Stacker compiled a list of myths about monkeypox and investigated their viability using news, scientific, and government reports.
Stacker compiled a list of frequently asked questions about the currently available monkeypox vaccine from governments, scientific sources, and health experts.
Stacker has collected information to help readers understand the varying hate crime laws across the U.S.
(BPT) - People go to great lengths to reduce their odds of getting cancer. Many of us wear sunscreen, avoid processed foods, have regular checkups and eat organic produce, but what if your risk is …
Clinical trials examine the safety and effectiveness of new treatments in people, and this research plays a key role in developing ways to prevent, detect and treat diseases.
Traumatic brain injuries are caused by an external force that injures the brain. Taxman, Pollock, Murray & Bekkerman, LLC looked at a CDC report on traumatic brain injuries, which used 2017 surveillance data to pull insights and trends about TBI-related hospitalizations in the U.S.
Gigacalculator used data from the Wisconsin Department of Health to determine which activities burn the most calories.
(BPT) - Living with chronic pain makes day-to-day life incredibly challenging. It can interfere with everyday activities such as cooking, housework, and even just running simple errands. Dealing with …
(BPT) - Heart health is an important issue for everyone but is a particular concern for the Hispanic community. According to the American Heart Association, 52% of Hispanic men and 43% of Hispanic women nationwide have a form of heart disease, which can often lead to death.
Celebrity chef, cookbook author and "Despierta América" star Jesus Diaz (AKA Chef Yisus) personally knows that behind these statistics are tragic family stories. Having recently lost his own mother due to related health issues, Chef Yisus is helping to spread awareness on this issue and urge the Hispanic community to think about what they consume in their day-to-day. That's why in honor of Cholesterol Education Month, he's teamed up with Mazola® Corn Oil to share easy-to-make recipes anyone can make, like the following Reina Pepiada Arepas, which replaces lard with corn oil.
A simple and effective change you can make this Cholesterol Education Month is to simply replace lard, butter, margarine or other higher saturated fat oils with heart-healthy1 Mazola® Corn Oil, which has natural cholesterol-blocking plant sterols that can help protect you from bad cholesterol2. In fact, Corn Oil has the highest amount of naturally occurring plant sterols per serving compared to any other popular cooking oil, containing three times more cholesterol-blocking plant sterols than olive oil and 40% more than canola oil3, a win-win for the whole family!
Reina Pepiada arepas
Prep time: 10-15 minutes; Cook time: 45 minutes; Servings: 6
Chicken-Avocado Salad (Filling)
To view this recipe (and others), find more inspiration, and learn more about how you can incorporate heart-healthy1 Mazola® Corn Oil into recipes this Cholesterol Education Month, visit www.Mazola.com.
1Very limited and preliminary scientific evidence suggests that eating about 1 tablespoon (16 grams) of Corn Oil daily may reduce the risk of heart disease due to the unsaturated fat content in Corn Oil. FDA concludes that there is little scientific evidence supporting this claim. To achieve this possible benefit, Corn Oil is to replace a similar amount of saturated fat and not increase the total number of calories you eat in a day. One serving of this product contains 14 grams of Corn Oil.
2USDA FoodData Central (2019). Corn oil has plant sterols content of 135.6 mg/serving vs. 29.8 mg/serving for olive oil. Based on analysis of corn oil and April 2019 USDA FoodData Central data for olive oil.
3Based on analysis of corn oil and 2013 USDA comparison of other cooking oils: Corn Oil has plant sterols content of 135.6 mg/serving vs. 30.0 mg/serving for Olive Oil, 40.8 mg/serving for Vegetable Oil and 93.9 mg/serving for Canola Oil.
(BPT) - The COVID-19 pandemic introduced unprecedented challenges and altered ways of living across the globe. Now, more than two years later, the effects are still felt widely. Many non-emergent clinical services were limited or suspended during the early stages of the COVID-19 pandemic in the US, which may have adversely impacted epidemics of public health importance, such as HIV, and access to testing, which is a cornerstone of prevention efforts. While adjusting to a new normal, it’s time to reprioritize making routine HIV screening a normal and important part of self-care.
