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Unichem Labs gets USFDA nod for arthritis drug – Hindu Business Line

April 17th, 2017 11:42 am

New Delhi, April 17:

Drug firm Unichem Laboratories today said it has received approval from the US health regulator for Piroxicam capsules, used in the treatment of osteoarthritis and rheumatoid arthritis, in the US market.

In a BSE filing, Unichem Laboratories said it has received ANDA approval from the US Food and Drug Administration (USFDA) for Piroxicam Capsules USP 10mg and 20mg.

The approved product is therapeutically equivalent to Feldene Capsules 10mg and 20mg of Pfizer Inc.

Piroxicam is a non-steroidal anti-inflammatory drug (NSAID) indicated for relief of the signs and symptoms of osteoarthritis (OA) and rheumatoid arthritis (RA).

Unichem Laboratories said the product will be commercialised from its Goa plant.

Active Pharmaceutical Ingredient will also be made in-house at Roha API Plant, it added.

Shares of Unichem Laboratories were trading 1.49 per cent higher at Rs 290 on BSE.

(This article was published on April 17, 2017)

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Melbourne woman travelling to Russia for ground-breaking MS stem cell treatment – 9news.com.au

April 17th, 2017 11:41 am

A Melbourne woman is attempting to raise $170,000 for her sister to travel to one of the world's pre-eminent stem cell treatment facilities in an attempt to stop the fatal progression of Multiple Sclerosis.

Chantelle Baker was first diagnosed with MS in May, 2016. In a six month period, 79 lesions had developed on her brain.

"There is no medication to stop the progression of MS," Mrs Baker told A Current Affair.

Chantelle Baker, 41, is hoping to travel to Russia for stem cell treatment to stem the progression of Multiple Sclerosis (Source: A Current Affair)

Mrs Baker, her husband Dara, five-year-old daughter, Lilly, and younger daughter, Edie, are hostages to the hope that Russian doctors can achieve what Australia doctors cannot.

The cost is high, so Mrs Baker's sister, Maxine Parker, has set up an online fundraising campaign to raise the money on her sister's behalf.

"That's my job, I am her big sister," Ms Parker said.

"I have spent 17 years sharing the same bedroom with her growing up and there was no way I was going to let anything take her away from me and I still won't. I am determined to fight this all the way, side-by-side with her."

Mrs Baker's sister, Maxine Parker, has launched a crowd-funding campaign to pay for her sister's treatment in Russia (Source: A Current Affair)

But the cost is nothing compared to the regret the family would face if they didn't give it their all to get Mrs Baker to Russia for the ground-breaking treatment.

"I am scared of not being able to walk, I am scared of waking up one day and not being able to see my kids again because I have gone blind," Mrs Baker said.

"My worst fear is not remembering my children in four or five years' time."

Ms Parker said she would do anything to keep her sister active for her children (Source: A Current Affair)

NSW mother of two Nikki Tatum has just finished the treatment at the same stem cell clinic in Moscow that Mrs Baker is hoping to attend.

Ms Tatum is now back in Australia and will have to wait months before she knows if the therapy worked.

"I have just recently returned from to have HSCT (Hematopoietic Stem Cell Therapy) to hold the progression of my MS," Ms Tatum said in a video message to Mrs Baker.

"I just want to wish you luck for July and let you know that you have made the best choice. The doctors and nurses are just outstanding and you are definitely well looked after."

Mrs Baker, her husband and their children (Source: A Current Affair)

The video message affirmed to Mrs Baker that she was making the right decision.

"It definitely gives me hope. I know I am making the right decision and that is just verifying that I am," Mrs Baker said.

Mrs Baker's husband, Dara, agrees.

"We need to make it work. We need the treatment to work. But of course, I love her to death anyway," Mr Baker said.

Mrs Baker's family have set up a Facebook page where her journey can be followed, Chantelle Fights Multiple Sclerosis.

Nine Digital Pty Ltd 2017

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Seattle girl hopes Canadian clinical trial will save her vision – KING5.com

April 16th, 2017 9:51 pm

A Seattle girl hopes a clinical trial will save her vision. She has a rare eye condition, that could someday make her legally blind.

Ted Land, KING 5:49 PM. PDT April 16, 2017

Calnan has a rare eye condition called Aniridia, a genetic mutation that prevents her eyes from developing. (Photo: KING)

A Seattle girl hopes a clinical trial in Canada will help save her vision. She has a rare eye condition that could someday make her legally blind.

Calnan Sorenson, 7, cannot see as well as other kids her age. She's able to bounce around on a trampoline with her brother in the yard of their Wedgwood home, but as she gets older, her family worries she won't be able to lead such an active, animated life.

It's terrifying, and it's really hard to adjust expectations for the future, said Matthew Sorenson, Calnans dad.

Calnan has a rare eye condition called Aniridia. A genetic mutation is preventing her eyes from developing. The most noticeable symptom is the absence of the iris, the colored part of the eye. The disease could eventually make her blind.

The situation of, there isn't really any option, is the situation we were in for the first couple of years after she was diagnosed, and it was tough, Matthew said.

Now there is an option. Calnan is among a few dozen patients, mostly kids, taking part in a clinical trial of a drug which researchers hope will halt the deterioration of her eyesight.

Every three months her family travels to Vancouver and the University of British Columbia, where a pair of researchers are testing a treatment for Aniridia.

Once it's the day of the appointment I feel a little scared and nervous, Calnan said.

The exams are uncomfortable, but Matthew says his family is hopeful the quarterly trips across the border could help save Calnans vision.

We've seen smaller indications of progress, things like how far away she can sit from the television. We've just sort of noticed that she doesn't need to stand in front of the TV anymore, he said.

This is still very much an experiment, and so Calnan is learning braille and working with a teacher who can help her prepare for the possibility of life with less eyesight.

For now, her family just wants her to enjoy being a kid, not worrying too much about a future that's still unclear.

2017 KING-TV

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How to take good care of your eyes? – The New Indian Express

April 16th, 2017 9:51 pm

VIJAYAWADA: Nowadays, majority of the people often ignore eye care. It is essential for every individual to take little attention and proper diet to keep many vision-related problems at bay. Theres no substitute for the quality of life good vision offers. Its best to be proactive and rectify certain vision problems at the young age itself.

According to eye specialists, a clear and stable vision is a much-needed requirement for every individual. However, patients generally dont give this issue the attention it deserves. At all ages, it is advised to keep a regular check on your eyesight. The constant change in power of glasses can be a serious outcome of an underlying ocular or systemic disease. Frequent change in eye power after 40 years may indicate development of cataract and needs to be addressed.

Farsightedness and nearsightedness are the two most commonly seen eyesight problems among the youth. Many children who suffer from these diseases will face difficulty in seeing the blackboard in the classroom, have to squint in order to see small text clearly, have to strain the eyes too hard to get a clear vision of something etc, said Tummala Sandhya Rani, an ophthalmologist at Gayatri Eye Care. We also observe that parents give their mobile phones to children to play games and keep themselves occupied. The constant exposure to screens has led to several eye problems. Instead they should encourage physical activity among their children to keep eye problems at bay, he added.

There is a misconception that using anti-glare monitors will help. Prolonged computer usage has reduced the rate of blinking among people. The ideal blinking rate should be 15 to 16 times a minute and if it is less than this, it can cause dry eyes. This new lab will enable us to explain to our patients all these problems in detail after a thorough analysis, said Dr P Ram Kumar of Chaitanya Eye Hospitals. We have hundreds of patients walking in every day with unexplained eye problems. Some of these problems are because of changing work culture, office environment and stress. Today, the scene is quite different. Children are riveted to their computers and cell phones. Games, playgrounds and physical activity are the forgotten preserve, he said.

He also pointed out that another cause for concern is the rise in eye problems among the young because of Vitamin B12 deficiency. If such problems are not detected in the early stage, it can lead to partial blindness in them. In-depth analysis of such problems needs high-end research, he added. The ophthalmologists also point out that Hypertension is another big reason for constant decline in vision. Some people suffering from hypertension dont realise it but it shows up in the form of regular decline in the vision. This causes Hypertensive Retinopathy and several other retinal diseases. Keeping a tab on your blood pressure can save you from the risk of developing such retinal diseases.

