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Free diabetes testing in Torrevieja and Murcia – RTN Newspaper

May 26th, 2017 2:45 pm

THE QUIRONSALUDhospitals in Torreviejia and Murcia will be conducting free testing for diabetes next Monday May 29, between the times of 09.00h and 11.00h to coincide with World Nutrition Day, which falls on Sunday.

Obesity, physical inactivity and poor nutrition increase the number of obese and diabetic people every year. People are unaware of the fatal consequences of this chronic disease as diabetes is a condition that is triggered when the body does not produce enough insulin or does not use it effectively.

There are several types: Type 1 diabetes is the most common childhood disease. The pancreas does not produce insulin, so an excess of blood sugar is created, which makes it necessary to provide the body with injected insulin.

According to Oscar Boullosa, coordinator of the Diabetes Unit of the Hospital Quirnsalud Torrevieja, type 2 diabetes is the most common, 90% of diabetic patients suffer with this type, they are generally over 40 years old, and their body does not produce enough insulin to take advantage of glucose or are resistant to it. These individuals require a balanced diet and exercise.

This multidisciplinary unit monitors all reviews of diabetic patients annually ensuring disease control.

In Spain, about 26,000 children under the age of 15 suffer from type 1 diabetes, 13% of all diabetics. More than 5,500,000 people are estimated to suffer with type 2, of whom 43% are undiagnosed, that is, they do not know they have the disease. Figures that are increasing and indicate that in 20 years could be increased by up to 55%. One in six adults are obese and one in four children are overweight, an excellent breeding ground for the illness. Diabetes can be cured and the data is clear: more than 70% of obese patients undergoing bariatric or metabolic surgery cease to become diabetic.

The effectiveness is immediate in patients with type 2 diabetes, who usually stop using insulin and medication in the weeks following the intervention, explains Dr. Juan Lujn, head of service and head of the Unit for Obesity and General Surgery and Digestive System of Hospital Quirnsalud Murcia.

Those interested in attending the Hospital Quirnsalud Murcia can request information by phone 968 011 197 or email prevencion.mur@quironsalud.es or through the web http://www.quironsalud.es/hospital-murcia

Those who wish to do so at the Hospital Quirnsalud Torrevieja can obtain all the information by phone 966 925 770 or by email prevencion.trv@quironsalud.es or through the web http://www.quironsalud.es/torrevieja/es

To perform the test it is necessary to be nil by mouth from the night before.

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Local youngster headed to DC to lobby for T1 diabetes research funding – The Bridgton News

May 26th, 2017 2:44 pm

Brady Chappell

By Wayne E. Rivet

Staff Writer

NAPLES He may be just nine years old, but Brady Chappell has an important message he plans to share with lawmakers.

The Naples boy is headed to Washington, D.C., this July, where he will lobby to increase funding for Type 1 Diabetes research.

Brady was selected to serve as one of two Maine delegates to the biennial JDRF Childrens Congress.

JDRF is the leading global organization funding Type 1 Diabetes (T1D) research.

Our strength lies in our exclusive focus and singular influence on the worldwide effort to end T1D, according to the JDRF website.

Just last weekend, Brady was honored to be invited by U.S. Senator Susan Collins to attend the annual JDRF Gala in Manchester, N.H., where the N.H. and Maine delegates were introduced to the attendees. Brady was able to meet both Sen. Collins and Sen. Shaheen (N.H.), who were in attendance to receive awards from JDRF for their work on behalf of the T1D community. Brady was even able to sit next to Sen. Collins at dinner.

Both senators are co-chairwomen of the Senate Diabetes caucus, which was also founded by Sen. Collins.

Brady was diagnosed with T1D at the age of six. Brady a very athletic, energetic and intelligent kid was diagnosed with T1D around Valentines Day of 2014. He had been recovering from a long bout with an illness when, thankfully, his grandmother noticed he was going to the bathroom a lot. He was also looking rather thin and was uncharacteristically lethargic. Just to be sure everything was okay, his parents Tait and Jeanette Chappell made an appointment with his doctor.

Needless to say, we were blown away when the doctor took his blood sugar and said, You need to take him to the hospital immediatelyhe has Type 1 Diabetes! What? Just like that? You dont need to do more tests? This wasnt something that was even on our radar as a possibility, the Chappells said. The doctors said that we were lucky and caught it relatively early before his blood sugar, at that point over 600, had gone even higher.

While it was a startling diagnosis, the Chappells were happy for Brady that he was being taken care of and was finally feeling better. Although a bit scared, Brady took the news in stride and was resolved to learn all he could about T1D.

The resilience of children is an amazing thing. Within two weeks, he was giving himself shots, taking his own blood sugar and counting carbs. He continues to amaze us! the couple said.

T1D can feel relentless at times, with all the finger sticks and sleepless nights, managing lows. Anything that can help alleviate that feeling is a tremendous thing. Brady now uses a Dexcom CGM and loves using the Omnipod insulin pump.Both of these devices have benefited from previous JDRF funding and help to make his daily diabetes care easier to manage.

But, the Chappells believed they could do better!

Three years ago, they were very happy to join the JDRF Walk to Cure Diabetes and help to raise money to find a cure. They were overwhelmed when Bradys Bunch raised over $20,000 in the first year. They were also very happy to sponsor a JDRF Kids Walk at Bradys school, which raised an additional $5,000.

The next Bradys Bunch fundraising effort is the JDRF One Walk 5K on Sunday, Sept. 17, starting at Thornton Academy in Saco. Check-in is at 10 a.m. with a start at 11 a.m. The goal is to raise $15,000. To make a donation to team Bradys Bunch, go to http://www.jdrf.org website, under events go to One Walk, a box allows you to enter your zip code for a walk near you, select the Saco walk and you will find teams signed up for the event, click Bradys Bunch, and make a donation.

When Brady grows up, he wants to be a professional baseball player or an engineer. He loves sports, especially baseball, football, basketball and skiing.

Although constantly tracking his blood sugar can be difficult, Brady says, Diabetes doesnt stop me from doing anything. I just always have to think about diabetesI was sad when my doctor told me that unless we found a cure, I would have diabetes for the rest of my life. That made me want to find a cure.

The JDRF 2017 Childrens Congress will take place on July 2426 in Washington, D.C. Every two years, more than 150 children living with Type 1 Diabetes (T1D) gather in Washington, D.C., to meet face-to-face with some of the top decision-makers in the U.S. government. The children, ages 4 to 17, represent all 50 states and the District of Columbia. The delegates in JDRFs Childrens Congress enjoy a once-in-a-lifetime opportunity to help members of Congress understand what life with T1D is like and why research to fund life-changing therapies until a cure can be found is so critical. They speak up on behalf of the millions of people living with T1D and the families and friends who love them.

The JDRF Childrens Congress T1D advocacy program was inspired by a boy from Massachusetts named Tommy Solo. One day, at age nine, he asked his mother, Why cant kids go to Washington and tell their representatives about what it is like to have Type 1 Diabetes and let them know that we want scientists to find a cure?

His mom and other JDRF volunteers agreed and, in 1999, the first-ever JDRF Childrens Congress took place in Washington, D.C.

Since then, ninesuccessful Childrens Congresses have been held, one every other year, and more than 1,000 kids with T1D have served as delegates. JDRF Childrens Congress has been essential to securing continued government funding of T1D research and to raise awareness of the daily burden of Americans living with this serious autoimmune disease.

Delegates form lifelong friendships, meet T1D role models, develop leadership skills, and leave Childrens Congress empowered to use their voices for the change that will improve their lives and the lives of all people affected by T1D.

