Guest guest Posted August 15, 2004 Report Share Posted August 15, 2004 its called disabled Medicaid . he use to get SSI and that was all the income that counted for his Medicaid now he gets nothing. I think you just have to prove that he is disabled which with wes that is physically with all the charge things and a slight mental delay. ask a Medicaid worker to help you get it that way KayRena Holweger wrote: > How does Wesley qualify on his own income? Cameron is only four > years old???? > > kayrenanew wrote:have you looked into > getting Medicaid just for your charge child? > we get too much money from husbands income for family to be on > Medicaid but wesley qualifies for disabled income on his own > income. > KayRena > > Holweger wrote: > > > Wow -- first of all let me thank everybody for all your replies. > You > > all have been real helpful and I'm going to use your ideas. I'm > going > > to answer questions all in one reply...... > > > > Cameron uses a formula called Compleat which is a special formula > just > > for tube feedings. We've tried Pediasure but Cam would always throw > > > up with it. I've looked into WIC and Medicaid, but my husband makes > > > too much money. Sometimes I just want to tell these people " If I > made > > too much money, I wouldn't be asking you for help! " Our insurance > > does help us with the formula but we have a high deductible($4000 > per > > person) and they pay very little on it. In fact we're having > > problems with the insurance company paying the correct amount. > > > > I've been looking into the vital-slim therapy lately. Alot of you > > mentioned that your child doesn't feel hunger with a g-tube. > Cameron > > does b/c if we are late feeding him he gets very cranky and then > he's > > fine after we feed him. > > > > Thanks again!!!!!!!!!!!!!!!!!!! > > > > Michele Westmaas wrote: > > - > > My daughter, Aubrie, had a Gtube for her first year and a half. She > > > had > > it removed before her 2nd birthday. She also had failure to thrive, > > > swallowing difficulties, and GE reflux. I would have to look back > at > > my > > notes from the time for details. I remember thinking she'd never > eat. > > > > She'd vomit just at the sight of the spoon. She never did master > the > > suck-swallow-breath thing with the bottle but went directly to a > sippy > > > > cup. When she first ate foods, she would pocket the difficult > > textures > > in between her lower lip and gum. I don't know how she could > > separate > > the hull from the popcorn, the meat from the veggies, etc, but she > > did. > > Then she'd spit the " yuckies " in a napkin. Eventually, she had less > > > and > > less yuckies pocketed and finally was able to eat everything. There > > > are > > very few foods that she does not manage fine now. In fact, I can't > > think of one off hand. > > > > We were stumped as to how to go from the tube to oral feeding. The > > ped > > didn't have any good suggestions except that she gave us her > blessing > > to > > do whatever during the spring when we expected no ear infections and > > > colds and could best afford any weight loss that might occur during > > the > > transition. So the SLP and I figured out a plan together. We did > > overnight tube feedings that ended early enough in the night so that > > > she'd hopefully wake up somewhat hungry. Then we did only oral > > feeding > > during the day. > > > > Some dr's had suggested oral feeding at meals followed by a tube > > feeding > > to " top off " whatever the child didn't take orally. But that didn't > > > make sense to us cuz then she'd never really get that feeling of > > hunger. I don't know how we did it, but we did make the transition. > > > At > > the time, we gave Aubrie Pediasure instead of milk to get as many > > calories in as possible. Now I wish we'd never given up the > Pediasure > > > > cuz she's still very small but now won't take the taste of it. > > > > So-- Perhaps I didn't give you much specific help, but I hope I gave > > > you > > some evidence that it is possible to wean from the tube to oral > > feeding. It will take work and it will be frustrating. In my > > experience, I needed a supportive SLP to work with me since the dr's > > > weren't so helpful. Our docs didn't care so much if she ever ate > > orally. They didn't care how she got it, they just wanted her to > get > > the nutrition. From a mom's point of view, the way the nutrition is > > > taken in is a huge issue. > > > > Best of luck to you and welcome to the list. I'm