tag:blogger.com,1999:blog-49540784386461017672024-03-12T19:28:26.644-04:00The Scoliosis FoundationScoliosis News and InfoThe Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.comBlogger32125tag:blogger.com,1999:blog-4954078438646101767.post-13850532952506757012012-07-16T10:20:00.000-04:002012-07-16T10:20:02.315-04:00Straightening out Scoliosis<strong> <div class="headline_area">
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Straightening out Scoliosis<span style="font-size: xx-small;"> (article from <a href="http://cincinnatichildrensblog.org/straightening-out-scoliosis/" target="_blank">CCHMC blog</a>)</span></h1>
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by <span class="author vcard"><a class="url fn" href="http://cincinnatichildrensblog.org/author-bios">Tanya Leach</a></span> on <abbr class="published" title="2012-06-20">June 20, 2012</abbr></div>
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<em>Did you know treatment for early onset scoliosis can begin when patients are babies? Experts at Cincinnati Children’s often correct curves in a child’s spine with a series of casts. June is National Scoliosis Awareness Month, and we invite you to learn more about early onset scoliosis.</em><br />
<strong>A bump on her back.</strong><br />
A mother’s instinct told Courtney Strotman something was wrong with her baby.<br />
Addyson Strotman was 4 weeks old when Courtney noticed the bump on her back. Courtney’s husband, Brandon, tried to ease her fears, telling her it was just a muscle. But Courtney insisted it was something more.<br />
Five months later, doctors at Cincinnati Children’s diagnosed Addyson with infantile scoliosis. An X-ray measured the curve in Addyson’s spine at 26 degrees. Two months later, it had worsened to 42 degrees. The Strotmans’ options were to do nothing and face the complications of spinal deformity, to put growing rods in Addyson’s spine, or to try to correct the problem with a series of casts that their baby would wear for about a year.<br />
<strong>Controlling curves with casting?</strong><br />
They decided on casting, a method that is quickly becoming the preferred treatment for early onset scoliosis. Orthopaedic surgeon Dr. Peter Sturm brought the Mehta casting technique to Cincinnati. “We can actually control curves and frequently get them better just with casting,” Sturm says. “It’s less invasive, and it works.”<br />
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<em>We need to act fast! If we can prevent anyone else from going through with a terribly invasive surgery like our son did, then we have succeeded! Early detection is key to overcoming this condition. It may not seem like a mainstream illness, but it does affect children negatively, often through difficult treatments. Casting is the preferred method because it is less invasive than surgery, but even casts can be difficult to treat with. We need your help to find a cure and better treatment options. Read this article, check out the </em><a href="http://www.facebook.com/#!/thecrawfordspinecenter" target="_blank"><em>CCHMC Crawford Spine Center </em></a><em>Facebook page and our website for more information. </em><br />
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</strong><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com2tag:blogger.com,1999:blog-4954078438646101767.post-39652173288945471222012-05-23T16:27:00.003-04:002012-05-23T16:28:12.851-04:00Weighing the Treatment Options for Scoliosis<strong>This article, one of the few times that scoliosis has been written in mainstream publication, outlines some information about scoliosis, as well as, new techniques for treating scoliosis. I will not be able to do justice to the importance of articles like these, so I will allow you to view it in its entirety:</strong><br />
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<a href="http://finance.yahoo.com/news/weighing-treatment-options-scoliosis-040100076.html">http://finance.yahoo.com/news/weighing-treatment-options-scoliosis-040100076.html</a><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com1tag:blogger.com,1999:blog-4954078438646101767.post-49767048312054543492012-04-07T10:50:00.000-04:002012-04-07T10:50:39.803-04:00Risk of Blood Loss in Childhood Spine Surgery<strong>After a study by Johns Hopkins Children's Center was completed and the results were shown, the risk of blood loss in spinal surgery for children is believed to be directly linked to the underlying condition. Children with Cerebral Palsy had the highest rate of blood loss during surgery while Adolescent Scoliosis patients the least. This is great news for the medical community, patients, and families since the medical staff can now use this information to prepare better for surgery. One element that was not discussed in this article was the risk to infants or young children ages 10 or less. From our discussions with the doctor, the risk for bleeding is higher in younger children. However, I will have to find more support for this claim. Please read the entire article <a href="http://www.hopkinschildrens.org/Risk-of-Blood-Loss-in-Childhood-Back-Surgery-Varies-with-Cause-of-Spine-Deformity.aspx" target="_blank">here</a>.</strong><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com3tag:blogger.com,1999:blog-4954078438646101767.post-25076412050132916802012-02-13T20:48:00.000-05:002012-02-13T20:48:57.167-05:00Jim Calhoun Taking Medical Leave Due to Spinal Issues<strong>Although this blog is for scoliosis, there is a story I wanted to share about Jim Calhoun, men's basketball coach at UConn. Jim Calhoun's legacy is marred with controversy and questionable ethical practices. For this reason, he is definitely not one of my favorite coaches. However, no one can tell me that I don't feel for the guy. A three time cancer survivor, Jim Calhoun's next major battle is with <a href="http://health.yahoo.net/channel/spinal-stenosis.html">Spinal Stenosis</a>. After speaking with several orthopedic doctors and spinal specialists, I have a new found respect for him....medically. Spinal stenosis is a narrowing of the spine at the base of the neck or lower back. It causes strain on the spinal nerves as well. From what I have read in the article on Jim Calhoun's medical leave from the team and what I have heard, he is in CONSIDERABLE pain. If any of you have ever had back pain, you can multiply that by 1000 and that may be close to what he is feeling right now. If a coach who hasn't missed more than 20 games in his lengthy career cannot even get out of bed, then spinal stenosis is no joking matter. Regardless of his legacy, and being mindful that this particular blog entry is about a spinal condition and not scoliosis, say a few positive thoughts for a speedy recovery. Any person going through something similar to scoliosis needs the support. See the full story <a href="http://news.yahoo.com/uconns-calhoun-taking-indefinite-medical-leave-202004854--spt.html">here</a>.</strong><br />
