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	<title>Medical blog &#187; first</title>
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	<description>Medical News and Health Information</description>
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		<title>Children’s health care bill expected to be one of Obama&#039;s first &#8230;</title>
		<link>http://www.raganvirtualworkshops.com/15628.php4</link>
		<comments>http://www.raganvirtualworkshops.com/15628.php4#comments</comments>
		<pubDate>Sun, 04 Jan 2009 18:42:24 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[bill]]></category>
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		<description><![CDATA[WASHINGTON &#8211; Congressman Mike Thompson (D-CA) last week joined a majority in the House of Representatives in support of bipartisan legislation to provide health care to 11 million children from working families.
 The Children&#8217;s Health Insurance Program Reauthorization Act (H.R. 2) was approved by a vote of 289-139.
 The bill is very similar to the [...]]]></description>
			<content:encoded><![CDATA[<p>WASHINGTON &ndash; Congressman Mike Thompson (D-CA) last week joined a majority in the House of Representatives in support of bipartisan legislation to provide health care to 11 million children from working families.<br />
 The Children&rsquo;s Health Insurance Program Reauthorization Act (H.R. 2) was approved by a vote of 289-139.<br />
 The bill is very similar to the legislation that President Bush vetoed twice in the 110th Congress.<br />
 &ldquo;Investing<span id="more-15628"></span> in children&rsquo;s health care is one of the wisest choices our federal government can make,&rdquo; Thompson said during a speech on the House of Representatives floor. &ldquo;Children have to be healthy to get an education and achieve their full potential as adults. When kids see the doctor more regularly, they receive the preventive services that keep them healthier longer &ndash; and they are less likely to end up in the emergency room, which saves everyone money.&rdquo;<br />
 Thompson said almost a million and a quarter children in California are uninsured, which he called &ldquo;simply unacceptable.&rdquo;<br />
 He said that, in contrast to President Bush&rsquo;s multiple vetoes of similar bills, President-elect Obama gave his enthusiastic support to providing coverage for 4 million additional children. &ldquo;That is truly change we can believe in,&rdquo; Thompson said.<br />
 SCHIP was created in 1997 to provide health care coverage for children in families that earn too little to afford health insurance for their children but too much to qualify for Medicaid.<br />
 The bill passed last week by the House of Representatives reauthorizes SCHIP through 2013 and preserves the coverage for all 7.1 million children currently covered by SCHIP, including 1,538,416 children in California.<br />
 Thompson&#39;s office has previously estimated that 1,600 Lake County children will receive coverage under the legislation.<br />
 The bill also extends health care coverage to 4.1 million additional low-income children, who are currently uninsured. The bill is fully paid for.<br />
 This bipartisan bill has been endorsed by dozens of organizations, representing millions of Americans &ndash; ranging from business groups such as the National Federation of Independent Businesses and Business Roundtable to the American Hospital Association, AARP and Families USA.</p>
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		<title>FDA Approves First Gout Drug For 40 Years</title>
		<link>http://www.raganvirtualworkshops.com/19738.php4</link>
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		<pubDate>Wed, 24 Dec 2008 16:16:06 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[Approves]]></category>
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		<category><![CDATA[Gout]]></category>
		<category><![CDATA[years]]></category>

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		<description><![CDATA[The US Food and Drug Administration has given marketing approval to a new drug that lowers levels of uric acid in the blood of patients with
gout: the current treatment for the condition was developed over 40 years ago.  The new drug is called ULORIC (generic name febuxostat) and Takeda
Pharmaceuticals North America is the sole [...]]]></description>
			<content:encoded><![CDATA[<p>The US Food and Drug Administration has given marketing approval to a new drug that lowers levels of uric acid in the blood of patients with<br />
gout: the current treatment for the condition was developed over 40 years ago.  The new drug is called ULORIC (generic name febuxostat) and Takeda<br />
