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3 11, 2025

Caring for a Partner with Prostate Cancer

By |2025-11-03T16:22:23+02:00November 3, 2025|Fitness News, News|0 Comments


November is National Family Caregiver’s Month.

I met my husband while I was registering for journalism classes at the University of Missouri 50 years ago. Dean was standing in line behind me and asked me out for a beer. I scoffed and said no.

When I got to the registration table, the class I needed was full. Dean stepped up and introduced me to the instructor. It turned out Dean had had dinner with him the night before, and the man had written a book on suburban journalism that included Dean’s father, a publisher of a chain of weekly newspapers in Ohio.

The instructor made room for me in the class, and I wound up going out for that beer.

After we got married, Dean and I realized it would be difficult for us both to stay in journalism. He decided to go into sales, while I pursued editing jobs. We moved seven times for my work, requiring him to find a new job each time. He never minded.

He championed my career, edited my resumes, provided tech support and wore a tux as my plus one to events I attended as an arts editor. He took care of me.

After we retired, he was diagnosed with stage 4 metastatic prostate cancer. We were dazed. I had always assumed I would receive the first life-threatening prognosis given my mother’s two bouts with breast cancer before she turned 50 and her eventual death from lymphoma.

There was no history of prostate cancer in Dean’s family. Neither of his parents, who lived to be 89 and 94, died from cancer.

It was my turn to take care of him. I became his nutritionist, personal trainer, cheerleader and sex therapist.

For the first two years, he was prescribed a treatment plan of radiation and androgen deprivation therapy (ADT), which is chemical castration. These drugs eliminate interest in sex as well as the ability to have an erection. For my husband, this was the cruelest part.

He mourned losing his libido. Despite the fact he no longer felt desire, he refused to give up on sex for me. We navigated this by using a calendar where I would draw hearts on days of intimacy. That way he was able to keep track and not let weeks pass. To declare his intent, he bought me a black silk nightgown weeks after his diagnosis.

There were other side effects. During this time, he suffered from mental fog, hot flashes, lost muscle tone, insomnia and weight gain.

I changed our diet to follow cancer nutrition guidelines — plant- and protein-based — and added pilates, yoga, weights and swimming laps to his regular pickleball practice.

To counter the mental fatigue, I write a to-do list daily, and created a check system to use before he leaves the house. Does he have his phone, keys, hat, water bottle, wallet?

Now in year four, Dean has castrate-resistant prostate cancer, meaning the basic drugs no longer work. He’s had two rounds of targeted radiation treatment, but more spots keep popping up. He’s undergoing chemo, which brings a whole new set of woes. He fights dizziness, increasing fatigue and appetite changes.

He stopped enjoying coffee or his cocktail of choice, an Old Fashioned. He needs to be reminded to drink water. He resists greens, which I put in his morning smoothie.

We program his daily naps. I lie down next to him, face-to-face, holding his hand until he falls into a deep sleep.

2025

A surprising consequence of the disease has been ghosting. While cancer isn’t contagious, a few family members and long-time friends have disappeared from our lives.

Fortunately, we found community and counseling at Wellness House, a cancer support center that offers hundreds of programs for free. Dean attends a prostate cancer support group, where he finds comfort in conversations with peers. He also goes to a general cancer group and receives individual counseling from an empathetic clinical psychologist there.

I frequent a cancer caregiver support group where I sometimes find stories sadder than mine.

The community we’ve found has helped us deal with the anxiety before PSA tests, PSMA-PET scans and messages on MyChart. We now understand we no longer live in the land of what ifs. We are planning for what’s next.

I put up two whiteboards in our house. One tracks what must be done: Revise the will, register the vehicles in both our names, simplify finances, write down passwords and have “The Will” discussion with our two adult children.

The other board is titled “Living Our Best Lives.” We may be running out of tomorrows, but we still have adventures to take.

We plan in quarterly increments: An October European trip to experience three of the world’s great opera houses, walking Aruba beaches in December, rally driving school for Dean in June, celebrating our daughter’s 40th birthday in Hawaii in December 2026 and making it to our 50th wedding anniversary May 2027.

But cancer takes no vacation in your mind. I wake up with a stomachache of despair and anticipatory grief. What will it be like to live without my best friend, the man I’ve cocooned with for 2/3 of my life?

We keep busy so we have little time to wallow. Even as we pass the tissues, we make conscious decisions to find pleasure and laughter. Sometimes we have a no-cancer-talk day.

Dean is happiest exercising with his pickleball gang, playing online poker with his brother-in-law and spending time with our grandchildren. He hopes to leave them with many memories.

Dean calls himself the luckiest unlucky guy around. He is serene with his choices. He loves and has been loved deeply.

We have found that even when there is no light at the end of the tunnel, joy can still be found along the way. It just takes resolve to look for it.

This educational resource was created with support from Bayer and Merck.

Have your own Real Women, Real Stories you want to share? Let us know.

