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		<title>April 9, 2010 &#8211; Matson Comes Home</title>
		<link>http://cj4nier44.wordpress.com/2010/04/10/april-9-2010-matson-comes-home/</link>
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		<pubDate>Sat, 10 Apr 2010 06:25:11 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<description><![CDATA[Today is the day Matson and his Mommy came home. They spent 19 days in San Diego. Matson was so happy to see his big brother, Tyler. And Tyler was so happy to see his Matson. They missed each other so much. I guess it is a mutual boy thing because they wouldn&#8217;t let Lily [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=212&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Today is the day Matson and his Mommy came home. They spent 19 days in San Diego. Matson was so happy to see his big brother, Tyler. And Tyler was so happy to see his Matson. They missed each other so much. I guess it is a mutual boy thing because they wouldn&#8217;t let Lily in. Lily came to me with her bottom lip out and said Matson is making her sad. I ask her why and she said &#8220;Matson wouldn&#8217;t say hi to me.&#8221; It was a boys only reunion for a couple of hours. Poor Lily.</p>
<p>We spent yesterday afternoon making a welcome home Matson and Mommy sign. We colored it and put all kinds of stickers on it. What fun!  Here is a picture of Tyler &amp; Lily with their welcome home sigh.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/04/p1010039.jpg"><img class="aligncenter size-medium wp-image-213" title="P1010039" src="http://cj4nier44.files.wordpress.com/2010/04/p1010039.jpg?w=225&#038;h=300" alt="" width="225" height="300" /></a></p>
<p>My daughter-in-law, Stephanie, said the last few days in San Diego were pretty good. She got out and walked Matson as much possible to build up his strength. They walked on the beach, around WalMart, and on Easter Sunday she took him to Sea World to have breakfast with the dolphins. Matson loves the dolphins. He said they have bendy backs just like him. He got to be wheeled around in a wheel chair and enjoyed the Shamu the killer whale show. And, they had a 7.2 earthquake while they were there. Matson said the hotel was bumping. The quake was in Mexicali but they felt it really good. They even felt several strong aftershocks. What an experience to top off their stay in San Diego.</p>
<p>All in all Matson is recovering well from his scoliosis surgery. He still get his pain meds at night but Steph has cut them down during the day. We took him to Tyler&#8217;s little league game this evening and he did great until the last 20 minutes when he started saying his back was hurting. He has already figured out his limitations. He can&#8217;t bend to pick up anything. That is where Lily comes in. We heard him telling Lily to pick up his toy because he can&#8217;t bend over. He can get himself up on a chair and he has figured out how to get himself on the floor to play with Tyler. Pretty remarkable considering he had his surgery on the 24th of March. Kids are so resilient. It is amazing how they bounce back. The doctor said to let him be a kid. He will figure out what he can do and can&#8217;t do. The brace will protect his spine until the graphs heal. He has an appointment in July with the doctor to see if he can discontinue wearing the brace. Then in October he will have another little surgery to lengthen the rods. His journey is just beginning but the hardest part is behind him.</p>
<p>Here he is getting ready to go to the airport to fly home.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/04/matson26414_1376132196047_1014114738_31187717_723512_n.jpg"><img class="aligncenter size-medium wp-image-214" title="matson26414_1376132196047_1014114738_31187717_723512_n" src="http://cj4nier44.files.wordpress.com/2010/04/matson26414_1376132196047_1014114738_31187717_723512_n.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>Playing with his brother, Tyler and his sister. Lily.</p>
<p><a style="text-decoration:none;" href="http://cj4nier44.files.wordpress.com/2010/04/p1010050.jpg"><img class="aligncenter size-medium wp-image-215" title="P1010050" src="http://cj4nier44.files.wordpress.com/2010/04/p1010050.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>Welcome home Matson. You were missed.</p>
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		<title>April 2, 2010 &#8211; Matson</title>
		<link>http://cj4nier44.wordpress.com/2010/04/03/april-2-2010-matson/</link>
		<comments>http://cj4nier44.wordpress.com/2010/04/03/april-2-2010-matson/#comments</comments>
