JJ’s MiniONE®
“The MiniONE® Balloon Button G Tube was such a life changer. We love the low-profile design. It is very durable, comfortable, and well made. It has made a huge difference for him and for us.”
JJ’s Mom
Hi, I’m Carrie, JJ’s mom, and I would love to share our journey with you and how much we love the MiniONE® Balloon Button G Tube.
JJ was born with a rare genetic disease. He was also diagnosed with FTT (failure to thrive) at birth. At his 2-year checkup, it was decided that getting a G-tube (gastrostomy tube) would be in JJ’s best interest. I was so nervous about the surgery, but after he healed, recovered, and started gaining weight, I knew that we had made the right decision for him.
The MiniONE® Balloon Button G Tube was such a life changer. We love the low-profile design. It is very durable, comfortable, and well made. It has made a huge difference for him and for us.
He is getting all of his nutrition now, and it has given us peace of mind. We don’t have to worry about him getting dehydrated or whether he got enough calories by mouth. Since he aspirates, he is not able to eat by mouth except for some tastes.
He has gotten stronger and healthier. We are extremely thankful and appreciative of such an amazing product that has helped our son in so many ways. Thank you for giving us peace of mind and being a part of our everyday life.