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Integrative Health or Complementary and Alternative Medicine Market Hit Stunning Double Digit CAGR +22% by end 2027 With Renowned Key Players Columbia…

Posted: July 21, 2021 at 1:46 am

The market is set to gain momentum in the coming years owing to the changing regulatory scenario, coupled with robust government initiatives, resulting in the establishment of strong transnational connections across healing pathways linking global, national, and local movements regarding alternative medicine. Additionally, government initiatives exploring norms related to the right to health in all its forms are set to supplement the participation of service providers and users in the field of alternative and complementary healthcare.

Integrative Health or Complementary and Alternative Medicine Market USD 82.27 billion in 2021 and is expected to expand at a CAGR of +22% from 2021 to 2027.

Top Key Players are covered in this report:

Columbia Nutritional; Nordic Nutraceuticals; Ramamani Iyengar Memorial Yoga Institute; The Healing Company Ltd.; John Schumacher Unity Woods Yoga Centre; Sheng Chang Pharmaceutical Company; Pure encapsulations, LLC.; Herb Pharm; AYUSH Ayurvedic Pte Ltd.

The report begins with a brief introduction and market overview, in which Integrative Health or Complementary and Alternative Medicine industry is first defined before estimating its market scope and size. Next, the report elaborates on the market scope and market size estimation. This is followed by an overview of the market segmentations such as type, application, and region. The drivers, limitations, and opportunities are listed for Integrative Health or Complementary and Alternative Medicine industry, followed by industry news and policies.

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This referential document assessing the market has been compiled to understand diverse market developments across specific regional pockets such as Europe, North and Latin American countries, APAC nations, as well as several countries across MEA and RoW that are directly witnessing maneuvering developments over the years.

In addition, the report provides insight into main drivers, challenges, opportunities and risk of the market and strategies of suppliers. Key players are profiled as well with their market shares in the global Integrative Health or Complementary and Alternative Medicine market discussed. Overall, this report covers the historical situation, present status and the future prospects of the global Integrative Health or Complementary and Alternative Medicine market for 2016-2026.

Market Segmentation

Product Type Segmentation

Industry Segmentation

Moreover, the impact of COVID-19 is also concerned. Since outbreak in December 2019, the COVID-19 virus has spread to over 100 countries and caused huge losses of lives and economy, and the global manufacturing, tourism and financial markets have been hit hard, while the online market increase. Fortunately, with the development of vaccine and other effort by global governments and organizations, the negative impact of COVID-19 is expected to subside and the global economy is expected to recover.

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Regional Analysis:

Studying and analyzing the impact of Coronavirus COVID-19on the Integrative Health or Complementary and Alternative Medicine industry, the report provides in-depth analysis and professional advices on how to face the post COIVD-19 period.

Table of Contents:

Chapter 1: Global Integrative Health or Complementary and Alternative Medicine Market Overview

Chapter 2: Market Data Analysis

Chapter 3: Technical Data Analysis

Chapter 4: Government Policy and News

Chapter 5: Global Integrative Health or Complementary and Alternative Medicine Market Manufacturing Process

and Cost Structure

Chapter 6: Productions Supply Sales Demand Market Status and Forecast

Chapter 7: Key Manufacturers

Chapter 8: Up and Down Stream Industry Analysis Art Supplies

Chapter 9: Marketing Strategy

Chapter 10: 2021-2027 Integrative Health or Complementary and Alternative Medicine Market Development Trend

Analysis

Chapter 11: New Project Investment Feasibility Analysis

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Integrative Health or Complementary and Alternative Medicine Market Hit Stunning Double Digit CAGR +22% by end 2027 With Renowned Key Players Columbia...

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Traditional Chinese Medicine Lessons Market is to Witness Significant Growth between 2021-2027|| Future Plans and Industry Growth with High CAGR by…

Posted: July 21, 2021 at 1:46 am

Another report named,Worldwide Traditional Chinese Medicine Lessons (COVID-19 Version) Markethas been added into its tremendous archive byMarket Research Store. The report investigates and assesses the Traditional Chinese Medicine Lessons (COVID-19 Version) market on a worldwide, provincial, and national level. The report offers information of earlier years alongside top to a bottom investigation from 2020 to 2025 based on income (USD Billion). Furthermore, the report offers a far-reaching investigation of the components driving and controlling the development of the market combined with the effect they have on the interest over the gauge time frame. Likewise, the report incorporates the investigation of worthwhile chances accessible in the Traditional Chinese Medicine Lessons (COVID-19 Version) market on a worldwide level.

The Top Leading players working in the market to Covered in this Report:AOMA Graduate School of Integrative Medicine, Five Branches University, American College of Acupuncture & Oriental Medicine, Bastyr University, Emperors College School of Traditional Oriental Medicine, European School of Acupuncture, American College of .