sure you'll find > > many > > helpful posts here. > > > > Michele W > > Aubrie's mom (6 yrs) CHaRgE > > > > > > > > Membership of this email support groups does not constitute > membership > > in the CHARGE Syndrome Foundation. > > For information about the CHARGE Syndrome > > Foundation or to become a member (and get the newsletter) > > please contact marion@... or visit > > the CHARGE Syndrome Foundation web page > > at http://www.chargesyndrome.org > > 7th International > > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > > Information will be available at our website > > www.chargesyndrome.org or by calling 1-. In Canada, you > > > may contact CHARGE Syndrome Canada at 1- (families), > visit > > www.chargesyndrome.ca, or email info@.... Thank you! > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 15, 2004 Report Share Posted August 15, 2004 , Forgot to mention, Kennedy is 6 and she is about 43 pounds, so she isn't huge but she's healthy and in her 'range'. To see a recent pic, go to http://ca.geocities.com/weirfamilyrogers/kennedy.html if you want an idea of her size. Weir Mom to Kennedy 6 yr old with CHARGE, 15, 13 and wife to Graeme. New Brunswick, Canada Weir homepage: http://ca.geocities.com/weirfamilyrogers CHARGE SYNDROME CANADA: http://www.chargesyndrome.ca Re: Hello & Need some advice > > > Wow -- first of all let me thank everybody for all your replies. You all > have been real helpful and I'm going to use your ideas. I'm going to answer > questions all in one reply...... > > Cameron uses a formula called Compleat which is a special formula just for > tube feedings. We've tried Pediasure but Cam would always throw up with it. > I've looked into WIC and Medicaid, but my husband makes too much money. > Sometimes I just want to tell these people " If I made too much money, I > wouldn't be asking you for help! " Our insurance does help us with the > formula but we have a high deductible($4000 per person) and they pay very > little on it. In fact we're having problems with the insurance company > paying the correct amount. > > I've been looking into the vital-slim therapy lately. Alot of you > mentioned that your child doesn't feel hunger with a g-tube. Cameron does > b/c if we are late feeding him he gets very cranky and then he's fine after > we feed him. > > Thanks again!!!!!!!!!!!!!!!!!!! > > Michele Westmaas wrote: > - > My daughter, Aubrie, had a Gtube for her first year and a half. She had > it removed before her 2nd birthday. She also had failure to thrive, > swallowing difficulties, and GE reflux. I would have to look back at my > notes from the time for details. I remember thinking she'd never eat. > She'd vomit just at the sight of the spoon. She never did master the > suck-swallow-breath thing with the bottle but went directly to a sippy > cup. When she first ate foods, she would pocket the difficult textures > in between her lower lip and gum. I don't know how she could separate > the hull from the popcorn, the meat from the veggies, etc, but she did. > Then she'd spit the " yuckies " in a napkin. Eventually, she had less and > less yuckies pocketed and finally was able to eat everything. There are > very few foods that she does not manage fine now. In fact, I can't > think of one off hand. > > We were stumped as to how to go from the tube to oral feeding. The ped > didn't have any good suggestions except that she gave us her blessing to > do whatever during the spring when we expected no ear infections and > colds and could best afford any weight loss that might occur during the > transition. So the SLP and I figured out a plan together. We did > overnight tube feedings that ended early enough in the night so that > she'd hopefully wake up somewhat hungry. Then we did only oral feeding > during the day. > > Some dr's had suggested oral feeding at meals followed by a tube feeding > to " top off " whatever the child didn't take orally. But that didn't > make sense to us cuz then she'd never really get that feeling of > hunger. I don't know how we did it, but we did make the transition. At > the time, we gave Aubrie Pediasure instead of milk to get as many > calories in as possible. Now I wish we'd never given up the Pediasure > cuz she's still very small but now won't take the taste of it. > > So-- Perhaps I didn't give you much specific help, but I hope I gave you > some evidence that it is possible to wean from the tube to oral > feeding. It will take work and it will be frustrating. In my > experience, I needed