Pharmaceuticals North America is the sole developer and marketer of the product in the US.<br />
 According to a statement from Takeda, febuxostat is a new highly potent<span id="more-19738"></span> non-purine selective inhibitor of xanthine oxidase, and has a completely<br />
different structure from the currently used xanthine oxidase inhibitor, which was developed over 40 years ago.  Xanthine oxidase is an enzyme<br />
involved in the production of uric acid.<br />
 Febuxostat lowers the concentration of uric acid in the blood of hyperuricemic patients with gout.  The drug has been proved to be safe and effective<br />
in clinical trials, and the dose does not need to be adjusted for patients with mild-to-moderate renal or hepatic impairment (kidney or liver<br />
problems).<br />
 ULORIC will be available as 40 mg or 80 mg tablets to be taken once a day.  It is not recommended for asymptomatic hyperuricemia, said the<br />
company&#8217;s press release.<br />
 Febuxostat was discovered by another Japanese company, Teijin Pharma.  Their president Osamu Nishikawa said in a press statement released jointly<br />
with Takeda that:<br />
 &#8220;This FDA approval granted to Takeda Pharmaceuticals North America, along with the EMEA (European Medicines Agency) approval given last year<br />
to Ipsen, our licensee for febuxostat in Europe, marks a significant milestone for our global business.&#8221;<br />
 He said Teijin  would be developing febuxostat themselves for the Asian market, as well as collaborating with other pharma companies.  The company<br />
wishes to strengthen its global operations by &#8220;expanding areas where febuxostat is available and increase the presence of the product to be widely used<br />
by patients worldwide,&#8221; he added.<br />
 President of the Takeda parent company in Japan, Yasuchika Hasegawa, said:<br />
 &#8220;The approval of ULORIC offers patients and healthcare providers in the US for the first time in 40 years, a novel treatment option for patients who<br />
have hyperuricemia with gout, where there are still unmet clinical needs.&#8221;<br />
 Gout is a common, painful form of arthritis that causes swollen, red, hot and stiff joints. It occurs when uric acid builds up in the blood,<br />
because the body produces too much or can&#8217;t get rid of it (some medications can slow down elimination), or from eating too many foods rich in<br />
purines, such as liver and dried beans.<br />
 Pseudogout  is sometimes confused with gout because the symptoms are similar; however, it is caused by calcium phosphate, not uric acid.<br />
 According to the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), there could be as many as 6 million Americans aged<br />
20 and older who have had gout at some time in their lives.  It is more common in men aged 40 to 50, and women rarely develop it before the<br />
menopause.  Also people who have had an organ transplant are more susceptible.<br />
 NIAMS suggest people may be at risk of developing hyperuricemia and gout if they are on certain medications, these include:<br />
 Diuretics, such as furosemide (Lasix1), hydrochlorothiazide (Esidrix, Hydro-chlor), and metolazone (Diulo, Zaroxolyn).<br />
 Drugs containing salicylate, such as aspirin.<br />
 Niacin, a vitamin also known as nicotinic acid.<br />
 Cyclosporine (Sandimmune, Neoral), a medication used to suppress the immune system.<br />
 Levodopa (Larodopa), a drug used in the treatment of Parkinson&#8217;s disease..<br />
 Takeda Pharmaceuticals North America, Inc, whose head office is in Deerfield, Illinois, is a wholly owned subsidiary of Takeda Pharmaceutical<br />
Company Limited whose head office is in Chuo-ku, Osaka, Japan.<br />
 Sources: Takeda Pharmaceutical Company Limited press release, NIAMS.<br />
 Written by: Catharine Paddock, PhD<br />
 For any corrections of factual information, or to contact the editors please use our<br />
 .</p>
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		<title>Safety first, for food and drugs</title>
		<link>http://www.raganvirtualworkshops.com/17667.php4</link>
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		<pubDate>Tue, 16 Dec 2008 01:24:00 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Drugs]]></category>
		<category><![CDATA[first]]></category>
		<category><![CDATA[Food]]></category>
		<category><![CDATA[safety]]></category>

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		<description><![CDATA[
With the peanut butter scare making news — the latest in a series involving salmonella-contaminated foods including tomatoes, jalapeno peppers and E. coli-contaminated spinach — there again rises the public clamor for doing something.