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CADH to host health fair; mobilizes resources through diabetes & hypertension screening and counseling – The Maravi Post

May 26th, 2017 2:44 pm

Community members at Chinsapo township in Lilongwe going through diabates screening for funds mobilization

LILONGWE-(MaraviPost)-The Community against Diabetes & Hypertension (CADH) in Malawi, has intensified its resource mobilization through diabetes and hypertension screening, and counseling, ahead of the health fair, slated for July 29.

The screening and counseling exercise is targeting individuals, companies, and institutions of goodwill. This enabled CADH to collect monies or material in return of the services.

The health fair, which will be held in Lilongwe, will be the first of its kind focussing on all non-communicable diseases (NCDs). The health fair comes barely two months after CADH opened its counseling centre in the capital, with the central quest to upscale awareness campaigns on diabetes and hypertension.

The fair aims to increase health awareness to the public, by providing health screenings, demonstrations, and information.

Speaking in an interview with The Maravi Post a head of the health fair, CADHs Programs Manager, Thomas Psyata, said diabetes and hypertension diseases were claiming many lives silently, hence the need for the mass awareness campaign.

Psyata said that the health fair will be a platform to demonstrate the effect of community peer supporting groups in prevention and treatment of diseases.

He added that this is the reason the organization launched the resource mobilization campaign, to meet the cost of the fair. He said the fair would also motivate participants to champion self-care practices, and make positive health behavioral change.

Since we opened the counseling centre, there have been overwhelming responses from communities as far as Mzimba for our services. But our limited resources, especially human and mobility, have been our main constraints to reach more people.

With the health fair slated for July 29, this year, we hope to increase awareness on NCDs particularly diabetes, hypertension, cancer among others. This is the reason we are visiting individuals, companies, institutions with our services, and that in return, they give us money or any material to support, to help finance the health fair preparation, said Psyata.

Psyata therefore asked people to support the initiative for their own good, as it focuses on improving the health status of the nation.

Established in 2016, CADH, is serving local communities in awareness campaigns, prevention and treatment of diabetes and hypertension. CADH is operational in six districts Lilongwe, Balaka, Salima, Dedza, Rumphi and Mzimba.

According to the World Health Organization, diabetes results in high healthcare costs, loss of labour productivity, and decreased rates of economic growth.

Globally, healthcare expenditure for diabetes totaled US$465 billion in 2011, equivalent to 11% of total health spending.

Without an investment in making effective treatments for preventing diabetes complications will arise widely, and predictably rise to US$595 billion by 2030.

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Geeks Vs Loneliness: face-blindness – Den of Geek UK

May 26th, 2017 2:42 pm

Welcome to Geeks Vs Loneliness, our spot on the site where we chat about things that may be affecting you, or people you know. This week, we're handing over to Shawm Kreitzman, who wants to talk about something we're betting many of you - us included - hadn't heard of before...

A few years ago, I stumbled across the trailer for Anomalisa on YouTube.

I had never heard of the film, but I watched the trailer with mild interest and thought it looked like a curious (if slightly melancholy) piece of stop-motion animation, nicely executed, but ultimately unremarkable. I let my mouse wander on to something else, and didnt give it another thought.

Until my girlfriend happened to see it, that is.

That was incredibly creepy, she said to me, after seeing the clip.

Creepy? I had thought the mood was a little on the glum side, the general tone rather drab. But creepy?

All the faces are exactly the same, she told me.

Apparently thats the whole point of the film. I hadnt actually noticed it.

From where I sit, you have a superpower. Congratulations. You may not have X-Ray vision, or Adamantium claws that spring out of your knuckles (and be honest, how useful would that really be at the office) but there is something that you do every day; something that is completely beyond my abilities. You can distinguish one face from another.

I happen to suffer from face-blindness (prosopagnosia, to its friends) which means I find it very, very difficult to tell faces apart.

Think for a moment about how many different faces you have seen in your life. Apart from your family and friends, there are the faces of your neighbours; there are the thousands of commuters you have passed on your way to work, and the total strangers you see in the supermarket. There were the faces of the other kids at your school, back in the day. And thats before we even start talking about the faces you see in the Media: politicians, actors, celebrities, lingerie models, football hooligans etc.

Somehow, those millions of faces all look different to you. I have absolutely no idea how you do it.

Never mind the faces in Anomalisa; all faces look alike to me. Jason Statham and Clark Gregg look alike to me, apart from the hair (dont tell the staff at Den Of Geek I said that). Show me a photo of the Beatles and I see four identical white kids with silly haircuts. With a gun to my head I couldnt tell you which one is which.

Im not blind; my vision is perfectly fine. I can read the bottom line of the eye-chart forwards and backwards without breaking a sweat. But if I should happen to bump in to my optician at the grocery store an hour later, I will have absolutely no idea who she is.

Most people, it seems, are hard-wired to distinguish the tiniest variations in facial features and perceive those variations as a unique individual without even realising they are doing it. I never got those wires. When I look at a human face, I see the eyes, nose and mouth right where theyre supposed to be. I can see that some people have brown eyes, some people have blue eyes and such like.

But to take all those features and use them to construct a unique person? That is completely beyond my ability.

Like many people with prosopagnosia, I spent most of my life with absolutely no idea I had it. Indeed, it wasnt until I was in my 30s that I even knew it could be a thing. Before that, I just assumed I simply wasnt paying enough attention. After all, everyone else seemed to recognise each other with ease. Why couldnt I do that?

There were plenty of socially awkward moments. I hated parties, or any situation where I would be expected to meet a large number of new people in a short time (I still do). When I worked in a shop, I was hopeless at recognising regular customers when they walked in (until they spoke to me, at which point I would recognise them at once. Im exceptionally good with voices.). If someone changed their look significantly (shaved their beard, lost a lot of weight, dyed their hair purple etc) they instantly became a stranger to me. And I was useless at spotting familiar actors in films.

Before I read about prosopagnosia, it had never occurred to me that others might be seeing faces differently. When I recognise people (and I do recognise people all the time) its usually by their hair; their voice; their body language. I just assumed that everyone else did the same thing, only much better.

The biggest problem with face-blindness is that most people have never heard of it. Tell someone youre colour-blind and they will understand immediately. Tell them youre dyslexic and they will nod, sympathetically. But prosopagnosia? Is that contagious? Do you take pills for it? (No, you dont, by the way. Theres no treatment per se.) And if you fail to recognise someone youre supposed know, they can become very offended very quickly. Even after I explain it (which I rarely bother to do) people are often sceptical.

So you really cant see my face? they ask.

Of course I can see your face; its right where you think it is. I just cant see what makes your face different from the countless other faces I have seen in my lifetime. (And my prosopagnosia is relatively mild. Some people are unable to recognise their own family, or even themselves in mirrors and photographs.)

Please dont be offended. Its nothing personal, but thats exactly the problem. For most people, The Face is the most personal thing there is (theres a reason they dont call it Voicebook).

The irony is that Im not troubled by any of this, although that wasnt always the case.

Before I knew what it was, I struggled with it quite a bit. I thought I must be doing something wrong; I thought I simply wasnt being observant enough. This is a story I have heard from many others with the same condition. Many of us are terrified of meeting people, of interacting with anyone, for fear of embarrassing ourselves or inadvertently causing offence. We simply dont realise that we truly see the world differently.

When you're different, you tend to experience things through a filter. If something happens and you react one way while everyone else reacts another way, your first response is generally to wonder why. If I wasnt reacting to things the way normal people do, then obviously we're seeing things differently. When I eventually realised I was face-blind, it didn't scare me or disturb me; it made perfect sense. I was literally seeing things differently.

Normal is my least-favourite word in the English language. Remember Malcolm McDowell's line from Star Trek: Generations? Normal is what everyone else is, and you are not. Best Line Ever.

