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	<title>heroes &#8211; Vicki Tapia</title>
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		<title>The Power of Softness</title>
		<link>https://vickitapia.com/2016/01/the-power-of-softness/</link>
		
		<dc:creator><![CDATA[Vicki Tapia]]></dc:creator>
		<pubDate>Sun, 03 Jan 2016 19:27:17 +0000</pubDate>
				<category><![CDATA[Blogging]]></category>
		<category><![CDATA[aging]]></category>
		<category><![CDATA[Alz]]></category>
		<category><![CDATA[author]]></category>
		<category><![CDATA[blog]]></category>
		<category><![CDATA[caregiver]]></category>
		<category><![CDATA[caregiver burnout]]></category>
		<category><![CDATA[daughter]]></category>
		<category><![CDATA[dementia]]></category>
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		<category><![CDATA[eldercare]]></category>
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		<guid isPermaLink="false">http://vickitapia.com/?p=281</guid>

					<description><![CDATA[The holidays have always been a time of togetherness for my family and some of my oldest memories are from this season. It’s only natural for me to “remember when,” so it never comes as a surprise when I develop that unmistakable longing for my mom. If only there were a way to satisfy such a longing with conversation or a hug! Of course, it’s impossible, since Mom passed away in 2008. Recently, a conversation I had with my friend, Jean, about our mothers gave me an idea, and while it can’t help fulfill my yearning as a daughter who has lost her mom, it might make a difference someday for you. After her mother’s death several years ago, Jean found herself hesitating over an old sweater as she cleaned out her mother’s belongings. Rather than going into the donation box, somehow the sweater found its way home with her. In our conversation, Jean told me there have been a few times over the ensuing years that she’s pulled the old sweater off the hanger and actually worn it. She shared that the softness of the sweater next to her skin feels like an embrace from her mom, a sense of being enveloped by her essence and her love. I’m touched by this lovely sentiment. Sadly, many of us will face the deconstructing of our parents’ household somewhere along life’s journey. Knowing first-hand the stress involved in this difficult endeavor, it’s not uncommon to become an automated machine with “donate, trash, sell, or giveaway” the words of the day. Dismantling a home of many years can become a chore to endure and rarely do we utter the word “keep.” In sorting through my mother’s belongings after she passed away, I chose to keep several of her decorative teacups, a ceramic cat, a &#8217;60&#8217;s &#8220;lady&#8221; vase, a few knickknacks and even her spurs. While in no way diminishing the sentimental value of these items, I’ve come to realize they simply can’t offer the same intrinsic experience as an article of clothing. No way can I cuddle with a spur! Saving an item of Mom’s clothing was the furthest thing from my mind during those disquieting days. I was all about tidying up and moving stuff out. It has taken time and distance for me to recognize what I will call the “power of softness” and what it would have meant to me to have one of my mom’s old sweaters or even her bathrobe. As a daughter, if you find yourself in the position of sorting through parents’ belongings, may I suggest stopping long enough to save something soft? Fold it up and tuck it away. Grieving happens in stages. It comes and goes. You may not even think about or touch this precious garment again for quite a while. If, however, somewhere down the road, like me, you experience this longing for your loved one, that “softness” might become a cherished treasure, more special than you ever imagined. I miss you, Mom. SaveSave]]></description>
