Guest guest Posted December 23, 2003 Report Share Posted December 23, 2003 Gracie just had her G tube placed three weeks ago, and I am so glad we did it. She is 18 months old and still does eat by mouth all the time. We decided to get the tube for security and ease of life. She is on 9 different meds now, and was really having a hard time taking them every day. It was getting to the point where she would refuse to eat, because everything had something hidden in it. It is also there to maybe help keep her out of the hospital when she is ill. We can always keep her hydrated now, and feed her if she is too ill to eat. The only complication was that she got very infected after the surgery. The GI did not know exactly why it got so infected, but Augmentin cleared it up and life is good now. Since the tube I know she is getting her medicine with the correct dose and absorbing it all. I may be crazy but I really think I can tell the difference with her meds working better now. She is also eating better, since food no longer has medicine in it anymore. Our next adventure is waiting another month or so to change the tube into a mic key button. That will be nice, the onesies are getting old. I know its a tough decision, but for us it was the right one. Good luck. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2003 Report Share Posted December 23, 2003 , Did Gracie have any trouble gaining weight prior to the G-tube? Was she in that awful termed category of "failure to thrive"? Glad to hear the tube is working so well. Anne R Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2003 Report Share Posted December 23, 2003 , Did Gracie have any trouble gaining weight prior to the G-tube? Was she in that awful termed category of "failure to thrive"? Glad to hear the tube is working so well. Anne R Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2003 Report Share Posted December 23, 2003 Hi. My son Matt will be 3 in January. He stopped gaining weight at a year and eventually stopped growing.He wsnt even on the charts anymore. He finally had a g tube placed in July and it was the best thing we ever did. he had an infection after and ran a fever and nobody knew why,but the antibiotics worked right away. He was in pain after and was afraid when we had to clean it. He didnt like getting in and out his car seat because it hurt him. This lasted only for a few days and then he was fine. It has worked miracles. He has gained 8 pounds, and even grew alittle. From what I have been told, the height takes longer to kick in. His foot finally grew,too. The last time I took him for shoes I actually wound up crying in the shoe store because his foot hadnt grown,but this time it went up almost 2 sizes!!! The tube has been a miracle for . He looks so much better now and has more energy. Another thing is that it is great if you have to give meds or if they get sick, you can try to keep them hydrated. He had the g tube for 3 months and in October he switced to a mic-key button. The button is even better for Matt because there is no tube sticking out when he isnt getting a feed. The g tube generally has around 8 inches ot tubing that sticks out. It helps if you put a piece of tape around it and then pin it to the inside of the shirt,this way if it gets tugged on, it is tugging more on the shirt. I can explain this to you in more deatil if you want. Feel free to email me privately, too. Jill, Matts mom scad Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 24, 2003 Report Share Posted December 24, 2003 No, she was never failure to thrive, but she was slow to gain weight. She was born in the 91% and now she is in the 50%, a drop but nothing to be excited about. The Drs. say this is pretty normal due to the mito and how sick she has been. The primary reason for the tube is the ease of giving her medicine. The tube is so great for that. For example, when she gets a shot she must take a large premed dose of motrin and hour before the shot and then every 6 hours for the next 2 days. Before the tube, this was awful to do. She would spit it out and then I would worry about it, the motrin protects her liver from inflammation. But now I am confident to get her shots without worrying about what they are doing to her, and know they are helping her. She also is taking 9 different meds, some are twice a day some are three times a day. The different dosing times gives me 4 different times a day for medicine. I do not know of many adults who would willingly do that. Now it takes less than 5 minutes, and no yucky medicine mouth. Hope this helps a little. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 24, 2003 Report Share Posted December 24, 2003 Anne, My DD has had a g-tube since she was about 16 months old. She is now almost six. It saved her life, much of her stature, and her intelligence. She was about 14 pounds at 16 months. She is now about 40 pounds. is eating most of her food orally now but still cannot eat enough to maintain her weight. We stopped tubing for several months but she lost five pounds, so I just started tubing her again. My DD has GERD, even post Nissen and with meds. She has some hypotonia issues, especially above the waist. She is mildly spastic below the waist. We have had about every g-tube problem one can have. Our had to have a new tube reinserted because of terrible granulation tissue. She almost had to have it done again but we figured things out in time to avoid another surgery. As a result, I know tons of tricks to avoid problems. If you start to have problems, I