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Division by item type:Acupuncture, Chinese Herbology, Others

Division by Application:Hospital, Clinic, Others

Comprehend the impact of COVID-19 on the Traditional Chinese Medicine Lessons (COVID-19 Version) Market with our examiners checking the circumstance across the globe. Solicitation Now

This report estimates income development at the worldwide, local, and neighborhood levels and gives an examination of the latest business patterns from 2021 to 2026 in every one of the sections and sub-portions. A portion of the significant topographies remembered for the market are given beneath:

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Significant Geographies referenced in this report are as per the following:

North America (the U.S. furthermore, Canada, and the remainder of North America)

Europe (Germany, France, Italy, and Rest of Europe)

Asia-Pacific (China, Japan, India, South Korea, and Rest of Asia-Pacific)

LAMEA (Brazil, Turkey, Saudi Arabia, South Africa, and Rest of LAMEA)

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Traditional Chinese Medicine Lessons Market is to Witness Significant Growth between 2021-2027|| Future Plans and Industry Growth with High CAGR by...

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Pet CBD Products Need Better Regulation, Researchers Say – Forbes

Posted: July 21, 2021 at 1:46 am

Buyer bewarepet products containing cannabidiol (CBD) are freely available and sold as supplements, but research shows labels arent always accurate and those products often get mixed with reputably-sourced brands.

Like clockwork, in early July, The U.S. Food and Drug Administrations (FDA) Center for Veterinary Medicine tweeted its yearly warning to pet owners about unregulated CBD products, ahead of the seasonal spike of CBD sales due to firework-induced dog anxiety. Distrust of the FDA abounds, but the organization may have a solid point when it comes to the sketchier side of CBD products marketed for pets.

Brett Hartmann gives his dogs Cayley, a six-year-old-Labrador Retriever drops of a cannabis based ... [+] medicinal tincture to treat hip pain and anxiety, June 8, 2017 at his home in Los Angeles, California. It's early morning, just after breakfast, and six-year-old Cayley is wide awake, eagerly anticipating her daily dose of cannabis. The black labrador, tail wagging, laps up the liquid tincture owner Brett Hartmann squirts into her mouth, a remedy he uses morning and evening to help alleviate Cayley's anxiety. As the multi-billion dollar medical and recreational marijuana industry for humans blossoms in the United States, so is a new customer base -- animals. / AFP PHOTO / Robyn Beck (Photo credit should read ROBYN BECK/AFP via Getty Images)

Recent findings from Leafreport found that 56% of pet CBD products that were sampled were mislabeled with inaccurate claims. Leafreport collected a sampling of 55 pet CBD products, and found over half had inaccurate labeling, most often, incorrect levels of CBD. Out of 55 pet products that were independently tested at Las Vegas-based Canalysis Laboratories, 31 contained the wrong amounts of CBD, and many also contained no THC despite being labeled as full-spectrum CBD.

Beyond pet products, the teams continued research also found an alarming amount of mislabeled delta-8-THC products (often converted from CBD-rich biomass or isolate in a lab) and on July 13, the team published findings detailing wildly different pricing standards between CBD products, meaning some companies scoop up newbieshook, line, and sinker.

One pet product was particularly deceptivecontaining only about 1.5% of the CBD the label claimed it contained, meaning that your pet might not even be getting amounts of the healing compound significant enough to do anything.

Instead, go with a brand that provides certificates of analysis and that is sold in a reputable store, such as a state-regulated dispensary or a CBD store that vets its vendors to ensure their products are safe.

What if we regulated pet CBD products better, consistently providing analytical data, or at the very leastallow veterinarians to properly guide pet owners?

Leafreportoriginally founded in 2019 in Tel Aviv, Israelis an online resource on CBD with discussions from medical doctors, clinical consultants, chemists, nutritional and natural health experts from around the world.

Dr. Zora DeGrandpre practices naturopathic medicine and is a medical and scientific writer and editor, specializing in naturopathic, functional, botanical, and integrative medicine. DeGrandpre writes online courses for medical students around the world including courses for continuing medical education and on the use of medical marijuana and CBD.

DeGrandpre explained that the same product caution that anyone uses for themselves should ideally be applied to their petsadding that consumers need to look into the companys history and reputation.

While different animals may respond differently to CBD, contaminants such as microbial products, heavy metals, toxins, and pesticides are often more toxic to pets than to humans, DeGrandpre says in an email. In addition, dogs appear to be particularly sensitive to THCso you should only use zero-THC products with dogs, and to be safer, with any animals. Also, there isnt a lot of research around CBD and animalsmany vets (for many reasons including legal and professional ones) urge caution when using CBD with your pet.

The effects of CBD on a 200-pound person is not going to work the same way on a 10-pound toy dog, which is why titration is a bit more imperative when dealing with pets, even though they are fully equipped with an endocannabinoid system. Source CBD, for instance, provides a dosing calculator for humans and pets, and relies an anecdotal reports from people who claim a variety of beneficial effects on both mammals and reptiles.

Luna, a pug with acne and seizures, takes her daily dose of CBD oil.

Finally, you should always use the same principle with pets that we recommend for humans! DeGrandpre adds. Start low and go slow, always monitoring the effects on your pet carefully. You want to ensure your pets health, after all! We also recommend checking with your vet to ensure that CBD products will not interfere with any medication that your pet may be on already.