		<pubDate>Sat, 03 Apr 2010 05:14:18 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<description><![CDATA[The kids are down for the night. I should be. This 66 year old grandma had a full day with Tyler &#38; Lily. Lily slept in this morning until 9:30. I was heading up the stairs to check on her when she was coming down. This little girl is always in the best mood. What [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=206&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>The kids are down for the night. I should be. This 66 year old grandma had a full day with Tyler &amp; Lily. Lily slept in this morning until 9:30. I was heading up the stairs to check on her when she was coming down. This little girl is always in the best mood. What a joy she is. Tyler did all his chores this morning like a trooper. It was a good day. Daddy got home around 5 with a pizza. Friday nights are sleep out nights in the living room. I did it with them last week when Daddy was in San Diego with Mommy and Matson. They do this really cute sumo wrestling with pillows under their shirts. Pretty rowdy too. I took some pictures but haven&#8217;t uploaded them to my computer yet. I will post the pictures another time.</p>
<p>Matson is doing really well today. Being out of the hospital has helped a lot. He was able to sit out by the pool in the sunshine  yesterday. It is amazing how much he has healed in 10 days. Mom walks him often so he can regain his strength. They still struggle with the bulky brace. In time it will seem like they have always dealt with it. He is having fun playing with his toys and watching his favorite movies. Here is a picture of him with his brace.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/04/24383_1366632078550_1014114738_31158694_7708595_n.jpg"><img class="aligncenter size-medium wp-image-207" title="24383_1366632078550_1014114738_31158694_7708595_n" src="http://cj4nier44.files.wordpress.com/2010/04/24383_1366632078550_1014114738_31158694_7708595_n.jpg?w=297&#038;h=300" alt="" width="297" height="300" /></a>This was taken when he was still in the hospital.</p>
<p>This is what his X-ray looks like after his surgery with the rods in place.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/04/24383_1371182672312_1014114738_31171163_3084199_n.jpg"><img class="aligncenter size-medium wp-image-208" title="24383_1371182672312_1014114738_31171163_3084199_n" src="http://cj4nier44.files.wordpress.com/2010/04/24383_1371182672312_1014114738_31171163_3084199_n.jpg?w=225&#038;h=300" alt="" width="225" height="300" /></a>It is just amazing that they were able to correct him this much.</p>
<p>Here is our happy Matson out of the hospital.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/04/24383_1371182752314_1014114738_31171165_145564_n.jpg"><img class="aligncenter size-medium wp-image-209" title="24383_1371182752314_1014114738_31171165_145564_n" src="http://cj4nier44.files.wordpress.com/2010/04/24383_1371182752314_1014114738_31171165_145564_n.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a>He still has a lot of healing to do. I know in the long run this will all be worth it. I just pray he doesn&#8217;t remember too much of all the pain he went through. We can&#8217;t wait to get him home. Tyler misses him so much. Matson has his post-op appointment next Wednesday. If all goes well he might get to come home early. I think the best thing for him is his normal day to day routine. In three months the brace will be history and he can get back  to just being a boy. The doctor said to let him do whatever he wants except contact sports. Matson, you are my little hero and I love you so much.</p>
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		<title>March 31, 2010 &#8211; Matson&#8217;s Recovery</title>
		<link>http://cj4nier44.wordpress.com/2010/04/02/march-31-2010-matsons-recovery/</link>
		<comments>http://cj4nier44.wordpress.com/2010/04/02/march-31-2010-matsons-recovery/#comments</comments>
		<pubDate>Fri, 02 Apr 2010 05:22:51 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<description><![CDATA[I can&#8217;t believe 7 days have passed since Matson&#8217;s  surgery. I had intended to post something daily on his progress. BUSY is all I can say. Matson had his surgery on the 24th. The surgery went well and the doctor was able to correct his spine from 60 degrees to 22, That was better than [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=200&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>I can&#8217;t believe 7 days have passed since Matson&#8217;s  surgery. I had intended to post something daily on his progress. BUSY is all I can say.</p>
