Guest guest Posted August 15, 2004 Report 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
Guest guest Posted August 15, 2004 Report 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
Guest guest Posted August 16, 2004 Report 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
Guest guest Posted August 16, 2004 Report 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
Guest guest Posted August 16, 2004 Report 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
Guest guest Posted August 16, 2004 Report 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
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