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	<title>Holly Eburne &#187; life balance</title>
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	<description>Enriching Lives, One Step at a Time</description>
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		<title>Slowing Down and Really Smelling the Roses</title>
		<link>http://hollyeburne.com/life-coaching/slowing-down-and-really-smelling-the-roses/</link>
		<comments>http://hollyeburne.com/life-coaching/slowing-down-and-really-smelling-the-roses/#comments</comments>
		<pubDate>Mon, 22 Aug 2011 18:43:23 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Life Coaching]]></category>
		<category><![CDATA[Choose from the most used tags]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[relieve overwhelm as a carer]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=1194</guid>
		<description><![CDATA[This morning I sat at my computer and was browsing through my journal when I came across a note (and reminder) I had written on July 21, 2011&#8230; I went for a run along our country road and it was full of surprises. There is an abundance of wildlife in our area but it seemed [...]]]></description>
			<content:encoded><![CDATA[<p>This morning I sat at my computer and was browsing through my journal when I came across a note (and reminder) I had written on July 21, 2011&#8230;</p>
<p>I went for a run along our country road and it was full of surprises. There is an abundance of wildlife in our area but it seemed more acute today. The list of birds is like opening the Audobon bird book. I saw a pair of western tanagers chasing each other, a group of cedar waxwings eating dogwood berries, juncos on the side of the road, yellow warblers in the bushes, and townsend solitaire with her young. There were brewer’s and red-wing blackbirds, male northern oriole feeding 2 of his youngsters (I’ve never seen a male bird feed their young), winter wrens singing their long song. Did you know that winter wrens are the smallest birds with the longest song. Eagles flying overhead teaching their young one how to fly and more bird sounds in the forest that I couldn&#8217;t identify.</p>
<p>I passed by a field of llamas munching on grass as their lower jaw slide sideways and then circle around. Snakes hiding in the tall grasses bordering the creek that flows gently along the side of the road. Even the horses were having a lazy day as they basked in the fields with the sun peeking in and out on this crisp summer day. A crisp 13 degrees Celsius&#8211;far below our typical 30 degrees.</p>
<p>It was a glorious run&#8211;no human-made sounds.</p>
<p>If I had decided to ride my bike instead of run I would have missed all of these sights and sounds. The pace would have been too fast and the wind rushing by my helmet would have blocked out many of these natural sounds.</p>
<p>Bike riding <em>versus</em> running/walking is a metaphor for my life: frenetic <em>versus</em> calm and peaceful.</p>
<p>Three years when I woke up to the reality of my husband&#8217;s dementia and stopped fighting it, I began to slow down enough to see the abundance that was all around me&#8211;life lessons in patience and surrendering to what is, healthy children, a beautiful home. Before then I was too busy to notice anything because I was &#8216;riding&#8217; away from the pain of the losses and changes in my life.</p>
<p>Over the past few years it has been a conscious effort to slow down and really smell the roses. It is healthy and necessary for me to face my dark side (sadness and anger) as much as my light side. It&#8217;s all part of who I am and it&#8217;s part of loving all of me.</p>
<p>This past month has been crazy busy and I reached my upper emotional and mental limit 3 times. When I lose my balance I have physical reminders&#8211;a chest cold, eye infection or fatigue. Dr. Bruce Lipton, a biochemist, has proven that over 85% of our physical illnesses have an emotional root cause.  I guess it won&#8217;t surprise you that I am recovering from a cold and a cough.</p>
<p>So reading my note from July 21st is a wonderful reminder of how life feels when I take the time to slow down, bend over and really smell the roses. Time to get back to my morning meditations, saying no to projects that completely fill my schedule, and time to bring out the knitting needles and cross stitching to spend more time with my feet up enjoying the company of my husband.</p>
<p><a href="http://hollyeburne.com/wp-content/uploads/2011/08/Unknown.jpeg"><img class="alignnone size-thumbnail wp-image-1198" title="Unknown" src="http://hollyeburne.com/wp-content/uploads/2011/08/Unknown-150x150.jpg" alt="" width="150" height="150" /></a></p>
<p>&nbsp;</p>
<p><strong>Note</strong>: If you have an experience of reaching your upper limits and what you did to regain your balance I would love to hear from you.</p>
<p>&nbsp;</p>
<p>&nbsp;</p>
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		<title>Food for Thought&#8211;SELF-LOVE</title>
		<link>http://hollyeburne.com/life-coaching/food-for-thought-self-love/</link>
