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	<title>Comments on: Down Syndrome Links</title>
	<atom:link href="http://giftsds.segullah.org/down-syndrome-links/feed/" rel="self" type="application/rss+xml" />
	<link>http://giftsds.segullah.org</link>
	<description>A Book about How Children with Down Syndrome Enrich our Lives</description>
	<lastBuildDate>Sat, 21 Jan 2012 16:27:20 +0000</lastBuildDate>
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		<title>By: Catherine Suarez</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-11071</link>
		<dc:creator>Catherine Suarez</dc:creator>
		<pubDate>Sat, 21 Jan 2012 16:27:20 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-11071</guid>
		<description>Hello:
I teach at Las Positas College in Livermore, California. Every year I host a week-long event called La Semana Cubana/ Cuban Week. This year I have invited an artist from Cuba, Jesus Carrete Rodriguez, along with his wife and daughter Liliana. Liliana was born with Down Syndrome. Mr. Carrete started an Art Therapy program for children and young adults with Down Syndrome out of his own house in Pinar del Rio, Cuba ten years ago. This year from Monday, March 12 through Friday, March 16th artwork from his students will be displayed at La Semana Cubana. The event is open and free to the public. I am hoping to have Mr. Carrete, his wife Coralina and his daughter Liliana there as well; their visas are pending. If they do come I would like to provide them with local opportunities(Bay Area and around) to meet with members of art therapy programs. Please contact me if you would like further information about our event of if you have a contact for me: csuarez@laspositascollege.edu.

Thank you,

Catherine</description>
		<content:encoded><![CDATA[<p>Hello:<br />
I teach at Las Positas College in Livermore, California. Every year I host a week-long event called La Semana Cubana/ Cuban Week. This year I have invited an artist from Cuba, Jesus Carrete Rodriguez, along with his wife and daughter Liliana. Liliana was born with Down Syndrome. Mr. Carrete started an Art Therapy program for children and young adults with Down Syndrome out of his own house in Pinar del Rio, Cuba ten years ago. This year from Monday, March 12 through Friday, March 16th artwork from his students will be displayed at La Semana Cubana. The event is open and free to the public. I am hoping to have Mr. Carrete, his wife Coralina and his daughter Liliana there as well; their visas are pending. If they do come I would like to provide them with local opportunities(Bay Area and around) to meet with members of art therapy programs. Please contact me if you would like further information about our event of if you have a contact for me: <a href="mailto:csuarez@laspositascollege.edu">csuarez@laspositascollege.edu</a>.</p>
<p>Thank you,</p>
<p>Catherine</p>
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	<item>
		<title>By: Katia Hauser</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-8137</link>
		<dc:creator>Katia Hauser</dc:creator>
		<pubDate>Wed, 12 Jan 2011 18:59:06 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-8137</guid>
		<description>Hello. The Down Syndrome Footprint Foundation and Store focuses on raising awareness, empowerment, and employment for individuals with Down syndrome with the Down Syndrome Footprint Symbol. As the mother of a child with Down syndrome I look forward to raising as many awareness and job opportunities as possible for the Down syndrome community. Please shop our storefront at www.DownSyndromeFootprint.com for your walk, fundraiser, or just for yourself as a personal celebration. This is the first Down Syndrome Awareness store that guarantees every item that we sell is made or packaged by an individual with Down syndrome!</description>
		<content:encoded><![CDATA[<p>Hello. The Down Syndrome Footprint Foundation and Store focuses on raising awareness, empowerment, and employment for individuals with Down syndrome with the Down Syndrome Footprint Symbol. As the mother of a child with Down syndrome I look forward to raising as many awareness and job opportunities as possible for the Down syndrome community. Please shop our storefront at <a href="http://www.DownSyndromeFootprint.com" rel="nofollow">http://www.DownSyndromeFootprint.com</a> for your walk, fundraiser, or just for yourself as a personal celebration. This is the first Down Syndrome Awareness store that guarantees every item that we sell is made or packaged by an individual with Down syndrome!</p>
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	</item>
	<item>
		<title>By: Catherine Grube</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-7695</link>
		<dc:creator>Catherine Grube</dc:creator>
		<pubDate>Thu, 18 Nov 2010 02:14:40 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-7695</guid>
		<description>Hi,

I just started Fabulous with 47! to support families in Southern Maryland with a child with Down syndrome and to raise awareness and acceptance of individuals with disabilities.  I am particularly interested in helping families cope with the stresses and emotions following the diagnosis.  I think Fabulous with 47! would be a good site to list!