<p>Matson had his surgery on the 24th. The surgery went well and the doctor was able to correct his spine from 60 degrees to 22, That was better than they had anticipated. Recovery was awful for him. He was in unimaginable pain and they could not stabilize his heart rate. Pretty scary five hours in recovery. They finally found a combination of drugs that helped with his pain. You would think such a little body would respond to any pain meds. Not the case with Matson.</p>
<p>On the 25th he is still in awful pain and the nasogastric tube in his nose has provided a lot of added pain, not suctioning, irritating his stomach wall and causing extreme stomach pain and bleeding. My heart aches for him.</p>
<p>On the 26th, my birthday, Matson was molded for his brace. He must wear a brace full time for at least 3 months post-op in order to protect and stablize his implants. It is a hard fiberglass brace. He hates it. He is still in a lot of pain and the nasogastric tube is still clogging and needs to be flushed out causing him pain.</p>
<p>Today is April 1st.  I haven&#8217;t had time to finish this post. My son came to take Tyler &amp; Lily to Karate. I have some free childless time to write some more.</p>
<p>Back to Matson&#8217;s recovery. On March 27th that awful nasogastric tube was removed. Yeah, that tube was a nightmare for him. He is able to eat soft foods and he was able to keep jello and gaterade down. His fever is better and his heart rate is finally stabilized. That was worrisome. A normal heart rate is around 90 and his was hovering around 130 to 150 for the last couple of days. He woke up smiling and wanted balloons for his room. He also wanted to go swimming. There is a pool at the motel where he will be recovering when he is released. He won&#8217;t be going swimming for a while. He has a brace to wear for 3 months while the graphs heal.</p>
<p>March 28th is an even better day. He is eating on his own and wants Mac and Cheese for lunch. He got his catheter out too. Now he can go potty on his own. Well, not quit on his own. I understand from his Mom that going potty is quit an ordeal because he can&#8217;t be upright without his brace. But, all in all it is a better day for him. He got to go outside to the garden in a wheel chair. Daddy made him laugh by shaking a tree and blossoms fell on Mommy&#8217;s head. Laughter is good. Matson also told his Mom that he was going to be doctor so if she got sick he could make her all better. He said &#8221; you will have to have a tube in your nose though.&#8221;</p>
<p>March 29th is one step forward and one step back. His Mommy&#8217;s words. He has to walk more so he can get out of the hospital. His Mom walks him down to the playroom for some fun. Matson has quite a bit of pain today and is very frustrated. The process to go the bathroom is time consuming. His Mom has to log roll him to one side, put the back part of his brace on, log roll back and put the front on then Velcro it together. All this while he is needing to go to the bathroom. Poor little guy. This will be his life for 3 months of having to wear the brace. My son came home today. My daughter in law&#8217;s mother goes to San Diego to be with her and Matson for the duration of his recovery. Tyler and Lily are so happy to have daddy home. They have been so good for me. Lily is just the easiest child ever. She pretty much goes with the flow and is a happy little girl of three. Tyler is more serious and misses him Mom. He is so funny and intelligent. He make me smile all the time. Tyler is 7. I taught him how to play Uno and he beats me at it all the time.</p>
<p>It&#8217;s getting late so I&#8217;d better close for now. March 30th Matson was discharged from the hospital. More on his recovery next time.</p>
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		<title>March 25, 2010 &#8211; Matson&#8217;s Recovery</title>
		<link>http://cj4nier44.wordpress.com/2010/03/25/march-25-2010-matsons-recovery/</link>
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		<pubDate>Thu, 25 Mar 2010 16:54:18 +0000</pubDate>
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		<description><![CDATA[Our little sweet boy, Matson has his surgery yesterday. All went well until recovery. They had a hard time stabilizing him. His heart rate was 220 and his pain level was awful. They tried different medicines to control his pain and nothing was working. His Mom reported that his body was racked with spasms. Finally [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=197&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Our little sweet boy, Matson has his surgery yesterday. All went well until recovery. They had a hard time stabilizing him. His heart rate was 220 and his pain level was awful. They tried different medicines to control his pain and nothing was working. His Mom reported that his body was racked with spasms. Finally they tried a strong pain medicine plus Valium. He was drifting in and out of sleep. Spasms would wake him up. Poor little guy. He was put in a room with another child that would screech and he would get mad. He told his Mom he was going over there and tell that boy to stop because his screeching was giving him a headache. His Mom told him he could not walk yet and he said then he would crawl over there. Always the little bossy one. His Mom has asked for another room when one comes available.  The good news is the doctors were able to correct his curve from 60 degrees to 22. That was better than they expected.</p>