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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30 10, 2025

Managing Atopic Dermatitis in Kids

By |2025-10-30T23:34:19+02:00October 30, 2025|Fitness News, News|0 Comments

October is Eczema Awareness Month.

If your childhood memories include scratching miserably at your itchy skin while an adult gently scolded you to stop or you’d make it worse, you’re far from alone.

More than 9.6 million children in the United States are affected by atopic dermatitis (AD), a chronic inflammatory skin condition that causes red, itchy patches all over the body. The most common type of eczema, AD often starts before the age 5 — and about one third of kids who have it are hit with a moderate to severe case.

Caring for children with AD can be tough on the whole family, said Teresa Wright, M.D., chief of pediatric dermatology at Le Bonheur Children’s Hospital in Memphis, Tennessee.

“If a child has more moderate to severe eczema and they’re miserable, they’re itchy, they’re scratching until they bleed, they’re getting infections, sometimes ending up in the hospital — all of this does affect the whole family,” Wright said.

She added that childcare providers and teachers don’t always know how to handle AD, so parents may get called away from work to pick up their kids. “It literally can interfere with a family’s ability to make a living,” Wright said.

Understanding AD treatment options, along with how to talk to healthcare providers (HCPs) about them, may help lighten your family’s load.

AD Treatments for Kids

Treating atopic dermatitis can be a big job that includes keeping skin hydrated, reducing itching and treating inflammation while also preventing or managing infections. Some of the treatments for kids with AD are:

  • Topical corticosteroids — creams or ointments to help with itching and inflammation (swelling)
  • Emollients (moisturizers) — lotions, gels, creams and ointments that help with dryness
  • Topical calcineurin inhibitors — creams or ointments that help calm the immune system and prevent itching and inflammation
  • Topical PDE4 inhibitors — creams and ointments that block an enzyme involved in inflammation
  • Biologics — injected medicines made from living cells that teach the immune system to target chemical messengers that cause inflammation
  • Phototherapy (light therapy) — involves shining UV light onto the skin to lower the number of certain cells that trigger inflammation
  • Antibiotics — medicines used to treat skin infections
  • Antihistamines — don’t treat AD, but may help itchy kids sleep better

Which of these treatments is right for your child depends on many variables.

“I think the main factor is how severe their atopic dermatitis is, and the age of the child might also determine what treatments we are able to recommend,” Wright said. “I also try to keep in mind parents’ resources and ability to access medications and treatments, and we have to consider what will be covered by insurance.”

Talking to providers about treatment for atopic dermatitis

With so many options for treating kids with AD, it’s important that caregivers and HCPs share as much information as possible.

For parents, this might involve an honest conversation about how AD affects their child’s daily life — physically, emotionally and socially. If AD is keeping your child (and your family) from living your best lives, a provider needs to know so they can help figure out a way to make it better.

Caregivers should also ask HCPs about the most common AD triggers (like dry air, heat, irritating fabrics, and allergens like pollen and pet dander). An HCP can also offer advice on how to track your child’s personal AD triggers and what to do about them.

Finally, if you’re consulting a new HCP, parents will want to be prepared with a list of AD treatments or remedies that have already been tried, along with some notes about how well they worked (or didn’t).

Keeping calm and connected

Caring for children with AD isn’t easy, but shifting your mindset may help your days go more smoothly. As hard as it can be to keep your cool in chaotic moments — like when you’re trying to apply ointment to a wriggling toddler — patience is key to treating your child’s AD. So is consistency, since many treatments take time (and regular application) to work.

Wright emphasized the importance of carefully following instructions and sticking to a regular, daily skincare routine. “I’m always saying the devil is in the details,” she said.

Staying in close contact with your child’s HCPs can also be helpful, particularly when it comes to sharing anything you notice about AD triggers and symptoms — or your concerns about treatments.

“If you’re nervous about using a particular thing or you’ve heard something that makes you reluctant to follow some advice I’m giving, we can talk about that,” Wright said. “I’m on your side.”

Importance of innovation in atopic dermatitis treatment

With so many kids struggling with AD, it’s no surprise that experts are always working to figure out new ways to treat this complicated condition.

“We have a number of new non-steroid topical options that can be appropriate for some situations,” Wright said. “And in more recent years, we’ve had more systemic medication options.”

As hard as it may be to watch your child suffer, you can take heart knowing that treatments are out there — it’s just a matter of finding the right one.

This educational resource was created with support from Organon, a HealthyWomen Corporate Advisory Council member.

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30 10, 2025

Types of Melanoma – HealthyWomen

By |2025-10-30T20:32:19+03:00October 30, 2025|Fitness News, News|0 Comments

Medically reviewed by Elizabeth Liotta, M.D.



