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Fact: Red yeast rice is the most colorful name in the supplement game. It certainly sounds cool as an acronym (#RYR vibes). But did you know red yeast rice is produced from a mold — not a yeast? We’re guessing “red mold rice” just doesn’t have the same ring to it.
If you have high cholesterol, you may have heard of red yeast rice as a possible alternative to prescription cholesterol-lowering medication. The ruby-red food and dietary supplement has also been thought to have anti-cancer properties.
But is it too good to be true?
Here’s what you need to know about the potential benefits and the red flags to consider before taking red yeast rice.
Red yeast rice has been around for centuries and is known as a “natural statin” in traditional Chinese medicine. It’s produced by fermenting rice with a type of mold called Monascus purpureus.
Depending on the strain and the conditions of fermentation, the fungus enhances the rice with compounds called monacolins, which can lower cholesterol levels in the body. One of those monacolins — monacolin K — has the same makeup as the medicine lovastatin, a prescription cholesterol-lowering medication.
The most celebrated benefit of red yeast rice is its ability to lower cholesterol thanks to monacolin K. Some studies have shown that taking red yeast rice on a daily basis for six to eight weeks can lower total cholesterol and LDL (“bad”) cholesterol levels.
Red yeast rice may also have anti-cancer benefits. One study found that red yeast rice stopped the growth of cancer cells in the colon. And a different study found that red yeast rice extracts stopped breast cancer cells from growing. But more research needs to be done regarding any anti-cancer benefits to taking the supplement.
Lower cholesterol levels are directly linked to the amount of monacolin K in red yeast rice supplements. Research shows taking up to 10 mg of monacolin K on a daily basis is associated with lower cholesterol levels.
This is where things get a little complicated. The FDA approved lovastatin — which is basically monacolin K — as a drug before it was marketed as a supplement. So, any product that lists lovastatin or enough monacolin K to work like a statin, is illegal to sell in the U.S. as a dietary supplement. Over the years, the FDA has issued warnings against companies who market added or enhanced supplements with lovastatin and monacolin K.
As a result, the red yeast rice products you see online and in the grocery store typically won’t list the amount of monacolin K on the product label. The product may not contain any monacolin K — although most will have some level of the cholesterol-lowering ingredient — but you won’t know for sure the actual amount.
Because red yeast rice can act like a statin, the same side effects may apply. These can include:
Some people experience other side effects. These can include:
Red yeast rice products may contain citrinin, which can cause kidney damage.
Red yeast rice may not be an option for everyone. You shouldn’t take it if you’re on cholesterol-lowering medications like a statin because it can increase the risk of serious side effects.
Also, people taking certain substrate drugs (CYP450 3A4 or P-glycoprotein), including some antibiotics and antifungals, shouldn’t take red yeast rice as it can affect how the body metabolizes medication. If you are taking any medication and you don’t know if it’s a substrate drug, be sure to ask your healthcare provider.
Red yeast rice isn’t recommended for people who are pregnant or lactating because there are no clinical studies — good or bad — that show the effect of taking the supplement while pregnant.
Overall, red yeast rice is considered safe and has few side effects. However, because the amount of monacolin K usually isn’t listed on supplement labels, you never know what you’re going to get. For example, one brand online says their red yeast rice supplement has “appropriate levels of naturally occurring monacolin compounds, especially monacolin K.”
If you’re thinking about red yeast rice for cholesterol, the supplement may not contain enough monacolin K to make a difference or have any benefits. High cholesterol can lead to serious health problems such as heart disease — the number one killer of women in the U.S.
Just like with any supplement, it’s a good idea to talk to your healthcare provider before you give red yeast rice the green light.
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There’s a lot at stake in this presidential election, and women’s health policy will be impacted by our new commander in chief and their administration, no matter who wins. So, as the 2024 presidential election fast approaches, make sure you know where Kamala Harris and Donald Trump stand on important issues related to women’s health and healthcare.
You can do a deep dive on each candidate’s stances on their websites (do your research at
KamalaHarris.com and DonaldJTrump.com) but here’s a quick snapshot of some of the key issues affecting the health of women and people assigned female at birth.
Health Insurance
Donald Trump wants to replace the ACA with “much better healthcare.” During the debate, he mentioned that he has a “concept of a plan” for healthcare reform but has not issued specifics.
Trump campaigned in 2016 on repealing and replacing the ACA. Though that effort failed, his administration made other changes, including zeroing out the penalty for not having insurance, ending certain subsidies, and reducing funding for outreach and enrollment support.
Trump
Trump’s platform makes no mention of Medicaid.
As President, Trump allowed states to require people to work in order to qualify for Medicaid. His failed efforts to repeal the ACA would have reversed Medicaid expansion. He also proposed restructuring Medicaid payments to the states using block grants or per person spending caps.
Harris
Harris has said she will protect Medicare by taxing millionaires and billionaires and closing tax loopholes.
As vice president, Harris cast the tie-breaking vote for the Inflation Reduction Act, which contained provisions to lower Medicare prescription prices.
The Harris-Biden administration expanded coverage for mental health services and extended coverage for telehealth through December 2024.
Trump
Trump has said he will make no cuts to Medicare and will not change the retirement age, although no specific policies have been shared.