		<comments>http://hollyeburne.com/life-coaching/food-for-thought-self-love/#comments</comments>
		<pubDate>Wed, 06 Jul 2011 17:29:35 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[caregiving]]></category>
		<category><![CDATA[Life Coaching]]></category>
		<category><![CDATA[changing perspective]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[life lesson]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=1180</guid>
		<description><![CDATA[There is a saying…’you teach what you need to learn’. This is what I’m doing by writing and sharing what I’m learning about self-love. These past few years have been a time of massive personal growth and uncovering the &#8216;real&#8217; Holly. It isn’t an easy process but definitely worth the sweat and tears that come [...]]]></description>
			<content:encoded><![CDATA[<p>There is a saying…’you teach what you need to learn’. This is what I’m doing by writing and sharing what I’m learning about self-love.</p>
<p>These past few years have been a time of massive personal growth and uncovering the &#8216;real&#8217; Holly. It isn’t an easy process but definitely worth the sweat and tears that come along with it. Living with a husband with dementia has taught me about unconditional love, patience, surrendering to what is, and living in the present moment. In addition, when our investments collapsed I had to search for a deep knowing or trust that I would feel happy again&#8211;despite my external circumstances.</p>
<p>This morning I was listening to a meditation about self-love in one of my energy/intuitive coaching courses. It seems that no matter how many times I practice or become aware of the need to love myself, I always learn a little bit more about how to do it. I&#8217;m finally understanding that if I&#8217;m to truly love someone without conditions, then I have live it myself. When I judge another person I am really finding something inside of me that I don’t like. For 57 years I have been looking for love <em>outside </em>of me when all this time, it has been <em><strong>inside</strong></em>.</p>
<p>Loving myself is far more difficult than I imagined. I didn’t realize how often I look in the mirror and pinch the extra soft tissue around my belly or upper hips. Or notice the abundance of wrinkles multiplying daily. How about the endless times that I beat myself up for the mistakes I made in investing our hard-earned money. How many more times do I have suffer? When will I truly surrender or accept what is and learn from it? When will I understand that I always do my best and that mistakes are fertile ground for learning. And in regards to my body image…how about learning to let go of my judgments and loving every bit of ME. Me&#8211;because I’m unique—just like YOU.</p>
<p>To help you on your path to loving yourself unconditionally, here is a shortened version of what I learned this morning. <em>It helps if you are in a quiet area with your eyes closed or slightly opened and relaxed.</em></p>
<p>First of all think about someone you LOVE with all of your heart and soul. Take a second and find out where you feel this emotion in your body. <em>For example, when I remember the moment our son or daughter was born, I feel a huge ball of love in my chest area. It feels so good to think about my family, pets, patients in my physiotherapy practice,  friends, and our home in the country.</em></p>
<p>Now I want you to focus on your heart or wherever you feel your love and turn up the volume on it. Turn it up as high as you want and feel it spread throughout your body. Then put your hand on your chest and say out loud…”I LOVE me” 3 times. Notice how you feel and whether it gets easier on the 3rd time. Turn up the volume knob again (without effort) and really feel the love you have for yourself. Then take a couple of ‘easy’ breaths and slowly open your eyes. Look around and notice how you feel and whether the room looks any brighter or sharper.</p>
<p>Like any new lesson, it takes ‘conscious’ practice before it becomes easier. To help you out over the next 21 days (that is how long it takes for a habit to form), I want you to look in the mirror every morning, and while looking into your eyes say…<strong>”I Love you, thank you for being so wonderful and for being you”.</strong></p>
<p>Don&#8217;t forget&#8230;to give love you need to love yourself first.</p>
<p><a href="http://hollyeburne.com/wp-content/uploads/2011/07/Unknown.jpeg"><img class="alignnone size-thumbnail wp-image-1182" title="Unknown" src="http://hollyeburne.com/wp-content/uploads/2011/07/Unknown-150x105.jpg" alt="" width="150" height="105" /></a></p>
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		<title>Ticket to Freedom In The World of Dementia</title>
		<link>http://hollyeburne.com/alzheimers-and-related-dementia/ticket-to-freedom-in-the-world-of-dementia/</link>
		<comments>http://hollyeburne.com/alzheimers-and-related-dementia/ticket-to-freedom-in-the-world-of-dementia/#comments</comments>
