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	<title>Comments for Caregiving Solutions</title>
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	<link>http://caregivingsolutions.wordpress.com</link>
	<description>Offering solutions and support for caregiving challenges</description>
	<lastBuildDate>Fri, 25 Sep 2009 18:16:49 +0000</lastBuildDate>
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		<title>Comment on Alan Stanford&#8217;s 10 Tips For Caregivers by Kim</title>
		<link>http://caregivingsolutions.wordpress.com/2008/07/10/stanfords-10-tips-for-caregivers/#comment-86</link>
		<dc:creator>Kim</dc:creator>
		<pubDate>Fri, 25 Sep 2009 18:16:49 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=45#comment-86</guid>
		<description>Such good points.  Like your web site very much.  Thank you for sharing your wisdom and practical suggestions.</description>
		<content:encoded><![CDATA[<p>Such good points.  Like your web site very much.  Thank you for sharing your wisdom and practical suggestions.</p>
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		<title>Comment on Decreased Eating In The Elderly by Pamela Larsen Schroeder</title>
		<link>http://caregivingsolutions.wordpress.com/2008/06/06/decreased-eating-in-the-elderly/#comment-84</link>
		<dc:creator>Pamela Larsen Schroeder</dc:creator>
		<pubDate>Thu, 04 Jun 2009 01:08:51 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=30#comment-84</guid>
		<description>Hi Stefanie,

It is most challenging trying to get a person with dementia to eat! Patience is important, as you state. I have &lt;em&gt;learned&lt;/em&gt; to not take refusal to eat personally. Mary, who I referred to in my post, still skips supper about 2-3 nights a week. It does help to have a routine; sit down and eat with her. She has always loved salads, so putting out the ingredients on the kitchen counter and engaging her in assembling her salad (like at a salad bar), sometimes works. We try to talk about other things and listen to music she likes, as well. She tends to snack on candy throughout the day, even though we attempt to minimize her stashes. She stays in bed until at least noon, so that is another factor limiting her intake. Her husband puts out orange juice and a half banana in the morning, so when she gets up to the bathroom, she sees them. Sometimes it is successful. When I am there visiting, I also mist Young Living&#039;s &lt;em&gt;Citrus Fresh &lt;/em&gt;in the air about 30 minutes before mealtime. This therapeutic-grade essential oil blend can help perk up an appetite (and mood), plus the room just smells clean and fresh. If you want to learn more about using essential oils and caregiving, please feel free to contact me. Do any other readers have additional suggestions?

Peace &amp; Blessings,

Pam</description>
		<content:encoded><![CDATA[<p>Hi Stefanie,</p>
<p>It is most challenging trying to get a person with dementia to eat! Patience is important, as you state. I have <em>learned</em> to not take refusal to eat personally. Mary, who I referred to in my post, still skips supper about 2-3 nights a week. It does help to have a routine; sit down and eat with her. She has always loved salads, so putting out the ingredients on the kitchen counter and engaging her in assembling her salad (like at a salad bar), sometimes works. We try to talk about other things and listen to music she likes, as well. She tends to snack on candy throughout the day, even though we attempt to minimize her stashes. She stays in bed until at least noon, so that is another factor limiting her intake. Her husband puts out orange juice and a half banana in the morning, so when she gets up to the bathroom, she sees them. Sometimes it is successful. When I am there visiting, I also mist Young Living&#8217;s <em>Citrus Fresh </em>in the air about 30 minutes before mealtime. This therapeutic-grade essential oil blend can help perk up an appetite (and mood), plus the room just smells clean and fresh. If you want to learn more about using essential oils and caregiving, please feel free to contact me. Do any other readers have additional suggestions?</p>
<p>Peace &amp; Blessings,</p>
<p>Pam</p>
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		<title>Comment on Decreased Eating In The Elderly by Stefanie</title>
		<link>http://caregivingsolutions.wordpress.com/2008/06/06/decreased-eating-in-the-elderly/#comment-83</link>
		<dc:creator>Stefanie</dc:creator>
		<pubDate>Wed, 03 Jun 2009 22:24:38 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=30#comment-83</guid>
		<description>Thanks for this. I am currently taking care of an elderly patient with dementia. Sometimes I get frustrated when she doesn&#039;t eat but I have learned to be patient.


