Published April 10, 2025
"Elijah doesn't see himself as sick," his mom says. "He sees himself as a normal kid. And that's exactly what his Aveanna team allows him to be."
Four-year-old Elijah has hypoplastic left heart syndrome. He spent the first five months of his life in…
Published April 3, 2025
Magnolia stopped eating around one year old.
She began only wanting to drink formula, then switched to milk primarily. By age 3, Magnolia was diagnosed with Avoidant/Restrictive Food Intake Disorder (ARFID). ARFID significantly limits the amounts …
Published Feb. 4, 2025
Kryssi lives with Crohn's disease and has had a feeding tube since 2011. Although she is an expert now, she spent many years feeling isolated and unsure when it came to her feeding tube. Then she joined the Aveanna Healthcare Medical Solutions (AHMS…
Published Feb. 7, 2024
This Feeding Tube Awareness Week, we're excited to spotlight Aveanna patient AJ. His journey is a testament to the life-changing impact a feeding tube and an incredible support system can have.
AJ was born at 29 weeks gestation, weighing only 2 poun…
Published Feb. 11, 2022
“Jacob is a medical miracle,” his grandmother shares. “His original prognosis was that he wouldn’t walk, wouldn’t talk, and would have a brain deficit. That’s not the case today. He’s exceptionally bright and can do anything he puts his mind to.”
J…
Published Feb. 8, 2022
Karissa lives with gastroparesis. It took years for her to receive her diagnosis and the treatments she needed. But she never stopped advocating for herself. “I decided that I wasn’t going to stop until I got answers,” Karissa says. “I don’t believ…
Published Feb. 7, 2022
Many people can benefit from a feeding tube or G-tube when they are receiving home health care. If tube feeding is done outside of a hospital setting, it is called enteral feeding. According to Mayo Clinic, people with the following conditions can …
Published Feb. 18, 2021
Melia was born with a rare genetic disorder called epidermolysis bullosa, which causes frequent blistering of the skin. Melia’s skin may be fragile, but she certainly isn’t! She’s an independent fighter through and through. But even the strongest f…
Published Feb. 14, 2020
“I have spinal muscular atrophy type two,” Cory shares. “Because of my condition, I’ve had to learn to adapt to every type of normal situation, including eating.”
Spinal muscular atrophy is a genetic condition that causes progressive muscle weakness…
Published Feb. 7, 2020
“There are different ways to feed your baby, and they are all beautiful,” Heather says. “I hope more people learn that during Feeding Tube Awareness Week.”
When her daughter Melia Grace was born last summer, Heather wasn’t familiar with all the dif…
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