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		<title>CMV Support</title>
		<description>News, Information, Friendship and Support for all.</description>
		<link><![CDATA[http://www.cmvsupport.org/site]]></link>
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		<item>
			<title><![CDATA[Dillon]]></title>
			<description><![CDATA[2006/11/15
Hi, I am Dillon. I am 6, and I live in Liverpool!]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/9.jpg]]></link>
			<guid>image-id:64</guid>
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			<media:title><![CDATA[Dillon]]></media:title>
			<media:description><![CDATA[2006/11/15
Hi, I am Dillon. I am 6, and I live in Liverpool!]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_9.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Me at 3lb 9oz]]></title>
			<description><![CDATA[2006/10/15
Me at 3lb 9oz and that's my Mummy's hand.]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/8.jpg]]></link>
			<guid>image-id:63</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/8.jpg' medium='image' />
			<media:title><![CDATA[Me at 3lb 9oz]]></media:title>
			<media:description><![CDATA[2006/10/15
Me at 3lb 9oz and that's my Mummy's hand.]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_8.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Me and My Mummy!]]></title>
			<description><![CDATA[2006/10/15
This is Me and Mummy going to Venice]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/7.jpg]]></link>
			<guid>image-id:62</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/7.jpg' medium='image' />
			<media:title><![CDATA[Me and My Mummy!]]></media:title>
			<media:description><![CDATA[2006/10/15
This is Me and Mummy going to Venice]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_7.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Howdy! My name is Jack.]]></title>
			<description><![CDATA[2006/10/15
I am 4 years old and like to play with all types of toys even the girly ones too. I am extremely active and like all sports especially the rough and tumble ones.
I was diagnosed with CMV from birth and i currently wear a CI (Cochlear Implant) which was fitted when i was around 2 years of age. I am unable to talk at the moment but not sure if this is due to autism or a communication disorder.]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/6.jpg]]></link>
			<guid>image-id:61</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/6.jpg' medium='image' />
			<media:title><![CDATA[Howdy! My name is Jack.]]></media:title>
			<media:description><![CDATA[2006/10/15
I am 4 years old and like to play with all types of toys even the girly ones too. I am extremely active and like all sports especially the rough and tumble ones.
I was diagnosed with CMV from birth and i currently wear a CI (Cochlear Implant) which was fitted when i was around 2 years of age. I am unable to talk at the moment but not sure if this is due to autism or a communication disorder.]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_6.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[David Higgins]]></title>
			<description><![CDATA[2006/9/13
David at 16 months. He is now almost 21 months and finally gaining weight due to a PEG tube emplaced a few weeks ago.]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/4.jpg]]></link>
			<guid>image-id:60</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/4.jpg' medium='image' />
			<media:title><![CDATA[David Higgins]]></media:title>
			<media:description><![CDATA[2006/9/13
David at 16 months. He is now almost 21 months and finally gaining weight due to a PEG tube emplaced a few weeks ago.]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_4.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Welsh Chick!]]></title>
			<description><![CDATA[2009/12/1]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/38.jpg]]></link>
			<guid>image-id:59</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/38.jpg' medium='image' />
			<media:title><![CDATA[Welsh Chick!]]></media:title>
			<media:description><![CDATA[2009/12/1]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_38.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Chloe XX]]></title>
			<description><![CDATA[2009/8/17
this is my daughter chloe,sh was born with cmv although we didnt find out until sh was a couple of days old.my doctors had told me 5 months pregnant that she wouldnt survive birth.Chloe is now little over 7 months old and is profoundly deaf.Chloe wears hearing aids which she shows some signs of them workin.She cant hold her head up straight but will be gettin physio to help.She also doesnt hold anythin in her hands or try to pick anything up.As a single mum at 21 i have found all of this hard to deal with especially as i dont get much help from family,but i would never change her as she is the best thing in my life and i love her with all my heart.There should be more awareness of cmv as i had never heard of it before chloe.There should also be more support groups where people can come together and swap stories.I have so many questions that no one can seem to answer and its very frustrating at times.]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/37.jpg]]></link>