<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com1tag:blogger.com,1999:blog-4954078438646101767.post-35328548538425435442012-01-20T12:06:00.000-05:002012-01-20T12:06:48.046-05:00Scoliosis medical device startup spun out of ABIA<strong>From the Akron-Beacon Journal 1.12.12 <a href="http://www.medcitynews.com/2012/01/scoliosis-medical-device-startup-spun-out-of-abia/?utm_source=rss&utm_medium=rss&utm_campaign=scoliosis-medical-device-startup-spun-out-of-abia">Full Article Here</a></strong><br />
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<div class="the-story-block"><div class="content content-the-story"><div class="clearer"></div><div class="story-main-text"><a href="http://www.medcitynews.com/2012/01/scoliosis-medical-device-startup-spun-out-of-abia/scoliosis/" rel="attachment wp-att-117083"><img alt="" class="aligncenter size-full wp-image-117083" height="333" src="http://www.medcitynews.com/wordpress/wp-content/uploads/scoliosis.jpg" title="scoliosis" width="285" /></a><br />
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<strong>The </strong><a href="http://www.medcitynews.com/tag/austen-bioinnovation-institute-in-akron/"><strong>Austen BioInnovation Institute in Akron</strong></a><strong> (ABIA) has created its first company: a firm that’s developing a noninvasive spinal fixation system for children with scoliosis.</strong><br />
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<strong>APTO Orthopaedics’ device is designed to eliminate the need for repetitive, painful and costly surgeries for children with scoliosis, who can require up to two surgeries per year to adjust implants for their growing spines, according to a statement from the ABIA.</strong><br />
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<strong>“This technology would allow surgeons to lengthen the spinal implants in an incision-less manner that would enable reduction in the expense, trauma and risk that accompany current procedures,” said </strong><a href="https://www.akronchildrens.org/cms/doctors/todd_ritzman/index.html"><strong>Dr. Todd Ritzman</strong></a><strong>, cofounder of the company and a physician at Akron Children’s Hospital.</strong><br />
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<strong>APTO’s key next steps involve continuing work to develop a prototype of the device, and after that, beginning to test the device on animals, an ABIA official said. </strong><br />
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<strong>The U.S. spinal implants market is valued at $6.8 billion annually, according to the statement.</strong><br />
<strong>The ABIA was formed in 2008 as a result of the collaboration among several Akron institutions: Akron Children’s Hospital, Akron General Health System, Northeast Ohio Medical University, Summa Health System, The University of Akron and the John S. and James L. Knight Foundation.</strong><br />
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<strong>Within a decade, the ABIA wants to create 2,400 new jobs and attract at least $50 million worth of investments annually in area healthcare companies.</strong></div></div></div><br />
<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-12781289348287227172011-12-05T09:04:00.000-05:002011-12-05T09:04:44.368-05:00Saving Julie From Scoliosis<span class="byttl">Published Thursday, December 01, 2011 3:01 AM at <a href="http://www.theeagle.com/health/Saving-Julie-from-Scoliosis">The Eagle</a></span><br />
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<div class="headline"><strong><u><span style="color: red; font-size: large;">Saving Julie from Scoliosis</span></u></strong></div><div class="headline"><strong><u><span style="color: red; font-size: large;"></span></u></strong> </div><div style="display: block; margin: 3px;"><strong>The following information was provided by a third party, and was not prepared or edited for accuracy by The Eagle.</strong><br />
</div><!-- BITSHeadlineEnd --><div id="byline"></div><div class="text"><strong>LOS ANGELES ( Ivanhoe Newswire) -- Look in the mirror ,do you see a slight curve on your<img align="right" alt="" border="0" src="http://www.ivanhoe.com/images/ivanhoe/3383a.jpg" /> back? 3% of us have scoliosis. It's a minor problem for most people, but for some children it's severe and requires treatment. </strong><br />
<strong>At 39, Julie Flores enjoys the little things in life but it wasn't too long ago Julie's routine was a lot different. </strong><br />
<strong>"I just felt like it was painful, it was no fun," Julie told Ivanhoe. </strong><br />
<strong>It started with a head tilt at the age of five. By the time Julie turned eight, her upper body was bent almost in half. She was diagnosed with dystonia, a movement disorder that causes involuntary muscle spasms. By then severe scoliosis had set in too. </strong><br />
<strong>"I'll never forget one comment someone made of a high school boy who saw her and said 'oh look at that giraffe'," Lidia Flores, Julie's mother, told Ivanhoe. </strong><br />
<strong>By the time Julie hit 30, even house work caused unimaginable pain. Then, her mom found <img align="left" alt="" border="0" src="http://www.ivanhoe.com/images/ivanhoe/3383b.jpg" />Dr. Frank Acosta. </strong><br />
<strong>"Hers was an extreme case where her spine was essentially shaped like an s," Frank Acosta, M.D., Director of Spinal Deformaty at Cedars-Sinai Medical Center, explained. </strong><br />
<strong>"This is a pretty severe case, yeah, one of the worst i have ever seen," Dr. Acosta stated. </strong><br />
<strong>After two operations doctor Acosta placed screws down Julie's spine with help from computer navigation. The goal was to take some pressure off her lung, organs and nerves and realign her spine. After 9 weeks at the hospital and 4 months of physical therapy the operation was a success. </strong><br />
<strong>"I sat next to her and Julia was I think two inches taller than me," Lidia said. </strong><a href="http://www.ivanhoe.com/cart/p_customerlogin.cfm?alert=yes"><strong><img align="right" alt="" border="0" src="http://www.ivanhoe.com/images/ivanhoe/HereForAlert40.jpg" /></strong></a><strong> </strong><br />
<strong>"When I got up and I sat up, I was like wow," Julie said. </strong><br />
<strong>Julie can now stand up straight for the first time in 31 years. </strong><br />
<strong>"I feel like God gave me this whole brand new life again," Julie said. </strong><br />
<strong>Eventually bone will grow up and down Julie's spine over the rods that were surgically implanted. The years of compression caused some damage to her lungs but Julie is now almost pain-free.</strong><br />
