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John F McCullagh Dec 2011
Young Liam loved Orange
and liked to wear ties.
To his firehouse friends
He was one of the guys.

He had his own locker
a slicker and hat.
He also had cancer,
and a bad one at that.

From early on in his life
he fought neuroblastoma ;
An invasive tumor
a metastatic carcinoma.

His family who loved him
labored to save
their dear little child
Prince Liam the Brave.

He faced surgery bravely,
engaged in his fight..
He endured radiation
Chemo and knife.

When many a New Yorker
complains about stress,
Prince Liam was stoic
When put to the test.

Then just before Christmas
he suffered a relapse
He became neutrapenic-
His immune system collapsed.

With blood in his *****
And a spot on his lung
Liam grew weak.
his defenses undone.




An Amethyst stone
he received from a friend
was his talisman of hope
that he held to the end.

The worst part of the journey
was when hope was gone.
Then Liam lay, still and silent
in his mother's arms.


There are brave fire fighters
Who’ll be fighting back tears
Brave Prince Liam has died,
He lived only six years

There are many old people
still avoiding the grave
Who know less about love
Than did Liam the brave

We will gather together
In St Francis’ nave
To remember the life of
Prince Liam the brave


i
When Liam Witt was diagnosed with Stage 4 cancer at 33 months of age, his parents began calling him Prince Liam the Brave.
After they moved Liam and his little sister Ella from New Jersey to New York to be closer to Memorial Sloan-Kettering Cancer Center, firefighters down the block saw a kindred spirit.
The men of Ladder Co. 24 and Engine Co. 1 made Liam an official firefighter and even gave him an equipped locker inside their firehouse on W. 31st St.
As Liam underwent surgeries and was treated with chemotherapy and radiation for four years, his irrepressible spirit inspired friends to help his parents, Gretchen and Larry, start the foundation Cookies for Kids' Cancer.
It has raised an astonishing $2.5 million for pediatric cancer research, mostly from small bake sales and the charity's online cookie orders.
"He never became 'that sick kid,'" said Fraya Berg, a family friend. "He never lost himself in the disease. He was just a kid who was sick."
judy smith Aug 2015
A terminally ill 5-year-old was given a dream day — an amazing birthday, prom and a wedding all in one.

Lila May Schow has spent most of her life in the hospital or at the doctor’s office. She has a rare childhood cancer, neuroblastoma, and doctors have not been able to successfully treat the disease.

Lila has stopped receiving chemotherapy treatments. Doctors told the family treatment is no longer an option because her body is not strong enough.

Sadly, she is not expected to live past Thanksgiving.

Lila’s parents, assuming it could be her last birthday, decided to make the day extra special. With the help of local businesses and volunteers, everyone gathered on July for the huge party.

“We don’t know how much time we have left,” Lila’s dad Ryan Schow tells KATU, “and we have put up one hell of a fight. We just want to give her everything she deserves.”

The family started a Facebook groupto ask for help. A local bank donated the use of their building, a DJ offered his services, women dressed as Disney characters volunteered to appear and bakers donated cakes. Over 1,000 people attended the huge bash.

Lila, dressed as her favorite princess Cinderella, attended her birthday/prom/wedding. The sweetest moment of the day was when Lila’s dad proposed and married his daughter.

“We wouldn’t have gotten this far and been able to fight this hard without all the help we’ve been given. We’re so very grateful for that. It’s all about making a little girl smile,” Lila’s dad, Ryan Schow, tells KATU. “It’s all about making a little girl smile.”

read more:www.marieaustralia.com/long-formal-dresses

www.marieaustralia.com/bridesmaid-dresses
Dear Well-Wisher,

I hope this message finds you in good health.

We, Vaishali and Tushar Purohit from Pune, come to you with a heavy heart and tears in our eyes, pleading for your help to save our 4-year old son Rishi's life. He is undergoing treatment for neuroblastoma (rare form of cancer) at the Tata Memorial Hospital, Mumbai.

Since April, our little warrior has been bravely battling cancer that is threatening to take him away from this world. Every rupee you contribute will be the difference between life and death for our 4-year old warrior.

We would also request you to forward this message to your family and friends, which will inspire them to contribute and aid in saving an innocent life.

Here's the fundraiser link:* https://www.impactguru.com/fundraiser/help-s-o-tushar

Thanking you for your consideration and support during these trying times.🙏🏼 *
Hello all I haven’t shared anything like this before! If any of you can share it further in any of your groups/ with people who can help would be nice
I know Tushar person personally 🙏

Please keep Rishi in your prayers🙏

https://www.impactguru.com/fundraiser/help-s-o-tushar
Celso Moskowitz May 2017
A child is dying,
neuroblastoma,
on the other side
of the world,
right now, right now, right now!
and I know of this
because I read of this
and maybe I'm dying
of cancer
as well,
but this
I do not
know.

