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The popularity of social sites offering support for people with medical conditions has exploded in recent years, especially as more people seek health information on their mobile phones.
For years, the chatty among us have relished the chance to swap stories in doctor's office waiting rooms. Hearing about the experiences of those with similar ailments has always offered affirmation and valuable information.Now, virtual waiting rooms have sprung up all over the internet. For millions of Americans with health issues, feelings of isolation have gone the way of the mercury thermometer. Social media pages hosted by patient advocacy groups, medical facilities, and health sites like Healthline.com offer information on everything from a mysterious rash to multiple sclerosis.Ariana Medina of Peekskill, N.Y. studies psychology and also suffers from mental illness. She embraces social media and participates on Healthline's Help For Depression page on Facebook.For Medina, such online communities are much more rewarding than simply coming home from a doctor's visit with a pamphlet. “Now, we have choices—read the article or watch the video or check out the pictograph,” she said. “Not only are [patients] able to get health information, they are also able to gain support due to social media and not feel so isolated in their illness, which is an amazing stride, especially for people who have mental illnesses, an invisible illness with so much stigma wrapped around it.”Medina is one of 250,000 fans of Healthline's 11 Facebook pages. Healthline's most popular condition-specific pages are for multiple sclerosis, Crohn's disease, bipolar disorder, osteoarthritis, rheumatoid arthritis, and HIV/AIDS.Slideshow: Depression Medications and Side Effects »Facebook Is Not a Doctor SubstituteMedina cautions that patients should always check with a doctor when seeking health advice. She said the Help For Depression page, like many other online forums, is “often loaded with horror stories of side effects” from visitors who are not medical professionals.Kevin Vicker, who handles social media for the National Stroke Association (NSA), told Healthline that the importance of drawing a line between medical advice and non-clinical information and support is an issue on their Facebook page as well.“Sometimes we have people that ask, either openly or directed at our page through a private message, that they're experiencing such and such symptoms, and they ask if it's a stroke,” he said. “We don't give medical advice, but we drop a link to stroke warning signs that tells them if they're experiencing stroke symptoms to call 911 immediately.”One symptom of stroke is a sudden severe headache with no known cause, he said. “But how often do we get headaches? How do we distinguish between a migraine and a stroke? We're not in the business of diagnosing, but we can get people connected with doctors,” Vicker said.Saving a Friend's LifeSusan Grupe Wahlmann is one of the NSA page's 43,000 fans. The Illinois woman suffered a stroke two years ago, and she had her husband share the terrifying experience on Facebook from the moment it happened.She told Healthline that she learned from a blood test that her stroke had been caused by taking a form of birth control that led to excess blood clotting. She shared that information on Facebook as soon as she learned it.After Wahlmann's post, a friend of hers taking the same contraceptive got checked by a doctor and learned that she also had a blood clot, Wahlmann said. “We all can get help through social media, I love it. I am so grateful for the Facebook pages. Things would be so different had this happened 20 years ago,” she said.Fans of Healthline's Facebook pages say the medium offers them validation and hope for a cure. Hearing about the suffering of others often puts their own illnesses into perspective. Plus, news about medical breakthroughs and new research keeps them at the forefront of managing their conditions.Slideshow: What are the Warning Signs of Stroke? »The Numbers Tell the StoryThe impact of social media on healthcare is staggering, especially among young patients ages 18 to 24. Ninety percent of them say they trust the health information they receive through social media, according to Search Engine Watch.More than 40 percent of people also said they would consider information obtained on social media when choosing a doctor, hospital, or other medical facility, according to Demi & Cooper Advertising DC Interactive Group.One out of five smartphone owners has a health app on their device, and almost half of the unique visitors to Healthline.com access the site via their mobile phones.As for sharing, 30 percent of adults said they would post information about their health on social media for other patients to view, Fluency Media reports. Almost half said they would share it with a doctor.Opening Doors For the IsolatedLenora Houseworth manages social media pages for the Crohn's & Colitis Foundation of America (CCFA). She told Healthline that social media engagement for her organization has grown 200 percent in the past three years. Houseworth said people who suffer from gastrointestinal illnesses not only face embarrassment, but often isolation and skepticism.“They don't necessarily look sick, but inside, they feel awful. Often times social media has become the only touch point that patients have for medical information. A lot of these people live in boondocks USA, or they're overseas, and don't have access to premier GI doctors.”