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28 10, 2025

8 cosas que debes considerar si tienes cáncer cervical

By |2025-10-28T20:04:16+03:00October 28, 2025|Fitness News, News|0 Comments

English

Someterse a tratamientos contra el cáncer no es una hazaña fácil. Las terapias intensivas, los cambios de tu cuerpo y los temores de recurrencia son comunes para mujeres que se han sometido a tratamientos contra cáncer cervical. Pero la recuperación no termina cuando concluye el tratamiento. Las sobrevivientes podrían tener que lidiar con cambios físicos, emocionales y sexuales a largo plazo.

Saber qué esperar después del tratamiento puede ser útil para que te prepares y sientas más calma para seguir adelante.

Aquí encontrarás 8 cosas que deberías saber si tuviste o tienes cáncer cervical.

1. La supervivencia podría significar ajustarse a un “nuevo estándar de normalidad”

La carga emocional, física y mental del tratamiento puede persistir durante mucho tiempo después del final del tratamiento. “Muchas sobrevivientes experimentan fatiga, cambios de la salud sexual, síntomas tempranos de la menopausia y angustia relacionada con una posible recurrencia”, dijo Kathryn Miller, M.D., oncóloga ginecológica certificada de Capital Women’s Care. “Lo más importante que debes saber es que no tienes que enfrentar estos desafíos sola, podemos anticipar muchas de estas dificultades y proporcionar tratamiento o facilitar acceso a asistencia temprana”.

2. El tratamiento podría afectar tu fertilidad y salud reproductiva

Los tratamientos contra el cáncer cervical tales como cirugías, radiación y ciertos fármacos quimioterapéuticos podrían afectar la fertilidad. Podrían causar daños a los ovarios, el útero y el cuello uterino, órganos clave para un embarazo.

La buena noticia es que hay métodos para preservar la fertilidad. “Para mujeres que todavía desean tener hijos [biológicos], siempre tratamos de hablar de opciones para preservar la fertilidad antes de que el tratamiento empiece, tales como cervicectomías uterinas (remoción del cuello uterino preservando el útero) o el congelamiento de óvulos o embriones”, dijo Miller.

Lee: El embarazo y el cáncer cervical: Conoce tus opciones >>

3. Es conveniente estar pendiente de linfedemas

El linfedema es una hinchazón que puede desarrollarse después de radioterapias, cirugías pélvicas o remociones de los ganglios linfáticos. Comúnmente se manifiesta en los brazos y piernas, pero también puede afectar otras áreas del cuerpo.

El linfedema es un síntoma frecuente después de tratamientos contra el cáncer cervical, por lo que reconocerlo es clave. “Si notas una sensación de pesadez, presión o hinchazón de las piernas, avisa a tu equipo de atención inmediatamente, entre más temprano lo abordes, mejor será el desenlace clínico”, dijo Miller.

4. Las relaciones sociales pueden cambiar

Un diagnóstico de cáncer puede cambiar la dinámica con tu familia, amigos y especialmente con tus parejas. Las sobrevivientes podrían tener que lidiar con la intimidad emocional y física después del tratamiento, lo cual podría afectar sus relaciones.

Miller dijo que tener una comunicación abierta es clave. “Asesoría, ya sea mediante terapia individual o para parejas, puede marcar una diferencia importante”, explicó. “Grupos de apoyo con otras sobrevivientes también podrían proporcionar una sensación de conexión social y solidaridad compartida”.

5. Los cambios vaginales son frecuentes, pero hay ayuda disponible

Muchas sobrevivientes notan cambios de sus vaginas después del tratamiento. Estos cambios podrían incluir sequedad, una vagina más corta o delgada y dolor durante las relaciones sexuales. Si sientes molestias, hay algunas opciones que puedes analizar con tu proveedor de atención médica (HCP, por sus siglas en inglés).

Estas incluyen:

“También es importante hablar abiertamente con tu proveedor médico acerca de cualquier dolor o sangrado, hay soluciones y no tienes que simplemente vivir con eso”, agregó Miller.

6. Las ostomías son infrecuentes, pero prepárate por si acaso

Una ostomía crea una apertura (un estoma) en tu estómago para recolectar heces u orina en una bolsa removible. Miller dijo que la mayoría de sobrevivientes de cáncer cervical no la necesitan a menos que el trastorno esté en etapas avanzadas o que la cirugía requiera la remoción de la vejiga o el recto.

“Si se requiere [una ostomía], pasamos mucho tiempo preparando a las pacientes para que sepan qué esperar y les brindamos acceso a enfermeras que tienen experiencia con la ostomía”, dijo. “Muchas personas pueden disfrutar de vidas plenas y activas con una ostomía”.

7. Podría ocurrir una menopausia quirúrgica

Cirugías tales como remociones de los ovarios (ooforectomías) o del útero (histerectomías) podrían desencadenar el inicio de la menopausia. Esto ocurre cuando se remueven los ovarios o el útero. Miller explicó que la menopausia quirúrgica puede reducir los niveles de estrógeno y progesterona.