The global pet CBD market is projected to witness considerable growth over the coming years of the forecast period 2018-2028, according to data compiled by San Francisco-based TMR Research. In Europe, researchers came to nearly the same conclusion: Data released on July 12 from Dublin, Ireland-based Research and Markets reported similar findings. The global CBD pet products market to rise with a CAGR of 41.3% during the forecast period (2021-2026). Research and Markets analysts attributed the rise in part to the 2018 Farm Bill, which set things off in the United States.

Some states in the U.S. are starting to allow specific provisions for veterinarians and medical cannabis, such as Nevadas forward-thinking Assembly Bill 101, allowing recommendations, sponsored by Assemblymember Steve Yeager. Then theres Californias Assembly Bill No. 2215, approved in 2018, which basically only allows veterinarians to discuss medical cannabis treatment without fears of repercussions. Californias Assembly Bill 384 would take it a step further, allowing them to give recommendations. Oregon and Washington State Veterinary Medical Associationspostedtheir owncautionary fact sheetsfor medical cannabis advice online. New Yorks Assembly Bill A5172 would offer similar provisions.

Eloise Theisen is a board certified Adult Geriatric Nurse Practitioner who specializes in cannabis therapy. For over 20 years, Theisen has worked primarily with cancer, dementia, and chronic pain patientsfocusing her efforts on cannabinoid therapies for the past five years. Theisen is the president of the American Cannabis Nurses Association.CBD products for pets and humans are still not regulated and testing is not required, Theisen says. It is important to look for companies that do independent 3rd party testing to ensure that the product label. matches the certificate of analysis. Some products may have THC levels that are above the legal limit and that could be unhealthy for pets. Additionally, some companies may have more or less CBD than listed on a label and you may not be giving your pet exactly what you expected.

Furthermore, some companies can be misleading about ingredients such as hempseed oil, which contains antioxidants and fatty acids, butno CBD.

I recommend only buying from a company that provides an independent 3rd party certificate of analysis, Theisen adds. It is important to know exactly what you are giving your pet. A comprehensive certificate of analysis from a reputable 3rd party testing lab will ensure that the product is free of contaminants and that the potency is accurate. If the company cannot provide a certificate of analysis, look for another company that does. There are enough companies out there providing transparency with their products.

In general, its on the consumer to vet the safety and ingredients in pet CBD productsfor the health of their pets, if for no other reason.

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Former Emmerdale star Leah Bracknell’s widower finds love again two years after her tragic death – Leeds Live

Posted: July 21, 2021 at 1:46 am

Former Emmerdale actress Leah Bracknell's widower has found love again two years after the star tragically passed away.

Leah, who played Zoe Tate in the ITV soap for 16 years, was diagnosed with stage four lung cancer in 2016.

She later passed away in September 2019, aged 55, following a three year battle with the illness, The Mirror reports.

READ MORE: Emmerdale star Samantha Giles quits Twitter after trolls hurl vitriolic abuse at her

The star also had television roles in Judge John Deed, A Touch of Frost, The Royal Today and DCI Banks, as well as performing on stage and in pantomime.

Leah and long term partner, Jez Hughes, were together for thirteen years before tiring the knot in March 2017, shortly after her diagnosis.

The pair opted to get married after the learnt that Leah's cancer was incurable.

To get the latest email updates from LeedsLive, click here.

It has been reported that the soap star's widower has been dating Precious Dunlop for over two months.

A source told The Sun: "Jez's friends are delighted for him and have wished them both well. It's been such a heartbreaking time losing Leah, but he is back in a happy place and is enjoying life once more."

"My husband is like my rock," she previously said of Jez. "He is by my side a lot of the time. He has been a great sounding board.

"I think we support each other as well. My family do OK. Im not positive all the time, but I am optimistic."

Leah was diagnosed in 2016.

In August 2017, it was announced her targeted biological therapy had stopped working and that she had been surviving solely on expensive alternative treatments for several months.

Her quest to undergo alternative treatments of immunotherapy and integrative medicine in Germany led many to donate to Leahs treatment.

READ MORE: Ex-Emmerdale star Catherine Tyldesley used 50,000 of taxpayers' furlough money to help her business

Within a few days, kind-hearted benefactors had donated 50,000.

The Emmerdale actress stayed positive about the situation, and in 2019 she confirmed she was on an immunotherapy clinical trial which kept her cancer stable.

However, she died in September that year and her husband paid tribute to her : "My darling wife, best friend and soul mate flies free in spirit.

"I have been the luckiest man in the world to spend time walking, dancing, laughing, praying, dreaming, singing, drumming, talking, travelling, crying, planning, hoping, loving, going wild, exploring, rebelling, forgiving, celebrating, playing, sharing secrets at dawn, opening hearts, minds and soul- alongside a woman of such depth, power, humour, humility, honour, intelligence and love- it is impossible to do justice to with the transient, flimsy power of words."

"Ali (Leah's real name) is the bravest person I've ever met and she faced the last three years of cancer with dignity, grace and light.

