Meet Chelsea & Tracy Ashworth

Tracy Ashworth never thought a warm autumn afternoon playing in a pile of leaves in the backyard eight years ago would lead to her daughter's need for a feeding tube.

A day of fun was followed with days of pain, and it would take more than a year before Chelsea Ashworth, then 10-years-old would be diagnosed with Lyme disease and a condition called Bartonella. Bartonella is a bacterial infection carried by ticks and other insects that can cause abdominal pain and gastroparesis, a delayed emptying of the stomach due to a partial paralysis of the stomach muscle. These co-infections shut down Chelsea's digestive system, leaving her unable to eat, drink or take any medication orally.

Path to Diagnosis

During the difficult path to her diagnosis, Chelsea was fed using a peripherally inserted central catheter (PICC) and total parenteral nutrition (TPN), but these were not long-term solutions as they were hard on her liver and kidneys. With her liver failing and the family running out of options, doctors recommended the MIC-KEY* jejunal gastrostomy tube as a healthier way for Chelsea to feed while they worked to diagnose the causes of her condition.

Using the MIC-KEY* TJ/GJ tube, Chelsea received 8-12 hour feedings at night. Her parents also liked the ability to rehydrate Chelsea quickly during the day by using the MIC-KEY* TJ/GJ tube as opposed to the hour and a half rehydration process they endured previously with the PICC line.

The convenience of the MIC-KEY* TJ/GJ tube enabled Chelsea to hydrate during school hours in the nurses office. In addition, the low profile of the MIC-KEY* TJ/GJ tube made everything from dressing to playing on the playground easier.

"The MIC-KEY* TJ/GJ tube is so much cleaner and easier to deal with and provides a better way to live," said Chelsea. "I was able to shower, take baths; even swim if I wanted to."

Road to Recovery

During high school, Chelsea underwent 160 hyperbaric oxygen therapy treatments for her disease. She graduated with honors last summer, and is now a freshman at Auburn University pursuing her passion - political science. Chelsea has not used a feeding tube in three years, but Tracy remains grateful for the work that Kimberly-Clark Health Care does to bring cutting edge technology to the world of enteral feeding.

"As a mother, it is heartbreakingly difficult when you can't feed your child the way nature intended," she said. "I know that Kimberly-Clark is working on educating doctors and nurses about the importance of enteral feeding options and creating feeding tubes that will work wonders for children and adults."

 

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