										<content:encoded><![CDATA[<p><a href="http://somebodystolemyiron.com/wp-content/uploads/2015/12/Spurs.jpg"><img loading="lazy" class="size-medium wp-image-506 alignleft" src="http://somebodystolemyiron.com/wp-content/uploads/2015/12/Spurs-300x225.jpg" alt="Spurs" width="300" height="225" /></a>The holidays have always been a time of togetherness for my family and some of my oldest memories are from this season. It’s only natural for me to “remember when,” so it never comes as a surprise when I develop that unmistakable longing for my mom. If only there were a way to satisfy such a longing with conversation or a hug! Of course, it’s impossible, since Mom passed away in 2008. Recently, a conversation I had with my friend, Jean, about our mothers gave me an idea, and while it can’t help fulfill my yearning as a daughter who has lost her mom, it might make a difference someday for you.<br />
<a href="http://somebodystolemyiron.com/wp-content/uploads/2016/01/IMG_5821.jpg"><img loading="lazy" class=" wp-image-513 alignright" src="http://somebodystolemyiron.com/wp-content/uploads/2016/01/IMG_5821-300x225.jpg" alt="IMG_5821" width="263" height="197" /></a>After her mother’s death several years ago, Jean found herself hesitating over an old sweater as she cleaned out her mother’s belongings. Rather than going into the donation box, somehow the sweater found its way home with her. In our conversation, Jean told me there have been a few times over the ensuing years that she’s pulled the old sweater off the hanger and actually worn it. She shared that the softness of the sweater next to her skin feels like an embrace from her mom, a sense of being enveloped by her essence and her love. I’m touched by this lovely sentiment.</p>
<p>Sadly, many of us will face the deconstructing of our parents’ household somewhere along life’s journey. Knowing first-hand the stress involved in this difficult endeavor, it’s not <a href="http://somebodystolemyiron.com/wp-content/uploads/2015/12/IMG_6278.jpg"><img loading="lazy" class="wp-image-504 alignright" src="http://somebodystolemyiron.com/wp-content/uploads/2015/12/IMG_6278-225x300.jpg" alt="IMG_6278" width="187" height="249" /></a>uncommon to become an automated machine with “donate, trash, sell, or giveaway” the words of the day. Dismantling a home of many years can become a chore to endure and rarely do we utter the word “keep.” In sorting through my mother’s belongings after she passed away, I chose to keep several of her decorative teacups, a ceramic cat, a &#8217;60&#8217;s &#8220;lady&#8221; vase, a few knickknacks and even her spurs. While in no way diminishing the sentimental value of these items, I’ve come to realize they <a href="http://somebodystolemyiron.com/wp-content/uploads/2015/12/IMG_6279-1.jpg"><img loading="lazy" class=" wp-image-505 alignleft" src="http://somebodystolemyiron.com/wp-content/uploads/2015/12/IMG_6279-1-300x225.jpg" alt="IMG_6279 (1)" width="263" height="197" /></a>simply can’t offer the same intrinsic experience as an article of clothing. No way can I cuddle with a spur! Saving an item of Mom’s clothing was the furthest thing from my mind during those disquieting days. I was all about tidying up and moving stuff out. It has taken time and distance for me to recognize what I will call the “power of softness” and what it would have meant to me to have one of my mom’s old sweaters or even her bathrobe.</p>
<p>As a daughter, if you find yourself in the position of sorting through parents’ belongings, may I suggest stopping long enough to save something soft? Fold it up and tuck it away. Grieving happens in stages. It comes and goes. You may not even think about or touch this precious garment again for quite a while. If, however, somewhere down the road, like me, you experience this longing for your loved one, that “softness” might become a cherished treasure, more special than you ever imagined.</p>
<p>I miss you, Mom.</p>
