Patient Ambassadors

Patient Ambassador Club - Allison

Allison

During a fun afternoon playing “capture the flag”, 14-year-old Allison attempted to jump over a stone bench to outrun her competitors. Allison’s foot did not clear the bench, resulting in a sprained ankle and a neck bone bruise. Allison’s physical therapist noticed her ankle wasn’t moving and requested brain and spine scans which all came back normal. She was then referred to Dr. Shawn Funk, a pediatric orthopedic surgeon at CHRISTUS Children’s. While on the path to healing from an Achilles tendon lengthening procedure, Allison’s left hand began to curl in, completely out of her control. Dr. Funk immediately knew this was a neurological issue and admitted Allison for further testing. Doctors diagnosed her with dystonia, a neurological movement disorder that causes involuntary muscle contractions, resulting in abnormal postures and repetitive movements. Specialists concluded that the traumatic sprain to Allison’s ankle and neck bone bruise likely caused the dystonia to begin to present itself. It has been almost three years since Allison’s initial diagnosis, and she continues to push forward every day while advocating for herself and for other patients who might be facing the same diagnosis. 

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Destany A.

Destany A.

Destany, a varisty cheerleader at 16 years old, was at the top of a pyramid when it unexpectedly collapsed. She endured a severe concussion, spinal shock, and was unable to walk on her own. She had major loss of motor strength on the right side of her body. She could not walk, write, or feel with her right hand. She had trouble reading and suffered from severe headaches. Destany underwent six months of extensive occupational and physical therapy and made a dramatic recovery.

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Arredondo Twins

Marceline and Phoebe A.

Marceline and Phoebe were born at 23-weeks-gestation at CHRISTUS Santa Rosa Hospital – New Braunfels. The twins both weighed just a little over one pound each and were extremely frail. Marceline and Phoebe were immediately airlifted to CHRISTUS Children’s for further treatment and were admitted to the Neonatal Intensive Care Unit (NICU). Upon arrival, doctors quickly got to work to care for these tiny girls. Phoebe underwent surgery right away to repair a small bowel perforation and continued to have surgeries on her GI tract. Marceline had extra blood flowing to her lungs and received surgery to close the artery as well as surgeries to correct cranial abnormalities. Today, Marceline and Phoebe are two fiery five-year-olds. 

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Holly and Heather

Holly and Heather C.

Holly and Heather were born severely premature, weighing just one pound, 10 ounces, and two pounds, respectively. The identical twins were rushed to the Neonatal Intensive Care Unit (NICU) at CHRISTUS Children’s and were fighting for their lives. Holly has undergone eight resuscitations, 17 brain surgeries, two lung surgeries, two intestinal surgeries, three eye surgeries, one cranial reconstruction, and more. Thanks to generous supporters like you, the sisters beat all the odds and continue to grow stronger together.

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Marc D.

Marc D.

In October 2016, 18-year-old Marc had an infected hair follicle and his mom knew something was not right. After several tests and hospital visits, Marc was referred to specialists at CHRISTUS Children’s. Doctors performed a biopsy and learned Marc had Leukemia. Marc underwent several rounds of chemotherapy, spinal taps, and radiation therapy over 3.5 years and completed his chemotherapy in January 2020. Marc tries to stay positive and plans to start sharing his story with the community with hopes of helping others in the fight against cancer.

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Camilla G.

Camilla G.

Camilla was born with Trisomy 21 – Down Syndrome and had two holes in her heart. She underwent emergency life-saving surgery. Camilla’s mom, Jennifer, had fundraised for Children’s Miracle Network Hospitals for several years as a Walmart associate. She had never seen where her fundraising efforts went, until she had to experience services at a children’s hospital first-hand when Camilla was born. Camilla continues to see several specialists at CHRISTUS Children’s.

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Violet G.

Violet G.

When 12-year-old Violet started losing weight, experiencing mild panic attacks, and losing color in her skin, her parents sought help from her pediatrician. After running labs on multiple occasions, results showed significant for moderate anemia, which prompted a referral to pediatric hematology at CHRISTUS Children’s. After more tests, Violet was diagnosed with myeloid-lymphoid neoplasm with eosinophilia (MLN-eo), a hematologic neoplasm in which, due to an underlying gene arrangement, the bone marrow makes too many copies of a type of blood cell called eosinophils. Her diagnosis is extremely rare in pediatric patients, especially in females, making the diagnosis very difficult and unusual. Violet’s doctors also did a baseline check of her organs and found that her heart had suffered some damage from her diagnosis. Violet started immunotherapy and heart treatment and she slowly began getting better. Violet is doing great today and hopes to grow up to pursue a career in the medical field to help other patients like herself.

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Maddie K.

Maddie K.

In December 2016, Maddie went in for a routine pediatric check-up where her pediatrician noted she was underweight. At four months old, Maddie weighed only nine pounds, when her expected weight should be 13-15 pounds. The family scheduled an appointment at CHRISTUS Children’s, were cardiologists diagnosed Maddie with a large ventricular septal defect (VSD), a small aortic valve, and a small hypoplastic aortic arch, all serious congenital heart defects. Maddie’s VSD and small hypoplastic aortic arch required immediate surgical repair. Physicians performed the life-saving surgery with no complications. Today, she is happy, healthy, and thriving – and busy, too! Maddie started kindergarten, plays T-ball, and takes dance classes.

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Emmalee M.

Emmalee M.

Emmalee was born with a cleft lip and nasal deformity, a partial left palate, and a hemangioma on her right eyelid. Her cleft lip was causing Emmalee to have difficulty bottle feeding and she was struggling to gain healthy and necessary weight. If left untreated, the hemangioma, a noncancerous, dense group of blood vessels, above her right eye could potentially damage her eyeball or even cause blindness. Corrective surgery was her best option for a healthy, normal life. From November 2015 to 2018, Emmalee underwent corrective surgery for her lip, nose palate, and eyelid. Month by month, her doctors noticed a drastic change in her appearance and health. The surgeries were all a complete success. Once Emmalee’s lip healed, she was able to bottle-feed properly and slowly began to gain weight. The hemangioma that was once present on her tiny face had disappeared. Because of her partial palate, she will require a bone graft when she is older, but for now, Emmalee is enrolled in Pre-K for SA and enjoying spending her days making new friends and learning.

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Maritza M.

Maritza M.

Maritza is Emmalee’s biological little sister, who was born exactly one year after Emmalee. Upon her birth, doctors noticed Maritza also had a cleft lip and nasal deformity, and a partial right palate that would all require corrective surgery. She underwent a cleft lip and nose reconstruction surgery at just nine weeks old. The family was overjoyed with another successful surgery. Maritza will also require a bone graft when she is older, but for now she is doing great and having fun in head start.

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