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Restoring sight to over 4M people – CBS News

April 16th, 2017 9:51 pm

Eye surgeons Sanduk Ruit and Geoff Tabin, along with the doctors they've trained, have helped restore sight to over 4 million people and aren't finished yet

The doctors were gods to an old, blind Burmese woman whose sight was restored by a quick operation. Cataracts had stolen her sight for years, while others had been blind for decades before the simple operation allowed them to see again. Bill Whitaker reports from Burma, also known as Myanmar, where two eye surgeons were bringing their program that has already reversed blindness in over 4 million people and could help to eliminate cataract and other reversible blindness in the developing world. Out of Darkness will be broadcast on 60 Minutes at 7 p.m. ET/PT.

Dr. Sanduk Ruit, center, and Dr. Geoff Tabin, right, examine patients

CBS News

Hallelujah! shouts the old woman as the bandages are removed. Her surgeons, Drs. Sanduk Ruit and Geoff Tabin look on and assure her they are not gods. But they are miracle workers to the sightless in Burma and their plan has already changed the lives of millions more blind people throughout the world.

Dr. Ruit, a Nepalese eye surgeon, had been restoring the sight of cataract suffers using a technique that requires no stitches. He met Dr. Tabin, an American eye surgeon and world-renowned mountain climber, and they created the Himalayan Cataract Project. Their revolutionary system goes beyond the surgery. They started a lens factory that produces implants for a fraction of the cost in the U.S. and they have a hospital in Nepal that has trained hundreds of doctors and nurses in their technique. During their visit to Burma, they were able to perform more surgeries in three days than are usually done in a year. They left behind a Burmese team trained in their techniques to carry on the work.

Their focus was originally in the Himalayas, but they have been so successful they renamed their group CureBlindness.org. Theyve operated in two dozen countries, including North Korea and Ethiopia, restoring sight to 150,000 people. The doctors theyve trained have given vision to 4 million others. Its the developing world, but people are getting first-rate treatment says Dr. Tabin For these advanced cataracts, Im performing the same quality of surgery that I would be doing in America. Tabin is currently a professor at the University of Utah Medical School in Salt Lake City.

Their surgical outcomes have been peer-reviewed by the leading American journal for eye doctors.

And as Dr. Tabin points out, they are doing more than restoring sight. You know, once someone goes blind in a developing world, their life expectancy is about one-third that of age and health matched peers, he says. And also in the developing world, it takes, often, a person out of the work force, or a child out of school, to care for the blind person. So when we restore sight to a blind person, were freeing up their family and restoring their life, Tabin tells Whitaker.

2017 CBS Interactive Inc. All Rights Reserved.

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Both Types of Diabetes Rise in US Children – WebMD

April 16th, 2017 9:51 pm

By Serena Gordon

HealthDay Reporter

WEDNESDAY, April 12, 2017 (HealthDay News) -- Two new studies on diabetes deliver good and bad news, but the overall message is that the blood sugar disease remains a formidable public health burden.

The first study looked at the incidence of type 1 and type 2 diabetes in U.S. children, and uncovered this troubling trend: From 2002 to 2012, the rates for both types of diabetes increased, especially among racial and ethnic minorities.

But a bit of hope was offered up in the second study: Swedish researchers reported a drop in the incidence of heart disease and stroke in adults with both types of diabetes.

"These studies highlight our concerns about the increasing prevalence of diabetes. Every 23 seconds, another person is diagnosed with diabetes [in the United States]," said Dr. William Cefalu, chief scientific, medical and mission officer for the American Diabetes Association (ADA).

Cefalu added that the Swedish study was encouraging and shows that things are "trending in the right direction. Because of research in diabetes, we've been able to improve the lives of millions of people with diabetes around the world, but the disease is still increasing worldwide. We still have a lot of work to do."

In the United States, approximately 29 million people have diabetes, according to the ADA. The vast majority of those have type 2 diabetes. About 1.3 million people have type 1 diabetes.

In people with type 2 diabetes, the body doesn't use insulin properly. This is called insulin resistance. Insulin is a hormone that helps usher sugar from foods into the body's cells to be used as fuel. When someone has type 2 diabetes, this process doesn't work well and blood sugar levels rise. Obesity is the main risk factor for type 2 diabetes, though it's not the only factor involved in the disease.

Type 1 diabetes is an autoimmune disease. The body's immune system mistakenly attacks the insulin-producing cells in the pancreas. This leaves someone with type 1 diabetes with little to no insulin. To stay alive, someone with type 1 diabetes must replace that insulin through injections.

"The specific genes and environmental/behavioral factors that cause type 2 diabetes are different than those that cause type 1 diabetes," explained Elizabeth Mayer-Davis, the author of the study on diabetes incidence in children.

Mayer-Davis and colleagues found that type 1 diabetes was increasing 1.8 percent a year. The increase was significantly larger for Hispanic children, at 4.2 percent a year. That compared with 1.2 percent for white children, the findings showed.

The factors underlying the increase aren't entirely clear, she said.

Although far fewer children have type 2 diabetes, the disease is increasing faster than type 1. Between 2002 and 2012, the rate of type 2 diabetes increased 4.8 percent a year. The annual increase in type 2 diabetes in black children was 6.3 percent. For Asian/Pacific Islanders, the yearly increase was 8.5 percent, and for Native Americans, it was almost 9 percent, the investigators found.

"The increase in incidence of type 2 diabetes is likely related primarily to the increases in overweight and obesity in youth, although this is not the only reason," said Mayer-Davis. She's a professor of nutrition and medicine at the University of North Carolina, Chapel Hill.

The second study looked at all of the people registered in a Swedish National Database from 1998 through 2012, and followed their health through 2014. The database has nearly 37,000 people with type 1 diabetes and more than 457,000 with type 2 diabetes. These patients were compared to similar people without diabetes (the "control" group).

The researchers saw roughly a 40 percent greater reduction in heart disease and stroke in people with type 1 diabetes compared to the matched controls. In people with type 2 diabetes, there was roughly a 20 percent greater drop in heart disease and stroke compared to the control group, the study showed.

When it came to deaths during the study period, people with type 1 diabetes had similar reductions in the number of deaths compared to controls. People with type 2, however, had smaller reductions in deaths versus the control group, the researchers found.

Even with these improvements, people with either type of diabetes still have much higher overall rates of premature death and heart disease than the control groups, the study authors noted.

"We believe the changes observed in our study most likely reflect a combination of advances in clinical care for patients with diabetes," said study author Dr. Aidin Rawshani. He is from the Institute of Medicine at the University of Gothenberg in Sweden.

"Perhaps the most important is improved management of cardiovascular risk factors," he said. These risk factors include high blood pressure, abnormal cholesterol, signs of early kidney damage and poor blood sugar control. He said treatment with high blood pressure medications and cholesterol-lowering drugs likely contributed to the improvement.

Both studies were published April 13 in the New England Journal of Medicine.

WebMD News from HealthDay

SOURCES: Aidin Rawshani, M.D. and Ph.D. student, Sahlgrenska University Hospital and the Institute of Medicine at the University of Gothenberg, Sweden; Elizabeth Mayer-Davis, Ph.D., professor, nutrition and medicine, University of North Carolina, Chapel Hill; William Cefalu, M.D., chief scientific, medical and mission officer, American Diabetes Association; April 13, 2017, New England Journal of Medicine

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Free Empower Diabetes Classes Begin May 2 At UT Health Northeast – Gilmer Mirror

April 16th, 2017 9:51 pm

Tyler, TX If you or a family member have diabetes, you are encouraged to learn more, get connected, and get on top of this serious disease by attending UT Health Northeasts free Empower Diabetes classes beginningMay 2in classroom 3207 at UT Health Northeast, located at 11937 U.S. 271 in Tyler, at the corner of U.S. 271 and State Highway 155.

Disease management is the goal of the Empower Diabetes program. Each session provides information for better diabetes self-management and guidelines for living a healthy lifestyle.Classes are freeand topics include:

May 2

9:00-10:00 a.m.- What is Diabetes?