<p>Here is our little guy in the hospital.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/03/25703_1363552241556_1014114738_31151425_2095747_n.jpg"><img class="aligncenter size-medium wp-image-198" title="25703_1363552241556_1014114738_31151425_2095747_n" src="http://cj4nier44.files.wordpress.com/2010/03/25703_1363552241556_1014114738_31151425_2095747_n.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a>Rest easy my sweet boy. You are loved so much.</p>
<p>I will update more later.</p>
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		<title>March 20, 2010 &#8211; Sacto Airport</title>
		<link>http://cj4nier44.wordpress.com/2010/03/20/march-20-2010-sacto-airport/</link>
		<comments>http://cj4nier44.wordpress.com/2010/03/20/march-20-2010-sacto-airport/#comments</comments>
		<pubDate>Sat, 20 Mar 2010 19:29:53 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<guid isPermaLink="false">http://cj4nier44.wordpress.com/?p=195</guid>
		<description><![CDATA[Here I am sitting in the Sacramento Airport waiting for my flight to Las Vegas. The time has come for Matson&#8217;s spine surgery. I get there today and Matson and his Mom and Dad leave on Sunday for San Diego. Monday is all the pre-op tests. Tuesday is going to be a fun day for [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=195&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Here I am sitting in the Sacramento Airport waiting for my flight to Las Vegas. The time has come for Matson&#8217;s spine surgery. I get there today and Matson and his Mom and Dad leave on Sunday for San Diego. Monday is all the pre-op tests. Tuesday is going to be a fun day for Matson. Anything fun for the day. Wednesday the 24th is the day. Surgery early in the morning. They were told it would be a 6 to 8 hour surgery. A long worrisome day for two wonderful parents.I know God will be with them. The new procedure with the magnetic rods has been denied by the hospital. Review boards and red tape because the FDA hasn&#8217;t fully approved it. The old procedure will be done with the dual growing rods. Hopefully in a year Matson can have them changed out eliminating the need for lengthtening every six weeks. Matson, my sweet boy, I know you will be just fine. You are a tough little cookie and I love you so much.</p>
<p>The last two weeks have been a whilwind of lunches and physical therapy appointments. Lunches with old school chums that I connected with on FaceBook and with the  Golden Girls. That is what Bev&#8217;s husband calls us. We three who retired from the County. A friendship that just keeps going on and on. I can&#8217;t imagine a month going by without us getting together.</p>
<p>Physical therapy on my foot. I haven&#8217;t a clue what I did to it. One day it is fine and the next it is painful. X-rays just showed some arthritis. But the pain is not where the arthritis is. Go figure. Hope it get better soon. Cortisone is a magic drug.</p>
<p>Need to sign off for now. More updates on Matson as I know.</p>
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		<title>Matson&#8217;s Curvy Journey</title>
		<link>http://cj4nier44.wordpress.com/2010/02/13/matsons-curvy-journey/</link>
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		<pubDate>Sat, 13 Feb 2010 00:12:31 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<description><![CDATA[Matson&#8217;s Curvy Journey is the name my Daugher in Law put on Matson&#8217;s CaringBridge website. This website is a way for her to keep family and friends updated on Matson&#8217;s journey with Progressive Infantile Scoliosis. Sounds like such a big name for a curvature of the spine. Matson is my grandson. He will be four on Valentine&#8217;s Day. [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=187&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Matson&#8217;s Curvy Journey is the name my Daugher in Law put on Matson&#8217;s CaringBridge website. This website is a way for her to keep family and friends updated on Matson&#8217;s journey with Progressive Infantile Scoliosis. Sounds like such a big name for a curvature of the spine. Matson is my grandson. He will be four on Valentine&#8217;s Day. I first notice his curve when he was about three months old.  