CDC panel recommends Pfizer, Moderna vaccines over J&J attributable to uncommon blood clot circumstances

A health care worker holds a dose of the Johnson & Johnson vaccine.

Phill Magakoe | AFP | Getty Images

An advisory board for the Centers for Disease Control and Prevention on Thursday recommended Pfizer and Modern‘s vaccines over Johnson & Johnson‘s shot for adults ages 18 and up after dozens of people found a rare blood clot after the J&J vaccination, all of whom were hospitalized and nine of them died.

The Advisory Committee on Immunization Practices has unanimously decided to recommend Pfizer and Moderna over the Johnson & Johnson vaccine. CDC director Rochelle Walensky has yet to accept the recommendation.

The CDC has confirmed 54 cases of people who develop blood clots and have low blood platelet levels, a new condition known as thrombosis with thrombocytopenia syndrome that mainly affects younger women. All patients were hospitalized, nine people died and 36 were treated in the intensive care unit.

The US has administered more than 17 million J&J doses since the Food and Drug Administration approved the emergency syringe in February.

“TTS case reporting rates after Janssen vaccines are higher in men and women in a wider age range than previous estimates,” said Dr. Keipp Talbot, chairman of the CDC’s vaccines and safety subgroup, the advisory body.

Although the panel’s recommendation was unanimous, some members struggled with the vote. The CDC experts could also have recommended giving up the shot altogether or restricting it to certain age or demographic groups.

Dr. Pablo Sanchez, a professor of pediatrics at Ohio State University, said he was not recommending J&J admission to any of his patients, despite ultimately standing for the panel’s proposal.

“I just can’t recommend a vaccine associated with a disease that can lead to death,” Sanchez told the committee. “I don’t recommend it to any of my patients’ parents.”

Seven of the patients who died were women and two men, with a mean age of 45 years. Most of the deceased had previous health conditions such as obesity, high blood pressure and diabetes. The death reporting rate was 0.57 deaths per million doses administered, according to the CDC.

“In reviewing these cases, we noticed how quickly patient status deteriorates and leads to death,” said Dr. Isaac See of the CDC’s Vaccine Safety Team joined the advisory board.

According to the CDC, patients typically developed symptoms 9 days after vaccination and were hospitalized 5 days after symptoms appeared. The overwhelming majority of patients were women, 37 total, and the mean age was 44. Seventeen men developed TTS.

Johnson & Johnson’s director of global therapeutic vaccines Penny Heaton defended the company’s shot during the meeting, saying it “saves lives here in the US and on every continent around the world”.

“It’s easy to store and transport,” said Heaton. “In many low- and middle-income countries, our vaccine is the primary and sometimes even the only option in the US as its permanent protection may be the preferred choice for people who cannot or do not want to return for multiple vaccinations.”

Heaton said J&J recognizes the incidents of TTS related to the vaccine and that the condition can be fatal, although cases are rare. She said patient safety and wellbeing remain a top priority for J&J, and the company has several studies underway to identify risk factors related to developing TTS.

In April, the Food and Drug Administration and the CDC stopped briefly the use of the Johnson & Johnson single vaccine after six adult women developed blood clots and low platelet counts at the same time.

A week later, the FDA and the CDC did canceled the break on J&J shots after the independent advisory panel said the benefits of the shots outweigh the risks. At the time, the panel did not recommend restricting admissions based on age or gender. It suggested that the FDA put a warning label on for women under 50.

The FDA has advised health care providers not to give a J&J booster to people who have developed TTS in the past after the first injection. The FDA also said the J&J syringe should not be given to people who received the vaccine from AstraZeneca, even though AstraZeneca is not approved for use in the United States

CDC experts said Thursday that people who received J&J booster doses have not seen any cases of TTS, although the number of boosters is relatively small.

“Currently available evidence supports a causal relationship between TTS and the Janssen COVID-19 vaccine,” the FDA said in the factsheet for healthcare providers.

In October, the FDA and CDC approved authorized J&J boosters for all adults at least two months after receiving their first J&J syringe. More than 800,000 people have received J&J boosters, according to CDC data. People who received their primary vaccination with the J&J shot can also be boosted with the Pfizer or Moderna vaccines.

This is the latest news. Please check again for updates.

Household elevating cash for analysis after daughter was identified with uncommon genetic dysfunction

CRESTVIEW, Fla. (WJHG / WECP) – At first glance, Carson Talbert looks like a normal, happy one-year-old, but was diagnosed with a rare genetic disorder when Carson was less than a month old.

