It’s Cool to be Kind: 5 Cyberbullying Prevention Tips

LinkedIn

Here are 5 cyberbullying prevention tips. Number one is The Golden Rule.

1. The Golden Rule. It’s important to remind ourselves that behind every username and avatar there’s a real person with real feelings. The “golden rule” is just as important online as it is in real life. Kids can take the high road by applying the concept of “treat others as you would like to be treated” to their actions online, creating positive impact for others and disempowering bullying behavior.

2. Promote Kindness. It’s important to teach kindness. But it’s just as important to model the lessons of kindness that we teach. How you and your friends treat each other online can model behavior for younger generations. Respect others’ differences and use the power of the Internet to spread positivity.

3. Move from bystander to upstander. Often kids want to help out a target of bullying but don’t know what to do. According to StopBullying.gov, only 20-30 percent of students notify adults about bullying. Encourage kids to speak up against and report online bullying. If they find themselves a bystander when harassment or bullying happens, they have the power to intervene and report cruel behavior. Kids can choose to be an upstander by deciding not to support mean behavior and standing up for kindness and positivity.

4. Turn negative to positive. Kids are exposed to all kinds of online content, some of it with negative messages that promote bad behavior. Teach your kids that they can respond to negative emotions in constructive ways by rephrasing or reframing unfriendly comments and becoming more aware of tone in our online communication. Reacting to something negative with something positive can lead to a more fun and interesting conversation – which is a lot better than working to clean up a mess created by an unkind comment.

5. Mind Your Tone. Messages sent via chat and text can be interpreted differently than they would in person or over the phone. Encourage kids to think about a time that they were misunderstood in text. For example, have they ever texted a joke and their friend thought they were being serious – or even mean? It can be hard to understand how someone is really feeling when you’re reading a text. Be sure you choose the right tool for your next communication – and that you don’t read too much into things that people say to you online. If you are unsure what the other person meant, find out by talking with them in person or on the phone

Supporting teachers and their classrooms:
Google has teamed up with DonorsChoose.org, a nonprofit with a web platform that is part matchmaker, part Scholastic Fairy Godmother. Teachers post their school project wishes on the platform and people like you—or companies like us—find projects we’d love to sponsor. With DonorsChoose.org, Google has built a $1 million Classroom Rewards program to encourage and celebrate classroom achievement with Be Internet Awesome. Upon completion of the program, K-6 teachers can unlock a $100 credit towards their DonorsChoose.org project. Teachers can kick off the Be Internet Awesome lessons with one called #ItsCoolToBeKind. 💚 Check out the details on DonorsChoose.

Be Internet Awesome is Google’s free, digital citizenship and online safety program that teaches kids the skills they need to be safe and smart online. Parents can find additional resources in English, Spanish and Portuguese, such as downloadable materials for the home at g.co/BeInternetAwesome.

From One Goal to the Next

LinkedIn
Parker Thornton about to Go Over the Edge

A crowded room quiets as Parker Thornton approaches the podium. He has been tasked with motivating Special Olympics Athlete Health Messengers to commit to being fit every day by working out more, eating healthy, and cutting down on soda.

He starts his speech by proclaiming the three words he says to himself in the mirror every day, “I’m happy, I’m healthy, and I feel fantastic!” Parker let those familiar words calm his nerves at speaking in front of the large crowd. After the speech has concluded, the audience erupts into applause, motivated and encouraged to take on the challenge of living a healthy life.

Parker’s life didn’t start at peak health. As a newborn, he contracted viral meningitis and was hospitalized at Boston’s Children’s Hospital for five weeks, much of it on life support. He survived his first challenge, but the result of the viral meningitis left Parker with significant learning disabilities, which resulted in an anxiety disorder and depression.

When Parker was eight years old, he was introduced to Special Olympics New Hampshire when local families came together to start a ski team for children with intellectual disabilities. That introduction has led to more than 28 years of involvement with Special Olympics. Parker has won numerous gold medals in sports ranging from basketball, golf, skiing, and pentathlons. “I realized that Special Olympics was more than just sports; it taught me how to be a better man, a proficient communicator, and how to be a mentor to other athletes who have their own challenges. Special Olympics tells you how to speak up, get healthy to be a better athlete, and blossom gifts in yourself and others,” Parker said.

Parker recently had an opportunity to make his own life healthier. “I wasn’t happy with my body, and Parker Thornton smiling to the cameraI was depressed,” Parker said. He signed up for a sprint triathlon, which motivated him to train for seven months. Parker lost 20 pounds and was able to go off prescribed medication. Seeing a positive change in his body and completing the triathlon showed Parker that even if it takes hard work, he can accomplish whatever he sets his mind to.

Parker has set his mind to tackling new challenges in the last few years. He speaks frequently on topics related to disabilities, Special Olympics, and the health disparities of people with disabilities. “Inclusive health is such a big issue. No one understands the health differences between people with and without intellectual disabilities. I want to motivate and get people thinking about how they can make changes to better the lives of people with intellectual disabilities,” he said.

Parker is now a consultant for Special Olympics International. He lead an Athlete Health Messenger training for a new cohort of athlete leaders who are tasked with taking the charge for equal access to health for people with disabilities. He co-edits a monthly health newsletter that goes out to thousands of recipients and is continuously tasked with being called upon to give motivational speeches. Speaking fills Parker with a sense of purpose. He wants to motivate others to see people with intellectual disabilities as part of human diversity and should be celebrated as such.