In exploring my own prosopagnosia, I have realised that the way we perceive the world around us is extremely subjective and personal. When I compare notes with people who have dyslexia for example, I hear them talking about written words the way I talk about faces.

When they see printed text on a shop window or a street sign, they don't see the text, they see the shapes. Once they recognise those shapes as text, they can consciously make a decision to attempt to read it. For my part, I cant imagine seeing text and not reading it. Where they see shapes, I see language.

When it comes to faces, I see shapes, while you see people.

We can never truly know what another person sees when they look at the world, but I feel sure that it's nothing the rest of us would recognise. People with synesthesia, for example, can hear colours, and, growing up, probably assumed that the rest of us do as well.

The only thing we have in common is the fact that we have almost nothing in common. Thats why everyone reacts differently, and its one of the reasons why so many people hate each other so much. I really wish more of us would realise that; it would solve so many problems in this world.

For my part, I rather like the fact that I'm seeing things the way you don't (or vice versa). It constantly reminds me that everyone sees something different when they look at the same things. That's what gives the world its diversity.

Sadly, some people are frightened by diversity. I will never understand that. It's as plain to me as the face on your nose.

If you think you might have prosopagnosia, my best advice is to talk about it with your family and close friends. Compare notes. Let them know what youre dealing with. It really helps.

There are various facial recognition tests that are freely available online. I recommend these two:

http://www.faceblind.org/facetests/ff/ff_intro.php and http://facememory.psy.uwa.edu.au/

There are also many chat rooms, forums and Facebook groups devoted to prosopagnosia, including this Yahoo group:

https://groups.yahoo.com/neo/groups/faceblind/info

And finally, here is the NHS information page about prosopagnosia:

http://www.nhs.uk/Conditions/prosopagnosia/Pages/Introduction.aspx

Thanks for reading.

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Is Puma Biotechnology, Inc. (PBYI) a good buy? – TopChronicle

May 26th, 2017 2:41 pm

Share Price and 1 Year Extreme Prices Analysis

The share of Puma Biotechnology, Inc. (PBYI) currently has a value of $78.05 while the companys 52 week low is at $27.64, the shares dropped to the 52 week low on 06/27/16. While the companys share hit the 52 week high on 05/25/17 stationing the value of $75.10.

The difference of 52 week low value as well as 52 week high value and the current price of the stock suggests the next move of the shares. If the share price is currently hovering near the 52 week low and the value is achieved in the current past then it can suggest that the price of the shares is likely to go up.

Share Volume Analysis

The volume of the particular stock is the shares bought and sold in a single trading day. The average volume of a stock suggests the liquidity of a particular company. If the average volume is low then the liquidity is low which means it is hard to buy or sell the stock as there are fewer buyers or sellers of the stock.

Currently the shares of Puma Biotechnology, Inc. (PBYI) has the trading volume of 5.7 Million shares with the average trading volume of 5180 shares.

Price to Earnings Ratio

P/E of the company is not reported.

Earnings per Share EPS

Yet another important factor while evaluating a good buy/sell decision for Puma Biotechnology, Inc. (PBYI) is its Earnings per Share or EPS. EPS breaks down the profitability of the company on a single share basis.

Currently, EPS of Puma Biotechnology, Inc. (PBYI) is -1.97 while the analysts predicted the EPS of the stock to be -1.98 suggesting the company fell short of the analysts expectations.

Market Capitalization Analysis

Market Capitalization can be thought of as the overall price to buy the company. Market Capitalization if basically the market value of the companys shares outstanding. Market Cap is also the figure use to determine companys size, as opposed to using sales or total asset figures.

Puma Biotechnology, Inc. (PBYI) has a market capitalization of 2.89 Billion which suggests the company is a huge company further suggesting that the shares of Puma Biotechnology, Inc. (PBYI) are stable and safe compared to the lower market capitalization companies.

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The Bears And Bulls Square Off On Puma Biotechnology, Inc. (PBYI) – NY Stock News

May 26th, 2017 2:41 pm

NY Stock News
The Bears And Bulls Square Off On Puma Biotechnology, Inc. (PBYI)
NY Stock News
Puma Biotechnology, Inc. (PBYI) has presented a rich pool of technical data in recent sessions. These are the trends we've been tracking and how we feel they should be played in the current environment. Successful trading professionals know that in ...

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Older adults might be able to stave off arthritis knee pain with fiber – Reuters

May 26th, 2017 2:41 pm

Older people who eat the most fiber are at lower risk of developing knee pain and stiffness due to osteoarthritis (OA), new research shows.

Diets rich in fiber from plant-based foods have clear health benefits, such as lower cholesterol, better-controlled blood sugar, and a healthier weight, but most people in the U.S. dont eat enough fiber, lead author Dr. Zhaoli Dai of Tufts University in Boston told Reuters Health.

The current average fiber intake among U.S. adults is about 15 grams, she noted. This is far below the recommended level, which is 22.4 grams for women and 28 grams per day for men 51 years and above, Dai said.

OA, which occurs when wear and tear on the joints degrades cartilage and leads to bone abnormalities, is extremely common in people 60 and older. It can be painful, and is also a leading cause of disability. There is no treatment for OA, aside from joint replacement, and therapies to address symptoms, such as anti-inflammatories for pain and swelling.

Given that dietary fiber is known to help prevent obesity and reduce inflammation, both of which are associated with arthritis, Dais team looked at diet and arthritis risk over time in two study groups. In the Osteoarthritis Initiative, which included 4,796 men and women with OA or at risk for OA, people who consumed the most dietary fiber at the start of the study were 30 percent less likely than those who ate the least fiber to develop knee pain, stiffness or swelling due to OA, or to worsening of OA, during four years of follow-up.

In the Framingham Offspring Study, which included 1,268 adults in their early 50s, on average, the top quarter of fiber consumers had a 61 percent lower risk of knee OA symptoms nine years later than the bottom quarter.

There are many mechanisms through which increased fiber intake could help ease knee arthritis symptoms, Dai said, for example by reducing inflammation and helping people to maintain a healthy weight. Fiber can also act as a pre-biotic, she added, meaning that it can help fuel the growth of beneficial microbes in the gut, which in turn also reduces inflammation.

This is the first study to show that consuming more dietary fiber is related to lower risk of painful knee osteoarthritis, Dai said. Changing diets by increasing intake of dietary fiber seems to be one of the most economic ways to reduce the risk of knee osteoarthritis.

Older adults, especially those who are overweight or obese, should consider increasing their fiber intake, she added.

SOURCE: bit.ly/2rVN8xU Annals of Rheumatic Diseases, May 4, 2017.

NEWTON, Mass. Former U.S. Army Specialist Tara Barney will never forget the 2013 night when a fellow soldier cried as he described holding a dying friend in his arms, a wartime memory he had not shared with anyone.

A moderate-intensity walking regimen may reduce symptoms of mild cognitive impairment that are linked to poor blood vessel health in the brain, a small study suggests.

LONDON The number of new drugs approved for sale in United States and Europe has bounced back this year, suggesting a marked slowdown in 2016 was an aberration rather than a sign of flagging research and development productivity.

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Arthritis in your hands? This new invention could change your life – Express.co.uk

May 26th, 2017 2:41 pm

GETTY

Arthritis can affect multiple parts of the body, including the fingers, hands and wrists.

This can cause trouble holding items, meaning cooking can become a challenge.

However, a university student has created a saucepan that can help sufferers of the condition retain their independence.

Emma Bucknell, who is studying for a BA (Hons) in Product Design at Nottingham Trent University, has designed it to make cooking more comfortable.

GETTY

It has a plastic handle on one side so users can slide their hand through it, meaning the saucepan can be lifted using the strength in the arm as opposed to the hand.