“It’s called homocystinuria because of severe MTHFR deficiency,” said Grace Talbert, Carson’s mother. “There are only about 50 documented cases worldwide.”

Since her diagnosis, Carson has been on drugs that appear to help.

“There are little things my daughter should probably be doing but not doing,” Talbert. “Fortunately, she is really fine because she was diagnosed early and started medication early. Of all MTHFR-severe patients, it is one of the better cases. Fortunately, but that’s because she started medication after three weeks. “

However one fears that her mother has the unknown.

“Personally, I have never met an adult with it. I mostly see younger children so I don’t know what their life will be like as she gets older. There really is no one to compare it to, and there really is no one to compare to being diagnosed so early. “

HCU has no cure, but the Talbert family has started Fundraiser To raise money for research to hopefully find one one day.

“My daughters write homocystinuria because of severe MTHFR deficiency, no studies are ongoing,” said Talbert. “We hope that maybe a cure will be found in about 20 years, hopefully. But realistically this may not be the case, especially if there are no funds for research. “

Until a cure is found, her parents will do whatever they can to make Carson laugh and have fun with their big sister.

According to Carson’s parents, after their daughters were diagnosed, they were tested for HCU and discovered they were both carriers.

Copyright 2021 WJHG. All rights reserved.

From Maine to North Carolina – barefoot. British solider raises cash to battle daughter’s uncommon illness

News 12 employees

09/22/2021, 12:06 am

Updated on: 22.09.2021, 00:54

British Army Major Chris Brannigan is stopping tonight on a long and difficult journey down the northeast coast to raise funds to help his daughter fight a rare genetic mutation.

His 9-year-old daughter Hasti has Cornelia de Lange Syndrome or CDLS – a genetic mutation that affects physical and mental development. Brannigan says it is difficult to raise funds to develop a therapy for the rare disease.

“She wants her daddy at home,” he told News 12 in Bridgeport on Tuesday night. “She wants her new medicine, but if I don’t complete this trip unless I collect the money, it just won’t happen.”

Brannigan works in a laboratory in Bar Harbor, stopping at hospitals and universities along the way to raise awareness of CDLS. He will be staying at a Bridgeport fire station overnight.

Denver7 On a regular basis Hero bikes throughout the nation to boost cash for uncommon most cancers analysis

DENVER – Alec Fraser and Jamie Meehan will tell you the idea of ​​cycling nearly 5,000 miles like most good ideas do.

“One evening over a mug of beer we decided to drive across the country,” said Meehan.

The real inspiration was born in a Connecticut hospital decades earlier.

“Julian was a very special person,” said his father Alec.

Julian Fraser was a kid with a big smile and an even bigger heart. An all-American swimmer and college water polo player, his father said he was happy and healthy until he turned 19 and received a devastating diagnosis.

“He had osteosarcoma, a bone cancer that mostly affects children and adolescents,” said Alec. “Unfortunately at the time of diagnosis it had already metastasized and it was in 14 different parts of his body and he had a huge tumor in his abdomen.”

After years of tough battle, Julian lost his battle with cancer in 2017.

“They gave him very little chance of survival. I remember once he took me aside and said, ‘Dad, I don’t care what they say, I’ll hit this.’ And he just fought this disease with all his might, ”said Alec.

The two draw from this strength when they cycle Julian’s Honor from Connecticut to California. Her goal is to raise half a million dollars for Cycle for Survival, which funds research into rare cancers.

“Over 50% of people with cancer have some form of rare cancer, and yet only 4 cents of every dollar raised for cancer research goes to rare cancer research. So it’s very important to us, ”said Alec.

This week, Team JF made it to Colorado. A crowd of supporters accompanied her for long distances while the teenager was never far from her thoughts.

“I think of the fight Julian went through and the fights he had and there is a huge reservoir of commitment to keep it going and that’s why I think of him in the harder times that I drive” said Meehan.

Nothing will fill the hole Julian left, but Team JF hopes this ride to honor the teenager gives hope to those still struggling.

“I do that every now and then, of course I think of Julian and think of his life, great memories we had with Julian and the feeling, alright, he looks down at us and smiles at what we’re doing, so feels that look really good, “said Alec.

If you would like to donate to Cycle for Survival, visit their website.