Thanks again, 
-Stefanie 

Chicago,IL</description>
		<content:encoded><![CDATA[<p>Thanks for this. I am currently taking care of an elderly patient with dementia. Sometimes I get frustrated when she doesn&#8217;t eat but I have learned to be patient.</p>
<p>Thanks again,<br />
-Stefanie </p>
<p>Chicago,IL</p>
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		<title>Comment on Sharing Solutions To Caregiving Challenges by Tigerlily</title>
		<link>http://caregivingsolutions.wordpress.com/2008/04/03/sharing-solutions-to-caregiving-challenges/#comment-82</link>
		<dc:creator>Tigerlily</dc:creator>
		<pubDate>Wed, 27 May 2009 20:20:10 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=3#comment-82</guid>
		<description>I have been a caregiver to my disabled Mom for 9 years and I have also started a website for caregivers filled with tips and tricks that have helped me.  Please visit my website: caregiverscove.org</description>
		<content:encoded><![CDATA[<p>I have been a caregiver to my disabled Mom for 9 years and I have also started a website for caregivers filled with tips and tricks that have helped me.  Please visit my website: caregiverscove.org</p>
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		<title>Comment on Sharing Solutions To Caregiving Challenges by Chrissy</title>
		<link>http://caregivingsolutions.wordpress.com/2008/04/03/sharing-solutions-to-caregiving-challenges/#comment-79</link>
		<dc:creator>Chrissy</dc:creator>
		<pubDate>Tue, 20 Jan 2009 02:12:09 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=3#comment-79</guid>
		<description>Terrell Dougan, author of That Went Well book written about caring for her &lt;a href=&quot;http://www.thatwentwellthebook.com/&quot; rel=&quot;nofollow&quot;&gt;special needs&lt;/a&gt;  sister brought me to tears and also made me burst out laughing. 
Warmed my heart in this cold season, and boy do we all need that. It shows you time and again that the human race is quite wonderful, when the chips are down.</description>
		<content:encoded><![CDATA[<p>Terrell Dougan, author of That Went Well book written about caring for her <a href="http://www.thatwentwellthebook.com/" rel="nofollow">special needs</a>  sister brought me to tears and also made me burst out laughing.<br />
Warmed my heart in this cold season, and boy do we all need that. It shows you time and again that the human race is quite wonderful, when the chips are down.</p>
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		<title>Comment on Alan Stanford&#8217;s 10 Tips For Caregivers by Bookmarks about Caregiving</title>
		<link>http://caregivingsolutions.wordpress.com/2008/07/10/stanfords-10-tips-for-caregivers/#comment-76</link>
		<dc:creator>Bookmarks about Caregiving</dc:creator>
		<pubDate>Wed, 29 Oct 2008 06:00:07 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=45#comment-76</guid>
		<description>[...] - bookmarked by 6 members originally found by antifuchs on 2008-10-10  Stanford’s 10 Tips For Caregivers  http://caregivingsolutions.wordpress.com/2008/07/10/stanfords-10-tips-for-caregivers/ - bookmarked [...]</description>
		<content:encoded><![CDATA[<p>[...] &#8211; bookmarked by 6 members originally found by antifuchs on 2008-10-10  Stanford’s 10 Tips For Caregivers  <a href="http://caregivingsolutions.wordpress.com/2008/07/10/stanfords-10-tips-for-caregivers/" rel="nofollow">http://caregivingsolutions.wordpress.com/2008/07/10/stanfords-10-tips-for-caregivers/</a> &#8211; bookmarked [...]</p>
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		<title>Comment on Assessing Caregiver Well-Being by bokjae</title>
		<link>http://caregivingsolutions.wordpress.com/2008/04/30/assessing-caregiver-well-being/#comment-75</link>
		<dc:creator>bokjae</dc:creator>
		<pubDate>Thu, 11 Sep 2008 00:17:49 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=19#comment-75</guid>
		<description>Thank-you for the useful information. I am a full-time caregiver to my wife a stroke survivor. I need to be informed and educated on caregiving and related issues. Thanks for blogs/sites like this!</description>
		<content:encoded><![CDATA[<p>Thank-you for the useful information. I am a full-time caregiver to my wife a stroke survivor. I need to be informed and educated on caregiving and related issues. Thanks for blogs/sites like this!</p>
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		<title>Comment on Caregivers Commonly Experience Anticipatory Grief by Pamela Larsen Schroeder</title>
		<link>http://caregivingsolutions.wordpress.com/2008/04/13/caregivers-commonly-experience-anticipatory-grief/#comment-73</link>
		<dc:creator>Pamela Larsen Schroeder</dc:creator>
		<pubDate>Sun, 24 Aug 2008 19:55:19 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=16#comment-73</guid>
		<description>Hi Sara,

Experiencing a massive stroke (from both the patient&#039;s and caregiver&#039;s points of view) would certainly create a sense of vulnerability. I can well imagine that missed calls on the cell phone would be a trigger for you.