		<pubDate>Wed, 29 Dec 2010 21:09:38 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Alzheimer's and related Dementia]]></category>
		<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[frontotemporal dementia]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[relieve overwhelm as a carer]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=1028</guid>
		<description><![CDATA[When my husband, Dave, was initially diagnosed with Frontotemporal dementia 4 years ago, I wondered if I would ever feel free again. Last December Dave must have wondered the same thing when he handed in his driver’s license. His truck, and the privilege of driving, was his ticket to freedom. Or so I thought. This [...]]]></description>
			<content:encoded><![CDATA[<p>When my husband, Dave, was initially diagnosed with Frontotemporal dementia 4 years ago, I wondered if I would ever feel free again. Last December Dave must have wondered the same thing when he handed in his driver’s license. His truck, and the privilege of driving, was his <em><strong>ticket to freedom</strong></em>. Or so I thought.</p>
<p><span id="more-1028"></span>This morning while riding my bike along our beautiful country road I had an AHA moment. As I was gliding over one of the cattle guards, I had an overwhelming sense of freedom. I thought of how Dave must feel when he hops on his bike and rides into town to pick up 1 or 2 items. His bike is his <em>new </em><em>ticket to freedom</em>. I wonder if this is one of the reasons why Dave isn’t complaining as much about not driving. Time has healed some of the pain, but I also believe that he has found his own little piece of freedom to fill the void.</p>
<div id="attachment_1030" class="wp-caption alignnone" style="width: 160px"><a href="http://hollyeburne.com/wp-content/uploads/2010/12/DSC_0689.jpg"><img class="size-thumbnail wp-image-1030" title="ticket to freedom" src="http://hollyeburne.com/wp-content/uploads/2010/12/DSC_0689-150x150.jpg" alt="" width="150" height="150" /></a><p class="wp-caption-text">ticket to freedom</p></div>
<div>
<dl id="attachment_1030">
<dd>I didn’t realize how much freer it feels to have brisk (-5 degree) air blowing on my face&#8211;than driving my car. The only sounds I heard were birds chirping in the berry bushes and horses neighing as I rode by. There are a couple of horses I like to visit along the way. It is so much fun watching as they gallop and kick up their heels when they see me riding along our road. (I’d like to think it is for my hugs and kisses on their soft noses but I know it’s for the carrots in my pack)</dd>
<dd>
<div id="attachment_1029" class="wp-caption alignnone" style="width: 160px"><a href="http://hollyeburne.com/wp-content/uploads/2010/12/love-my-horse-kisses.jpg"><img class="size-thumbnail wp-image-1029" title="love my horse kisses" src="http://hollyeburne.com/wp-content/uploads/2010/12/love-my-horse-kisses-150x150.jpg" alt="" width="150" height="150" /></a><p class="wp-caption-text">love kissing that soft spot on their nose</p></div>
</dd>
</dl>
</div>
<p>There are times when living with the challenges and unpredictability of dementia feels suffocating. But it doesn&#8217;t take long to get a dose of  ‘oxygen’ and start breathing easier. It’s as simple as stepping outdoors.</p>
<p>How about you? What&#8217;s your <em><strong>ticket to freedom</strong></em>?</p>
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		<title>Laughter is the Best Medicine</title>
		<link>http://hollyeburne.com/alzheimers-and-related-dementia/laughter-is-the-best-medicine/</link>
		<comments>http://hollyeburne.com/alzheimers-and-related-dementia/laughter-is-the-best-medicine/#comments</comments>
		<pubDate>Mon, 15 Nov 2010 13:31:08 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Alzheimer's and related Dementia]]></category>
		<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[having fun]]></category>
		<category><![CDATA[life balance]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=965</guid>
		<description><![CDATA[There is nothing better than laughing until you cry. The studies have proven that it releases endorphins that are 50 times more potent than morphine. We produce our own anti-depressant with NO side effects. How great is that? When was the last time you laughed until you cried? Can you remember how good you felt [...]]]></description>
			<content:encoded><![CDATA[<p>There is nothing better than laughing until you cry. The studies have proven that it releases endorphins that are 50 times more potent than morphine. We produce our own anti-depressant with NO side effects. How great is that?</p>
<p><span style="font-size: 13.3333px;">When was the last time you laughed until you cried? Can you remember how good you felt afterwards?</span></p>