"She shone bright in this world with fire in her heart and water in her soul. The great mystery of existence always visible through her beautiful eyes.

"She inspired and changed the lives of so many, loved ones and strangers alike.

"Every day I learn of more people who she helped which brings the warmth of pride and gratitude to have known her into my heart.

"She taught me more than I'm able to comprehend and we shared more than I dreamt was possible in this life. More than either of us thought was possible."

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Mental Health Screening Tools for CF Patients, Caregivers – ubmd.com

Posted: July 21, 2021 at 1:46 am

Jacobs School of Medicine and Biomedical Sciences researchers are finding mental health screenings to be an important component for cystic fibrosis (CF) patients and their caregivers.

CF is a genetic, progressive disease that causes persistent lung infections and impacts the most basic physical processes. While recent breakthroughs have significantly extended the lifespan of patients with CF, the disease presents patients and their caregivers with significant, lifelong daily challenges.

Disease Takes Mental Toll on Patients, Caregivers

The primary purpose of CF clinics is to treat the physical disease, but providers are well aware of the mental toll it takes on patients and caregivers.

It can be challenging for people with CF and their families to sustain daily therapies and to live with a life-limiting disease, saysDanielle M. Goetz, MD, clinical associate professor of pediatrics and director of the Cystic Fibrosis Center of Western New Yorkat UBMD Pediatrics and Oishei Childrens Hospital.Our team began to feel that mental health screening was an important part of care to look at.

The Jacobs School/Oishei team effort was led by Goetz and Carla A. Frederick, MD, associate professor of medicine, with guidance from Drucy S. Borowitz, MD, clinical professor emeritus of pediatrics, and Beth A. Smith, MD, professor of psychiatry and pediatrics.

Depression Linked With Worse Health Outcomes

In 2013, the Buffalo researchers began systematically using efficient tools for screening for anxiety and depression in patients and their caregivers, both of whom exhibit higher rates of these conditions than the general population.

The researchers also developed an algorithm to determine which type of treatment would be necessary.

The screening process has been shared with other centers and was piloted at a larger CF center at the Ann and Robert H. Lurie Childrens Hospital of Chicago.

These tools and the research it is based on are described in apaperpublished in May in the British Medical Journal Open Quality.

CF is a disease that affects the whole body, including the ability to breathe and digest food, explains Goetz, who is also a pediatric pulmonologist with UBMD Pediatrics. The burden of taking two-to-three hours per day to clear the airways of mucus and taking multiple medicines can be so difficult and cause feelings of isolation.

The disease also can cause diabetes and liver problems.

It is a lot to think about and address, says Goetz, adding that previous studies have shown that depression in CF patients is linked with worse health outcomes, including decreased lung function, lower body mass index and increased exacerbations and hospitalizations.

Restrictions Can Lead to Feelings of Isolation

Due to the grave risk of passing infections to each other, people with CF are also not supposed to gather, as depicted in the book and adapted Hollywood film Five Feet Apart, which tells the story of a romance between two teens with CF.

In reality, CF patients are advised to stay six feet apart from each other (even before the COVID-19 pandemic), a restriction that by itself can lead to feelings of isolation and depression.

At the same time, since most CF patients are diagnosed as young children, parents or caregivers of CF patients are intimately involved with their care.

Parenting is hard, and parenting a child who has multiple medical and perhaps social needs is challenging, Goetz says.It makes sense that depression and anxiety are more common in these parents and caregivers. Watching and helping their child go through multiple stressors is painful.

We support the parents and caregivers, oftentimes talking to them about how they are dealing with their child or loved ones illness and how we can help them to seek help when needed.

Questionnaires Used With Clinical Assessments

In 2013, the center began to assess all of its 180 pediatric and adult CF patients for depression. The center is now screening between 95 and 99 percent of patients and caregivers.

The first step was a simple screening questionnaire (the Patient Health Questionnaire-2, or PHQ-2), which asks about the degree to which the individual has experienced either depression or anhedonia (lack of pleasure in activities the patient used to find pleasurable).

A positive response to either question triggers a more detailed questionnaire (the Patient Health Questionnaire-9 or PHQ-9) or Generalized Anxiety Disorder-7 (GAD-7) questionnaire, which the center now uses as the initial screening tools.

With these questionnaires, along with clinical assessments, the center assesses patients as having mild, moderate, moderately severe or severe depression or anxiety.

Patients are then referred to mental health specialists or treated at the CF center by its own mental health coordinator. They receive follow-up assessments to determine effectiveness of treatment.

Suicide Ideation Included in Screening Process

The researchers reported a higher prevalence of both depression and anxiety in the CF center than has been reported in the literature.

They also found that 5 to 10 percent of patients and caregivers had thought about committing suicide. The researchers had made the decision to include suicidal ideation in the screening process, and all clinic staff were trained to assess for this.

We looked at it this way, Goetz says. If we choose not to screen for suicidal ideation, it just means we may be missing it, not that suicidal ideation is not occurring.It is a challenging thing to screen for, though, if you dont know what to do with a positive screen.

