Guest guest Posted May 5, 1999 Report Share Posted May 5, 1999 Tina - Im not sure what the doc's long term plans are. If he thinks he is going to " train " her to drink that ##)(#$@*#$*()#, I would beg to differ. We CHOSE NG tubes than to drink that stuff; that is testimony to how bad it really is. If he thinks it is tolerable ask HIM to try it. WE had to use NGs long enough to prove the formula was beneficial, then we quickly placed GTubes. OUr quality of life is INFINITELY better. Id be glad to clue him in for you. (idiopathic eosinophilic esophagitis, GT, former TPN'r) and mom to five boys, all with EE, three with GTs and one on TPN (kody) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 5, 1999 Report Share Posted May 5, 1999 Tina - Im not sure what the doc's long term plans are. If he thinks he is going to " train " her to drink that ##)(#$@*#$*()#, I would beg to differ. We CHOSE NG tubes than to drink that stuff; that is testimony to how bad it really is. If he thinks it is tolerable ask HIM to try it. WE had to use NGs long enough to prove the formula was beneficial, then we quickly placed GTubes. OUr quality of life is INFINITELY better. Id be glad to clue him in for you. (idiopathic eosinophilic esophagitis, GT, former TPN'r) and mom to five boys, all with EE, three with GTs and one on TPN (kody) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 5, 1999 Report Share Posted May 5, 1999 Tina - Im not sure what the doc's long term plans are. If he thinks he is going to " train " her to drink that ##)(#$@*#$*()#, I would beg to differ. We CHOSE NG tubes than to drink that stuff; that is testimony to how bad it really is. If he thinks it is tolerable ask HIM to try it. WE had to use NGs long enough to prove the formula was beneficial, then we quickly placed GTubes. OUr quality of life is INFINITELY better. Id be glad to clue him in for you. (idiopathic eosinophilic esophagitis, GT, former TPN'r) and mom to five boys, all with EE, three with GTs and one on TPN (kody) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 18, 1999 Report Share Posted May 18, 1999 Tina, I have been on propulsid for years now for no troubles - to my knowledge. If your childs troubles with the med is tummy problems then I guess I could be having trouble with it and just not know. My tummy hurts all the time so its hard to tell. What exactly does your child experience and what is he on it for? I have EG. Best of luck, Reynolds _____________________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 19, 1999 Report Share Posted May 19, 1999 Hi Tina My kids (and me) have been on and off this drug for years. It just did not seem to be of any significant help. We eventually decided to stop it, why risk it if there is no definitive advantage. Steph Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 19, 1999 Report Share Posted May 19, 1999 Hi Tina My kids (and me) have been on and off this drug for years. It just did not seem to be of any significant help. We eventually decided to stop it, why risk it if there is no definitive advantage. Steph Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 19, 1999 Report Share Posted May 19, 1999 Hi Tina My kids (and me) have been on and off this drug for years. It just did not seem to be of any significant help. We eventually decided to stop it, why risk it if there is no definitive advantage. Steph Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 On Clayton's first endoscopy at 3 months of age his villi were compeltely flattenecd - but since he had not been exposed to wheat it would have been hard for it to be celiac's athough they did do further testing for celieacs - they did a d-xylose test I believe and of course it was negative. Love, Sharon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 NO, doubt! My cousin has it and it is very, very treatable with minimal intervention. Re: [eosinophilic gastroenteritis] EG > Yes, but I think that probably all of our kids were first tested for celiac. > Boy, I sort of wish that was what BJ had, the answers would have been > simple. > > Dawn, Loving mommy to 2 girls and a super strong little boy > > > > ------------------------------------------------------------------------ > Now the best and coolest websites come right to you based on your > unique interests. eTour.com is surfing without searching. > And, it's FREE! > http://click.egroups.com/1/3013/5/_/474479/_/955478731/ > ------------------------------------------------------------------------ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 In a message dated 4/11/00 4:07:58 PM Eastern Daylight Time, jpotter@... writes: << how can a baby that young be exposed to whea >> Tracey he was not - the GI at that time was crazy - it was a clear sign to the 2 other docs that saw him Dr. Katz at kennedy Kreiger in Baltimore and Dr. that he had EG and it was the formulas (he had been on similac, isomil, nutramgin, aleimentum - you name it) that caused the damage. He was put on Neocate Infant formula at 6 months of age at 4 months later