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Kendra Scarrow - Urgent Surgery for Eagle Syndrome
Kendra suffers from Eagle Syndrome and Ehlers-Danlos Syndrome, two rare conditions which are sometimes found together. There is poor awareness...
Heims Family: Love Never Fails
This love story begins in 1995 when Ben and Tanya Heims met during their junior year of high school. They...
Brad's New Lease on Life
If someone you dearly loved were given a second chance at life, what would you give? How about a third...
Mike Duroe PinCancer
Mike Duroe was a legend. Not only was he a legendary coach of men and women in the sport of wrestling, his coaching encompassed many avenues of...
Barb's Nickels and Dimes
Barb – We are making and selling shirts so that when we put one on we can take a deep breath...
#TalynnStrong
Wednesday, September 12, 2018, Five month old Talynn was diagnosed with a tumor in her brain. By the grace of...
#DigMeeker
It’s a PINK OUT! *Orders must be in by August 27th. Come support the Mustangs and Spartans and WEAR your pink...
Misty Koebrick's Battle with Cancer: Keep Calm and Warrior On!
Misty was diagnosed with lupus in Feb. of 2005 and has been on numerous meds to manage her diagnosis. In Feb. of...
Friends of Marsha Light
Marsha Light was diagnosed with breast cancer twelve years ago, shortly after the birth of their youngest of three children....
Cara’s Journey
Carolyn Marie Armstrong – daughter, granddaughter, sister, niece, cousin, student, mentor, and friend – has soft tissue sarcoma in her...
Grant and his Gang: Supporting Grant in his journey with Type 1 Diabetes
This is Grant, our brave & amazing 4 year old. Grant was diagnosed with Type 1 diabetes on March 4,...
Neil and Anna Tunnicliff Medical Support Fund
Neil Tunnicliff was diagnosed with stage IV rectal cancer in January 2018, at 29 years old. After undergoing major abdominal...
Shaun Strong
Shaun gained his angel wings on June 3rd, after a long, courageous battle with AML. Thank you to everyone who supported...
Fighting For Preston Scott
In October of 2014, with autumn’s colors in full prime, I held my 4-year old son Preston tightly after hearing...
Mikey's Therapy
Michael is a 6 year old boy, full of laughter and smiles. He loves the Little Einsteins and Doc McStuffins,...
Sudden Cardiac Arrest Awareness
It’s been a year…and some. July 1st I celebrated my first “re birth day”. It was a stormy day in a park...
Accessibility for Jordan
The Beginnings of a Champion Jordan’s life began on July 29, 2009, which happened to be her parents’, Steve and Jen,...
Lori Poulsen Fighting Cancer
Lori Poulsen is fighting cancer again, with Stage 4 breast cancer. Weekly medical tests, doctor visits and treatment co-pays are...
Assist in another goal for Kenny!!
At the end of February 2017, Ken was seriously injured in a car accident. He had many injuries including a concussion...
PKU AWARENESS
Boston has a rare genetic disease called PKU. PKU affects 0.004% of the U.S. population. PKU is the body’s inability to...
Team Reed - Find a Cure for VWM
Our son Reed was diagnosed in 2015 with a very rare genetic and terminal brain disease called Vanishing White Matter, he...
THINK I CAN'T? TRI [so] ME!
Know someone with Down syndrome? Then you know the sheer determination that rides on that extra chromosome. Whether it’s learning how...
Phase 4: Adam Craig's Road to Recovering His Dreams
We have some difficult news to share. This 4th of July weekend, our son, Adam Craig, experienced a horrific diving accident at Lake...
Zay and Ellies PKU Fundraiser
Our kiddos, Zay & Ellie Austerman were born with a rare genetic disorder called Phenylketonuria (PKU). We like to say...
The Jack of our Hearts
Meet Jack: Jack has Lissencephaly, Miller-Dieker’s Syndrome. He was born with a very rare brain malformation. His brain did not form...Do you, a family member, or friend need help meeting the financial demands of a medical condition? Let us help!
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