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A mom, a dad and their 2-year-old little boy went to sleep Sunday night.By Monday morning, all three were gone.Dillon Ev...
08/27/2026

A mom, a dad and their 2-year-old little boy went to sleep Sunday night.

By Monday morning, all three were gone.

Dillon Evans, his wife Isabella and their son Easton Lee died after a devastating fire tore through their Kansas home early Monday morning.

According to reports, firefighters were called around 1:30 a.m. to a home near Galesburg. Crews learned that a family of three could still be inside and attempted to search the home.

Tragically, none of them survived.

Dillon and Isabella were building their life together, surrounded by the laughter and little moments that make a family.

And then there was their son, Easton.

Just 2 years old. ❤️

Friends remember Dillon and Isabella as a couple who brought happiness wherever they went, sharing a relationship filled with laughter and love.

One of Isabella’s friends remembered being there after Easton was born, spending time with the new mother and her tiny baby.

Now, their loved ones are preparing to say goodbye to all three.

Family and friends will gather Tuesday, September 1, with funeral services scheduled for Wednesday morning in Parsons.

The loss is almost impossible to comprehend.

Three members of one young family were here one day, and suddenly they were gone.

Dillon.

Isabella.

Easton.

Please keep their parents, relatives, friends and everyone who loved this family in your prayers. 🙏

Pray especially for those who now have to face the unimaginable pain of burying a loved one while grieving the loss of an entire family.

May Dillon, Isabella and little Easton never be forgotten. ❤️

UPDATE: She risked her own life to keep her unborn baby alive for five more weeks.Then, shortly after giving birth, Ashl...
08/27/2026

UPDATE: She risked her own life to keep her unborn baby alive for five more weeks.

Then, shortly after giving birth, Ashlie and her tiny son were separated as both faced serious medical battles in different hospitals.

Now, they are finally together. ❤️

Ashlie’s aunt, Autumn, shared the update so many people had been praying for.

Ashlie was already dealing with kidney failure when her pregnancy became dangerous. At just 18 weeks, ending the pregnancy was presented as an option because continuing could put Ashlie’s life at serious risk.

She chose to keep fighting for her baby, Liam.

She made it to 23 weeks and 3 days before her blood pressure became dangerously high and she began losing her vision.

Liam was then delivered by C-section.

But their battle was far from over.

While Liam fought in the NICU, Ashlie became extremely ill herself and had to be transferred to another hospital because of stage 4 kidney failure and other serious complications.

She couldn’t simply stay beside the baby she had risked so much to bring into the world.

Now, thankfully, that has changed.

Ashlie is still very sick, but she is receiving outpatient care and can finally spend time with her son.

And Liam has reached **2 pounds.** 💙

He remains extubated and is receiving breathing support through NIPPV.

There are still concerns. Liam developed an infection, and a recent scan revealed brain issues that doctors will continue monitoring.

So their journey is far from over.

But look at how far they have already come.

A mother who risked everything for her son.

A baby born at just over 23 weeks who has now reached 2 pounds.

And after being forced to fight separately, Ashlie and Liam can finally face the journey together.

Please keep this mother and her tiny son in your prayers.

Pray that Ashlie remains strong enough to continue outpatient care, that Liam overcomes his infection, and that his doctors receive encouraging news as they continue monitoring his brain. 🙏💙

**Cycle 8, Day 15 | 194 days fighting childhood c*ncer** 🎗️💛Baker received vincristine today, and the best news is that ...
08/27/2026

**Cycle 8, Day 15 | 194 days fighting childhood c*ncer** 🎗️💛

Baker received vincristine today, and the best news is that his labs were great! 🙌🏼

He also had so much fun searching for the little creatures that another young boy, who is also fighting c*ncer, leaves around the hospital for the younger kids to find. Today is that little boy’s final treatment, and although he hasn’t been there recently, Baker still looks for his tiny treasures every week. 🥺💛

It’s something so small, but it makes Baker’s entire day. And honestly, I have just as much fun searching for them with him. 🤭 We may have to share our whole collection sometime!

His lab numbers are the highest they’ve ever been, which honestly surprised me, especially with him starting school. I’m SO thankful to see that his body is doing what it needs to do and continuing to stay strong. 💪🏼

His side effects during these quick chemo weeks have been very minimal. He’s tired, but otherwise he’s doing well. 🫶🏻

We did find a tick on him this morning, so we bagged it and saved it. The doctors aren’t too concerned right now, but we’ll definitely be keeping a close eye on the bite and watching for any changes.

Next week will be a much busier one. We’ll be at the hospital every day for chemo, so Baker won’t be going to school at all.