10:00-11:00 a.m.- Managing High and Low Blood Sugars and Sick Days

May 9

9:00-10:00 a.m.- Medications/Insulin

10:00-10:30 a.m.- Monitoring

10:30-11:00 a.m.- Stress/Coping

May 16

9:00-10:00 a.m.- Exercise

10:00-11:00 a.m.- Foot Care

May 23

9:00-10:30 a.m.-Meal Planning

10:30-11:00 a.m.- Goal Setting

July 11

9:00-11:00 a.m.- Reunion (Follow-Up)Class

Blood sugar and blood pressure testing are provided at the first class and at the reunion class.

Space is limited, and early registration is encouraged. Sessions include educational materials and door prizes.

To register, call(903) 877-7569or emailkrista.lindley@uthct.edu

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Ten-year-old, family, explain life with Type 1 Diabetes – WAAY

April 16th, 2017 9:51 pm

It was Leland Jeffrey's fourth birthday, but instead of a day filled with cake and ice cream, Leland was in Huntsville Hospital with a blood sugar level ten times higher than what it should be. Doctors told Leland's parents, Beverly and David, it was astonishing their son was still conscious.

At the time, the Jeffreys couldn't have anticipated the news they'd receive from their doctor. Leland, a perfectly happy and healthy child, was a Type 1 diabetic.

Commonly referred to as Juvenile Diabetes, we now know the condition can affect people of all ages. Actress Mary Tyler Moore was diagnoses when she was in her 20s, and battled the disease until she passed away this year.

As for Leland, his mom said there were signs in recent weeks that suddenly made sense post-diagnosis. Her typically sweet little boy would anger easily, was consuming a tremendous amount of liquid, and had dropped a good ten pounds.

It was in his son's hospital room that David described the "rapid fire" of questions and information being hurled toward him and his wife. Gradually Leland's condition improved. His blood sugar stabilized, and after a hospital stay that included terrifying words like "brain swelling," he was allowed to go home.

For the Jeffreys it was the start of a new way of life.

Six years removed from that day, Beverly said the routine of daily blood testings - approximately six between home and school - have now become commonplace.

Diets were altered and her little boy was given some very grown up instructions regarding his health. He learned to check his own sugars, and ro recognize the signs his sugars were crashing.

Leland is able to run and play like any active 10-year-old. He told WAAY-31 he just needs to be aware if his body starts tingling. That is when he knows to go inside his house, have some juice, then rest for a bit before going outside.

It is those kinds of signs that Pam Glover hopes to educate diabetics and their families about through her work as director of the diabetes management program at Huntsville Hospital.

Her first order of business is to make people understand the difference between Type 1 and Type 2 diabetes.

Type 1 is the result of a virus which attacks the pancreas. Some people have a predisposition, but it is something totally beyond their control. Child, such as Leland, who are diagnosed at a young age must spend their entire life looking for warning signs of an impending crash. Glover said it can quite literally mean the different between life and death.

Type 2 diabetes is usually the result of lifestyle, things like diet or lack of exercise. However, she said that isn't an across the board cause for all Type 2 cases, and that each can vary depending on things like smoking or even family history.

Regardless, Glover said it is crucial for those with both types to be aware of the seriousness of their respective disease and to manage it effectively and carefully.

As for Leland, this little boy learned how to do it. While at first he said he "hated having diabetes," and "wanted to go back to life before," he's learned to manage it and realizes it will be part of his daily routine if he wants to live a happy life.

The Jeffreys have been very active in the Huntsville chapter of the JDRF. Beverly said it was the support system provided by JDRF that helped her and David to cope with the initial diagnosis. They've remained active participants in the annual One Walk, which takes place each spring to raise money to fight - and hopefully one day cure - diabetes.

This year's race is happening on Saturday, April 22, at the Jackson Center in Cummins Research Park. You can register by clicking right here.

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Scientists have made a 3D-printed patch that can help heal the damaged heart tissue – Tech2 (blog)

April 16th, 2017 9:48 pm

Scientists have created a revolutionary 3D-bioprinted patch that can help heal scarred heart tissue after a heart attack. The discovery is a major step forward in treating patients with tissue damage after a heart attack, researchers at University of Minnesota in the US said. During a heart attack, a person loses blood flow to the heart muscle and that causes cells to die.

Our bodies can not replace those heart muscle cells so the body forms scar tissue in that area of the heart, which puts the person at risk for compromised heart function and future heart failure. Researchers used laser-based 3D-bioprinting techniques to incorporate stem cells derived from adult human heart cells on a matrix that began to grow and beat synchronously in a dish in the lab.

When the cell patch was placed on a mouse following a simulated heart attack, the researchers saw significant increase in functional capacity after just four weeks. Since the patch was made from cells and structural proteins native to the heart, it became part of the heart and absorbed into the body, requiring no further surgeries. This is a significant step forward in treating the No 1 cause of death in the US, said Brenda Ogle, an associate professor at the University of Minnesota.

We feel that we could scale this up to repair hearts of larger animals and possibly even humans within the next several years, said Ogle. Ogle said that the research is different from previous ones as the patch is modelled after a digital, three- dimensional scan of the structural proteins of native heart tissue. The digital model is made into a physical structure by 3D printing with proteins native to the heart and further integrating cardiac cell types derived from stem cells.

Only with 3D printing of this type can we achieve one micron resolution needed to mimic structures of native heart tissue, researchers said. We were quite surprised by how well it worked given the complexity of the heart. We were encouraged to see that the cells had aligned in the scaffold and showed a continuous wave of electrical signal that moved across the patch, Ogle said.

Ogle said they are already beginning the next step to develop a larger patch that they would test on a pig heart, which is similar in size to a human heart. The study was published in the journal Circulation Research.

Publish date: April 16, 2017 12:57 pm| Modified date: April 16, 2017 12:57 pm

Tags: 3D-Bioprint, Brenda Ogle, cells, Heart, heart attack, heart failure, Journal Circulation Research, scientists, structural proteins, University of Minnesota

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More Resources About Blindness and Visual Impairment

April 16th, 2017 9:48 pm

American Action Fund (AAF) for Blind Children and Adults

Baltimore, MD 410-659-9315 actionfund@actionfund.org

A service agency that specializes in providing to blind people help that is not readily available to them. The Tarzana office houses a postage-free national lending library of braille and Twin Vision(R) books for blind children. They also publish and distribute a braille weekly newspaper and calendars.

American Council of the Blind (ACB)

Arlington, VA 800-424-8666 info@acb.org

National consumer organization with local, state, and special interest affiliates; providing support, information, referral, and advocacy.

American Foundation for the Blind (AFB)

New York, NY 800-232-5463 afbinfo@afb.net

Provides comprehensive information on every aspect of blindness and visual impairment and a searchable database of nationwide services.

American Printing House for the Blind, Inc. (APH)

Louisville, KY 800-223-1839 info@aph.org Shopping site

Worlds largest company devoted solely to researching, developing, and manufacturing products for people who are blind and visually impaired. Founded in 1858, it is the oldest organization of its kind in the United States.

Babies Count

Alamogordo, NM

Babies Count is a national registry of young children aged birth to 36 months of age with visual impairments that works in conjunction with public and private agencies to collect standardized epidemiological and demographic data regarding children, their visual conditions, and the systems created to support them and their families.

Blinded Veterans Association (BVA)

Alexandria, VA 800-669-7079 bva@bva.org

An organization of blinded veterans helping blinded veterans. All legally blinded veterans are eligible for BVAs assistance whether they become blind during or after active duty military service.

Bookshare

Palo Alto, CA 650-352-0198 info@bookshare.org

An initiative of Benetech, a nonprofit organization, a person with print disabilities can read a newspaper the same day it hits the newsstand or a best-selling book online as soon as it is released.

Books Aloud

San Jose, CA 408-808-2613 info@booksaloud.net

The Books Aloud "Reading by Listening" Program provides a wide variety of recorded reading literature to eligible individuals of all ages. This is a FREE service.

Canadian National Institute for the Blind

Toronto, ON 1-800-563-2642

CNIB is a registered charity, passionately providing community-based support, knowledge and a national voice to ensure blind and partially sighted Canadians have the confidence, skills and opportunities to fully participate in life.

