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Uisneach and 1p36

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Tuesday 17 January 2012. On TV talking about Uisneach and 1p36. Tuesday 3 January 2012. After Santa and preparing for a new year. Christmas morning Uisneach didn't wake too early so his Mam and Dad were pleased with that. We went down for breakfast together and sitting o...

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Uisneach and 1p36 | uisneach-1p36.blogspot.com Reviews
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Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Tuesday 17 January 2012. On TV talking about Uisneach and 1p36. Tuesday 3 January 2012. After Santa and preparing for a new year. Christmas morning Uisneach didn't wake too early so his Mam and Dad were pleased with that. We went down for breakfast together and sitting o...
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Uisneach and 1p36 | uisneach-1p36.blogspot.com Reviews

https://uisneach-1p36.blogspot.com

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Tuesday 17 January 2012. On TV talking about Uisneach and 1p36. Tuesday 3 January 2012. After Santa and preparing for a new year. Christmas morning Uisneach didn't wake too early so his Mam and Dad were pleased with that. We went down for breakfast together and sitting o...

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uisneach-1p36.blogspot.com uisneach-1p36.blogspot.com
1

Uisneach and 1p36: Summer holiday, sick child – and some nice surprises!

http://uisneach-1p36.blogspot.com/2011/07/summer-holiday-sick-child-and-some-nice.html

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Wednesday 20 July 2011. Summer holiday, sick child – and some nice surprises! The view from every room in the house overlooking Clew Bay. Heaven. We all even managed to go out for a meal together without any major mishaps or incidents involving the kids. 29 July 2011 at 17:31.

2

Uisneach and 1p36: Christmas, communication and back to Crumlin

http://uisneach-1p36.blogspot.com/2011/11/christmas-communication-and-back-to.html

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Friday 25 November 2011. Christmas, communication and back to Crumlin. All snug in his winter jacket while taking a stroll in Dún Laoghaire with Dad. It's been an eventful couple of months and perhaps chronologically its best to work backwards as things come to mind. He insi...

3

Uisneach and 1p36: January 2012

http://uisneach-1p36.blogspot.com/2012_01_01_archive.html

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Tuesday 17 January 2012. On TV talking about Uisneach and 1p36. Tuesday 3 January 2012. After Santa and preparing for a new year. Christmas morning Uisneach didn't wake too early so his Mam and Dad were pleased with that. We went down for breakfast together and sitting o...

4

Uisneach and 1p36: On TV talking about Uisneach and 1p36

http://uisneach-1p36.blogspot.com/2012/01/blog-post.html

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Tuesday 17 January 2012. On TV talking about Uisneach and 1p36. 3 May 2014 at 05:29. Their program is unlike any other. Subscribe to: Post Comments (Atom). View my complete profile. What is 1p36 deletion syndrome? On TV talking about Uisneach and 1p36. Unique - Rare chromo.

5

Uisneach and 1p36: November 2011

http://uisneach-1p36.blogspot.com/2011_11_01_archive.html

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Friday 25 November 2011. Christmas, communication and back to Crumlin. All snug in his winter jacket while taking a stroll in Dún Laoghaire with Dad. It's been an eventful couple of months and perhaps chronologically its best to work backwards as things come to mind. He insi...

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raisingadisabledchild.blogspot.com raisingadisabledchild.blogspot.com

Adventures in Raising a Disabled Child: A Cast Is A Lousy Birthday Present

http://raisingadisabledchild.blogspot.com/2014/01/a-cast-is-lousy-birthday-present.html

Adventures in Raising a Disabled Child. Raising a daughter with 1p36 Deletion Syndrome. Thursday, January 23, 2014. A Cast Is A Lousy Birthday Present. We celebrated Whitney's 10th birthday list past week. Many family members came by to celebrate and spend time with her. She got some really fun gifts. (We decided against the iPad, by the way. It seemed like a bit much for a 10 year old.). I'm wondering if her bone density is an issue. So we'll have to do a good job of protecting her from falls and bu...

raisingadisabledchild.blogspot.com raisingadisabledchild.blogspot.com

Adventures in Raising a Disabled Child: Taking Responsibility

http://raisingadisabledchild.blogspot.com/2014/02/taking-responsibility.html

Adventures in Raising a Disabled Child. Raising a daughter with 1p36 Deletion Syndrome. Monday, February 17, 2014. During the daily rush of helping Whitney get dressed, off to school on time and countless other things, it's easy to set aside teaching important lessons. Melanie is better than I am about taking advantage of teaching moments. So when I see something new it often comes as a surprise. Even when it's been something Melanie has been working on for some time. Subscribe to: Post Comments (Atom).