Molly Hendrickson anchors at Denver7 from 4:30 a.m. to 7:00 p.m. It also features a different 7Everyday Hero on Denver7 every week. Follow Molly Facebook here and Twitter here. To appoint a hero in your life Click here.

Dad strolling barefoot down Atlantic Coast to boost cash for daughter’s uncommon well being situation

Posted: 09/17/2021 / 12:07 PM EDT
Updated: 09/17/2021 / 12:07 PM EDT

JACKSONVILLE, NC (WNCT) – Finding hope for Hasti. That’s what keeps father Chris Brannigan going.

Brannigan wanders from Maine to North Carolina without shoes. Everything to give his daughter a better life.

“Hasti and I took little barefoot walks just half a mile around our house and we really enjoyed that, we talked the whole time,” said Brannigan. “It has occurred to her now that this walk will allow me to take her new medicine home with me.”

Hasti needs gene therapy. She has CdLS, a rare disease that affects growth, cognition, and more. This makes it difficult for the little girl to lead a normal life.

“Like all 9-year-old girls, she loves trampoline jumping, swimming and ballet lessons,” said the father. “Her passion is cooking. She is always in the kitchen, peeling carrots and potatoes and chopping everything up. She would really like to become a cook one day. “

The clock is ticking to get this treatment as her condition is expected to worsen around the age of 12. The problem is that it costs $ 3.5 million to conduct a clinical trial for the disease.

“The thought that we might change their fate keeps me going,” said Brannigan. “It’s huge, it’s all I can really think about every day.”

That’s why her father runs 1,200 miles … barefoot!

“Every time someone sees me walking barefoot they double-take because it’s so bizarre and very painful, and that’s the idea of ​​getting people to look twice,” he said.

Brannigan’s final destination will be in Jacksonville at Camp Lejeune. He hopes to end his trip there by the end of October.

“I served in the British Army for 14 years, I thought it would be great to deal with my people and my military family,” said Brannigan.

He has more than 800 miles to go.

“My feet get a little more sensitive and a little more bruised every day,” he said. “I just have to keep going. I keep thinking about what Hasti wants and what she deserves, and that drives me to take steps. “

The nonprofit has raised over $ 1 million. Brannigan said although this looks like a lot of money, they still have to double it up to help his daughter and others like her.

Brannigan said every donation is important. To donate, visit this link.

Marblehead mom raises cash to combat uncommon cancers

Jacqui Lewis is a Marblehead mom who does everything by herself and raises two adopted children while running a travel company. “I’ve lived my best life,” she told top women owned businesses like six years in a row, (then) one day I just had this pain in my shoulder and that started my journey with cancer -19 shutdown. “That actual Friday, which was Friday the 13th, I was told I had a cancer called cholangiocarcinoma,” said Lewis. “Most people would probably know it as bile duct cancer, if they even knew it. I was shocked, but what really shocked me was when they told me I had rare cancer and the prognosis was poor. ”Rather than slowing down, Lewis aimed for the drive that kept her long and successful in business to be on a new mission to instill hope for people with rare cancers. “These statistics made me say, ‘You have to stop and do something. Something has to change.’” Lewis started the RARE initiative to raise at least $ 1,000,000 for the Henri and Belinda Termeer Center for Targeted to collect therapies at the Mass General Cancer Center. Dr. Lipika Goyal explained that advances in fighting one rare cancer can lead to answers for others, but then you can actually fertilize each other and borrow that knowledge into other rare cancers, ”Goyal said. Lewis is now asking people who want to support the fight against rare cancers to wear a wig for a day and raise funds for WigOut for a Cure. “All we asked is to donate $ 22 and support someone who is ready to take on a challenge,” she said. “That $ 22 represents all of us, the 22% who rarely have cancer.” Lewis said she was almost halfway to her $ 1,000,000 goal, and she recently passed the $ 435,000 mark . Information on the WigOut challenge and the RARE initiative can be found here.

Jacqui Lewis is a Marblehead mom who does everything by herself and raises two adopted children while running a travel company.

“I’ve lived my best life,” she said. “(I’m) an entrepreneur and had shouldered the best women-run businesses for six years in a row, and that started my journey with cancer.”

Lewis says she was diagnosed in March 2020, the week of the COVID-19 shutdown.

“That actual Friday, Friday the 13th, I was told I had a cancer called cholangiocarcinoma,” said Lewis. “Most people would probably know it as bile duct cancer, if they even knew. I was shocked, but what really shocked me was when they told me I had rare cancer and the prognosis was poor.”