Dialogue Magazine

Salem, OR 800-860-4224 info@blindskills.com

Each quarterly issue of DIALOGUE Magazine, from the non-profit Blinds Skills, Inc., contains a wide range of subject matter and comes in four formats: cassette, 18-point print, braille and on computer e-mail.

Family Connect

familyconnect@afb.net

FamilyConnect is an online, multimedia community created by the American Foundation for the Blind (AFB) and the National Association for Parents of Children with Visual Impairments (NAPVI). This site gives parents of visually impaired children a place to support each other, share stories and concerns, and link to local resources.

Hadley School for the Blind

Winnetka, IL 800-323-4238 info@hadley.edu

Provides academic, personal enrichment, and compensatory, or rehabilitation education through free home study courses for parents, family members, professionals, and paraprofessionals.

Helen Keller National Center for Deaf-Blind Youths and Adults (HKNC)

Sands Point, NY 516-944-8900 hkncinfo@hknc.org

The Center is a national vocational and rehabilitation program exclusively serving youths and adults who are deaf-blind. Their mission is to enable each person who is deaf-blind to live and work in the community of their choice.

Learning Ally (formerly Recording for the Blind and Dyslexic)

Princeton, NJ 800-221-4792 custserv@LearningAlly.org

Founded in 1948 as Recording for the Blind, Learning Ally creates and maintains over 80,000 audio recordings of textbooks, reference, and professional materials that are not available on tape or disc from other sources. There is a registration fee for this service.

Lighthouse Guild

New York, NY 800-829-0500 info@lighthouseguild.org

A worldwide organization dedicated to preserving vision and to helping people of all ages overcome the challenges of vision loss. Provides vision rehabilitation services, and partners with organizations to ensure that all individuals suffering vision loss have access to the services they require.

Lions Club International

Oak Brook, IL 630-571-5466

By conducting vision screenings, equipping hospitals and clinics, distributing medicine and raising awareness of eye disease, Lions work toward their mission of providing vision for all. They have extended their commitment to sight conservation through countless local efforts and through their international SightFirst Program, which works to eradicate blindness.

Matilda Ziegler Magazine for the Blind

New York, NY 212-242-0263 editor@matildaziegler.com

Editors at the Ziegler magazine scan four national newspapers a day and over 30 magazines a month selecting a broad selection of articles to be reprinted in the Ziegler. The magazine is free-of-charge to legally blind subscribers and is published in a variety of formats including: contracted braille, four track cassette, on-line and by e-mail.

National Braille Association

Rochester, NY 585-427-8260

National Braille Association (NBA) is the only national organization solely dedicated to the professional development of individuals who prepare and produce braille materials.

National Braille Press (NBP)

Boston, MA 888-965-8965 contact@nbp.org

The National Braille Press focuses on practical information to enable persons who are blind and visually impaired to be responsible and productive individuals. Categories include childrens braille literacy, computer access, and self-help books.

National Camps for Blind ChildrenChristian Record Services

Lincoln, NE 402-488-0981 info@christianrecord.org

An international organization serving blind and visually impaired individuals in approximately 80 countries worldwide that operates summer camps throughout North America for children and adults who are blind and visually impaired.

National Federation of the Blind (NFB)

Baltimore, MD 410-659-9314 pmaurer@nfb.org

National consumer organization, with local and state chapters and special-interest divisions that provide information, advocacy, and employment programs.

National Organization of Parents of Blind Children (NOPBC)

Baltimore, MD 410-659-9314 parentoutreach@nfb.org

(part of National Federation of the Blind/click on Info about Vision Loss for Parents and Teachers)

Focuses on the needs of parents and families. Find resources to help children thrive at home, school, and in the community.

National Prison Braille Network

Supports and promotes braille production facilities in prisons across the U.S. and helps ensure that inmate transcribers are well prepared for successful careers as braille transcribers upon release.

Newsreel Magazine

Columbus, OH 888-723-8737

Newsreel Magazine by and for the Blind is a unique monthly interactive audio magazine produced in the voices of its blind or visually impaired subscribers.

Perkins School for the Blind

Watertown, MA 617-924-3434 info@perkins.org

Conducts training activities for programs and staff serving children who are multiply disabled with blindness or deafblind and provides support services for parents.

Seedlings Braille Books for Children

Livonia, MI 800-777-8552 info@seedlings.org

Seedlings Braille Books for Children provides high quality, low cost braille books for children at every level of development, from toddler board books to classic literature for older children.

U.S. Association of Blind Athletes

Colorado Springs, CO 719-866-3224

This Association enhances the lives of blind and visually impaired people by providing the opportunity for participation in sports and physical activity. Offers training camps and competitions in swimming, track and field, wrestling, gymnastics, goal ball, skiing, skating, power lifting, judo, and tandem cycling.

WonderBaby.org

Watertown, MA email hidden; JavaScript is required

WonderBaby.org, a project funded by Perkins School for the Blind, is dedicated to helping parents of young children with visual impairments as well as children with multiple disabilities. Here youll find a database of articles written by parents who want to share with others what theyve learned about playing with and teaching a blind child, as well as links to meaningful resources and ways to connect with other families.

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Restoring eyesight with a simple, inexpensive surgery – CBS News

April 16th, 2017 9:48 pm

60 Minutes followed the Himalayan Cataract Project in their fight against preventable blindness to Burma.

Eric Kerchner

Blindness and partial blindness are not epidemic here in the U.S. but they are in certain parts of the world. Our story is about two doctors who decided to do something about it. And incredibly, to date, theyve restored sight to more than 150,000 people. Doctors theyve trained have restored sight to four million more. Their partnership seems improbable. One is a hard-charging, Ivy-League, American, adrenaline-junkie; the other a serene, Buddhist surgeon from the remote mountains of Nepal. We joined them on one of their most challenging missions -- in the isolated country of Burma. Their goal: to lead Burma out of darkness one patient at a time.

One by one the patches are peeled away and the world comes back into focus youre witnessing the moment when the people in this room realize they can see for the first time in years.

Bill Whitaker: Can you see my fingers?

60 Minutes correspondent Bill Whitaker watches Dr. Geoff Tabin perform eye surgery.

Eric Kerchner

Their eyes and their faces begin to light up with a quiet sort of joy and wonder at the gift of sight. As they look around, they see who changed their world, with an operation the day before that took just minutes. Doctors Geoff Tabin and Sanduk Ruit are eye surgeons. And now, they are life savers. To hear Doctors Ruit and Tabin speak, they are the beneficiaries.

Bill Whitaker: Whats it like when that bandage is taken off and that person sees for the first time, sees you?

Sanduk Ruit: I may have seen it thousands of times, but every time, theres a new tickle there. And I feel like my batterys been recharged.

Geoffrey Tabin: I still get such a thrill when people dont expect or realize theyre gonna have their sight restored. And then a transformation when they see, and the sort of moment of hesitation, what are they seeing, and then the smile.

Burma, also known as Myanmar, is one of the poorest countries in Asia.

CBS News

U Myint Oo hadnt seen for two years, until this moment. Others here had been blind for decades. They all had cataracts a milky, white build-up of protein that clouds the lens of the eye. In the U.S. they mainly afflict the elderly; removing them a routine operation. But here in Burma, also known as Myanmar, cataracts go untreated and blindness is a way of life.

Geoffrey Tabin: Its a Buddhist population, theyre very fatalistic. Theyre very accepting. And theres almost an acceptance that you get old, your hair turns white, your eye turns white and then you die. And the idea that you can actually have your sight restored has not really permeated all levels of Myanmar society.

Bill Whitaker: What does that tell you about the state of eye care here?

Geoffrey Tabin: Well, its a place we can make a difference.

Burma is one of the poorest countries in Asia, slowly emerging from the darkness of decades of dictatorship. After years of trying, Tabin and Ruit finally were permitted to bring their treatment here. We met them in Taunggyi in central Burma, where the lack of care has led to some of the highest rates of cataracts in the world. Through radio and pamphlets and conversation, word of the doctors visit spread.