So, it is important for the whole team to understand how to do the screening and how to make an emergency plan with patients, she adds. Anyone on the team can learn, especially nurses and providers, but really anyone, in case there isnt a social worker or psychologist on the team.

The centers emergency plans are tailored to each patient and may involve development of a suicide risk management plan, namely, a safety net for the patient, or urgent or emergent referral to a mental health professional.

Goetz explains that the stepped process, beginning with the short questionnaire, allows for quick screening for all people with CF and their caregivers.

A provider can then hone in on what needs to be done for each patient, with a focus on those who need more interventions, she says.

It has been so meaningful to have a social worker and psychologist in our clinic who can help support the providers in providing the best mental health care or referrals for care, Goetz adds. I cant say enough good things about this integrative approach and the importance of mental health and its impact on physical health.

Essential Role in Quality Improvement Efforts

CF Care Center teams also include nutritionists, respiratory therapists, nurse coordinators and research coordinators, all of whom play essential roles in quality improvement efforts.

The toolkit and related resources have now been disseminated on an international listserv for CF mental health and medical providers.

The CF Center of WNY at UB and Oishei Childrens Hospital, a Cystic Fibrosis Foundation-accredited center that treats patients from eight counties, has been involved in the CFFoundations Quality Improvement Network.

Goetz notes that the mental health screening project demonstrates a key premise of the quality improvement effort.

We know now that people with CF should be involved with our projects from their inception, Goetz says. That is an excellent aim for all teams looking to improve clinical care: The people who know best how to improve the process for disease assessment and management are likely the people living with the disease.

Other Co-Authors Are From Jacobs School

Along with Goetz, Frederick, Borowitz and Smith, other Jacobs School co-authors are:

Adrienne Savant, MD, of the Ann and Robert H. Lurie Childrens Hospital of Chicago, is also a co-author.

The research was funded by Cystic Fibrosis Foundation Therapeutics, part of the Cystic Fibrosis Foundation.

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Is Healthy Eating Too Expensive? You Can’t Afford Not to Try. – Mpls.St.Paul Magazine

Posted: July 21, 2021 at 1:46 am

On the surface, healthy eating seems like an easy enough task. After all, the most nutritious foods come straight from the earth; pure and unprocessed. But fresh whole foods are not always accessible to everyone. With obstacles like food deserts, expensive organics, and high-priced meats, eating healthy on a budget seems nearly impossible.

According to Amrit Devgun, naturopathic doctor and applied ayurvedic practitioner at Northwestern Health Sciences University, healthy eating falls on a spectrum. Like exercising, eating well can start with small steps. For example, introducing conventional produce into your diet is better than not eating fruits and vegetables at all. "If you can't afford fresh organic produce, shop for pesticide-free fruits and vegetables in the freezer aisle," she says. "If expensive meats aren't doable, substitute with tofu or other alternatives, like beans or lentils."

When trying to save on your grocery bill, start by filling your pantry with shelf-stable items like beans, rice, and lentils. Dried foods, devoid of water, cost less because they are cheaper for manufacturers to store and ship. Packed with essential vitamins and minerals, these kitchen staples last months in your cupboard and yield substantial portions.

Shopping for nutritious food on limited funds requires a bit of strategy. Pay close attention to grocery store sales so you can stock up on discounted staples. Big box stores like Target and Costco offer easy-to-use digital coupons for their growing stock of organic and health food products. These large retailers usually provide private label options that eliminate marketing costs associated with household name brands. For the same reason, buying in bulk saves moneyand without packaging costs, bulk foods are discounted even further.

Weekly meal planning is another cost-saving measure that will pay off in spades. Spending just 30minutes preparing for the week ahead helps you spend less money and waste less food. Instead of throwing away leftover sauteed veggies, add them to your eggs the following morning. Grill chicken for dinner and save some to pair with leafy greens for lunch. And, consider which fruits and vegetables are in season. Food grown closer to home is less expensive. Importing grapes from Chile or peppers from Peru in the winter will increase the price dramatically.

The World Health Organization's (WHO) International Agency for Research of Cancer (IARC) lists five commonly used industrial pesticides as probably and possibly carcinogenic. Glyphosate, the main ingredient in Monsanto's Roundup, is the most widely used agricultural pesticide in the U.S. According to the Environmental Working Group (EWG), "250 million pounds of glyphosate are sprayed on American crops" each year. These toxic pesticides are so prevalent that researchers have even found residue of pesticides in breast milk.

"If you buy conventional produce, use a vegetable wash or drop of soap and water to remove pesticides on the surface.For harder foods, like potatoes, you can clean the skin with a food brush. Removing the skin works too, but you lose some important nutrients in the process. It's a balancing act." Amrit Devgun, Northwestern Health Sciences University

Reducing your exposure to harmful pesticides is as essential as ever. While it may seem overwhelming, community organizations like EWG can help you make informed decisions that protect your health and the health of your family. EWG publishes an annual "Shopper's Guide to Pesticides in Produce." Named the Dirty Dozen and Clean Fifteen, these lists make shopping for safer, conventional (non-organic) fruits and veggies simple.