<p><span style="border-top-left-radius: 2px; border-top-right-radius: 2px; border-bottom-right-radius: 2px; border-bottom-left-radius: 2px; text-indent: 20px; width: auto; padding: 0px 4px 0px 0px; text-align: center; font-style: normal; font-variant-caps: normal; font-weight: bold; font-stretch: normal; font-size: 11px; line-height: 20px; font-family: 'Helvetica Neue', Helvetica, sans-serif; color: #ffffff; background-image: url(data:image/svg+xml; base64,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); background-size: 14px 14px; background-color: #bd081c; position: absolute; opacity: 1; z-index: 8675309; display: none; cursor: pointer; border: none; -webkit-font-smoothing: antialiased; background-position: 3px 50%; background-repeat: no-repeat no-repeat;">Save</span><span style="border-top-left-radius: 2px; border-top-right-radius: 2px; border-bottom-right-radius: 2px; border-bottom-left-radius: 2px; text-indent: 20px; width: auto; padding: 0px 4px 0px 0px; text-align: center; font-style: normal; font-variant-caps: normal; font-weight: bold; font-stretch: normal; font-size: 11px; line-height: 20px; font-family: 'Helvetica Neue', Helvetica, sans-serif; color: #ffffff; background-image: url(data:image/svg+xml; base64,phn2zyb4bwxucz0iahr0cdovl3d3dy53my5vcmcvmjawmc9zdmciighlawdodd0imzbwecigd2lkdgg9ijmwchgiihzpzxdcb3g9ii0xic0xidmxidmxij48zz48cgf0acbkpsjnmjkundq5lde0ljy2mibdmjkundq5ldiyljcymiaymi44njgsmjkumju2ide0ljc1ldi5lji1nibdni42mzismjkumju2idaumduxldiyljcymiawlja1mswxnc42njigqzaumduxldyunjaxidyunjmyldaumdy3ide0ljc1ldaumdy3iemymi44njgsmc4wnjcgmjkundq5ldyunjaxidi5ljq0oswxnc42njiiigzpbgw9iinmzmyiihn0cm9rzt0ii2zmziigc3ryb2tllxdpzhropsixij48l3bhdgg+phbhdgggzd0itte0ljczmywxljy4nibdny41mtysms42odygms42njusny40otugms42njusmtqunjyyiemxljy2nswymc4xntkgns4xmdksmjquodu0idkuotcsmjyunzq0iem5ljg1niwyns43mtggos43ntmsmjqumtqzidewljaxniwymy4wmjigqzewlji1mywymi4wmsaxms41ndgsmtyuntcyidexlju0ocwxni41nzigqzexlju0ocwxni41nzigmteumtu3lde1ljc5nsaxms4xntcsmtqunjq2iemxms4xntcsmtiuodqyideyljixmswxms40otugmtmuntiyldexljq5nsbdmtqunjm3ldexljq5nsaxns4xnzusmtiumzi2ide1lje3nswxmy4zmjmgqze1lje3nswxnc40mzygmtqundyylde2ljegmtqumdkzlde3ljy0mybdmtmunzg1lde4ljkznsaxnc43ndusmtkuotg4ide2ljayocwxos45odggqze4ljm1mswxos45odggmjaumtm2lde3lju1niaymc4xmzysmtqumdq2iemymc4xmzysmtauotm5ide3ljg4ocw4ljc2nyaxnc42nzgsoc43njcgqzewljk1osw4ljc2nya4ljc3nywxms41mzygoc43nzcsmtqumzk4iem4ljc3nywxns41mtmgos4ymswxni43mdkgos43ndksmtcumzu5iem5ljg1niwxny40odggos44nzismtcunia5ljg0lde3ljczmsbdos43ndesmtgumtqxidkuntismtkumdizidkundc3lde5ljiwmybdos40miwxos40nca5lji4ocwxos40otegos4wncwxos4znzygqzcunda4lde4ljyymia2ljm4nywxni4yntigni4zodcsmtqumzq5iem2ljm4nywxmc4yntygos4zodmsni40otcgmtuumdiyldyundk3iemxos41ntusni40otcgmjmumdc4ldkunza1idizlja3ocwxmy45otegqzizlja3ocwxoc40njmgmjaumjm5ldiylja2miaxni4yotcsmjiumdyyiemxnc45nzmsmjiumdyyidezljcyocwyms4znzkgmtmumzayldiwlju3mibdmtmumzayldiwlju3miaxmi42ndcsmjmumdugmtiundg4ldizljy1nybdmtiumtkzldi0ljc4ncaxms4zotysmjyumtk2idewljg2mywyny4wntggqzeylja4niwyny40mzqgmtmumzg2ldi3ljyznyaxnc43mzmsmjcunjm3iemyms45nswyny42mzcgmjcuodaxldixljgyocayny44mdesmtqunjyyiemyny44mdesny40otugmjeuotusms42odygmtqunzmzldeunjg2iibmawxspsijymqwodfjij48l3bhdgg+pc9npjwvc3znpg==); background-size: 14px 14px; background-color: #bd081c; position: absolute; opacity: 1; z-index: 8675309; display: none; cursor: pointer; border: none; -webkit-font-smoothing: antialiased; background-position: 3px 50%; background-repeat: no-repeat no-repeat;">Save</span></p>
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		<item>
		<title>An Unsung Hero…The Family Caregiver</title>
		<link>https://vickitapia.com/2015/11/an-unsung-herothe-family-caregiver/</link>
		
		<dc:creator><![CDATA[Vicki Tapia]]></dc:creator>
		<pubDate>Mon, 09 Nov 2015 19:22:16 +0000</pubDate>
				<category><![CDATA[Blogging]]></category>
		<category><![CDATA[aging]]></category>
		<category><![CDATA[Alz]]></category>
		<category><![CDATA[author]]></category>
		<category><![CDATA[blog]]></category>
		<category><![CDATA[caregiver]]></category>
		<category><![CDATA[caregiver burnout]]></category>
		<category><![CDATA[daughter]]></category>
		<category><![CDATA[dementia]]></category>
		<category><![CDATA[eBook]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[heroes]]></category>