It has a plastic handle on one side so users can slide their hand through it, meaning the saucepan can be lifted using the strength in the arm as opposed to the hand.

The design does away with a traditionally straight saucepan handle, and instead aims to reduce weight and pressure that is placed on peoples fingers and hands.

Bucknell said: I know from my grandparents that arthritis is a painful and uncomfortable condition. My nan struggles with lifting saucepans so I took the opportunity to find a solution to help them.

During research she discovered that long, thin handles can prove a problem for arthritic people, because the hand is forced to perform an unnatural grip while holding on to them.

Getty

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She added: I can see that arthritis does not just affect a person with its painful symptoms, it affects their whole life. What many people would see as a simple task, can become difficult and sometimes impossible for those with the condition.

This can destroy independence; the one thing elderly and retired people desire to keep.

The aluminium saucepan is light to hold, and its handle can fit a range of different hand sizes.

It will go on display at the universitys 2017 Degree Show from 3 to 10 June at the City Campus.

GETTY

James Dale, principal lecturer in Product Design at Nottingham Trent University, said: Emma has seen first-hand how difficult it can be for people with arthritis to carry out tasks such as cooking and she has used this experience to create a product that could improve peoples confidence and independence.

The saucepan has the potential to go beyond the elderly market and reach others who have the same condition.

According to Arthritis Care, approximately 10 million people suffer from arthritis in the UK.

Both osteoarthritis and rheumatoid arthritis can affect the joints in the hands.

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Arthritis: Suffering from arthritis? Vitamin D supplements may help – Economic Times

May 26th, 2017 2:41 pm

SYDNEY: Vitamin D supplements, combined with good sleeping habits, could help manage pain-related conditions including fibromyalgia, arthritis, menstrual cramps and chronic back pain, says a study.

The findings, published in the Journal of Endocrinology, suggest that vitamin D supplements combined with good sleep quality could increase the effectiveness of pain management treatments.

Previously published studies have shown that vitamin D can affect the body's inflammatory response, which also alters pain sensation.

This simple approach, if effective, could reduce the burden on health services and improve the lives of patients, the researchers said.

"The research is very exciting and novel. We are unravelling the possible mechanisms of how vitamin D is involved in many complex processes, including what this review shows -- that a good night's sleep and normal levels of vitamin D could be an effective way to manage pain," said Sof Andrikopoulos, Assistant Professor at University of Melbourne in Australia.

For the study, the team conducted reviews of the most relevant studies that have examined the role of vitamin D in pain-related conditions or sleep disturbances.

The results indicate that vitamin D levels may have an important role in the relationship between pain and sleep.

"It is necessary to understand the possible mechanisms involved in this relationship, including immunological and neurobiological pathways related to inter-relationship among sleep, vitamin D and pain," added Monica Levy Andersen from Universidade Federal de Sao Paulo in Brazil.

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How to protect yourself against vision loss, a growing problem – Chicago Tribune

May 25th, 2017 11:52 pm

Ask Americans to name the ailment they fear most, and blindness ranks at the top, along with Alzheimer's and cancer, according to a recent survey by the Wilmer Eye Institute at Johns Hopkins University. And yet each year, 50,000 Americans go blind, nearly half from eye diseases that are treatable or preventable.

What's worse, the number of Americans who are either blind or visually impaired is expected to double by 2050, most of it driven by an aging population and the growing number of people with chronic conditions that can cause vision loss, such as diabetes, says James Jorkasky, executive director of the National Alliance for Eye and Vision Research.

The challenge for vision experts is to make Americans aware of the things they can do to protect their eyesight, including getting a regular eye exam. Only half of the estimated 61 million Americans at high risk of losing their eyesight had an eye exam in the past 12 months partly due to a lack of insurance coverage for preventive eye care and glasses, noted a National Academies of Sciences, Engineering and Medicine report last fall, but also because many eye diseases don't show symptoms in the early stages, so people don't realize they have a problem.

Doctors, too, may need to step up their game. A new study in the journal JAMA Ophthalmology found that in one of four cases, trained eye professionals missed the early, more treatable signs of age-related macular degeneration (AMD) an irreversible loss of vision that affects 14 million Americans.

But there is some good news for those already diagnosed with eye disease, including new treatments and cutting edge research that could bring hope to millions in the near future. There are also simple changes everyone can do to greatly reduce their risk of eye disease. Here's what you need to know:

Cutting edge technologies

Glaucoma is caused by a buildup of damaging pressure within the eye and requires a daily dose of medicated eye drops to hold the disease at bay. Unfortunately, getting patients to follow that regimen daily for years is difficult, says Dr. Andrew Iwach, board chairman for the Glaucoma Research Foundation. Instead, clinical trials have started testing a thin polymer ring to be worn in the eye that would slowly release medication throughout the day. "It's like drip irrigation, rather than flooding the eye," Iwach says.

Using stem cells to regenerate healthy cells in disease-damaged eyes is the holy grail for researchers. This is especially true for incurable conditions that damage the retina, the layer of light-sensitive cells at the back of the eye.

Earlier this year, a Japanese man became the first person to receive retinal stem cells created from donated skin cells to stop his macular degeneration from getting worse.

And scientists at the Jules Stein Eye Institute at the University of California at Los Angeles report promising results from transplanting stem cells from embryonic cells into patients who had been blind for decades from AMD and another disease. A study in 2014 reported that 10 of the 18 patients who received the cells experienced significantly improved vision.

The Argus II, a bionic retina approved by the Food and Drug Administration, is now being used by more than 100 people with retinitis pigmentosa and other related conditions. It also recently was implanted in the first person with macular degeneration.

This "bionic eye" uses a tiny camera attached to glasses that sends visual data to a microchip implanted in the eye, which then sends light signals to the brain. So far, the vision it provides is rudimentary, but patients say even some vision can greatly improve the quality of life for a blind person.

Ways to help your eyes

To keep your eyes healthy, says the National Eye Institute, get a dilated eye exam to detect problems early; know your family history and whether you're at risk for eye disease; wear sunglasses to block out ultraviolet rays that can increase the risk of cataracts; and control your diabetes to prevent damage to the retina.

Here are five other surprising things that can help:

Adjust your yoga and sleep position: Those with glaucoma should avoid head-down positions in yoga (downward facing dog, for example), which can cause a dangerous rise in internal eye pressure, a study last year found. Other studies show that habitually sleeping on one side can cause greater pressure and worsening vision loss in the eye facing downward.

Got dry, irritated eyes? Add more fish to your diet. The omega-3 oils in fish not only can cut the risk of dry eyes, studies show, but omega-3 fish oil supplements may improve dry eye symptoms. A new study published in the journal Cornea found that taking a daily omega-3 supplement improved dry eye symptoms after six weeks.

Think of it as Vitamin See. A diet high in vitamin C oranges, red peppers, strawberries, broccoli may help curb cataracts by 33 percent. British researchers believe vitamin C helps prevent the clouding of the lens that causes cataracts, but their findings only pertain to vitamin C from food, not supplements.

Send your children outside. Adults aren't the only ones with dry eye woes. A new study finds the same problem among children ages 7 to 12 who spend more than three hours daily looking at a smartphone. Playing outside could help. Researchers at the University of Cambridge report that for every hour children play outside in natural light with far-away horizons, they reduce their risk of near-sightedness by 2 percent.

Exercise (and spinach) helps glaucoma. A brisk walk for 20 minutes four times a week can lower the pressure inside the eye, which helps protect the retina, according to the Glaucoma Research Foundation. Adding more dark, leafy greens spinach, kale to your diet could help too. A recent study found that those who ate the most greens were 21 percent less likely to develop glaucoma.

Candy Sagon is a freelance writer.

