Help and Hope Happen Here

6 year old Miriam Koska was experiencing leg pain, abdominal pain, fevers, night sweats and fatigue in the fall of 2025 when she was diagnosed with an offshoot of Neuroblastoma known as Ganglioneuroblastoma. This form of Pediatric Cancer has a similar treatment protocol to the more well known Neuroblastoma. Miriam has been through difficult treatment but is doing as well as possible as she enters her next phase of treatment at the Mayo Clinic in Rochester, Minnesota.  

Megakaryoblastic Leukemia is an even more aggressive form of Acute Myeloid Leukemia, which always is a difficult form of Pediatric Blood Cancer.  Olivia White was 15 months old in February of 2024 when she was diagnosed with this disease. After some very difficult struggles with her treatment, Olivia has been feeling much better over the past months as she approaches her 4th birthday this coming November.

For the second time in just a few months on this podcast, we heard the story of a Fungal Infection that attacked a child who was in treatment for Acute Lymphoblastic Leukemia and this infection could not be stopped for causing a child to pass away. This time it was Lola Aguilar, the 6 year old daughter of Alyssa who spoke beautifully on our podcast about what her beloved daughter had to go through after falling to the floor on Halloween in 2024, just as she was about to go Trick or Treating. 

Harper Wengrod was born on January 12th of 2024 and by the end of that year , a lump on her abdomen that her dad Joe found after Thanksgiving that was thought to be Neuroblastoma was the probable cause. That was not to be the case however as Joe and Melanie were to learn that Harper was actually suffering from Stage 3 Sertoli Cell Ovarian Cancer. This is such a rare diagnosis for a child not even a year old to receive, as Ovarian Cancer is found in women decades older than that. Harper continues to fight her battle on a daily basis and physically it looks as if she is a completely healthy toddler.

After hearing the story of a friend that had a child who was diagnosed with a form of Pediatric Cancer, Mike Dechristopher got involved in this Pediatric Cancer cause in 2012 and started the Dylan Project. This Non-Profit now has helped hundreds of families in the New England area and brings joy to these kids by buying gifts each holiday season and delivering them to their homes, giving him the nickname of the Real Life Santa Claus, a nickname that is well deserved. 

Lainy Sharpe began to feel numbness in her legs, followed by paralysis when she was 12 years old in the summer of 2023. Her diagnosis was Mesenchymal Chondrosarcoma, which as rare of a diagnosis as it gets. Lainy fought as hard as possible before passing away in January of 2025 and was very much a part of the Pediatric Cancer community during her fight, which was proven by her winning the Children's Healthy Hero Award for her dedication to helping others at Banner Children's Hospital in Tucson, Arizona.

Elena Lappostato was complaining of mouth pain in September of 2025 and just a couple of weeks later, she was diagnosed with Neuroblastoma when she was 3 years old. Since that time , Elena has undergone difficult treatment including 2 autoglous stem cell transplants and is now doing well and has recently begun the next phase of her treatment which is Post Consolidation.

After winning the Vault event and finishing 2nd in the All Around Competition in the Hawaii Gymnastics Championship in November of 2017, 11 year old Kaylan Haywood competed for the first time since her winning performance in January of 2018. What resulted was Kaylan's side being weak, her foot was dragging, and her arm was hanging. In February she was diagnosed with DIPG and only was able to live for 6 more months, as she passed away on August of 2018 from this most dreaded form of Pediatric Brain Cancer.

Dana Quiroga felt a pain in her knee during her entire soccer season in 2023 and during that summer this pain did not go away, leading to her diagnosis of the Bone Cancer Osteosarcoma. Dana underwent a replacement for her knee and tibia with a prosthetic substitute and now 3 years later, Dana is feeling well and has already chosen what she plans to do with her career which will involve Pediatric Nursing.

Grace Fulcher was 16 years old in 2015 when she began to complain about double vision. Her double vision led to a diagnosis of a non curable Pediatric Brain Tumor known as an Anaplastic Astrocytoma. Grace was given 3 years to live and she did her very best in trying to make those 3 years meaningful. Grace continued with her high school studies, being a member of the National Honor Society for 3 years, and graduating Summa Cum Laude with a 4.4 Grade Point average. Because of the acceleration of her brain cancer, Grace went to college for only her first semester of freshman year in which she hoped to become involved in Neo Natal care. Grace passed away at the age of 19 on October 24th of 2018.