may be able to help you. I would never do an NG tube for more than a week or so. They are dangerous and the risk of aspiration is high. My DD is on periactin for migraine prevention. There is another med that helps stim appetite. It is called megace. Have you tried that? We also use feeding therapy. Our feeding therapist has done wonders. She has helped me to feed . The stress about 's feeding is mine. has a great relationship with food. I am very thankful for that. We also calorie load. Have you tried Carnation Instant Breakfast with whole milk and cream? Lots of calories and it is really good for you. Unfortunately, our is lactose intolerant. Anne, I am so glad that we have the g-tube. Recently, a pulmonary hospital suggested removing her g-tube. They figured that she would start eating enough when we discovered that is lactose intolerant. I said NO. I insisted that we had to go at least through a winter with all the winter illnesses before we removed it. Well, she has lost five pounds and we are using the tube again. Go with your gut about this decision. If you think that a tube would help you, it probably will. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 25, 2003 Report Share Posted December 25, 2003 Anne R, Our son Lucas was 4 when he received his G-button and J-button. He had reflux with severe vomiting up to 10-12 times after every meal. He lost 5-6 lbs at the time. It was discovered that his pituitary gland was malfunctioning and that his thyroid was not producing. He was put on Synthroid at the time but he has been tube fed ever since. The past 2 months he went from J-tube feeding to G-tube feedings and our hopes are that we will soon return back to oral feeds. I can say he even has a spare tire now. I believe that his stamina, development and susceptability to illness has all improved with the tube feedings. It seems like such a scary process but you do get used to it. Unfortunately Lucas developed fistulas (abnormal opening whereby the intestine created an open area to his skin near the stoma instead of having one pathway from his J-button stoma site. Lucas had his tube pulled out at school and we spent 4 hours in ER to have it replaced. However, Lucas is one of the few if only child I know who has two seperate buttons (one in the stomach and one in the jejuneum (part of the intestine)). His G-button has not really caused any major difficulties since original surgery (Lucas is currently 7 years old). Best of luck in your decision. Feel free to contact me with further questions. Happy Holidays, Loriann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 25, 2003 Report Share Posted December 25, 2003 Anne R, Our son Lucas was 4 when he received his G-button and J-button. He had reflux with severe vomiting up to 10-12 times after every meal. He lost 5-6 lbs at the time. It was discovered that his pituitary gland was malfunctioning and that his thyroid was not producing. He was put on Synthroid at the time but he has been tube fed ever since. The past 2 months he went from J-tube feeding to G-tube feedings and our hopes are that we will soon return back to oral feeds. I can say he even has a spare tire now. I believe that his stamina, development and susceptability to illness has all improved with the tube feedings. It seems like such a scary process but you do get used to it. Unfortunately Lucas developed fistulas (abnormal opening whereby the intestine created an open area to his skin near the stoma instead of having one pathway from his J-button stoma site. Lucas had his tube pulled out at school and we spent 4 hours in ER to have it replaced. However, Lucas is one of the few if only child I know who has two seperate buttons (one in the stomach and one in the jejuneum (part of the intestine)). His G-button has not really caused any major difficulties since original surgery (Lucas is currently 7 years old). Best of luck in your decision. Feel free to contact me with further questions. Happy Holidays, Loriann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 25, 2003 Report Share Posted December 25, 2003 Anne R, Our son Lucas was 4 when he received his G-button and J-button. He had reflux with severe vomiting up to 10-12 times after every meal. He lost 5-6 lbs at the time. It was discovered that his pituitary gland was malfunctioning and that his thyroid was not producing. He was put on Synthroid at the time but he has been tube fed ever since. The past 2 months he went from J-tube feeding to G-tube feedings and our hopes are that we will soon return back to oral feeds. I can say he even has a spare tire now. I believe that his stamina, development and susceptability to illness has all improved with the tube feedings. It seems like such a scary process but you do get used to it. Unfortunately Lucas developed fistulas (abnormal opening whereby the intestine created an open area to his skin near the stoma instead of having one pathway from his J-button stoma site. Lucas had his tube pulled out at school and we spent 4 hours in ER to have it replaced. However, Lucas is one of the few if only child I know who has two seperate buttons (one in the stomach and one in the jejuneum (part of the intestine)). His G-button has not really caused any major difficulties since original surgery (Lucas is currently 7 years old). Best of luck in your decision. Feel free to contact me with further questions. Happy Holidays, Loriann Quote Link to comment Share on other sites More sharing options...
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