Rather than slowing down, Lewis aimed for the drive that long drove her to be successful in business on a new mission and to instill hope for people with rare cancers.

“What we’re getting now is 3% of the funding, and we represent 22% of the people with cancer,” she said. “These statistics motivated me to say: ‘You have to stop and do something has to change.'”

Lewis started the RARE initiative to raise at least $ 1,000,000 for the Henri and Belinda Termeer Center for Targeted Therapies at the Mass General Cancer Center.

Dr. Lipika Goyal explained that advances in fighting a rare cancer can lead to answers for others too.

“In rare cancers, sometimes you see a mutation with a cancer, you find a drug that works for that mutation in that cancer, but then you can actually fertilize each other and borrow that knowledge into other rare cancers,” Goyal said.

Lewis is now asking people who want to support the fight against rare cancers to wear a wig for a day and raise funds.

She calls the challenge WigOut for a Cure.

“All we asked is to donate $ 22 and support someone who is ready to take on a challenge,” she said. “That $ 22 represents all of us, the 22% who have rare cancer.”

Lewis said she was almost halfway to her $ 1,000,000 goal and recently passed the $ 435,000 mark.

Find information about the WigOut challenge and the RARE initiative here.

Mattress Bathtub and Past will get uncommon purchase ranking, however 2 merchants would not chunk

Bed bath and beyond can be out of reach.

Although the retailer received a rare buy rating this week from B. Riley, who initiated the name with a price target of $ 44 and an upbeat argument for its new management and cost-cutting strategies, the stock doesn’t look particularly attractive at its current levels, two said Dealer to CNBC “Trading nation” on Thursday.

The $ 3.5 billion company Profit and sales growth forecasts looks maybe better than those of its industry peers, but still lags behind the broader market, said Gina Sanchez, founder and CEO of Chantico Global, in an interview on Thursday.

“It’s really hard to get upset,” she said. “We think they’re the right price and that’s not necessarily a screaming buy.”

Bed Bath and Beyond has already risen 78% since the beginning of the year and is trading at a multiple of almost 20.5 times the forward price / earnings ratio.

The history of the stock as a Reddit favorite is also doing investors a disservice, Sanchez said.

“Once that momentum takes hold in the market, you’re pretty late because these momentum trades on some of these meme stocks have nothing to do with fundamentals,” she said. “If you buy it just for the momentum, that’s the worst reason to buy because you will inevitably be the bigger fool in this story.”

One possibility that could develop has to do with Bed Bath and Beyond’s brief interest, said Matt Maley, chief marketing strategist at Miller Tabak, in the same “Trading Nation” interview.

Both times this year the stock got swept up in Reddit trading – first when GameStop rallied in January and again when AMC skyrocketed in June – it had remarkably high short interest, Maley said.

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“Now it’s down again. If anything, it’s got incredibly low short interest, not a high one. So people have to be very, very careful,” warned Maley. “If we … get another short squeeze, Bed Bath and Beyond won’t be one of the stocks being squeezed like that.”

While the company’s recovery history may sound promising, it will likely take time for the stock to reflect, the strategist said.

“They’ve made some good changes and their revenue has been pretty good, but I just don’t think people should be looking for another rocket ship like we’ve seen twice this year,” he said hey.

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Marvel Leisure to Launch NFTs — Followers Can Quickly Hunt for Uncommon NFT Comedian Books – Bitcoin Information

Marvel Entertainment has announced that it is entering the non-fungible token (NFT) space. The wholly owned subsidiary of Walt Disney Company and popular comic book creator, says Marvel fans can purchase “Official Marvel NFT Digital Collectibles, Digital Comics, and more.”

Marvel publishes NFT digital comics and collectibles through the Veve app

  • The comic and film giant Marvel entertainment is getting into NFTs, according to a press release published on Thursday. The announcement indicates that Marvel aims to bring digital collectibles, digital comics, and other NFT products to market.

Marvel Entertainment is launching NFTs - fans will soon be able to look for rare NFT comics“Since the beginning, collecting has always gone hand in hand with being a Marvel fan,” said Dan Buckley, president of Marvel Entertainment, in a statement. “Like us, Veve understands that collecting is as much about the experience as it is about the product, and we look forward to expanding that experience for our fans in the years to come,” added Buckley.