Esta disminución puede causar síntomas tales como:

Si notas cualquiera de estos síntomas, comunícate con tu proveedor de atención médica para hablar sobre opciones terapéuticas. “Trabajamos de cerca con las pacientes para controlar estos síntomas, a veces con reemplazo hormonal (si es seguro para su tipo específico de cáncer), a veces con medicamentos no hormonales y siempre con asistencia relacionada con el estilo de vida para mantener la salud de los huesos y del corazón”, dijo Miller.

8. Las disparidades pueden afectar la supervivencia

No todas las sobrevivientes obtienen el mismo acceso a la atención. Factores tales como el racismo, la falta de acceso a atención de buena calidad, el estatus socioeconómico, la edad y retrasos de diagnósticos podrían dificultar la recuperación. Estos desafíos frecuentemente afectan principalmente a sobrevivientes de bajos ingresos y a mujeres de color.

Un estudio demostró que las mujeres de raza negra e hispanas eran más propensas a no tener seguro médico que las mujeres de raza blanca no hispanas. Las mujeres de raza negra también tienen las mayores tasas de mortalidad y las menores tasas de supervivencia para un tipo de cáncer cervical denominado adenocarcinoma cervical.

“Puesto que somos proveedores médicos, tenemos la responsabilidad de reconocer estas disparidades y ayudar a remover obstáculos dando acceso a las pacientes a recursos comunitarios, a programas de orientación para pacientes y a asesoría financiera”, dijo Miller. “Todas las sobrevivientes merecen el mismo acceso a atención de alta calidad, independientemente de sus antecedentes”.

La vida después del tratamiento puede acarrear muchos desafíos, pero no tienes que enfrentar los sola. Si notas cualquier cambio de tu salud emocional, mental o física, por favor, comunícate con tu proveedor de atención médica. El podrá ayudarte a preparar un plan terapéutico personalizado. Este plan puede ser útil para controlar los síntomas, fomentar la recuperación y mantener tu calidad de vida.

Este recurso educativo se preparó con el apoyo de Merck.

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28 10, 2025

Stroke Risk for Women – HealthyWomen

By |2025-10-28T18:03:16+03:00October 28, 2025|Fitness News, News|0 Comments

Medically reviewed by Nieca Goldberg, M.D., FACC



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28 10, 2025

As a Breast Surgeon I was Diagnosed with Breast Cancer

By |2025-10-28T16:02:25+03:00October 28, 2025|Fitness News, News|0 Comments


October is Breast Cancer Awareness Month.

As told to Marnie Goodfriend

All I ever wanted to do was become a doctor. My dad was a surgeon, and my mom was a nurse. I received a PhD in the genetics of cancers and spent my 30s training to become a breast surgeon. I loved the human body, and I loved operating. It was my life. But I never checked my own breasts. I thought, “I’m a doctor. I’m not going to get breast cancer.” I was healthy, had no history of breast cancer in my family and felt invincible. I had recently gotten engaged and had just signed up for my first triathlon when I saw a lump. It ended up being just a cyst, and I still didn’t check my breasts.

Two and a half years later, a month after I had cycled up the Stelvio Pass, a major mountain pass in Italy, I found another lump. My mammogram was normal, but when I got my ultrasound scan, I looked at the screen and saw cancer. The surgeon was my friend and a mentor who had trained me. She saw what I saw and asked me, “Who do you want to treat you because I don’t think I can?”

I had a week of waiting for the formal results, but as a doctor, I knew too much. I told my parents, “In a week, I’ll be telling you I have breast cancer.” It’s like I dissociated from myself. The results were positive for stage 3b breast cancer, and I started chemotherapy to shrink it down. Suddenly, I was about to undergo every treatment that I gave my patients, realizing how little I knew, how scared I was and how huge the decisions are that women with breast cancer need to make in a very short period of time.

The chemotherapy drugs — every three weeks for five months — were horrible. You lose everything — your fertility, your dignity, your power, your hair, your nails, your sense of pride. I didn’t know how to navigate being intimate with my husband: Do you touch the breast or not? How do I function in the world? The chemo treatments brought on instant menopause, so I had brain fog, hot flashes, and night sweats so bad I thought I wet myself in bed. You’re dealing with these instant changes to your body and your life while being really ill.

(Photo/Liz O’Riordan)

The week before Christmas in December 2015, I had a mastectomy with an implant reconstruction, and they took a couple of my lymph nodes out. But sadly, there were 13 centimeters of cancer left in my breast, and it had spread to my lymph nodes. So, the following month, I had another surgery to remove all my lymph nodes, and in April 2016, I had radiotherapy (that’s what we call radiation in the UK) and was put on a drug to try and stop the cancer coming back. During this time, I couldn’t work, and it took about another eight months once treatment had finished to get my energy levels and immune system back up to be able to work again.

When I returned, I was shadowing another doctor to make sure I was safe to practice. As a cancer patient, it was extremely difficult to tell patients they had cancer. It felt like I was reliving my own diagnosis, and knowing how much they would hurt post-surgery was mentally challenging. Everyone was asking me how I felt after the cancer, but I just wanted to be Liz.