I asked my Daughter in Law about it and, yes, they had noticed it also. The pediatrician told them that it might correct itself. It didn&#8217;t. Several trips to Shriner&#8217;s Hospital and several castings didn&#8217;t correct his curve. He has such a reaction to the casting material that he had deep purple and blue bruises on his body that took  months to heal. They even had to take him to their friend, who was a veterinarian, to have the cast cut off. The local hospitals wouldn&#8217;t do it because they didn&#8217;t put the cast on.  A trip to Salt Lake&#8217;s Shriner&#8217;s Hospital was a six hour drive or an hour and a half flight.  Poor little guy couldn&#8217;t wait that long. Enough of the casts. My Daughter in Law became an expert at Scoliosis research. She found a doctor in San Diego who was an expert in growing rods. After several visit with him and a countless tug of war with the insurance company it was finally approved. He was scheduled for the surgery on February 10th. Then the doctor called them about a new procedure where you put in magnetized rods that can be lengthened with a remote control device. One invasive surgery to put the rods in and then no more until the rods had to be replaced when they have reach the extended length. With the old growing rod procedure there would have been two small incisions made at the top and bottom of his spine to manually extend the rods as he grows about every six months. Of course we are thrilled with the new procedure. Matson will be the first child in the US to have this procedure. From what my Daughter in <span style="text-decoration:line-through;">Law</span> tells me there are five children in the UK who have had this new <span style="text-decoration:line-through;">innovative</span> procedure and one in Japan. She also told me the FDA hasn&#8217;t fully aprroved this procedure here in the US but they are going ahead with it anyway. I found this website that explains the procedure a little better.</p>
<p><a href="http://www.news-medical.net/news/20091202/Ellipse-Technologies-presents-clinical-results-of-its-MAGEC-System-study.aspx">http://www.news-medical.net/news/20091202/Ellipse-Technologies-presents-clinical-results-of-its-MAGEC-System-study.aspx</a></p>
<p>Matson is scheduled for this new procedure on the 24th of March. They will leave for San Diego on the 20th of March. I will fly to Las Vegas and take care of  Matson&#8217;s brother and sister while they are gone. He will have to stay in San Diego for at least three weeks to make sure there isn&#8217;t any infections. He will have to wear a protective brace for six months. The doctor said once he heals to let him play anything he wants except contact sports. He can play baseball, soccer and go swimming.  I think I would worry about both baseball and soccer. All the what ifs would drive me crazy. But, the doctor said he needs to be a kid through all of this. Of course, being his Grandma, my heart breaks that he has to go throught this at all. My Son has a good attitude about all of this. I know he worries but he said at least he can be fixed. He doesn&#8217;t have cancer or a life threatening disease. He&#8217;s right. My head knows that. It&#8217;s my heart that has a hard time.</p>
<p>Matson&#8217;s back</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/02/matsons-back.jpg"><img class="aligncenter size-medium wp-image-188" title="Matson's back" src="http://cj4nier44.files.wordpress.com/2010/02/matsons-back.jpg?w=225&#038;h=300" alt="" width="225" height="300" /></a></p>
<p>This is my sweet boy Matson</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/02/matson19069_1324040293782_1014114738_31050249_1067785_n.jpg"><img class="aligncenter size-medium wp-image-190" title="Matson19069_1324040293782_1014114738_31050249_1067785_n" src="http://cj4nier44.files.wordpress.com/2010/02/matson19069_1324040293782_1014114738_31050249_1067785_n.jpg?w=300&#038;h=224" alt="" width="300" height="224" /></a></p>
<p>I know God will be watching over you. You are a very brave little boy and I love you so much.</p>
<p>This is going to be a ten year journey and I will post often about his progress. Please pray for our little guy.</p>
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			<media:title type="html">Matson's back</media:title>
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		<title>February 1, 2010 &#8211; Curves, My Good Habit</title>
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		<pubDate>Tue, 02 Feb 2010 01:57:37 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<guid isPermaLink="false">http://cj4nier44.wordpress.com/?p=182</guid>
