com

Space to Change | Special Needs Facilities | Firefly Community

http://community.fireflyfriends.com/campaigns/space-to-change

A place for special needs families to meet, talk and break down life's barriers. Don't be a stranger, log in. Space to Change Accessible Toilets. Space to Change Accessible Toilets. Search for locations near you that provide GoTo Shop Trolleys or Space to Change and Changing Places toilets. Why support this campaign? Space to Change provides alternative guidance where space is restricted, more likely to be the case in small buildings and refurbishments. 97% of families said changing my child is a problem.

swanarchie07.wordpress.com 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 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.

swanarchie07.wordpress.com 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 swanarchie07.wordpress.com

Archie’s Story | half a decade old

https://swanarchie07.wordpress.com/2011/11/30/archies-story-2

Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. November 30, 2011. OH HOW I WAS WRONG. I was told that Archie needed a pot on once a week for 8 weeks and each time they would manipulate it into position, he would then go into some little shoes called Dennis brown boots and bars, I was shown pictures of other children and their stories and then handed a DLA FORM. HERE IS WHERE THE JOURNEY REALLY BEGAN. Once upon time was a child ready to be born,. The chi...

swanarchie07.wordpress.com swanarchie07.wordpress.com

What’s the point of a parent carer’s needs assessment? | half a decade old

https://swanarchie07.wordpress.com/2015/04/02/whats-the-point-of-a-parent-carers-needs-assessment

Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. 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). What we have for parent carers of disabled children is. 1,245 more words. It Must Be Mum.

swanarchie07.wordpress.com swanarchie07.wordpress.com

October | 2015 | half a decade old

https://swanarchie07.wordpress.com/2015/10

Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. Monthly Archives: October 2015. How a year can change things. October 14, 2015. So I decided to brush the cob webs off and try write today,. Last year was hell for me but not hell due to Archie well not direct anyway,. After all the fights I went through to get the respite I felt we needed as a family my actually family fell apart a few months after we received the support package we needed, how ironic.

swanarchie07.wordpress.com swanarchie07.wordpress.com

June | 2013 | half a decade old

https://swanarchie07.wordpress.com/2013/06

Half a decade old. Sharing my journey of living with a child with a undiagnosed genetic condition. Monthly Archives: June 2013. June 16, 2013. Love, Belief and Balls. June 16, 2013. Love, Belief and Balls. It Must Be Mum. A whole load more. Love, Belief and Balls. The World of Gorgeous Grace. Authors of our lives. Definitely Not The Walton's. As Alex Grows Up. Star In Her Eye. Making rights make sense. Friends of Ty Gwyn Special School. They Call Me Mummy. The angel and the soldier. Sun, Moon and Stars.

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Please Enable Javascript and download the updated version of Flash Player. Brody McKinley was born on December 17th, 1980 in Lima, Ohio. He attended Shawnee Senior High School. He remained in Lima, Ohio until he enrolled at Miami University in Oxford, Ohio. There his studies ranged from Zoology and Psychology to Computer Science. While in Oxford, Brody played the lead in three independent short films, two of which he co-produced. BrodyMcKinley.com 2010 info@BrodyMcKinley.com.

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Hey, New Guy! Workout - fitness - nutritional advice. Brody's got a new website. Welcome - Brody has a new website we hope you will visit! Http:/ www.brodymcvittie.com. April 14th, 2014. We have had numerous requests to see B's video work-outs that he finally gave the okay to allow them to be shown through this forum. In this first video he is pulling himself up by only 2 fingers on each hand. In the third video he has a weighted vest on . December 06th, 2013. LONDON FREE PRESS ARTICLE - BY RANDY RICHMOND.

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brodymeandgdd.wordpress.com brodymeandgdd.wordpress.com

Brody, Me and GDD – Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility & no primary diagnosis.

Brody, Me and GDD. Our journey with Global Development Delay, Autism, Epilepsy, Hypotonia, Hypermobility and no primary diagnosis. December 5, 2016. January 2, 2017. Posted in SWAN UK. Sorry For The Inconvenience. We Are Trying To Change The World. October 25, 2016. January 2, 2017. I Am ‘One In Four’, But Why Do I Feel Like I Shouldn’t Talk About It? October 14, 2016. October 14, 2016. Why Isn’t This News Worthy? October 11, 2016. October 14, 2016. Thousands of disabled children and adults in the UK hav...

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