 In the not distant past, studies have confirmed that the people reasonably enough are very much concerned about the safety of [...]]]></description>
			<content:encoded><![CDATA[<p><object width="425" height="355"><param name="movie" value="http://www.youtube.com/v/sHzdsFiBbFc&#038;rel=1"></param><param name="wmode" value="transparent"></param><embed src="http://www.youtube.com/v/sHzdsFiBbFc&#038;rel=1" type="application/x-shockwave-flash" wmode="transparent" width="425" height="355"></embed></object></p>
<p>With the peanut butter scare making news — the latest in a series involving salmonella-contaminated foods including tomatoes, jalapeno peppers and E. coli-contaminated spinach — there again rises the public clamor for doing something.<br />
 In the not distant past, studies have confirmed that the people reasonably enough are very much concerned about the safety of the food they eat.<br />
 Only government has the expertise and authority to do something<span id="more-17667"></span> about it. Food producers who are by tradition and lack of federal resources mainly relied upon to monitor themselves fall short, as the record demonstrates.<br />
 The Food and Drug Administration oversees some 80 percent of America&#8217;s food supply, excluding meat, poultry and processed egg products. As its name makes plain, it is also the overseer of the nation&#8217;s medical supplies.<br />
 As the peanut butter brouhaha was gathering force, the General Accountability Office, the investigative arm of Congress, put medical products on their High-Risk List on Jan. 22.<br />
 While Americans ponder whether in the face of 500 illnesses and eight deaths to continue to send their kids off to school with the popular peanut butter and jelly sandwiches, or if they should go on nibbling on cookies and other goodies containing peanut paste, they should be no less wary about the medicinal pills they are ingesting in ever increasing quantities. Placement on the High-Risk List was earned because &#8220;the American consumer may not be adequately protected from unsafe and ineffective medical products&#8221; resulting in part from &#8220;the globalization of the medical products industry.&#8221;<br />
 In the recent past you might recall when consumers, allied with state governments that helped them pay for needed drugs, wanted to import drugs from Canada and elsewhere at a much lower cost.<br />
 Among the arguments in opposition put forward by the pharmaceutical industry was that their products were American made and therefore safe.<br />
 Neglected by Pharma, surely by oversight, is that for years U.S. drug makers were importing ingredients for their pills that were made in America. And, you might well ask, where from did those ingredients come? The answer, of course, is the country that makes a host of lower-cost products, namely China, now the world&#8217;s dominant supplier of medicinal ingredients.<br />
 Yes, folks, that&#8217;s the same China that recently sentenced two of its citizens to death for purveying milk and milk products adulterated with melamine. Melamine is a toxic chemical that can cause cancer and renal failure, among other dire illnesses. It was inserted into baby formula to disguise the fact that the milk had been watered and to give it the appearance of a higher protein value. It caused at least six deaths and some 300,000 illnesses in China.<br />
 In the U.S., it led to a clampdown by the FDA that imposed new testing to keep tainted products out of our country. Melamine has also been detected in more than a dozen countries in eggs, yogurt, chocolates and frozen desserts.</p>
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		<title>First child fatality resulting from it in state this winter</title>
		<link>http://www.raganvirtualworkshops.com/20042.php4</link>
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		<pubDate>Sat, 13 Dec 2008 21:26:54 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Health]]></category>
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		<category><![CDATA[child]]></category>
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		<category><![CDATA[Winter]]></category>

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		<description><![CDATA[A 12-year-old  Boston Latin Academy student died over the weekend from complications of the flu, Boston school and public health officials confirmed yesterday, one of only a handful of deaths nationwide so far this flu season.
 Hunter Pope was a seventh-grader  at the school, according to a statement from the city&#8217;s school system. [...]]]></description>
			<content:encoded><![CDATA[<p>A 12-year-old  Boston Latin Academy student died over the weekend from complications of the flu, Boston school and public health officials confirmed yesterday, one of only a handful of deaths nationwide so far this flu season.<br />
 Hunter Pope was a seventh-grader  at the school, according to a statement from the city&#8217;s school system. He is the first Massachusetts child known to have died of the flu this winter.<br />
 Dr. Anita Barry, director of the infectious<span id="more-20042"></span> disease bureau for the Boston Public Health Commission, said yesterday that the boy&#8217;s death is still being investigated, but  there was no evidence he had serious health conditions or was suffering from another infection that would heighten his risk.<br />
 Last winter four children in Massachusetts died of the flu, including two who had simultaneous infections with methicillin-resistant staphylococcus aureus, or MRSA, a bacterial infection to which people are more vulnerable when they have the flu. MRSA can be lethal because many antibiotics are powerless against it.<br />
 Health officials also did not know yet  whether Pope had been vaccinated against the flu.<br />
 This was the first flu season for which the US Centers for Disease Control and Prevention recommended that all children over 6 months old get flu shots.<br />