the vili were back to normal. Sharon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 > > , My son (now 1) has went through the same problems but has > been diagnosed with severe protein intolerences and not EG. At four months > of age he was hospitalized for vomiting, diarreha and dehydration. At that > time he was on Alimentum. When we started him on the Neocate he also had > constipation problems for a few weeks. I used a glycerine suppository > every two to three days until the constipation let up. He still has a > rough time having bowel movements (unless he gets a hold of a " bad " food) > but for the most part it is better than the alternative. If you would like > more information on my experiences let me know. Take care. > > Tracey > > > > > > jpotter@... on 04/11/2000 09:47:50 AM > > Please respond to eosinophilic gastroenteritis (AT) e > > To: eosinophilic gastroenteritis (AT) e > cc: > Subject: [eosinophilic gastroenteritis] eg > > > My son is 5 months old. he was 3 months and hospitalized for severe > diarreha and dehydration. we almost lost him. i was breastfeeding > at the time. when i resummed breastfeeding he began having loose > stools again. the dr placed him on Alimentum. he's had trouble on > that too, blood in the stool. he was on neocate for 2 days and got > terribly constipated. he's back on alimentum. he's had several > biopsies and all ahow high levels of eosinophils and the dr. believes > it to be EG. i need some information > > tracy > > > > ---------------------------------------------------------------------- -- > Get paid for the stuff you know! > Get answers for the stuff you don't. And get $10 to spend on the site! > http://click.egroups.com/1/2200/5/_/474479/_/955472126/ > ---------------------------------------------------------------------- --Tracey, what kind of tests did they do to determine a protein intolerance? i was using the suppositories on karson,when he was on the Neocate but was worried about him becoming dependent on them. the dr had only given us one can of the Neocate so we had to stop, and go back to the Alimentum. i don't know anything about this. Is your son able to eat regular foods. I have only been able to give Karson rice cereal. He's on Miralax now for the constipation. He had 5 loose stools yesterday so i haven't given him any today. my dr is talking about using a steroid to treat this, Prednizone? Did your son have to be on that? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 > Hi , > > I would first put your son back on Neocate or Elecare. If you have a > constipation problem you can give him things to soften his stool. See if > that helps with the blood. > > [eosinophilic gastroenteritis] eg > > > My son is 5 months old. he was 3 months and hospitalized for severe > diarreha and dehydration. we almost lost him. i was breastfeeding > at the time. when i resummed breastfeeding he began having loose > stools again. the dr placed him on Alimentum. he's had trouble on > that too, blood in the stool. he was on neocate for 2 days and got > terribly constipated. he's back on alimentum. he's had several > biopsies and all ahow high levels of eosinophils and the dr. believes > it to be EG. i need some information > > tracy > > > > ---------------------------------------------------------------------- -- > Get paid for the stuff you know! > Get answers for the stuff you don't. And get $10 to spend on the site! > http://click.egroups.com/1/2200/5/_/474479/_/955472126/ > ---------------------------------------------------------------------- --Hi , I was giving him suppositories for the constipation, but was afraid he would rely on them too much. The Dr. had only given us one can of the Neocate, so we had to put him back on the Alimentum. He was still constipated. We gave him Miralax, and he had 5 loose stools yesterday, no blood. I didn't give him any today, and he hasn't gone yet. I have to call the Dr. tomorrow to see if I should continue with the Miralax. I don't know anything about EG. So far we have only been able to give him rice cereal, will he ever be able to tolerate regular food? Where do you get the Neocate from, we were told you had to order it direct. Our insurance will not cover it. Any info you have i would really appreciate, i am very concerned. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 > On Clayton's first endoscopy at 3 months of age his villi were compeltely > flattenecd - but since he had not been exposed to wheat it would have been > hard for it to be celiac's athough they did do further testing for celieacs - > they did a d-xylose test I believe and of course it was negative. > > Love, > Sharon Sharon, how can a baby that young be exposed to wheat. They think my son has EG, but they are not sure. I don't know if they tested for Celiac's disease, but my husband had a cousin who had it. Can it be heriditary? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 > Most insurances will cover it but sometimes you have to fight to get them to > do it. > > Dawn, Loving mommy to 2 girls and a super strong little boy Dawn, Does your son have EG? Are there differing degrees? What were his symptoms? What clinic is he treated at? Our dr has talked about refering Karson somewhere else. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 Hello , Well since you don't have a bunch of the Neocate already, I would recommend trying the Elecare. It's a little bit less expensive and a lot less disgusting!! LOL. Well, I don't know how it tastes but for your own sake it smells better. Have you tried Mineral Oil for the constipation? Sometimes that works and sometimes it doesn't. I am not sure how much to give though I know that Sharon tried it on Clayton.....right Sharon? It probably seem very overwhelming right now. Everything is so new and strange, but hopefully it will get better. You are in a good position right now that your son is young enough that he will drink the formula. A lot of parents are struggling b/c their child is too old to notice how awful the stuff tastes. Then they have to go to other extremes such as G-tube etc. I wouldn't try the steroids unless the eos's still remain after being on one of these two formula's. The steroids just cause too many problems. Spencer is experiencing so many side effects and it is really scary. He has to be on them, and most likely will be forever at some sort of dose. Hopefully this is not E.G. and something a little easier to handle, where once under control you can give him food. Even if it is E.G. you can begin to give food to your child, trying one at a time. There are many different methods and tests used to tell what they can tolerate. Most of the time though it is through symptoms that you figure out what they can and can not have. Although Spencer doesn't eat anything, not even by G-tube there are many, many kid's and adults that eat food with E.G.. Also, is WIC available to you in your state? This may be an option for you. The state may pay for this formula. But the insurance may just need a good, good fight before they will even think about paying for it. My son has E.G. very badly to where he has to be supported nutritionally solely on IV food called TPN. I have E.G. but can eat a lot of things but need to take medication. I have it to where it is very bothersome. My son has it and it is life threatening to him. I think this is why it is so hard for them to learn about this disease is that it varies so much. Keep your chin up!!! You are in the right place for support. BTW: Where do you live? If you live anywhere close to Ohio I would recommend coming to Cincinnati Children's. Have they done a colonoscopy on your son......this may be key in diagnosing him. ---- Original Message ----- To: eosinophilic gastroenteritis (AT) e> Sent: Tuesday, April 11, 2000 4:00 PM Subject: Re: [eosinophilic gastroenteritis] eg > > > Hi , > > > > I would first put your son back on Neocate or Elecare. If you have > a > > constipation problem you can give him things to soften his stool. > See if > > that helps with the blood. > > > > [eosinophilic gastroenteritis] eg > > > > > > My son is 5 months old. he was 3 months and hospitalized for severe > > diarreha and dehydration. we almost lost him. i was breastfeeding > > at the time. when i resummed breastfeeding he began having loose > > stools again. the dr placed him on Alimentum. he's had trouble on > > that too, blood in the stool. he was on neocate for 2 days and got > > terribly constipated. he's back on alimentum. he's had several > > biopsies and all ahow high levels of eosinophils and the dr. > believes > > it to be EG. i need some information > > > > tracy > > > > > > > > > ---------------------------------------------------------------------- > -- > > Get paid for the stuff you know! > > Get answers for the stuff you don't. And get $10 to spend on the > site! > > http://click.egroups.com/1/2200/5/_/474479/_/955472126/ > > > ---------------------------------------------------------------------- > --Hi , > > I was giving him suppositories for the constipation, but was afraid > he would rely on them too much. The Dr. had only given us one can of > the Neocate, so we had to put him back on the Alimentum. He was > still constipated. We gave him Miralax, and he had 5 loose stools > yesterday, no blood. I didn't give him any today, and he hasn't gone > yet. I have to call the Dr. tomorrow to see if I should continue > with the Miralax. I don't know anything about EG. So far we have > only been able to give him rice cereal, will he ever be able to > tolerate regular food? Where do you get the Neocate from, we were > told you had to order it direct. Our insurance will not cover it. > Any info you have i would really appreciate, i am very concerned. > > > > > ------------------------------------------------------------------------ > Get your money connected @ OnMoney.com - the first Web site that lets > you see and manage all of your finances all in one place. > http://click.egroups.com/1/3012/5/_/474479/_/955483224/ > ------------------------------------------------------------------------ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 Hello , Well since you don't have a bunch of the Neocate already, I would recommend trying the Elecare. It's a little bit less expensive and a lot less disgusting!! LOL. Well, I don't know how it tastes but for your own sake it smells better. Have you tried Mineral Oil for the constipation? Sometimes that works and sometimes it doesn't. I am not sure how much to give though I know that Sharon tried it on Clayton.....right Sharon? It probably seem very overwhelming right now. Everything is so new and strange, but hopefully it will get better. You are in a good position right now that your son is young enough that he will drink the formula. A lot of parents are struggling b/c their child is too old to notice how awful the stuff tastes. Then they have to go to other extremes such as G-tube etc. I wouldn't try the steroids unless the eos's still remain after being on one of these two formula's. The steroids just cause too many problems. Spencer is experiencing so many side effects and it is really scary. He has to be on them, and most likely will be forever at some sort of dose. Hopefully this is not E.G. and something a little easier to handle, where once under control you can give him food. Even if it is E.G. you can begin to give food to your child, trying one at a time. There are many different methods and tests used to tell what they can tolerate. Most of the time though it is through symptoms that you figure out what they can and can not have. Although Spencer doesn't eat anything, not even by G-tube there are many, many kid's and adults that eat food with E.G.. Also, is WIC available to you in your state? This may be an option for you. The state may pay for this formula. But the insurance may just need a good, good fight before they will even think about paying for it. My son has E.G. very badly to where he has to be supported nutritionally solely on IV food called TPN. I have E.G. but can eat a lot of things but need to take medication. I have it to where it is very bothersome. My son has it and it is life threatening to him. I think this is why it is so hard for them to learn about this disease is that it varies so much. Keep your chin up!!! You are in the right place for support. BTW: Where do you live? If you live anywhere close to Ohio I would recommend coming to Cincinnati Children's. Have they done a colonoscopy on your son......this may be key in diagnosing him. ---- Original Message ----- To: eosinophilic gastroenteritis (AT) e> Sent: Tuesday, April 11, 2000 4:00 PM Subject: Re: [eosinophilic gastroenteritis] eg > > > Hi , > > > > I would first put your son back on Neocate or Elecare. If you have > a > > constipation problem you can give him things to soften his stool. > See if > > that helps with the blood. > > > > [eosinophilic gastroenteritis] eg > > > > > > My son is 5 months old. he was 3 months and hospitalized for severe > > diarreha and dehydration. we almost lost him. i was breastfeeding > > at the time. when i resummed breastfeeding he began having loose > > stools again. the dr placed him on Alimentum. he's had trouble on > > that too, blood in the stool. he was on neocate for 2 days and got > > terribly constipated. he's back on alimentum. he's had several > > biopsies and all ahow high levels of eosinophils and the dr. > believes > > it to be EG. i need some information > > > > tracy > > > > > > > > > ---------------------------------------------------------------------- > -- > > Get paid for the stuff you know! > > Get answers for the stuff you don't. And get $10 to spend on the > site! > > http://click.egroups.com/1/2200/5/_/474479/_/955472126/ > > > ---------------------------------------------------------------------- > --Hi , > > I was giving him suppositories for the constipation, but was afraid > he would rely on them too much. The Dr. had only given us one can of > the Neocate, so we had to put him back on the Alimentum. He was > still constipated. We gave him Miralax, and he had 5 loose stools > yesterday, no blood. I didn't give him any today, and he hasn't gone > yet. I have to call the Dr. tomorrow to see if I should continue > with the Miralax. I don't know anything about EG. So far we have > only been able to give him rice cereal, will he ever be able to > tolerate regular food? Where do you get the Neocate from, we were > told you had to order it direct. Our insurance will not cover it. > Any info you have i would really appreciate, i am very concerned. > > > > > ------------------------------------------------------------------------ > Get your money connected @ OnMoney.com - the first Web site that lets > you see and manage all of your finances all in one place. > http://click.egroups.com/1/3012/5/_/474479/_/955483224/ > ------------------------------------------------------------------------ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 Hello , Well since you don't have a bunch of the Neocate already, I would recommend trying the