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Goold: Working to save his vision, Pham never loses sight of goal – STLtoday.com

May 25th, 2017 11:52 pm

There will be times during games, perhaps between pitches or during pitching changes, that Tommy Pham will give himself an impromptu eye test in the outfield.

Hell pinch one eye shut and make sure the signs around the ballpark are still as crisp as they were the day before, still as clear as they were a few innings ago. Then hell check the other eye. The Busch Stadium carved into the wall behind home plate offers a constant to focus on, but any of the advertisements or scoreboards can become a personal, daily eye chart. This past week, against Boston, Pham actually switched the contact lens in his left eye between innings because he didnt like what he saw or, rather, couldnt see.

To thrive at a game that can change in a blink, this is how vigilant the Cardinals resurfacing outfielder must be to avoid being betrayed by his vision, again.

I look at all of them Busch Stadium, KMOX, the scoreboard, all of that, Pham said. Ive got to make sure this is the best lens because the best lens gives me the best opportunity. If my left eye gets any worse, Im in trouble. If my right eye gets any worse, Im in trouble.

Pham, 29, returned to the majors two weeks ago, and before going on a tear with a .304 average and a .587 slugging percentage in his first 12 games, he warned people they were about to hear a familiar tale. After an aggravating spring, his offensive awakening came immediately after he got new contact lenses. Since first being diagnosed in 2008 with a degenerative eye condition, keratoconus, Pham has had a breakthrough surgery to halt the erosion and since cycled through a variety of contact lenses looking for the right fit, even if its just fit for right now.

Keratoconus causes structural abnormalities in the cornea, warping it and leaving it similar to the shape of a footballs tip. Instead of light bending toward the retina to be processed as an image, the light scatters, splinters. Halos or double images can appear. Pham said he is legally blind in his left eye due to keratoconus.

Its like driving a car with someone who is holding a jar of Vaseline, said Dr. Brian Boxer Wachler, a Beverly Hills, Calif.-based surgeon and ophthalmologist, and then they smear it all over your windshield.

Before Boxer Wachler pioneered a non-invasive treatment, the remedy for the keratoconus was a corneal transplant, and the combination of vanishing vision and that extreme correction has forced athletes from their games. It led one Olympic bobsledder, the late Steven Holcomb, to deep depression and a failed suicide attempt. Boxer Wachlers treatment allowed Holcomb to race again, for a Gold Medal. Keratoconus affects one in 500, Boxer Wachler said, and it was Holcombs recovery and Winter Olympics success that brought new attention to the disease.

Boxer Wachler said hes treated several elite athletes, including an NHL player, but few have a career based around striking a small, fast-moving object with a round stick. Pham is one.

What Tommy Pham sees is different than what we see, said Dr. Edward S. Bennett, a professor and assistant dean for student services and alumni relations at UMSLs College of Optometry. He has been Phams doctor in St. Louis. Its like looking through a window and there might be a smudge, there might be a crack, but there isnt that crisp clear view. If somebody would tell me an individual could play Major League Baseball with keratoconus, Id say, Absolutely not. Only Tommy Pham. I think Tommy is one in a million.

Pham was back at Dr. Bennetts office Friday to get another pair of contact lenses because his backup just wasnt right. Before the Cardinals played recently in Miami, Pham tore two left lenses and had to have a new one flown in from Las Vegas just to play. Most players have a guy who gets them bats, or a guy who can get them fly shoes, or, like Carlos Martinez, a guy they frequent for haircuts. Pham is considering flying home to Las Vegas on Monday, an off day, because hes got a guy who can sharpen my lenses.

His pursuit of better vision hasnt ended since it began, in Jupiter, Fla.

The Cardinals selected Pham in the 16th round of the 2006 draft, and they billed him as an athletically gifted shortstop with bat speed to create havoc. They saw it only in flashes those early years, but Pham mostly struggled. Teammates described seeing details in the spin of breaking pitches he never could and never has, he said Friday. He presumed as a young player that his talent, not his eyesight, was outmatched.

It was new to me, Pham said. Everyone was throwing harder. I was facing competition older than me. So, I just felt, man, this is what I have to do to catch up. I just thought I had to adjust.

In 2008, he hit .203 for the season but also slugged 18 home runs in 394 at-bats. He returned to Florida to pick up the car he left behind, and was greeted there by then-farm director Jeff Luhnow. Pham explained his average was the result of his swing. Luhnow suggested it was his sight. After a flight to St. Louis and a checkup there, Pham was diagnosed with keratoconus. Now he had an explanation.

To save his career, he needed a solution.

Vision is the most important thing (in baseball). Youve got to see it to hit it. Simple as that, said Dr. Don Tieg, a consultant for the New York Yankees who oversees a sports vision institute. Ive worked with (multiple) major-league teams and there was usually one player with some vision issue that youd think would not let them get to the top, and they won a Cy Young Award or are in the Hall of Fame. Athletes compensate. The question becomes how do you do that if youre impaired by keratoconus? More power to him.

During the 2011 offseason, Pham visited Boxer Wachler and had the treatment now named Holcomb C3-R Cross Linking System. The procedure uses a vitamin application and ultraviolet light to strengthen the cornea. Boxer Wachler said hes performed about 6,000 of the procedures, which gained FDA approval last year, and the success rate is 99.3 percent. In a video filmed shortly after he had Holcomb C3-R, Pham describes how hes had other surgeries that brought him to tears.

This one put something else in his eyes: relief.

If I never had it, who knows where I would be right now, Pham said.

Since LASIK was never an option, Pham had a set of contact lenses that improved his eyesight, from 2009 until he landed 52 games in the majors in 2015. He once experimented with a new type of lenses only to have them slide and shift and blot out his vision when he tracked fly balls. He experienced similar issues last season, even as he hit nine home runs. During the All-Star break, he, Dr. Bennett, and Phams handful of self-improvement books drove to Iowa to meet with a specialist for assistance. Another set of contacts came. The issues continued into the spring and undermined his bid for the opening-day roster. Nine years after he learned it wasnt his swing, it was his sight, he had the same lesson. Experimenting with new contacts had backfired on me.

With the help of his optometrist in Vegas and Dr. Bennett in St. Louis, Pham concluded that he needed to use a brand of contacts that uses a corneal topographer literally a map-maker for the eye to create curvatures that allow for a snugger fit on irregular corneas. One flaw can throw his vision off. This is why Pham does his daily check of the advertisements.

K-M-O-X spells clear.

Clear means his career.

With Tommy Pham a mild change can turn a home run into a strike out, said Dr. Bennett, who had Phams permission to speak with the Post-Dispatch. He is just so totally dedicated. He is consumed. Thats why hes been successful.

When Boxer Wachler first met Steven Holcomb, the U.S. bobsled driver had already been to the brink. As he recounted in his book, But Now I See, and elsewhere, Holcomb washed down 73 sleeping pills with whiskey in attempt to escape the blindness swallowing his eyes. Keratoconus was about to force him from his beloved sport, until Boxer Wachler told him about his procedure.

He was still skeptical, Boxer Wachler recalled this past week. All he had heard was this kind of prison sentence of corneal transplant.

What became known as Holcomb C3-R offered more than parole. It improved his vision from 20/1,000 to 20/20, according to reports, and he led the U.S. bobsledders to gold in Vancouver and won two Bronze Medals in Sochi 2014. Earlier this month, Holcomb was found dead in his room at the Olympic training facility in Lake Placid, N.Y. Boxer Wachler became close friends with Holcomb and relayed what the bobsledder often said about the role he came to play for others with keratoconus, now his legacy.

He saw it as a bigger purpose.

Gives them hope, Boxer Wachler said. Gives them hope that they can be helped. You dont have to just wait and wait and lose and then get a corneal transplant. Others see him succeed and know its possible. Tommys story, in that bigger purpose, can give hope, too.