As president, Trump enacted tax reductions that sped up the depletion of the Medicare Part A Trust Fund and repealed a federal board that was intended to slow Medicare spending. He increased Medicare premiums for higher-income beneficiaries. He also relaxed Medicare telehealth rules to make remote care more accessible during the Covid pandemic.
Harris
Harris supports a $6,000 tax credit for parents of newborns and enhanced child tax credits ($3,600 for children under 6 and $3,000 for older children).
Harris supports creating federal paid family and medical leave (the current Family and Medical Leave Act guarantees unpaid leave) and enhanced funding for childcare providers. She proposes a cap on childcare costs to no more than 7% of a family’s income
.
Trump
Trump has not issued specific policy proposals, but at a New York Economic Club event, Trump stated that his proposals to increase tariffs on foreign imports would reduce the costs of childcare. He also said of childcare, “You have to have it.” Trump’s running mate, JD Vance, has said he supports a $5,000 child tax credit. A more modest proposal failed to pass in the Senate due to Republican opposition.
Harris
Harris has made a campaign commitment to pass the Equality Act, which protects LGBTQ+ people from discrimination.
The Biden-Harris administration reinstated Section 1557 of the ACA, which provides the broadest protections to date for healthcare based on gender identity and sexual orientation, for transgender people, and for gender-affirming care.
Trump
Trump has pledged to prohibit gender-affirming care for young people and block the use of federal funds for gender-affirming care.
Trump has also pledged to “Keep men out of women’s sports” as part of the 2024 Republican pledge to “end left-wing gender insanity.”
As president, Trump created the Division of Conscience and Religious Freedom at HHS and issued final conscience regulation expanded religious protections, which created opportunities for LGBTQ-based discrimination in certain circumstances.
Harris
Harris supports expanding the number of drugs that the government can negotiate and extending the $35 insulin cap for Medicare recipients to all Americans.
Harris cast the tie-breaking vote to pass the Inflation Reduction Act (IRA), which requires the government to negotiate drug prices on certain drugs, caps out-of-pocket drug costs and limits insulin costs to $35 per month for Medicare enrollees.
Trump
The Trump administration created a voluntary model for Medicare prescription plans to limit insulin costs to $35 per month and allowed states to import medicines from Canada; however that was later rescinded. Trump initially supported creating a “Most Favored Nation” status for Medicare to limit government spending on certain drugs but has since backed away from that position.
Trump
Trump has taken credit for the Supreme Court’s decision to overturn Roe v. Wade, which removed the constitutional right to abortion. He favors letting states decide their own abortion laws, and he personally supports exceptions to abortion bans in cases of rape, incest, and threats to the mother’s life.
Although Trump has held a variety of positions on abortion rights over the years. Recently, he said that laws banning abortion after six weeks go too far, but later stated that he plans to vote for such a measure in Florida, his home state. Trump previously would not commit to vetoing a federal abortion ban if Congress passes one, but more recently posted on social media that he would veto such a ban.
Harris
Harris supports the FDA decision to improve access to medication abortion pills by allowing them to be mailed.
The Biden-Harris administration opposes the interpretation and enforcement of the Comstock Act to prevent sending abortion medication through the mail.
Trump
Trump has suggested he would block availability of medication abortion pills at times and suggested that he would not block them at other times. Support for leaving abortion policy to the states allows states to block access to all abortion, including medication abortion pills.
Trump has not publicly spoken on his position on the Comstock Act, but many Republican leaders, including his running mate JD Vance, have called for the enforcement of the Comstock Act to prohibit the mailing of medication abortion pills.
Harris
Harris supports the proposed Right to Contraception Act, which protects the right to contraceptives.
The Biden-Harris administration is fighting a federal lawsuit that challenges ACA requirements to cover preventive services (including contraceptives). The administration has issued executive orders in support of contraception.
Trump
Earlier in the 2024 campaign, Trump said he was open to restrictions on contraceptives but later promised never to ban birth control.
Trump administration policies paved the way for employers with religious objections to exclude birth control from employee health plans. Most Republican members of Congress, including Vance, opposed the Right to Contraception Act.
Harris
Harris supports guaranteed rights to IVF and supports the ACA, which includes access to coverage before, during and after childbirth. She advocated against a ruling from the Alabama Supreme Court that embryos are children, and therefore cannot be destroyed.
She took a stand against Republicans blocking a bill that would have protected IVF.
Trump
Trump supports access to IVF and said he would require insurance companies to cover the costs but did not detail how he would implement such a requirement.
The Republican platform opposes research using embryonic stem cells (which can be derived from the IVF process).
Harris
In the past, Harris supported 12 weeks of paid leave for most workers, including new parents, caregivers and victims of intimate partner violence. During her presidential run, she has expressed support for paid family and medical leave but has not shared details.
Eye Injury Prevention Month is observed every October to promote awareness about eye safety and prevent injuries
“Wearing colored contacts may seem harmless. But beware: colored contact lenses can severely damage your eyes if you don’t buy them with a prescription. They can even cause permanent blindness if they’re not fitted by an eye specialist.” according to American Academy of Opthamology (AAO)
“Consumers need to know that permanent eye damage can occur from using non-prescription lenses,” says Thomas Steinemann, MD, an ophthalmologist at MetroHealth Medical Center in Cleveland, Ohio, and member of the American Academy of Ophthalmology. “I have seen far too many serious cases in both children and adults from using decorative lenses.”