After hearing of the doctors visit, hundreds of Burmese came to Taunggyis hospital in central Burma.

Eric Kerchner

Hundreds of Burmese whod lost their sight found their way to Taunggyis hospital with the help of care givers many trekking for days. Here, cataracts are not just a malady of old age; they take the sight of the very young too, caused by infections and malnutrition.

By the time the doctors scrubbed in, the corridors were choked with people hoping to have their sight restored.

Bill Whitaker: Is it ever daunting? I mean, you look out there and you see that line of people, all who need this surgery.

Geoffrey Tabin: Its daunting on a worldwide basis. It may be a long line but this individual person Im gonna give the very best care I can.

Dr. Ruit set a rapid pace. He repaired an eye; the patient got up; the next patient was ready on an adjoining table. Just minutes an eye, then onto the next. Dr. Tabin performed the delicate surgery just feet away.

Geoffrey Tabin: Want to take a look. See how nice and clear that is. I dont know what that was - maybe 4-5 minutes. And its going from total blindness to great vision.

They kept up this pace until 7:00 in the evening.

Bill Whitaker: Its almost like an assembly line. But assembly line sounds too mechanical. I mean, this is peoples eyes.

Geoffrey Tabin: Its peoples lives. You know, once someone goes blind in a developing world, their life expectancy is about one-third that of age and health matched peers. And for a blind child, the life expectancy is five years. And also in the developing world, it takes, often, a person out of the work force, or a child out of school, to care for the blind person. So when we restore sight to a blind person, were freeing up their family and restoring their life.

Among the throng waiting to have their lives restored we found Kancchi. Her son, a farmer, had been her eyes and devoted caretaker since cataracts took her sight. 15-year old Yawnu had been blind since age seven. He was overwhelmed, but grateful.

In four days in Taunggyi, Dr. Ruit and Dr. Tabin -- with the help of local doctors -- performed 503 cataract surgeries.

Eric Kerchner

Thank you, he said. Doctors Ruit and Tabin heard that a lot. In four days in Taunggyi, with the help of local doctors they were training, they performed 503 cataract surgeries. Her eyes now bandaged, Kancchi waited with her son.

Bill Whitaker: You are going to be performing as many cataract surgeries as the hospital does normally in a year.

Sanduk Ruit: we are basically here to ignite fire. Ignite fire of the possibility of doing high quality, high volume cataract surgery. It is still possible.

Bill Whitaker: You want to ignite a fire here.

Sanduk Ruit: Ignite a fire here.

As long as he can remember, Sanduk Ruit has been burning to change the world around him. He grew up desperately poor, in this village with no electricity or running water, high in the Himalayas of Nepal.

The nearest school was a 15-day walk away. Ruits illiterate parents saw education as the way out for their children, but the grip of poverty and poor health was too strong to escape. His younger sister, with whom he was very close, died of tuberculosis.

Sanduk Ruit: I saw her pass away in front of me. And then it was a very strong determination from inside that maybe this is the profession that I should take and make healthcare available for my countrymen.

Eye surgeons Sanduk Ruit, left, and Geoff Tabin have restored eyesight to more than 150,000 patients in 24 countries.

CBS News

That determination took him to medical school in India. He came back to Nepal an eye doctor, committed to bringing modern care to remote mountain villages. The documentary Out of the Darkness showed them carrying equipment on their backs. His team hiked for days. His goal as revolutionary as it was simple: to cure blindness in the Third World with a quick, cheap technique to remove cataracts. Soon the medical world took notice and so did a young Geoff Tabin.

Geoffrey Tabin: I imposed myself on Sanduk and came to work in Nepal.

Bill Whitaker: What did you think of him when he first showed up?

Sanduk Ruit: You know, I was a bit scared in the beginning, you know. He had tremendous energy. He would never get tired. Energy in working, energy in eating, energy in drinking. Energy in talking, you know?

It was like being hit by a human avalanche fitting since Geoff Tabins passion was mountaineering more than medicine. Hed raced through Yale, Oxford and Harvard medical school. But he had made his name as one of the first people to climb the highest peak on every continent. He met Dr. Ruit and thought hed found his next challenge. Ruit was skeptical this frenetic young man had the same dedication to ophthalmology he had to adventure.

Sanduk Ruit: I sent him to an-- to a hospital in eastern part of Nepal in the middle of summer. And I said, Hes not gonna survive there.

Geoffrey Tabin: During the summer, in the monsoon, its quite oppressive. Its sort of 100, 105, with a 99 percent humidity, and lots of mosquitoes.

Bill Whitaker: Wait a minute. You sent him to-- a difficult place on purpose--

Sanduk Ruit: Difficult place. Difficult-- definitely. Yeah.

Bill Whitaker: Did you know thathe was testing you?

Geoffrey Tabin: No. I thought he sent me there because there was so much need. I scratched my mosquito bites and was excited to go to work that there were all of these blind people that, you know, I could make a difference in their life.

Bill Whitaker: He won you over?

Sanduk Ruit: Yes, yes, definitely.

Their relationship has grown from teacher student to collaborators and friends. Like yin and yang, these opposites complement each other. They created the Himalayan Cataract Project, started here at Tilganga, Ruits hospital in Kathmandu. They perfected the procedure called small incision cataract surgery: just one small splice the cataract comes out, a new man-made lens goes in, no stitches required. Its quick and costs about $20.

Bill Whitaker: How does the quality of care youre providing here, compare to the quality of care youd be able to provide in the U.S.?

Geoffrey Tabin: For these advanced cataracts, Im performing the same quality of surgery that I would be doing in America.

A Burmese woman celebrates her restored eyesight.

Eric Kerchner

Dr. Tabin spends most of his year at the University of Utah where cataract surgery costs a couple thousand dollars an eye. He might do four or five a day. Here, he does that many in a half hour, removing cataracts hed never see in the U.S., because theyd never go untreated so long.

Their project is funded by donations and grants. Theyre able to keep costs down because they dont use expensive equipment and they make their own lenses at their factory in Nepal. The lenses are crucial to the process theyre a permanent implant. Each costs about four dollars. In the U.S., because of strict, safety requirements, they can cost 50-times more.

Bill Whitaker: Comparable quality?

Sanduk Ruit: Very comparable. Id put that in my mothers eyes.

So far theyve operated in two dozen countries, including North Korea, Ethiopia and now Burma. Theyve brought hundreds of doctors, including the Burmese doctors working with them, to Tilganga for training. And everywhere they go, they train other doctors to carry on their work once theyve moved on.

Sanduk Ruit: How many fingers?

We saw the immediate benefit the morning after surgery.

The patients gathered in a Buddhist monastery. As the bandages came off, first wonder; then smiles and celebration. Remember U Myint Oo, blind for two years? His family sent us this picture. He can read again, his favorite pastime.

Fifteen-year-old Yawnu, blind half his life, seemed somewhat bewildered by this new world of sight.

For Kancchi the wait was over. Her son was overcome when she saw his face for the first time in years.

Then there was this woman.

Bill Whitaker: Is this the first time shes been able to see in months?

Man: Yes.

She called Doctors Ruit And Tabin gods. They assured her they are not. But in this room it certainly seemed they had performed miracles.

Hallelujah!

The doctors recently got more good news. The Himalayan Cataract Project is one of eight semifinalists for a $100 million grant from the MacArthur Foundation.

For more information on The Himalyan Cataract Project, visit their website or call888-287-8530.

Produced by Henry Schuster and Rachael Morehouse.

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ProShares Ultra Nasdaq Biotechnology (NASDAQ:BIB) Carving out Recent Gains For the Week – The Herald

April 16th, 2017 9:47 pm

All three benchmark US indexes closed lower on Friday after fluctuating throughout the session.

ProShares Ultra Nasdaq Biotechnology (NASDAQ:BIB) performed nicely this week, continuing its impressive near-term upward movement. The stock has moved north1.52% over the past week of trading.

Looking further out, over the past twelve months, ProShares Ultra Nasdaq Biotechnologys stock was -0.08% and 7.76% over the last quarter and 12.38% for the past six months.