raisingadisabledchild.blogspot.com raisingadisabledchild.blogspot.com

Adventures in Raising a Disabled Child: Unlucky Break

http://raisingadisabledchild.blogspot.com/2005/08/unlucky-break.html

Adventures in Raising a Disabled Child. Raising a daughter with 1p36 Deletion Syndrome. Thursday, August 04, 2005. A few months ago the developmental specialists encouraged my wife and I to have our daughter stand next to the couch in order to help her feel independent when standing up and to gain strength in her legs and trunk. I hung up and rushed from work to the hospital. Once the the orthopedic surgeon saw my daughter's X-Rays he told us there was no need to insert pins or operate. What a relief!

laurens1p36deletionjourney.blogspot.com laurens1p36deletionjourney.blogspot.com

Laurens 1p-36 Deletion Journey: January 2012

http://laurens1p36deletionjourney.blogspot.com/2012_01_01_archive.html

Laurens 1p-36 Deletion Journey. Thursday, 19 January 2012. Welcome to Lauren's Blog. This is our gorgeous daughter Lauren-Mary Hayden. Lauren is just gone three years old. She lives with a very rare genetic disorder known as 1P-36 deletion syndrome. 1P-36 deletion syndrome is characterised typically by delayed physical and mental development. Typically this is most apparent in areas such as growth, limited speech ability, low muscle tone, hypotonia, seizures, heart problems and distinct facial features.

raisingadisabledchild.blogspot.com raisingadisabledchild.blogspot.com

Adventures in Raising a Disabled Child: Knee Improvements

http://raisingadisabledchild.blogspot.com/2014/03/knee-improvements.html

Adventures in Raising a Disabled Child. Raising a daughter with 1p36 Deletion Syndrome. Monday, March 24, 2014. Next we headed to see a rheumatologist. After examining Whitney, he diagnosed her with knee effusion. He ordered some blood tests to determine the cause. He was leaning toward arthritis but wanted more information. So after the blood tests came back, we've been able to rule out rheumatoid arthritis. It's good to be on the road to recovery again. Thanks to everyone who's been so concerned ab...

raisingadisabledchild.blogspot.com raisingadisabledchild.blogspot.com

Adventures in Raising a Disabled Child: Willing Protector

http://raisingadisabledchild.blogspot.com/2014/03/willing-protector.html

Adventures in Raising a Disabled Child. Raising a daughter with 1p36 Deletion Syndrome. Tuesday, March 18, 2014. Three years after Whitney was born with all of her complications and challenges, Melanie and I welcomed a son to our family. We named him Liam in the hope that someday he can help be a protector for his older sister. Liam is a short form of William or Wilhelm, which means willing protector in German. Labels: Meanderings from Dad. Subscribe to: Post Comments (Atom). Summer is Coming to an End.

raisingadisabledchild.blogspot.com raisingadisabledchild.blogspot.com

Adventures in Raising a Disabled Child: Weak in the Knees

http://raisingadisabledchild.blogspot.com/2014/03/weak-in-knees.html

Adventures in Raising a Disabled Child. Raising a daughter with 1p36 Deletion Syndrome. Monday, March 03, 2014. Weak in the Knees. So what is going on with her knee? Labels: General Medical Treatment. Subscribe to: Post Comments (Atom). Carter and 1p36 Deletion Syndrome. Summer is Coming to an End. Nothing Beats A Quickie! Taylor's Adventures and that 1P36 Thing. A few of my favorites. On TV talking about Uisneach and 1p36. The Ins and Outs of 1p36 parenting. 1p36 Conference in MN and Doctor Appt Updates.

raisingadisabledchild.blogspot.com raisingadisabledchild.blogspot.com

Adventures in Raising a Disabled Child: Stressed About Birthday Shopping

http://raisingadisabledchild.blogspot.com/2014/01/stressed-about-birthday-shopping.html

Adventures in Raising a Disabled Child. Raising a daughter with 1p36 Deletion Syndrome. Wednesday, January 15, 2014. Stressed About Birthday Shopping. Whitney doesn't really care for typical age appropriate play. She really doesn't care about her clothes or hair. Although she does like books. So maybe there's an idea there. I'll have to think about this decision a bit more. But time is running out. Someone please tell me that gift giving for her will get easier someday! Labels: Meanderings from Dad.

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uisneach-1p36.blogspot.com uisneach-1p36.blogspot.com

Uisneach and 1p36

Uisneach is our son. In February 2011, at 18 months of age, he was diagnosed with having a genetic disorder called 1p36 micro-deletion syndrome. This is our blog charting the ups and downs of raising a child with developmental delay. Tuesday 17 January 2012. On TV talking about Uisneach and 1p36. Tuesday 3 January 2012. After Santa and preparing for a new year. Christmas morning Uisneach didn't wake too early so his Mam and Dad were pleased with that. We went down for breakfast together and sitting o...

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