Thanks!
Catherine Grube</description>
		<content:encoded><![CDATA[<p>Hi,</p>
<p>I just started Fabulous with 47! to support families in Southern Maryland with a child with Down syndrome and to raise awareness and acceptance of individuals with disabilities.  I am particularly interested in helping families cope with the stresses and emotions following the diagnosis.  I think Fabulous with 47! would be a good site to list!</p>
<p>Thanks!<br />
Catherine Grube</p>
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	<item>
		<title>By: Ria Haag</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-3517</link>
		<dc:creator>Ria Haag</dc:creator>
		<pubDate>Fri, 15 May 2009 03:22:42 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-3517</guid>
		<description>Almost a month ago, I started a blog &quot;Bill and Ria&quot; to share experiences about our life, parenting, and Down syndrome. Our son Matthew was diagnosed with Down syndrome after his birth in 2007.  I hope to be added to your list. Thanks!</description>
		<content:encoded><![CDATA[<p>Almost a month ago, I started a blog &#8220;Bill and Ria&#8221; to share experiences about our life, parenting, and Down syndrome. Our son Matthew was diagnosed with Down syndrome after his birth in 2007.  I hope to be added to your list. Thanks!</p>
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		<title>By: Kim Duffy</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-3496</link>
		<dc:creator>Kim Duffy</dc:creator>
		<pubDate>Mon, 11 May 2009 18:18:48 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-3496</guid>
		<description>I am president of the Gulf Coast Down Syndrome Society, Inc., and this is our new website.  We would appreciate your including it in your links.
Thank you,
Kim Duffy</description>
		<content:encoded><![CDATA[<p>I am president of the Gulf Coast Down Syndrome Society, Inc., and this is our new website.  We would appreciate your including it in your links.<br />
Thank you,<br />
Kim Duffy</p>
]]></content:encoded>
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		<title>By: Annemarie Jansen</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-3211</link>
		<dc:creator>Annemarie Jansen</dc:creator>
		<pubDate>Sat, 28 Feb 2009 13:36:31 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-3211</guid>
		<description>Dear readers, 

We would like to have a link on your site although our site is in dutch. 

We are building a small-scale holidaypark in France especially for families with disabled children. This 2009 the park opens with a minicamping for children with Downsyndrome and their families. The park will be build further year by year en become more prettier than it already is. We are a non-profit organisation and work with volunteers and sponsors because we think that a holiday at our place must be reachable for every family. 

Because we have no marketing budget, we must find other ways to reach families with Downsyndrome children and you can help us with this. We are very thankfull if you can arrange al link to us at your website. 

Kind regards, 
Annemarie Jansen
volunteer from the start of Puylagorge</description>
		<content:encoded><![CDATA[<p>Dear readers, </p>
<p>We would like to have a link on your site although our site is in dutch. </p>
<p>We are building a small-scale holidaypark in France especially for families with disabled children. This 2009 the park opens with a minicamping for children with Downsyndrome and their families. The park will be build further year by year en become more prettier than it already is. We are a non-profit organisation and work with volunteers and sponsors because we think that a holiday at our place must be reachable for every family. </p>
<p>Because we have no marketing budget, we must find other ways to reach families with Downsyndrome children and you can help us with this. We are very thankfull if you can arrange al link to us at your website. </p>
<p>Kind regards,<br />
Annemarie Jansen<br />
volunteer from the start of Puylagorge</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Renee Forrestall</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-1694</link>
		<dc:creator>Renee Forrestall</dc:creator>
		<pubDate>Sun, 04 Jan 2009 04:38:56 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-1694</guid>
		<description>Hello,

I am sending you some information and links on our group for you to consider for your website. 

I am the founder of the Team Possibles - an integrated studio art program for young adults. In Spring 07, I was invited by the NSDSS to develop a pilot art class for our young people with DS.  Since that time, we have grown into a rich and integrated program that includes partners and volunteers from the broader community. The results have been startling, and a testament to the importance of providing quality resources and never underestimating our members.

We have worked with the Atlantic Fim Festival,  Atlantic Film-makers Coop, Halifax Regional Municipality Junior Leaders, the Art Gallery of Nova Scotia, and Forrestall Fine Art. Starting January 09, we will be working with the Visual Connections Art Gallery and the Duke Of Edinburgh Award organization.

Team Possibles operates with the support of our local Recreation Department, the NSDSS, and other granting organizations. Centred around studio projects, punctuated by social and physical activities, the group serves youth from NSDSS and their peers from university and high school. 

I am a mother to Marie (she is 18 years old with T-21). I have over twenty years experience as an Art Specialist Teacher, and as a professional artist. In recent years, I have taught with the Education Departments at NSCAD and Mount Saint Vincent Universities as an art education Instructor for their BEd programs. I am also a studio Instructor for the NSCAD University’s BFA program. I currently work with the Halifax Regional School Board as a full-time art education teacher/consultant. 