In 2019, an estimated one in eight people living with HIV in the US were unaware of their status, and in 2016 nearly 80 percent of new HIV infections were transmitted by people who didn’t know they had HIV or were not in care. Further, HIV diagnoses have greatly declined during the COVID-19 pandemic. According to a recent analysis, the number of Centers for Disease Control and Prevention (CDC) funded HIV tests conducted by the country’s health departments plunged by nearly half from 2019 to 2020. Another report indicates that HIV diagnoses dropped by 17% from 2019 to 2020, after declining by no more than 3% annually since 2016, likely due to disruptions to HIV-related services caused by the COVID-19 pandemic.4
To help normalize HIV testing, Gilead launched Press Play, a resource to encourage routine testing as a regular part of self-care and help deter negative emotions or stigma associated with HIV screenings. HIV testing is for everyone – the CDC recommends people between the ages of 13 and 64 get tested for HIV at least once as part of routine health care, and some people may benefit from getting tested more often. Press Play provides information about what you can expect during an HIV test, next steps to take after a test, and other tools – including options for finding an HIV testing site or ordering a free at-home test – to help make test taking easier.
“With Press Play, our goal is to normalize routine HIV screening as an important part of self-care by providing resources to help you get tested and information on your options once you have your test results – no matter the outcome,” said David Malebranche, MD, MPH, Senior Director of Global HIV Medical Affairs at Gilead. “Once you know your HIV status, you’re on your way to moving forward. You can connect with your HCP to understand options to help prevent or treat HIV.”
While it’s natural to feel nervous about getting tested for HIV, no matter the test result, there is power in knowing your HIV status. By knowing your status, you are better equipped to discuss prevention or treatment options with a health care provider. Although there is currently no cure for HIV, there are several options available to help prevent or treat HIV.
The only way to know your HIV status is through testing. It’s time to reintroduce testing into self-care routines and work together to help put an end to the HIV epidemic. To learn more about HIV testing, find HIV testing sites, or order a free at-home test, visit Press Play’s website at hivtestnow.com.
 Moitra E, et al. Impact of the COVID-19 pandemic on HIV testing rates across four geographically diverse urban centres in the United States: An observational study. Lancet Reg Health Am. 2022;7:100159. doi:10.1016/j.lana.2021.100159
 Centers for Disease Control and Prevention (CDC). CDC fact sheet: HIV in the United States and dependent areas. Accessed May 31, 2022. https://www.cdc.gov/hiv/pdf/statistics/overview/cdc-hiv-us-ataglance.pdf
 CDC. Gaps in HIV testing and treatment hinder efforts to stop new infections. Accessed March 18, 2019. https://www.cdc.gov/media/releases/2019/p0315-gaps-hinder-hiv-testing.html
 CDC. HIV Surveillance Report, 2020; vol. 33. Accessed May 31, 2022. https://www.cdc.gov/hiv/library/reports/hiv-surveillance/vol-33/index.html
 Patel D, et al. HIV testing services outcomes in CDC-funded health departments during COVID-19. J Acquir Immune Defic Syndr. 2022. doi:10.1097/QAI.0000000000003049
 “Should I get tested for HIV?” Centers for Disease Control and Prevention. HIV: Getting tested. Accessed May 31, 2022. https://www.cdc.gov/hiv/basics/hiv-testing/getting-tested.html
(BPT) - For U.S. Air Force Veteran and father, Juan Reyes, being diagnosed with amyotrophic lateral sclerosis (ALS) was a “devastating blow.” Reyes, who had just adopted three children, knew his diagnosis would redefine their lives. According to the National Institutes of Health, ALS — more commonly known as Lou Gehrig’s Disease — is an incurable, progressive disease of the nervous system that leads to muscle weakness and eventual loss of function including walking, speaking, swallowing, eating and breathing. Veterans, like Reyes, are twice as likely to be diagnosed with ALS than those who have not served in the military. Despite the difficult news, Reyes and his family made a conscious choice to “embrace their now” and live each day with purpose and happiness.
“We had a choice to make — allow ALS to consume us, or live our lives boldly,” says Reyes. “We could have lost control of our future had we decided to let ALS be our compass. This disease infiltrates many aspects of our lives, yet we simply don’t let it consume us.”
To fully “embrace their now,” Reyes and his family have decided to create unforgettable memories together by traveling and going on adventures with each other. In fact, together with his wife and caregiver, Meg, Reyes is taking a series of RV trips across the U.S. this year to help spread awareness of ALS and meet others living with the disease. Acting as an advocate and mentor, Reyes is open about his experience with ALS, sharing what he's learned along his journey, to help encourage others to “embrace their now.”
Reyes and his family are focused on making the most of every moment they have with each other, and they encourage others living with this fatal disease to do the same. Here are five tips from Reyes that help him cope:
1. Live in the present
“Embrace your now,” without worrying too much about the future. This mindset can help you “take life by the horns” and enjoy the time you have with your loved ones.