<p><span style="font-size: 13.3333px;">I was chatting with my friend, Sue, on the phone and she was complaining about her house being a mess, her business not doing as well as she expected, and that her life felt like a struggle. I reminded her of when we went snowshoeing last year and how much fun she had falling backwards into the deep snow and making snow angels. She laughed like a kid and called Emma, our youngest springer spaniel, a ‘silly goose’ when Emma would bury herself in 10 foot snow banks searching for rabbits. I was curious and asked Sue&#8230; <em>what have you been doing lately for fun? </em>Nothing. <em>Well, you need to do something about that</em>. We came up with a plan for her to take Friday afternoon off and spend time doing whatever she wanted. No cell phones, no computer, no thinking about work. The next day she emailed me with everything she had done for herself and was thrilled at how great she felt.</span></p>
<p>How can YOU put some fun and laughter into your life?</p>
<p>#1 <span style="text-decoration: underline;"><span style="color: #ff0000;">Make time to have fun EVERY day</span></span><span style="text-decoration: underline;">:</span></p>
<p><span style="text-decoration: underline;"> </span><span style="font-size: 13.3333px;">If you aren’t feeling happy and good about your life, it is time to <strong>schedule </strong>some fun into it. Yes…schedule some time every day. You can choose to take a block of time or mini breaks. These are times when you don’t answer the cell phone, check emails or do any of those ‘should’ activities. Do something different—maybe even something that you haven’t done since you were a kid. It can be as simple as watching a funny video on YouTube (David after the dentist, Charlie Bit Me, or Mrs. Hughes) or walking to a dog park to watch the dogs wrestle and play with each other.</span></p>
<p>#2 <span style="text-decoration: underline;"><span style="color: #ff0000;">Hang out with people who are fun to be around</span></span><span style="text-decoration: underline;">:</span></p>
<p><span style="text-decoration: underline;"> </span></p>
<p>Think about the people who are in your world. Notice how you feel after spending time with them. I want you to give them a number between 1 and 10. <span style="font-size: 13.3333px;">If you feel more stressed, they would be closer to a 1 and would be considered ‘emotional vampires’. These are the people who <em>deplete</em> your precious energy. </span><span style="font-size: 13.3333px;">If you want to <em>fill </em>your energy tank, then make a habit of spending more time with friends and family who are above 8. They support &amp; encourage you and make you laugh; you feel better after being with them.</span></p>
<p>Remember if you want to stay healthy and enjoy life, schedule 30 minutes of fun into <strong>every</strong> day. It is easy to do when you write out your daily schedule the night before. Also make a list of people you want to spend more time with and make a luncheon date with one of them…this week!</p>
<p><strong>NOTE: </strong>if you haven’t signed up for my free newsletter, <strong>Dementia Hope Tips for Caregivers</strong>, click <a href="www.dementiahopeformula.com">this link.</a> Feel free to pass it along&#8211;Thanks!</p>
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		<title>Living with Dementia: Enjoying the Present Moment</title>
		<link>http://hollyeburne.com/alzheimers-and-related-dementia/living-with-dementia-enjoying-the-present-moment/</link>
		<comments>http://hollyeburne.com/alzheimers-and-related-dementia/living-with-dementia-enjoying-the-present-moment/#comments</comments>
		<pubDate>Fri, 03 Sep 2010 17:36:11 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Alzheimer's and related Dementia]]></category>
		<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[changing perspective]]></category>
		<category><![CDATA[dementiahope]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[life lesson]]></category>
		<category><![CDATA[Overcoming Dementia]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=829</guid>
		<description><![CDATA[I just came back from a run with my husband, Dave. It is an absolutely gorgeous fall morning&#8211;sun is shining, with wispy clouds and a feel of coolness in the air. Perfect for running. As we are heading towards the sun, I look up to see many layers and shapes of clouds, on a backdrop [...]]]></description>
			<content:encoded><![CDATA[<p>I just came back from a run with my husband, Dave. It is an absolutely gorgeous fall morning&#8211;sun is shining, with wispy clouds and a feel of coolness in the air. Perfect for running. As we are heading towards the sun, I look up to see many layers and shapes of clouds, on a backdrop of the deep blue sky. What is interesting, and particularly beautiful, are the colours around the sun&#8211;shades of mint green and fuchsia-almost like a rainbow but without the rain. I mention it to Dave, who isn&#8217;t wearing sunglasses, and he can&#8217;t see anything but the blinding sunshine. When I comment about the gorgeous sky, he quickly points out the dark clouds in the distant. Hmmm&#8230;..I guess he&#8217;s right. When I take off my rose-coloured sunglasses there isn&#8217;t any mint and fuchsia colours around the sun and I have to admit there are dark clouds in the east. All of this is true for Dave. But for me, the truth is&#8230;the sun is shining, I am enjoying the feel of the crisp air and I am happy to be running with my husband. <span style="font-size: 12.7315px;">I also know that if I focus on the dark clouds and the chance that it might rain, then I will miss these magical moments.</span></p>