With cancer, your identity suddenly changes. People didn’t recognize me because I used to have long hair, and now it was short and gray. I went to a local hospital where I’d worked as a junior doctor and saw the woman who had trained me. The only way she could treat me was to stop being my friend to try to reduce the emotional toll of operating on someone you know. It was really hard to be operated on and treated by colleagues of mine and my husband who is also a surgeon.

As a Breast Surgeon I was Diagnosed with Breast Cancer (Photo/Liz O’Riordan)

I found myself at home alone, unable to have children. I lived in a small village and didn’t have many friends. I’d lost my job, my purpose, my identity and my financial security. I started blogging weekly about my experience and decided the day after I got my diagnosis, to “come out” on Twitter. I used to tweet about triathlons and baking. Now, I was flooded with information and support from people all over the world. They told me, a breast cancer surgeon, how to cope with chemotherapy, what toothpaste is best if your mouth is sore and recommended cookbooks. Overnight, I had an instant network of women supporting me. With my writing, I wanted to offer a sensible opinion that wasn’t reactionary — and doctors and nurses thanked me for doing so. I realized I could help people in a different way.

I began explaining breast cancer with videos, writing and posts on social media, using my dual experiences as a surgeon and patient to reach people around the world to help them navigate cancer. In some ways, it was more fulfilling than being a doctor. I could connect with patients on an intimate level and encourage healthcare providers to talk about sex, menopause and how to help people live after you’ve operated on them, not just be alive. The growing community also shared important resources like CoppaFeel!, a UK-based organization that teaches you how to examine yourself properly and sends a text reminder on the first of every month to check your breasts.

In the spring of 2018, I noticed a nodule on my chest underneath my left armpit. It was a recurrence on my chest wall, and that meant I had to have my implant taken out, and more surgery and radiotherapy. I had my ovaries removed in September 2018, and I was put on a different hormonal blocking tablet to stop the cancer from coming back. I received a lot of therapy and treatment for my left arm because I couldn’t lift it very high, and to perform reconstructions, you have to contort yourself into awkward positions. Psychologically, I was a mess. I was so fearful of the cancer returning that I couldn’t be around women who were having recurrences, so I ended up retiring at 43.

This led to a collaboration with another local doctor who’d been diagnosed with breast cancer around the same time as me. Between us, we had bought 20 books about being a breast cancer patient and read questions on the internet like, “Is it safe to have sex during chemo?” “Will my husband’s hair fall out, too?” “Should I be detoxing?” You want to connect and be hugged, but there are men out there who are sleeping in separate bedrooms because they’re scared they’re going to catch cancer. We wanted to tell younger women to start taking preventive measures now, and if you’re already getting mammograms, the importance of checking your breasts in between.

Liz receiving Humanitarian Award, 2024 Liz receiving Humanitarian Award, 2024

To dispel misinformation online and support patients, we decided to write a common-sense book about breast cancer, answering every question patients have from diagnosis to death. I’m deeply concerned about the rise of false information and people pushing alternative therapies and scams to make money. People believe them, and women in their 30s and 40s are dying because they’re doing something on TikTok instead of believing healthcare providers. Our book covers sex, exercise and mental health. We now know that exercise can reduce the physical and mental side effects of cancer and the risk of recurrence. It also helps fight fatigue. Before cancer, I was all about the data, my heart rate and ideal heart rate zones. Now, I show up to local park runs and cycle with people because I’ve made lasting friendships, and it brings me joy. I’ve got into wild swimming as well, swimming in rivers in the wintertime.

In 2022, six months after my mother passed from metastatic cancer of her right arm, my breast cancer came back in the skin near my mastectomy scar. I had more surgery, and now I get monthly injections and take a low-dose form of chemo I’ll be taking for the rest of my life, but the fact that I could use this horrible experience for good changed me. Sharing my writing online paved the way to becoming a published author and being asked to give a TEDx talk to help and protect breast cancer patients and the people who love them. I talk about how I never thought I’d feel like a woman again — I just looked like an alien. Then, I remembered when I was operating, all I could see of people was their eyes, which made me realize I don’t need external attributes to define me. Having a different relationship with ourselves and our bodies starts from the inside.

Today, I speak at events and conferences around the world, have a robust following on social media, and in 2024, I received a Humanitarian Award presented to me by Elizabeth Hurley. My new book, The Cancer Roadmap, will be released this November, and I’m working on another book about food and going into season four of my podcasts. But, I also have to remind myself that I have breast cancer, which means taking more time for myself. More river swimming, more walking the dog, more peaceful moments in the garden.

Resources

The Brem Foundation

The Get in Touch Foundation

Susan G. Komen Foundation

Breast Cancer Research Foundation

Have your own Real Women, Real Stories you want to share? Let us know.