 &#8220;It&#8217;s tragic when a child dies, but to put it in context, it&#8217;s not a frequent event,&#8221; said Dr. Alfred DeMaria, director of Communicable Disease Control at the state Department of Public Health. &#8220;It&#8217;s not something that we see a lot of cases  &#8211; one to two a year.&#8221;<br />
 The boy&#8217;s death adds to this season&#8217;s nationwide child flu death toll that, as of Feb. 7, stood at four. No more recent statistics were available yesterday.<br />
 &#8220;We are extremely saddened by this news,&#8221; School Superintendent Carol R. Johnson said in a statement. &#8220;Our thoughts and prayers are with the Pope family, and with the entire Boston Latin Academy community, during this difficult time.&#8221;<br />
 A letter is being sent home to families of Boston Latin Academy students, expressing sorrow  and urging parents to get flu shots for their children.<br />
 When classes resume Monday after this week&#8217;s vacation, counselors will be available for students and staff.<br />
 State and national disease trackers began counting flu deaths in children after 153 children died in the 2003-2004 flu season. Since then, one child in Massachusetts died in 2005-2006, one child who was not a resident died here in 2006-2007, and four children in the state died last winter.<br />
 Across the country, 83 children died from flu last winter, according to the CDC.<br />
 Flu season, which can stretch into April, is climbing toward its peak statewide, with 1,229 cases reported for the week ending Feb. 7, up from 725 the week before.<br />
 Health specialists say that hand-washing, covering up when one coughs, and staying home with the flu can help reduce spread of the illness.<br />
 Barry of the Boston Public Health Commission recommended calling a healthcare provider if a person has the following symptoms: breathing problems; difficulty keeping fluids down; a fever that will not come down after taking drugs such as acetaminophen;  appearing to get better only to see a fever go up again, which might indicate a secondary infection such as pneumonia;  a change in mental status; and  underlying conditions such as heart problems, or lung conditions illnesses, including asthma.<br />
 &#8220;People should take care not to transmit it if they have it, and not to get it if they can avoid it,&#8221; DeMaria said.<br />
 .</p>
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		<title>FDA Panel Gives Blessing to First Drug Manufactured in &#8230;</title>
		<link>http://www.raganvirtualworkshops.com/14447.php4</link>
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		<pubDate>Wed, 10 Dec 2008 05:50:43 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[blessing]]></category>
		<category><![CDATA[Drug]]></category>
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		<category><![CDATA[Panel]]></category>

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		<description><![CDATA[,
 ,
 The first drug ever manufactured in genetically-modified animals is likely coming soon to the U.S. market. A panel of expert advisers to the FDA
 that an experimental anti-clotting product developed by Framingham, MA-based GTC Biotherapeutics looks safe and effective enough to become a marketed product.
 , based on documents that were made publicly [...]]]></description>
			<content:encoded><![CDATA[<p>,<br />
 ,<br />
 The first drug ever manufactured in genetically-modified animals is likely coming soon to the U.S. market. A panel of expert advisers to the FDA<br />
 that an experimental anti-clotting product developed by Framingham, MA-based GTC Biotherapeutics looks safe and effective enough to become a marketed product.<br />
 , based on documents that were made publicly available Wednesday morning. The FDA still hasn&#8217;t made a final decision; its deadline<span id="more-14447"></span> for doing so is Feb. 7.<br />
 The product in question, a human protein called antithrombin, is isolated from the milk of goats who have been genetically modified to produce copious amounts of the protein. The drug, marketed as ATryn, has been cleared for sale in Europe since 2006. It hasn&#8217;t been a financial boon for GTC, but the company hopes that winning this FDA panel blessing will set a precedent that its manufacturing method, sometimes called &#8220;pharming,&#8221; can be used for other, more profitable medicines.<br />
 who will now gear up in hopes of marketing the drug.<br />
 &#8220;We are very pleased with the Advisory Committee&#8217;s recommendation,&#8221; said Geoffrey Cox, CEO of GTC Biotherapeutics, in a statement after the panel&#8217;s recommendation.<br />
 Pharming&#8217;s appeal,<br />
 , comes from its ability to churn out large quantities of protein drugs in a cheap way. Scientists already know how to make genetically engineered protein drugs through fermentation-style techniques using standard lab organisms like E. coli, yeast, or hamster cells, although these methods are more costly and time-consuming than milking a goat.<br />
 GTC was able to successfully point out that all protein drugs have to go through a rigorous purification process to separate the drug from all the gunk it brews with. Since they proved the end product is pure and consistent, who cares if it came from a modified goat?<br />
 Luke Timmerman is the National Biotechnology Editor for Xconomy. You can email him at ltimmerman@xconomy.com or call 206-624-2374.</p>
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		<title>Updated 1/5: Resurrection Medical Center&#039;s first baby is from Des &#8230;</title>
		<link>http://www.raganvirtualworkshops.com/13738.php4</link>
		<comments>http://www.raganvirtualworkshops.com/13738.php4#comments</comments>
		<pubDate>Sat, 06 Dec 2008 08:25:39 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Family Health]]></category>
		<category><![CDATA[Medical Stories]]></category>
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		<category><![CDATA[Updated]]></category>

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		<description><![CDATA[The first baby born in 2009 at Resurrection Medical Center, 7435 W. Talcott Ave., Chicago, is a girl &#8212;  7-pound 13-ounce Julia Oleksy. She was delivered by Dr. Steven Bujewski, an obstetrician/gynecologist.