Is It Safe To Wear Non-Prescription Colored Contacts?
It is not safe to wear contact lenses that were not prescribed especially for you. This includes contact lenses purchased without a prescription and contact lenses prescribed for someone else. Your eyes are at risk of serious harm — and potentially blindness — when you wear contact lenses that were not prescribed specifically for you.
Contact lenses advertised as ‘one size fits all’ or ‘no need to see an eye doctor’ are not safe. The ‘one size fits all’ claim is misleading and dangerous. Contact lenses must be tailored to each individual. Lenses that are not the correct size for your eye may result in serious harm and could destroy your vision.
Poorly fitting contact lenses can scratch your eye — or worse
Colored contacts also might let less oxygen through to the eye. This is because the paints and pigments make the lenses thicker and less breathable.
Treating this damage can require eye surgery, like a corneal transplant. And treatment doesn’t always work. People have been blinded by colored contact lenses.
For further details visit: https://www.aao.org/eye-health/halloween-cosplay-colorful-contacts-eye-safety
Disclaimer
The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.
Do you remember the scene in “Alice in Wonderland” when Alice nibbles on a mushroom so she doesn’t grow too big or shrink too small? That’s pretty much the thought process behind microdosing. You don’t take enough of the psychedelic drug to experience a real notable change, but the tiny dose may have mental perks, like reducing anxiety and depression.
Interest in microdosing and magic mushrooms seems to be at an all time high right now. A recent report found that 8 million people in the U.S. used psilocybin, the psychedelic component of magic mushrooms, last year. And about half of those people reported microdosing the last time they used it.
Read: Are Medical Mushrooms Really Magic? >>
The increase in curiosity around microdosing psilocybin may be due, in part, to the its decriminalization over the past few years in several states and cities across the U.S. Decriminalization of magic mushrooms, or shrooms, means that there are no criminal penalties for personal use. However, it’s important to note that psilocybin is still illegal on the federal level, even in states where it’s decriminalized. And the lack of regulation can mean whatever product you’re buying could be fake or contain harmful ingredients.
We asked Jim Grigsby, Ph.D., director of the University of Colorado Denver Center for Psychedelic Research, what you need to know about microdosing and magic mushrooms.
Microdosing is taking a very small amount of a psychoactive substance to enhance your mood without the mind-altering side effects.
“Microdosing puts too little of the stuff in your brain to produce a psychedelic experience,” Grigsby said. “Some people report that they get a little buzz off of it, and if so, they may have taken slightly more than needed.”
When you microdose mushrooms, you take a much smaller dosage (5% to 10%) than you would if you wanted to hallucinate or “trip.” And people who microdose generally take these doses on a semi-regular basis — two or three days a week.
iStock.com/los_angela
A microdose typically involves eating about 0.1 grams – 0.3 grams of mushrooms each time.
There are different ways to microdose mushrooms. The mushrooms can be chewed up dry or added into a hot tea or a broth/soup. They can also be crushed or put in a coffee grinder and mixed in chocolate or put in gelatin capsules and taken orally.
A microdose works the same way as a regular dose, just with different effects. The psilocybin is first converted to psilocin, the active ingredient. When it reaches the brain. The psilocin binds to serotonin receptors — especially one called 5-HT2A — which play a role in brain functions like perception and mood. That triggers, on a small scale, a biochemical cascade which is thought to eventually cause reactions at dopamine receptor sites. (Dopamine receptors affect emotions, movement and the reward system in the brain.)
While at least one survey found that people microdosing psilocybin reported improved mood, feeling more connected to other people and cognitive enhancement, the jury is still out on the benefits to and safety of microdosing mushrooms.
“There isn’t any good research on the subject, only observational studies that rely on self-report — no clinical trials or experiments,” Grigsby said. Some research shows people reported improved mood, more energy, productivity, creativity and clear thinking, but there’s no control group for comparison. “Statistically, it’s possible to take into consideration people’s expectations, and that can then explain the entire effect. So, it could be a placebo effect.”
There is little research on the effects of microdosing mushrooms and no guidelines regarding who shouldn’t try it. That said, some research suggests repeated microdosing of psilocybin can cause valvular heart disease, so people with cardiac conditions and heart valve problems should be aware of this possible side effect.
Microdosing may also not be good for people with a history of psychosis or a family history of psychosis. “Again, we don’t know for sure, but if someone with schizophrenia asked me about it, I’d probably advise against it,” Grigsby said.
Microdosing psilocybin is not recommended for people who are pregnant. “Although the dose is very small, and psilocybin is safe and basically non-toxic, like with many drugs, pregnant and lactating women ought not to try microdosing,” Grigsby said.
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Nearly 20,000 women in the United States will receive an ovarian cancer (cancer of the ovaries) diagnosis in 2024.
“The silent killer”
There is no screening test for ovarian cancer, so it can go a long time without being caught.
Symptoms of ovarian cancer often go unnoticed or are mistaken for other conditions.
Ovarian cancer is often diagnosed at an advanced stage, making it harder to treat.
Black women are 20% more likely to be diagnosed with late-stage ovarian cancer than white women.
BEAT ovarian cancer — know the signs and symptoms
Bloating
Eating less and feeling full quickly
Abdominal and pelvic pain that is ongoing
Trouble with your bladder or bowels
Know your risk
Because there’s no screening for ovarian cancer, knowing your genetic risk factors is key to prevention.