Parker is planning on accomplishing his next goal in 2019: attending professional stunt school in California. “It’s been a lifelong dream of mine to get trained to do professional stunts like you see in the movies,” he said. “I can’t wait to see what’s next.”

Living With LGMD

LinkedIn
Keisha Greaves

I have Limb-Girdle Muscular Dystrophy (MD); I was diagnosed at the age 24. Keisha Greaves, founder of  Girls Chronically Rock shares her story.

I was born and raised in Cambridge, MA and went to high school in Cambridge. I received my bachelor’s degree in Fashion Design and Merchandising and then furthered my education in getting my Master’s degree in Business.

When I first discovered my symptoms of my MD, it was crazy to me because I started to get symptoms around 2009, while in graduate school. I began to repeatedly fall, and my leg would just give out on me without notice. I would fall to the ground and not be able to pick myself back up, I would need assistance from someone to lift me up with all their might, because it was something I just wasn’t capable of doing on my own. I also began notice when I tried to reach for certain things in the kitchen cabinets or try to exercise I was unable to lift my right arm up all the way. I kind of just thought to myself maybe I need to go on a diet and lose weight, but in the back of my mind I knew it something more.

So I went to see an orthopedic, but I was told that this was more of a neuro-muscular issue, so I then went to see a Neurologist. Once I saw the Neurologist, she then tested me and gave me a muscle biopsy, MRI, an EMG and every other test you can think of. So after multiple tests, I was finally diagnosed with Limb-Girdle Muscular Dystrophy. Limb-Girdle is a form of MD that affects the limb of the shoulders all the way down to the legs, which progressively over time eventually gets worse.

The first thing I thought was how long am I going to live, will I be in a wheelchair soon, and what is my life going to be like from now on. I knew I had to be strong and continue to do what I have to do so I started doing some research on it and read what eating healthy and exercising would help. I joined weight watchers with my cousin, I lost over 36 pounds and I felt great. I’ve able to keep half the weight still off, and I am still determined to lose more.

They have multiple types of Limb-Girdle Muscular Dystrophy, and 5 years later my doctor’s are still trying to figure which type I have exactly. The only thing they know at this point is from the types I may have, can affect my heart which is why I often have to go get a echo-cardiogram test that tests my heart to make sure everything is ok.

Living with Limb-Girdle Muscular dystrophy is still new to me every day. I wake up every day not knowing how my legs are going to feel, or what pain I may have when leaving my house. I try to be very careful when walking because I don’t want to fall and because I won’t be able to pick myself back up. Although I’m on my feet a lot for work, after a certain amount of hours, my legs start to weaken. I am currently a visual merchandiser at different locations for a very popular clothing store. I enjoy my job because it keeps me and my legs active and I enjoy traveling to the different store locations, doing what I love and my part in the fashion industry.

I have the wonderful support from my family and friends but at the end of the day, they have NO IDEA what I go through on daily basis or what I’m feeling. I try to explain to them how my legs feel, but it’s just so hard to explain. I still go out and enjoy my life as normal, but sometimes I always have certain things in the back of my mind.

When going out, I find myself researching about where I am going first, like does this place have stairs? Does it have an elevator? Do they accommodate handicapped people? So all of these things I worry about when I go out, and my friends and family have no idea. Living with MD has made me realize how strong I am and knowing I have no choice but to deal with this. I sometimes get stares because people wonder what a young girl like me is doing either walking with a limp, with a cane, or parking in a handicap parking spot. But I don’t mind because they just don’t know me or know what I have. Although my MD has progressed over the years and getting worse, I have learned to accept it and make certain changes in to my life, such as now walking with a cane in order to keep my balance and helping me not to fall. At this point, I am just taking everything day by day and staying strong. But there is one thing I want people to know by reading this quote.

“There’s no “cure” or a pill will “fix it”, but at one point I thought it may help. And, I thought the same with therapy and food. But it’s my endless support from family and friend that helps. It is hardest thing that I have ever done, and I found myself much stronger for doing it. Never, ever, underestimate the power of your desire. If you want to live badly enough, you can live. The greater question, at least for me was: How do I decide I want to live? That is the question I’m still working on?”

girlschronicallyrock.com

6 things Deaf activist Nyle DiMarco wants you to know about sign language

LinkedIn
Nyle DiMarco signing on stage

You may know Nyle DiMarco from America’s Next Top Model, where he was crowned the victor of the show’s 22nd season, in 2015. You may have seen DiMarco demonstrate perfect rhythm on Dancing With the Stars, where he went home with yet another grand prize. DiMarco, in short, is a winner.

But DiMarco, who is deaf, believes he owes his good fortune in life to a childhood experience: learning language — both spoken and signed — at an early age. Language acquisition, he says, helped him understand and engage with the world, which led to life-changing educational opportunities.

Now DiMarco is using his fame to try to help millions of deaf children around the world also gain access to language through his eponymous foundation. As part of that work, he appeared at the 2018 Social Good Summit in New York City to recognize International Day of Sign Languages and will appear at International Week of the Deaf, annual events that highlight the importance of access to sign language as part of achieving full human rights for deaf people.

Here are six things DiMarco wants you to understand about sign language and the importance of language acquisition for Deaf people:

1. You are a fierce advocate for early language acquisition among Deaf children. How did learning sign language at an early age change your life?

