The daughter of our beloved actress has just passed away… See more (vvh)

Heartbreaking news for Julia Roberts, we announce… See more
But when filming alongside Ewan McGregor, the 44-year-old actress was unrecognizable as the actress who rose to fame as Vivian Ward in 1990’s Pretty Woman.
Without makeup and dressed in frumpy clothes, Julia transformed while filming emotional scenes for August: Osage County in Bartsville, Oklahoma.
On set: Actress Julia Roberts and co-star Ewan McGregor were filming their new movie August: Osage County on Thursday.
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Hysterical performance: The brunette performed a tearful act
The movie star, who in real life has three children with her husband, cinematographer Daniel Moder, wore a white shirt over a cream blouse and paired it with loose-fitting blue jeans.
Her long brown hair wasn’t glamorously styled to play Barbara Weston, a character from a family that overcomes certain differences when their alcoholic patriarch disappears.
During the intense scene, Ewan held Julia’s hand with great anticipation as they walked toward a boat dock to identify a body for a sheriff.
Mummy look: The Pretty Woman actress looked a little disheveled while filming the intense scene in which they had to identify a corpse for a sheriff.
Upon seeing the body, Julia begins to cry, seeking comfort from Ewan’s character, Bill Fordham, as she continues to cry in his arms.
She may have been hysterically upset during the scene, but moments later, between takes, Julia was dying of laughter.
The actress appeared alongside Julianne Nicholson, who appeared to be pointing something rather amusing to the group.
It’s not her usual look: she wore jeans and multi-layered blouses for the role of Barbara Weston.
The Boardwalk Empire star also looked disheveled, sporting a pair of navy blue slacks, brown bell-bottoms, and her hair tied back in a ponytail.
Other stars of the 2013 film include Benedict Cumberbatch as ‘Little Charles Aiken’ and Meryl Streep and Violet Weston.
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The film’s IMBd page states that Renée Zellweger and Andrea Riseborough were considered for the role.
Riseborough was cast, but dropped out due to scheduling conflicts. Juliette Lewis replaced her as Karen Weston.
Chloë Moretz auditioned for the role of Jean Fordham, but lost to Abigail Breslin.
Quite an act: The group seemed to find something quite funny while working with Julianna Nicholson
Every Day a Battle: Supporting Olek Through Spasticity and Care.1968

Dear Supporters,
It has been a long time since we last shared news about our son, and unfortunately, the past months have been incredibly difficult for our family. Between constant hospital check-ups, rehabilitation sessions, and bouts of illness, it has felt like an endless cycle of challenges. Every day brings new concerns, new obstacles, and a persistent worry about the health and well-being of our little boy, Olek.
On August 26, we spent several days at the hospital in Bydgoszcz for a series of tests focused on Olek’s heart. We were relieved to learn that the results had not shown any significant changes compared to his previous examinations. While this news was somewhat comforting, it was far from the resolution we had hoped for. His condition still requires careful monitoring, and we remain vigilant, knowing that each small step in progress is hard-won and precious.
In recent weeks, we have noticed a growing concern: Olek’s muscle tension has been steadily increasing. He is experiencing spasticity, which affects him daily and causes him significant discomfort. This constant state of heightened muscle tension is both painful and exhausting for him. It also presents a new challenge for us as his parents, as we try to find ways to ease his suffering. Unfortunately, this means that we will need to purchase specialized rehabilitation equipment, which is extremely costly. Such equipment is vital if we are to provide even a small relief from the pain that Olek endures each day.
As parents, it is heartbreaking to watch your child struggle and not be able to fully alleviate their suffering. Olek’s resilience is remarkable—he faces each day with courage far beyond his years—but it pains us to see him limited by his condition. The therapies and exercises that we perform at home are not enough on their own. The proper equipment would allow him to receive targeted rehabilitation and help maintain his mobility, even in the face of increasing muscle stiffness. Every device, every tool, represents hope—hope that Olek can regain some measure of comfort and independence.
Looking ahead, October 20 will bring another daunting challenge. Olek is scheduled to travel to the Children’s Health Center in Warsaw for a series of more detailed cardiological and neurological tests. These examinations are critical for understanding his condition and planning further treatment, but they carry significant risks. General anesthesia, necessary for some of the procedures, raises the possibility of complications, including a temporary halt in his heart function. As parents, the thought of this procedure fills us with fear and anxiety. We know it is essential, but we cannot help the worry that grips us each time we consider it.
Alongside these medical concerns, we have also noticed troubling issues with Olek’s growth. Despite changes in his diet and the addition of vitamins, his weight has stalled at just 10 kilograms. Watching him struggle to gain weight is agonizing. Each kilogram, each gram, is a symbol of his fragility and the fragility of the journey we are on together. His stalled growth reminds us of how much he relies on our care and how critical every intervention is for his health.
Life for Olek is a daily battle, and life for us as his parents is a constant exercise in vigilance, compassion, and perseverance. Every day, we manage a delicate balance: attending to his medical needs, ensuring he receives nutrition, and providing him with love and comfort in a world that is often frightening and overwhelming for such a small child. On top of this, we must coordinate therapy sessions, transport him to appointments, and monitor his progress, all while navigating the emotional toll of seeing him suffer. The weight of responsibility is immense, and we know we cannot manage it alone.
That is why we are reaching out to you. Your support—whether through donations, sharing our story, or simply sending messages of encouragement—gives us hope. It reminds us that we are not alone, that others care, and that together we can provide Olek with opportunities that might otherwise be impossible. Each contribution, no matter the size, is a lifeline. It allows us to purchase the specialized equipment he needs, cover the costs of transportation to hospitals, and ensure that he receives the highest quality care available.
Despite the challenges, Olek continues to amaze us. His courage and resilience shine through even in the most difficult moments. When he smiles, despite the pain and discomfort, we see a reminder of why we fight every day. His laughter, his curiosity, his small victories—they are the sparks that keep us moving forward. We dream of a day when his muscle tension is eased, when he can grow and thrive without constant medical interventions, and when he can enjoy the simple pleasures of childhood that many take for granted.
The journey ahead will not be easy. There will be more hospital visits, more therapies, and more obstacles to overcome. But with your support, we can provide Olek with the resources he needs to face these challenges. Your generosity can help us ease his pain, support his development, and offer him a future filled with hope and possibility.
We ask you to stand with us. Do not leave us to face this alone. Every act of kindness, every donation, every shared message reminds us that we are part of a community that cares. It reminds us that hope exists even in the hardest of times. And most importantly, it gives Olek a chance—a chance to grow stronger, healthier, and happier.
Olek is our son, our joy, and our inspiration. His journey has been marked by fear and uncertainty, but also by courage, resilience, and love. We are committed to doing everything we can to give him the best possible care, but we need your help to continue this fight. Together, we can provide him with the tools, therapies, and support that will allow him to thrive.
Thank you for believing in Olek, for supporting him, and for helping us navigate this challenging path. Every contribution is a symbol of hope, every gesture of kindness a step toward a brighter future for our beloved son.
—Olek’s Parents
“From Stomach Pain to a Life-Changing Diagnosis”.711