Questions to ask yourself
Talk to your healthcare provider. Being proactive about ovarian cancer is important.
This educational resource was created with support from Merck.
Natálie Taschlerová is a Czech ice dancer. With her brother and skating partner, Filip Taschler, she is the 2020 Nebelhorn Trophy champion and two-time Czech national champion (2022–2023). They represented the Czech Republic at the 2022 Winter Olympics.
On the junior level, she is the 2019 JGP USA bronze medalist and has competed in the final segment at three World Junior Championships, their highest placement being fourteenth in 2019. Nationally, she is a three-time Czech national junior champion.
Taschlerová began learning to skate in 2004 and subsequently began learning ice dance alongside her brother Filip following the end of his partnership with Karolína Karlíková. Years later, Taschler would say that “our relationship is better since we started skating together. When we were younger, we fought like small kids, but now we are adults. We respect each other.”
Taschlerová/Taschler made their international junior debut in the 2017–18 season, including two appearances on the ISU Junior Grand Prix, placing twelfth in Poland and thirteenth in Austria. After winning what would be the first of three Czech junior national titles, they made their first appearance at the World Junior Championships, where they finished eighteenth.
Competing their second season on the Junior Grand Prix, Taschlerová/Taschler were thirteenth at JGP Lithuania and eleventh at their home JGP Czech Republic. They then won their first international junior medals competing at minor events, a bronze at the Open d’Andorra and a silver at the junior category at the Inge Solar Memorial. Junior national champions for the second time, they finished the season placing fourteenth at the 2019 World Junior Championships.
Women Fitness President Ms. Namita Nayyar catches up with Natálie Taschlerová an exceptionally talented Czech ice dancer and two-time Czech national champion here she talks about her fitness routine, her diet, and her success story.
You were born in Brno, Czech Republic. You started skating at the age of three years and subsequently, you began learning ice dance alongside your brother Filip Taschler. In 2017–18 season you won first of three Czech junior national titles. This later propelled your career to the height where you have been at the top of the world of ice dancing. Tell us more about your professional journey of exceptional hard work, tenacity, and endurance?
I started with figure skating at the age of two, initially just to learn how to skate. Out of all the sports I’ve tried, I fell in love with figure skating the most. Alongside this, I was also engaged in sports gymnastics. However, a time came when I had to make a choice between the two. I had talent in both disciplines, but it was becoming increasingly difficult to maintain my commitment to each. Consequently, at the age of 11, I chose to continue with figure skating and stepped away from gymnastics.
My transition to ice dancing was prompted by a previous injury; I severely broke both bones in my right forearm for the second time, which resulted in a lengthy and difficult recovery. When I returned to the ice, the fear of jumping was overwhelming. I found myself contemplating whether to leave figure skating altogether to lead a more conventional life focused on school. The alternative was to switch disciplines, and I always had strong skating skills and an intuitive feel for music on the ice. It was then that my brother, Filip, suggested we try skating together. Now, here we are in a different country, chasing our dreams. Sometimes, it all feels quite surreal.
Our first junior medals gave us a glimpse of a promising future in the sport. These achievements fueled our ambition to reach higher levels. During the 2018-2019 season, we were still skating and living in our hometown, Brno, training under our former coach Nikola Višnová. Our coach had trained and lived in Milan during her professional career. Although home was comforting, we knew that to improve, we needed to step outside our country. We explored staying home as long as possible, trying to find suitable training conditions. However, this proved very challenging.
The first major change was our schooling. With training starting at 11 a.m. and ending around 5-6 p.m., attending school daily became nearly impossible. Some teachers were unsupportive of our journey, causing more problems. As a result, we switched to online homeschooling, which was a tremendous help. We both graduated high school and found we actually enjoyed studying. The best part just needed a computer and Wi-Fi to connect to our classes’ haha!
That season, we began collaborating with Matteo Zanni, travelling to Milan for weeks at a time to prepare for significant competitions like the 2018 Nationals and the 2019 Junior Worlds in Zagreb. After the season, Matteo invited us to move to the USA with him, offering us a chance to start a new life there. It was a pivotal opportunity, and we knew if we wanted to excel, we had to seize it. Our former coach, who was pregnant for the second time and planning to retire from coaching, supported this move. Leaving our family was tough, especially since our father was ill, but he encouraged us to pursue our dreams.
In the summer of 2019, we relocated to Chicago. It was a huge change – new country, different language – everything was unfamiliar, but it was exciting. We even spent the first week sleeping on the floor without beds, which is now one of my fondest memories. Exploring the USA, experiencing new culture, and meeting athletes and coaches were incredible. Besides training with Matteo Zanni, we worked with Collin Brubacker and Oleg Ebstain. Everything seemed perfect. It was the summer of my dreams. Until our lives were turned upside down.
In July 2019, our father passed away from cancer. It was devastating and brought everything to a halt. We returned to the Czech Republic, uncertain about our next steps – whether to continue skating or stay home to support our mom. The financial aspect was a significant concern since figure skating is very expensive. However, we tried to keep going. Skating became one of the things that saved us. While we didn’t have much time to process our grief, we continued, knowing this was what our dad wanted – for us to always fight and follow our dreams. Figure skating is a long journey where patience, passion, and a love for hard work are very important.