I was born into a large, multigenerational Deaf family — my great grandparents, grandparents, parents, and my two brothers are all Deaf. I am the fourth generation and have been exposed to American Sign Language and English since birth.

Knowing sign language saved my life. I was never alone. My entire family used sign language, so I never missed dinner table conversations. Growing up, I attended Deaf schools including Gallaudet University, the only Deaf university in the world. You could say it was a utopia for me.

With sign language, I was able to embrace my own identity as Deaf. I did not let being Deaf define me. Instead, I defined it.

2. Why is it often difficult for Deaf children to access sign language education?

Audism. Audism is a set of beliefs that include: hearing people are superior to Deaf people; Deaf people should be pitied for having futile and miserable lives; Deaf people should become like hearing people as much as possible; and that sign languages should be shunned. The stigma that notion has created positions sign language as a “lesser option” and pushes people consciously, or unconsciously, to prioritize hearing and speech therapies over sign language education. Materials and information become less available to the less popular option, and when you’re a new parent to a Deaf baby or child you look to the most available materials.

That is something my foundation, The Nyle DiMarco Foundation, is looking to change.

3. What myths about sign language and language acquisition are most harmful to the human rights of Deaf people?

In this bizarre world we live in, there are doctors, early interventionists, and audiologists that tell hearing parents not to expose their Deaf child to sign language because it will hinder their ability to learn English. That is a myth. A foundation in sign language helps your Deaf child learn how to read and write.

People believe that sign language is not a language. That is false. Sign language is a full language with its own grammar, syntax, and structure.

4. If you could immediately change anything about the representation of Deaf people and sign language in popular culture, what would it be?

Representation behind and in front of the camera. Empowering Deaf people as actors, writers, directors, producers, etc. There is no true representation if we’re not part of the stories being told — nothing about us without us. Sign language is being exploited and that only adds irreparable errors.

5. What does the International Week of the Deaf principle “nothing about us without us” mean to you?

It means that society needs to empower Deaf people as decision makers. This is true for every minority group. In order to improve our society as a whole, every marginalized group needs to be included in the conversation whether it’s political, social, or within the entertainment industry. I know that is easier said than done, but I feel like people are taking charge of their cultural and personal narratives more and more and it’s inspiring to see that.

Continue on to Mashable to read the complete article

Forget managing chronic arthritis pain, prevent it from happening!

LinkedIn
smiling doctor in hospital lab

MARINA DEL REY, California–According to the National Institutes of Health, over 25 million American adults suffer from pain on a daily basis. More than 23 million of them report that they are in a lot of pain.

The majority of these people will have a poor health status, use more health care, and suffer from more disability as a result of their chronic pain. Oftentimes people don’t know how to successfully go about managing it, or preventing it from happening in the first place. One pain expert, Dr. Akash Bajaj, is helping patients beat chronic pain through Alpha Mac, or Alpha 2 Macro-Globulin treatment.

“The beauty of this new treatment is that it doesn’t just attack the pain that is there and make it stop, it prevents inflammation which is the cause of the pain from happening in the first place,” explains Dr. Bajaj, board-certified interventionist, pain specialist and medical director at Remedy Spine & Pain Solutions in Marina Del Rey, Calif. “Being able to stop pain is great, but when you can prevent it from happening, it just doesn’t get any better or more powerful than that.”

Chronic pain can result from a variety of issues, including sports injuries, poor lifestyle choices, traumatic injury, and arthritis, among other issues. Chronic pain is often the result of chronic inflammation. Being able to nix the chronic inflammation ultimately prevents the pain from ever happening. That’s exactly what the Alpha Mac treatment does. While many people are familiar with stem cell treatments and Platelet Rich Plasma (PRP) treatments, the Alpha Mac treatment takes it one step further.

Popular treatments that people often use for arthritis joint and degenerative disc chronic pain only provide temporary relief, and then the patients are usually subjected to repeated exposure to harmful chemicals, such as steroids. The Alpha 2 Macro-Globulin treatment blocks or inhibits the inflammatory reaction, which decreases the body’s ability to create inflammation in the affected joints. Alpha 2 Macro-Globulin therapy, like PRP treatment, is a very simple in-office procedure.

“Millions of people suffer from pain every year. Pain can occur from sporting injuries, everyday activities or just from getting older,” says Dr. Bajaj. “Traditional treatments include steroid injections, physical therapy, chiropractic care or a combination of these as well as pain medications. While these are useful treatments the problem with them is there is really no end point in sight for the patient. Patients placed on medications may need to continue their use on an ongoing basis with the risk of developing side effects or even addiction. The same applies to physical therapy and steroid based injections.”

Now a new treatment is available that is natural, non-toxic and is derived from the patient’s own blood to eliminate pain. Alpha Mac therapy utilizes the body’s own healing properties to help decrease inflammation, which typically is the underlying source of the pain. Inflammation can affect virtually any area of the body including the joints, lower back, the neck or other areas.