Darline Medina's daughter Brooklyn was full of health for the 1st 2 years of her life until the winter of 2023 when Brooklyn began to experience abnormal movements in her left eye. Her eye looked okay when examined by an eye doctor but her walking did not look okay and this led to her diagnosis of DIPG. Brooklyn's diagnosis took place in April of 2023 but her life span from that day until her passing on February 17th of 2024, was just 10 months, and took place one month before her 4th birthday.

Jameson Doud was nearing his 8th birthday in August of 2024 when he was diagnosed with a Midline High Grade Glioma Pediatric Brain Cancer. In March of 2025 the Doud family got very good news that there were no signs of any cancer from the most recent scans but just a couple of months later, Jameson's scans showed that his cancer had spread to his bone and Jameson was not expected to last until Christmas of 2025. That expectation went too far unfortunately and James on passed away from this disease on August 12th of 2025.

In May of 2025, 5 year old Rosie Wittmayer was found to have a double ear infection and then began to develop fevers every 2-4 weeks. These fevers were checked out regularly but no solution was found , with one possibility floated that she had the Mumps. Finally on August 27th, Rosie and the Wittmayer family received her diagnosis of B Cell Acute Lymphoblastic Leukemia. Rosie has been through nearly 11 months of treatment and still has more than a year left as her scheduled date to end her treatment protocol will be in November of 2027. Fortunately Rosie is doing well physically .

Zach Arter had been serving youths in Omaha Nebraska for 15 years in various capacities and then decided to focus on helping Pediatric Cancer patients in August of 2024. That is when he started his HELP 1 PERSON TODAY with this non-profit which tries in a number of ways to help these kids who have to go through difficult treatment during their individual cancer battles.

As Toni and Dylan Franklin were in the playground with their children Noelle and Dylan in the spring of 2024, Noelle asked her dad to look at a bump that had formed on her leg. Withing a week Noelle was diagnosed with Osteosarcoma, a very difficult Bone Cancer. After being treated at the Pediatric Cancer hospital at Duke University which did not go well, Noelle was transferred to the Pediatric Cancer hospital at the University of North Carolina. Despite the treatment that was more to the benefit to Noelle, she was unable to recover and passed away on May 12th of 2025, almost exactly one year after her original diagnosis. 

After being shuttled back and forth between her home and hospital emergency rooms for months in 2015 because of recurring fevers, Addie Stiverson received the very difficult diagnosis of Hepatoblastoma in the autumn of 2015 while visiting family in Colorado. Although her doctors were optimistic that Addie would recover from this Liver Cancer, her body said otherwise as after a Liver Transplant, Addie's cancer spread to her lungs and then her brain. Addie passed away on December 20th of 2016, having lived for only 3 years and 17 days.

A massive Malignant Rhabdoid Tumor was found on 4 month old Kinley Mercer's left kidney in the summer of 2022 and she was diagnosed with Stage 4 Kidney Cancer.  Upon undergoing chemotherapy treatment, Kinley went through scans that showed that her cancer had spread very quickly, so much so that her doctors declared that her cancer was no longer curable. Kinley passed away from this very difficult form of pediatric cancer on November 12th of 2022, only 7 1/2 months after her birth.

Andrea Wilson had two very difficult health crises on her hands, one with her younger daughter Phoenix who was diagnosed with Stage 3 High Risk  Neuroblastoma when she was 3 years old in 2017,  and one with her older daughter Liberty who contracted Septic Pneumonia while Phoenix was in treatment. Phoenix was on the 7th floor of Phoenix Children's Hospital while Liberty was on the 9th floor. Fortunately both girls are surviving and doing well and Andrea and her family are looking onto the possibility of trying to build a Western Style Ranch with horses, so that Pediatric Cancer families can have a place to go to for healing purposes. 

The counties of Knox, Laurel, and Whitley, in Southeastern Kentucky have seen 10 DIPG diagnoses since 2024, an extraordinarily high number of cases in such a condensed area. Shay McAlister is an Independent Journalist who has been investigating this issue and will discuss the problems that are related to this most deadly form of Pediatric Brain Cancer, which normally sees 1 or 2 cases in the entire state each year. Shay has written 2 major articles on this issue and will be continuing her goal to find some answers that are needed as to why this is happening.