I&#039;m wondering if your mother has a personal emergency response system that she is physically able to use. They certainly add to one&#039;s peace of mind.

It is common for individuals who have suffered a stroke to experience clinical depression at some point in their recovery. I have no idea whether or not this applies to your mother&#039;s situation. When present, it can affect their day to day outlook, as well as hopes and plans for the future. Most health professionals are pretty savvy about screening for, and treating depression that often coexists with any kind of life-threatening or chronic condition. 

Many people who have had a massive stroke (or heart attack, etc.) wonder if and when it&#039;s going to happen again...and whether the next one will be fatal. Sometimes it&#039;s verbalized, often it&#039;s not. It&#039;s not always comfortable to start conversations about such topics, but it can be very meaningful to discuss, when the timing seems right. I think that patients experience anticipatory grieving, as well as caregivers.

I wish I had done more with my mother when she was more mobile. But it was great to see her delight with different things on our recent trip. 

I hope you both enjoy planning and making your trip to Ireland!  

Peace &amp; Blessings,

Pam</description>
		<content:encoded><![CDATA[<p>Hi Sara,</p>
<p>Experiencing a massive stroke (from both the patient&#8217;s and caregiver&#8217;s points of view) would certainly create a sense of vulnerability. I can well imagine that missed calls on the cell phone would be a trigger for you.</p>
<p>I&#8217;m wondering if your mother has a personal emergency response system that she is physically able to use. They certainly add to one&#8217;s peace of mind.</p>
<p>It is common for individuals who have suffered a stroke to experience clinical depression at some point in their recovery. I have no idea whether or not this applies to your mother&#8217;s situation. When present, it can affect their day to day outlook, as well as hopes and plans for the future. Most health professionals are pretty savvy about screening for, and treating depression that often coexists with any kind of life-threatening or chronic condition. </p>
<p>Many people who have had a massive stroke (or heart attack, etc.) wonder if and when it&#8217;s going to happen again&#8230;and whether the next one will be fatal. Sometimes it&#8217;s verbalized, often it&#8217;s not. It&#8217;s not always comfortable to start conversations about such topics, but it can be very meaningful to discuss, when the timing seems right. I think that patients experience anticipatory grieving, as well as caregivers.</p>
<p>I wish I had done more with my mother when she was more mobile. But it was great to see her delight with different things on our recent trip. </p>
<p>I hope you both enjoy planning and making your trip to Ireland!  </p>
<p>Peace &amp; Blessings,</p>
<p>Pam</p>
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		<title>Comment on Traveling With The Elderly &amp; Disabled by Pamela Larsen Schroeder</title>
		<link>http://caregivingsolutions.wordpress.com/2008/06/30/traveling-with-the-elderly-disabled/#comment-72</link>
		<dc:creator>Pamela Larsen Schroeder</dc:creator>
		<pubDate>Sun, 24 Aug 2008 19:06:20 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=35#comment-72</guid>
		<description>Hi Sara,

I don&#039;t have experience traveling in Europe. Perhaps some of our readers can offer specific resources.

Here&#039;s a few suggestions based on my recent travel with my mother. 

We used a transport chair, rather than a wheelchair. It&#039;s lighter and more portable. The wheels are smaller (so she couldn&#039;t use them to propel herself). It doesn&#039;t go over crushed rock though, it needs a solid surface such as cement or asphalt. We rented it, but purchased one when we returned from our trip. It&#039;s nice to have a side or back pocket to store small items and hold a water bottle. The one we purchased didn&#039;t have one, so we bought a separate one to attach.

There are so many people traveling with wheelchairs these days. It was great to see! I think you&#039;d get a lot of assistance from working with a travel agent who knows your mother&#039;s requirements. 

The trip did fatigue my mother. We just scheduled a rest break a couple times each day; mom actually needed to lie down for 30 minutes or so. She chose which activities were most important for her to experience, in person. DVDs and picture travel books were a strategy to fill in the gap. I think that a DVD on touring Ireland would be a great resource now, to both motivate your mother and help plan where you all want to go on your trip.

