Upgrade to the __tier_name__

You’re attempting to view exclusive content only for members in the __tier_name__.

Upgrade to the __tier_name__

You’re attempting to view exclusive content only for members in the __tier_name__.

Current Plan

Skip to content

25% Off Site Wide through July 17th! 🎉 Automatically applies at checkout.

Walli Cases
Previous article
Now Reading:
Pearson Family
Next article

Pearson Family

Meet the Pearson family! Jake and Kailee found out in June of 2021 that their daughter Mailee would be born with gastroschisis, a condition where the small intestines are on the outside of the body. They were told it appeared to be a simple case and Mailee would spend six weeks in the NICU. At 34 weeks, they went for a scan and the surgeon said they needed to deliver immediately. Mailee’s stomach had begun to close, which caused the intestines to cut off from the other intestines. Mailee spent 6 months in the NICU. She had 3 surgeries during that time and a couple weeks ago had an intense operation where they had to taper and staple 60 centimeters of bowel and connect it to an ostomy, and then connect the other lower intestines to a J tube. Because Mailee’s intestines don’t work, she gets all of her nutrients through TPN, which is a central line. Two times a day when they open the line for feeding, they risk the chance of getting an infection in the blood. This infection would be very dangerous to Mailee.

In the midst of dealing with all of this, Cooper, their almost 2-year-old son, stopped eating. He wasn’t gaining weight and lost close to all his body fat. Jake and Kailee had him in and out of doctors and hospitals with no answers. In June 2022, his eye started having random movements. They went in for an MRI and found a large brain tumor. It’s located on the hypothalamus, optic nerve, and pituitary glands going back towards his brain stem. It has also metastasized down his spine. Cooper started oral chemo in July in hopes that the tumors would stop growing. In September they went for an updated MRI to find that the tumor has grown almost a full centimeter bigger and the spine has a new small tumor. Due to the location of the tumor, it is inoperable. Cooper has been on two different types of chemo for treatment.

Jake and Kailee said it has been a journey, and it’s far from over. On November 16th, the Walli Gives Back Foundation showed our love and support for the Pearsons and had a fundraiser for the family.

About the Walli Gives Back Program:
When Walli Cases was created, owners Nick and Jenna Emery were recently married and both emerging from what they would describe as the darkest times of their lives. They are both passionate about reaching out to others in need because of the huge outpouring of love and support they received during their trials, including Jenna becoming a widow with an 8-month-old son and more recently losing her mother to cancer, and Nick going through divorce. When they created Walli cases, they wanted to help others feel the same hope and encouragement, and the Walli Gives Back program was created. Each month, Walli chooses a family to support.
This quote by Natalie Norton sums up why they are both devoted to "giving back" to others in their time of need: "There is always a light. Find it. Follow it. And then turn around and shine it as brightly as you can for those still feeling their way through the darkness."
Cart Close

Your cart is currently empty.

Start Shopping
Select options Close