Little Liam’s world changed in an instant. One morning, he complained of stomach pain—something that, at first, seemed minor. But within hours, what seemed like a routine discomfort spiraled into a nightmare no parent should ever face. The words hung heavy in the air: “Your child has cancer.”
Doctors discovered a tumor pressing against his kidneys, a stage 4 neuroblastoma. Aggressive. Rare. Cruel. For a child so small, the diagnosis was overwhelming. What should have been a world full of playgrounds, laughter, and bedtime stories became a maze of hospital corridors, IV lines, and medical jargon. Every day is a battle for Liam—a battle he never asked for, a battle he fights with courage beyond his years.
Since that day, life has been a whirlwind. Chemotherapy sessions, countless tests, and long nights in the Pediatric Intensive Care Unit have become the rhythm of his family’s days. There were moments when Liam had to be placed on a ventilator after a severe reaction to medication, and his tiny body has struggled under the strain of high blood pressure caused by the tumor itself. Each beep of the monitor, each change in his condition, sends ripples of fear and hope through the hearts of his parents.
Yet amid the fear and exhaustion, there is also unwavering love. His parents sit at his bedside for hours on end, holding his hand, whispering encouragement, and sharing stories of better days to come. They have learned to find hope in small victories: a smile after a painful treatment, a calm night without fever, a moment of laughter amid tears. Every gesture, no matter how small, becomes a celebration of resilience, courage, and life itself.
The road is long, and the challenges immense, but Liam’s family refuses to give in to despair. They have reached out to the world, asking for prayers, support, and positive energy for their little boy. Their plea is simple but profound: “Please help Liam. Please hope with us. Please stand with him as he fights.” ❤️🩹
Liam needs all of us. He needs our collective prayers, our messages of encouragement, our belief that he can survive and thrive. This story is not only about a child battling cancer—it is about the power of community, the strength of love, and the courage that shines brightest when hope feels fragile. It is about parents who refuse to let fear overshadow the possibility of miracles and a little boy whose bravery reminds us all of the preciousness of life.
Every day Liam fights, he teaches a lesson in courage. Every day his parents remain by his side, they teach a lesson in unconditional love. And every time someone offers a prayer, a kind word, or a gesture of support, they teach a lesson in humanity. Liam’s story is heartbreaking, yes, but it is also inspiring. It is a reminder that even in the darkest battles, hope, love, and community can light a way forward.
So today, we lift Liam up in our hearts and in our thoughts. We send strength to his tiny body, courage to his family, and faith to everyone watching his journey unfold. What would you say to them? What words of comfort, encouragement, or hope would you offer? Now is the time to stand together, for Liam needs us, and together, perhaps we can help carry him through this fight.