Like the caduceus and the lab coat, the stethoscope is a symbol of modern medicine. But some doctors are starting to doubt its worth. “It’s a relic,” said Eric Topol, a cardiologist and geneticist who directs the Scripps Translational Institute in La Jolla, California. In the video above, he demonstrates how to use a new alternative: a small ultrasound machine that looks like a flip phone.
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Approximately 1.1 billion people have Facebook accounts, and the number of social media sites and users just keeps growing. Whether this trend forges relationships or increases isolation is an ongoing debate, but in the realm of medicine, social media that goes beyond the Yelp-like physician rating sites might enhance the patient experience and benefit physicians and their institutions as well, according to a group of experts who recently addressed the topic at a panel for gastroenterologists.“As physicians, we can no longer ignore [social media]; we have to understand how patients are wanting to connect with us,” said M. Bridget Duffy, MD, chief medical officer at Vocera Communications, an information technology company that develops mobile communication devices and services for use in health care and other industries.Dr. Duffy moderated a session on the emergence of social media in medicine at the 2014 GI Roundtable, a conference dedicated to exploring challenges and their solutions for gastroenterology and the field’s future.“Historically, we’ve focused on the intervention, but patients want us to connect with them before they arrive at the clinic or hospital. They want us to understand their preferences; they want a personalized plan and a path to their well-being; and they want a connectivity after they leave,” said Dr. Duffy, who has spent the past 20 years researching ways to improve the patient, staff and physician experience.Dr. Duffy leads the Experience Innovation Network, a group of health care organizations committed to accelerating innovation on patient and staff experience. In addition, Vocera partners with Rock Health, a start-up incubator in San Francisco that mentors and supports medical tech companies dedicated to that goal. Dr. Duffy and her team participate in this mentoring and support, and help connect the companies to providers to test and adopt their novel products and services.“We need to find technologies and process improvements that create consistent, seamless experiences of care, and that empower and engage patients to be partners in their care,” she added.Cancer Connect—A Platform for PatientsSocial media, by definition, refers to the virtual communities and networks in which people generate, distribute and discuss information. Charles Weaver, MD, an oncologist and founder of Cancer Connect—a popular cancer information website—predicts this is how patients will interact with each other from now on. “The question for all of us is how do we become a part of it? How do we participate, and how do we use it to everyone’s best advantage?”A pioneer of Internet-based patient education, Dr. Weaver got the idea to add a social media component to Cancer Connect after his elder son developed a rare sarcoma. Treatment required a long commute from their remote home in Sun Valley, Idaho, to the University of Utah Hospital. “I got to experience the fear, anxiety, confusion and isolation that any parent or patient experiences when they’re diagnosed with a significant illness,” Dr. Weaver said.Fast forward several years, and Dr. Weaver found his sons engaged on Facebook one afternoon when they should have been doing homework. He was on the verge of scolding them when the younger one said, “‘Think if there was a Facebook just for cancer patients. Wouldn’t it be neat if they could connect with each other? They wouldn’t have to go through what [my brother] went through in a small town,’” Dr. Weaver recalled.His older son chimed in, “That would have been really helpful.” He had, in fact, already been using Facebook to locate and connect with other kids who had cancer.The next day, Dr. Weaver called his programmers to discuss creating a Facebook-type of application just for cancer patients. Now, a little more than two years after Cancer Connect added its social media component, 52,000 people have registered to participate. Some 9,000 patients visit the physician-moderated virtual communities every month.Users “are looking for validation of what their physician told them, for translations of what their physician said, and for support from others who have gone through their experience,” Dr. Weaver said. They “also told us that it was very important for them to give back. In fact, the patients we surveyed rated that as the most important aspect.”Private-Label CommunitiesCancer Connect’s social media platform is free and open to any patient who wants to join, but