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Actor Patrick Swayze who starred in “Dirty Dancing,” “Point Break” and “Ghost” died on Monday, September 14, 2009 after 20 months of battling with pancreatic cancer. He was 57 years old.
According to its website, TalentSpring’s resume search engine reviews an organization’s open job descriptions, identifies the relevant attributes being sought (experience, skill, location, education, etc.), and then matches those attributes to tens-of-thousands of resumes found on social networking sites, job boards and the organization’s ATS. The search results are ranked and ordered based on candidate quality and relevance, saving recruiters and hiring managers time, improving hire quality, and reducing overall time-to-hire.
She adds, "It's also outdated in terms of the belief that that we all want to separate work from personal time. Today, with people so connected all the time, there's a belief that it's bad to be on vacation and check e-mail."
could have. I was constantly fatigued, I had numbness over much of my body, a loss of hearing, twitching muscles, vertigo. You name the symptom, and I had it.” Now, thanks to LDN, Linda is almost back to normal, and works tirelessly to raise money and awareness of LDN. “This drug has saved my life,” she says. “Along with hundreds of other people, I am working hard to get the word out about LDN. Many patients who don’t yet know about this drug, desperately need it.” Linda adds that LDN has virtually no side effects – unlike most of the much costlier, highly toxic medications doctors routinely prescribe to treat the disease. Vicki Finlayson, of Auburn, California, tells a story of a life that was filled with 9 years of side-effect-laden medications approved by the FDA for MS. “I was on just about every one of these medications,” she says, “and often, I was on several at one time – along with medications for the pain. Yet, my MS was getting progressively worse, until I was virtually bedridden.” Happily, in 2005, she found LDN, and she hasn’t looked back. “I felt improvement in two days,” she says. She is now back to normal, and all of her symptoms are gone. In fact, in May, 2008, she walked 53 miles to the State Capitol Building in Sacramento to meet with state officials to raise awareness about LDN. She will be back on the Capitol steps this October 21st, as part of the ongoing effort to educate the public, doctors and government officials about the importance of this inexpensive, effective, patient-driven treatment. “LDN gave me my life back. I feel that it’s very important to spread the word about it.” Because low dose naltrexone treatment represents an inexpensive, off-label use for a drug approved long ago by the FDA, pharmaceutical companies -- who carry out most of today’s research on medications -- aren't much interested in funding research on LDN. But the incredible thing is that hundreds of patients – and several doctors, too – who have experienced remarkable results in themselves and in their patients, are conducting research and raising money and awareness on their own. In fact, one group of patients in the US raised enough money to help fund a successful trial at the University of California in San Francisco, and there are now trials being conducted in Mali, Africa, as well as in Milan, Italy. In addition, Dr. Ian Zagon and his colleagues at Penn State are doing both animal and human trials for several disorders, including multiple sclerosis, Parkinson's disease and various cancers; and Stanford University is entering into a Phase II trial for fibromyalgia. It is estimated that hundreds of doctors throughout the United States, the UK and Canada, as well as in countries as far-reaching as Italy, Israel, Australia, and even Nigeria, prescribe LDN for their patients.
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