The doctor takes a small amount of blood, which is processed through a centrifuge to extract the Alpha 2 Macro-Globulin. Then, the Alpha Mac is injected at the source of the inflammation. This leads to a decrease in chronic pain in joints and the spine that are due to arthritis, sports injuries, etc. Alpha 2 Macro-Globulin seeks out and removes pro inflammatory enzymes. The procedure works quickly, is not very painful, and provides effective chronic arthritis pain relief. Alpha Mac uses components derived from a patient’s own blood, primarily enzymes that act quickly to eliminate inflammatory chemicals, allowing the regenerative properties of PRP to work more quickly. Together these therapies, both derived from the patient’s own blood, are bringing superior outcomes compared to single modality approaches.

“I’ve been suffering from chronic pain for a number of years; one of the worst parts about it is the anticipation…waiting for the symptoms to rear their ugly head. Alpha Mac has changed my life, I no longer have to nervously wait for the onset of pain,” says David Graham, a 57-year old pro golfer. “Cutting it off at the pass has greatly improved my quality of life. I thank Dr. Bajaj for that.”

The procedure is performed by Dr. Akash Bajaj, who is an award-winning surgeon, and highly regarded pain management specialist. For more information on services provided or to book an appointment, visit their site at: remedypainsolutions.com.

About Remedy Spine & Pain Solutions
Founded and run by award-winning surgeon and pain management expert Dr. Akash Bajaj, the center is located in Marina Del Rey, Calif. They provide advanced solutions for those who suffer from all types of chronic pain. They also offer a minimally invasive, highly effective implant surgery for those with chronic back pain. Remedy Spine & Pain Solutions has won numerous awards, including multiple times winning Super Doctors award and the Best of Marina Del Rey award. For more information on services provided, visit their site at: remedypainsolutions.com.

# # #

Huey Lewis Opens Up About Sudden Hearing Loss: ‘I Haven’t Come to Grips with the Fact That I May Never Sing Again’

LinkedIn
huey lewis holding microphone on stage

In mid-April, Huey Lewis shocked fans when he canceled all upcoming tour dates, citing a battle with Meniere’s disease that robbed him of his hearing. While he hopes the health problems are treatable, the “Power of Love” rocker says he’s facing the possibility that he may never return to live performance.

It’s a reality that Lewis, 67, admits he’s finding hard to accept. “I haven’t come to grips with the fact that I may never sing again,” the Huey Lewis and the News frontman said in an interview with the Today show on Monday. “I’m still hoping I’m gonna get better. They say a positive attitude is important.”

Meniere’s disease is an inner ear disorder that produces feelings of vertigo, as well as tinnitus (or ringing) and hearing loss. Lewis says he first noticed the symptoms in March during a performance in Dallas. “As I walked to the stage, it sounded like there was a jet engine going on,” he continued. “I knew something was wrong. I couldn’t find pitch. Distorted. Nightmare. It’s cacophony.”

In a tragic twist, the lifelong rocker says his hearing loss is most severe when it comes to music. “Even though I can hear you, we can talk, I can talk on the phone — I can’t sing,” he told Today‘s Jenna Bush Hager. “I can’t hear music. I can do everything but what I love to do the most, which is a drag.”

While there’s no known cure for the disease, Lewis says that his hearing may improve with a new dietary regimen. “No caffeine, lower salt, and keep your fingers crossed. It can get better. It just hasn’t yet.”

On April 13, Lewis posted a message to social media announcing the cancellation of all upcoming tour dates because his condition made it “impossible” to continue singing for the time being.

Continue onto PEOPLE to read the complete article.

CVS Health Fights Back on High Cost Drugs by Launching Industry’s Most Comprehensive Approach to Saving Patients Money

LinkedIn

New CVS Health initiative seeks to solve one of the nation’s most pressing problems and a major source of consumer financial worry.

Recognizing the threat of rising drug prices and high out-of-pocket costs, CVS Health providing most advanced solutions for prescribers, pharmacists and patients.

CVS Pharmacists are key resource for patients in identifying opportunities to maximize their prescription benefits and save money at the pharmacy counter in communities nationwide.

CVS Caremark mitigating impact of high drug costs by providing members and prescribers with robust information and innovative tools to choose lower-cost prescription drugs.

The high cost of prescription drugs is one of the nation’s most pressing problems and a major source of financial worry for consumers across the nation. While CVS Health (NYSE: CVS) has made significant progress in mitigating the impact of high list prices set by pharmaceutical manufacturers, for too many Americans annual out-of-pocket drug costs are still significant. In response, CVS Health announced today that it is fighting back by launching the most comprehensive program in the industry to help patients save money on their medications.

According to a recent national poll, commissioned by CVS Health, 83 percent of Americans said they were concerned personally about the impact of rising prescription drug prices.[1] As prescription drug prices continue to rise and enrollment in high deductible health plans grows, many patients are shouldering higher costs for their prescription medicine.

CVS Health will address this problem with a robust set of initiatives, including the new CVS Pharmacy Rx Savings Finder, which will enable the company’s retail pharmacists for the first time to evaluate quickly and seamlessly individual prescription savings opportunities right at the pharmacy counter. This new tool further enhances existing savings opportunities the company’s pharmacy benefit manager (PBM) CVS Caremark is currently offering its clients such as the preventive drug lists that make medications for many common, chronic conditions available at a $0 copay. In addition, CVS Caremark provides real-time, member-specific drug costs and lower-cost alternatives to prescribers through their electronic health record system and to CVS Caremark members through the member portal and newly updated app. These programs are part of CVS Health’s commitment to helping consumers find the lowest cost prescription drugs by offering more pricing transparency for prescribers, pharmacists and patients.