 Julia&#8217;s official arrival time was shortly after midnight &#8212;  at 12:39 a.m. Jan. 1. She is the first child of Joanna [...]]]></description>
			<content:encoded><![CDATA[<p>The first baby born in 2009 at Resurrection Medical Center, 7435 W. Talcott Ave., Chicago, is a girl &#8212;  7-pound 13-ounce Julia Oleksy. She was delivered by Dr. Steven Bujewski, an obstetrician/gynecologist.<br />
 Julia&#8217;s official arrival time was shortly after midnight &#8212;  at 12:39 a.m. Jan. 1. She is the first child of Joanna Kosmowska and Krzysztof Oleksy, of Des Plaines. The couple&#8217;s extended family members live in Poland.<br />
 To welcome the new arrival,<span id="more-13738"></span> Resurrection assembled a gift bag containing onesies, a blanket, bibs and toys. The gifts were presented to Julia&#8217;s mother, said Evelyn O&#8217;Connor, public relations manager.</p>
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		<title>eDiets.com(R) and Lady of America Fitness Centers Complete First &#8230;</title>
		<link>http://www.raganvirtualworkshops.com/20935.php4</link>
		<comments>http://www.raganvirtualworkshops.com/20935.php4#comments</comments>
		<pubDate>Tue, 02 Dec 2008 09:54:27 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Health]]></category>
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		<category><![CDATA[America]]></category>
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		<category><![CDATA[lady]]></category>

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		<description><![CDATA[eDiets.com(R) and Lady of America Fitness Centers Complete First Phase of Meal Delivery Marketing Program
 FORT LAUDERDALE, Fla., Feb. 24 /PRNewswire-FirstCall/ &#8211;
 eDiets.com, Inc.
    (NASDAQ: DIET)
  ,
 a leading provider of convenient at-home diet, fitness and healthy lifestyle solutions, today announced that it has completed the first phase of its marketing [...]]]></description>
			<content:encoded><![CDATA[<p>eDiets.com(R) and Lady of America Fitness Centers Complete First Phase of Meal Delivery Marketing Program<br />
 FORT LAUDERDALE, Fla., Feb. 24 /PRNewswire-FirstCall/ &#8211;<br />
 eDiets.com, Inc.<br />
    (NASDAQ: DIET)<br />
  ,<br />
 a leading provider of convenient at-home diet, fitness and healthy lifestyle solutions, today announced that it has completed the first phase of its marketing program to promote the Company&#8217;s fresh meal delivery service at Lady of America Franchise<span id="more-20935"></span> Corporation&#8217;s (&#8220;LOAFC&#8221;) fitness centers.<br />
 This first phase included rolling out the meal delivery program to the entire LOAFC franchise system, providing training to many of the largest and most successful LOAFC fitness centers and working with the leaders of the franchise system to optimize the success of the program.<br />
 Phase 2 of the planned rollout is now underway.  This phase consists of refining the sales process and working with individual clubs and trainers to better support their day to day activities, including meal sampling at all regional member events. Lady of America is the second largest chain of women&#8217;s fitness clubs, with clubs in the U.S. operating under the brands LOA Fitness for Women, Lady of America, Ladies Workout Express, Workout Express and Health Clubs of America.<br />
 &#8220;Our partnership with Lady of America is a great example of how health and fitness facilities are the ideal platform to help expand the distribution of our meal delivery program,&#8221; said Kevin McGrath, President and Chief Executive Office of eDiets.com.  &#8220;I am pleased with the progress we have made to-date; training almost two hundred franchise owners, sales reps and fitness trainers. Now the very important second phase   begins: optimizing the program to accelerate sales to Lady of America clients and taking our lessons learned and applying them directly to the next franchise systems. Lady of America&#8217;s clubs provide a dynamic and supportive environment to thousands of women who want to work on their fitness and lifestyle goals and our fresh meal delivery program is a perfect complement to their mission. We were particularly impressed with their reputation for excellent customer service, which is essential to our mutual clients.&#8221;<br />
 &#8220;Lady of America&#8217;s family of fitness centers is delighted to be able to offer the eDiets fresh meal delivery service to our members,&#8221; said Gerry Weber, CEO of Lady of America Franchise Corporation. &#8220;Lady of America&#8217;s members will now enjoy working out at their local clubs with the added benefit of healthy, and delicious meals delivered to their homes.&#8221;<br />
 eDiets.com, Inc. is a leading provider of personalized nutrition, fitness and weight-loss programs. eDiets currently features its award-winning, fresh-prepared diet meal delivery service as one of the more than 20 popular diet plans sold directly to members on its flagship site,<br />
 . The company also provides a broad range of customized wellness and weight management solutions for Fortune 500 clients. eDiets.com&#8217;s unique infrastructure offers businesses, as well as individuals, an end-to-end solution strategically tailored to meet its customers&#8217; specific goals of achieving a healthy lifestyle. For more information, please call 310-954-1105 or visit<br />
 .<br />