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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28 10, 2025

Exercise For Building Better Bones

By |2025-10-28T14:01:16+03:00October 28, 2025|Fitness News, News|0 Comments


Exercise is an important component in the overall strategy for improving the health and strength of your bones. The optimal exercise regime for preventing osteoporosis has yet to be established, but these guidelines are based on our current state of knowledge. We do know that exercise works best when you have adequate levels of estrogen, calcium intake and vitamin D. The diet should be low in fat with emphasis on cereals ,fruits and vegetables.

We think of bones as solid, rocklike structures, instead they’re living tissue that is constantly changing. Peak bone mass usually occurs between age 20 and 30 and then slowly declines. Bone loss accelerates during the first several years following menopause. A Recent study indicated that a fat-laden diet could lead not only to obesity and heart disease but to the thinning, fragile bones of osteoporosis. The foods we eat, the amount of physical activity we perform and various environmental and genetic factors contribute to bone health. If you have been diagnosed with osteoporosis , check with your physician before starting any exercise program.

Effect of good/bad Posture:

How we work, play, sit and move can determine the chronic stress placed on our spine. Viewed from the side, the spine is shaped like an S-curve. It is ten times stronger when these natural curves are maintained. Good posture and body mechanics can alleviate/prevent back pain and protect your spine against fracture.

Posture:

  • When standing, an imaginary vertical line should connect your ear, shoulder & hip.
  • Don’t lock your knees. Stand with feet straight ahead or slightly turned out.
  • Pull in your stomach muscles so as to prevent a sag.
  • Maintain a normal (not flat or exaggerated) curve in your low back.

Sitting:

  • Do NOT sit or stay in the same position for prolonged periods of time.
  • Sit in a firm, straight-back chair with your buttocks all the way back.
  • Use a lumbar roll to maintain the natural curve in your low back.
  • Tuck your chin in and pull your head straight back.
  • To get out of a chair, slide forward without slouching and then stand up.
Exercise For Building Better Bones

Moving & Lifting:

  • Keep an upright back.
  • Use your legs instead of your back ,when you lift even the lightest object. Keep a wide base of support. Squat down, keeping your chest upright.
  • Avoid forward bending. If you must lean forward, bend where your legs meet your trunk, NOT at your waist.
  • When lifting, hold objects close to you. Keep the activity close to your body.
  • Avoid twisting movements. Always point your feet in the direction you’re moving.
  • It requires lots of practice before new ways of performing daily tasks become a habit. But the payoff is long-term back health. Observe how many times you bend over and how many hours you’re sitting during a typical day: ie. cleaning the bathtub, picking up a child, reaching for your workout bag or purse, gardening, commuting, watching t.v. or working on the computer. Start off with a few changes. Make a consistent effort to be aware of your movements and protect the normal curves of your spine.

Flexibility:

Much of our day is spent sitting or bending ,thanks to advancement of science. This can tighten some muscles and put a lot of stress on the spine. As part of an overall program of stretching, develop good flexibility in your spine, hamstrings (back thigh), hip flexors (front thigh) and pectoral (chest) muscles. Avoid forward bending exercises to prevent extra stress on the bones and discs of the spine. Stretch the muscles to a point of tension, not pain, and hold the stretch for 15-30 seconds at least 3 -5 times daily or as directed by your physical therapist.

Strength Training:

Strength training is probably one of the most important things you can do to build or maintain strong bones. During exercise muscles are challenged, to pull on their bony attachments stimulating bone formation. If you want to increase bone mass in a particular bone, the exercise must recruit muscles that attach to that bone. It has been observed that a certain strength training intensity stimulates bone growth. You must challenge a muscle to fatigue after about 8-10 repetitions, 2-3 times/week. It’s important to gradually increase resistance as your muscles become stronger, instead of cruising through a workout that has become easy. Use of free weights appears to stimulate bone growth in the hips (probably due to weight-bearing). To increase bone density in the spine, utilize either free weights or exercise machines. Have an exercise professional design a well-balanced strength program for you involving major muscle groups, particularly in the hips, wrists and spine (common osteoporosis fracture sites). Learn proper exercises for the upper/lower back and abdominals to give you strength for good posture.

Weight Bearing Exercise:

Each time we step, jump, run or balance on part of our body, the impact causes compressive force on the bone which in turn encourages bone building. That’s why it’s important to participate in regular weight-bearing exercise which is appropriate for your fitness level and current bone health. For example: very fast walking, uphill walking, stair-stepping, jump rope or jumping activities, high-impact aerobics, jogging, certain types of dancing, soccer, tennis, squash and basketball can be good exercise choices for bone-building. High impact forces and a variety of movement patterns cause a stronger bone response.

However, your strength, heart health and bone integrity must be adequate for safe exercise. Your doctor or physical therapist can tell you what’s safe and effective for you. Strength training exercises done standing (or when balancing your weight on a leg or hand) are also an important part of a weight-bearing exercise program.