🎗️💛 **Prayer requests:**
• That Baker stays healthy
• That he makes count next week
• For a good appetite
• Less fatigue
• That the tick bite heals quickly
• And please pray for cooler weather because he is officially over this heat! 😂

**Hebrews 10:23**

“Let us hold unwaveringly to the hope we confess, for the one who made the promise is trustworthy.”

His promises are true, and we continue holding onto them every single day.

Thank you for continuing to stand beside Baker and our family in prayer. 💛🎗️

And here’s a little look at his collection of treasures and the picture frame he made with Mrs. Kay. 💛

And no… that is definitely NOT his coffee. 😅☕️

Elias was born with **Double Inlet Left Ventricle (DILV)**, a rare and serious **congenital heart defect**.This conditio...
08/27/2026

Elias was born with **Double Inlet Left Ventricle (DILV)**, a rare and serious **congenital heart defect**.

This condition means that both of the heart’s upper chambers connect to the same lower chamber instead of having separate pathways. As a result, oxygen-rich and oxygen-poor blood can mix, making it harder for the heart to deliver enough oxygen to the body.

DILV is a complex heart condition that often requires multiple procedures and surgeries as a child grows. Elias has already been through several heart procedures and recently underwent the **Glenn procedure**, an important step in his treatment.

Despite everything he has faced, Elias is now recovering and has been successfully taken off the breathing machine. ❤️‍🩹🙏

When Scarlett was born, her mother Louise imagined all the beautiful moments ahead—watching her daughter grow, talk, run...
08/27/2026

When Scarlett was born, her mother Louise imagined all the beautiful moments ahead—watching her daughter grow, talk, run, and enjoy a happy childhood. ❤️

But everything changed on Scarlett’s first birthday when she experienced a prolonged seizure.

After months of testing, doctors finally discovered that Scarlett has **BPAN**, a rare genetic d*sorder that can gradually lead to dementia-like symptoms and affect movement, speech, and memory.

Despite the uncertainty surrounding her future, Scarlett remains a joyful little girl. She loves singing, Disney princesses, and spending precious time with her family. 💕

Her mother knows there are difficult questions about what lies ahead, but Louise refuses to give up.

Instead, she is turning her fear into hope and continuing to fight for research and treatments that could help protect Scarlett’s future.

A mother’s love is driving a race against time—and Louise is determined to keep fighting for her little girl. ❤️‍🩹

*sorder *sorderAwareness *seaseAwareness

**HE KEPT BUMPING INTO THINGS—THEN DOCTORS DISCOVERED WHAT WAS INSIDE HIS BRAIN 🧠**Benjamin Gutierrez’s early years seem...
08/27/2026

**HE KEPT BUMPING INTO THINGS—THEN DOCTORS DISCOVERED WHAT WAS INSIDE HIS BRAIN 🧠**

Benjamin Gutierrez’s early years seemed normal at first, but his parents soon began noticing unusual signs.

As a baby, Benjamin experienced strange episodes and frequent seizures. His face would also turn red while he was eating. As he grew, another concerning problem became noticeable—he often bumped into things and struggled to see where he was going.

Doctors eventually ordered an MRI, which revealed a large **cavernous malformation** deep inside his brain.

A cavernous malformation is an abnormal cluster of small blood vessels that can cause serious neurological problems, including seizures and vision difficulties.

When follow-up scans showed that the malformation was growing, doctors faced a difficult decision. They determined that delicate brain surgery was necessary to address the condition.

Benjamin’s journey has been filled with uncertainty, but his family continues to hope for the best as he receives the care he needs. ❤️‍🩹🙏

**“IT WAS LIKE HIS SKIN HAD 𝖬𝖤𝖫𝖳𝖤𝖣.” 🔥**What started as an attempt to recreate a viral online experiment turned into a t...
08/26/2026

**“IT WAS LIKE HIS SKIN HAD 𝖬𝖤𝖫𝖳𝖤𝖣.” 🔥**

What started as an attempt to recreate a viral online experiment turned into a terrifying accident for 12-year-old Caden Ballard. 💔

Caden was trying an experiment involving rubbing alc*hol when he believed the flames had gone out. But as soon as he picked up the bottle, he realized his shirt had caught f*re. 😢

Thankfully, Caden’s older brother reacted quickly and managed to put out the flames before the situation became even more serious. ❤️‍🩹

Caden later required surgery and is now focused on healing through specialized medical care.

His doctors expect his recovery to be a long process and will continue monitoring him as he grows.

What began as a viral experiment became a life-changing moment for this young boy and his family.