 Statements which are not historical in nature are forward-looking statements. Forward-looking statements involve known and unknown risks and uncertainties which could cause the actual results, performance or achievements to be materially different from those which may be expressed or implied by such statements. These risks and uncertainties include, among others, that we will not be able to obtain sufficient and/or acceptable outside financing (when and if required);, changes in general economic and business conditions; changes in product acceptance by consumers; a decline in the effectiveness of sales and marketing efforts; loss of market share and pressure on prices resulting from competition; significant investments in our technology platform, marketing plans, and product development to remain competitive with other online providers of healthy living and weight loss plans, many of which may be found to offer superior and more varied features than our plans and may also be offered for free;<br />
 volatility in the advertising markets; any delay, disruption, or suspension of our supply of prepared meals from our vendor;<br />
 ;  product liability and other risks from the sale of ingested products; regulatory actions affecting our marketing activities; and the outcome of litigation pending against us. For additional information regarding these and other risks and uncertainties associated with eDiets.com&#8217;s business, reference is made to our Annual Report on Form 10-K for the year ended December 31, 2007, and other reports filed from time to time with the Securities and Exchange Commission. All forward-looking statements are current only as of the date on which such statements are made. We do not undertake any obligation to publicly update any forward- looking statements.<br />
 For more than 25 years, Lady of America Franchise Corporation (LOAFC) has been an innovator in the constantly evolving business of women&#8217;s fitness.  LOAFC was established in 1984 with the goal of providing a safe and rewarding environment to women working on their fitness and lifestyle goals while enjoying the company and support of other women. Today, LOAFC is the world&#8217;s largest full-service chain of women&#8217;s fitness centers with over 400 franchises in operation across 45 states and nine countries under the brands; Lady of America, Ladies Workout Express, Workout Express and Health Clubs of America fitness centers. For more information or to find a Lady of America location, visit<br />
 .</p>
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		<title>Spinning Launches First Heart Rate &amp; Fitness App for iPhone &amp; iPod &#8230;</title>
		<link>http://www.raganvirtualworkshops.com/11860.php4</link>
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		<pubDate>Mon, 24 Nov 2008 11:10:43 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[first]]></category>
		<category><![CDATA[Fitness]]></category>
		<category><![CDATA[Heart]]></category>
		<category><![CDATA[iPhone]]></category>
		<category><![CDATA[iPod]]></category>
		<category><![CDATA[Launches]]></category>
		<category><![CDATA[Rate]]></category>
		<category><![CDATA[Spinning]]></category>

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		<description><![CDATA[Lawrence, KS    Dec 21, 2008 in
 [prMac.com] Venice &#038; Santa Barbara, California &#8211; Spinning, the worldwide leader in indoor group cycling, has announced the iSPINNING fitness application available on the Apple(R) iPhone App Store. iSPINNING, free for a limited time only, is an innovative new cardio and cycling application that compiles real-time data for fitness tracking. [...]]]></description>
			<content:encoded><![CDATA[<p>Lawrence, KS    Dec 21, 2008 in<br />
 [prMac.com] Venice &#038; Santa Barbara, California &#8211; Spinning, the worldwide leader in indoor group cycling, has announced the iSPINNING fitness application available on the Apple(R) iPhone App Store. iSPINNING, free for a limited time only, is an innovative new cardio and cycling application that compiles real-time data for fitness tracking. iSPINNING is the first of a suite of health and fitness apps enabled by<span id="more-11860"></span> iTMP Technology, a pioneering developer of smartphone hardware and software applications.<br />
 For iPhone and iPod touch users interested in cutting edge fitness applications, and for Spinning enthusiasts eager to integrate their fitness data with Apple&#8217;s mobile computing platforms, the new iSPINNING iPhone application is a breakthrough in fitness tracking.<br />
 iSPINNING is an iPhone-based Spinning computer and cardio fitness system that is compatible with leading fitness heart rate transmitters and a growing list of other fitness sensors. In addition to heart-related data, iSPINNING receives speed, cadence, and power data from cycling sensors so users can track cycling metrics from their road and mountain bikes too.<br />
 &#8220;For years the fitness industry has struggled with the complexities of tracking and displaying fitness data in ways that are appealing to the end user. iTMP has raised the bar with their suite of iPhone apps that collect data from body and equipment sensors to track and present it in a simple and usable format,&#8221; said John Baudhuin, CEO of Mad Dogg Athletics, Inc., creators of the Spinning indoor cycling program.<br />