it also is used by practices as a virtual home base for their patients. Dana-Farber Cancer Institute, Memorial Sloan-Kettering Cancer Center and Fred Hutchinson Cancer Research Center are just a few of the institutions that use Cancer Connect to supplement supportive care of their patients and patients’ families.For such centers and practices, creating private-label communities has several advantages. On a practice’s website, Cancer Connect is part of the patients’ experience as it relates to that particular institution, an approach that may improve patient retention, increase patient referrals and enhance patient satisfaction, Dr. Weaver said.The model works fairly simply. For example, from Dana-Farber’s home page, a click on “My Dana-Farber” brings the visitor to an invitation to join their online cancer community. “It explains the rules of the community and how you participate in it. From that point on, the patient never leaves the experience of your brand and what you’re providing,” Dr. Weaver said.Once a patient becomes part of Dana-Farber’s online community, he or she can participate in both local and national conversations. They can choose to interact only with Dana-Farber patients, with patients from other centers using Cancer Connect, or both.“The beauty of this is that for [cancers] that are common, you can build a community on your own website because you’ll have enough patients to benefit from the experience,” Dr. Weaver said. “With rare conditions, even a place like Dana-Farber won’t have a critical mass of patients who can support each other, but by sharing the community with other large centers, you aggregate patients so they can get the support they need.”This need, of course, varies from one patient to another. Some visit Cancer Connect communities looking for an answer to a specific question or problem, whereas others desire a stronger connection.“The ones who want a deeper relationship tend to find others who are also looking for a deeper level,” Dr. Weaver said. “People initially join up because they want support and information. Those who stay want to share information and provide support, to give back,” he noted.GI Connection, a New Kid on the BlockWhen Klaus Mergener, MD, PhD, MBA, of Digestive Health Specialists in Tacoma, Wash., learned about Cancer Connect and its offshoot, The RA Connection, for people with rheumatoid arthritis, he quickly envisioned the utility of the concept for gastroenterology.“We have a huge number of chronic diseases,” Dr. Mergener said, from irritable bowel syndrome to cirrhosis. “If we can get a few hundred [GI] patients to start talking and connecting about their illnesses, I think that might be very useful.”He proposed the idea of a GI-specific platform to Dr. Weaver, and the two worked together to develop GI Connection, which is scheduled to go live this summer. “GI and cancer have a couple of things in common,” Dr. Weaver said. “The most important is that both specialties deal with chronic conditions, and people with chronic conditions want to stay connected.“Also, they are both subspecialties that get their patients from someplace else—you’re typically not diagnosed with cancer by an oncologist,” Dr. Weaver continued. “This gives the subspecialties an opportunity to create communities to aggregate around the experience at their center.”Aside from patients with chronic GI diseases, those worried about an upcoming procedure might take comfort in the support of others, too. “Connecting with someone who has had a colonoscopy or multiple colonoscopies and can tell you that it’s OK is very powerful,” Dr. Weaver said. “Sorry to say, but patients put a lot more value on one-to-one interactions with other patients than with health care providers.”Before the launch of GI Connection, Dr. Mergener began raising awareness among practices that he hopes will be early adopters, mentioning the site to patients and increasing visibility with business cards and scannable QR codes. “Charles [Weaver] tells me that once you get up to 100 or 200 patients, involvement snowballs by word of mouth,” he said.CrohnologyAs Sean Ahrens took the podium at the GI Roundtable to discuss Crohnology, the platform that he developed to capture the experiences of patients with inflammatory bowel disease (IBD), he acknowledged that physicians are his toughest audience.