Pham, who has hit his way into a larger role with the Cardinals, acknowledged that hes been asked to embrace a larger role as spokesperson. He noted its something he must consider. In the clubhouse Friday, Pham recounted details of his latest apportionment and during his answers he would close an eye, squint, and open it wide. He was trying to read the nameplate on his locker from the other side of the room. Asked what kept him chasing the game through all this, Pham opens both eyes wide.

Even as his vision failed, his focus remained.

I would regret quitting on my ability before I made it to the major leagues, Pham said. I saw other guys make it to the majors, and there were times I think I was better, that I was good enough.

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Healthy Vision Month a perfect time to focus on eye care – San Angelo Standard Times

May 25th, 2017 11:52 pm

Julian Roberts, National Association of Vision Care Plans 5:32 a.m. CT May 23, 2017

Throughout the year many Texans make the time for a routine visit to their physician and dentist, and rightly so. But one fundamental area of our health that can unfortunately be overlooked is vision.

May is Healthy Vision Month and an excellent reminder that eye care should be a top priority for all Texans. Vision care is essential health care. And in my role as executive director of the National Association of Vision Care Plans (NAVCP), I am committed to furthering that notion by ensuring people throughout this great state have access to exceptional vision care at an affordable price.

This is an extremely important issue because virtually every age group from young children to the elderly, and everyone in between requires some form of vision care. Consider that more than 80 percent of adults in the U.S. need vision correction. An aging population means that even more Texans will in the coming years need vision correction and eye exams to ensure and protect their sight.

A number of experts have expressed concerns that the rise in use of digital devices with screens will result in the need for increased vision correction at even younger ages. This is concerning because approximately three-quarters of all childhood learning is visual. Proper eye care that commences at an early age is more important than ever.

It is also worth noting that regular eye exams are an affordable, noninvasive way to detect serious medical conditions such as hypertension, diabetes, neuromuscular disorders and cancer. Its staggering to think how much we could drive down healthcare costs and even save lives here in Texas and elsewhere if we are able to catch serious health issues earlier through routine eye exams.

The results of a recent study commissioned by NAVCP the most extensive review ever of available data indicate that consumers exhibit healthier eye care behavior when they have vision care benefits. The study found that nearly 90 percent of Americans with vision benefits planned on getting an eye exam within the next year, while 67 percent of those who did not have vision benefits had no intention of receiving an eye exam. Once the exam had been completed, almost twice as many people with a benefit planned to get new eyewear compared to those without a benefit. This data establishes a clear link between managed vision care plans and healthier vision habits. It also underscores the value of these plans for promoting better overall health.

Yet, even in the face of compelling data such as this, there have in recent years been legislative efforts in the Lone Star State that have increased consumers out-of-pocket costs and limited their eyewear choices. Texans deserve better.

I encourage you to observe Healthy Vision Month by getting an eye exam or accompanying a family member to the eye doctor. Take control of your vision. Now, see to it.

Julian Roberts is the Executive Director of the National Association of Vision Care Plans (NAVCP).

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Scientists Use the Tweaked Genes of a Virus to Halt Vision Loss – Mental Floss

May 25th, 2017 11:52 pm

Dogs are a lot more complicated than we give them credit for. As a result, sometimes things get lost in translation. Weve yet to invent a dog-to-English translator, but there are certain behaviors you can learn to read in order to better understand what your dog is trying to tell you. The more tuned-in you are to your dogs emotions, the better youll be able to respondwhether that means giving her some space or welcoming a wet, slobbery kiss.

1. What youll see: Your dog is standing with his legs and body relaxed and tail low. His ears are up, but not pointed forward. His mouth is slightly open, hes panting lightly, and his tongue is loose. His eyes? Soft or maybe slightly squinty from getting his smile on.

What it means: Hey there, friend! Your pup is in a calm, relaxed state. Hes open to mingling, which means you can feel comfortable letting friends say hi.

2. What youll see: Your dog is standing with her body leaning forward. Her ears are erect and angled forwardor have at least perked up if theyre floppyand her mouth is closed. Her tail might be sticking out horizontally or sticking straight up and wagging slightly.

What it means: Hark! Who goes there?! Something caught your pups attention and now shes on high alert, trying to discern whether or not the person, animal, or situation is a threat. Shell likely stay on guard until she feels safe or becomes distracted.

3. What youll see: Your dog is standing, leaning slightly forward. His body and legs are tense, and his hacklesthose hairs along his back and neckare raised. His tail is stiff and twitching, not swooping playfully. His mouth is open, teeth are exposed, and he may be snarling, snapping, or barking excessively.

What it means: Dont mess with me! This dog is asserting his social dominance and letting others know that he might attack if they dont defer accordingly. A dog in this stance could be either offensively aggressive or defensively aggressive. If you encounter a dog in this state, play it safe and back away slowly without making eye contact.

4. What youll see: As another dog approaches, your dog lies down on his back with his tail tucked in between his legs. His paws are tucked in too, his ears are flat, and he isnt making direct eye contact with the other dog standing over him.

What it means: I come in peace! Your pooch is displaying signs of submission to a more dominant dog, conveying total surrender to avoid physical confrontation. Other, less obvious, signs of submission include ears that are flattened back against the head, an avoidance of eye contact, a tongue flick, and bared teeth. Yupa dog might bare his teeth while still being submissive, but theyll likely be clenched together, the lips opened horizontally rather than curled up to show the front canines. A submissive dog will also slink backward or inward rather than forward, which would indicate more aggressive behavior.

5. What youll see: Your dog is crouching with her back hunched, tail tucked, and the corner of her mouth pulled back with lips slightly curled. Her shoulders, or hackles, are raised and her ears are flattened. Shes avoiding eye contact.

What it means: Im scared, but will fight you if I have to. This dogs fight or flight instincts have been activated. Its best to keep your distance from a dog in this emotional state because she could attack if she feels cornered.

6. What youll see: Youre staring at your dog, holding eye contact. Your dog looks away from you, tentatively looks back, then looks away again. After some time, he licks his chops and yawns.

What it means: I dont know whats going on and its weirding me out. Your dog doesnt know what to make of the situation, but rather than nipping or barking, hell stick to behaviors he knows are OK, like yawning, licking his chops, or shaking as if hes wet. Youll want to intervene by removing whatever it is causing him discomfortsuch as an overly grabby childand giving him some space to relax.

7. What youll see: Your dog has her front paws bent and lowered onto the ground with her rear in the air. Her body is relaxed, loose, and wiggly, and her tail is up and wagging from side to side. She might also let out a high-pitched or impatient bark.

What it means: Whats the hold up? Lets play! This classic stance, known to dog trainers and behaviorists as the play bow, is a sign shes ready to let the good times roll. Get ready for a round of fetch or tug of war, or for a good long outing at the dog park.

8. What youll see: Youve just gotten home from work and your dog rushes over. He cant stop wiggling his backside, and he may even lower himself into a giant stretch, like hes doing yoga.

What it means: OhmygoshImsohappytoseeyou I love you so much youre my best friend foreverandeverandever!!!! This ones easy: Your pup is overjoyed his BFF is back. That big stretch is something dogs dont pull out for just anyone; they save that for the people they truly love. Show him you feel the same way with a good belly rub and a handful of his favorite treats.

The best way to say I love you in dog? A monthly subscription to BarkBox. Your favorite pup will get a package filled with treats, toys, and other good stuff (and in return, youll probably get lots of sloppy kisses). Visit BarkBox to learn more.