There are many reasons why a stock might advance so much, so quickly. The total market, including country, continent, or global, might have gone up due to macro reasons. The company might have reported better than expected (consensus) earnings results. A sell-side firm might have issued a buy report on the company. The company might have announced a major change in the business, such as a buyout, M&A, spin-off, R&D results or the acquisition of a new large client. The company might have announced its involvement in a lawsuit. The company might have changed its yearly guidance. The institutional investors might have bought a large chunk of stocks of the company.

Over the past 50 days, ProShares Ultra Nasdaq Biotechnology (NASDAQ:BIB) stock was -8.62% off of the high and 9.22% removed from the low. Their 52-Week High and Low are noted here. -10.28% (High), 39.45%, (Low).

ProShares Ultra Nasdaq Biotechnology (NASDAQ:BIB) may have great momentum, but how has it been performing relative to the market? The stocks price is $47.37 and their relative strength index (RSI) stands at 48.31. RSI is a technical oscillator that shows price strength by comparing upward and downward movements. It indicates oversold and overbought price levels for a stock.

Disclaimer: The views, opinions, and information expressed in this article are those of the authors and do not necessarily reflect the official policy or position of any company stakeholders, financial professionals, or analysts. Examples of analysis performed within this article are only examples. This is not a recommendation to buy or sellProShares Ultra Nasdaq Biotechnology (NASDAQ:BIB).

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Rheumatoid arthritis sufferers given early and aggressive treatment live ‘better and longer lives’ – The Sun

April 16th, 2017 9:47 pm

Over 20 years, patients given drugs were apparently more able to walk, get dressed and less likely to die

RHEUMATOID arthritis sufferers given early and aggressive treatment have better and longer lives, researchers say.

Experts studied 602 patients with one in four receiving drugs within six months of showing symptoms.

Alamy

Over 20 years they were more able to walk, get dressed and less likely to die, said teams from Manchester and East Anglia Universities.

Author James Gwinnut said: Though there is a broad range in terms of how people are affected by the disease, the number of patients whose lives have improved has increased thanks in part to early treatment.

The good news is that early intervention has become more and more common in the NHS over these past 20 years.

Alamy

Dr Natalie Carter, head of research liaison and evaluation at Arthritis Research UK, added: This study confirms how important early diagnosis and the commencement of treatment is.

It is also encouraging to hear about the progress that has been made over the last 20 years.

Now the scientific community must continue to build on this so that together we can continue to harness the power of exceptional science and make everyday life better for all people with arthritis.

Biomedcentral.com

The study was published in Arthritis and Rheumatology.

There are 400,000 Brits with incurable rheumatoid arthritis.

It causes inflammation in your joints with main symptoms being joint pain and swelling and flare ups.

The incurable disease leads to progressive joint destruction which leads to disability and premature death.

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FDA rejects drugmaker’s much-anticipated arthritis pill – | WBTV … – WBTV

April 16th, 2017 9:47 pm

(CBS News/AP) -

Drug company Eli Lilly says their much-awaited pill forrheumatoid arthritishas been rejected by the Food and Drug Administration. Its the companys second drug development setback since November.

A letter to the company from the FDAsaid that they needed more information about baricitinibs safety and the best doses, Lilly said Friday in a statement.

The drugmaker disagrees with FDAs conclusions but will work with the agency on a plan to eventually get baracitinib approved for U.S. patients.

In November, Lillys experimental medicinesolanezumabflopped in a closely watched test in patients with mildAlzheimers diseaseafter already failing in patients with more advanced Alzheimers.

The arthritis drug, which has the proposed brand name Olumiant and was approved for use in Europe in February, was expected to be a big seller in part because most other new rheumatoid arthritis drugs are injected, making them less appealing for patients.

We are disappointed with this action, said Christi Shaw, president of the Lilly division that developed the drug, in the companys statement, adding that the company remains confident in the drugs ability to safely treat moderate and severe rheumatoid arthritis.

About 23 million people worldwide -- three-fourths of them women -- have rheumatoid arthritis, an autoimmune disorder that happens when the immune system mistakenly attacks a persons own body tissues. The chronic disorder causes painful swelling and progressive destruction of joints, which can leave them deformed and, in severe cases, lead to disability. It can also damage other body parts, including the skin, eyes, lungs, heart and blood vessels.

Rheumatoid arthritiscan strike at any age, but typically begins between the ages of 40 and 60, and if someone in your family has had it, your odds for the condition may be higher.

Eli Lilly & Co. and Incyte Corp., its partner in developing baracitinib, applied for FDA approval of the drug in January 2016. Normally the review process takes 10 months, but this January, FDA said it needed three additional months to review more information. Still, drug industry analysts as recently as this week were advising clients that approval of baracitinib was likely.

Despite the setback, Lilly reaffirmed its 2017 financial forecasts Friday, for earnings per share of $2.69 to $2.79, excluding one-time items, and revenue between $21.8 billion and $22.3 billion. It said Incyte, which is based in Wilimington, Delaware, was evaluating the rejections impact on its position and would update investors when it reports first-quarter results, likely in mid-May. Lilly is expected to report its quarterly results on April 25.

2017 CBS Interactive Inc. All Rights Reserved. This material may not be published, broadcast, rewritten, or redistributed. The Associated Press contributed to this report.

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Pedometers tied to less fatigue for rheumatoid arthritis patients – Geo.tv – Geo News, Pakistan

April 16th, 2017 9:47 pm

Patients with rheumatoid arthritis who receive pedometers may be more active and feel less fatigued even if they are not told to use the trackers to aim for a specific number of steps, a small study suggests.

All 96 study participants had rheumatoid arthritis, an immune system disorder that causes debilitating swelling and pain in the joints. Researchers randomly assigned patients to get a pedometer with or without a daily step goal, or to get only educational brochures with advice on becoming more active.

After 21 weeks, all of people with pedometers were walking more on average each day: 1,441 additional steps without a step goal and 1,656 extra steps with a goal. But the patients who didnt get pedometers actually got 747 fewer steps a day on average by the end of the study.

Patients with pedometers reported statistically meaningful declines in fatigue during the study, but people who only got education did not.

We found that increasing activity just through walking decreased fatigue, said lead study author Dr. Patricia Katz of the University of California, San Francisco.

Most of us probably dont realize how inactive we are until we start measuring our daily activity, Katz said by email. Having a concrete goal, such as the number of daily steps, seems to help people become and stay active.

Every patient received the same educational brochure at the start. In the two groups that received pedometers, all of the participants were asked to keep a daily diary to record how many steps they logged.

For one group with pedometers, researchers also assessed their activity levels at the start of the study and set goals for them to increase their average daily steps by 10 percent every two weeks.

At the start of the study, participants were 54 years old on average and were typically getting about 4,891 steps a day, which researchers classified as sedentary. Very few of them were getting at least 8,000 steps a day, which the researchers say is a healthy activity level.

Beyond its small size, another limitation of the study is that researchers lacked data on how often participants wore the devices, which makes it difficult to get an accurate daily step count, the authors note in Arthritis Care and Research.

Its also possible that the pedometer groups might not have improved as much if they hadnt also been recording their steps in a daily diary, which increases their engagement with the effort to be more active, said Dr. Mitesh Patel, a researcher at the University of Pennsylvania in Philadelphia who wasnt involved in the study.

Research indicates that for most people, pedometers and wearable devices are more likely to help change health behaviors if they are combined with an engagement strategy, Patel said by email.

Generally, pedometers are most useful for people who are sedentary and unaware of their own level of inactivity, said Dr. Lucas Carr, a physiology researcher at the University of Iowa who wasnt involved in the study.

This relatively simple intervention helped a very sedentary group of rheumatoid arthritis patients increase their activity at a level that is considered clinically significant, Carr said by email. The largest health benefits are realized when an individual changes from doing nothing to doing something.

While the study included only people with rheumatoid arthritis, its possible pedometers might be useful for people with other chronic medical problems, said Dr. David Geier, an orthopedic surgeon sports medicine specialist in Charleston, South Carolina who wasnt involved in the study.

It seems reasonable to think they could help stimulate activity, Geier said by email. Physical activity would be helpful for almost everyone.