<p><span style="font-size: 12.7315px;"> According to several studies, 91-97% of what we worry about never comes to fruition. You can bet I have tested this theory many times and it has held true for me. I am learning to spend less energy worrying about something that &#8216;might&#8217;, but usually doesn&#8217;t, happen. For example, if Dave was late coming home from shopping, I would worry that he had a seizure while driving&#8211;that was before his license was taken away due to the complications of his frontotemporal dementia. When he arrived home safely, I would remind myself of the wasted energy, not to mention the negative impact on my health.</span></p>
<p>There are times when I get scared looking down the road at the dark clouds of our future (with dementia), but I have to remind myself that we aren&#8217;t there yet. Right now Dave is still physically able to do many things and I am going to keep treasuring the moments&#8230;just like our run this morning.</p>
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		<title>Magic Moments</title>
		<link>http://hollyeburne.com/alzheimers-and-related-dementia/magic-moments/</link>
		<comments>http://hollyeburne.com/alzheimers-and-related-dementia/magic-moments/#comments</comments>
		<pubDate>Sat, 28 Aug 2010 18:35:26 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Alzheimer's and related Dementia]]></category>
		<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[frontotemporal dementia]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[Overcoming Dementia]]></category>
		<category><![CDATA[peace]]></category>
		<category><![CDATA[relieve overwhelm as a carer]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=822</guid>
		<description><![CDATA[Living as a carer for my husband, Dave with dementia (frontotemporal dementia) is a challenging and life changing experience. There have been times (too numerous to count) when I have wanted to hand the job over to someone else. This isn&#8217;t what I had planned for the years when our kids left home and we were [...]]]></description>
			<content:encoded><![CDATA[<p>Living as a carer for my husband, Dave with dementia (frontotemporal dementia) is a challenging and life changing experience. There have been times (too numerous to count) when I have wanted to hand the job over to someone else. <em>This isn&#8217;t what I had planned for the years when our kids left home and we were still young enough to travel,</em> <em>hike and bike wherever</em>. But this is what life is handing us and I finally figured out that I can&#8217;t fight it and I had better learn to accept it. This is why the &#8216;magic&#8217; moments in my day are so important. They keep me from going insane or becoming depressed for long periods.</p>
<p><span id="more-822"></span>Last week we spent a few days on a beautiful fishing boat with great friends and gorgeous scenery. Dave was excited to be some place other than at home with his daily routine of exercising and working on his puzzles. But when he doesn&#8217;t get his 11 hours of sleep and a 1-2 hour nap (combined with adapting to a different environment) he withdraws into his own world. There was a moment when 7 of us were sitting around the table enjoying a delicious halibut dinner and I noticed our friends laughing &amp; chatting. Then I looked at Dave, sitting at the head of the table wearing sunglasses and a ball cap, mechanically putting his fork to his mouth and oblivious to those around him. I noticed the contrast between Dave (and us as a couple) with our friends. I was reminded of the change in our relationship and for a few hours, I felt really sad inside. Instead of crying, I wrote in my journal and by the next morning, I was feeling better. I began to pay attention to the &#8216;magic moments&#8217;&#8230;catching my first deep sea fish, the crystal blue sky as the fog lifted, 3 humpback whales blowing and diving, and for the wonderful friends who accept Dave for who he is now. Not who he was a few years ago.</p>
<p>Every day has magic moments, even though they are hard to find sometimes. You can identify them when you see, hear or feel something that makes you laugh, feel good, tingle inside, or smile. When you take a few extra moments to appreciate those moments, I guarantee they will sustain you through the tough times when you are fed up and want to throw in the towel.</p>
<p><a href="http://hollyeburne.com/wp-content/uploads/2010/08/DSC_0265.jpg"><img title="DSC_0265" src="http://hollyeburne.com/wp-content/uploads/2010/08/DSC_0265-150x150.jpg" alt="" width="150" height="150" /></a> Dave&#8217;s halibut</p>
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		<title>Living with Dementia: Organized Chaos</title>