Full Interview is Continued on Next Page
This interview is exclusive and taken by Namita Nayyar President of womenfitness.net and should not be reproduced, copied, or hosted in part or full anywhere without express permission.
All Written Content Copyright © 2024 Women Fitness
Disclaimer
The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.
September 2024 is National Ovarian Cancer Awareness Month.
Like most cancers, ovarian cancer has better outcomes if it’s treated early. However, it’s tough to find ovarian cancer early because it often has no symptoms. In the U.S. alone, there are almost 20,000 new cases of ovarian cancer each year — and more than 14,000 deaths.
Ovarian cancer, which occurs when abnormal cells in the ovaries grow uncontrollably, is more common in white women — yet, Black women have lower survival rates. And the difference is pretty big. The five-year survival rate in Black women is 41% — a full 7% lower than the 48% five-year-survival rate seen in white women.
And for early- and late-stage ovarian cancer, Black women’s survival rates are worse not just than that of white women, but of all other races and ethnicities.
We reached out to Holly Harris, MPH, ScD, the lead researcher of a 2022 study designed to better understand why Black women have worse survival rates and outcomes of ovarian cancer than other races and ethnicities.
Harris, an associate professor of epidemiology at Fred Hutchinson Cancer Research Center, said a lot of the disparities in ovarian cancer outcomes for Black women come down to access. Unfortunately, Black women are less likely to get offered the treatments that are recommended by professional medical guidelines. In fact, one 2019 study found that Black women were 25% less likely than white women to get the recommended ovarian cancer treatments.
“Black women are less likely to receive guideline-adherent care, and that’s likely impacted by the areas they live in and their access to different resources,” Harris said.
Social determinants of health (SDoH) can contribute to the health disparities and inequities Black women face. SDoH are nonmedical factors, such as socioeconomics (job type, level of education and income) and where you live, work and play, that affect the quality of life, opportunities and health outcomes.
According to the National Women’s Law Center, in almost every state, Black women are more likely to be uninsured, live in poverty, have limited access to food and face issues securing housing than non-Hispanic white women. All of these factors can make it challenging for Black women to access and afford healthcare.
“Socioeconomic factors likely explain some of the disparities [Black women with ovarian cancer face],” Harris said. “The area that you live impacts [your ability to receive] quality care. For ovarian cancer, it’s really important that people are able to receive guideline-adherent care, and that’s something that socioeconomic status is likely impacting.”
Even with good care, Harris added that Black women may face racism from healthcare providers (HCPs) when seeking treatment. She notes that structural racism may play a role in disparities among Black women with ovarian cancer. Structural racism is the various ways in which society limits resources, opportunities, power and well-being of people based on their race and/or ethnicity.
A 2022 research article found that structural racism that affected Black women’s finances led some to go without reproductive healthcare or face barriers to seeking care, which can include:
Researchers also discovered that individual racism led to some women choosing to receive healthcare from same-race HCPs.
Because racism can play a large role in health outcomes for Black women, Harris also said that HCPs need to address their biases to provide better care to Black patients.
“[HCPs must] uncover their own unconscious bias and make sure that they’re giving patients the best care they can,” Harris said.
Here are ways you can advocate for yourself to get the healthcare you need and increase your chances of survival from ovarian cancer:
This educational resource was created with support from Merck.
En los setentas y ochentas, el aroma de piñas coladas flotaba en la brisa marina en todas las playas de EE.UU. Durante los veranos, antes del invento de protectores solares en latas de aerosol, mis amigas y yo nos bañábamos en aceites con esencias de frutas tropicales en búsqueda de un bronceado perfecto. Estábamos sumamente seguras de que protegíamos nuestras pieles responsablemente contra los peligrosos rayos del sol. Después de todo, los frascos de Hawaiian Tropic alardeaban un factor de protección solar (FPS) de 2. No tienes que ver las fotos Polaroid tan de cerca para ver que estábamos efectiva y eficazmente friéndonos en aceite.
Algunas de nosotras pagamos por nuestros bronceados (y, siendo honesta, algunas quemaduras de sol) con pieles deterioradas por el sol. Pero, ¿fue nuestra búsqueda por el brillo perfecto también la causa de las nuevas tasas alarmantes de cáncer de la piel? Este año, la Sociedad estadounidense contra el cáncer pronostica que Estados Unidos alcanzará un nuevo y macabro récord: Por primera vez se anticipan 2 millones de diagnósticos de cáncer. Y el tipo más mortal de cáncer de piel, el melanoma, tiene uno de los mayores crecimientos.
El melanoma es el quinto tipo más frecuente de cáncer en EE.UU. y cada vez se vuelve más común. De hecho, las tasas de melanoma han aumentado por más de un 320% desde 1975 en la mayoría de países en los que viven principalmente personas de pieles claras. Y en 10 años desde 2013 a 2023 hubo un aumento del 27%.
Entonces, ¿qué causó este aumento?
Un estudio sugiere que el aumento de las tasas de obesidad es un factor importante. La obesidad es un factor de riesgo conocido de melanoma porque causa cambios corporales, tales como inflamación continua y mayores niveles de insulina, los cuales pueden causar cáncer. Y las tasas de obesidad casi se han triplicado para las mujeres y cuadruplicado para los hombres desde 1975.