Wishing Caden strength, healing, and a full recovery ahead. ❤️‍🩹🙏

My phone pinged last night, and my heart sank.It was a message from our friend Tom Fritz of Titus, Alabama.Tom is the hu...
08/26/2026

My phone pinged last night, and my heart sank.

It was a message from our friend Tom Fritz of Titus, Alabama.

Tom is the husband who has been transforming a school bus into a pink home on wheels so he could take his wife, Jo Jo, through Alabama, Florida, and Georgia for cancer events.

For 50-year-old Jo Jo, the journey was meant to be a chance to say goodbye to friends while continuing to raise awareness in the fight against cancer.

Twelve months ago, doctors gave Jo Jo 18 months to live after she was diagnosed with stage 4 breast c*ncer.

She fought hard through treatment, and together, she and Tom created a plan called “Where’s Jo Jo? The Pink Bus Journey of a Lifetime,” with 21 stops planned across 31 days in October.

Just weeks ago, Jo Jo was feeling great. Tom was working on the bus, and Jo Jo was helping wherever she could.

Then everything changed.

“Jo Jo had a reaction to her chemo last Thursday,” Tom told me.

“There are toxins in Jo Jo’s blood, and she’s suffered a big setback.”

Doctors have now placed Jo Jo in home hospice and told the family she may have only days to weeks left.

The news has devastated everyone around her.

“There are 23 people at the house right now surrounding Jo Jo,” Tom said.

He hopes people will leave messages for Jo Jo that the family can read to her.

Tom still hopes his wife will somehow make a comeback. He wants nothing more than for her to live forever.

But he isn't sure he can continue the Pink Bus Tour if Jo Jo passes before October.

“I’m just not sure I can get through it,” he whispered.

For now, the bus, the tour, and all the plans have been put aside.

Tom isn't thinking about traveling across the Southeast right now.

He's thinking about loving his wife, holding her close, and comforting her through what may be the hardest days of their lives.

Tom says he welcomes your prayers for Jo Jo and their family.

When you see the crushed truck after the rollover, it’s hard to believe a Texas teenager survived behind the wheel.But 1...
08/26/2026

When you see the crushed truck after the rollover, it’s hard to believe a Texas teenager survived behind the wheel.

But 17-year-old Junior did.

Now, his family is facing the possibility that his life may never look the same again.

According to his family, Junior was ejected from the truck during a devastating crash in East Texas on August 11.

He survived, but the extent of his injuries became clear when his family reached the hospital.

Junior suffered fractures to his spine in three places, a broken femur, and other serious injuries. Doctors have told his family that he is paralyzed from the waist down.

He was flown by helicopter twice—first to Conroe and then to Memorial Hermann in Houston, where he underwent major surgery.

Just think about how quickly everything changed.

One photo shows Junior standing on a football field in his Groveton uniform—a 17-year-old who loves football, basketball, video games, and spending time with his friends and siblings.

Then came one crash.

One rollover.

And suddenly, his family is facing a completely different future.

Rehabilitation. Mobility equipment. Accessibility changes. And learning how to navigate everyday life in ways Junior never expected to at 17.

There are still many unknowns, and his family is taking things one day at a time.

They are asking for prayers and words of encouragement.

Pray for Junior’s healing.
Pray for his strength as he processes everything he has been through.
Pray for his parents and siblings as they walk this difficult road beside him.

And pray that Junior never forgets what that mangled truck already proves:

**He is still here.**

Her leg. Then her head. Then somewhere else.That’s how the pain is moving through little Jazzy’s body right now—shifting...
08/26/2026

Her leg. Then her head. Then somewhere else.

That’s how the pain is moving through little Jazzy’s body right now—shifting without warning and never staying still long enough for her to truly rest.

Jazzy is facing neurobla*stoma for the third time.

She has been sleeping for much of the day, and doctors have given her a significant amount of medication to help keep her comfortable. So far, it hasn’t been enough.

Her strength has declined so much that she is no longer walking. During the brief moments when she is awake, her family gently helps her stand and encourages her to take a few steps whenever she can.

“We just help her stand when she’s ready,” her family shared. “Even a few steps matter right now.”

Before things became this difficult, Jazzy’s family had been preparing to travel to California for treatment. The appointment was postponed, and they lost the Airbnb and rental car they had booked, although they received travel credit for when a new appointment is scheduled.

Now, the family has another concern. They fear Jazzy may be experiencing increased swelling in her brain.

Tomorrow, after an important blood test that cannot be done at their hospital in New York, Jazzy is expected to go to the hospital. Despite how exhausted everyone already is, they know this test cannot be missed.

Tonight, Jazzy needs all the love and prayers surrounding her.

Pray that her pain finally eases. Pray for her strength to return. And pray that her body finds the strength to face this third fight.

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