		<link>http://hollyeburne.com/alzheimers-and-related-dementia/living-with-dementia-organized-chaos/</link>
		<comments>http://hollyeburne.com/alzheimers-and-related-dementia/living-with-dementia-organized-chaos/#comments</comments>
		<pubDate>Sat, 14 Aug 2010 17:54:35 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Alzheimer's and related Dementia]]></category>
		<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[Overcoming Dementia]]></category>
		<category><![CDATA[peace]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=800</guid>
		<description><![CDATA[Organized chaos&#8230;it must look like my life is busy from the outside with balancing work, home, family, caring for my husband, Dave, with frontotemporal dementia, and fitting in &#8216;me&#8217; time, but I found a secret for staying calm&#8211;most of the time. It is called exercise. Sometimes it is a bike ride, a run, Nordic hike, [...]]]></description>
			<content:encoded><![CDATA[<p>Organized chaos&#8230;it must look like my life is busy from the outside with balancing work, home, family, caring for my husband, Dave, with frontotemporal dementia, and fitting in &#8216;me&#8217; time, but I found a secret for staying calm&#8211;most of the time. It is called exercise. Sometimes it is a bike ride, a run, Nordic hike, kayak or gardening. Whatever it is&#8211;without exception&#8211;I feel better afterwards. This morning was a good example&#8230;</p>
<p><span id="more-800"></span>For the past few days I have been busy getting ready (making lists, shopping, chores) for a big fishing trip up north with some friends. (I have never caught a fish and I am quite excited) Anyway, I noticed that my mind was starting to feel like it was in overdrive so I hopped on my mountain bike for a cruise along our country road. Within minutes I started noticing the crystal blue skies (all of the wildfire smoke has disappeared) against the green hills, the smell of fresh air, and the sounds of the birds flitting among the bushes lining the creek. The wind against my face and the feeling of gliding along on my bike was freedom. I was reminded of all of the things in my life that I am grateful for&#8211;living on a quiet country road among nature, our sweet animals, my health and Dave&#8217;s health&#8211;who has done very well since his diagnosis 3 1/2 years ago. It is amazing how great I feel when I quiet the chatter in my brain and surround myself with nature.</p>
<p>Stepping out of the commotion of &#8216;living with dementia&#8217; is key to seeing the bigger picture of my life. Last year I was standing within a foot of a hummingbird feeder and there were 5 territorial male hummingbirds (3 calliopes &amp; 2 rufous) fighting for a spot on the feeder. It was fascinating to be inside of their &#8216;organized chaos&#8217; because they managed to buzz around me&#8211;without touching me or each other. What an incredible sight. It wasn&#8217;t until I stepped back out of their energy that I noticed how calm it was to be on the outside. My bike ride this morning was like stepping out of my chaotic mind chatter. I came back relaxed and rejuvenated. So&#8230;any time you feel yourself winding up, lace up your shoes and go for a walk, run, pick weeds or any activity that will get your body moving and in touch with nature. It is a win-win for everybody!</p>
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		<title>News-fasting is Healthy</title>
		<link>http://hollyeburne.com/alzheimers-and-related-dementia/newsfasting-is-a-healthy-habit/</link>
		<comments>http://hollyeburne.com/alzheimers-and-related-dementia/newsfasting-is-a-healthy-habit/#comments</comments>
		<pubDate>Sun, 01 Aug 2010 20:11:36 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Alzheimer's and related Dementia]]></category>
		<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[relieve overwhelm as a carer]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=791</guid>
		<description><![CDATA[The other morning my mother-in-law phoned me at 6 am (she knows I like to get up at 4 am and read, meditate or write) to ask me how the wildfire was. What fire? She said&#8230;&#8221;the one in your part of town&#8221;. We live in the country among sage brush, miniature cacti and pine beetle [...]]]></description>
			<content:encoded><![CDATA[<p>The other morning my mother-in-law phoned me at 6 am (she knows I like to get up at 4 am and read, meditate or write) to ask me how the wildfire was. What fire? She said&#8230;&#8221;the one in your part of town&#8221;. We live in the country among sage brush, miniature cacti and pine beetle (dead) trees so summer fires aren&#8217;t uncommon.</p>
<p>Anyway, I looked outside and saw a bit of smoke but knew we weren&#8217;t in immediate risk of evacuation. We chatted some more, I thanked her and then checked out the details on the internet. The wildfire was about 10 km away and they had plenty of firefighters and helicopters working on it, so I didn&#8217;t plan any further.</p>