  • The comics started in 1939, but Marvel’s entertainment line started in 1998 and is based in New York City. The corporate unit with 1,786 employees makes an estimated $ 366 million per year in revenue.
  • For the NFT venture, Marvel has partnered with Orbis Blockchain Technologies Limited, a company that operates the Veve Digital Collectibles app. The application is available for iOS and Android. The app allows Marvel fans to buy and trade the company’s unique offers.
  • The announcement also states that users of the Veve app can also “search for rare (and even secret) NFT comics and collectibles and showcase their hard-earned collection in fully customizable virtual showrooms.”
  • Veve’s in-app currency called Gems is required to purchase official Marvel NFT products, and NFT owners can also resell them through Veve’s secondary marketplace.
  • About Veves Platform, vice president of business development and strategy for Marvel Entertainment, says Daniel Fink, the company hopes “to push the boundaries of what Marvel fandoms can be, starting with personal and interactive digital collectibles that fans really get through NFTs and can share ”. and enjoy in a way you couldn’t before. “
  • Marvel follows the comic book maker’s competitor, Dc comics, which revealed that NFTs would hit the market in March 2021. This followed a Letter to freelance artists by the legal representative of DC Comics, who urged freelance artists to stop making DC Comics-related NFTs.
  • “More details on Marvel’s exciting new digital collectibles coming to Veve will be announced in the next few weeks,” Marvel added on Thursday. “Comic book fans should also be excited for some exciting new revelations coming soon,” added the entertainment company.

What do you think of Marvel Entertainment getting into NFTs? Let us know what you think on this matter in the comments below.

Tags in this story

Blockchain, Comic fans, comics, Dan Buckley, Daniel Fink, Dc comics, Marvel Comics, Marvel entertainment, Marvel fans, Marvel NFT, Movies, nft, Not fungible token, Non-fungible token (NFT), Veve app

Photo Credit: Shutterstock, Pixabay, Wiki Commons, Marvel Comics,

Disclaimer of liability: This article is for informational purposes only. It is not a direct offer or solicitation of an offer to buy or sell, or a recommendation or approval of any product, service, or company. does not provide investment, tax, legal or accounting advice. Neither the company nor the author are directly or indirectly responsible for any damage or loss caused or allegedly caused by or in connection with the use of or reliance on any content, goods or services mentioned in this article.

CDC says there’s probably hyperlink between uncommon coronary heart irritation in younger individuals after Covid shot

The headquarters of the Centers for Disease Control and Prevention (CDC) in Atlanta, Georgia.

Tami Chapel | Reuters

A CDC safety group said there was a “likely link” between rare heart inflammation in adolescents and young adults, mostly after they received their second Covid-19 vaccine, citing the latest available data.

There have been more than 1,200 cases of myocarditis or pericarditis, mostly in those under the age of 30 who Pfizer‘s or Modern ”s Covid vaccine, according to a series of slide presentations released Wednesday for a meeting of the Advisory Committee on Immunization Practices of the Centers for Disease Control and Prevention.

Myocarditis is the inflammation of the heart muscle while pericarditis is the inflammation of the membrane that surrounds the heart.

“The clinical picture of myocarditis cases after vaccination was variable and most often appeared within a week of the second dose, with chest pain being the most common,” said Dr. Grace Lee, Chair of the Committee’s Security Group. CDC officials are collecting more data to fully understand the potential risks, how to deal with them and if there are any long-term issues, she said.

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The agency said 267 cases of myocarditis or pericarditis were reported after receiving one dose of the mRNA vaccines and 827 cases after two doses by June 11. There are 132 additional cases where the number of doses received is unknown, the CDC said.

The agency announced that around 300 million shots had been administered by June 11.

“This is still a rare occurrence,” said Dr. Tom Shimabukuro at the meeting. For both vaccines combined, there were 12.6 cases of heart inflammation per million doses. Cases were more common among Moderna vaccine recipients at 19.8 cases per million than eight cases per million at Pfizer, he said.

Men under 30 make up the bulk of cases, the CDC said, and most cases appear to be mild. Of the 295 people who developed the disease and were discharged, 79% made a full recovery, according to the presentation. Nine people were hospitalized, according to the agency, two of them in the intensive care unit.

CDC officials said the benefits of the Covid vaccine still outweigh the risks.

Cases in younger people are increasing as older people are vaccinated at higher rates. The US vaccinated 177.6 million people with at least one dose, according to the CDC, that’s about 53% of the population. Only 13.6% of 18- to 24-year-olds in the United States received at least one dose of vaccine, compared with 26% of people ages 50 to 64, the data shows.

