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Miracle Families
Miracle families are what make Dance Marathon's across the country as special as they are. ELONTHON is blessed to have several families that visit our event yearly. With miracle families talking during our event, the dancers really get a chance to realize what Dance Marathon and Children's Miracle Network are all about.
If you or your family would like to share your story with the students of Elon, please contact Nancy Rusell at nrussell2@elon.edu.
Below are the Miracle families that have participated at ELONTHON in the past. We hope that you got to meet them and listen to their stories while you were dancing at ELONTHON!
*Our Miracle Angels*
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Mason Lindley
12/10/1998-5/11/2005
Diagnosis: Lawn mower accident
Parents: Chuck and Tracey Lindley
Siblings: Lizzy
Mason Lindley was 3 years old when he was accidentally run over by a lawn mower. After several surgeries you would have never known. He really enjoyed ELONTHON and met one of his good friends, Joshua Holdner, an ELONTHON. Unfortunately, Mason passed after the 2005 Dance Marathon following complications from surgery. Mason is known on campus as one of our Miracle Angels and our first Miracle Child. The Lindleys are a permanent part of the Elon family. View Mason's memory page.
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Sherilyn Adams
7/11/91-11/14/07
Diagnosis: AML (Leukemia)
Parent: Laura Adams
Siblings: Veronica, Dustin, and Nicolette
Sherilyn was diagnosed with AML (Leukemia) when she was just 11 years old. After going into remission, she relapsed in 2005 and again in 2007. Although Sherilyn was unable to attend ELONTHON, her story has been shared with Elon students for the past few years. At a past ELONTHON, dancers wrote cards to Sherilyn. She is now one of our Miracle Angels |
ELONTHON Miracle Children
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Joshua Holdner, age 11
DOB: 6/26/98
Diagnosis: Tyrosinemia Type I
Parents: Mike and Teri Holdner
Siblings: Danielle
Website: www.joshuascure.org
Joshua has a rare, devastating genetic metabolic disorder known as Tyrosinemia Type I. Joshua is one of approximately 100 children in the United States and the only one in the state of North Carolina to have this rare genetic disorder. Josh has an older sister named Danielle. His favorite movie is Star Wars and favorite animals are dogs and dinosaurs. He and his family have joined us for ELONTHON a number of times and he always enjoys playing ping-pong and jumping in the moon bounce.
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Ashley Larimore, age 11
DOB: 6/9/98
Diagnosis: Distolic Dysfunction
Parents: Linda and Greg Larimore
Siblings: Daniel and Matthew (who passed away shortly after birth)
Now 9 years old, it is hard to believe that Ashley was born two-thirds of the way through a normal pregnancy. Ashley and her twin suffered from Distolic Dysfunction, but her twin, Matthew, only lived for thirty days. At birth, Ashley weighed one pound twelve ounces and stayed in the hospital four months, weighing less than five pounds when she finally came home. Ashley’s only continuing complications are asthma and a chronic heart condition. Ashley wants to work in neonatology (baby doctor) when she grows up and her favorite subject in school is math. Ashley looks up to her parents and grandparents and her favorite memory of ELONTHON is jumping in the moon bounce!
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Nick Marriam, age 16
DOB: 11/24/92
Diagnosis: Cancer survivor
Parents: Fred and Angel Marriam
Siblings: Alex
Nick is a 15 year old cancer survivor. When Nick was 6 years old, he was diagnosed with T-Cell Lymphoma cancer. He was in and out of the hospital, having to miss 2 years of school because of treatments. After Nick was feeling better, he wanted to help other children who have to spend long amounts of time in hospitals, like he had to. In March 2001 Nick and his cousin, Shelby, founded Nickelby Project, where they assemble and deliver gift bags for children who are battling serious illnesses. Their project has won many awards and recognition, as it has helped many parents and children. Nick and his younger brother Alex are regulars at ELONTHON who have spent the entire night for two years straight. Nick’s favorite ELONTHON game is dodge ball and his favorite memory is swimming in the pool.
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Jackson Payne, age 14
DOB: 11/17/95
Diagnosis: Cancer
Parents: Ann and John Payne
Siblings: Davis and Mitchell
We met the Payne family at Radiothon 2006 at Duke Children’s Hospital! They have attended ELONTHON for the past two years, sharing a slideshow about Jackson’s battle with cancer at a very young age. Jackson likes to read and play basketball. Jackson looks up to J.J. Reddick and he would love to learn to play the electric guitar. We look forward to seeing Jackson and his family at future ELONTHON events!
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Leigha Martinelli, age 15
Diagnosis: Cancer
Parent: Denise and Steve Martinelli
Siblings: Dustin and Tanner
Leigha has been a member of our ELONTHON Family for a couple of years. She is an enthusiastic 12 year old middle-schooler who has battled cancer throughout her life. She has been in remission for two years. Leigha is known for bringing her friends to ELONTHON and has stayed early into the morning for the past few years. Last year, she and her friends organized a dance contest for some of the ELONTHON dancers. Leigha’s father, Steve Martinelli is one of our most memorable speakers every year, and donates his bounce castle for our event. Mr. Martinelli is an Elon Alumni as well as the founding President of Kappa Alpha Order.