We operate in terms to parallel the school/college calendar. During Winter 09, we will be offering Team Possibles Zine. We are working with our City Recreation program and Anchor Archive Screen–Printing Cooperative to establish a print shop for the Team to learn photo-screen printing and other printing methods. The work will culminate in exhibitions at the recreation centre and at the Visual Connections gallery and hopefully at the CDSS conference. 

Here are some links to our Blogs - you may be interested to see what we do.
Hope you enjoy our work.
Thank you
Renee Forrestall


http://teampossiblesmovie.blogspot.com/
2008 Winter and Spring:  Team Possibles - The Movie
The Team created two films with the Viewfinders Film Festival and the Atlantic Film-maker’s Coop.
They worked on a mask-making and costume design project for an exhibition at the Art Gallery of Nova Scotia, and made a film using shadow puppets that they had made.


http://teampossibles.blogspot.com/
2007 Fall Term:   Teen Exhibition
We created an exhibition of photographs and had an opening at the Forrestall Fine Art Gallery: the exhibit was attended by the Lieutenant Governor of N.S..


http://teampossiblescamp.blogspot.com/
2008 Summer Term:  Team Possibles - Outdoor Adventure Art Camp
The Team hiked around many city parks and created art works in a natural environment using found materials. The adventures also included visiting a museum and the Busker’s Festival. 

http://teampossiblesstylefashion.blogspot.com/
2008 Fall Term:  Team Possibles -  Style and Fashion 
The Team opened their second public art exhibition at the Art Gallery of Nova Scotia. 
The Team worked with a local artist on creating wearable art and a fashion show.
They created fashion photographs and posters and had their first experience working in a Darkroom.</description>
		<content:encoded><![CDATA[<p>Hello,</p>
<p>I am sending you some information and links on our group for you to consider for your website. </p>
<p>I am the founder of the Team Possibles &#8211; an integrated studio art program for young adults. In Spring 07, I was invited by the NSDSS to develop a pilot art class for our young people with DS.  Since that time, we have grown into a rich and integrated program that includes partners and volunteers from the broader community. The results have been startling, and a testament to the importance of providing quality resources and never underestimating our members.</p>
<p>We have worked with the Atlantic Fim Festival,  Atlantic Film-makers Coop, Halifax Regional Municipality Junior Leaders, the Art Gallery of Nova Scotia, and Forrestall Fine Art. Starting January 09, we will be working with the Visual Connections Art Gallery and the Duke Of Edinburgh Award organization.</p>
<p>Team Possibles operates with the support of our local Recreation Department, the NSDSS, and other granting organizations. Centred around studio projects, punctuated by social and physical activities, the group serves youth from NSDSS and their peers from university and high school. </p>
<p>I am a mother to Marie (she is 18 years old with T-21). I have over twenty years experience as an Art Specialist Teacher, and as a professional artist. In recent years, I have taught with the Education Departments at NSCAD and Mount Saint Vincent Universities as an art education Instructor for their BEd programs. I am also a studio Instructor for the NSCAD University’s BFA program. I currently work with the Halifax Regional School Board as a full-time art education teacher/consultant. </p>
<p>We operate in terms to parallel the school/college calendar. During Winter 09, we will be offering Team Possibles Zine. We are working with our City Recreation program and Anchor Archive Screen–Printing Cooperative to establish a print shop for the Team to learn photo-screen printing and other printing methods. The work will culminate in exhibitions at the recreation centre and at the Visual Connections gallery and hopefully at the CDSS conference. </p>
<p>Here are some links to our Blogs &#8211; you may be interested to see what we do.<br />
Hope you enjoy our work.<br />
Thank you<br />
Renee Forrestall</p>
<p><a href="http://teampossiblesmovie.blogspot.com/" rel="nofollow">http://teampossiblesmovie.blogspot.com/</a><br />
2008 Winter and Spring:  Team Possibles &#8211; The Movie<br />
The Team created two films with the Viewfinders Film Festival and the Atlantic Film-maker’s Coop.<br />
They worked on a mask-making and costume design project for an exhibition at the Art Gallery of Nova Scotia, and made a film using shadow puppets that they had made.</p>
<p><a href="http://teampossibles.blogspot.com/" rel="nofollow">http://teampossibles.blogspot.com/</a><br />
2007 Fall Term:   Teen Exhibition<br />
We created an exhibition of photographs and had an opening at the Forrestall Fine Art Gallery: the exhibit was attended by the Lieutenant Governor of N.S..</p>
<p><a href="http://teampossiblescamp.blogspot.com/" rel="nofollow">http://teampossiblescamp.blogspot.com/</a><br />
2008 Summer Term:  Team Possibles &#8211; Outdoor Adventure Art Camp<br />
The Team hiked around many city parks and created art works in a natural environment using found materials. The adventures also included visiting a museum and the Busker’s Festival. </p>
<p><a href="http://teampossiblesstylefashion.blogspot.com/" rel="nofollow">http://teampossiblesstylefashion.blogspot.com/</a><br />
2008 Fall Term:  Team Possibles &#8211;  Style and Fashion<br />
The Team opened their second public art exhibition at the Art Gallery of Nova Scotia.<br />
The Team worked with a local artist on creating wearable art and a fashion show.<br />
They created fashion photographs and posters and had their first experience working in a Darkroom.</p>
]]></content:encoded>
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		<title>By: email from Barbara Curtis</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-1207</link>
		<dc:creator>email from Barbara Curtis</dc:creator>
		<pubDate>Wed, 12 Nov 2008 19:27:02 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-1207</guid>
		<description>This article appeared on the front page of the early edition of the Washington Post last Sunday, and on the front page of the Metro Section in subsequent editions.