“Today’s consumers are faced with higher prescription drug prices than ever before and many of them are now paying for a larger share of their prescription drug costs out of their own pockets at the pharmacy counter due to growth in high deductible health plans,” said Thomas Moriarty, Chief Policy and External Affairs Officer, CVS Health. “Until now, patients haven’t had the appropriate tools available to them to help them manage these costs. To address this, CVS Health is giving expanded tools to patients, prescribers and pharmacists so they can evaluate prescription drug coverage in real-time and identify lower-cost alternatives. We are committed to finding the right drug at the lowest possible cost for patients to ensure they are able to access and stay on the medications they need. That’s our promise.”

At the Pharmacy Counter

The new CVS Pharmacy Rx Savings Finder enables the retail pharmacist to quickly and seamlessly review a patient’s prescription regimen, medication history and insurance plan information to determine the best way for them to save money on out-of-pocket costs – with the primary goal of helping the patient find the lowest cost alternative under their pharmacy benefits plan.

“Our direct experience is that patients who are confronted with high out-of-pocket costs at the pharmacy counter are less likely to pick up their prescriptions and are less likely to be adherent to their prescribed therapy,” said Kevin Hourican, Executive Vice President, Retail Pharmacy, CVS Pharmacy.

“Armed with the information available through our Rx Savings Finder, our more than 30,000 CVS pharmacists can play an important role by helping patients save money on their medications, providing advice on how and when to take them, and ultimately helping them achieve better health outcomes,” Hourican added. “We are beginning this process with our CVS Caremark PBM members and expect to roll it out more broadly throughout the year.”

The Rx Savings Finder will show pharmacy teams:

  1. First, if the prescribed medication is on the patient’s formulary and is the lowest cost option available.
  2. Second, if there are lower-cost options covered under the patient’s pharmacy benefit – such as a generic medication or therapeutic alternative with equivalent efficacy of treatment.
  3. Third, if the patient may be able to save money by filling a 90-day prescription rather than a 30-day prescription.
  4. Finally, if neither a generic nor a lower-cost alternative is available, other potential savings options for eligible or uninsured patients where allowed by applicable laws and regulation.[2]

Pharmacists can also help patients enroll in the ExtraCare Loyalty Program and sign them up for Pharmacy and Health Rewards. Through Pharmacy and Health Rewards, patients receive $5 in ExtraBucks for every 10 prescriptions filled, earning up to $50 in ExtraBucks annually.

At the Doctor’s Office

Another component of the company’s comprehensive savings approach is the recently launched real-time benefits program, which helps bring greater drug price transparency to prescribers and CVS Caremark members. At the point-of-prescribing, providers are able to see the member-specific cost for a selected drug, based on a member’s coverage, along with up to five lowest-cost, clinically appropriate therapeutic alternatives based on the patient’s formulary. PBM members have access to the same information on the CVS Caremark app and member portal. Early results show that prescribers accessing the real-time benefits information through their electronic health record switched their patient’s drug from a non-covered drug to a drug on formulary 85 percent of the time. In addition, when the patient’s drug is covered, prescribers using real-time benefits switch their patient to a lower-cost alternative 30 percent of the time. When the prescriber switched to a lower-cost drug, the difference was approximately $75 per prescription.
“We have been working hard to keep prescription medications affordable for patients,” said Troyen A. Brennan, M.D., Executive Vice President and Chief Medical Officer, CVS Health. “In fact, in 2017, nearly 90 percent of our PBM plan members spent less than $300 out-of-pocket for their prescription medicines. While this signals progress, for those patients that cost is not insignificant. That is why we are committed to doing even more across our enterprise to help patients find and access the lowest cost drug at the pharmacy which ultimately will help improve clinical outcomes and remove higher downstream medical costs from the system.”

Using Pharmacy Benefit Management Solutions

CVS Health is also making a variety of PBM solutions available to help further drive down drug trend for its PBM clients and drug costs for the patients they support. The company’s Point of Sale (POS) rebate offering allows the value of negotiated rebates on branded drugs to be passed on directly to patients when they fill their prescriptions – and the savings from this program can be significant. In 2013, CVS Health led the industry with the introduction of POS rebates to clients, and today nearly 10 million members are covered by and able to benefit from the program.

In 2017, despite manufacturer brand list price increases on drugs near 10 percent, CVS Health PBM strategies reduced drug trend for CVS Caremark commercial clients to the lowest level in five years, keeping drug price growth at a minimal 0.2 percent. In fact, 42 percent of CVS Caremark commercial clients spent less on their pharmacy benefit plan in 2017 than they had in 2016. CVS Caremark helped members reduce monthly out-of-pocket costs and improve adherence to its highest level in seven years in key categories such as diabetes, hypertension and hyperlipidemia.

Prescription drug trend is the measure of growth in prescription spending per member per month. Trend calculations take into account the effects of drug price, drug utilization and the mix of branded versus generic drugs as well as the positive effect of negotiated rebates on overall trend. The 2017 trend performance is based on a cohort of CVS Health PBM commercial clients, employers and health plans.