Se necesita más investigación, pero evidencia sugiere que los factores medioambientales también juegan un papel importante. Se sospecha que el cambio climático es un factor importante del aumento de casos de melanoma y se estima que una reducción del 10% del ozono estratosférico causará 300,000 casos adicionales de cáncer de piel.
Otra causa puede ser el uso de camas bronceadoras en interiores. Afortunadamente, el uso de dispositivos para bronceado en interiores ha disminuido en años recientes. Pero la popularidad de su uso en los noventas podría ser la causa de algunos de los casos que estamos viendo hoy.
Con todo el progreso de concientización que se logró para que las personas no se bronceen sin protección, tendencias nuevas de las redes sociales podrían estar poniendo este progreso en riesgo. Una tendencia reciente de TikTok invita a personas jóvenes a que se bronceen cuando los índices de luz UV son más altos, cuando los rayos solares son más fuertes, el cual es el momento más peligroso en el que se puede tener exposición.
La exposición a la radiación ultravioleta (UV) sin protección siempre ha sido el mayor factor de riesgo de melanoma, pero el color de la piel, de los ojos, las pecas, sistemas inmunológicos debilitados y los antecedentes familiares también juegan un papel importante (aproximadamente 1 de cada 10 personas que reciben diagnósticos de melanoma tienen un familiar cercano con antecedentes de la enfermedad).
Independientemente del riesgo que tengas de melanoma, puedes tomar medidas para reducirlo. La forma más efectiva para lograrlo es hacer que la protección solar sea un hábito y someterte a examinaciones en una forma regular.
Protección solar: A pesar de lo que mis amigas y yo solíamos pensar, un protector solar con un FPS de 2 no proporciona realmente protección contra el sol. La Skin Cancer Foundation [Fundación contra el cáncer de piel] recomienda usar un producto con un FPS de entre 30 y 50 y usar protectores solares de espectros amplios, es decir que bloquean ambos tipos de rayos UV solares: UVA y UVB.
Y el uso de protección solar no debería limitarse a la playa. Siempre que haya luz, necesitas protección contra los rayos UV. Los protectores solares que son seguros para los ecosistemas de los arrecifes tienen dos funciones: Mientras protegen tu piel usando dióxido de titanio u óxido de zinc para desviar los rayos solares, estos protectores solares también son más seguros para los arrecifes de corales, los cuales juegan un papel importante en el equilibrio del clima porque absorben gases dañinos de CO2 y producen oxígeno.
La Administración de medicamentos y alimentos (FDA, por sus siglas en inglés) de EE.UU., entidad que regula los protectores solares, advierte que ningún protector solar es realmente a prueba de agua, solo son resistentes al agua, y ningún protector solar bloquea completamente los rayos solares. Para obtener la mejor protección, aplica el protector solar varias veces y con frecuencia.
Según la Skin Cancer Foundation, ropa con FPS es otra forma muy efectiva de protegerte contra los efectos dañinos del sol y contra el cáncer de piel.
Examinaciones regulares: Puedes examinar tu piel para detectar señales tempranas de melanoma. Es importante indicar que el melanoma puede manifestarse en cualquier parte del cuerpo, no solo en las partes que puedes ver. Puede formarse debajo de las uñas de tus pies o del cabello o en las membranas de la nariz o de la boca. Adopta el hábito de revisar regularmente cambios de tu piel en el espejo, incluyendo áreas que son difíciles de inspeccionar. Registra el tamaño y la forma de lunares y marcas en la piel. Puedes medir un lunar con una regla o tomar fotos para hacer comparaciones. También puedes pedir a tu peluquero o barbero que te diga si hay protuberancias o lunares sospechosos en tu cuero cabelludo. La American Academy of Dermatology [Academia estadounidense de dermatología] recomienda que tengas consultas con un dermatólogo certificado si notas cualquier protuberancia o cambio nuevo sospechoso que te preocupe o si tienes una herida que no sana.
Lee: El ABCDE para identificar melanomas >>
En tu cita, tu proveedor de atención médica inspeccionará tu piel en todo tu cuerpo, medirá y examinará cuidadosamente los elementos de tu piel tales como lunares y registrará cualquier cambio que hayas tenido en comparación con consultas previas.
Aunque las personas de color son menos propensas a desarrollar melanoma, tienen más posibilidades de recibir diagnósticos con cánceres en etapas más avanzadas y tienen más posibilidades de morir por la enfermedad. Estas desigualdades resaltan claramente la importancia de la prevención, la examinación y el acceso a tratamientos.
¿La lección? Todos, no solo los exusuarios de protectores solares con un FPS de 2, deben estar alerta.
Este recurso educativo se preparó con el apoyo de Merck.
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As told to Jacquelyne Froeber
October is Breast Cancer Awareness Month.
December is my birthday month. It was also the month I scheduled all my yearly health exams, including my mammogram.
But December 2014 was busy, I guess. (I burned all my journals from that time — but that’s another story.) I don’t remember why I didn’t go for my mammogram, but I didn’t get one until June 2015.
The day after the exam I got a phone call. There was something abnormal in the imaging, and I needed to have a biopsy. I was a nurse, so I knew that wasn’t great news, but I had the biopsy that week and went about my normal routine.