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</div><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-13705247247798946272011-11-21T17:12:00.000-05:002011-11-21T17:12:01.724-05:00I said it once, and I will say it again...<strong>Its amazing to me how resilient and confident children are nowadays. As Amber and I prepared for Aiden's surgery today, we felt the gambit of emotions ranging from anxiety to despair. All the while, the person going through the surgery, Aiden, is calm, cool, and collected. His spine is being operated on and we are the ones exhibiting these emotions. Aiden, once again, showed us a very valuable lesson. His calm demeanor is evidence that those afflicted with trauma, pain, or a medical condition can still touch those around them. As well as set an example for how to deal with adversity!</strong><br />
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<strong>Thank you to everyone for their positive thoughts. They truly work!</strong><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-59353269998790403072011-10-06T11:25:00.000-04:002011-10-06T11:25:07.842-04:00What Does Surgery Mean to Him?<strong>On November 21, 2011, our son, Aiden, will go into Cincinnati Children's Hospital Medical Center (CCHMC) for surgery to help treat his Infantile Scoliosis. This surgery, the Grow Rods, will be used to help correct the abnormal curve of his spine, as well as, attempt to impede further increases in degree curvature (his curve is currently 70 degrees+). The surgery for a 5 year old is not performed very often and comes with some risks. However, our doctor, Peter Sturm, is one of the best. We are hoping his experience and knowledge will change Aiden's life forever.</strong><br />
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<strong>At only 5 years old, Aiden has had 2 different types of braces and 14 body casts to help alleviate the curve of his spine. Although about 3% of the population has some type of scoliosis, those patients with degree curves of 50 degrees and higher is only 0.03%. Needless to say, what Aiden has is rare. Amber and I have always been open about his treatment and talk to Aiden regularly about his condition. He takes his limitations with a grain of salt and strives to be as normal as possible. However, his daily life has been altered due to the casting and doctor appointment. People always ask him why he wears a cast, his clothes never fit properly, people stare, and school is altered because of all the appointments at the doctors. Now that we have neared the time when surgery is inevitable, Amber and I know what the benefits (and drawbacks) are for our son. But what does this surgery mean for him?</strong><br />
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<strong>Aiden knows that he will never be able to play football. He knows that he has 6 pre-op appointments October 27, 2011 to prepare for the surgery (i.e. Cardiology, blood work, EKG, Titanium and Nickel Testing, Pulmonary Testing, etc). He knows that his back will be cut open from the base of the neck to the top of his buttocks. He knows he will have hundred of stitches to close his surgical wound. He knows that he will be in pain. He knows he will spend time in ICU after the surgery. He knows we will spend Thanksgiving at the Hospital. He knows that he will have to go back in to CCHMC for additional surgeries every 9-12 months. He knows that eventually he will have to have another major surgery to add new rods. He knows that he will have 3 months of no contact or play. He knows that his diet will change. He knows that he will have to wear a brace for 3 months. He knows that his back is a part of him and he needs it. He knows that it will be a long road for his recovery. Aiden knows all these things at the young age of 5. </strong><br />
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<strong>After telling him all these things, we asked him if he was ok with his surgery. We asked him if he wanted to go through with it. And this is when Aiden showed that there was one thing he didn't know. He asked me "I don't have to wear any more casts? That means I will be normal?". And with a few short inquisitive questions, Aiden showed me that I didn't know everything. Aiden will always be normal. His scoliosis is normal to us. But to him, he wants to be like the other kids. Not only will this surgery attempt to help his scoliosis, it will begin a new chapter for him and his quest to be normal. Now that is a question only time will answer.</strong><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-90747101048278633662011-09-06T14:55:00.000-04:002011-09-06T14:55:49.676-04:00A Step in the Right Direction<strong>A doctor in New York is in the beginning stages of a minimally invasive surgery to correct spinal deformities caused by scoliosis. The doctor, Vishal Sarwahi, M.D., Director of Spine Deformity Surgery at Montefiore Medical Center, stated that he could minimize the number of incisions, x-ray exposure, and recuperation time with this new procedure. Although his control group consisted of adolescent scoliosis patients, his work seems promising. These advances in the fight against scoliosis are important, even if they are not on a grand scale. Please check out the full article at </strong><a href="http://www.prnewswire.com/news-releases/minimally-invasive-surgery-now-an-option-for-children-with-scoliosis-128678133.html"><strong>PR Newswire</strong></a><strong>.</strong><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-43717813984145817382011-08-11T16:26:00.000-04:002011-08-11T16:26:47.947-04:00New Initiatives with CCHMC<div style="text-align: center;"><strong>The Scoliosis Foundation is once again partnering with Cincinnati Children's Hospital Medical Center on new initiatives involving patient care, mainframe database access for scoliosis patients & doctors, and doctor/nurse practictioner training. We are hoping to get started quickly so more detailed information to come soon! </strong></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-83044240496669928932011-08-06T10:16:00.000-04:002011-08-06T10:16:24.681-04:00'One Degree at a Time' Golf Outing Update<strong>The Scoliosis Foundation has updated the information for the golf outing to be held on August 27, 2011 at Glenview Golf Course. This information can be found on the Auction Items and Golf Info link from the outing page. Some of the updated event info includes:</strong><br />
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<span class="text"><b><span style="color: black; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">$100 Golf Registration Fee includes:</span></span></b></span><br />
<ul style="margin: 0px 0px 0px 40px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">18 holes of golf with cart</span></span></b></li>