Elecare. It's a little bit less expensive and a lot less disgusting!! LOL. Well, I don't know how it tastes but for your own sake it smells better. Have you tried Mineral Oil for the constipation? Sometimes that works and sometimes it doesn't. I am not sure how much to give though I know that Sharon tried it on Clayton.....right Sharon? It probably seem very overwhelming right now. Everything is so new and strange, but hopefully it will get better. You are in a good position right now that your son is young enough that he will drink the formula. A lot of parents are struggling b/c their child is too old to notice how awful the stuff tastes. Then they have to go to other extremes such as G-tube etc. I wouldn't try the steroids unless the eos's still remain after being on one of these two formula's. The steroids just cause too many problems. Spencer is experiencing so many side effects and it is really scary. He has to be on them, and most likely will be forever at some sort of dose. Hopefully this is not E.G. and something a little easier to handle, where once under control you can give him food. Even if it is E.G. you can begin to give food to your child, trying one at a time. There are many different methods and tests used to tell what they can tolerate. Most of the time though it is through symptoms that you figure out what they can and can not have. Although Spencer doesn't eat anything, not even by G-tube there are many, many kid's and adults that eat food with E.G.. Also, is WIC available to you in your state? This may be an option for you. The state may pay for this formula. But the insurance may just need a good, good fight before they will even think about paying for it. My son has E.G. very badly to where he has to be supported nutritionally solely on IV food called TPN. I have E.G. but can eat a lot of things but need to take medication. I have it to where it is very bothersome. My son has it and it is life threatening to him. I think this is why it is so hard for them to learn about this disease is that it varies so much. Keep your chin up!!! You are in the right place for support. BTW: Where do you live? If you live anywhere close to Ohio I would recommend coming to Cincinnati Children's. Have they done a colonoscopy on your son......this may be key in diagnosing him. ---- Original Message ----- To: eosinophilic gastroenteritis (AT) e> Sent: Tuesday, April 11, 2000 4:00 PM Subject: Re: [eosinophilic gastroenteritis] eg > > > Hi , > > > > I would first put your son back on Neocate or Elecare. If you have > a > > constipation problem you can give him things to soften his stool. > See if > > that helps with the blood. > > > > [eosinophilic gastroenteritis] eg > > > > > > My son is 5 months old. he was 3 months and hospitalized for severe > > diarreha and dehydration. we almost lost him. i was breastfeeding > > at the time. when i resummed breastfeeding he began having loose > > stools again. the dr placed him on Alimentum. he's had trouble on > > that too, blood in the stool. he was on neocate for 2 days and got > > terribly constipated. he's back on alimentum. he's had several > > biopsies and all ahow high levels of eosinophils and the dr. > believes > > it to be EG. i need some information > > > > tracy > > > > > > > > > ---------------------------------------------------------------------- > -- > > Get paid for the stuff you know! > > Get answers for the stuff you don't. And get $10 to spend on the > site! > > http://click.egroups.com/1/2200/5/_/474479/_/955472126/ > > > ---------------------------------------------------------------------- > --Hi , > > I was giving him suppositories for the constipation, but was afraid > he would rely on them too much. The Dr. had only given us one can of > the Neocate, so we had to put him back on the Alimentum. He was > still constipated. We gave him Miralax, and he had 5 loose stools > yesterday, no blood. I didn't give him any today, and he hasn't gone > yet. I have to call the Dr. tomorrow to see if I should continue > with the Miralax. I don't know anything about EG. So far we have > only been able to give him rice cereal, will he ever be able to > tolerate regular food? Where do you get the Neocate from, we were > told you had to order it direct. Our insurance will not cover it. > Any info you have i would really appreciate, i am very concerned. > > > > > ------------------------------------------------------------------------ > Get your money connected @ OnMoney.com - the first Web site that lets > you see and manage all of your finances all in one place. > http://click.egroups.com/1/3012/5/_/474479/_/955483224/ > ------------------------------------------------------------------------ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 > > > > Does your son have EG? Are there differing degrees? What were his > > symptoms? What clinic is he treated at? Our dr has talked about > > refering Karson somewhere else. > > > > > > , > My son has EG. I definitely think there are differing degrees. Of course, > I think