http://www.washingtonpost.com/wp-dyn/content/article/2008/11/08/AR2008110802462.html?sub=AR

The first interview for this was done October 7, the day before Tripp went back to the hospital the first time.  The second was done the next day, when Justin&#039;s birth parents arrived from Taiwan to visit and the photos were taken.

I thank God that perhaps some baby with Down syndrome might be saved to live a full life and to increase the fullness of all the surrounding lives.  That&#039;s the beauty of God&#039;s work - I don&#039;t even know how or when it happens.  I just know it will.</description>
		<content:encoded><![CDATA[<p>This article appeared on the front page of the early edition of the Washington Post last Sunday, and on the front page of the Metro Section in subsequent editions.</p>
<p><a href="http://www.washingtonpost.com/wp-dyn/content/article/2008/11/08/AR2008110802462.html?sub=AR" rel="nofollow">http://www.washingtonpost.com/wp-dyn/content/article/2008/11/08/AR2008110802462.html?sub=AR</a></p>
<p>The first interview for this was done October 7, the day before Tripp went back to the hospital the first time.  The second was done the next day, when Justin&#8217;s birth parents arrived from Taiwan to visit and the photos were taken.</p>
<p>I thank God that perhaps some baby with Down syndrome might be saved to live a full life and to increase the fullness of all the surrounding lives.  That&#8217;s the beauty of God&#8217;s work &#8211; I don&#8217;t even know how or when it happens.  I just know it will.</p>
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		<title>By: Tara</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-689</link>
		<dc:creator>Tara</dc:creator>
		<pubDate>Thu, 25 Sep 2008 23:41:51 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-689</guid>
		<description>A big Welcome to our new blogs:

Matthew Nicholas Vawter
Days with Dylan
Finnian’s Journey
Beneath the wings
ever forward, Maya
Raising Reid
Cornish Adoption Journey
A story of Down syndrome

Thank you for sharing your journeys with us…….</description>
		<content:encoded><![CDATA[<p>A big Welcome to our new blogs:</p>
<p>Matthew Nicholas Vawter<br />
Days with Dylan<br />
Finnian’s Journey<br />
Beneath the wings<br />
ever forward, Maya<br />
Raising Reid<br />
Cornish Adoption Journey<br />
A story of Down syndrome</p>
<p>Thank you for sharing your journeys with us…….</p>
]]></content:encoded>
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		<title>By: Diane Grover</title>
		<link>http://giftsds.segullah.org/down-syndrome-links/comment-page-1/#comment-258</link>
		<dc:creator>Diane Grover</dc:creator>
		<pubDate>Thu, 31 Jul 2008 03:05:37 +0000</pubDate>
		<guid isPermaLink="false">http://giftsds.segullah.org/?page_id=18#comment-258</guid>
		<description>We thought you might enjoy seeing our blog.  It might be one you would want to pass along to parents.  There are 3 parts to it.  The first attached is an introduction with a fabulous montage.  The second is made up of stories from parents all over the world.  The third is an ongoing blog, with the girls who inpspired the whole project.  The main page is called Hidden Treasures Our T21 Journey.  The next is Hidden Treasures Our T21 Journey~ Our Stories.  The final one is called Erin and MaryEllen&#039;s Excellent Adventures. All of them can be found in the link above.  We hope you enjoy them, and will consider passing them along to others.  God bless. Diane Grover</description>
		<content:encoded><![CDATA[<p>We thought you might enjoy seeing our blog.  It might be one you would want to pass along to parents.  There are 3 parts to it.  The first attached is an introduction with a fabulous montage.  The second is made up of stories from parents all over the world.  The third is an ongoing blog, with the girls who inpspired the whole project.  The main page is called Hidden Treasures Our T21 Journey.  The next is Hidden Treasures Our T21 Journey~ Our Stories.  The final one is called Erin and MaryEllen&#8217;s Excellent Adventures. All of them can be found in the link above.  We hope you enjoy them, and will consider passing them along to others.  God bless. Diane Grover</p>
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