After experiencing a number of illness when he was 2 years old going into the spring of 2025, Caitlyn and CJ Jennings thought that their beloved son Brooks was experiencing normal illnesses that many toddlers may experience. Unfortunately that was not the case. Brooks was diagnosed with a Fusion Mesenchymal Tumor that was located in his lung and then spread to his Pelvic Bone. Brooks continued to feel well until August of last year when his health went downhill, leading to his passing on October 25th of 2025.

Shaya Rees Frum was 14 years old when her then 11 year old sister Jessie was diagnosed with DIPG on March 3rd of 2011.  Jessie passed away from this terrible Pediatric Brain Cancer on January 5th of 2012, but not before laying the groundwork for the Jessie Rees Foundation that has been directed by her father Eric for the past 14 years. I spoke with Erik about Jessie and the Foundation back in April. Shaya has taken on a major role in the Foundation, it is her full time job, and hopefully she will be the person to take on its Leadership Role, when Erik and Shaya decide that the time is right .

Maribeth Ditmars has suffered plenty of heartache and loss for the past 25 years, beginning with the diagnosis of Acute Lymphoblastic Leukemia in 1997 and the subsequent passing of her son Christopher at the age of 14 in 2001. This was followed by the passing of her younger son Jarrod when he was 21 years old from an accident on July 4th of 2015, which left him unconscious for the last 4 days of his life. In between those years, Maribeth successfully battled her own demons with her dependence on alcohol, to the point where she has been able to counsel many people who have had similar problems and she is now very involved in helping others. Maribeth has now been sober for 22 years . 

During Alisha Harper's pregnancy, she was told that there was a 60 percent chance that her son would be born with Down Syndrome. That statement turned out to be a correct one as Chase was born in December of 2016 with this illness and by the time Chase was 4 years old, Alisha saw that his Down Syndrome was manageable. One month after feeling as good as possible about how Chase was doing, he developed a body rash which turned out to be a symptom of Acute Lymphoblastic Leukemia. Despite having this 1-2 punch thrown at him, Chase is doing well as he is now 9 years old and living his best life possible. 

10 year old Charli Martin hurt her shoulder while competing in the New York State School Wrestling Tournament when she was in 5th grade in 2023. While going for Physical Therapy, Charli noticed a lump on her neck and after taking antibiotics and still in therapy, the pain in her shoulder did not go away. Charli then had this lump biopsied and the result was her diagnosis of High Risk B Cell Acute Lymphoblastic Leukemia. Charli has now completed her 8th grade year and at 13 years of age is back playing sports and living the life of a normal and healthy 13 year old teenager.  

Gwen Mysiak worked in the field of Public Broadcasting for 19 years in Buffalo and during that time, her friend's cousin Andrew Pawlak was 13 years old and in 7th grade when he was diagnosed with a form of Pediatric Cancer and passed away 2 years later. Not too much time went by after that before Gwen switched carriers to become the Punt Pediatric Cancer Collaborative's Executive Director in 2012. This Collaborative focuses on 6 major programs to help families deal with a Pediatric Cancer situation, with a special emphasis on their bereavement program.

Sydney Belsher has been through a great deal in her still very young life as she is 12 1/2 years old, which started with stomach issues almost from her birth in the fall of 2013, and then her diagnosis of Infantile Acute Lymphoblastic Leukemia which came when she was 6 months old in April of 2014. Right after her diagnosis Sydney's lifespan was very uncertain as her doctors feared she would have a stroke and may not survive. This did not happen thankfully but Sydney has battled both physical and mental issues over the years . Fortunately Sydney has survived all of her issues and is trying to live her best life possible.

When she was 4 months old on November 14th of 2023, Kalia Arrayan was diagnosed with High Risk B Cell Acute Lymphoblastic Leukemia. This diagnosis came as a complete shock to her parents Heather and Casey who did not see any clear symptoms before a routine checkup showed a lump on her spleen. Kalia went through a very difficult treatment process for the next 8 months before she underwent a Bone Marrow Transplant with her 11 year old brother being her donor. Kalia has been doing much better over the past nearly two years as she approaches her 3rd birthday.