Balance:

Good levels of strength and flexibility guarantee that you’ll keep your balance more easily. To help prevent falls, activities that require balance are also good to practice. Many forms of dance
can promote good balance.

A simple exercise: Practice standing on one foot for 30 seconds. Repeat with the other leg. When you can do this easily, try it with your eyes closed or while moving the “air leg” forward-and-back or out-and-in. There are all kinds of balance games and activities you can do. Remember to progress gradually and provide for something to grab if you need a balance check.

As an adolescent or young woman, exercise can boost your bone mass. After the mid-thirties, success means keeping the bone you have (or slowing the rate of bone loss). Whatever your age, exercise is good medicine for your body and your bones.

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.



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27 10, 2025

How Biosimilars Help with Chronic Conditions

By |2025-10-27T21:53:14+03:00October 27, 2025|Fitness News, News|0 Comments

Biosimilars are medicines used to treat many chronic diseases. And they’re close copies of biologics.

What are biologics?

Medicines made from living cells

Biologics are complex medicines made from living cells, like yeast or bacteria.

  • Regular medicines (like aspirin or antibiotics) are small molecule drugs. They’re made with chemicals. They have a simple structure and can be copied exactly. These copies are called generics.
  • Biologics are large, complex molecules. They target certain cells or processes in the body to help fight diseases. They can treat many chronic conditions, but they’re often very expensive.

What are biosimilars?

Close copies of biologics

Biologics are too complicated to copy perfectly. Instead, scientists make medicines that are very close to the original biologic. These are called biosimilars .

  • Biosimilars deliver the same amount of the active ingredient into the body at the same rate as the biologic .
  • They work the same way, are just as safe and usually cost less.

How do biosimilars work?

They block damaging cells and signals

Biosimilars help stop inflammation and damage.

  • Many chronic diseases come from overactive immune responses that cause too much inflammation.
  • For example, special proteins called cytokines send inflammation signals in the body.
  • When cytokines overreact, they cause chronic inflammation.
  • This inflammation makes symptoms worse and causes damage.
  • Biosimilars target these cells and block the signals to reduce inflammation.

What do biosimilars treat?

Biosimilars can treat chronic conditions

Biosimilars block the inflammation signals that cause symptoms and damage in different chronic conditions.

  • Crohn’s disease
    • Stop the immune system from attacking the gut.
  • Multiple sclerosis
    • Keep certain immune cells from getting into the nervous system.
  • Rheumatoid arthritis
    • Block proteins that cause joint inflammation.
  • Ulcerative colitis
    • Stop immune cells that cause inflammation in the bowel.
  • Psoriatic arthritis
    • Block damaging signals that cause joint pain and swelling.

Why do biosimilars matter?

Biosimilars offer more access to effective treatments

Biologics take many years and a lot of money to develop. So they have a very high cost.

Biosimilars:

  • Can be made at a lower cost.
  • Are just as safe and effective as the original biologics.
  • Give more people access to the best medicines.
  • Help people with chronic conditions get needed treatment at a lower cost.

Are biosimilars right for you?

Like all medicines, biosimilars may have side effects. Always talk to your healthcare provider about the best options for you.

This educational resource was created with support from Sandoz.



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27 10, 2025

Migraine Toolkit – HealthyWomen

By |2025-10-27T19:52:25+03:00October 27, 2025|Fitness News, News|0 Comments

If you or someone close to you has migraine disease, you may already know that it’s more than “just a headache.”

Many people think of migraine as a severe headache, but migraine is actually a neurological condition with many different symptoms. Yes, the most common symptom of a migraine attack is head pain, which can be severe or moderate and long-lasting. But there are many other symptoms as well.

Migraine symptoms can include:

  • Sensitivity to light, sound and smells
  • Eye pain
  • Vision problems like tunnel vision, blurry vision or seeing flashing lights
  • Nausea
  • Dizziness, numbness and tingling
  • Sweating
  • Increased urination
  • Fatigue
  • Frequent yawning
  • Constipation

And migraine may come with or without aura, which is a warning that a migraine headache is coming on.

There’s a wide variety of ways to experience migraine and a wide variety of treatments available as well.

Migraine toolkit

We’ve put together a migraine toolkit to help you navigate this complicated disease or care for someone who’s living with it.

Here, you’ll find a journal to help track triggers and symptoms so you and your healthcare provider (HCP) can try to find patterns that will help get the disease under better control, a migraine action plan you can put together with your HCP, a checklist to help support dialogue with an HCP, and a list of resources where you can learn more about the disease and find support. We’ve also included a migraine health plan for school and a pediatric migraine action plan you can use if you’re caring for a child with migraine.

And finally, we’ve included some screening quizzes you can take if you think you may be living with migraine disease. If you are experiencing migraine, it’s important to talk to an HCP about managing your condition.