<li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">City BBQ dinner</span></span></b></li>
<li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Gift bag</span></span></b></li>
<li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Entry into Longest Drive contest</span></span></b></li>
<li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Entry into Closest to the Pin contest</span></span></b></li>
<li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Entry for Door Prizes</span></span></b></li>
<li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Beer - at golf course and after party</span></span></b><span style="font-family: Arial; font-size: xx-small;"><span style="font-size: 10px; line-height: 13px;"><br />
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<b><span style="font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"><span style="color: black;">Extras - with cost</span></span></span></b><ul style="margin: 0px 0px 0px 40px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><li style="color: #000066; line-height: 0px;"><span style="color: black;"><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Gimme/Mulligan/Throw Package </span></span></b><b><u><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">$20</span></span></u></b></span><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"><br />
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</ul><b><span style="color: black; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"> Limit 2 per team</span></span></b><br />
<ul style="margin: 0px 0px 0px 40px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><li style="color: #000066; line-height: 0px;"><span style="color: black;"><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">$10,000 Hole In One Contest </span></span></b><b><u><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">$20</span></span></u></b></span><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"><br />
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</ul><b><span style="color: black; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"> Limit 1 per player - played on South Course Hole #5</span></span></b><br />
<ul style="margin: 0px 0px 0px 40px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><li style="color: #000066; line-height: 0px;"><b><span style="color: black; font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Split-the-Pot </span></span></b></li>
</ul><span style="color: black;"><b><span style="font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"> </span></span></b><b><u><span style="font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">1 for $1/10 for $5/20 for $10</span></span></u></b></span><b><span style="font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"><br />
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<ul style="margin: 0px 0px 0px 40px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><li style="color: #000066; line-height: 0px;"><span style="color: black;"><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Cornhole Tournament </span></span></b><b><u><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">$20 per team</span></span></u></b></span><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"><br />
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</ul><b><span style="color: black; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"> Played during after-party at the Century Inn</span></span></b><br />
<ul style="margin: 0px 0px 0px 40px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><li style="color: #000066; line-height: 0px;"><span style="color: black;"><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Silent Auction </span></span></b><b><u><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;">Price Varies</span></span></u></b></span><b><span style="font-family: Arial; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"><br />
</span></span></b></li>
</ul><b><span style="color: black; font-size: x-small;"><span style="font-size: 12px; line-height: 15px;"> See below for detailed items - items subject to change</span></span></b><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/GolfOuting.html">http://www.thescoliosisfoundation.org/GolfOuting.html</a><a href="http://www.thescoliosisfoundation.org/"></a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-12534970537874838462011-07-19T19:36:00.000-04:002011-07-19T19:36:06.336-04:003rd Annual 'One Degree at a Time' Golf Outing<div style="text-align: center;"><strong>The Scoliosis Foundation is accepting groups for the 2011 golf outing. The outing will be on August 27, 2011 at the Glenview Golf Course. There will be food, fun, prizes, games, silent auction, and an after party at the Century Inn down the street from the golf course. Please signup via the website or send an email to <a href="mailto:andrew@thescoliosisfoundation.org">andrew@thescoliosisfoundation.org</a>. Space is limited so please confirm your group quickly to reserve your spot. Thank you for your support!</strong></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-9373038322138193672011-07-11T16:36:00.000-04:002011-07-11T16:36:50.368-04:00Recap of Spinal Fusion Study<strong>A recent return to spinal fusion patients 10 years after surgery treatment for scoliosis returned surprising results. There seemed to be very little degeneration with the spine, as well as, limited effect on balance and movement. Although this study was for scoliosis patients 21 years and younger, it provides positive results for the future. As the treatments, surgeries, and medical plans evolve and progress, scoliosis patients both young and old can find a little solace in the long lasting effects. Please find the full article <a href="http://news.health.com/2011/04/09/spinal-fusion-for-scoliosis-seems-effective-years-later-study/">here</a>.</strong><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-90223227885072462672011-06-30T10:26:00.000-04:002011-07-05T23:55:33.122-04:00NASCAR EVENT JULY 8th<div><div class="separator" style="clear: both; text-align: center;"><a href="http://4.bp.blogspot.com/-LYKDir4-rJ4/TgyHZjCY2yI/AAAAAAAAABI/JiUSBHzz7g4/s1600/NASCAR.bmp" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" height="417px" i$="true" src="http://4.bp.blogspot.com/-LYKDir4-rJ4/TgyHZjCY2yI/AAAAAAAAABI/JiUSBHzz7g4/s640/NASCAR.bmp" width="640px" /></a></div><br />