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Feds reject Lilly’s rheumatoid arthritis pill – Indianapolis Star

April 16th, 2017 9:47 pm

LINDA A. JOHNSON, AP Medical Writer 1:09 p.m. ET April 14, 2017

Eli Lilly made the list.(Photo: Joe Vitti/IndyStar)Buy Photo

Eli Lilly said U.S. regulators have rejected its much-anticipated pill for the immune disorder rheumatoid arthritis, the drugmakers second drug development setback since November.

The Food and Drug Administration said in a letter to the company that it needed more information about the drugs safety and the best doses, Lilly said Friday in a statement.

Lilly said it disagrees with FDAs conclusions but will work with the agency on a plan to eventually get the drug, baracitinib, approved for U.S. patients.

In November, Lillys experimental medicine solanezumab flopped in a closely watched test in patients with mild Alzheimers disease, after having already failed in testing in patients with more advanced Alzheimers.

The arthritis drug, which has the proposed brand name Olumiant and was approved for use in Europe in February, was expected to be a big seller in part because most other new rheumatoid arthritis drugs are injected, making them less appealing for patients.

Christi Shaw, president of the Lilly division that developed the drug, said the company remains confident in the drugs ability to safely treat moderate and severe rheumatoid arthritis.

About 23 million people worldwide, three-fourths of them women, have rheumatoid arthritis, a chronic disorder in which the immune system attacks the bodys tissues. It causes painful swelling and progressive destruction of joints, which can leave them deformed and, in severe cases, lead to disability. It can also damage other body parts, including the skin, eyes, lungs, heart and blood vessels.

Eli Lilly & Co. and Incyte Corp., its partner in developing baracitinib, applied for FDA approval of the drug in January 2016. Normally the review process takes 10 months, but this January, FDA said it needed three additional months to review more information. Still, drug industry analysts as recently as this week were advising clients that approval of baracitinib was likely.

Despite the setback, Lilly reaffirmed its 2017 financial forecasts Friday, for earnings per share of $2.69 to $2.79, excluding one-time items, and revenue between $21.8 billion and $22.3 billion. It said Incyte, which is based in Wilimington, Delaware, was evaluating the rejections impact on its position and would update investors when it reports first-quarter results, likely in mid-May. Lilly is expected to report its quarterly results on April 25.

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HEALTH LINES: Arthritis common condition, but not easily … – Northeast Mississippi Daily Journal

April 16th, 2017 9:47 pm

Lifestyle HEALTH LINES: Arthritis common condition, but not easily understood by all

WILLIAM PILLOW

Arthritis is a condition that is very common, but not well understood by most. It is not a single disease. There are actually more than 100 types of arthritis.

More than 50 million adults and 300,000 children have some type of arthritis. It is more common in women and is the leading cause of disability in America. Common arthritis complaints are joint pain, swelling and stiffness.

Inflammatory arthritis (rheumatoid, lupus) is an overreaction of the bodys immune system. The body attacks the cartilage and destroys it. Metabolic joint disease (gout) occurs when crystals are deposited in the joints and cause acute pain. These are best treated by a primary care physician, nurse practitioner or specialist (rheumatologist) with medications and changes in diet. Blood tests are often used in the diagnosis.

Osteoarthritis (wear and tear arthritis) is the most common type. Cartilage is the thick cushioning surface on the ends of bones. With time this cartilage can wear down (thinning/mild arthritis) and progress to the point where bone rubs on bone (severe arthritis).

Orthopaedic Sports Medicine has significantly advanced the diagnosis and treatment of arthritis. As a physician at NEO Sports Medicine, I am often asked when someone should seek medical treatment. Anyone in their teenage years or younger with a joint that stays swollen for more than a few days should be seen urgently to rule out cartilage damage or juvenile rheumatoid arthritis.

Mild non-traumatic joint pain in someone 30 or older can start initial treatment with weight loss, anti-inflammatory medication (Aleve, Advil, Tylenol), and reasonable exercise that does not cause pain. Primary care physicians can prescribe stronger anti-inflammatories.

If this does not provide relief, a referral to an orthopaedist is the next step. Patients should not assume an appointment means imminent surgery. X-rays will give the doctor a good idea of the condition of the joint. At NEO Sports Medicine, physicians look at the whole person not just a joint. Many times a course of physical therapy to strengthen the muscles (the shock absorbers of a joint) will help. A steroid injection into the joint can also provide relief. Braces can also be used on a short-term basis to give the joint a rest.

Joint pain is not always arthritis. Torn cartilage can often be repaired with an outpatient arthroscopic surgery using a small camera that is quite minor. An MRI can be helpful to get a better picture of the joint. For major joint damage that has failed conservative treatment, a joint replacement can provide life-changing relief. Replacements are available for the knee, hip, shoulder and even finger joints.

Modern joint replacements are now meant to last longer than 15 years and can allow patients to get back to a more active lifestyle. My partners and I provide accurate diagnoses and seek to exhaust all forms of conservative treatment. If surgery is indicated, we provide minimally invasive joint surgery to get patients back to the lifestyle they desire.

Dr. William Pillow is an orthopedic surgeon at North East Orthopaedics and Sports Medicine.

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Psoriatic arthritis: ‘It is very much an invisible illness because I look and appear fine’ – thejournal.ie

April 16th, 2017 9:47 pm

Sandra Quinn Journalist and editor living with psoriatic arthritis

I SUFFER FROM psoriatic arthritis. Its a bit of a pain, literally, and often decides to flare up at the most inconvenient times.

It is the best form of arthritis to have in fairness, as it is not degenerative. It can be treated effectively with weekly injections, steroids, medication to prevent stomach ulcers, pain killers, anti-inflammatories and a host of other things.

My diagnosis

I was diagnosed when I was in college at the age of 19.It is a dehabilitating and life-long auto-immune disease, which when flared up causes severe pain, swelling and reduced mobility in my major joints, with my hips, spine, shoulders and knees being the worst affected.

The disease is relatively well controlled through a strict cocktail of daily maintenance drugs and weekly injections. Then for the flare-ups, which are unpredictable in nature, severity and duration, there are stronger medications, such as painkillers, anaesthetic topical patches (like plasters), anti-inflammatories, steroids and more.

It is very much an invisible illness because I look and appear to be fine and while I may be in a lot of pain, I would often still try to be in good form.

People often tell me I seem fine, not realising that they only see me when Im well enough to be seen. If I am really bad and in a lot of pain, I will be at home in bed hiding away from the world.

Managing flare ups

So, when it flares up, I have a list (its intimidatingly long to be frank) with a secondary bag of medication to match, which I can refer to and there are stages and steps to follow.

I have been going through the motions of the first steps since last week and all was going according to plan-ish, until I woke at 5am on Saturday (never a good sign) and had an upset stomach and bouts of vomiting from the severe waves of pain coming over me.

As it was a Saturday and my own GP practice was closed, I rang SouthDoc and got great medical advice and help. But as they were in Mallow and I was in Rockchapel (both in Cork, but a good 40-minute drive away from each other), it was not practical for me to go there, with the possibility of then having to go onto Limerick to the hospital.

I rang my own GP and left messages. Then I rang the assigned 24 hour rheumatology nurse specialist, then the rheumatology secretary and then the hospital itself.

No service available until Monday

The upshot of all those calls and chasing people was that there is no rheumatologist on call and the service is not available until Monday.

Armed with that knowledge, I assessed what SouthDoc had told me and started a process of self-medication and dosage.

The options were to self-medicate in the comfort of my own home or go to hospital, where they would only be able to give me pain relief, but nothing to treat the direct source of the flare up, without consulting a rheumatologist.

So, I ask you, is it fair or right that anyone with a severe illness or disability has to schedule their flare ups to tie in with the supposed schedule of Monday to Friday, 9 to 5, within business hours service of specialist care?

Its unacceptable

I think this story will evolve quite a lot, as it is clearly unacceptable in this day and age to only have access to vital medical experts and services within regular business hours.

I appreciate that people need time off and that services have wind down times, but the health system should not be one of those un-manned areas.

Sandra Quinn is a journalist and editor. Shes from Cork and lives in Limerick. Youll find her personal blog over onwww.quinnsquandries.blogspot.ie, while her work has been published in daily and weekly local, regional and national publications.