			<guid>image-id:58</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/37.jpg' medium='image' />
			<media:title><![CDATA[Chloe XX]]></media:title>
			<media:description><![CDATA[2009/8/17
this is my daughter chloe,sh was born with cmv although we didnt find out until sh was a couple of days old.my doctors had told me 5 months pregnant that she wouldnt survive birth.Chloe is now little over 7 months old and is profoundly deaf.Chloe wears hearing aids which she shows some signs of them workin.She cant hold her head up straight but will be gettin physio to help.She also doesnt hold anythin in her hands or try to pick anything up.As a single mum at 21 i have found all of this hard to deal with especially as i dont get much help from family,but i would never change her as she is the best thing in my life and i love her with all my heart.There should be more awareness of cmv as i had never heard of it before chloe.There should also be more support groups where people can come together and swap stories.I have so many questions that no one can seem to answer and its very frustrating at times.]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_37.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Molly]]></title>
			<description><![CDATA[Molly
2009/5/13
Molly was born 3/9/07 at 25 weeks weighing 800gms and was diagnosed with CMV at about 4 weeks. Molly is a beautiful and very happy girl, doing everything she should be. Molly was born with various different problems and is being monitored very closely.  Molly's twin brother Ben also diagnosed with CMV sadly was not so lucky and passed away after 28 days. Very glad to have joined this site. Molly is with her big sister Jess in this picture. Thank you.]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/34.jpg]]></link>
			<guid>image-id:57</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/34.jpg' medium='image' />
			<media:title><![CDATA[Molly]]></media:title>
			<media:description><![CDATA[Molly
2009/5/13
Molly was born 3/9/07 at 25 weeks weighing 800gms and was diagnosed with CMV at about 4 weeks. Molly is a beautiful and very happy girl, doing everything she should be. Molly was born with various different problems and is being monitored very closely.  Molly's twin brother Ben also diagnosed with CMV sadly was not so lucky and passed away after 28 days. Very glad to have joined this site. Molly is with her big sister Jess in this picture. Thank you.]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_34.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Ms Alexis]]></title>
			<description><![CDATA[2009/5/4
Alexis was born on August 3, 2008. She was shortly after diagnosed with CMV. She was in the NICU for 2 months and had to take Gancycloveir for 6 of those weeks. So far she is doing good *crosses fingers* She recently had an MRI that showed the calcium deposits on her brain, but I am NOT going to let that worry me. She is a strong girl and I know she will live her life to the fullest. Shes my heart. I am so glad there is a support group. Thank you.]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/33.jpg]]></link>
			<guid>image-id:56</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/33.jpg' medium='image' />
			<media:title><![CDATA[Ms Alexis]]></media:title>
			<media:description><![CDATA[2009/5/4
Alexis was born on August 3, 2008. She was shortly after diagnosed with CMV. She was in the NICU for 2 months and had to take Gancycloveir for 6 of those weeks. So far she is doing good *crosses fingers* She recently had an MRI that showed the calcium deposits on her brain, but I am NOT going to let that worry me. She is a strong girl and I know she will live her life to the fullest. Shes my heart. I am so glad there is a support group. Thank you.]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_33.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
		</item>
		<item>
			<title><![CDATA[Chris in Cornwall]]></title>
			<description><![CDATA[2009/2/28
I love being outdoors, I live in lancashire. Here i am with my Dad Mick on holiday in Cornwall, where we stay each year in an adapted farm cottage. I have Epilepsy as well as my disabilities and have a seizure every day, but we dont let that stop us having fun !]]></description>
			<link><![CDATA[http://www.cmvsupport.org/site/wp-content/gallery/archive/32.jpg]]></link>
			<guid>image-id:55</guid>
			<media:content url='http://www.cmvsupport.org/site/wp-content/gallery/archive/32.jpg' medium='image' />
			<media:title><![CDATA[Chris in Cornwall]]></media:title>
			<media:description><![CDATA[2009/2/28
I love being outdoors, I live in lancashire. Here i am with my Dad Mick on holiday in Cornwall, where we stay each year in an adapted farm cottage. I have Epilepsy as well as my disabilities and have a seizure every day, but we dont let that stop us having fun !]]></media:description>
			<media:thumbnail url='http://www.cmvsupport.org/site/wp-content/gallery/archive/thumbs/thumbs_32.jpg' width='100' height='75' />
			<media:keywords><![CDATA[]]></media:keywords>
			<media:copyright><![CDATA[Copyright (c) CMV Support (http://www.cmvsupport.org/site)]]></media:copyright>
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