 &#8220;While there are a handful of fitness apps for the iPhone, until now none of them have incorporated real-time user data in their calculations. With our wireless virtual bridge, SMHEART LINK, we connect distributed health and fitness sensors to Apple&#8217;s iPhone and iPod touch. In other words, we enable Apple&#8217;s incredible mobile computers to double as heart monitors and cycling computers,&#8221; said Michael Williams, founder and CEO of iTMP.<br />
 The iSPINNING application will run with simulated data so users can see how the application will monitor and manage cardio fitness metrics. Additional hardware, including iTMP&#8217;s SMHEART LINK, will be required to allow the app to &#8220;listen&#8221; to your heart and your Spinner(R) bikes or outdoor bikes. SMHEART LINK stores an entire workout&#8217;s worth of data, compiling information even while the iPhone app is interrupted by a call or if the iPhone is not present. The result is an uninterrupted workout profile that can be reviewed real-time during or after a workout. iTMP&#8217;s SMHEART LINK has a suggested retail price of $149.95 (USD) and will be available for the holiday and resolution seasons online, where users can also find additional product information, accessories and receive updates. Spinning&#8217;s website, will also carry SMHEART LINK and Spinning&#8217;s cadence sensor.<br />
 iTMP Technology, Inc. was founded to revolutionize the world of fitness and health metrics monitoring. iTMP partnered with industry leaders to bring cardiovascular training and cycling metrics to the iPhone and iPod computing platforms. With iTMP&#8217;s SMHEART LINK wireless bridge, athletes can track their cardio workouts anywhere, with no syncing or additional uploading software.<br />
 About Mad Dogg Athletics, Inc.<br />
 The Spinning program offers an energizing, cycling-inspired group exercise training program with expert coaching, exhilarating music and a unique mind/body philosophy &#8211; all at a self-directed pace. The Spinning program has reached more than 30,000 clubs and millions of enthusiasts in 80 countries worldwide. Mad Dogg Athletics, Inc. is the worldwide leader in indoor group cycling bikes, education and products. The company works closely with Star Trac(R) on its patented line of Spinner bikes and develops and markets Spinning instructor orientations, &#038; continuing education programs. iSPINNING is a trademark and Spin, Spinning, Spinner and the Spinning logo are registered trademarks of Mad Dogg Athletics, Inc. logo.</p>
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		<title>National men&#039;s health policy is first in the world</title>
		<link>http://www.raganvirtualworkshops.com/17957.php4</link>
		<comments>http://www.raganvirtualworkshops.com/17957.php4#comments</comments>
		<pubDate>Mon, 24 Nov 2008 04:22:04 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Health]]></category>
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		<category><![CDATA[National]]></category>
		<category><![CDATA[Policy]]></category>
		<category><![CDATA[World]]></category>

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		<description><![CDATA[Tuesday, February 3, 2009
 THE PUBLICATION of a national policy on men&#8217;s health has been hailed as groundbreaking.
 But the failure to provide additional resources to assist in the implementation of the recommendations contained in the document has been criticised.
 The National Men&#8217;s Health Policy 2008-2013, launched last week by the Minister of State at [...]]]></description>
			<content:encoded><![CDATA[<p>Tuesday, February 3, 2009<br />
 THE PUBLICATION of a national policy on men&#8217;s health has been hailed as groundbreaking.<br />
 But the failure to provide additional resources to assist in the implementation of the recommendations contained in the document has been criticised.<br />
 The National Men&#8217;s Health Policy 2008-2013, launched last week by the Minister of State at the Department of Health and Children (DOHC) Mary Wallace, highlights the need<span id="more-17957"></span> for a specific focus on men&#8217;s health needs and offers a series of recommendations on how to support men to take more responsibility for their own well-being.<br />
 In publishing the document, which was developed by the DOHC in conjunction with the Health Service Executive (HSE), Ireland has become the first government in the world to develop a national policy on men&#8217;s health.<br />
 Among the recommendations in the policy are: the establishment of a centre for research and development in men&#8217;s health; the piloting of a national men&#8217;s health helpline; and the provision of specific training courses for those working with men.<br />
 &#8220;To have this report out is just so important,&#8221; said Dr Ian Banks, a Belfast-based GP and chief executive of the European Men&#8217;s Health Forum. &#8220;It really is a milestone in terms of men&#8217;s health and the recognition from Government that something needs to be done.&#8221;<br />
 That such a policy is needed is evident by looking at the figures. According to the national policy, male life expectancy in Ireland is currently 76.8 years, compared to 81.6 years for women. In addition, men have higher death rates for most of the leading causes of death across all age groups and, on average, experience some form of ill-health or disability during the last 13.7 years of their lives.<br />
 The burden of ill health and mortality is borne, in particular, by men from lower socio-economic groups, who are, on average, up to six times more like to die from the leading causes of death than men from higher socio-economic groups.<br />