		<description><![CDATA[On January 12, 2004 I did something very good for myself. I joined our local Curves. They were offering a two for one so I got my Mom to join with me. We started out going the three days a week that they recommended. After a few weeks my Mom suggested that we go every [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=182&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>On January 12, 2004 I did something very good for myself. I joined our local Curves. They were offering a two for one so I got my Mom to join with me. We started out going the three days a week that they recommended. After a few weeks my Mom suggested that we go every morning, Monday throught Friday. It has been six years and we are still going every morning except when I am out of town. Mom has managed to surpass me by almost 100 workouts. Good for you Mom! Mom is 86 years old and still going strong. I credit our exercise program with keeping her healthy. She isn&#8217;t on blood pressure or cholesterol medicines. Unlike her daughter, Me, who is on blood pressure meds. My Mom is this little 5&#8242;, 126 pound person who I don&#8217;t resemble at all. I am 5&#8242; 7&#8243; and I won&#8217;t give my weight. Let&#8217;s say I would love to lose 25 pounds. I know working out at Curves has had great benefits to both of us. My knees don&#8217;t hurt anymore and I have more energy than most almost 66 year olds. Curves is the best part of my mornings. I could be in a Curves commercial, huh? Here is the picture I took this morning. I took it because the circuit was full. Fuller than we have seen it in a long time. These are my friends, some old renewed friendships and some new friendships.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/02/p1000701.jpg"><img class="aligncenter size-medium wp-image-183" title="P1000701" src="http://cj4nier44.files.wordpress.com/2010/02/p1000701.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>Here is my Mom on the stretching machines after her workout.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/02/p10007021.jpg"><img class="aligncenter size-medium wp-image-185" title="P1000702" src="http://cj4nier44.files.wordpress.com/2010/02/p10007021.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>Oh, and another thing I am going to do for myself starting today. Eating better and no skipping meals. Maybe this will be the year I lose those 25 pounds.</p>
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		<title>January 31, 2010</title>
		<link>http://cj4nier44.wordpress.com/2010/01/31/january-31-2010/</link>
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		<pubDate>Sun, 31 Jan 2010 23:04:42 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<description><![CDATA[Homemade sourdough rolls rising in the oven and housework done. Time to finally update this blog.  I spent last week in Las Vegas with my son, Matt, and his family. I went for Lily&#8217;s 3rd birthday. We also celebrated Matson&#8217;s 4th birthday since he will be in the hospital for his birthday on February 14th. Yes, [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=169&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Homemade sourdough rolls rising in the oven and housework done. Time to finally update this blog. </p>
<p>I spent last week in Las Vegas with my son, Matt, and his family. I went for Lily&#8217;s 3rd birthday. We also celebrated Matson&#8217;s 4th birthday since he will be in the hospital for his birthday on February 14th. Yes, he is a Valentine&#8217;s baby. Matson will undergo spine surgery to correct his Scoliosis on February 10th if  everything falls into place. The doctor called my daugher in law and told her about a new procedure that has only been done five times in England and once in Japan. It involves magnitized rods that can be adjusted with a remote control. The problem is the FDA hasn&#8217;t fully approved the procedure here in the States. The hospital in San Diego has to approve the procedure also. So, the waiting begins. If things don&#8217;t fall into place the old procedure will have to be done. That will be double growing rods that will have to be lengthened surgically every six months. I will write more about this when we know which procedure will be done.</p>
<p>The birthday party for the little ones was fun. Lots of activities were planned through out the week. My favorite was visiting the Build a Bear Workshop. You pick out which animal you want, select a sound, and stuff it. What fun for the kids. The man who works there was so good with the kids. He said he had been working there for four years and he really enjoyed it. You could tell he did. Lily picked out a pink bear and dressed her in a fancy dress. She named her Lullaby. I was amazed that she came up with that name on her own. She is only three. Matson picked out Alvin the Chipmunk and named him Matson-Alvin. Tyler picked out a cat and had him dressed as a fireman cat. He named him Whiskers. What a fun afternoon.</p>