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Stem Cell Institute of America | Stem Cell Therapy …

April 16th, 2017 9:47 pm

Stem Cell Institute of America

The Stem Cell Institute of America trains physicians in your community on the amazing benefits of Stem Cells so they in turn are able to share their now extensive knowledge in this exciting subject with you. These Physicians have decided to educate local clubs, churches, business, organization in their community etc. on one of the most significant medical breakthroughs in natural medicine. Their purpose is to educate and answer questions on how you or someone you know can live a life without pain.

Chronic pain robs suffers of their quality of life and often leads to unnecessary pain medications and even depression. It is possible to turn the clock of time backwards and get your life back.

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Diabetes drives children to help others – Jackson Clarion Ledger

April 16th, 2017 1:44 am

John Webb, Special to The Clarion-Ledger 8:02 p.m. CT April 15, 2017

Type 2 diabetes can wreak havoc on your health. While lifestyle changes can help keep diabetes under control, many patients require oral medications or insulin injections as forms of treatment, too. Watch the video for how diabetes affects your body. Time

Mary Fortune, executive vice president of the Diabetes Foundation of Mississippi, pictured here with Bailey, one of DFM's Diabetic Alert Dogs, has lived with the disease 50 years.(Photo: Special to The Clarion-Ledger)

To invert a popular adage, it can take a child to raise a village or, in this case, a child who grew up with diabetes and as an adult vividly recalls what it was like.

A self-described free spirit, Mary Fortune has trekked the world despite a particularly brittle case of type 1 diabetes, traveling the Pacific Coast Highway on the back of a motorcycle, even in the immediate aftermath of a low blood sugar episode, and riding the rails of Europe, where she remembers asking for food from a train window in Hamburg during another hypoglycemic moment (blood glucose monitoring was not available in those days).

But she had one limitation.

She was told that because of her condition she should never try to get pregnant. That was the conventional wisdom in those days.

Yet, as she marks her 50th anniversary with diabetes a demanding and often unforgiving life partner Fortune says she feels as if she has raised an enormous family of those from across the state who like her had to come to terms in their youth or childhood with multiple daily insulin injections, finger sticks, blood sugar highs and lows, rigorous attention to diet and exercise and the kind of health complications that can beset even the most conscientious.

Theyre all my children, hundreds who have grown up with diabetes, and Im still in touch with quite a few, said Fortune, executive vice president of the Diabetes Foundation of Mississippi. Ive followed their lives and careers, engagements, weddings, births, successes and failures, times of crisis and grief, and times of joy.

And making this Mississippi matriarch of diabetes particularly proud this week are those children and adults she has mentored over the years who will be participating in the Diabetes Foundations 14th Annual Ultimate Fashion Show and Champagne Luncheon from 11 a.m to 1 p.m. Thursday at the Country Club of Jackson.

Proceeds will go to support the foundations Camp Kandu for children with diabetes and their families. The need has never been greater, because new studies have shown the rates of children being diagnosed with both Type 1 and Type 2 diabetes have increased dramatically, especially among racial and ethnic minorities.

Nationally between 2001 and 2009,the prevalence of Type 1 diabetes increased 21 percent among children up to age 19, according to astudy funded by the Centers for Disease Control and Prevention and the National Institutes of Health. The prevalence of Type 2 diabetes among those ages 10 to 19 rose 30 percent during the same period, the study, released in 2014, found.Type 1 diabetes is a chronic condition in which the pancreas produces little or no insulin, the hormone needed to allow sugar into cells to produce energy. Type 2 diabetesoccurs when the body becomes resistant to insulin or doesn't make enough insulin.

We are up at Batson Childrens Hospital seeing newly diagnosed children far more than we used to be, Fortune said.

RELATED:Diabetes and children: A balancing act

SEE ALSO:UMMC Delta diabetes project improves use of telehealth

Among those taking to the runway will be Charlie Mozingo, 41, the founder of Mozingo Clothiers in Fondren, who was introduced to Fortune after his diagnosis at the age of 10 and who in adulthood has been working with the foundation as a volunteer and board member.

Mozingo Clothiers is excited to be a part of this years fashion show, he said. We are dressing seven gentlemen in everything from custom clothing to some of our more casual attire. (As GQ might advise, Look for bold windowpanes in sport coats with lightweight materials that are both soft and comfortable, Mozingo said.)

Also taking part will be the foundations communications coordinator, Kaitlan Alford, 23, who was diagnosed with Type 1 at age 9 after spending two days in a coma.

My diagnosis was dramatic for everyone, really intense, and I saw how it affected my family, she said. We were all in a sense diagnosed. My mother saw me going through all this, the 2 a.m. blood sugar checks every night, but she knew I could handle it and take care of myself, which made me feel like I could do anything.

Kaitlan Alford, diagnosed as a child with Type 1 diabetes, was 14 when she walked the runway nine years ago at the Ultimate Fashion Show and Champagne Brunch in Jackson to raise money for the Diabetes Foundation of Mississippi's children's programs. Now an adult, she is the foundation's communications coordinator.(Photo: Special to The Clarion-Ledger)

Soft-spoken and demure, Alford had to fight back tears as she recalled how the disease has affected her mother, as well as the way Fortune reached out to her, first as a friend and mentor but then as the one who hired her after college.

I get emotional when I talk about it, Alford said. I dont just work here. Its not just us helping others. Mary helps me. We talk about things we both go through, trying to juggle the complex set of challenges that diabetes presents while at the same time trying to live a normal life.

Kaitlan Alford, 23, communications coordinator for the Diabetes Foundation of Mississippi, first walked the runway at the foundation's Ultimate Fashion Show and Champagne Brunch in Jackson. Alford, who has Type 1 diabetes, still participates in the event that raises money for the foundation's children's programs.(Photo: Special to The Clarion-Ledger)

At one of the foundations many statewide fund-raising walks, a child touched Alfords life in a way that she said still stands out in her mind.

My mom walked over to me and introduced me to this tiny, blond curlyhaired boy with blue eyes that could melt anyones heart, Alford said. He was 3 years old, and he had been diagnosed with Type 1 at 18 months."

She said that her eyes immediately filled with tears. Describing how I felt is nearly impossible, Alford said. I was hurting for him because I knew what he was going through, and I was empowered by him because he was 3 and dealing with challenges I didnt have to face until I was 9.

Ayden Wolken, 10, seen here with a bull at this year's Dixie National Rodeo Show, was diagnosed with diabetes when he was 18 months old.(Photo: Special to The Clarion-Ledger)

Alford said the boy, Ayden Wolken of Mendenhall, now 10 and competing on the soccer field and at livestock shows, inspired her to be even more courageous and determined while living with diabetes. Seeing him thriving now continues to inspire me, she said.

These are the kinds of moments that those at the Diabetes Foundation of Mississippi make possible because of their passion for not merely helping others, but for changing lives.

The Diabetes Foundation of Mississippis 14th Annual Ultimate Fashion Show and Champagne Luncheon will feature models of all ages in spring and summer fashions, giveaways and an array of raffle items, as well as a Champagne lunch and a drawing for the 2017 Patty Peck Honda Car 4 a Cure. All money raised by the foundation remains in Mississippi to be used to improve the quality of life of children and adults with diabetes.

Being honored will be the foundations 2017 Women of Excellence, Dr. Jane-Claire Boyd Williams of GI Associates and Dr. Beverly Hogan, president of Tougaloo College.

What: The Diabetes Foundation of Mississippis 14th Annual Ultimate Fashion Show and Champagne Luncheon

Where: The Country Club of Jackson

When:11 a.m.-1 p.m. April 20

Cost: $70 per ticket

For more information, call 601-957-7878 or visit msdiabetes.org (click on Events).

Type 1 diabetes, formerly known as juvenile or insulin-dependent diabetes, isa chronic condition in which the pancreas produces little or no insulin, the hormone needed to allow sugar into cells to produce energy.

Type 2 diabetes, once call adult-onset diabetes, occurs when the body becomes resistant to insulin or doesn't make enough insulin.

Source: Mayo Clinic

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