Marissa Metcalf does not remember many details from her treatment during her battle with Acute Lymphoblastic Leukemia which took place in 2010 when she was 3 1/2 years old. What she does know, now that she is 19 years old and looking at possible careers, is that this form of Pediatric Blood cancer has affected her in different ways as she approaches 20 years of age, and wants to help others who have been diagnosed with cancer by becoming an Oncology Nurse, which would be a great accomplishment for her and a good thing for her future patients.

Lily and Sebastian McGrath's 2 1/2 year old son Bryson was first thought to have a Wilms Tumor before his Pediatric Cancer diagnosis was changed to Stage 4 Neuroblastoma in the early days of 2023. Lily and Sebastian had to put up with a number of more than questionable medical decisions during Bryson's fight and also had to endure the final days of Bryson's life who while in Hospice Care, was  promised 24 hour round the clock availability should they be needed and when they were needed the most, they were nowhere to be found. Lily also had to watch after Bryson passed away while one of the Hospice nurses attempted to rip off all of Bryson's dressings, instead of treating her son with the kid gloves that he more than deserved. 

Cherie Colbom is not only an expert Nutritionist, she has written 35 books, including her Juicing For life which has sold 2 million copies and her current book which became available on April 28th entitled The Truth About Seed Oils. Cherie will talk about how Seed Oils can have negative health effects for consumers and will discuss the link between Seed Oils and Pediatric, Adolescent and Young Adult, and Adult Cancer. Cheire has been on television many times discussing this issue and has also written many articles on this subject.

Brody Bailey is one of possibly two children in the World who have been born with a Congenital Diaphragmatic Hernia and then diagnosed with Neuroblastoma. Lauren and TJ Bailey are Brody's parents and will talk about his journey with the good news being that he is more than 3 years old and is doing as well as possible health wise. The Bailey family has received great support from their Township of Deptford New Jersey community, especially from Rich Nardiello who is the head of the great Pop Pop Custom Cars Non-Profit and a wonderful advocate for the cause of Pediatric Cancer. 

Jordan Belous has always had a soft spot for Pediatric Cancer Patients and when she was 16 years old in 2015 she issued a "challenge", much like the Ice Bucket Challenge, when she created a video that went viral by dancing for 14 seconds to the song WHIP/NAE NAE by Rapper Silento to either Dance or Donate. More than 7000 people took up her challenge and donated more than $100,000 to Memorial Sloan Kettering to fight the cause of Pediatric Cancer. That was the birth of her WHIP PEDIATRIC CANCER Non- Profit. Since that time Jordan has personally developed long standing and iron clad friendships with more than 300 Pediatric Cancer patients and has done extraordinary work for these kids, their families and the cause of Pediatric Cancer. 

Matt Giegerich has been the Chief Executive Officer of The Matthew Larson Foundation for Pediatric Brain Tumors for the past 18 months. This foundation, also known as the Iron Matt Foundation, was started by young Matt's parents Kelly and Greg after Matt passed away from the Pediatric Brain Cancer Choroid Plexus Carcinoma in 2007, when he was 7 years old. This Foundation focuses on helping families with financial assistance as well as focusing on raising money to award Grants to researchers who are trying to help solve the many issues that are involved with Pediatric Brain Cancer.  This Foundation has now awarded over 100 Grants to researchers in the United States and Canada. 

Mason Fox was 10 years old when he was diagnosed with Acute Lymphoblastic Leukemia in April of 2023. Mason then went through treatment and was doing very well with his recovery before a Fungal infection got the best of him quickly in February of 2024, and led to his surprising and unfortunate passing, not even 10 full months past his original diagnosis. His parents Leslie and Michael detail the amazing persona that Mason had as he was most concerned with helping others even during treatment for this blood cancer, as he bought toys with his own money and would walk down the halls at St. Joseph's Children's Hospital with these toys in a wagon, hooked up to his IV pole, and would deliver them to the other Pediatric Cancer patients on his floor. 

Liam Bascle was only able to live 7 1/2 years because of an Ependymoma Brain Tumor that he was diagnosed with in April of 2015. His persona resonated with many people despite his tender age and many tributes came his way after his very unfortunate passing in November of 2021, after fighting with this Brain Tumor for 6 1/2 years . To honor the memory of their beloved son his father Nick, with support from his mom Sarah, started the Links Fore Liam Golf Tournament in New Hampshire to help raise money for the cause of Ependymoma and Pediatric Cancer. This tournament is now held in  New Hampshire, Colorado, and Louisiana, with at least 4 more locations on the horizon. 