“Partly, I think that’s because there is a wave, a front, of patients connecting back toward each other; the case I want to make to you is toward [the acquisition of] medical knowledge,” Mr. Ahrens said. “We are moving from the era of traditional media, where people are receiving information, to one in which they are contributing to the knowledge source.”Mr. Ahrens was 12 years old when he experienced the onset of Crohn’s disease. Now 28, he has gone through a host of different treatments, or as he thinks of them, experiments. “These include physicians prescribing different medications, and me doing things like changing my diet,” he said.Mr. Ahrens began to develop Crohnology as a college student, but the concept for the site gelled a few years later during one of his more unusual self-experiments. Remicade (Janssen Biotech; infliximab) was no longer controlling his symptoms, but he feared making the leap to Humira (AbbVie; adalimumab). Under the supervision of a physician who thought the novel therapy probably wouldn’t hurt him, Mr. Ahrens started inoculating himself with a pig whipworm solution he’d ordered from a company in Germany.“During this treatment, it occurred to me that the very least I could do, as a favor to humanity, was leave a paper trail so that others could learn from this experiment,” he said.It became clear about two-thirds of the way through that the pig whipworm therapy wasn’t working, as Mr. Ahrens’ symptoms remained severe. For the sake of his health, he adopted a specific carbohydrate diet, although he knew that it would compromise the quality of the data. But the experience further supported his theory that patients are vast silos of information, and that there should be a system to capture those experiences and learn from them, instead of dismissing each patient’s experience as anecdotal.In 2011, Rock Health selected Crohnology as part of its inaugural class of start-ups to nurture. The support solidified development of Crohnology’s website and mobile platform. To date, the network has about 5,500 patient contributors with irritable bowel disease, representing 70 different countries.As for that physician audience? Reactions have been mixed. “On the whole, physicians like the concept of connecting patients and giving them emotional and social support,” Mr. Ahrens said. “But they’re also generally of the school of thought that medical knowledge needs to be very carefully collected and dispensed inside the physician system, through rigorous clinical trials.”He views Crohnology as a model that can accrue useful knowledge without the staggering costs of clinical trials.Catching Up to the ConsumerIronically, although the increasing presence of technology has been criticized for creating barriers between physicians and patients, in the right hands, social media technology may be a way to start tearing down those walls, Dr. Duffy said.“I think there is a way that technologies can be humanizing if you pick the right ones,” she said. “That’s what patients are doing through sites like Cancer Connect and Crohnology, using technology to create human connections with others who have conditions like theirs.”One of her concerns with these technological innovations, however, is that physicians, who historically have been a bit recalcitrant with social media in their profession, are falling behind what their patients want and need.“Doctors on the delivery side have to figure out how to find those resources that help restore people to a full life versus just a great technical outcome,” Dr. Duffy said. “And we have to move faster to catch up with where consumers are going.”
"Your child is as white as he is Asian… Why embrace one label and not the other?”
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“Your child is neither white nor Asian. I once heard this description: When you have a glass of milk and add chocolate to it, you no longer have just a glass of milk and you no longer just have chocolate because you have created something completely different. A bi-racial or multi-racial child is not either/or.”
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The British Heart Foundation (BHF) has launched a series of online videos and DVDs to help healthcare professionals ease their patients' fears about common heart tests and treatments including ECGs, echocardiograms and stent surgery.The launch comes as the heart charity release new online research that shows half the nation (48%) has turned to the internet for information about tests or treatments they've been referred for by their doctor.Of those who have searched on the internet for this medical information: - Over half (52%) said they wanted to find out more about the side effects for their test or treatment - Over two in five (42%) said they were concerned about what the test or treatment involved - Over one in five (22%) said they didn't feel their doctor gave them enough information - Nearly a quarter (23%) said they wanted to get information to reassure their familyThe online survey of over 2,000 UK adults also reveals that around one in five patients (19%) feel uncomfortable asking their doctor all of their questions at an appointment. A similar number (20%) who have been for an appointment with their doctor say they feel unsure if their condition or concern is being correctly diagnosed.
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