Gunner's Magic Train Offical Page

Gunner's Magic Train Offical Page Gunner Henry Gillespie – “Forever 8” – committed to providing information and support for families affected by childhood cancer and promoting awareness.

Gunner Gillespie, also known as “G-Man”, was born prematurely at 26 weeks gestation. He weighed just 1 pound, 14 ounces and began his life fighting. During his first few years he struggled to develop and gain weight. But eventually, Gunner began to thrive and grow into a happy little boy. The Gillespie’s took a collective sigh of relief and began to focus on a healthy future for their family. But

unfortunately, just when they thought they were over the hump, they began to see changes in Gunner that concerned them. After a misdiagnosis and, almost too late, a correct diagnosis, the Gillespie’s were told that their son had cancer and that he would not live a year. On November 30, 2007, when Gunner Henry Gillespie was only 7 years old, he was diagnosed with a DIPG (Diffused Intrinsic Pontine Glioma) Brain Tumor. It was located on his brain stem and the doctors told his parents it was inoperable. On October 23, 2008, after fighting this tumor for eleven months, Gunner lost his fight with pediatric cancer and will forever be 8 years old. Gunner had always loved trains, and had a large collection of trains and train memorabilia. It was Gunner’s love, passion and obsession with trains that sparked the idea for the Gunner’s Magic Train Pediatric Cancer Foundation. As Gunner’s mother, Janna does not want his death to be in vain. “I dream of a cure for children with cancer and their families,” she told me. I know that Gunner would want his train to continue chugging along, offering support and help to children battling this deadly disease.” - Read more at: http://www.purchasefamilymag.com/gunners-magic-train-pediatric-cancer-foundation/


We are using the childhood cancer motto Behold The Gold and going GOLD on all social media. Do your part by making your Facebook, Twitter, and Instagram accounts GOLD for awareness! This September during childhood cancer awareness month we are doing pies in the face and calling our blast . This is where we are using whip cream/cool whip and throwing pies in friends or family members faces. Much like the Ice Bucket Challenges that have been going on, our goal is to go viral. You can video yourself or someone else getting pied, post your video to social media, nominate or challenge a friend, and encourage donations to different research organizations such as Gunner's Magic Train foundation or any Childhood Cancer foundation of your choice! DON'T FORGET to use the hashtag on your videos/photos, follow Gunner's Magic Train on Instagram () and like us on Facebook to stay up to date and see who is getting pied! For more information, questions, comments, or to find out how you can get even more involved please contact Janna Gillespie or Savana Smothers.

01/31/2021

16 brave individuals who have lost their lives to DIPG. DIPG knows no race, age, ethnicity, gender, or economic status. It can happen to anyone, at anytime, and is incredibly unpredictable. We need to do better for our children, and all of those who are affected by DIPG. This is so incredibly unfair.
Team Nichols -
DaphnesFight
DIPG Online
The braveheart Vs the big lump
Gunner's Magic Train Offical Page
Monkey In My Chair
Easton Roy’s Journey “BEaston”

Today in 2007, we found out that Gunner had a tumor on his brain stem.  A DIPG.  Please help other children from losing ...
12/01/2020

Today in 2007, we found out that Gunner had a tumor on his brain stem. A DIPG. Please help other children from losing their lives from this deadly disease.

Tomorrow is giving Tuesday. Donations will be tripled if you donate tomorrow! Please think about giving if you can!

Starting at 8am tomorrow, we have the opportunity to triple all donations made on Facebook.

https://p2p.thecurestartsnow.org/265?fbclid=IwAR1u_u65UenBGSsOLEgWMc-vec0oTizyHgwXrMBAkQLSS7V4dZE4yr2YIWA

Fundraiser for The Cure Starts Now: 100 Families Strong Giveathon

To all Gunner’s Magic Train followers.....if you would like to donate, share or spread the word.  We would greatly appre...
11/18/2020

To all Gunner’s Magic Train followers.....if you would like to donate, share or spread the word. We would greatly appreciate you supporting children’s cancer. Please and thank you.

Fundraiser for The Cure Starts Now: 100 Families Strong Giveathon

“There’s no more serious diagnosis in all of human medicine than a brain tumor because it not only is a medical issue th...
05/21/2020

“There’s no more serious diagnosis in all of human medicine than a brain tumor because it not only is a medical issue that has to be treated, but it actually affects the psyche, the soul of the entire personhood of a human being,” Dr. Steven Kalkanis, chair of neurosurgery at Henry Ford Health System and medical director of the Henry Ford Cancer Institute in Detroit, told TODAY.

This is Gunner and he received that serious diagnosis in 2007. It was really hard to watch the tumor change his appearance but to also change him mentally too.