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Cooper Thomas, age 11
DOB: 11/30/97
Diagnosis: Born premature at Duke
Parents: Britt and Michael Thomas
Siblings: Eli
Cooper Thomas weighed just 1 pound, 3 ounces when he was born. His fathers wedding band fit up to his thigh . . . that is how small he was. Born nearly 16 weeks early, Cooper was rushed to Duke Children's intensive care nursery, where for more than five months he received the most advanced round the clock care. Cooper loves to dance and proved it to everyone, when he did the ELONTHON morale dance on stage at our last ELONTHON! He loved all the banners that students made for him, along with playing in the family room.
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Caden Turley, age 5
DOB: 8/13/04
Diagnosis: Seizure Disorder
Parents: Nikki and Brian Turley
Siblings: None
The Turley Family joined us in 2006 and shared their story with the ELONTHON dancers. His parents, Brian and Nikki, both work at Elon University.
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Vincent Fry, age 17
Diagnosis: Cancer
Parents: Don and Barbara
Now 15 years old, one would never know of the struggles that Vincent Fry endured during the early part of his childhood. He is fully recovered and has participated in ELONTHON for the past 3 years to share his story. |
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Caedon Baute, age 4
Parents: Brian and Gretchen Baute
Siblings: Cameron, Kierstin, and Raegan
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Jamie Cathell, Senior
ELON student!
Diagnosis: Cystic Fibrosis
Jaime Cathell is a senior at Elon University . She is very involved in Elon’s Campus Outreach and Phi Mu sorority. Jaime has battled with cystic fibrosis since she was young and has been a dancer at ELONTHON in the past. Jaime is studying history and is very outgoing!
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London and Jordan Gleason, age 9
Diagnosis: Twin to Twin Syndrome
Parent: Joy Gleason
Siblings: None
London and Jordan Gleason are twins who had twin-to-twin syndrome in the womb. London and Jordan are in elementary school and both are ELONTHON participants in past years. The girls have enjoyed playing in the play room and meeting dancers at past ELONTHON events.
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Emily Coleman, age 13
Diagnosis: Juvenile Rheumatoid Arthritis
Parent: Michelle Coleman
Siblings: Ellen and Elizabeth
We were fortunate to meet Emily and her mother at Duke Children’s Hospital’s Radiothon in 2006. Emily is a cheerful 11 year-old with juvenile rheumatoid arthritis. Although her condition is not life threatening, arthritis is a chronic condition that Emily will live with for the rest of her life. Emliy has both an older and younger sister who accompanied her on her Make a Wish Foundation trip to Walt Disney World!
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Abron Kelly, age 14
DOB: 8/26/95
Diagnosis: Nephronophthisis
Parents: Donovan and Debra Kelly
Siblings: Zach, Jacob, Devon, and Daniel
Website: http://www.caringbridge.org/nc/abronkelly/
The Kelly family joined us for the first time at ELONTHON 2007 and we even had the honor of hearing Abron sing in the morning! She was diagnosed in 2003 with Nephronophthisis, which is a rare genetically linked disease that destroys the kidneys. Abron has had an unsuccessful kidney transplant in 2005 and was placed on dialysis. In 2006, Abron received the gift of life from a 16-year-old that was tragically killed in an automobile accident. She continues on her way to recovery adjusting to the many necessary medications to support her kidney transplant.
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Sarah May, age 18
Diagnosis: Acute Myeloid Leukemia
Parents: Mike and Renee May
Sarah was diagnosed in 1999 with acute myeloid leukemia (AML) and was treated at Duke Children's Hospital. She received six months of chemo over a seven month period of time. Sarah hopes to become a doctor so that she can help others. ELONTHON 2007 was their first time at our event and we hope to see them again! |
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Matt Cooper, age 14
Diagnosis: Brain Tumor
Parents: Dan and Wendy Cooper
Siblings:
ELONTHON executive members were fortunate enough to run into Matt and his dog, Bluenose, at Radiothon at Duke Children’s Hospital in 2006. Matt is a 12 year old California native who was diagnosed with having a brain tumor at a young age. Matt loves his guide dog and loves speaking about Duke Children’s Hospital.
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Veronica Adams, age 22
Diagnosis: AML
Parent: Laura Adams
Sibling: Sherilyn
Veronica has AML, along with her sister Sherilyn. She is currently an impatient at Duke and is undergoing her 5th and final treatment. |
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Emily Hollis, age 8
Diagnosis: Anaplastic Medulloblastoma
Parents: Eddie and Dawn
Sibling: Trey
Website: www.emilyhollis.info
Emily just finished treatment for anaplastic medulloblastoma, which is a cancerous brain tumor. Although she was not able to join us for ELONTHON 2007, her mother, aunt and cousin Addision Ottaway (a junior at Elon) came and spoke about her time at Duke. The have a group called "Emily's Encouragers" that has been diligently raising funds for her medical expenses since August 2006. |
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Madison 'Madi' Smith, age 9
Diagnosis: Leukemia
Parents: Allison and Howard
Madi had leukemia whens she was younger and is currently doing much better! She collects money at school for Duke Children's Hospital and encourages everyone else to join as well. Although her family was not able to join us last year, we hope to see them in upcoming years!
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