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<div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-89866217617451137592011-06-27T09:36:00.000-04:002011-06-27T09:36:42.775-04:00NASCAR Event July 8, 2011<strong> <div class="MsoNormal" style="margin: 0in 0in 0pt;"><b style="mso-bidi-font-weight: normal;"><i style="mso-bidi-font-style: normal;"><span lang="EN-AU" style="color: #cc0000; font-family: Arial; mso-bidi-font-size: 14.5pt;">Join us for a special evening of NASCAR Fun! </span></i></b></div><div align="left" class="MsoBodyTextIndent" style="margin: 3pt 0in 2pt; text-align: left; text-indent: 0in;"><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #17365d; font-family: Wingdings; font-size: 11pt; mso-ascii-font-family: 'Times New Roman'; mso-char-type: symbol; mso-hansi-font-family: 'Times New Roman'; mso-no-proof: no; mso-symbol-font-family: Wingdings;"><span style="mso-char-type: symbol; mso-symbol-font-family: Wingdings;">Ø</span></span></b><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #17365d; font-size: 11pt; mso-no-proof: no;"> Silent Auction of One-of-a-Kind NASCAR and <city w:st="on"><place w:st="on">Cincinnati</place></city> Sports Memorabilia!</span></b></div><div align="left" class="MsoBodyTextIndent" style="margin: 3pt 0in 2pt; text-align: left; text-indent: 0in;"><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #17365d; font-family: Wingdings; font-size: 11pt; mso-ascii-font-family: 'Times New Roman'; mso-char-type: symbol; mso-hansi-font-family: 'Times New Roman'; mso-no-proof: no; mso-symbol-font-family: Wingdings;"><span style="mso-char-type: symbol; mso-symbol-font-family: Wingdings;">Ø</span></span></b><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #17365d; font-size: 11pt; mso-no-proof: no;"> Showing of the NASCAR/CMT movie “PettyBLUE” in HD on a 12 Foot Screen!!</span></b></div><div align="left" class="MsoBodyTextIndent" style="margin: 3pt 0in 2pt; text-align: left; text-indent: 0in;"><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #17365d; font-family: Wingdings; font-size: 11pt; mso-ascii-font-family: 'Times New Roman'; mso-char-type: symbol; mso-hansi-font-family: 'Times New Roman'; mso-no-proof: no; mso-symbol-font-family: Wingdings;"><span style="mso-char-type: symbol; mso-symbol-font-family: Wingdings;">Ø</span></span></b><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #17365d; font-size: 11pt; mso-no-proof: no;"> Meet and talk with the Director about the making of “PettyBLUE” !!!<span style="mso-spacerun: yes;"> </span>Benefit for the Scoliosis Foundation of <city w:st="on"><place w:st="on">Cincinnati</place></city>.<span style="mso-spacerun: yes;"> </span></span></b><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #cc0000; font-size: 11pt; mso-no-proof: no;">Event from 5:30pm to 9:00pm<span style="mso-spacerun: yes;"> </span>– $20 donation for admittance.<span style="mso-spacerun: yes;"> </span></span></b><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #17365d; font-size: 11pt; mso-no-proof: no;"><span style="mso-spacerun: yes;"> </span>100% of donations benefits educational programs for families with children fighting Infantile Scoliosis, and treatment research at <city w:st="on"><place w:st="on">Cincinnati</place></city> Children’s Hospital.<span style="mso-spacerun: yes;"> </span></span></b><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #cc0000; font-size: 11pt; mso-no-proof: no;">ActionCOACH matches donations up to $20 for GrowthCLUB attendees!!!!</span></b></div><div align="left" class="MsoBodyTextIndent" style="margin: 3pt 0in 2pt; text-align: left; text-indent: 0in;"><br />
</div><div align="left" class="MsoBodyTextIndent" style="margin: 3pt 0in 2pt; text-align: left; text-indent: 0in;"><b style="mso-bidi-font-weight: normal;"><span lang="EN-AU" style="color: #cc0000; font-size: 11pt; mso-no-proof: no;">Location is the Oasis Convention Center - 902 Loveland-Miamiville Road, Loveland, Ohio</span></b></div><br />
<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></strong>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-73946215804219753772011-06-08T22:17:00.000-04:002011-06-16T08:37:33.979-04:00NASCAR EVENT JULY 8th<div><div style="text-align: center;"><strong>On July 8, 2011, The Scoliosis Foundation will hold a special event at <b>The Hilton Garden Inn 5300 Cornell Road Cincinnati, OH 45242. </b></strong></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong><b>This is one day prior to the NASCAR event at the Kentucky Speedway on July 9, 2011. </b></strong></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong><b>The Scoliosis Foundation proudly presents a special limited viewing of the CMT movie "Petty Blue" in HD. For a suggested donation of $20 per person, each attendee will be able to view the movie in HD on a 12' screen, interact in a question/answer session with the director <a href="http://www.mikeviney.com/">Mike Viney</a>, and bid through a silent auction on select NASCAR and Cincinnati sports memorabilia. All donations will benefit research through the Cincinnati Children's Hospital Medical Center. As you may already know, each donation is tax deductible to the extent allowed by law. Please register for the event through the foundation website and secure your spot at this one time event. </b></strong></div><div style="text-align: center;"><strong><b> </b></strong><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-15994535128500020652011-06-06T10:09:00.000-04:002011-06-16T08:37:34.706-04:00Even the Royals are not Immune<div><div style="text-align: center;"><strong>Princess Eugenie, the younger child of Prince Andrew and the original Fergie, endured a lengthy surgery to place pins on her spine to correct scoliosis when she was 12 years old. She is an inspiration for those following her and those preparing for treatment against this condition. </strong></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong>The full article can be read at <a href="http://www.usmagazine.com/healthylifestyle/news/princess-eugenie-i-had-8-hour-surgery-at-age-12--201126">http://www.usmagazine.com/healthylifestyle/news/princess-eugenie-i-had-8-hour-surgery-at-age-12--201126</a></strong></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-36523025687741519502011-06-03T14:58:00.001-04:002011-06-03T14:58:59.613-04:00JUNE IS NATIONAL SCOLIOSIS AWARENESS MONTH<div style="text-align: center;"><strong>Since 2008, when the NSF and the government declared June as <a href="http://sites.google.com/site/wwwscoliosisorgawareness/2009-nsam-campaign-overview">National Scoliosis Awareness Month</a>, the programs involved in this awareness has grown significantly. Please take some time to look at our website, become acquainted with the various types of scoliosis, and take action in the fight to find a cure for this condition! Your help is vital in making progress towards a cure and The Scoliosis Foundation thanks you for your help!!!</strong></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-56140834754948677562011-06-02T15:07:00.000-04:002011-06-02T15:07:40.617-04:00New Blog Site<div style="text-align: center;"><strong>Due to Yahoo! discontinuing their blog service at Yahoo! Pulse, I have moved the blog website to </strong><a href="http://scoliosisfoundation.blogspot.com/"><strong>http://scoliosisfoundation.blogspot.com/</strong></a><strong> . I have moved over all of the previous blogs and will use this trusted site from now on. Please feel free to re-read the previous posts and follow my blog in the future. Thanks for your continued support!</strong></div><div style="text-align: center;"><strong><br />