“Everything else takes a back seat to being present. This is not complicated, but it can be difficult for some,” Reyes says. “Being present means exactly that, nothing more: visiting, helping, learning. Enjoy your life the best you can.”
2. Be open about ALS
Don’t avoid difficult topics when it comes to ALS, but instead, have very honest, real conversations with your family — even with children.
“Our family is very pragmatic — we just say that ALS is something Dad has,” Reyes explains. “My wife and I choose to remain in control by talking about and communicating all aspects of this disease with our children.”
3. Accept support from others
ALS brings a multitude of changes for the person living with the disease and their families. Willing to be open and accept help and support from others can make a huge difference.
“ALS impacts your physical, emotional and mental health,” Reyes says. “But there is one aspect that can impact all of the above: self-imposed isolation. Accepting support from family, friends and my community has helped reduce my feelings of isolation.”
4. Partner with healthcare providers
Stay actively engaged with your healthcare team. Communicate frequently and discuss treatment options with your providers so they can help to find the best treatment options for you.
“Once the gravity of ALS settles in, allow yourself to catch your breath, then start planning with your healthcare team,” advises Reyes. “Your plan should encompass solutions for daily living, long-term arrangements, and treatment options.”
“When the prescription drug RADICAVA® (edaravone) came up, we discussed pursuing this course. My doctor and I reviewed the benefits and risks of treatment, and while RADICAVA is not a cure, it has been shown to help slow the decline of physical function in a medical study,” says Reyes. “I felt comfortable moving forward with this option, but I encourage anyone diagnosed with ALS to actively work with their doctor on a treatment plan that’s right for them.”
RADICAVA® and RADICAVA ORS® (edaravone) are indicated for the treatment of ALS. Do not receive RADICAVA® or RADICAVA® ORS if you are allergic to edaravone or any of the ingredients in RADICAVA and RADICAVA ORS. See IMPORTANT SAFETY INFORMATION below.
5. Share Your ALS Story
People in the ALS community have a lot to share. Questions and fears, as well as stories of courage and hope. Whether someone living with ALS is searching for more answers about the disease, or for new ways to live each day with purpose, hearing from others with similar experiences may make a world of difference. The Share Your Story program allows real people living with ALS and/or their caregivers to share their own experiences of living with ALS and why treatment with RADICAVA® (edaravone) matters to them.
Sharing your story could help you cope with ALS through self-expression. "Releasing my thoughts, feelings and emotions about the disease has given me a sense of relief," Reyes noted.Whether you Share Your Story by video or post, you could help others who live with ALS feel like they’re part of a larger community of support and understanding.
“I share my story because I want more people living with ALS to feel inspired and to understand they are not alone,” says Reyes. “By sharing your story, you could make an impact on how others live with ALS, too.”
Interested in sharing your experience with others? Call a JourneyMateTM Resource Specialist toll-free 1-855-457-6968 or visit www.ShareYourALSStory.com to sign-up for a chance to share your story.
In addition to sharing his experiences online, Reyes will continue to share his story with others as he travels around the country. “I try to be as optimistic as possible. 'How?' you may ask? My answer is, 'Why the heck not!'” said Reyes. “Let me be clear though, it is immensely difficult to maintain a healthy outlook with such a relentless disease. Just know you are not alone on this journey.”
This content is sponsored by Mitsubishi Tanabe Pharma America, Inc. (MTPA) and is intended for U.S. audiences only. Juan Reyes is an actual patient and is being compensated by MTPA.
IMPORTANT SAFETY INFORMATION
Do not receive RADICAVA (edaravone) or RADICAVA ORS (edaravone) if you are allergic to edaravone or any of the ingredients in RADICAVA and RADICAVA ORS.
Before you take RADICAVA or RADICAVA ORS, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
What are the possible side effects of RADICAVA and RADICAVA ORS?
RADICAVA and RADICAVA ORS may cause serious side effects, including hypersensitivity (allergic) reactions and sulfite allergic reactions.
Your healthcare provider will monitor you during treatment to watch for signs and symptoms of all the serious side effects and allergic reactions.
The most common side effects include bruising (contusion), problems walking (gait disturbance), and headache.
These are not all the possible side effects of RADICAVA or RADICAVA ORS. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects to www.fda.gov/medwatch or Mitsubishi Tanabe Pharma America, Inc. at 1-888-292-0058.
RADICAVA and RADICAVA ORS are indicated for the treatment of amyotrophic lateral sclerosis (ALS).
For more information, including full Prescribing Information, please visit www.RADICAVA.com.
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