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Columbus Lions help transport donor eye tissue – Columbus Journal

May 25th, 2017 11:52 pm

The Columbus Lions Club transports donor eye tissue two months out of the year, in May and October. Lion Linda Madsen and Lion Bob Groh act as the Columbus Lions eye coordinators. This year the Columbus Lions are celebrating their 30th anniversary as a club, and over these years have transported countless numbers of boxes containing donor eye tissue. Many of the clubs members and their family and friends drop what they are doing to transport eye tissue when they receive a call from Madsen or Groh, to ensure that the donor eye tissue is delivered in a timely manner. So far this month, 26 boxes of donor tissue have been transported (with 11 days left in May that might add to this total).

Lion Jack Sanderson was delivering three boxes of donor eye tissue to the Lions Eye Bank of Wisconsin on Saturday May 13 when Jimmy Cliffs song I Can See Clearly Now came on the radio. He said it was very inspirational to him since he knows that delivering donor eye tissue could lead to someone regaining their sense of sight. Sanderson transported a total of five boxes of tissue that day, because the Lions Eye Bank had processed tissue that was intended for transplantation that needed to be sent out.

The Columbus club is part of the Cornea Express, a statewide relay of Lions Club members who transport tissue throughout Wisconsin. The Lions Eye Bank of Wisconsin uses this unique process of transporting donor eye tissue, and it makes a huge impact. When a donation occurs, local Lions clubs are called upon to transport the corneal tissue to the Lions Eye Bank of Wisconsin via a relay system. Volunteers use their own vehicles to transport the donor tissue.

The Lions Eye Bank of Wisconsin needs eye and corneal tissue from donors of most ages. The eye tissue is used for more than just restoring vision: It can also be used to further research for certain diseases such as glaucoma and macular degeneration. The Lions Club has a focus of helping people prevent blindness, and this is just one of the examples of what Lions do to serve their communities.

To read donor stories and learn more about Lions Eye Bank of Wisconsin, go online to lebw.org.

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Gaston 5-year-old lobbying Congress for Type 1 diabetes cure – Gaston Gazette

May 25th, 2017 11:52 pm

Eric Wildstein Gazette staff TheGazetteEric

Hes only 5 years old, but hes preparing to advocate for juvenile diabetes research before Congress.

Miles Bone spent Wednesday morning engaged in a wild, water war with his pre-kindergarten classmates at Gaston Day School to celebrate the end of the year. After toweling off, he readied to eat a chicken nuggets lunch from Chick-fil-A with everyone.

But first, he had to prick his finger with a needle to test his blood glucose level, a ritual he must repeat several times each day as a Type 1 diabetic. He entered his glucose number into an insulin pumpwhich he wears basically 24/7that injects him with the correct amount of insulin through a tube attached to his arm to keep his blood glucose stable after eating.

We talked about last night how he wants to show people what its like to have Type 1 diabetes because a lot of people dont know, said Sara Bone, Miless mother. A lot of people dont understand what Type 1 diabetes is and how much it affects his life and how hard he has to work to take care of himself.

Type 1 diabetes, also known as juvenile diabetes, is an autoimmune disease in which a persons pancreas stops producing insulin, a hormone people need to get energy from food. Children and adults can be diagnosed suddenly at any age. It cannot be prevented and there is no cure.

Miles, who lives in Dallas with his parents and older brother, will advocate for Type 1 diabetes research on Capitol Hill in late July. He applied and was selected to be part of a delegation of about 160 children from each U.S. state and several countries representing the Juvenile Diabetes Research Foundation 2017 Childrens Congress, a bi-annual event.

The delegates will be lobbying their representatives of Congress to remind them of the vital need to continue supporting Type 1 diabetes research that could reduce the burden of the disease and ultimately find a cure.

CC 2015 Highlights from JDRF on Vimeo.

These childrenages 4 to 17will participate in a number of activities on the Hill, including a Congressional Committee hearing to share personal testimonies that highlight the daily struggles of living with Type 1 diabetes and the need for continued funding for research projects such as the Special Diabetes Program, which provides $150 million annually for Type 1 diabetes research at the National Institutes of Health.

I want Miles to one day be able to eat some pizza and not feel bad three hours later for doing it, said Sara Bone. I think that were almost there and I want him to actually know a day where he doesnt have to worry about it.

Miles was diagnosed with Type 1 diabetes just three days after his first birthday. His parents noticed he was feeling ill and scheduled a visit with his pediatrician. Miles was hospitalized with diabetic ketoacidosis, a potentially-deadly result of extremely high blood glucose and remained there for three days before his release. It was a scary time for his parents and brother, who had no family history of Type 1 diabetes and were new to caring for the condition.

It was the scariest thing that first day we brought him home, said Sara Bone. You just think how am I ever going to do this.

They would learn to balance the high and low blood glucose fluctuations that result from diabetes and how to maintain them with a proper diet. That includes keeping a close eye on what Miles eats, delivering insulin at the proper times and boosting low blood glucose with juice boxes, glucose tablets or another form of carbohydrate.

At school, Miless teachers help him to keep track of his health, though hes already handling a lot of the heavy lifting on his own. Sara Bone says its a constant balancing act and it causes Miles to miss out on or delay certain activities so that he can care for his diabetes. But she feels its already made him a stronger person.

Its made him more compassionate, she said. Its made his brother a compassionate kid. He really cares about Miles and wants to see him OK and cares about his future.

And Miles will work toward that brighter future by joining a long list of other advocates with Type 1 diabetes, such as celebrities including the NHL Hall of Fame hockey player Bobby Clarke, musicians Bret Michaels and Nick Jonas, and the late actress Mary Tyler Moore.

NASCAR Xfinity series driver Ryan Reed, 23, was diagnosed with Type 1 diabetes in 2011. He later began his nonprofit organization, Ryan's Mission, which advocates and raises money for Type 1 diabetes research.

Reed will host the Lilly Diabetes #DriveYourHealth Track Walk from 2 to 4 p.m. Friday at the Charlotte Motor Speedway. Lilly Diabetes will make a donation to the American Diabetes Association Charlotte Chapter for each participant who reaches the finish line.

Reed will also sport the Lilly Diabetes logo on his No. 16 Ford Mustang at the NASCAR Xfinity series events at the speedway this weekend.

Miles and his family have already been doing their part. The family has participated in five Juvenile Diabetes Research Foundation One Walks and mentored several families who are new to Type 1 diabetes.

As for what Miles hopes his talks with Congress will yield for type 1 diabetes, he says optimistically a cure.

You can reach Eric Wildstein at 704-869-1828 or Twitter.com/TheGazetteEric.

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Nutrition Corner: Control diabetes with low-carbohydrate vegetable – The Sunday Dispatch

May 25th, 2017 11:52 pm

The Sunday Dispatch
Nutrition Corner: Control diabetes with low-carbohydrate vegetable
The Sunday Dispatch
The number of people affected by diabetes and pre-diabetes continues to grow. In our area, 11 percent of the population more than one out of 10 people have diabetes. How many are undiagnosed? Nationwide, 9.3 million, or 21 percent of the ...

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HRRMC receives grant for diabetes prevention outreach – Chaffee County Times

May 25th, 2017 11:52 pm

Heart of the Rockies Regional Medical Center Foundation was one of seven local nonprofit organizations awarded a grant by the Climax Area Community Investment Fund on May 3. The fund supports programs and projects that promote health and wellness.

The $41,500 grant will support a unique partnership between Heart of the Rockies Regional Medical Center in Chaffee County and St. Vincent Hospital in Lake County to implement the National Diabetes Prevention Program, a nationally recognized diabetes prevention program. Education and improved access to quality health care can help individuals at risk for diabetes. The funds will also be used to increase the availability of fitness, nutrition and other health education in the region.