<p>Lily and her Lullaby</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/01/p1000551.jpg"><img class="aligncenter size-medium wp-image-170" title="P1000551" src="http://cj4nier44.files.wordpress.com/2010/01/p1000551.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a>  </p>
<p>Tyler and his Whiskers</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/01/p1000548.jpg"><img class="aligncenter size-medium wp-image-171" title="P1000548" src="http://cj4nier44.files.wordpress.com/2010/01/p1000548.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>I didn&#8217;t get a good picture of Matson and his chipmunk as he wasn&#8217;t very cooperative that day. He is pretty head strong and difiant when he doesn&#8217;t want his picture taken. I did get some good pictures of him on other days.</p>
<p>Here is his pensive look while watching TV.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/01/p1000611.jpg"><img class="aligncenter size-medium wp-image-172" title="P1000611" src="http://cj4nier44.files.wordpress.com/2010/01/p1000611.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>With his birthday cake.</p>
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<p>I raised three boys so I didn&#8217;t get to dress up little girls. Our Lily is going to be a flower girl in her Aunt&#8217;s wedding in June. We went to a bridal salon so Lily could try on her flower girl dress. The dress is exactly like her Aunt&#8217;s wedding dress. We had such fun taking pictures of her. She is a little angel and loved every minute of playing dress up. Here are pictures of our day at the salon.</p>
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<p>I left stormy California for Las Vegas on the 20th. It was storming in Vegas also. Very cold and windy. It snowed in the surrounding foothills near my Son&#8217;s home.</p>
<p>I took this picture from the car.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/01/p1000661.jpg"><img class="aligncenter size-medium wp-image-177" title="P1000661" src="http://cj4nier44.files.wordpress.com/2010/01/p1000661.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>I had a couple of good days there but by the time I was to leave and come home another storm came. I was stranded in the airport for a few hours before being able to board the plane for the trip home. The ride was pretty smooth by the time we got out of the Vegas valley.</p>
<p>I heard there was an awful wind storm here while I was away. My neighbor told me there were 70 mile an hour winds. My Dad&#8217;s fence blew over as did several in our neighborhood. Two big Cypress trees blew down in my neighbor&#8217;s yard. No damage, thank goodness. The last two days here have been blue skies and sunshine. The kind of days I like because the heater doesn&#8217;t come on. All natural sunshine through the windows.</p>
<p>The sourdough rolls are done. Time to munch.<a href="http://cj4nier44.files.wordpress.com/2010/01/p1000696.jpg"><img class="aligncenter size-medium wp-image-180" title="P1000696" src="http://cj4nier44.files.wordpress.com/2010/01/p1000696.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
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		<title>January 17, 2010</title>
		<link>http://cj4nier44.wordpress.com/2010/01/18/january-17-2010/</link>
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		<pubDate>Mon, 18 Jan 2010 00:19:45 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<description><![CDATA[The rains have finally come. A pretty good downpour. We need the rain so much so no complaining here. It was a good day to do laundry and put a pot of homemade soup on to cook. I have never made homemade Split Pea Soup before. It smells so good. It was easy but a little [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=164&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>The rains have finally come. A pretty good downpour. We need the rain so much so no complaining here. It was a good day to do laundry and put a pot of homemade soup on to cook. I have never made homemade Split Pea Soup before. It smells so good. It was easy but a little messy to blend. It TASTES so good. I love Split Pea Soup. I love all homemade soups.  Can&#8217;t stand the canned stuff.</p>