<p>As you know sensational, bad news sells. In fact, we are bombarded by sad, violent or depressing news for 87% of our day. Not just from the paper and TV, but from other well-meaning friends and family. When I started news-fasting about 15 years ago I was concerned about keeping up with the current events and being able to contribute to an intelligent conversation. But bad news travels quickly.</p>
<p>I challenge you to not watch or read news for a week and notice how quickly the news gets back to you. Then it is your choice of finding out more details&#8211;or not.</p>
<p><span style="font-size: 13.1944px;">I remember feeling sick as I watched the twin towers coming down on 911, and on boxing day in 2004, listening to people screaming as they hung onto tree branches during the tsunami in Thailand. I didn&#8217;t need to see that repeated every hour on the hour to be more informed. Once is enough.</span></p>
<p>I use this same philosophy for living with my husband&#8217;s dementia. I am fully aware of the pain and challenges of being a carer, but I choose to focus on what it great about my life. I like to use this analogy. When I am sitting in a room, I look around at all of the solid objects&#8211;chairs, table, lamps etc. Then I look at the space around those solid objects. The desk, table and lamps (which take up little room) are the aggravations and challenges of dementia; the ABUNDANT space represents what is great about my life..physically healthy husband, great family &amp; friends, comfortable home and remembering I&#8217;m not the one dealing with a dying brain.</p>
<p>Let me know how you feel when you spend more time noticing the space instead of the solid objects. And whether you feel happier and more optimistic when you reduce your exposure to news that sells.</p>
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		<title>Working through moments of sadness</title>
		<link>http://hollyeburne.com/alzheimers-and-related-dementia/working-through-moments-of-sadness/</link>
		<comments>http://hollyeburne.com/alzheimers-and-related-dementia/working-through-moments-of-sadness/#comments</comments>
		<pubDate>Sun, 28 Feb 2010 19:30:32 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[Alzheimer's and related Dementia]]></category>
		<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[frontotemporal dementia]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[Overcoming Dementia]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=636</guid>
		<description><![CDATA[This morning Dave had just left with the dogs for a walk and I was getting ready for a run. I was sitting in the den when I noticed how tired I was feeling. It was emotional fatigue from a week of household challenges—the furnace breaking down, the central vacuum not working and a whole [...]]]></description>
			<content:encoded><![CDATA[<p>This morning Dave had just left with the dogs for a walk and I was getting ready for a run. I was sitting in the den when I noticed how tired I was feeling. It was emotional fatigue from a week of household challenges—the furnace breaking down, the central vacuum not working and a whole electrical circuit out.</p>
<p>Since my husband, Dave, was diagnosed with <a href="http://hollyeburne.com/wp-admin/post.php?action=edit&amp;post=18">Frontotemporal dementia</a> 3 years ago, I have gradually taken over his chores; chores that came easily to his ‘male’ brain. I had no idea how much he did until I had to pick up his end. Well, I finally have to admit that I am reaching my tipping point. I am putting up my white flag and calling for help. I realize that if I want to keep a balance in my life—working, having personal &amp; family time, and managing our house&#8211;I need some assistance. No longer do I think I can do this by myself. My &#8216;dream&#8217; plan is to hire a retired couple&#8211;4 hours/ day for 2 days a week. The husband can take care of the mechanical issues around the house, be a driver for Dave (he lost his driver’s license in December and the nearest bus stop is 9 km.), run errands and keep Dave company. His wife can help me with the house chores, including cleaning and cooking.</p>
<p><span id="more-636"></span>Besides feeling tired this morning, I was feeling sad. That isn’t a usual emotion for me and in the past, I would busy myself with work or something else to take my mind off the pain. This time I decided to sit with the pain and let the tears flow. I didn’t make a phone call to complain or to get sympathy from a friend or family member. I decided to work through it myself. As I was having a small ‘pity’ party, I looked out the windows at the chickadees, goldfinches and pine siskins eating at the feeders. I watched as the birds flew in and out, sometimes stopping at the bird bath for a drink. I started feeling better. This is what happens when I am out with nature. I notice that when I feeling a bit down, it only take seconds of being outside before I feel the weight off my shoulders, and the lightness and happiness coming back.</p>