About CVS Health

CVS Health is a pharmacy innovation company helping people on their path to better health. Through its more than 9,800 retail locations, more than 1,100 walk-in medical clinics, a leading pharmacy benefits manager with more than 94 million plan members, a dedicated senior pharmacy care business serving more than one million patients per year, expanding specialty pharmacy services, and a leading stand-alone Medicare Part D prescription drug plan, the company enables people, businesses and communities to manage health in more affordable and effective ways. This unique integrated model increases access to quality care, delivers better health outcomes and lowers overall health care costs. Find more information about how CVS Health is shaping the future of health at https://www.cvshealth.com.

###

[1] The Morning Consult poll was conducted from February 22-26, 2018, among a national sample of 1992 registered voters. The interviews were conducted online and the data were weighted to approximate a target sample of registered voters based on age, race/ethnicity, gender, educational attainment, and region. Results from the full survey have a margin of error of plus or minus 2 percentage points.

[2] Prescriptions submitted for reimbursement to Medicare, Medicaid or other federal or state programs are not eligible.

Have a lower leg injury? Don’t just sit there and suffer, get moving!

LinkedIn
iwalkfree

LOS ANGELES, Calif.– Each year, there are millions of people who end up with lower leg injuries. Those who have experienced it know all too well the way it can make something like mobility a new challenge to conquer.

Yet the majority of people need to still be able to get around to go to school, work, run errands, and just continue to participate in life. Time and duties don’t come to a halt with a lower leg injury, so knowing how to get around easier can make a world of difference.

“The last thing people want when they have a lower leg injury is to be holed up in the house and stuck on the couch waiting it out,” explains Brad Hunter, the innovator of iWALK2.0 and the chief executive officer of the company, iWALKFree, Inc.  “There are things people can do to help make it easier during this challenging period. Taking steps to make it easier will help keep people more mobile and less frustrated.”

According to the National Institutes of Health, there are 6.5 million people in the country who need to use some type of device to assist with their mobility. Here are some tips for helping make mobility easier while having a lower leg injury:

1. Consider using the iWalk2.0. Those who use crutches often find that they make mobility more challenging. They keep both hands busy, making it difficult to carry things or even open doors. The iWALK2.0 has been designed to help people easily get around with their lower leg injury and at the same time do so hands-free.

2. Plan ahead. Taking the time to plan out errands and tasks will give people an opportunity to determine which will be the easiest routes and schedules to take. Planning ahead will help people stay organized, determine the routes that are the best for increasing mobility, and will reduce the stress of backtracking.

3. Ask for help. Many people shy away from asking others for help. They don’t want to burden them or feel like they are being a pest. The truth is that most people won’t mind one bit helping out. Don’t shy away from asking for help when it is needed.

4. Look for obstacles. When you arrive at your destination, take a moment to scan the area for what could be potential obstacles. If you know stairs will be difficult, for example, or if you see the sidewalk is blocked off for repair, determine the best way to navigate around it before approaching the area.

5. Getting around. If your lower leg injury is preventing you from being able to drive, determine your other options. Ask friends and family members for rides, and if that is not an option check with your local bus company to see what they can provide. Many public transportation systems offer a home pickup and drop-off option for those in need.

“The important thing to remember is that this is a temporary challenge and you can take measures that will help to make mobility easier during it,” adds Hunter. “We routinely hear from people who love how the iWALK2.0 has made their mobility easier. Our system has helped countless people to navigate the challenge of a lower leg injury with more ease and confidence.”

The IWALK2.0 was developed as a way to help make healing from a lower leg injury more comfortable and to increase the ease of mobility. The original prototype was created by a farmer in Canada.  The concept continued to develop, and the iWALK2.0 was launched in late 2013. Sales really took off when Harrison Ford was photographed wearing it.

The iWALK2.0 is hands-free, easy to learn to use, it’s intuitive, and safe. From the knee up, the leg is doing the same walking motion that comes naturally to it. The device is essentially a temporary lower leg, which gives people their independence and mobility back as they recover from an injury. The device is pain-free, and makes it possible for people to engage in many of their normal routine activities, such as walking the dog, grocery shopping, and walking up or down stairs.

Clinical research, the results of which are on the company website, shows that patients using the iWALK2.0 heal faster, and have a higher sense of satisfaction and a higher rate of compliance. The iWALK2.0 sells for $149 and is available online and through select retailers. Some insurance companies may cover the cost of the device. The device can be used with a cast or boot, and comes with a limited warranty. For more information on the iWALK2.0, visit the site at: http://iwalk-free.com. To see a video of the iWALK2.0 in action, visit: iWalkFree

About iWALKFree
The iWALK2.0 is a hands-free knee crutch, made by iWALKFree, Inc.  It’s a mobility device used instead of traditional crutches and knee scooters. It offers more comfort and independence, with the hands and arms remaining free. The device offers people a functional and independent lifestyle as they are recovering from many common lower leg injuries. For more information on the iWALK2.0, visit the site at: http://iwalk-free.com

# # #

Source:

National Institute of Health: How many people use assistive devices? https://www.nichd.nih.gov/health/topics/rehabtech/conditioninfo/people

Move Over Crutches and Knee Scooters, Now There’s Something Hands-Free and Much Better

LinkedIn
iwalkfree

According to the National Institutes of Health, there are around 6.5 million people in the country who use a cane, walker, or crutches to assist with their mobility. Many of these people are prescribed crutches or knee scooters for lower leg injuries. Yet those devices come with their own set of problems, making them difficult to use.