a supportive SLP to work with me since the dr's > weren't so helpful. Our docs didn't care so much if she ever ate > orally. They didn't care how she got it, they just wanted her to get > the nutrition. From a mom's point of view, the way the nutrition is > taken in is a huge issue. > > Best of luck to you and welcome to the list. I'm sure you'll find many > helpful posts here. > > Michele W > Aubrie's mom (6 yrs) CHaRgE > > > > Membership of this email support groups does not constitute membership in > the CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 Your daughter is absolutely precious!!!! Thanks for the pic!!! Weir wrote: , Forgot to mention, Kennedy is 6 and she is about 43 pounds, so she isn't huge but she's healthy and in her 'range'. To see a recent pic, go to http://ca.geocities.com/weirfamilyrogers/kennedy.html if you want an idea of her size. Weir Mom to Kennedy 6 yr old with CHARGE, 15, 13 and wife to Graeme. New Brunswick, Canada Weir homepage: http://ca.geocities.com/weirfamilyrogers CHARGE SYNDROME CANADA: http://www.chargesyndrome.ca Re: Hello & Need some advice > > > Wow -- first of all let me thank everybody for all your replies. You all > have been real helpful and I'm going to use your ideas. I'm going to answer > questions all in one reply...... > > Cameron uses a formula called Compleat which is a special formula just for > tube feedings. We've tried Pediasure but Cam would always throw up with it. > I've looked into WIC and Medicaid, but my husband makes too much money. > Sometimes I just want to tell these people " If I made too much money, I > wouldn't be asking you for help! " Our insurance does help us with the > formula but we have a high deductible($4000 per person) and they pay very > little on it. In fact we're having problems with the insurance company > paying the correct amount. > > I've been looking into the vital-slim therapy lately. Alot of you > mentioned that your child doesn't feel hunger with a g-tube. Cameron does > b/c if we are late feeding him he gets very cranky and then he's fine after > we feed him. > > Thanks again!!!!!!!!!!!!!!!!!!! > > Michele Westmaas wrote: > - > My daughter, Aubrie, had a Gtube for her first year and a half. She had > it removed before her 2nd birthday. She also had failure to thrive, > swallowing difficulties, and GE reflux. I would have to look back at my > notes from the time for details. I remember thinking she'd never eat. > She'd vomit just at the sight of the spoon. She never did master the > suck-swallow-breath thing with the bottle but went directly to a sippy > cup. When she first ate foods, she would pocket the difficult textures > in between her lower lip and gum. I don't know how she could separate > the hull from the popcorn, the meat from the veggies, etc, but she did. > Then she'd spit the " yuckies " in a napkin. Eventually, she had less and > less yuckies pocketed and finally was able to eat everything. There are > very few foods that she does not manage fine now. In fact, I can't > think of one off hand. > > We were stumped as to how to go from the tube to oral feeding. The ped > didn't have any good suggestions except that she gave us her blessing to > do whatever during the spring when we expected no ear infections and > colds and could best afford any weight loss that might occur during the > transition. So the SLP and I figured out a plan together. We did > overnight tube feedings that ended early enough in the night so that > she'd hopefully wake up somewhat hungry. Then we did only oral feeding > during the day. > > Some dr's had suggested oral feeding at meals followed by a tube feeding > to " top off " whatever the child didn't take orally. But that didn't > make sense to us cuz then she'd never really get that feeling of > hunger. I don't know how we did it, but we did make the transition. At > the time, we gave Aubrie Pediasure instead of milk to get as many > calories in as possible. Now I wish we'd never given up the Pediasure > cuz she's still very small but now won't take the taste of it. > > So-- Perhaps I didn't give you much specific help, but I hope I gave you > some evidence that it is possible to wean from the tube to oral > feeding. It will take work and it will be frustrating. In my > experience, I needed a supportive SLP to work with me since the dr's > weren't so helpful. Our docs didn't care so much if she ever ate > orally. They didn't care how she got it, they just wanted her to get > the nutrition. From a mom's point