</strong></div><div style="text-align: center;"><strong>Please visit </strong><a href="http://www.thescoliosisfoundation.org/"><strong>http://www.thescoliosisfoundation.org/</strong></a><strong> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-78767997929412057622011-06-02T14:48:00.000-04:002011-06-02T14:48:48.532-04:00When It Hit Home.....<div style="text-align: center;"><span style="text-decoration: underline;"><span style="color: #0000bf; font-size: xx-small;"><strong>As previously posted on May 18, 2011 on original blog</strong></span></span></div><div style="text-align: center;"><br />
</div><div style="text-align: center;">A little while ago, Aiden starting complaining about how his 13th Mehta cast was hurting him. Through his crying and whimpering, the triage on the open wounds caused by the rubbing of his skin against the cast, and the obvious size constraint, Amber and I didn't know what to do at this point. We called Dr. Peter Sturm at Cincinnati Children's Hospital Medical Center (CCHMC) and his nurses agreed to get us in right away. In the past, we would wait to get into CCHMC and only see the nurses. However, this time, Aiden was able to see the nurses, radiology technicians, surgery technicians, AND the doctor. They all agreed the cast was too tight and hurting Aiden, but made the choice to keep it on until his June appointment (his regular visit where he will have the cast taken off and degree curve measured). They broke the cast around the belly hole and re-petaled the rough edges so they didn't hurt him as much. Through all of this, Aiden showed remarkable strength. It was not until that night that our last 4 1/2 years really hit home for me. <br />
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Aiden and I were sitting on the couch and I was looking at his cast. I kept on saying how good it looked and repeatedly asked how it felt to him. Aiden began to tear up and looked down at the floor. I asked him what was wrong. For the first time in his entire treatment, he looked at me with tears in his eyes and "Daddy, I don't ever want to have a cast again!". We talked about how he has had many casts but he told me how he was sick of getting them and didn't want anymore. Amber and I are very frank with our children, so I told him that what would happen if he didn't get the casts. After a brief pause, he said, "It's ok daddy, we will be ok without a cast."<br />
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I couldn't help but grab him and hold him. Even knowing the negative consequences, he had finally hit the wall with his treatment. Aiden never complained one bit, but now, he was willing to take a serious gamble with his health in order to gain relief. It was difficult and eye opening, but long overdue. With everything he has had to endure, Aiden always showed strength. Now, he looked to his parents for comfort and relief. We explained how it wouldn't be long before he got it off and he seemed to find solace in our approach for the time being. <br />
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Amber and I know there are parents out there who endure daily struggles with their children. There are some of these parents who endure much more than we could imagine. Some of them are sources of strength for us to deal with Aiden's treatment. For all of you that have to deal with adversity, we thank you for your strength and courage!!! We wish you the best of luck in all future treatment. Just remember, there will be a time when every aspect of your child's condition will hit home, and when it does, embrace it. Be honest, be strong, and be diligent! Your child will always be your child, so cherish every moment, even when it is difficult!<br />
</div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-12103501691523201812011-06-02T14:47:00.000-04:002011-06-02T14:47:00.111-04:001st Annual 'Sprint for Spines' 5K Run / Walk - SIGN UP TODAY!.<div style="text-align: center;"><span style="text-decoration: underline;"><span style="color: #0000bf; font-size: xx-small;"><strong>As previously posted on May 6, 2011 on original blog</strong></span></span></div><div style="text-align: center;"><br />
</div><div class="MsoNormal" style="text-align: center;"><span class="text"><span style="font-family: Garamond; font-size: 14pt;"><span style="color: black;">We cordially invite you to participate in <strong>The Scoliosis Foundation’s 1st Annual ‘Sprint for Spines’ 5k Run / Walk</strong> on <strong>Saturday, June 25, 2011</strong> at <strong>Kestrel Point @ Winton Woods Park</strong>.</span></span></span><span style="font-family: Garamond; font-size: 14pt;"><br />
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<span style="color: black;"><span class="text">Your entry fee will be used in an ongoing effort to help find a cure for scoliosis. Your fee will cover your race entry, race t-shirt, refreshments, event </span><span class="text">activities, and official scoring. There will also be awards for the top winners </span><span class="text">in each division. The participant fee for each runner / walker is $25. There </span><span class="text">are additional prizes for reaching one of the fundraising milestones listed on </span><span class="text">the information sheet. ALL proceeds will directly benefit The Scoliosis </span><span class="text">Foundation.</span><br />
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<span class="text">You will receive your official participant number for the event via email one </span><span class="text">week prior to the event.</span><br />
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<span class="text">You can register via phone, email, online form submission or mail and payments can be made by check or online submission. You can also register </span><span class="text">to race on the day of the event. If you choose to register on the day of the </span><br />
<span class="text">event, the entry fee will be $30 per participant. To register online, please visit </span></span></span><span class="text"><span style="font-family: Garamond; font-size: 14pt;"><span style="color: windowtext;"><span style="color: #4f93df;"><a href="http://www.sprunning.com/register.html">www.sprunning.com/register.html</a></span></span><span><span style="color: black;"> and find The Scoliosis Foundation's event </span></span></span></span><span style="font-family: Garamond; font-size: 14pt;"><span style="color: black;"><span class="text">and click register.</span><br />