Once home, you can further decontaminate your food."If you buy conventional produce, use a vegetable wash or drop of soap and water to remove pesticides on the surface," says Devgun. "For harder foods, like potatoes, you can clean the skin with a food brush. Removing the skin works too, but you lose some important nutrients in the process. It's a balancing act."

When deciding whether to invest in organics, Devgun suggests a shift in perspective. "With our exposure to the high amounts of pesticides in some of the foods we eat, many of us develop serious health issues. We end up spending significant amounts of money on health care," she says. "If you can, why not invest in the prevention of disease instead?"

A rule of thumb when shopping for healthy foods is shopping the perimeter. This strategy keeps you away from the temptations in the snack aisle and focuses your shopping trip on rainbow eating. Full of phytonutrients, colorful fruits and vegetables protect us from illnesses such as cancer, diabetes, and heart disease. Each color has disease-fighting superpowers, so eating the whole rainbow is ideal.

A Rainbow of Health-Boosting Phytonutrients

*Pro Tip: Growing your fruits and vegetables is one of the cheapest ways to get variety in your diet. With minimal care, a backyard garden is plentiful in the summer months. For apartment dwellers, a windowsill is a perfect place to grow fresh herbs. When neither works, you can share the cost with neighbors and build (or find) a community garden. At the end of the growing season, you can freeze or can your bounty for winter cooking.

As Michael Pollan famously writes in his book, In Defense of Food: An Eater's Manifesto, "Eat food. Not too much. Mostly plants." Devgun couldn't agree more. "Plant-based diets bring the best results for overall longevity and quality of life," she says. "Eating a plant-based diet is cheaper and helps us prevent chronic disease."

When prescribing a healthy diet to clients, Devgun often suggests cutting down on meat. "By reducing meat consumption, you naturally decrease your toxic burden." Plant-based eating optimizes your health by reducing inflammation, boosting your immune system and decreasing your cancer risk. It also helps you maintain a healthy weight.

Located in Bloomington,Northwestern Health Sciences Universityis a pioneer in integrative natural health care education, offering degree programs in chiropractic, acupuncture, Chinese medicine, massage therapy, medical assisting, medical laboratory programs, post-bac/pre-health, radiation therapy, and B.S. completion. ItsBloomington Clinicis open to the public andprovides chiropractic treatment,acupuncture, Chinese medicine, massage therapy, naturopathic medicine, and cupping.

See more content fromNorthwestern Health Sciences University.

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What is Stem Cell Research? – WorldAtlas

Posted: July 6, 2021 at 2:49 am

Stem cells are those that don't have a specific purpose.

A stem cell is a cell in a living body with the potential to develop into different types of cells during the early stage. Most cells in a living organism are differentiated cells, meaning they are found in a specific organ and perform particular functions. Red blood cells, for example, are specifically designed to transport oxygen through the blood. Human beings start out as a single cell known as a zygote, which is a fertilized egg. The zygote undergoes cell division into two, then four, eight, sixteen, and so on. The cells begin to differentiate and specialize in specific functions in the body as the zygote develops. The cells that haven't acquired specific purpose are known as stem cells; they can replicate indefinitely unlike differentiated cells that begin to break down after replicating. Once a stem cell divides, it remains as a stem cell or turns into a differentiated cell. This makes them especially intriguing for scientific research.

There are two types of stem cells: embryonic and adult stem cells. Embryonic stem cells are derived from embryos developed through in vitro fertilization in a fertilization clinic. The fertilized eggs are then donated for research purpose with the consent of the donors. Embryonic stem cells develop into specialized cells as the embryo develops. Adult stem cells are found among differentiated cells in an organ or tissue. Their main functions are to repair and maintain the tissue. Unlike embryonic stem cells that are produced by the embryo, researchers are still trying to understand the source of adult stem cells.

Stem cells have three distinct properties regardless of their source; they replicate and renew themselves infinitely, they are unspecialized, and they give rise to differentiated cells. Unlike a nerve cell, blood cells, or muscle cells, stem cells can proliferate. Research conducted in laboratories have revealed that stem cells can yield millions of unspecialized cells with the properties of the parent stem cell.

The properties of stem cells make them excellent and intriguing candidates for research. The embryonic human stem cells provide information concerning the complex process that occurs during the development of life. The primary objective of the research is to understand how undifferentiated cells end up with specific functions. Human stem cells are used to test new drugs and observe how a human body would respond to the medication. Stem cells are also helping researchers study diseases such as cancer and diabetes and how they can be treated. The immediate potential application of stem cell research is the generation of tissues and cells that replace organs once destroyed or removed. A breakthrough would eliminate the dependency on organ transplant, but instead, patients would receive stem cells that would generate the organ. Preliminary research in rodents shows that transplanted stem cells from the bone marrow can generate heart muscle tissues and repair the heart. A bone marrow transplant is already being used as a treatment for some form of cancer in humans.