You may want to determine if there&#039;s a preferred time to travel during the summer (assuming you have some flexibility). I&#039;m thinking of potential impact on weather, crowds, special events, promotions, etc.

There may be a guided tour on a bus, train, or other motorized vehicle that is both a convenient and efficient way to visit some sights.

Hope you enjoy planning your trip together! My mom wasn&#039;t very &quot;gung-ho&quot; at the beginning (lots of reservations), but she really &quot;got into it&quot; as time went by. It was a special and memorable trip for all of us. We took lots of pictures, so she could show friends and relatives and re-live some memories whenever she wishes.

Peace &amp; Blessings,

Pam</description>
		<content:encoded><![CDATA[<p>Hi Sara,</p>
<p>I don&#8217;t have experience traveling in Europe. Perhaps some of our readers can offer specific resources.</p>
<p>Here&#8217;s a few suggestions based on my recent travel with my mother. </p>
<p>We used a transport chair, rather than a wheelchair. It&#8217;s lighter and more portable. The wheels are smaller (so she couldn&#8217;t use them to propel herself). It doesn&#8217;t go over crushed rock though, it needs a solid surface such as cement or asphalt. We rented it, but purchased one when we returned from our trip. It&#8217;s nice to have a side or back pocket to store small items and hold a water bottle. The one we purchased didn&#8217;t have one, so we bought a separate one to attach.</p>
<p>There are so many people traveling with wheelchairs these days. It was great to see! I think you&#8217;d get a lot of assistance from working with a travel agent who knows your mother&#8217;s requirements. </p>
<p>The trip did fatigue my mother. We just scheduled a rest break a couple times each day; mom actually needed to lie down for 30 minutes or so. She chose which activities were most important for her to experience, in person. DVDs and picture travel books were a strategy to fill in the gap. I think that a DVD on touring Ireland would be a great resource now, to both motivate your mother and help plan where you all want to go on your trip.</p>
<p>You may want to determine if there&#8217;s a preferred time to travel during the summer (assuming you have some flexibility). I&#8217;m thinking of potential impact on weather, crowds, special events, promotions, etc.</p>
<p>There may be a guided tour on a bus, train, or other motorized vehicle that is both a convenient and efficient way to visit some sights.</p>
<p>Hope you enjoy planning your trip together! My mom wasn&#8217;t very &#8220;gung-ho&#8221; at the beginning (lots of reservations), but she really &#8220;got into it&#8221; as time went by. It was a special and memorable trip for all of us. We took lots of pictures, so she could show friends and relatives and re-live some memories whenever she wishes.</p>
<p>Peace &amp; Blessings,</p>
<p>Pam</p>
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		<title>Comment on Traveling With The Elderly &amp; Disabled by Sara</title>
		<link>http://caregivingsolutions.wordpress.com/2008/06/30/traveling-with-the-elderly-disabled/#comment-71</link>
		<dc:creator>Sara</dc:creator>
		<pubDate>Sat, 23 Aug 2008 02:12:18 +0000</pubDate>
		<guid isPermaLink="false">http://caregivingsolutions.wordpress.com/?p=35#comment-71</guid>
		<description>Wow--this is so helpful, thank you.  Do you have any suggestions or resources for getting in out of places with a wheelchair?  I am wanting to take my mom, post-stroke, to Ireland next summer and getting in and out of castles, restaurants, etc. is my biggest concern.  She can walk with a quad cane shorter distances with limited stairs and in the US it&#039;s really not that hard--but Europe is a whole other story.  I would hate to get there and only just &quot;drive around.&quot;  I want to show her that she CAN enjoy things like that again :)
thank you
~caregiversara</description>
		<content:encoded><![CDATA[<p>Wow&#8211;this is so helpful, thank you.  Do you have any suggestions or resources for getting in out of places with a wheelchair?  I am wanting to take my mom, post-stroke, to Ireland next summer and getting in and out of castles, restaurants, etc. is my biggest concern.  She can walk with a quad cane shorter distances with limited stairs and in the US it&#8217;s really not that hard&#8211;but Europe is a whole other story.  I would hate to get there and only just &#8220;drive around.&#8221;  I want to show her that she CAN enjoy things like that again <img src='http://s.wordpress.com/wp-includes/images/smilies/icon_smile.gif' alt=':)' class='wp-smiley' /><br />
thank you<br />
~caregiversara</p>
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