<p>Throughout this past year, I am learning that the key to my happiness is within. It isn’t dependent on other people or circumstances. I am also learning that it is okay to feel sadness and grief, as long as I don’t get stuck in that stage. It seems the more I practice ‘leaning’ into my emotions and letting them ‘be’, the easier life flows for me. I have a different perspective on my life and I am realizing that abundance doesn’t come from a large bank account.</p>
<p>I wanted to share my latest insight with you while it was fresh inside. I just came back from a run and I am feeling 100% better. There are 3 horses down the road, which gallop towards me when they see me. I’d like to think it is for more than the carrots I bring! Anyway, they let me kiss them while I feed them and I love listening to the crunching sounds of the carrots. On my way home I heard the spring sounds—warblers in the creek, robins, belted kingfishers waiting for the ice to melt from the streams and the trill of the red-wing blackbirds. How can I feel sad listening to the cheeriest sounds in the world?</p>
<p><a href="http://hollyeburne.com/wp-content/uploads/2010/02/love-my-horses.jpg"><img class="alignright size-medium wp-image-637" title="love my horses" src="http://hollyeburne.com/wp-content/uploads/2010/02/love-my-horses-300x168.jpg" alt="" width="300" height="168" /></a></p>
<p>Have a wonderful day!</p>
<p><a href="http://hollyeburne.com/wp-content/uploads/2010/02/love-my-horses.jpg"></a> </p>
<p><a href="http://hollyeburne.com/wp-content/uploads/2010/02/love-my-horses.jpg"></a> </p>
<p><a href="http://hollyeburne.com/wp-content/uploads/2010/02/love-my-horses.jpg"></a></p>
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		<title>Walking in my shoes&#8211;living with a spouse with frontotemporal dementia</title>
		<link>http://hollyeburne.com/frontotemporal-dementiadementia/walking-in-my-shoes-living-with-a-spouse-with-frontotemporal-dementia/</link>
		<comments>http://hollyeburne.com/frontotemporal-dementiadementia/walking-in-my-shoes-living-with-a-spouse-with-frontotemporal-dementia/#comments</comments>
		<pubDate>Wed, 24 Feb 2010 18:01:09 +0000</pubDate>
		<dc:creator>Holly</dc:creator>
				<category><![CDATA[frontotemporal dementia;dementia]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[frontotemporal dementia]]></category>
		<category><![CDATA[life balance]]></category>
		<category><![CDATA[walking in my shoes]]></category>

		<guid isPermaLink="false">http://hollyeburne.com/?p=632</guid>
		<description><![CDATA[Every time  my sister or children come to visit, I learn a little bit more about how I am managing my new life—a life with my husband, Dave who has Frontotemporal dementia. I am more aware of how I speak to him&#8211;including my tone and patience. I am also more aware of how I ‘respond’ [...]]]></description>
			<content:encoded><![CDATA[<p>Every time  my sister or children come to visit, I learn a little bit more about how I am managing my new life—a life with my husband, Dave who has Frontotemporal dementia. I am more aware of how I speak to him&#8211;including my tone and patience. I am also more aware of how I ‘respond’ or ‘react’ to comments from people who step into our lives for a few hours or a few days; people who have good intentions, but aren’t walking in my shoes. A good example was the other night…</p>
<p>Dave was tired and wanted to go to bed soon after dinner, but he hadn’t done the dishes. There is a courtesy rule in our household that the cook doesn’t wash dishes. He said he would do them in the morning and I quickly said “oh no, you need to do them now.”</p>
<p>My sister was sitting on the couch and her eyes popped wider and said “that’s okay, Dave, I’ll do them for you.” I paused, took a breath, and then quietly told her that it helps both of us if he does them tonight.</p>
<p>I can understand that if you are visiting us for a short time, it may seem cruel to insist on the dishes when Dave wants to go to bed. After all, Dave is the one with the illness, the one who needs assistance and protection. What they don’t see is the growing list of responsibilities and chores that are piling up on my shoulders. They don’t realize that something as small as doing the dishes is one less chore for me. Fortunately Dave has enough insight to see how much work I do around the house (in addition to running 2 businesses) and he wants to contribute to the best of his ability. As his condition changes, so does his ‘honey-do’ list. It is a win-win for both of us.</p>
<p>This little story teaches me not to be upset when someone makes a comment. I am not walking in their shoes either and they are doing the best they can. Living with dementia is a novel experience and like parenting, it is trial and error—not just for Dave and me, but for our family and friends. I must remind myself to stay ‘grounded’ in my belief that I am caring for Dave (and me) in the best way I can. And so far, it seems to be getting easier.</p>
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