that some of the kids have other things to deal with too. BJ had > severe, severe diarrhea, dehydration (all the time), stomach pain, weakness, > hard time gaining weight and growing. He is treated at Children's Mercy in > Kansas City, KS although our doctor has conferred with other doctors such as > Dr. Sampson on ways to treat BJ. > > Dawn, Loving mommy to 2 girls and a super strong little boy Dawn, My son was 3 months old and had severe diarrhea, vomitting, and dehydration. We almost lost him. I had been breastfeeding up until his hospitalization. When we left the hospital I resumed breastfeeding but he began to have loose stools with blood in them. He went on the Alimentum and continued to have loose stools with blood. He went on the Neocate and got terribly constipated. He has been gaining weight all along and outside of some discomfort when he was constipated, he's a really good, happy baby. i'm just worried in time it will get worse? Does it ever go away or is this something he will always have to deal with? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 Yes, but I think that probably all of our kids were first tested for celiac. Boy, I sort of wish that was what BJ had, the answers would have been simple. Dawn, Loving mommy to 2 girls and a super strong little boy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 Most insurances will cover it but sometimes you have to fight to get them to do it. Dawn, Loving mommy to 2 girls and a super strong little boy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 > > Does your son have EG? Are there differing degrees? What were his > symptoms? What clinic is he treated at? Our dr has talked about > refering Karson somewhere else. > > , My son has EG. I definitely think there are differing degrees. Of course, I think that some of the kids have other things to deal with too. BJ had severe, severe diarrhea, dehydration (all the time), stomach pain, weakness, hard time gaining weight and growing. He is treated at Children's Mercy in Kansas City, KS although our doctor has conferred with other doctors such as Dr. Sampson on ways to treat BJ. Dawn, Loving mommy to 2 girls and a super strong little boy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 Do I have the Kak? I keep on checking and can't find it. It is your system or mine? Re: [eosinophilic gastroenteritis] eg > No , I take Gastrochrom. I think it is considered safe during > pregnancy, but can understand your reluctance to take anything that might > harm the baby. > > I had a letter from someone reguarding something to do during the last > trimester to help with the baby's digestive system.... I hope they will > post that here.. I will try to find that letter, but deleted a lot because > of the virus.....Didn't want to take any chances... I also keep changing > your messages to plain text because Kak is transmitted with HTML...... > > Judy > > > > ------------------------------------------------------------------------ > Avoid the lines and visit avis.com for quick and easy online > reservations. Enjoy a compact car nationwide for only $29 a day! > Click here for more details. > http://click.egroups.com/1/3011/5/_/474479/_/955490577/ > ------------------------------------------------------------------------ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 Do I have the Kak? I keep on checking and can't find it. It is your system or mine? Well I hope neither one of us have it. I keep checking too. I sent from the Archive until I got the all clear.... I just read that it transmits itself in HTML and not is Basic.... I sure don't want to get it again... It was a nightmare for me trying to get rid of it..... I am not very computer literate...... I like to use HTML for sending pics and stationery, but have been refraining for now..... Just leary I guess.... Until I get a message that has it and my system warns me I will be nervous... Judy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 put on Neocate Infant formula at 6 months of age at 4 months later the villa > were back to normal. Sharon, I wonder if Spencer's Villa would show up damaged right now? Since he hasn't eaten anything by gut for about 8 months now. Interesting thought. Steph, do you know if this is a symptom of 100 % tpn dependant children? Re: [eosinophilic gastroenteritis] EG > In a message dated 4/11/00 4:07:58 PM Eastern Daylight Time, > jpotter@... writes: > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 put on Neocate Infant formula at 6 months of age at 4 months later the villa > were back to normal. Sharon, I wonder if Spencer's Villa would show up damaged right now? Since he hasn't eaten anything by gut for about 8 months now. Interesting thought. Steph, do you know if this is a symptom of 100 % tpn dependant children? Re: [eosinophilic gastroenteritis] EG > In a message dated 4/11/00 4:07:58 PM Eastern Daylight Time, > jpotter@... writes: > > Quote Link to comment Share on other sites More sharing options...
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