I look at the clock
and think about
some woman,
someone,
still,
above the information
undercurrent.

And if I don't know
what this makes of me,
much less
of her.
Gallagher et al. 2010 J Toxicol Env Health A “Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002” PMID 21058170.  

The study authors investigated the National Health Inventory Survey (a very large national database) and found that boys receiving the full HepB series were 3 times as likely to receive  an autism diagnosis as compared to those not receiving any HepB vaccine (statistically significant).  Non-white boys had a significantly worse outcome.

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20. Minami et al. 2010 Cell Biol Toxicol “Induction of metallothionein in mouse cerebellum and cerebrum with low-dose thimerosal injection” PMID 19357975.  

The study authors determined that in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.

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25. Young et al. 2008 J Neurol Sci “Thimerosal exposure in infants and neurodevelopmental disorders: an assessment of computerized medical records in the Vaccine Safety Datalink” PMID 18482737.  

The study authors determined that significantly increased risk ratios were observed for autism and autism spectrum disorders as a result of exposure to mercury from Thimerosal containing vaccines using the CDC’s Vaccine Safety Datalink.

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26. Geier et al. 2008 Neuro Endocrinol Lett “Neurodevelopmental disorders, maternal Rh-negativity, and Rho(D) immune globulins: a multi-center assessment” PMID 18404135.  

Mothers receiving thimerosal via Rho(D) immune globulin injection saw a significantly higher rate of autism in the children exposed to mercury in utero.  Overall, twice as much autism was seen in the exposed group of children versus the non-exposed control group.
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33. Geier et al. 2006 J Toxicol Env Health A “An evaluation of the effects of thimerosal on neurodevelopmental disorders reported following DTP and Hib vaccines in comparison to DTPH vaccine in the United States” PMID 16766480.  

This study shows significantly increased risk ratios for autism, speech disorders, mental retardation, infantile spasms, and thinking abnormalities reported to VAERS found following thimerosal-containing DTP vaccines in comparison to thimerosal-free DTPH vaccines, with minimal bias or systematic error.
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­38. Burbacher et al. 2005 Environ Health Perspect “Comparison of blood and brain mercury levels in infant monkeys exposed to methylmercury or vaccines containing thimerosal” PMID 16079072.

Infant macaques retained significantly higher levels of elemental mercury in their brain tissue when exposed to thimerosal in infant vaccines versus methylmercury.  The half-life of the mercury associated with thimerosal exposure was indefinite as it lasted much longer than the overall testing period.

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39. Yel et al. 2005 Int J Mol Med “Thimerosal induces neuronal cell apoptosis by causing cytochrome c and apoptosis-inducing factor release from mitochondria” PMID 16273274

Thimerosal at levels comparable to infant exposure via vaccines caused neuronal cell death through changing the mitochondrial microenvironment.  Thimerosal induced cell death was associated with mitochondrial depolarization and a significant level of reactive oxidative stress intracellularly.
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4­2. Parran et al. 2005 Toxicol Sci “Effects of Thimerosal on NGF signal transduction and cell death in neuroblastoma cells” PMID 15843506.

Thimerosal exposure caused programmed cell death (apoptosis) in neuroblastoma cells.  At 48 hours incubation, concentrations of thimerosal typical of those present in the blood stream after vaccination caused neuronal death.

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43. James et al. 2004 Am J Clinical Nutrition “Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism” 80:1611.  

Children with autism have a diminished methylation capacity leading to higher sustained levels of oxidation stress, due to deficiencies primarily in glutathione.  Vaccines produce a very high level of oxidation stress to the body upon administration.

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­51. Bernard et al. 2002 Mol Psychiatr “The Role of Mercury in the Pathogenesis of Autism” PMID 12142947.

This paper links thimerosal exposure via infant vaccines to autism based on the pathologies associated with autism as well as the timing of autistic regression.  Emphasis is made on the total mercury exposure to infants in the vaccination schedule used in the 1990’s and early 2000’s.

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53. Verstraeten et al. 1999 Internal CDC Abstract for the Epidemic Intelligence Service Meeting of 2000 “Increased risk of developmental neurologic impairment after high exposure to thimerosal-containing vaccine in first month of life.”  This original version of the Verstraeten et al. paper (that was ultimately “watered down” before it was published in final form in 2003) shows risks of autism at 7.6-fold for children exposed to thimerosal in the first month of life compared to unexposed controls.

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