***May is National Brain Tumor Awareness Month. Pediatric brain cancer is one of the deadliest forms of childhood cancer and impacts thousands of children every year. We are Going Gray for the month of May in support and solidarity with the many who battle brain tumors every year, and especially with those children and parents who deal with this disease every day. It sure is tough to go through.

Joan E Reynolds Gillespie Jon Pope Anna Mae Henry

I don’t know the exact day of these pictures but I know it was diagnosis week.  After leaving PICU we were placed on the...
05/08/2020

I don’t know the exact day of these pictures but I know it was diagnosis week. After leaving PICU we were placed on the 6th floor. Gunner’s room was at the end of the hallway and so as I went up and down the hallway 3-4 times, I had the realization......we were on the Cancer floor. Although, we had met with many doctors and I knew his diagnosis and I knew the survival statistics(0% by the way), it still had not sunk in. They never used the word cancer. We heard mass on the brainstem. We heard Diffused Intrinsic Pontine Glioma(DIPG) but never the word cancer. We heard have hope but know that it is not good. Then after several walks up and down the hallway a voice in my head said, “My child has cancer. Wait?! What?! This can not be! “

In this picture, meet Anthony. Gunner and Anthony would meet in this lounge room close to Gunner’s room and we would play games. In these pictures we are playing Candyland and Go Fish. It was these times that gave us some normalcy in the moment. Gunner was beginning to feel and look himself from the strong doses of steroids. It was a bandaid fix until we started the radiation treatments.

I have thought a lot about kids now having to go through being in the hospital with cancer or any other illness with all the covid scare and it saddens me even more. We would never have made it through the week on this floor without making friends or speaking with other parents going through this similar crisis. I’m sure if we were in this hospital on this floor now we would not be in this lounge playing games with other patients. We would probably have to stay in our rooms. Sad, sad, state we are in.

I’m sorry to say I can’t remember what type of cancer Anthony had but he passed away as well. I don’t forget the families, their faces....they are in my heart and mind so often. I’m so grateful I met Anthony and his mother. There was another family that we met on this floor and I still follow her mother. It’s a club you don’t want to be a part of but you meet some amazing people in it.

***May is National Brain Tumor Awareness Month. Pediatric brain cancer is one of the deadliest forms of childhood cancer and impacts thousands of children every year. We are Going Gray for the month of May in support and solidarity with the many who battle brain tumors every year, and especially with those children and parents who deal with this disease every day. It sure is tough to go through.

I’m talking more about symptoms today  because Gunner was misdiagnosed and many times kids are.   We had to push and pus...
05/06/2020

I’m talking more about symptoms today because Gunner was misdiagnosed and many times kids are. We had to push and push for Gunner’s doctors to listen to us. Because he was premature we had many specialized doctors and it was our local doctor that paid attention to our cries. Mamas and daddys be alert and trust your guts.

This is my son, Gunner Henry Gillespie and he is forever 8 because of Pediatric Brian Cancer. There is a year difference in these photos. I have often wondered why did I not notice how he was looking. He had changed so much personality wise but I didn’t realize how much he had changed physically. We were having lots of fits. He was having night terrors. He was paranoid about things. He definitely didn’t want to go to school which he had never been like that before. He had been in daycare since he was 2. He attended preschool at iKids and Central Elementary, and two years of Kindergarten. He never didn’t want to walk into the buildings. However, that fall of his first grade year was awful when I would pull up to drop him off at school. I would have the line backed up to Parcell’s. Ms. Fran would try so hard to get him out of the van. The picture on the left was fall of his Kindergarten year. The one on the right is fall of first grade. He had lost a lot weight. He was hungry but when he sat down to eat....well he would say I don’t feel like eating or he would have trouble swallowing. He was complaining of feeling sick. I chalked that up to because he didn’t want to go to school. Sadly, he didn’t want to leave me. He was scared but he could not vocalize to us what he was feeling or the symptoms he was experiencing. There are many other symptoms but I will discuss more of them later.

***May is National Brain Tumor Awareness Month. Pediatric brain cancer is one of the deadliest forms of childhood cancer and impacts thousands of children every year. We are Going Gray for the month of May in support and solidarity with the many who battle brain tumors every year, and especially with those children and parents who deal with this disease every day. It sure is tough to go through.

Gunner went through radiation treatment for his tumor.  He lost his hair just behind the ears where the radiation beams ...
05/06/2020

Gunner went through radiation treatment for his tumor. He lost his hair just behind the ears where the radiation beams targeted through his head. The radiation changed a few things about Gunner. His hair was darker when it came back in. His eyes also changed color. They were also darker.