While hospitalization rates have decreased in older age groups, they have barely moved in adolescents and young adults, said Dr. Megan Wallace from the CDC.

“Teenagers and young adults make up a larger proportion of the total cases, 33% of the cases reported in May were people ages 12-29, compared with 28% last December,” she said. Since the pandemic began, 2,767 people aged 12 to 29 have died of Covid, she said, noting that 316 of these deaths had occurred since April 1.

The CDC is coordinating its investigation with the Food and Drug Administration, which last month the PfizerBioNTech Vaccine for adolescents aged 12 to 15 years. Symptoms, which include chest pain and shortness of breath, typically develop within a week of receiving the vaccination, with most developing within four days, the agency said.

This is a developing story. Please check again for updates.

CNBC’s Rich Mendez contributed to this article.

Correction: Most of the cases of people who had myocarditis occurred in people under the age of 30. In a previous version, the age was incorrectly stated. The number of cases per million doses administered was 12.6. In an earlier version, the number was incorrectly specified.

Meghan Markle Provides Uncommon Have a look at Off-Responsibility Model Throughout Her Look in ‘The Me You Cannot See’ Trailer

Eat that, not that!

The frightening link between ultra-processed foods, sugar, and cancer, Doctor reveals

It’s no news that processed foods, whether you eat salty snacks or sugary treats, aren’t good for your waistline – especially if you eat them in place of fresh fruits and vegetables and other healthy foods like legumes and nuts. More worrisome, however, is the ability of processed foods to damage your health significantly later on. In his new novel, Metabolical, which recently hit bookshelves everywhere, Dr. Robert H. Lustig, MD, MDL, a pediatric neuroendocrinologist explored the many ugly truths of our current food system and modern medicine. Delving into the depths of eight pathologies in cells that believe in all chronic diseases, he argues that drugs are not an adequate solution to preventing or treating them. Instead, it shows how the food we eat is the real cure (and enemy) for conditions like heart disease, type 2 diabetes, and even cancer. Ultra-processed foods like potato chips, candy bars, cheese, and even sausages are often full of added sugars, partially hydrogenated oils, and nitrates. In “Metabolical”, a title that combines the functioning of the body (metabolism) with that of mass products, Big Pharma and Big Government (devilish), Lustig shows how all these components in processed foods can lead to type 2 diabetes and heart disease regular and prolonged consumption. Even more petrifying is the idea that these foods can contribute to cancer growth. How can consuming processed foods lead to cancer? “In the gut, nitrates are first converted into nitrites and then into nitrosoureas, which are known to be carcinogenic and cause colon cancer,” Lustig said in an interview with Eat This, Not That! Recent research has even suggested that nitrates alone, found in cured meats like pancetta, ham, salami, and other processed meats like bacon, beef jerky, and sausages, could increase your risk of developing cardiovascular disease . “And refined carbohydrates lead to insulin release and insulin resistance,” he says. “Insulin is a growth factor that makes cancer cells grow, and glucose is their main fuel.” Some cancers, such as pancreatic cancer, feed on fructose (which makes up 50% of table sugar or sucrose), which makes them stronger and more harmful. “While sugar is not a specific cause of cancer cell differentiation, it is a major driver of cancer cell growth,” adds Lustig. How has the mass production of food ruined society’s health in the past few decades? With the exception of 2020, Funny If you look at what people have died from in the past 50 years, it has changed dramatically from an infectious disease (like influenza) to a chronic non-communicable disease that includes heart disease, cancer, and dementia. “These are the diseases we now have evidence of how ultra-processed foods – especially sugars, but also trans fats – disrupt the mitochondria to cause these chronic diseases,” he says. “In other words, food has gone from providing health to disease. The point is, it’s not the food, it’s what was done with the food that makes it toxic.” What do you suggest we do to improve our own metabolic function and avoid chronic and inflammatory diseases? It’s easy. Funny says the answer can be found in three words: Eat real food. “Real food is anything that came out of the ground or any animal that ate that came out of the ground,” he adds. When the animal is fed something processed or the plant-based products have been stripped of nutrients and fiber (think whole wheat versus white bread), or chemicals are added to the animals’ feed and growing plants. The feed becomes a threat to our health. “We have a limited capacity to metabolize these chemicals, and we are well over our limit,” says Lustig. For more information, see 26 Worst Habits That Slow Your Metabolism Down, Science Says.