of view, the way the nutrition is > taken in is a huge issue. > > Best of luck to you and welcome to the list. I'm sure you'll find many > helpful posts here. > > Michele W > Aubrie's mom (6 yrs) CHaRgE > > > > Membership of this email support groups does not constitute membership in > the CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 Your daughter is absolutely precious!!!! Thanks for the pic!!! Weir wrote: , Forgot to mention, Kennedy is 6 and she is about 43 pounds, so she isn't huge but she's healthy and in her 'range'. To see a recent pic, go to http://ca.geocities.com/weirfamilyrogers/kennedy.html if you want an idea of her size. Weir Mom to Kennedy 6 yr old with CHARGE, 15, 13 and wife to Graeme. New Brunswick, Canada Weir homepage: http://ca.geocities.com/weirfamilyrogers CHARGE SYNDROME CANADA: http://www.chargesyndrome.ca Re: Hello & Need some advice > > > Wow -- first of all let me thank everybody for all your replies. You all > have been real helpful and I'm going to use your ideas. I'm going to answer > questions all in one reply...... > > Cameron uses a formula called Compleat which is a special formula just for > tube feedings. We've tried Pediasure but Cam would always throw up with it. > I've looked into WIC and Medicaid, but my husband makes too much money. > Sometimes I just want to tell these people " If I made too much money, I > wouldn't be asking you for help! " Our insurance does help us with the > formula but we have a high deductible($4000 per person) and they pay very > little on it. In fact we're having problems with the insurance company > paying the correct amount. > > I've been looking into the vital-slim therapy lately. Alot of you > mentioned that your child doesn't feel hunger with a g-tube. Cameron does > b/c if we are late feeding him he gets very cranky and then he's fine after > we feed him. > > Thanks again!!!!!!!!!!!!!!!!!!! > > Michele Westmaas wrote: > - > My daughter, Aubrie, had a Gtube for her first year and a half. She had > it removed before her 2nd birthday. She also had failure to thrive, > swallowing difficulties, and GE reflux. I would have to look back at my > notes from the time for details. I remember thinking she'd never eat. > She'd vomit just at the sight of the spoon. She never did master the > suck-swallow-breath thing with the bottle but went directly to a sippy > cup. When she first ate foods, she would pocket the difficult textures > in between her lower lip and gum. I don't know how she could separate > the hull from the popcorn, the meat from the veggies, etc, but she did. > Then she'd spit the " yuckies " in a napkin. Eventually, she had less and > less yuckies pocketed and finally was able to eat everything. There are > very few foods that she does not manage fine now. In fact, I can't > think of one off hand. > > We were stumped as to how to go from the tube to oral feeding. The ped > didn't have any good suggestions except that she gave us her blessing to > do whatever during the spring when we expected no ear infections and > colds and could best afford any weight loss that might occur during the > transition. So the SLP and I figured out a plan together. We did > overnight tube feedings that ended early enough in the night so that > she'd hopefully wake up somewhat hungry. Then we did only oral feeding > during the day. > > Some dr's had suggested oral feeding at meals followed by a tube feeding > to " top off " whatever the child didn't take orally. But that didn't > make sense to us cuz then she'd never really get that feeling of > hunger. I don't know how we did it, but we did make the transition. At > the time, we gave Aubrie Pediasure instead of milk to get as many > calories in as possible. Now I wish we'd never given up the Pediasure > cuz she's still very small but now won't take the taste of it. > > So-- Perhaps I didn't give you much specific help, but I hope I gave you > some evidence that it is possible to wean from the tube to oral > feeding. It will take work and it will be frustrating. In my > experience, I needed a supportive SLP to work with me since the dr's > weren't so helpful. Our docs didn't care so much if she ever ate > orally. They didn't care how she got it, they just wanted her to get > the nutrition. From a mom's point of view, the way the nutrition is > taken in is a huge issue. > > Best of luck to you and welcome to the list. I'm sure you'll find many > helpful posts here. > > Michele W > Aubrie's mom (6 yrs) CHaRgE > > > > Membership of