I see so many people opposed to G tubes and just let me tell you, from experience, that it is the best decision we ever made. My son was 10 years old and weighed 40 pounds. We resisted the tube also, like many of you are, thinking "we will just add more butter to his food" "give him whole milk and half and half", "we can do this on our own, we dont need a g-tube". Let me tell you, you cant.
When he was 10, he is now 16, we gave in and got the tube. It was very upsetting, I felt like a failure. Within a few months, he began to gain weight, his lung function improved and his quality of life got better. There were no more struggles at meal time..if he ate, he ate, if he didnt, we just gave him a little extra tube feed. Eating became a pleasureable experience for him. We no longer had to nag and beg for "just one more bite".
He has had troubles with his weight still, we just got done with acourse of IV antibiotics and since then he has gained 5 pounds in 2 weeks. He still gets nightly feeds.
Weight is definitely correclated to lung function. When we have trouble breathing, we burn more calories...CF kids (and adults) need a little extra cushion to fall back on when the times get tough! With the malabsorption, nutrition, not just weight is important..with a tube feed, the formulas provide 100% complete nutrition, which in turn makes the body heal better and lung function improve.
Oh! The best part of the g-tube...giving icky medicines...anything tough to swallow got shot through the g-tube..lol.
He has always been short for his age, probably because of the mal-nutrition. Weight gain is important for height growth. The taller you are, the bigger your lungs are and the better off a CF person will be. He is on growth hormone and it is working beautifully. His height would not be there if his nutritional staus was down.
In closing...if your child is in the lower percentiles, just bite the bullet and get the tube. The benefits outweigh the risks, and the sooner the nutritional status is met, the better. Dont let the opportunity for growth pass by...and once the damage is done, it is done.
Remember, its about NUTRITION as much as WEIGHT.
Susan
When he was 10, he is now 16, we gave in and got the tube. It was very upsetting, I felt like a failure. Within a few months, he began to gain weight, his lung function improved and his quality of life got better. There were no more struggles at meal time..if he ate, he ate, if he didnt, we just gave him a little extra tube feed. Eating became a pleasureable experience for him. We no longer had to nag and beg for "just one more bite".
He has had troubles with his weight still, we just got done with acourse of IV antibiotics and since then he has gained 5 pounds in 2 weeks. He still gets nightly feeds.
Weight is definitely correclated to lung function. When we have trouble breathing, we burn more calories...CF kids (and adults) need a little extra cushion to fall back on when the times get tough! With the malabsorption, nutrition, not just weight is important..with a tube feed, the formulas provide 100% complete nutrition, which in turn makes the body heal better and lung function improve.
Oh! The best part of the g-tube...giving icky medicines...anything tough to swallow got shot through the g-tube..lol.
He has always been short for his age, probably because of the mal-nutrition. Weight gain is important for height growth. The taller you are, the bigger your lungs are and the better off a CF person will be. He is on growth hormone and it is working beautifully. His height would not be there if his nutritional staus was down.
In closing...if your child is in the lower percentiles, just bite the bullet and get the tube. The benefits outweigh the risks, and the sooner the nutritional status is met, the better. Dont let the opportunity for growth pass by...and once the damage is done, it is done.
Remember, its about NUTRITION as much as WEIGHT.
Susan