Crutches often lead to muscle atrophy, make it difficult to use the stairs, and if they fall to the floor it can become a gymnastics maneuver to try and pick them up. Millions of people are prescribed crutches or knee scooters for lower leg injuries. Now, those with lower leg injuries have a better option to consider, the iWALK2.0, which gives them hands-free ability to continue walking and having full use of their arms and hands.

“When people have the ability to try out the hands-free iWALK2.0, they can feel what a major difference and step up it is from using crutches or a knee scooter,” explains Brad Hunter, the innovator of iWALK2.0 and the chief executive officer of the company, iWalk Free. “It’s a revolutionary device that helps give people back their independence and mobility while they are healing from an injury. It doesn’t get much better than that.”

Crutches are known for being uncomfortable, often making it difficult for people to remain independent. They take full use of someone’s arms and hands. Leg scooters are also difficult to use because they lack the ability for the person to feel they are getting around in a somewhat normal fashion. These problems are what motivated the iWALK2.0 innovator to find a better, more comfortable way to help heal a broken ankle. The original prototype was created by a farmer named Lance, and when Brad found it he purchased half of the company and innovated the device. Sales really took off when Harrison Ford was photographed wearing it. The rest, as they say, is history.

The muscles around your upper leg and hip atrophy by as much as 2% a day while on crutches. That’s not so with iWALK2.0. Also, one’s blood flow to the lower extremities is typically reduced when using crutches, thus hampering the healing process and the transition between using crutches and walking without them can be difficult, but the iWALK2.0 makes the transition seamless. The iWALK2.0 is an alternative to 2,000-year-old crutches, and won the I-Novo Award for “best design” of any medical product, as voted on by 120,000 medical experts from around the world at an international conference held in Germany.

The iWALK2.0 is hands-free, easy to learn to use, it’s intuitive, and safe. From the knee up, the leg is doing the same walking motion that comes naturally to it. The device is essentially a temporary lower leg, which gives people their independence and mobility back as they recover from an injury. The device is pain-free, and makes it possible for people to engage in many of their normal routine activities, such as walking the dog, grocery shopping, and walking up stairs.

Since 1999, the company has brought thousands of people a more comfortable way to heal from many common lower leg injuries. Made of lightweight aluminum and engineered plastic, the device fits onto the leg, and allows people to do what they have always done. The crutches and knee scooter alternative, it has been the subject of numerous scientific studies and has won multiple awards from Medtrade, the largest medical device show in North America.<

“If you hurt your leg, you have a choice between arm crutches or our leg crutch, the iWALK2.0,” adds Hunter. “With all the benefits of the iWALK2.0 there is no reason to ever want to choose crutches or a leg scooter. The iWalk will keep you moving comfortably throughout the duration of your recovery.”

Clinical research, the results of which are on the company website, shows that patients using the iWALK2.0 heal faster, have a higher sense of satisfaction, and a higher rate of compliance. The iWALK2.0 sells for $149 and is available online and through select retailers. Some insurance companies may cover the cost of the device. The device can be used with a cast or boot, and comes with a limited warranty. For more information on the iWALK2.0, visit the site at: http://iwalk-free.com. To see a video of the iWALK2.0 in action, visit:  iWalkFree.

About iWalk Free

The iWALK2.0 is a hands-free knee crutch, made by iWalk Free, that is a mobility device used instead of traditional crutches and knee scooters. It offers more comfort and independence, with the hands and arms remaining free. The device offers people a functional and independent lifestyle as they are recovering from many common lower leg injuries. For more information on the iWALK2.0, visit the site at: http://iwalk-free.com.

# # #

Source:

National Institutes of Health. How many people use assistive devices? https://www.nichd.nih.gov/health/topics/rehabtech/conditioninfo/Pages/people.aspx

DAV’s 2017 Outstanding Disabled Veteran of the Year

LinkedIn
Dr. Kenneth Lee

Dr. Kenneth K. Lee president of the Wisconsin Adaptive Sports Association

Disabled American Veterans (DAV) named Dr. Kenneth K. Lee, a combat-injured Operation Iraqi Freedom and Army veteran, its 2017 Outstanding Disabled Veteran of the Year.

Lee, who deployed as the commander of the Army’s Company B, 118th Area Support Medical Battalion, was injured in November 2004 by a suicide car bomber in Iraq. The explosion resulted in an open head traumatic brain injury and severe shrapnel wounds to his legs, which led to his evacuation back to the states, where he would later be diagnosed with post-traumatic stress disorder (PTSD).

While recovering from his injuries, Lee, a rehabilitation specialist, saw how long and difficult recovery could be, often leaving lasting changes. Lee, who resides in Brookfield, Wisconsin, is a volunteer physician at the National Disabled Veterans Winter Sports Clinic, which the Department of Veterans Affairs and DAV co-host, so he was no stranger to using adaptive sports as therapy. Through his own recovery, Lee propelled himself into the world of adaptive sports to help him deal with the psychological and physiological effects that can often cause an individual to hit bottom.

Within a year of Lee’s retirement in 2013, he formed the Milwaukee Wheelchair Lacrosse team and is now the president of the Wisconsin Adaptive Sports Association (WASA) which runs numerous adaptive sports programs.

DAV National Commander David W. Riley presented Lee the award at the organization’s 96th National Convention in New Orleans.