this email support groups does not constitute membership in > the CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 Your daughter is absolutely precious!!!! Thanks for the pic!!! Weir wrote: , Forgot to mention, Kennedy is 6 and she is about 43 pounds, so she isn't huge but she's healthy and in her 'range'. To see a recent pic, go to http://ca.geocities.com/weirfamilyrogers/kennedy.html if you want an idea of her size. Weir Mom to Kennedy 6 yr old with CHARGE, 15, 13 and wife to Graeme. New Brunswick, Canada Weir homepage: http://ca.geocities.com/weirfamilyrogers CHARGE SYNDROME CANADA: http://www.chargesyndrome.ca Re: Hello & Need some advice > > > Wow -- first of all let me thank everybody for all your replies. You all > have been real helpful and I'm going to use your ideas. I'm going to answer > questions all in one reply...... > > Cameron uses a formula called Compleat which is a special formula just for > tube feedings. We've tried Pediasure but Cam would always throw up with it. > I've looked into WIC and Medicaid, but my husband makes too much money. > Sometimes I just want to tell these people " If I made too much money, I > wouldn't be asking you for help! " Our insurance does help us with the > formula but we have a high deductible($4000 per person) and they pay very > little on it. In fact we're having problems with the insurance company > paying the correct amount. > > I've been looking into the vital-slim therapy lately. Alot of you > mentioned that your child doesn't feel hunger with a g-tube. Cameron does > b/c if we are late feeding him he gets very cranky and then he's fine after > we feed him. > > Thanks again!!!!!!!!!!!!!!!!!!! > > Michele Westmaas wrote: > - > My daughter, Aubrie, had a Gtube for her first year and a half. She had > it removed before her 2nd birthday. She also had failure to thrive, > swallowing difficulties, and GE reflux. I would have to look back at my > notes from the time for details. I remember thinking she'd never eat. > She'd vomit just at the sight of the spoon. She never did master the > suck-swallow-breath thing with the bottle but went directly to a sippy > cup. When she first ate foods, she would pocket the difficult textures > in between her lower lip and gum. I don't know how she could separate > the hull from the popcorn, the meat from the veggies, etc, but she did. > Then she'd spit the " yuckies " in a napkin. Eventually, she had less and > less yuckies pocketed and finally was able to eat everything. There are > very few foods that she does not manage fine now. In fact, I can't > think of one off hand. > > We were stumped as to how to go from the tube to oral feeding. The ped > didn't have any good suggestions except that she gave us her blessing to > do whatever during the spring when we expected no ear infections and > colds and could best afford any weight loss that might occur during the > transition. So the SLP and I figured out a plan together. We did > overnight tube feedings that ended early enough in the night so that > she'd hopefully wake up somewhat hungry. Then we did only oral feeding > during the day. > > Some dr's had suggested oral feeding at meals followed by a tube feeding > to " top off " whatever the child didn't take orally. But that didn't > make sense to us cuz then she'd never really get that feeling of > hunger. I don't know how we did it, but we did make the transition. At > the time, we gave Aubrie Pediasure instead of milk to get as many > calories in as possible. Now I wish we'd never given up the Pediasure > cuz she's still very small but now won't take the taste of it. > > So-- Perhaps I didn't give you much specific help, but I hope I gave you > some evidence that it is possible to wean from the tube to oral > feeding. It will take work and it will be frustrating. In my > experience, I needed a supportive SLP to work with me since the dr's > weren't so helpful. Our docs didn't care so much if she ever ate > orally. They didn't care how she got it, they just wanted her to get > the nutrition. From a mom's point of view, the way the nutrition is > taken in is a huge issue. > > Best of luck to you and welcome to the list. I'm sure you'll find many > helpful posts here. > > Michele W > Aubrie's mom (6 yrs) CHaRgE > > > > Membership of this email support groups does not constitute membership in > the CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 No problem, thanks Weir Mom to Kennedy 6 yr old with CHARGE, 15, 13 and wife to Graeme. New Brunswick, Canada