It’s hard to believe that Gunner would be gone 3 months from this picture. This picture was taken the summer after the radiation treatments were finished up. It seemed that the tumor caused Gunner trouble holding his head up and it caused his eyes to look out of the top of his head. We were living in Arizona receiving an holistic treatment and decided to go to Disneyland for a break. We loved it there and Gunner really did a great job traveling and spending a few days at Disneyland. He would tire easily but we would just get a wheel chair to help out. We made some fabulous memories. The radiation/holistic treatments bought us 11 more months with Gunner. I thank God for that time.

May is brain tumor awareness month.

And awareness is sorely needed.

Why? Because brain cancer is one of the most deadly and expensive cancers and brain tumor research is chronically underfunded.



Anna Mae Henry Jon Pope Jon Pope Joan E Reynolds Gillespie

It makes me so sad to see this sweet little face and know that he had to suffer going through a brain tumor.  I think of...
05/04/2020

It makes me so sad to see this sweet little face and know that he had to suffer going through a brain tumor. I think of all the littke kids and big kids having to go through cancer before Gunner, during the time of Gunner’s illness and after Gunner and it just makes me sad. It’s a hard road to travel and knowing what I do it’s so hard to see kids, parents, siblings, families walk that similar road today. We must do better. 😞

May is brain tumor awareness month.

And awareness is sorely needed.

Why? Because brain cancer is one of the most deadly and expensive cancers and brain tumor research is chronically underfunded.

This picture of Gunner was taken at school in the Spring of 2007.  It was the last professional picture I have of him wh...
05/03/2020

This picture of Gunner was taken at school in the Spring of 2007. It was the last professional picture I have of him where he looks healthy. I often look at this picture and wonder........was he sick here. Was the tumor growing and we just didn’t know. It was in the summer of 2007 that he would come inside from playing and complain of a headache. I would tell him that he probably was just getting too hot. So he would lay down and rest. This was one of the first signs. Many times children are misdiagnosed of having cancer. The symptoms are chalked up to being normal children’s illnesses. Be diligent and research. It’s always good to trust your guts mamas!

***May is National Brain Tumor Awareness Month. Pediatric brain cancer is one of the deadliest forms of childhood cancer and impacts thousands of children every year. We are Going Gray for the month of May in support and solidarity with the many who battle brain tumors every year, and especially with those children and parents who deal with this disease every day. It sure is tough to go through.

Gunner was born prematurely at 26 weeks weighing 1 lb 13 ounces.  He had to fight from the get go.  We spent 3 months in...
05/02/2020

Gunner was born prematurely at 26 weeks weighing 1 lb 13 ounces. He had to fight from the get go. We spent 3 months in NICU. We learned about two great organizations through Gunner’s prematurity.....March of Dimes and The Ronald McDonald which we try to donate funds to regularly.

So of course, after the diagnosis we were trying to find out if it was caused because of being born too early. What we found out was there are not many DIPG kiddos that were preemies. So it was not due to his prematurity. Once you hear your child has cancer, your mind is spinning but for some reason you need to know that it was nothing you did. The guilt is big. All of a sudden you are a member of a club that you really want nothing to do with. When the doctors finally shared what kind of tumor they obviously had very little good news to tell us. DIPGs are a very aggressive brain tumor with almost no survival rate. We were devastated to hear all this but we kept the faith and prayed very hard for a miracle.

May is Brain Tumor Awareness Month.   I would like to introduce to you my son, Gunner Henry Gillespie. He suffered from ...
05/01/2020

May is Brain Tumor Awareness Month. I would like to introduce to you my son, Gunner Henry Gillespie. He suffered from a brain tumor. A Diffused Intrinsic Pontine Glioma (DIPG) to be exact. Gunner was 7 years old when we found his brain tumor. He was misdiagnosed for awhile. We were lucky that we kept digging for answers because we were able to get 11 more months with him. I will continue to share his story over the month of May and continue to bring awareness to an awful disease.

Anna Mae Henry Joan E Reynolds Gillespie

02/05/2020

On World Cancer Day.....I would like to share that the MHS Student Council is a very active group at Marion High. They are the heartbeat of the school. They are are so involved in so many things that help our school and our community. Most recently, they raised money for Children’s Cancer at the Gold Rush Game in Memory of Gunner Gillespie and his organization Gunner’s Magic Train. They raised almost $1,000 from the sale of t-shirts, bracelets and socks! We opted to pay the money forward to The Cure Starts Now in hopes of making a difference in the lives of children! As I said the student council works hard and this week they had a blood drive to save lives! Please consider giving blood every chance you can!

Way to go MHS Student Council and thank you for all you do!

Marty Calcaterra Cameron

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