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laurens1p36deletionjourney.blogspot.com

Laurens 1p-36 Deletion Journey

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.

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Laurens 1p-36 Deletion Journey | laurens1p36deletionjourney.blogspot.com Reviews
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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.
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Laurens 1p-36 Deletion Journey | laurens1p36deletionjourney.blogspot.com Reviews

https://laurens1p36deletionjourney.blogspot.com

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.

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laurens1p36deletionjourney.blogspot.com laurens1p36deletionjourney.blogspot.com
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Laurens 1p-36 Deletion Journey: Welcome to Lauren's Blog

http://laurens1p36deletionjourney.blogspot.com/2012/01/welcome-to-laurens-blog.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.

2

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.

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

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.

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

Uisneach and 1p36: September 2011

http://uisneach-1p36.blogspot.com/2011_09_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. Thursday 1 September 2011. Uisneach’s 2nd birthday and other things. Uisneach turned two and we cannot believe how fast time flies! We left a little early. Subscribe to: Posts (Atom). Are the proud parents of Uisneach. He is our first and only child at present. We li...Welco...

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Laurens 1p-36 Deletion Journey

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.

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