“Dr. Kenneth Lee is a shining example of everything that is good about our nation and its veterans,” said Riley. “The compassion he shows for other veterans and his work to help them find success is truly the hallmark of this award, and we’re very proud of what he’s doing for this community. At DAV, we truly value the importance and therapeutic effectiveness of adaptive sports and it is vital to have experienced leaders like Dr. Lee involved and carving out a path ahead.”

Despite his injuries and the constant pain in his lower extremities, Lee speaks with gratitude about his time in the Army.

“I got a lot more from the Guard than I put into it,” said Lee. “I joined the military with my eyes wide open. I volunteered to join. I have no regrets.”

Lee and his wife Kate currently live in Brookfield, Wisconsin, with their two children. As a youth volunteer, in 2014 his daughter Leah earned a $10,000 scholarship by volunteering for the DAV at the Milwaukee VA Medical Center. On the same day he will be honored as the charity’s veteran of the year, his son Jonathan has earned the charity’s largest scholarship of $20,000 and will be honored the same morning. They both hope ultimately to serve veterans as physicians through the VA.

About DAV
DAV empowers veterans to lead high-quality lives with respect and dignity. It is dedicated to a single purpose: fulfilling our promises to the men and women who served. DAV does this by ensuring that veterans and their families can access the full range of benefits available to them; fighting for the interests of America’s injured heroes on Capitol Hill; providing employment resources to veterans and their families and educating the public about the great sacrifices and needs of veterans transitioning

About DAV
DAV empowers veterans to lead high-quality lives with respect and dignity. It is dedicated to a single purpose: fulfilling our promises to the men and women who served. DAV does this by ensuring that veterans and their families can access the full range of benefits available to them; fighting for the interests of America’s injured heroes on Capitol Hill; providing employment resources to veterans and their families and educating the public about the great sacrifices and needs of veterans transitioning back to civilian life. DAV, a non-profit organization with nearly 1.3 million members, was founded in 1920 and chartered by the U.S. Congress in 1932.

Learn more at dav.org.

Fiesta Educativa Serves Latinos with Developmental Disabilities

LinkedIn
Dancers

By Ling Woo Liu

In the mid-1970s, long-time Spanish teacher Irene Martinez received a dinner invitation from a friend that would change her life.

Her friend’s husband, Joe Sanchez, was the executive director of one of California’s Regional Centers, which were established in 1966 to serve people with developmental disabilities and their families. That night over dinner, a conversation with Sanchez piqued Martinez’s interest. “It was a combination of what he said and how he said it—he had a deep commitment to what he was doing,” says Martinez. Soon afterward, she applied and was hired to serve as a counselor at the Eastern Los Angeles Regional Center. “From the first day, it just fit,” she says. “I loved what I was doing.”

At the time, center staff had noticed that non-English-speaking families weren’t receiving Regional Center services to the same extent as English-speaking families. As one of the early Spanish speakers on staff, Martinez organized a workshop to inform Latino families about Regional Center services. “There were people from wall to wall,” says Martinez, describing her first outreach event. “Parents talked to each other and word got out to the other Regional Centers. Things started to snowball.”

By 1978, that snowball had grown into an independent organization called Fiesta Educativa (“Educational Party”), founded by the Eastern Los Angeles Regional Center. It was one of the first organizations in the country to serve Latino families with children who have developmental disabilities. The concept of a “party” stemmed from the fact that Latino families respond better to information imparted in casual, familiar settings, like the homes of fellow families, rather than in agency offices. Martinez served as one of Fiesta’s original board members, and since 1998 she has led the organization as its executive director.

Nearly 40 years after its founding, Fiesta’s headquarters remains in Lincoln Heights, a predominantly Latino and Asian neighborhood in eastern Los Angeles, in an office above a strip mall. Signs throughout the building are printed in English, Spanish, Chinese, and Vietnamese. Today, Fiesta Educativa is California’s largest nonprofit organization serving Latino families with children who have special needs. Fiesta has eight parent coordinators on staff and more than 30 volunteers based in offices in Los Angeles, Orange County, Riverside, San Bernardino, and San Jose. The organization works with Latino clients at 10 of the state’s 21 Regional Centers. Funding comes from Regional Centers as well as from event sponsorships.

Fiesta’s programs include family conferences throughout the state that attract thousands of attendees, an autism education program for parents, and a partnership with a counterpart Chinese American organization that trains parents on special education advocacy. In addition, staff members organize regular “Fiestas Familiares” (“Family Parties”) in the homes of families to discuss topics such as special education eligibility and access to Regional Center services. These outreach events, conducted in Spanish and featuring food and music, reach entire families in safe, comfortable settings. “Immigrants have a tremendous amount of knowledge, but our structures don’t always fit them,” says Martinez. “It’s like having a CD but all you have is a cassette player. Fiestas Familiares come from the families themselves—they are organic.”

To reach Latino families who might benefit from their services, Fiesta utilizes a range of culturally appropriate outreach strategies, including a radio talk show, workshops at schools, libraries, and community centers, a monthly email newsletter, and, because many families do not use email, WhatsApp texts and phone “blasts” that play a recording about their upcoming events.

After 19 years at the helm, Martinez, 74, soon will be looking for a successor to lead Fiesta into its fourth decade. Her dream for the organization echoes the dreams that many Fiesta parents have for their children. “Fiesta is my baby,” she says. “And I don’t want it to rely on me. I want it to be independent.”

Source: lpfch.org