After being diagnosed with Acute Myeloid Leukemia when he was 3 years old in 2012, Cullen Cisneros was able to live the next 8 years of his life free of cancer until 2020 when leg pain during a baseball game led to a diagnosis of Ewings Sarcoma. Cullen's parents Amy and Matt will talk about their beloved son, who fought from 2020 until May of 2025 to try and do everything he could to stay alive, only to pass away from this Bone Cancer when he was 15 years old. 

Amelia Mijach's then 2 year old son Hayes was diagnosed with High Risk Acute Lymphoblastic Leukemia when he was 2 years old in August of 2024 and the reason for his high risk status was because of his extraordinarily high white blood cell count at diagnosis. Hayes then contacted a serious fungal infection during his consolidation phase of his treatment and during the next year and a half of treatment he needed to fight off a battle of Neutropenic Fever and he experienced other battles as well. Finally in  December of 2025 Hayes turned the corner and is doing much better physically and is as active as possible. 

Erik Rees became an amazing Cancer Dad and Pediatric Cancer advocate during and after his daughter Jessie battled with and passed away from DIPG at the age of 12 in January of 2012. Erik talks about his beloved daughter and then details the Jessie Rees Foundation which was started because of Jessie's wish to help Pediatric Cancer patients who were at Children's Hospital of Orange County in California. Jessie started her Jessie's Joy Jars while battling her Pediatric Brain Cancer, and nearly 600,000 patients have received these Joy Jars in the United States and across the globe since Jessie was able to donate 3000 of these to patients before her passing. This foundation now raises 5 1/2 million dollars each year.

Ben Shroyers then  2 year old daughter Hannah was diagnosed with Stage 4 Neuroblastoma in 2018, then was diagnosed with Histiocytosis which ended up in her brain before she became cancer free in 2021. Now 10 years old and in 3rd grade, Hannah is doing well health wise. Ben started the Casting For The Kids Foundation in 2020 during the pandemic as a way to help families both emotionally and financially through a fishing tournament which has now raised $460,000 over the past 6 years . Ben is an amazing advocate for families in the Sarasota, Florida area and what he has accomplished through his foundation for many individuals and families in the Pediatric Cancer world is truly outstanding.

When Kelly DiGiammo's son Brayden was 13 years old in early 2024 he developed troubling health symptoms, including going from being one of the fastest runners in the school to losing his breath and running very slowly, experiencing continuing colds, and then having a bout with the flu. Brayden was diagnosed late in February of that year with Acute Myeloid Leukemia. Brayden successfully completed a Stem Cell Transplant and has been in remission since May of 2024. Kelly and Brayden will talk about his journey which has been a successful one and Kelly will also talk about her experiences getting involved in advocacy work for the cause of Pediatric Cancer. 

The bill AB 703 which was signed into law by California Governor Gavin Newsom and which I talked about with Sahil Metha on my podcast a few weeks ago is just one of the important accomplishments that was led by the Society Of Emerging Leaders, which was co founded by Mary Kemp in 2022 and is under the direction of Kaitlyn Lee. This law now gives the voters in California the option to check off a box on their state tax form if they would like to donate to the cause of Pediatric Cancer. Mary and Kaitlyn will talk about many of the other programs that The Society For Emerging Leaders have started in California to benefit the cause of Pediatric Cancer.

Jacob Orlick is now a senior in High School and making plans to attend Penn State University in the fall. Jacob was 11 when he was diagnosed with the Bone Cancer Ewings Sarcoma, had his right leg amputated, but has been able to live a fulfilling life which includes his work as a Motivational Speaker and his Podcast entitled Motivational Mic. Jacob is hoping that his career path leads him into becoming a Professional Sports Broadcaster. 

Dr. Katerina Levy decided to write her book THE HEALING Garden while she was a resident at the Broward Medical Health Center in South Florida. This book was based on the Healing Garden that she saw while at that Medical Center and is full of strategies that work for kids who are trying to cope with being diagnosed with any form of Pediatric Cancer. Dr. Levy is still in the very early stages of her career as a Pediatric Psychologist.