As an on-call hospice nurse, my schedule was pretty consistent. I worked seven days on, seven days off and — most important — I took a nap between 2 p.m. and 4 p.m.
My husband and kids knew not to call me during that time, so when my phone started buzzing during my nap, I was pretty annoyed. It was the provider’s office. “This isn’t a good time to talk,” I said.
“You have breast cancer,” the woman on the phone said.
“OK, can you call me back tomorrow? I’m on call at 5.”
She was startled. But she said OK. I hung up, rolled over and went back to sleep.
I know it sounds strange to just fall back asleep, but my patients depended on me. And I needed that nap. The next day my provider called and I made the time to listen. He said the cancer was small enough for a lumpectomy. So we scheduled the surgery for the following week.
By that Thursday, though, I’d noticed new imaging requests in my patient portal but no one could tell me why they were ordered.
When I finally got the nurse on the phone, I started asking her questions, and she cut me off. “Don’t worry about the tests — I do this all the time,” she said. “All you have to do is show up on Monday.”
I paused and felt the sting of being dismissed. “You may do this every day, but I’m not diagnosed with breast cancer every day,” I said. “And I will call the doctor and let him know why I’m not having the surgery with you. Have a good day.”
I hung up the phone. My mind and heart were racing. I’d just fired my provider! But I couldn’t stay with an office that wouldn’t answer my questions … right? Tears sprang to my eyes.
My husband helped calm me down and we found a different provider. I’d have to wait another month for the lumpectomy — but that was fine with me. During that time, I had the other tests that were ordered, including a PET scan. That scan showed the cancer had spread to the bone.
I had stage 4 breast cancer.
When I heard the news I was shocked. Within a week, I went from “small” cancer and a lumpectomy to plans for a bilateral mastectomy and chemotherapy. I learned that stage 4 — also called metastatic — cancer meant I would need ongoing treatment probably for the rest of my life.
Amid all the confusion and depressing news — there was a bright spot. My daughter had just found out that she was pregnant despite being told she couldn’t have children. The thought of holding my grandchild gave me extra hope that I could get through the surgeries and treatments and also keep my quality of life so I could enjoy time with my family.
The months went on, and after the baby was born, I’d put him on my chest despite the double mastectomy, and we would sleep like babies on my days off of work.
I continued working as much as I could through chemo but it was tough. I felt weak. I couldn’t even drive to work — my husband had to drive me. But I put on my bandana and pushed forward. In 2016, I got the best news: My scans showed no evidence of disease.
In 2017, I felt good enough to move, and my husband, John, and I relocated to a small town in eastern North Carolina. I got a new job as a hospice nurse.
We were only there for about six months when I had a blood clot in my left lung. Then, because of the blood thinners I was on, I had a ministroke. And then one more devastating blow: My provider said I couldn’t work anymore.
I was crushed. I’d been working for almost 40 years. I was the primary breadwinner in our family. Now, I wasn’t going to have income or insurance.
I spent the next seven days looking for financial resources that could help me pay for my medical treatments. I applied for disability — and got it — but it wouldn’t kick in for five months.
Then I came across an organization called Living Beyond Breast Cancer that offered funding and resources for people with metastatic breast cancer. They were hosting an annual conference in Philadelphia, and I decided to go.
At the time, I really didn’t know much about metastatic breast cancer outside of my personal experience. I’d also never met another Black woman with metastatic breast cancer. When I walked into the conference hall, I was blown away by the sheer number of people there. I probably looked like a deer in headlights going from booth to booth, but everyone was so kind and helpful. I got the financial guidance I needed. I heard stories from women who were eight and nine years into their diagnosis and thriving. I bonded with other Black women with metastatic breast cancer. All of it changed my life.
After the conference, I signed up for everything I could do as far as advocacy work for the organization. I traveled all over the U.S. and learned about the disease and new treatments and brought information back to my rural community in North Carolina. I’d learned that breast cancer rates are higher in women who live in rural areas and death rates are higher too compared to the national average. And these numbers are worse for women of color.
Early on, it became clear to me that information regarding Black people and metastatic breast cancer was lacking. But it wasn’t clear why. In 2019, I started working with an epidemiologist, Marina Pomare Kaplan, on a research project and survey that focused on the reasons why Black people weren’t being included in these clinical trials.
Unfortunately, Marina passed away in 2020. I thought that meant our research efforts were done, but a few months later, the Metastatic Breast Cancer Alliance contacted me and wanted to move forward.
We started the BECOME research project based on the research Marina and I had been doing. BECOME stands for Black Experience of Clinical Trials and Opportunities for Meaningful Engagement. And what we found with our survey was a big shocker. The overall reason why Black people weren’t being involved in clinical trials? It was because no one was asking us to participate. No one was having a conversation with us.
From there, I thought, Let’s find a way to get this information to providers. We planned an event the day before the San Antonio Breast Cancer Symposium in 2022, which is basically the biggest breast cancer conference in the world. It was my goal to have 100 people there — or fill half the seats in the room.
But that didn’t happen. The event was so packed I had to grab spare folding chairs. People lined up against the wall to listen to our research.
As I looked out at all the different faces in the room, I was overcome with emotion. I felt so proud to get all these people — providers, pharmaceutical reps, women of color — together in the same room to learn about the importance of including Black people in clinical trials for metastatic breast cancer.