The National Diabetes Prevention Program is the most effective intervention for lifestyle change that I've seen in my 20-year career, said HRRMC Wellness Supervisor Jon Fritz.The group class is led by a trained coach and encourages increased activity and decreased caloric intake. The answers are simple but the process is challenging and that's why trained coaches follow an evidence-based curriculum which has proven effective.

Chaffee County has had an NDPP program since 2013. Lake County and St. Vincent Hospital have identified diabetes prevention as a focus in their community. HRRMC will offer assistance in starting an NDPP program while expanding classes throughout Chaffee County.

HRRMC Foundation director Kimla Robinson accepted the award along with Fritz on behalf of the hospital. We are so honored to receive the Freeport-McMoRan Climax Area Community Investment Fund Grant and partner with St. Vincent Hospital to implement a diabetes prevention program, she said.

The Climax Area Community Investment Fund was established in 2011 to focus on programs and projects that help create sustainability and reduce dependency on any single industry. Eligible programs and projects include those in the areas of education, community and economic development, environmental stewardship, and health and wellness. A committee comprised of community leaders representing diverse organizations and two Freeport-McMoRan representatives governs the Fund.

For more information on the NDPP program, call the HRRMC Wellness Department at 530-2057.

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A potential game-changer to battle lung disease in premature babies. – CTV News

May 25th, 2017 11:49 pm

Joanne Schnurr, CTV Ottawa Published Thursday, May 25, 2017 3:33PM EDT Last Updated Thursday, May 25, 2017 6:55PM EDT

An Ottawa doctor and scientist has been awarded more than half a million dollars for ground-breaking research into using umbilical stem cells to fight chronic lung disease in premature babies.

It is research that Dr. Bernard Thbaud calls a game-changer. Right now, Dr. Thbauds work is in the early stages but there are indications that this could dramatically help the outcome for babies who are born weeks before they are due. And, the protective power of these stem cells may have multiple applications.

May 24th is the day that Olivia Eberts should have been born. But she and her twin brother Liam decided to come into the world 115 days early at just 23 weeks and 4 days gestation.

Liam passed away at 3 weeks, says his mother, Jamie Eberts, He unfortunately didn't make it; he was much sicker than Olivia.

Olivia has had her struggles, too. Born at just over one pound, she's had heart surgery, kidney problems and lung problems from the artificial help to keep her tiny lungs working.

Theres a lot of issues that come along with being born as young as they are, says Jamie, and it's going to be a lifelong battle for her and we don't know what the future will bring.

Dr. Bernard Thbaud is working on that future. Dr. Thbaud, a neonatologist and senior scientist at The Ottawa Hospital and CHEO, and professor at the University of Ottawa, is doing research into the possibility of using stem cells from the umbilical cord to combat lung disease in premature babies.

What we see in lab is very promising, he says, We think this will be a game changer, because the way these cells act is like something we have never seen before.

Right now, 40% of all premature babies have a lung disease called bronchopulmonary dysplasia or BPD. It can cause a lifetime of problems, even death. And there is no treatment. With funds from the Ontario Institute for Regenerative Medicine, Dr. Thbaud hopes to find a treatment using these miracle stem cells.

We have harnessed the healing potential of stem cells that we can take out of the umbilical cord, Dr. Thbaud adds.

Thbaud is also examining the impact these stem cells can have on septic shock in premature babies and their potential for helping with brain functioning in the babies.

We think these cells will improve the overall outcome of these pre-term babies. Now we have to make sure this is happening in a proper way and allow them to fulfill their promise.

Treatment would have to start, about a week after birth. So while Olivia may not benefit, her parents are still on board with the research

Tim Eberts is her father, The thought that other kids that will come through here could be helped by it, that's encouraging for us and we'd like to be involved in it.

Olivia is getting stronger. She now weighs 6 and a half pounds but will still be in hospital for a while yet.

Dr. Thbaud hopes to start his clinical trials in two years time.

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Blindness no barrier to massage therapist – Addison County Independent

May 25th, 2017 11:49 pm

Addison County Independent
Blindness no barrier to massage therapist
Addison County Independent
MASSAGE THERAPIST STEVEN Fidler has been running his own practice in Middlebury for the last three years. He believes his blindness has become an asset to providing his services. Independent photo/Trent Campbell. MIDDLEBURY Just another day ...

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Blindness no barrier to massage therapist - Addison County Independent

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Lakeland Community College biotechnology sciences students getting boost from grant – News-Herald.com

May 25th, 2017 11:49 pm

Thanks to a $40,320 grant from the Ohio Department of Higher Education, some hard-working Lakeland Community College biotechnology students will be eligible for scholarships to cover their tuition and fees.

The program is called Choose Ohio First and is aimed at helping students pursuing degrees in science, technology, engineering, mathematics and medicine or STEMM, its associated web page shows.

In Lakelands case, the grant applies to biotechnology science students who meet certain criteria, a media release from the school confirms.

Students who receive this scholarship will have their tuition fully covered at Lakeland, said Joe Deak, chairman of the schools biotechnology science program.

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He added that two Lakeland Community College students are now using this funding.

The scholarship covers up to $4,000 in tuition and fees for biotechnology students who dont receive PELL grants, according to Lakelands release.

It goes on to explain that high school graduates who passed chemistry with a C or better are encouraged to apply if they fit the following criteria:

Have an interest in a career in the laboratory biological sciences or data/analysis management as it pertains to biological data

Have a 3.0 overall GPA

Place into college algebra

Reside in Ohio.

Lakelands recent investments in its science and health technology programs and facilities have been making headlines in recent years, especially with the 2015 passage of its capital improvement bond issue, which is being used to fund a $40 million renovation and expansion of the colleges 20-year-old Health Technologies Building, bring the science hallway renovation to completion and help with other infrastructure improvements.

This is the stuff of the future, confirmed Arts & Sciences Division Dean Steven Oluic, who was on hand at a Sept. 1 open house for the renovated, third-floor science wing, when students, teachers, staff and anyone interested could see it, tour the classrooms and labs and learn about all the new, cutting-edge technology there.

I will submit to you that our biology, chemistry and physical science labs are among the best in the area, Oluic said. Really, youd be hard-pressed to find better labs.

College President Morris W. Beverage agreed.

When I went to Lakeland in 1972 and 1973, in the original labs up there, they were new, he said. This is the sort of thing you do every 40 or 50 years and you do it right. And, to do it right, you make sure the equipment and technology the students will be using are the standard of what theyll be using when they leave here. We want our students to experience what theyre going to experience in the world when they move on from here.

For Deak, theres no question thats exactly what Lakelands students are getting.

Deak said that, in his 20 years with the schools program, hes always been able to find grant money to keep it at the cutting edge and, thanks to this latest round of funding, the department is able to offer an unprecedented level of training to students who will likely go on to hit the ground running in roles which may not even exist yet.

Our folks wind up in research and development, quality control and medical lab technology, he said, just naming a few, and he added that the lab in which he answered these questions would pretty much be the envy of anyone at Case Western Reserve or Cleveland State University.

There are numbers to prove it, too.

According to Lakelands statement about the Choose Ohio First grant, Lakelands biotechnology science program has more than a 95 percent placement rate into jobs or transfer to a four-year school.

Institutions where graduates matriculate include Case Western Reserve University, Cleveland State University, Indiana Wesleyan University, John Carroll University, Lake Erie College and Youngstown State University, the statement reads. Lakeland also has a 2+2 articulation with Ursuline College, which allows students to transfer all of their credits and graduate with a bachelors degree in two additional years or less.

Deak said some students are even fortunate enough to land jobs with employers who actually pay their tuition for them.

After graduating from Lakeland, many students are then able to receive tuition waivers or reimbursements from their employers to reduce, or eliminate, the cost of the bachelors degree, he said.

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Lakeland Community College biotechnology sciences students getting boost from grant - News-Herald.com

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