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		<guid isPermaLink="false">http://vickitapia.com/?p=274</guid>

					<description><![CDATA[In 2004, my father was diagnosed with Parkinson’s-related dementia and a few months later, my mother with Alzheimer’s disease. That was the year I became a caregiver. While my parents didn’t reside with me, I was still intimately involved in their daily care for the next 4 and 5 years. Traveling down that rabbit hole of dementia with my parents was difficult and sad. I watched helplessly as this disease steadily and ruthlessly chipped away at their brains, one memory at a time. That said, it was also a time of considerable personal growth for me. I learned to parent my parents with patience and compassion, caring for them much as they’d cared for me as a child so many years before. Interspersed with the challenges were times of fleeting lucidity, as well as moments of poignant tenderness, which I still remember and cherish, even today. These are moments I would have missed forever, had I not been a family caregiver. According to Alzheimer’s Association’s 2015 Facts and Figures, 85 % of unpaid caregiving help provided to older adults in the U.S. is provided by family members; 2/3 of them women. And, over half of us caring for people with dementia are taking care of parents. How many of us actually plan on being an unpaid caregiver? Whether it’s a spouse, parents or a well-loved aunt, it’s unlikely most of us ever anticipate the reality of wearing the label “caregiver.” As the boomer population continues to age, the number of unsung heroes caring for a family member is on the upswing. According to the report *Caregiving in the U.S. 2015, there are currently an estimated 34.2 million American adults taking care of a loved one 50 years or older. Caregiving can be overwhelming, both emotionally and physically, bringing with it a myriad of emotions, all of which I experienced at one time or another, including: Frustration Helplessness Anger Sadness Depression Guilt Caregiving can be lonely! At times, I remember feeling like I was on a deserted island, with nary a person who really understood what it was like. While speaking at a caregiver’s meeting recently, two women approached me afterwards to share their stories. One woman told me her spouse with Alzheimer’s is slowly becoming more than she can handle, but her children are insisting that she keep him at home. The other woman suspects that her elderly father, who lives next door to her, is showing signs of dementia, but he flatly refuses to go to the doctor. They were both searching for answers. Like growing old, caregiving is not for sissies. I sensed in these 2 women what experts label caregiver burnout, a very real phenomenon and a number one reason why it’s imperative for all caregivers to recognize the importance of self-care. If you or someone you know is experiencing these symptoms, I encourage you, please make time for a doctor’s visit. Anxiety Irritability Social withdrawal Sleeplessness Exhaustion Poor concentration More susceptible to illness *Caregiving in the U.S. 2015 – A Focused Look at Caregivers of Adults Age 50+ was published by The National Alliance for Caregiving (NAC) and the AARP Public Policy Institute Amazon Praeclarus Press SaveSave]]></description>
										<content:encoded><![CDATA[<p style="text-align: center;"><a href="http://somebodystolemyiron.com/wp-content/uploads/2015/10/img_1169536238_15292_1321949118.jpg"><img loading="lazy" class="alignnone size-medium wp-image-451" src="http://somebodystolemyiron.com/wp-content/uploads/2015/10/img_1169536238_15292_1321949118-300x89.jpg" alt="img_1169536238_15292_1321949118" width="300" height="89" /></a></p>