 Moreover, while the gap in male and female mortality for all causes of death is consistent across all ages groups, it is most pronounced between the sexes aged 20-30 years, with men in this age bracket 3.5 times more likely to die than their female counterparts.<br />
 &#8220;Most of the problems we have with men can&#8217;t simply be fixed using the medical model alone because they are connected to the environment, and cover such issues as class, ethnicity, unemployment, social isolation and suicide.<br />
 &#8220;Doctors can&#8217;t do anything about these issues but the politicians can, which is why the policy is so important because it now embraces politics rather than just medicine &#8211; so this is a massive step forward,&#8221; said Dr Banks.<br />
 The policy&#8217;s co-author, Dr Noel Richardson from the Centre for Men&#8217;s Health Research and Training at the Institute of Technology, Carlow, said that the publication of the document is significant because traditionally the spotlight hasn&#8217;t been on men&#8217;s health. He stressed that the issue of men&#8217;s health concerns everyone.<br />
 &#8220;Targeting men&#8217;s health can have a beneficial impact on men&#8217;s lives, and can also lead to a positive spin-off on the lives of women and children. If you take single-income families where the man is the main breadwinner for example, if he&#8217;s out of work for an extended period due to illness, then that has huge repercussions, not just for himself, but also for those closest to him,&#8221; said Dr Richardson.<br />
 He added that from a preventative point of view, encouraging men to take care of their health will also lead to savings in the health service over the long-term because, at present, men tend to present themselves later than women for diagnosis and therefore often have a greater impact on services.<br />
 While hugely enthusiastic about the policy, Dr Banks has expressed criticism over Minister Wallace&#8217;s announcement that there will be no additional resources to assist in the implementation of any of the recommendations and actions contained in the policy.<br />
 &#8220;To be part of such a groundbreaking move, but then to say that there&#8217;s not enough money to address the problem is frankly just not good enough,&#8221; said Dr Banks.<br />
 &#8220;It is a huge step forward that the Government has accepted this as part of their policy and that has to be commended, but the fact that they don&#8217;t have sufficient funds to put that policy into practice shows that saving the banks is considered more of a priority than saving men&#8217;s health,&#8221; he added.</p>
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		<title>FDA approves first eyelash-lengthening drug</title>
		<link>http://www.raganvirtualworkshops.com/12728.php4</link>
		<comments>http://www.raganvirtualworkshops.com/12728.php4#comments</comments>
		<pubDate>Sat, 22 Nov 2008 21:47:45 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Approves]]></category>
		<category><![CDATA[Drug]]></category>
		<category><![CDATA[Eyelash]]></category>
		<category><![CDATA[first]]></category>
		<category><![CDATA[lengthening]]></category>

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		<description><![CDATA[BEIJING, Dec. 29 (Xinhuanet) &#8212; The Food and Drug
Administration (FDA) recently approved the first drug that will help with
producing longer eyelashes, according to media reports Monday.
 Latisse, produced by the company of Allergan, is
supposed to treat those who have hypotrichosis, a condition in which a person
does not have enough eyelashes. It will be available by [...]]]></description>
			<content:encoded><![CDATA[<p>BEIJING, Dec. 29 (Xinhuanet) &#8212; The Food and Drug<br />
Administration (FDA) recently approved the first drug that will help with<br />
producing longer eyelashes, according to media reports Monday.<br />
 Latisse, produced by the company of Allergan, is<br />
supposed to treat those who have hypotrichosis, a condition in which a person<br />
does not have enough eyelashes. It will be available by prescription starting in<br />
the first quarter of 2009.<br />
 The active ingredient<span id="more-12728"></span> in the once-daily prescription<br />
treatment is bimatroprost, the same ingredient that is in Allergan&#8217;s glaucoma<br />
treatment Lumigan.<br />
 Allergan states that &#8220;Latisse users can expect to<br />
experience longer, fuller, and darker eyelashes in as little as eight weeks,<br />
with full results in 16 weeks.&#8221; If Latisse is stopped, eyelashes will gradually<br />
return to their previous appearance as new eyelashes grow in.<br />
 The company also stated, &#8220;Latisse is the first and<br />
only science-based treatment approved by the FDA to enhance eyelash prominence<br />
as measured by increases in length, thickness and darkness of eyelashes.&#8221;<br />
 Allergan noted that Latisse may cause darkening of<br />
the eyelid skin, which may be reversible, and it &#8220;may also cause increased brown<br />
pigmentation of the colored part of the eye, which is likely to be permanent.&#8221;<br />
 The drug is the first prescription product for<br />
lengthening eyelashes, making sales forecasting a little difficult although<br />
Allergan said it estimates global peak sales could top 500 million U.S.<br />
dollarsa year.</p>
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