<p>I had lunch with my friends on Friday. We are called the Golden Girls by Bev&#8217;s husband. I guess it fits. We are retired with gray hair. Well, not me, I dye mine. It&#8217;s no secret. We get together for lunch once a month for our gab fests. We have been known to sit in the restaurant for 4 hours at a time. We have a lot of world problems to solve and our own. Don&#8217;t suppose the world would listen to us?  This Friday we were joined by a fellow retiree of the County. She is a funny lady and had so many funny stories to tell. We enjoyed our lunch with her.</p>
<p>Here is our picture.</p>
<p>The Golden Girls plus One.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/01/p1000501.jpg"><img class="aligncenter size-medium wp-image-165" title="P1000501" src="http://cj4nier44.files.wordpress.com/2010/01/p1000501.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>The plus one is on the left.</p>
<p>Jury Duty on the 12th was a bust. We sat in the jury room for three hours  then the judge came out and dismissed all of us. I almost read a whole book while sitting in there. I don&#8217;t usually like mysteries but this book was small enough to fit in my purse so that is the reason I choose it. It was a book by Mary Higgins Clark called On The Street Where You Live. It wasn&#8217;t too scary and it kept my interest while wiling away the afternoon in the jury room. Time served. I don&#8217;t have to go back until my names comes up again in two years. Let&#8217;s hope it doesn&#8217;t!</p>
<p>I stuck my head outside and it is still coming down. I took some pictures of that stuff falling from the sky. We don&#8217;t see it very often.</p>
<p><a href="http://cj4nier44.files.wordpress.com/2010/01/p1000503.jpg"><img class="aligncenter size-medium wp-image-166" title="P1000503" src="http://cj4nier44.files.wordpress.com/2010/01/p1000503.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p>I sure hope the dentist is working tomorrow. I have had an aching tooth since Thursday night. He doesn&#8217;t work on Fridays and Monday is a holiday but not for him, I hope.  This tooth has had two root canals in it. The last one only a few months ago. How can a tooth without a nerve hurt???  I am leaving on Wednesday for Las Vegas to visit my Son and his family so I have to get this tooth out of pain. If he isn&#8217;t working on Monday then Tuesday is my only day. That&#8217;s cutting it close.  Wish me luck.</p>
<p>One of my favorite shows is back on tonight. I love the suspense of 24 and you gotta love that Jack Bower. Two hours tonight and two hours tomorrow night. Can&#8217;t wait.</p>
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		<title>Tonsils Out</title>
		<link>http://cj4nier44.wordpress.com/2010/01/12/tonsils-out/</link>
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		<pubDate>Tue, 12 Jan 2010 03:21:21 +0000</pubDate>
		<dc:creator>cj4nier44</dc:creator>
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		<description><![CDATA[Today was finally the day to have the tonsils out. My little grandson, Matson, was finally well enough for the procedure. They were supposed to take him in at 7 AM. He had to wait until 8:45. I think they made the best of it because this picture shows him pretty relaxed and smiling  playing [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=cj4nier44.wordpress.com&amp;blog=5614292&amp;post=160&amp;subd=cj4nier44&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Today was finally the day to have the tonsils out. My little grandson, Matson, was finally well enough for the procedure. They were supposed to take him in at 7 AM. He had to wait until 8:45. I think they made the best of it because this picture shows him pretty relaxed and smiling  playing with a stuffed animal.<a href="http://cj4nier44.files.wordpress.com/2010/01/matspmimg00299.jpg"><img class="aligncenter size-medium wp-image-161" title="MatspmIMG00299" src="http://cj4nier44.files.wordpress.com/2010/01/matspmimg00299.jpg?w=300&#038;h=225" alt="" width="300" height="225" /></a></p>
<p> My daughter in law called to tell me they were taking him in. An hour later she called and said he was out and screeming. That must be awful with your throat feeling like someone sliced it open. She said he finally went to sleep in recovery. Around noon she called to tell me they were home and he was not wanting anything to drink or eat. I can&#8217;t blame him. I called this evening and he had been vomiting off and on all afternoon. He is either having a reaction to the anesthetic or he swollowed some blood. Poor little guy. I hope he is doing better tomorrow.  He is such a character when he feels good. Hopefully with his tonsils out he will have less sick days and more days like an almost four year old should have. Full of happy fun and mischief.</p>
<p>Not much else to report today. It is an overcast gloomy day here. Exercising at Curves was pretty much the highlight of my day.  Jury duty tomorrow, Uggg!!!</p>
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