Migraine Journal

HealthyWomen Migraine Journal

Migraine Action Plans

American Headache Society Pediatric Migraine Action Plan

American Headache Society Migraine Action Plan

Migraine at School Health Plan

Healthcare Provider Dialogue Checklist

Migraine Dialogue Checklist

Screening Quizzes

Migraine Again

National Headache Foundation Screener



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27 10, 2025

8 Things to Consider If You Have Cervical Cancer

By |2025-10-27T17:51:17+03:00October 27, 2025|Fitness News, News|0 Comments

Getting through cancer treatment is no easy feat. The intensive therapies, changes to your body and fears about recurrence are all common for women who’ve completed cervical cancer treatment. But recovery doesn’t end when treatment does. Survivors may deal with long-term physical, emotional and sexual changes.

Knowing what to expect after treatment can help you prepare and feel more at ease as you move forward.

Here are 8 things you should know if you’ve had or have cervical cancer.

1. Survivorship can mean adjusting to a “new normal

The emotional, physical and mental toll of treatment can linger long after it’s over. “Many survivors experience fatigue, changes in sexual health, early menopause symptoms and anxiety about recurrence,” said Kathryn Miller, M.D., a board-certified gynecologic oncologist at Capital Women’s Care. “The most important thing to know is that you don’t have to face these challenges alone — we can anticipate many of them and provide treatment or connect you with support early.”

2. Treatment may affect your fertility and reproductive health

Cervical cancer treatments like surgery, radiation and certain chemotherapy drugs can affect fertility. They may damage the ovaries, uterus and cervix — key organs for pregnancy.

The good news is that there are ways to preserve fertility. “For women who still want to have [biological] children, we always try to discuss fertility-preserving options before treatment begins, such as trachelectomy (removal of the cervix but preserving the uterus) or egg/embryo freezing,” Miller said.

Read: Pregnancy and Cervical Cancer: Know Your Options >>

3. Lymphedema is worth keeping an eye out for

Lymphedema is swelling that can develop after radiation therapy, pelvic surgery or lymph node removal. It typically appears in the arms and legs, but can also affect other areas of the body.

Lymphedema is a common symptom after cervical cancer treatment, so early recognition is key. “If you notice leg heaviness, tightness or swelling, let your care team know right away — the earlier we address it, the better the outcome,” Miller said.

4. Relationships can shift

A cancer diagnosis can shift dynamics with family, friends and especially partners. Survivors may struggle with emotional and physical intimacy after treatment, which can strain their relationships.

Miller said that open communication is key. “Counseling, whether individual or couples therapy, can make a big difference,” she explained. “Support groups with other survivors can also provide a sense of connection and shared understanding.”

5. Vaginal changes are common — but help is available

Many survivors notice changes in their vagina after treatment. These changes can include dryness, a shorter or narrower vagina, and pain during sex. If you’re feeling discomfort, there are several options you can explore with your healthcare provider (HCP).

These include:

“It’s also important to talk openly with your provider about any pain or bleeding — there are solutions, and you don’t have to simply live with it,” Miller added.

6. Ostomies are rare — but be prepared if needed

An ostomy creates an opening (stoma) in your stomach to collect stool or urine in a removable bag. Miller said most cervical cancer survivors won’t need one unless the disease is in the advanced stages or surgery requires the removal of the bladder or rectum.

“If [an ostomy is] necessary, we spend a lot of time preparing patients for what to expect and connecting them with ostomy nurses,” she said. “Many people are able to live full, active lives with an ostomy.”

7. Surgical menopause may occur

Surgeries such as removal of the ovaries (oophorectomy) or removal of the uterus (hysterectomy) can start menopause. This happens when the ovaries or uterus are removed. Miller explained that surgical menopause can lower estrogen and progesterone levels.

This drop can cause symptoms like:

If you notice any of these symptoms, contact your HCP to discuss treatment options. “We work closely with patients to manage these symptoms — sometimes with hormone replacement (if it’s safe for their cancer type), sometimes with non-hormonal medications, and always with lifestyle support to keep bones and heart healthy,” Miller said.

8. Disparities can affect survivorship

Not every survivor gets the same access to care. Factors like racism, lack of access to quality care, socioeconomic status, older age and delayed diagnosis can make recovery more difficult. These challenges often affect low-income survivors and women of color the most.

A study showed that Black and Hispanic women were more likely to be uninsured than non-Hispanic white women. Black women also have the highest death rates and lowest survival rates for a type of cervical cancer called cervical adenocarcinoma.

“As providers, we have a responsibility to recognize these disparities and help remove obstacles by connecting patients with community resources, patient navigation programs and financial counseling,” Miller said. “Every survivor deserves equal access to high-quality care, regardless of background.”

Life after treatment can bring many challenges, but you don’t have to face them alone. If you notice any changes in your emotional, mental or physical health, please reach out to your HCP. They can help you make a personalized treatment plan. This plan will help manage symptoms, support recovery and maintain your quality of life.

This educational resource was created with support from Merck.

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