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What is Stem Cell Research? - WorldAtlas

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New global guidelines for stem cell research aim to drive …

Posted: July 6, 2021 at 2:49 am

The International Society for Stem Cell Research (ISSCR) today released updated guidelines for stem cell research and its translation to medicine.

Developed in response to recent scientific and clinical advances, the revised guidelines provide a series of detailed and practical recommendations that set out global standards for how these emerging technologies should be harnessed.

Stem cell research has huge potential it could help pave the way for new therapies for ailments ranging from Parkinsons disease to childhood kidney failure. But scientific advances in this field can present unique ethical and policy issues beyond that seen in other areas of medical research.

The science is advancing at breakneck pace. Just in the past couple of months, we have seen model human embryos grown from skin cells, and the creation of human-monkey embryos for use in research.

The ISSCR has long recognised the need to set clear ethical boundaries for stem cell research. Previous guidelines have provided advice on techniques such as the use of human embryos to create stem cells, and set the required standards when using these technologies to create new medicines.

They have also explicitly banned certain practices, such as reproductive cloning and the sale of unproven therapies that claim to be made of stem cells.

The 2021 guidelines an update on the previous version, released in 2016 aim to set standards for the many recent advances in stem cell and human embryo research. These include chimeric embryos containing cells from humans and other animals, organoids grown from stem cells to create tissue that resembles particular human organs, and models of human embryos arrangements of human cells that mimic the early stages of embryo development.

The guidelines contain a clear requirement for certain new stem cell research approaches only to be conducted after a specialised review process. This review should be independent of the researchers, and include community members as well as people with expertise in the relevant science, ethics and law.

This is beyond what is typically required by a university or research institute where medical research is conducted. Besides evaluating the merit of the proposed research, the new reviews should also consider whether there are alternative ways to do the research, the source of stem cells and how they were obtained, and the minimum time required to reach the research goals, particularly in relation to human embryo and related research.

Specialised review is not a new concept. The previous guidelines required it when researchers made stem cells from human embryos or sought to culture human embryos in the lab. But now researchers will now also be required to seek higher review when they create model embryos such as blastoids, or study the development of animal-human embryos in animal wombs.

Researchers developing new therapies for mitochondrial disease will also be required to seek higher-level review before attempting to transfer to the uterus of a woman human embryos in which affected mitochondria (a part of the cells energy-production apparatus) have been replaced.

Importantly, the revised guidelines also clearly rule out certain activities. These continue to include reproductive cloning and attempts to form a pregnancy in a woman from genetically edited human embryos or from model embryos made from stem cells. Prohibited activities also now include using eggs and sperm made from human stem cells for reproduction, or transferring a human-animal chimeric embryo into the uterus of a woman or an ape.

Read more: China's failed gene-edited baby experiment proves we're not ready for human embryo modification

The guidelines also call for a public conversation about whether we should allow limited lab research on human embryos beyond the existing limit of 14 days development. Historically, it has not been possible to support human embryonic development outside the body beyond this stage. However, recent advances in human embryo culture raise the possibility that this may now be technically feasible.

Extending the amount of time in culture - in terms of days - could potentially yield new treatments for developmental conditions or infertility, but will also raise concerns about whether possible benefits justify this research. Any decisions to overturn this long-held signpost would need to be carefully deliberated and take into consideration existing law, community values and discussion around what the new limit should be.

The revised guidelines also reinforce the need for informed consent for the collection of human material and participation in stem cell clinical trials, and reiterate that no new stem cell treatment should be made available before it is tested for safety and effectiveness in well-designed and publicly visible clinical trials. The ISSCR continues to condemn the commercial use of unproven stem cell treatments.

While stem cell science holds much promise, it is paramount that research is scientifically and ethically rigorous, with appropriate oversight, transparency and public accountability.

The fact these guidelines are driven by experts including stem cell scientists, doctors, ethicists, lawyers and industry representatives from across 14 countries indicates a deep sense of responsibility and integrity within the research community, and a desire to ensure science remains in step with community values.

However, these guidelines are recommendations, not laws.

Researchers will need to abide by their respective national or state regulations and ethical standards. Some countries already have regulatory frameworks that are consistent with the new recommendations. In other places there is no national guidance around laboratory and clinical stem cell research at all, or existing law touches on some but not all of the emerging applications of stem cell research.

Read more: As scientists move closer to making part human, part animal organisms, what are the concerns?

For example, in Australia there is already an established pathway for higher-level review of embryo models created from stem cells. However, the same legislation currently bans any attempt to use mitochondrial transfer techniques to create embryos for research or to achieve a pregnancy both of which are permissible under the new ISSCR guidelines.

Rather than attempting to impose a set of hard-and-fast rules on an ever-evolving research field, the new guidelines attempt to address emerging issues and drive important discussions at domestic level. Ultimately, it is the public and the regulators who will need to set the standards.

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$6.3 million for ground-breaking stem cell research projects – News – The University of Sydney

Posted: July 6, 2021 at 2:49 am

The Federal Minister for Health and Aged Care, the Hon Greg Hunt, has announced$18.7 million in funding for the 2020 Stem Cell Mission, which focuses on research that develops and delivers innovative, safe and effective stem cell medicines to improve health outcomes.