Weir homepage: http://ca.geocities.com/weirfamilyrogers CHARGE SYNDROME CANADA: http://www.chargesyndrome.ca Re: Hello & Need some advice > > > Wow -- first of all let me thank everybody for all your replies. You all > have been real helpful and I'm going to use your ideas. I'm going to answer > questions all in one reply...... > > Cameron uses a formula called Compleat which is a special formula just for > tube feedings. We've tried Pediasure but Cam would always throw up with it. > I've looked into WIC and Medicaid, but my husband makes too much money. > Sometimes I just want to tell these people " If I made too much money, I > wouldn't be asking you for help! " Our insurance does help us with the > formula but we have a high deductible($4000 per person) and they pay very > little on it. In fact we're having problems with the insurance company > paying the correct amount. > > I've been looking into the vital-slim therapy lately. Alot of you > mentioned that your child doesn't feel hunger with a g-tube. Cameron does > b/c if we are late feeding him he gets very cranky and then he's fine after > we feed him. > > Thanks again!!!!!!!!!!!!!!!!!!! > > Michele Westmaas wrote: > - > My daughter, Aubrie, had a Gtube for her first year and a half. She had > it removed before her 2nd birthday. She also had failure to thrive, > swallowing difficulties, and GE reflux. I would have to look back at my > notes from the time for details. I remember thinking she'd never eat. > She'd vomit just at the sight of the spoon. She never did master the > suck-swallow-breath thing with the bottle but went directly to a sippy > cup. When she first ate foods, she would pocket the difficult textures > in between her lower lip and gum. I don't know how she could separate > the hull from the popcorn, the meat from the veggies, etc, but she did. > Then she'd spit the " yuckies " in a napkin. Eventually, she had less and > less yuckies pocketed and finally was able to eat everything. There are > very few foods that she does not manage fine now. In fact, I can't > think of one off hand. > > We were stumped as to how to go from the tube to oral feeding. The ped > didn't have any good suggestions except that she gave us her blessing to > do whatever during the spring when we expected no ear infections and > colds and could best afford any weight loss that might occur during the > transition. So the SLP and I figured out a plan together. We did > overnight tube feedings that ended early enough in the night so that > she'd hopefully wake up somewhat hungry. Then we did only oral feeding > during the day. > > Some dr's had suggested oral feeding at meals followed by a tube feeding > to " top off " whatever the child didn't take orally. But that didn't > make sense to us cuz then she'd never really get that feeling of > hunger. I don't know how we did it, but we did make the transition. At > the time, we gave Aubrie Pediasure instead of milk to get as many > calories in as possible. Now I wish we'd never given up the Pediasure > cuz she's still very small but now won't take the taste of it. > > So-- Perhaps I didn't give you much specific help, but I hope I gave you > some evidence that it is possible to wean from the tube to oral > feeding. It will take work and it will be frustrating. In my > experience, I needed a supportive SLP to work with me since the dr's > weren't so helpful. Our docs didn't care so much if she ever ate > orally. They didn't care how she got it, they just wanted her to get > the nutrition. From a mom's point of view, the way the nutrition is > taken in is a huge issue. > > Best of luck to you and welcome to the list. I'm sure you'll find many > helpful posts here. > > Michele W > Aubrie's mom (6 yrs) CHaRgE > > > > Membership of this email support groups does not constitute membership in > the CHARGE Syndrome Foundation. > For information about the CHARGE Syndrome > Foundation or to become a member (and get the newsletter) > please contact marion@... or visit > the CHARGE Syndrome Foundation web page > at http://www.chargesyndrome.org > 7th International > CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. > Information will be available at our website > www.chargesyndrome.org or by calling 1-. In Canada, you may > contact CHARGE Syndrome Canada at 1- (families), visit > www.chargesyndrome.ca, or email info@.... Thank you! > > > > Quote Link to comment Share on other sites More sharing options...
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