I thought about how far I’d come in my own journey — although I hate to call it a journey. It just doesn’t sound right when you’re talking about being bald and going to chemo. But being a patient advocate helped me help other people when I couldn’t through nursing anymore.
None of us signed up to be in this club. But all of us deserve representation and research to help us live our best lives with metastatic breast cancer.
BECOME – Black Experience of Clinical Trials and Opportunities for Meaningful Engagement
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Our Real Women, Real Stories are the authentic experiences of real-life women. The views, opinions and experiences shared in these stories are not endorsed by HealthyWomen and do not necessarily reflect the official policy or position of HealthyWomen.
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In the 1970s and ’80s, the smell of piña coladas wafted through the ocean breeze at every U.S. beach. In the summers before the invention of spray-canned sunscreen, my friends and I basted ourselves with tropical-fruit-scented tanning oils in a quest for the perfect tan. We felt smugly confident we were responsibly protecting our skin from the sun’s harmful rays. After all, our Hawaiian Tropic bottles boasted a sun protection factor (SPF) of 2. You don’t have to look too closely at the Polaroid pictures from this time to see that we were effectively and efficiently deep-frying ourselves in oil.
Some of us have paid for our tans (and, to be honest, a few sunburns) with sun-damaged skin. But was our youthful search for the perfect sun-kissed glow also behind the new alarming rates of skin cancer? This year, the American Cancer Society predicts the United States will reach a new, grim milestone: 2 million cancer diagnoses are expected for the first time ever. And the deadliest form of skin cancer, melanoma, is among the most quickly growing types of cancer.
Melanoma is the fifth most common cancer in the U.S., and it’s only getting more common. In fact, melanoma rates have risen by more than 320% in mostly fair-skinned countries since 1975. And in the 10 years from 2013-2023, there was a 27% increase.
So what’s behind this increase?
One study points to the rise in obesity rates as a factor. Obesity is a known risk factor for melanoma because it causes changes in the body, like ongoing inflammation and increased insulin levels, that can lead to cancer. And obesity rates have nearly tripled in women and quadrupled in men since 1975.
More research is needed but some evidence points to environmental factors playing a role as well. Climate change is suspected to be a factor in the rising cases of melanoma, and it’s estimated that a 10% reduction in stratospheric ozone will cause 300,000 additional skin cancer cases.
Indoor tanning bed usage could be another culprit. We can breathe a sigh of relief that indoor tanning usage has decreased in recent years. But the surge in usage in the 1990’s could be accounting for some of the cases we’re seeing today.
With as much progress as we’ve made getting the word out not to tan without protection, new social media trends could be putting this progress at risk. A recent TikTok trend encourages young people to tan during the highest UV indexes, when the sun’s rays are the strongest, which is the most dangerous time to be exposed.
Ultraviolet (UV) exposure without protection has always been the biggest risk factor for melanoma, but skin color, eye color, freckles, weakened immune systems and family history also play a role. (Around 1 in 10 people diagnosed with melanoma have a close family member with a history of the illness.)
No matter what your risk for melanoma is, you can take steps to reduce it. The most effective way to do this is by making sun protection a habit and having regular screening.
Sun Protection: Despite what my friends and I used to think, sunscreen with an SPF of 2 is not really sunscreen. The Skin Cancer Foundation recommends using a product with an SPF ranging between 30 and 50, and using broad spectrum sunscreen, meaning one that helps to block both types of the sun’s UV rays: UVA and UVB.
And sunscreen use shouldn’t be limited to the beach. Anytime it’s light out, you need protection from UV rays. Sunscreens that are reef-safe do double-duty: While protecting your skin using titanium dioxide or zinc oxide to deflect the sun’s rays, these sunscreens are also safer for coral reefs, which play a role in climate balance by absorbing harmful CO2 gases and creating oxygen.
The U.S. Food and Drug Administration (FDA), which regulates sunscreen, warns that no sunscreen is truly waterproof — just water-resistant — and no sunscreen completely blocks the sun’s rays. For the best protection, reapply your sunscreen frequently.
According to the Skin Cancer Foundation, SPF clothing is another very effective way to protect yourself against sun damage and skin cancer.
Regular Screening: You can screen your own skin for early signs of melanoma. It’s important to note that melanoma can appear on any part of the body, not just the parts you can see. It can form under toenails or hair, or in the membranes of the nose or mouth. Make a habit of regularly checking for skin changes in the mirror, taking care to investigate hard-to-inspect areas. Note the size and shape of moles and skin markings. You can measure a mole with a ruler or take pictures for comparison. You can also ask your hairdresser or barber to point out suspicious growths or moles on your scalp. The American Academy of Dermatology recommends that you see a board-certified dermatologist if you notice any suspicious changes or new growths that concern you, or if you have a wound that won’t heal.
Read: The ABCDEs of Spotting Melanoma >>
At your appointment, your healthcare provider will inspect your skin over your entire body, measuring and closely examining skin features such as moles and noting any changes from previous visits.
While people of color are less likely to get melanoma, they are more likely to get diagnosed with a more advanced stage cancer and are more likely to die from the disease. These disparities clearly outline the importance of prevention, screening and access to treatment.
The takeaway? Everyone — not just the recovering SPF2 sunscreen users — should be vigilant.
This educational resource was created with support from Merck.
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