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<span class="text"><span style="text-decoration: underline;">Your registration fee is tax-deductible.</span></span></span></span></div><div class="MsoNormal" style="text-align: center;"><span class="text"><span style="text-decoration: underline;"><span style="font-family: Garamond; font-size: 14pt;"><span style="text-decoration: none;"><span style="color: black;"></span></span></span></span></span></div><span style="font-family: Garamond; font-size: 14pt;"><span style="color: black;"><div class="MsoNormal" style="text-align: center;"><br />
<strong><span style="text-decoration: underline;">Registration Information</span></strong></div><div class="MsoNormal" style="text-align: center;"><br />
</div><div class="MsoNormal" style="text-align: center;"><span style="color: black;"><span class="text"><span style="font-family: Garamond; font-size: 14pt;"><strong>The Scoliosis Foundation's 'Sprint for Spines' 5K Run / Walk</strong> will be coordinated and monitored by Steve Prescott Race Coordination. The online registration will be conducted by Steve Prescott and payments can be made via secured online payment submission at <span class="text"><span style="font-family: Garamond; font-size: 14pt;"><span style="color: windowtext;"><span style="color: #4f93df;"><a href="http://www.sprunning.com/register.html">www.sprunning.com/register.html</a></span></span></span></span></span><span class="text"><span style="font-family: Garamond; font-size: 14pt;"><span>. If you choose to fill out the form and mail in the registration, please send form and check made payable to The Scoliosis Foundation to:</span></span></span></span></span> </div><div class="MsoNormal" style="text-align: center;"><br />
</div><div class="MsoNormal" style="text-align: center;"><span class="text"><span style="font-family: Garamond; font-size: 14pt;"><span style="color: black;"><strong>The Scoliosis Foundation</strong></span></span></span><span style="color: black;"><strong><span class="text"><span style="font-family: Garamond; font-size: 14pt;"><br />
PO Box</span></span><span class="text"><span style="font-family: Garamond; font-size: 14pt;"> 31158</span></span></strong></span></div><div class="MsoNormal" style="text-align: center;"><span style="color: black;"><span class="text"><span style="font-family: Garamond; font-size: 14pt;"><strong>Cincinnati, OH 45231<br />
</strong></span></span></span><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div></div></span></span>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com1tag:blogger.com,1999:blog-4954078438646101767.post-33472303444544640982011-06-02T14:45:00.002-04:002011-06-02T14:47:16.559-04:00Another New DNA Genetic Test That Benefits Scoliosis Patients.<div style="text-align: center;"><span style="text-decoration: underline;"><span style="color: #0000bf; font-size: xx-small;"><strong>As previously posted on April 27, 2011 on original blog</strong></span></span></div><br />
<div class="MsoNormal"><span style="font-family: Times New Roman; font-size: small;">What if you could test DNA from a saliva sample of a scoliosis patient and determine, with clear cut fact, the best course of treatment for him/her? The day has come for this dream to become a reality! </span></div><div class="MsoNormal"><br />
</div><div class="MsoNormal"><span style="font-family: Times New Roman; font-size: small;">Ten years in the making, ScoliScore is a newer DNA genetic test that does just what it is supposed to do. By testing DNA in the saliva of any scoliosis patient, it can determine, through high or low scores, the probability that the current degree curvature will become better or worse over time. This information is vital to treating scoliosis patients because it accurately assesses the need for x-rays, braces, casting, and/or surgery. </span></div><div class="MsoNormal"><br />
</div><div class="MsoNormal"><span style="font-family: Times New Roman; font-size: small;">By limiting x-rays, the patient is subjected to less radiation and health concerns from the procedures. The doctors using this test take the guesswork out of the treatment plans given to scoliosis patients and base them on clear cut facts. The genetic testing used is complicated and involved, yet becoming more and more widespread due to its significance in scoliosis treatment. </span></div><div class="MsoNormal"><br />
</div><div class="MsoNormal"><span style="font-family: Times New Roman; font-size: small;">Dr. Mark Locke, Director of Pediatric Orthopedics at Moore Orthopedic Clinic, loves the new test. He discussed the impact of the test on diagnosing treatment options for scoliosis patients. He gives an example of how a scoliosis patient with a 15 degree curve who has a high test score will eventually have that curve increase exponentially. Conversely, if the test had come back with a lower score, the curvature would remain the same. In general, a high test score indicates the curve will increase in degree measurement where a low score indicates the curvature will remain low. </span></div><div class="MsoNormal"><br />
</div><div class="MsoNormal"><span style="font-family: Times New Roman; font-size: small;">The ScoliScore DNA genetic test is another example of how advancements in medicine can benefit scoliosis patients and their treatment options. This line of medicine needs more advancements similar to this DNA test in order to gain ground on this debilitating condition. The information contained in this post came from </span><span style="color: purple; font-family: Times New Roman; font-size: small;"><a href="http://www.midlandsconnect.com/news/video.aspx?list=195149&id=577018">http://www.midlandsconnect.com/news/video.aspx?list=195149&id=577018</a></span><span style="font-family: Times New Roman; font-size: small;">. </span></div><div class="MsoNormal"><br />
</div><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-87385231494758429412011-06-02T14:43:00.000-04:002011-06-02T14:43:31.576-04:00ATTENTION ALL NASCAR FANS.<div style="text-align: center;"><span style="text-decoration: underline;"><span style="color: #0000bf; font-size: xx-small;"><strong>As previously posted on April 22, 2011 on original blog</strong></span></span></div><br />
<div align="center" style="text-align: center;">The Scoliosis Foundation is preparing to offer a special viewing of the movie "Petty Blue" (about the life of Richard Petty and his family) with special guest Mike Viney. Mike Viney is the Director of the movie and his resume includes:</div><div style="text-align: center;"><span style="text-decoration: underline;">CREDITS </span></div><div style="text-align: center;">Director -<em> Petty Blue</em> (CMT, 2010)<br />