Being treated terribly by her swimming coach and eventually belittled and made fun of by her teammates, Meghan Macantee was diagnosed with Acute Myeloid Leukemia in the fall of 2023, during her sophomore year at SUNY Potsdam where she was a member of the swimming team. Before her diagnosis, Meghan went to the emergency room 11 times where she was also treated poorly. In short, no one believed this wonderful young woman The fact that she was diagnosed with such a difficult form of Pediatric Cancer says it all. Meghan is now doing well health wise and giving back to others with her non-profit MEGHANSMISSIONINC. Meghan never received an apology from any of the people who so terribly wronged her. SHAME ON THEM.

Payton Alexander was living a healthy and normal life for a 14 year old until late in 2017 when she began experiencing symptoms that needed to be checked out. These symptoms led to her diagnosis of Ewings Sarcoma in January of 2018. Payton continued to try and live as good of a life as possible as she joined the Make A Wish and Little Warrior Foundations to try and help other patients suffering from Pediatric Cancer. Payton fought for 3 1/2 years with this Bone Cancer before her passing in November of 2021 when she was 19. Her mom Kim, who talked beautifully about her beloved daughter during our podcast, has been involved in the cause of Pediatric Cancer since Kim's passing, with her Payton Alexander Foundation. 

Tamy Bell's son Griffin was born 3 months prematurely in June of 2017 and 16 months later was diagnosed with Neuroblastoma in September of 2018. Griffin relapsed on two occasions after that but then in April of 2023, had a 3rd relapse that was more severe as his cancer had spread to his orbital bone. This relapse took away any realistic hope of further treatment that would help Griffin, and he passed away on March 18th of 2024, 3 months before his 7th birthday,

Sahil Mehta's older brother Ronil wanted to donate his brain to Stanford University after his passing from DIPG in 2018 in the hope that it would help another DIPG Victim in the future. Sahil took this request as his personal responsibility and then got so involved in the cause of Pediatric Cancer that he eventually worked with California Assemblyman Alex Lee to form the bill AB703, that would give the California State Taxpayers the option on their tax forms to check a box that would allow them to donate to the cause of Pediatric Cancer. This bill was fully formed and ready by July of 2025 to have Governor Gavin Newsom sign it into law. California is now only the 8th state in the country to have this provision on their tax form and Sahil is hoping that many other states will join in this effort to bring much more money into the cause of Pediatric Cancer.

Carrigan Nelson was diagnosed with Osteosarcoma in March of 2019 and fought for the next 69 months with this form of Pediatric Bone Cancer until her passing on Christmas Day in 2025 when she was 24 years old. Carrigan was a truly Iconic young woman who did so much for the cause of Pediatric and Adolescent Cancer and was beloved by everyone that knew her. A very well accomplished Singer, Dancer, and Artist, she looked at life with Joy and nothing mattered to her more than trying to inspire other young patients with her singing and reaching out in compassion to help others in any way possible. Her mom Tammy, her Aunt Bonnie, and her greatest friends Deaven Pierpoint, Hannah Nasser, and Madison Quinn will talk about their beloved daughter, niece, and friend in this Tribute To Carrigan.

Tony Garcia will talk about his early in life Pediatric Cancer battle which began in 1973 when he was diagnosed with Leukemia  when he was 2 1/2 years old. Tony's treatment finally ended nearly 10 years later in 1983 and since that time he has been doing as well as possible for the past 43 years, as a long term Pediatric Cancer survivor. Now 55 years old, Tony just published his first book (memoir) at the end of January called MY CHILDHOOD CUT SHORT. SURVIVING LEUKEMIA AND FINDING PURPOSE BEOND PAIN. Tony also is involved in supporting Pediatric Cancer patients through fundraising, volunteering, and advocacy work. 

Sydney Leandro was 5 years old on Easter Sunday of 2020 when she was diagnosed with Acute Lymphoblastic Leukemia. Now at age 11, Sydney is feeling and doing well and is able to live a good life. In 2025 her brother Jack, who is now 9 years old, decided to start a non-profit called PUCKS FOR BUCKS in which he shot approximately 200 pucks a day from his driveway into a hockey goal and raised $1.00 for each puck he shot, which he donated in Sydney's honor and to help other Pediatric Cancer Patients. He donated this money to the A Wish Come True Non- Profit which had treated the Leandro family to a trip to San Diego in 2023. Jack will continue his non profit after his current hockey season ends and will begin from where he left off last summer in which he had totaled 10,027 pucks shot.