Researchers from the University of Sydney have been awarded $6.3 million for three projects which will address blindness in adults, chronic heart failure, and help to improve decisions about access to stem cell interventions.

Deputy-Vice-Chancellor (Research), ProfessorDuncan Ivisoncelebrated the funding success.

This funding will allow our health and medical researchers to undertake important research for the benefit of many Australians and their families, through trials that use stem cell grown heart muscle in patients with no option end-stage heart failure," he said.

Medical Research Future Fund (MRFF) 2020 Stem Cell Mission grants awarded to Sydney researchers include:

The Stem Cell Mission is a priority of the Morrison Governments $20 billion Medical Research Future Fundand will provide $150 million towards research over 9 years.

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Limits for human embryo research have been changed: this calls for public debate – The Conversation CA

Posted: July 6, 2021 at 2:49 am

For 40 years, research into early human development has been guided by the principle that after 14 days, an embryo should not be used for research and must be destroyed. This rule has been part of the law of more than 12 countries. But new guidelines released by the International Society for Stem Cell Research have removed this rule. This makes it possible to conduct research on human embryos that are at more advanced stages of development.

Now, countries must revise their laws, policies and guidelines to reflect this change. But first, public debate is crucial to determine the limits of what sort of research should be allowed.

Over the decades human embryo research has allowed us to understand normal and abnormal human development, as well as early genetic diseases and disorders. Studying human embryos, as the earliest forms of human life, can give us insight into why miscarriages occur, and how our complex body systems develop. Human embryos are also important for stem cell research, where researchers try and create cell-based therapies to treat human diseases.

Often, extra embryos are created during in vitro fertilisation procedures. These extra embryos may be donated for research. They are cultured (or grown) in a laboratory and can be studied until they reach day 14 post-creation.

The 14-day rule has served as an international standard since 1990 when it was included in the Human Fertilisation and Embryology Act in the UK. At the time that it was introduced, it was not possible to keep human embryos alive in a laboratory for more than a few days. However, scientists have been recently been able to keep embryos alive for longer periods, between 12 and 13 days. The ethical, legal and social consequences of such research were also important considerations.

Although the 14-day rule has been criticised as being arbitrarily decided, there are a number of reasons for the time frame.

After an egg cell is fertilised by a sperm cell, the resulting embryo consists of a few identical cells. Most embryos will implant in the uterus after the 14th day. After this point, the primitive streak appears, which is the first sign of an embryos developing nervous system. The rule also identified the point at which the embryo shows signs of individuation, because it is no longer possible for the embryo to split into twins after 14 days. Some people reason that due to these events, it is at this stage that a moral being comes into existence, and it would not be ethical to perform research on embryos after this time.

There has been increasing pressure from some researchers to remove the 14-day rule, or at least extend it, as it prevents critical research from being undertaken. Extending the rule would allow important research into early human development to be done. The new guidelines make it possible to do research on embryos older than 14 days if the approval processes of the relevant ethics committees are followed.

A significant problem, however, is that there is no longer any limit on the time frame for research. Would it be permissible to do research on human embryos that are 20 days old or 40 days old? The guidelines specify no limit. The longer a human embryo is allowed to grow, the more recognisably human it becomes. At what point would we regard the research unethical, and at what point does the moral cost outweigh the benefits of research?

Countries around the world take a variety of approaches to human embryo research. Some like Italy and Germany dont allow it at all. Others, like the UK, allow research to continue until the embryo is 14 days old, after which it must be destroyed. There are also some which permit embryo research without identifying a limit. Some, like the US, do not have any law regulating it (but there are guidelines which contain reference to the 14-day rule).

In South Africa, reference to the rule is found in the National Health Act (2003), which states that human embryo research may only be done with permission of the minister, and that the embryos must not be older than 14 days.

International guidelines are not legally binding. But the effect of the revised guidelines is that the international standard for best practice in scientific research has now changed. This means that countries which have implemented the rule in their laws will need to revise them so that they are in line with best practice in science.

Human embryo research is a sensitive topic because people are divided on the moral status of the human embryo. Some people believe that the embryo, as the earliest form of human life, should be protected and not subjected to research at all. Others believe that while an embryo has some moral status, it cannot be protected in the same way as humans are, and may be used for some important research which could ultimately benefit people.

The decision to discard the 14-rule appears to have been made without public input. That does not encourage the public to trust in science, and public engagement should have come before such an an important rule was changed.

There are a number of approaches to working with the revised guidance. Bioethicist Franoise Baylis has suggested that project-specific time limits should be identified, based on the minimum amount of time required to address the stated research objectives. This would mean that some research would still be subject to the 14-day limit, while other studies would be permitted to exceed it. Another approach would be to keep the 14-day limit as the norm, and consider applications to exceed it case by case. Or the limit could be extended to 28 days.

The coming conversations surrounding embryo research will prove to be very important. The proverbial genie is out of the bottle, and public debate is crucial.

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