<p>In 2004, my father was diagnosed with Parkinson’s-related dementia and a few months later, my mother with Alzheimer’s disease. That was the year I became a caregiver. While my parents didn’t reside with me, I was still intimately involved in their daily care for the next 4 and 5 years. Traveling down that rabbit hole of dementia with my parents was difficult and sad. I watched helplessly as this disease steadily and ruthlessly chipped away at their brains, one memory at a time. That said, it was also a time of considerable personal growth for me. I learned to parent my parents with patience and compassion, caring for them much as they’d cared for me as a child so many years before. Interspersed with the challenges were times of fleeting lucidity, as well as moments of poignant tenderness, which I still remember and cherish, even today. These are moments I would have missed forever, had I not been a family caregiver.</p>
<p>According to <a href="https://www.alz.org/facts/downloads/facts_figures_2015.pdf"><em>Alzheimer’s Association’s 2015 Facts and Figures</em></a>, 85 % of unpaid caregiving<br />
help provided to older adults in the U.S. is provided by family members; 2/3 of them women. And, over half of us caring for people with dementia are taking care of parents.</p>
<p>How many of us actually plan on being an unpaid caregiver? Whether it’s a spouse, parents or a well-loved aunt, it’s unlikely most of us ever anticipate the reality of wearing the label “caregiver.” As the boomer population continues to age, the number of unsung heroes caring for a family member is on the upswing. According to the report *<a href="http://www.aarp.org/content/dam/aarp/ppi/2015/caregivers-of-older-adults-focused-look.pdf"><em>Caregiving in the U.S. 2015</em></a>, there are currently an estimated 34.2 million American adults taking care of a loved one 50 years or older.</p>
<p>Caregiving can be <em>overwhelming</em>, both emotionally and physically, bringing with it a myriad of emotions, all of which I experienced at one time or another, including:</p>
<ul>
<li>Frustration</li>
<li>Helplessness</li>
<li>Anger</li>
<li>Sadness</li>
<li>Depression</li>
<li>Guilt</li>
</ul>
<p>Caregiving can be <em>lonely</em>! At times, I remember feeling like I was on a deserted island, with nary a person who really understood what it was like.</p>
<p>While speaking at a caregiver’s meeting recently, two women approached me afterwards to share their stories. One woman told me her spouse with Alzheimer’s is slowly becoming more than she can handle, but her children are insisting that she keep him at home. The other woman suspects that her elderly father, who lives next door to her, is showing signs of dementia, but he flatly refuses to go to the doctor. They were both searching for answers. Like growing old, caregiving is not for sissies.</p>
<p>I sensed in these 2 women what experts label <em>caregiver burnout,</em> a very real phenomenon and a number one reason why it’s imperative for all caregivers to recognize the importance of <em>self-care</em>.</p>
<p>If you or someone you know is experiencing these symptoms, I encourage you, <em>please </em>make time for a doctor’s visit.</p>
<ul>
<li>Anxiety</li>
<li>Irritability</li>
<li>Social withdrawal</li>
<li>Sleeplessness</li>
<li>Exhaustion</li>
<li>Poor concentration</li>
<li>More susceptible to illness</li>
</ul>
<p><em>*Caregiving in the U.S. 2015</em> –<em> A</em> <em>Focused Look at Caregivers of Adults Age 50+ </em>was published by The National Alliance for Caregiving (NAC) and the AARP Public Policy Institute</p>
<p><a href="http://www.amazon.com/gp/product/1939807077/ref=as_li_tf_tl?ie=UTF8&amp;camp=211189&amp;creative=373489&amp;creativeASIN=1939807077&amp;link_code=as3&amp;tag=ssmibook-20">Amazon</a></p>
<p><a href="http://praeclaruspress.com/books/somebody-stole-my-iron/">Praeclarus Press</a></p>
<p style="text-align: center;"><a href="http://somebodystolemyiron.com/wp-content/uploads/2015/11/3.jpg"><img loading="lazy" class="size-medium wp-image-476 aligncenter" src="http://somebodystolemyiron.com/wp-content/uploads/2015/11/3-300x150.jpg" alt="3" width="300" height="150" /></a></p>
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