His parents told him his blood was sick when he was diagnosed with cancer. Rocco said he was sad, but he wanted to get better so he could donate his blood to help other people. This unselfish kindness and compassion are rare qualities in a five-year-old. But this is Rocco.
This was written by Hudson’s mom, Jessica McKearney.
I work as a Nurse Practitioner and Kyle works as a Project Manager. We live in a small town in Northeast Iowa. Before March 2019, Hudson was an energetic, Mickey Mouse and car loving toddler. He was spirited, happy, loved to dance and kept us on our toes. In November 2018, Hudson became a big brother to his sister Violet. Two under two was exciting and exhausting. Hudson was caring, empathetic, and always wanted to be with Violet. They had an incredible bond, and we were grateful to have two happy and healthy toddlers.
What is acute lymphoblastic leukemia?
Acute lymphoblastic leukemia (ALL) is a cancer of the white blood cells that normally fight infection. The cells do not grow and develop properly, filling up the bone marrow inside bones, where blood is normally made.
ALL is the most common type of childhood cancer, accounting for 35% of all cancers in children. Each year, there are about 2,900 new cases of children and adolescents diagnosed with ALL in the United States alone.
Its signs and symptoms resemble other common illnesses, which often leads to other treatments before the leukemia diagnosis is made.
When their daughter Kimmy was diagnosed with leukemia, Daniel and Taimi Hachey were told her disease had a 90% survival rate. Later tests showed Kimmy had Philadelphia chromosome-like precursor B-cell acute lymphoblastic leukemia, a rare type, difficult to treat. The adjusted survival rate? Only 50-60%. Her diagnosis went from, “The cure rate is high,” to “We are very concerned about her outcome.”
The Alliance for Childhood Cancer Action Days in Washington, D.C., is an opportunity for members of the childhood cancer community – from kids and their families to health care professionals and volunteers – to advocate for childhood cancer issues before Congress.
St. Baldrick’s Honored Kid, Scott, a 10-year-old whose cancer is in remission, attended Action Days with his mom Nancy and has provided us with the following report on his experiences in Washington.Scott (left) attended Childhood Cancer Action Days in Washington, D.C., in late March.
As we wrap up National Volunteer Week, today we’ll meet two more volunteers with very different stories: one is the mom of a child diagnosed with cancer; the other, a researcher who’s devoted her career to early detection of childhood cancers.
Both will show us that it doesn’t matter how you get involved – just that your involvement is crucial to the work of the St. Baldrick’s Foundation.
It’s Valentine’s Day and that means exchanging cards, chocolates, teddy bears, and flowers with loved ones. The prevailing symbol of Valentine’s Day is the heart – which makes sense, given that the day is all about showing love and affection.
Because the heart is so central to Valentine’s Day, it’s a useful time to reflect on how childhood cancers impact this vital organ. Unfortunately, childhood cancers affect far more than the parts of the body in which they emerge – brain cancer doesn’t just harm the brain; leukemia doesn’t just affect the blood; and bone cancers often spread to the major organs.
The League of Legendary Heroes is an order of dedicated volunteers who’ve participated in St. Baldrick’s Foundation events for three or more years. Each year, St. Baldrick’s names a League Champion to lead and inspire this group to raise money for lifesaving childhood cancer research.
Georgia Moore, our newest League Champion of the League of Legendary Heroes, just celebrated her 19th birthday on Dec. 30. The following day, New Year’s Eve, marked nine years since Georgia was diagnosed with acute lymphoblastic leukemia (ALL).
Our 2019 League Champion, Georgia Moore (third from left), appears with her family at Tufts University.
Each year, the St. Baldrick’s Foundation picks five kids to serve as Ambassadors. In this role, they represent the thousands of kids affected by childhood cancers and remind us of the importance of supporting childhood cancer research.
Take any group of kids and they’ll all have their own way of talking, their own opinions on books, movies, and video games, their own favorite foods.
But there is one thing the St. Baldrick’s 2019 Ambassadors have in common: childhood cancers. Beyond that, they share the support of loving families and a desire to inspire others to raise money for childhood cancer research.
Our 2019 Ambassadors, from left to right: Aiden, Arianna, Sullivan, Gabby, and Brooke.
With 2018 winding down, it’s time to thank this year’s St. Baldrick’s Ambassadors for their help raising funds and awareness for pediatric cancer research. This group of five kids and their families inspired us with their unique stories of courage and their refusal to give up hope.
We’ll be welcoming a new group of Ambassadors in the new year. For now, let’s check in on the 2018 team to see how they’re doing and what they enjoyed about the Ambassador experience.
Our 2018 Ambassadors, from left: Brooks, Kellan, Maya, Zach, and Julia.
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