Director - Demons For Angels (Narrative Short, 2008)<br />
Director - <em>Chasing Sunday</em> (FOX, 2007)<br />
Director/Editor - <em>Dale</em> (CMT, 2007)</div><div style="text-align: center;">Show Head/Senior Producer - <em>NASCAR Hot Wired</em> (Speed, 2010)<br />
Senior Producer - <em>NASCAR Confidential</em> (Speed, 2008)<br />
Senior Producer - <em>Road To Daytona</em> (ABC, 2008)<br />
Show Head/Senior Producer - <em>NASCAR: Chasing Glory</em> (ESPN2, 2007)<br />
Senior Producer - <em>Beyond The Wheel</em> (Speed, 2005-6)<br />
Producer - <em>Hey Rookie, Welcome To The NFL</em> (FOX, 2004-5)<br />
Segment Producer - <em>NFL Films Presents</em> (ESPN2, 2004)<br />
Segment/Field Producer - <em>NFL Under The Helmet</em> (FOX, 2003-4)<br />
Producer - <em>3 Games To Glory I, II, III</em> (DVD, 2002, 4-5) <br />
Associate Producer - <em>Hard Knocks: Dallas Cowboys</em> (HBO, 2002)</div><div style="text-align: center;"><span style="text-decoration: underline;">AWARDS &amp;amp; NOMINATIONS</span></div><div style="text-align: center;">EMMY Nominee, Outstanding Sports Documentary - <em>Dale</em> (2007)<br />
EMMY Winner, Outstanding Live Event Turnaround - <em>Beyond The Wheel</em> (2006)<br />
EMMY Nominee, Outstanding Live Event Turnaround - <em>Beyond The Wheel</em> (2005)<br />
EMMY Nominee, Outstanding Sports Series - <em>Hard Knocks: Dallas Cowboys </em>(2002)<br />
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There will be a a short update on the foundation and then the movie. There will be time after the movie to ask Mike some questions on what it was like to work with Richard Petty, the Earnhart family, and countless other drivers and celebrities. Mike will be coming up to Cincinnati from Charlotte for the NASCAR Race in July at Kentucky Speedway. There will be limited seating so check back at <span style="color: #4f93df;">www.thescoliosisfoundation.org</span> for more information.<br />
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<span style="font-size: 9px;">All credits and references taken from </span><span style="color: #4f93df; font-size: 9px;"><a href="http://www.mikeviney.com/">http://www.mikeviney.com/</a></span></div><div style="text-align: center;"><br />
</div><div style="text-align: center;"><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-76896880114697733482011-06-02T14:39:00.000-04:002011-06-02T14:39:46.615-04:00Recent Scoliosis News at Cincinnati Children's Hospital<strong></strong><strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong> <div style="text-align: center;"></div><br />
<div style="text-align: center;"><span style="text-decoration: underline;"><span style="color: #0000bf; font-size: xx-small;"><strong>As previously posted on April 12, 2011 on original blog</strong></span></span><br />
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<strong><span style="text-decoration: underline;">Dr. Peter Sturm Joins CCHMC</span></strong><br />
Dr. Peter Sturm, recently named The Alvin H. Crawford Chair of Spine Surgery and Co-Director, Crawford Spine Center, came to Cincinnati Children's Hospital Medical Center (CCHMC) after leading the Shriner's Hospital in Chicago, IL. He brings with him decades of service to orthopedics and specifically, scoliosis. He was trained under the infamous Dr. Min H. Mehta (the Mehta cast is named after her) on specialized casting for infantile scoliosis. Dr. Sturm brings a wealth of knowledge to the Orthopedic Department already known for its advances in medicine. Dr. Sturm is an advocate for casting as an alternative to spinal fusion surgery which can hamper spinal development in children. His work in this area will continue as he is the lead investigator on a multi-center study regarding this issue. <br />
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<strong><span style="text-decoration: underline;">HemiBridge Spinal Clip</span></strong><br />
The HemiBridge Spine Clip, a 2 inch square device, is a breakthrough in scoliosis treatment created by Dr. Eric Wall. A medical device 17 years in the making, the HemiBridge Spine Clip is a plastic square that promotes straighter growth by using the power of the spine in correcting a curvature. This device controls the growth in each vertebrae and acts as a counter device for scoliosis. The HemiBridge Spine Clip was just granted FDA approval for Phase I clinical trial. “It’s the only current FDA-approved study of a class 3 pediatric orthopedic device of any sort,” Wall says. “We’ve now got approval to start using it in humans.”<br />
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CCHMC continues to make advances in the field of scoliosis research. These doctors, along with the other fantastic doctors and support staff at CCHMC, make scoliosis treatment more bearable and practical. Please visit www.thescoliosisfoundation.org for more information regarding scoliosis and ways to help out the cause of finding a cure. <br />
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Full Article from <a href="http://www.cchmc.org/">Cincinnati Children's Hospital Medical Center</a><br />
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</div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0tag:blogger.com,1999:blog-4954078438646101767.post-64122498330600696422011-06-02T14:32:00.003-04:002011-06-02T14:37:03.379-04:00Stacy Lewis - Scoliosis Patient and America's Next Great Golfer<div style="text-align: center;"><span style="text-decoration: underline;"><span style="color: #0000bf; font-size: xx-small;"><strong>As previously posted on April 4, 2011 on original blog</strong></span></span></div><br />
<div style="text-align: center;"><span style="color: red; font-size: 21px;"><span style="text-decoration: underline;"></span></span>Stacy Lewis is an inspiration to everyone from little girls, female athletes, and female golfers to scoliosis patients, surgery patients, and those afflicted with conditions affecting their passions in life. Stacy's just recently won her first LPGA event at the Kraft Nabisco tournament. She is a source of inspiration for any scoliosis patient, but more importantly, to anyone looking for a way to overcome adversity in their life. Congratulations to Stacy Lewis. <br />
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<a href="http://stacysback.com/">Article reporting on Stacy's 1st LPGA Win</a><br />
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<a href="http://stacysback.com/bio.php">Biography of Stacy Lewis - an Inspirational Story </a><br />
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<strong>Please visit <a href="http://www.thescoliosisfoundation.org/">http://www.thescoliosisfoundation.org/</a> for more information.</strong></div>The Scoliosis Foundationhttp://www.blogger.com/profile/03269775690155674335noreply@blogger.com0