Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 jeannie, My daughter has a therapy vest she's had it for about 5 or 6 years and at that time it was $17,000 - $18,000, my insurance company paid for it. I think they start children on it when they're 5. Good Luck mom to 14 w/cf, Cody 11wocf, Zoey 3 wocf, Evan 11 wks w/cf Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 jeannie, My daughter has a therapy vest she's had it for about 5 or 6 years and at that time it was $17,000 - $18,000, my insurance company paid for it. I think they start children on it when they're 5. Good Luck mom to 14 w/cf, Cody 11wocf, Zoey 3 wocf, Evan 11 wks w/cf Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 jeannie, My daughter has a therapy vest she's had it for about 5 or 6 years and at that time it was $17,000 - $18,000, my insurance company paid for it. I think they start children on it when they're 5. Good Luck mom to 14 w/cf, Cody 11wocf, Zoey 3 wocf, Evan 11 wks w/cf Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 You are very wise gal....ALL the lists are great. EACH one has something special to offer each of us..Everyone should be on all. & pass the info & caring around. One other is www.cysticfibrosis@... .Comes out thru group at Yale. No charge either. You mentioned CYSTIC-L . so I assume you already know how to be on that one........It is www.Cystic-L.org Directions on each ones home page to sign up. CFParents is growing by leaps & bounds which shows you how great it is too.'Each one has folks from all over the world.They all have links to other CF info too. All Lists are super ...........:) I love them all dearly .ENJOY. remember, you can also always go to the search & put in name of list & then , just click:):) LOVE & HUGS, GrandmomBEV other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 You are very wise gal....ALL the lists are great. EACH one has something special to offer each of us..Everyone should be on all. & pass the info & caring around. One other is www.cysticfibrosis@... .Comes out thru group at Yale. No charge either. You mentioned CYSTIC-L . so I assume you already know how to be on that one........It is www.Cystic-L.org Directions on each ones home page to sign up. CFParents is growing by leaps & bounds which shows you how great it is too.'Each one has folks from all over the world.They all have links to other CF info too. All Lists are super ...........:) I love them all dearly .ENJOY. remember, you can also always go to the search & put in name of list & then , just click:):) LOVE & HUGS, GrandmomBEV other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 You are very wise gal....ALL the lists are great. EACH one has something special to offer each of us..Everyone should be on all. & pass the info & caring around. One other is www.cysticfibrosis@... .Comes out thru group at Yale. No charge either. You mentioned CYSTIC-L . so I assume you already know how to be on that one........It is www.Cystic-L.org Directions on each ones home page to sign up. CFParents is growing by leaps & bounds which shows you how great it is too.'Each one has folks from all over the world.They all have links to other CF info too. All Lists are super ...........:) I love them all dearly .ENJOY. remember, you can also always go to the search & put in name of list & then , just click:):) LOVE & HUGS, GrandmomBEV other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 Get your Pulmo doc to write a prescription for The Vest Airway Clearance System. He'll have to send some sort of info to the company that makes them...he should know how to do this. The company that makes them will probably call you for info (they called me anyhow, to find out about our insurance and my daughter's symptoms, etc...), and then they'll write a letter to your Pulmdoc, and have him write them a letter about the medical necessity. Then, after they get that, they're fully armed to talk to your insurance company about how it's Durable Medical Equipment and is medically necessary for your child's continued wellbeing, etc. Also, they have a deal where even if they haven't gotten approval from your insurance by 60 days, they'll still send one to you and they have other avenues like payment plans and a Vest Foundation that helps people who can't afford to pay for one. They say it can take up to 60 days to get the vest to you after they get the letter of medical necessity from the Pulmdoc. Reason I know all this is because I just talked to the lady from the company yesterday and got further into the process of getting Triana's vest...we're hoping to get it all cleared by the insurance company before the end of the year so it'll go on this year's coverage and we won't have a huge deductible to pay in one lump sum in January or February. Our insurance has already told me that they do cover it 100%, but I'm betting that the paperwork will take a little while. As for the cost, the docs at the hospital when Triana got dx'd a couple of months ago said it runs about $15,000 or so. I about fell out of my seat on that one! Holy cow! On the upside, it's got a lifetime guarantee on it, and getting bigger vest sizes as your kid grows is included in the price tag, so there's no extra cost for those later on down the line. Hope this helps some... Shanna mom of Triana, age 2 wcf other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 Get your Pulmo doc to write a prescription for The Vest Airway Clearance System. He'll have to send some sort of info to the company that makes them...he should know how to do this. The company that makes them will probably call you for info (they called me anyhow, to find out about our insurance and my daughter's symptoms, etc...), and then they'll write a letter to your Pulmdoc, and have him write them a letter about the medical necessity. Then, after they get that, they're fully armed to talk to your insurance company about how it's Durable Medical Equipment and is medically necessary for your child's continued wellbeing, etc. Also, they have a deal where even if they haven't gotten approval from your insurance by 60 days, they'll still send one to you and they have other avenues like payment plans and a Vest Foundation that helps people who can't afford to pay for one. They say it can take up to 60 days to get the vest to you after they get the letter of medical necessity from the Pulmdoc. Reason I know all this is because I just talked to the lady from the company yesterday and got further into the process of getting Triana's vest...we're hoping to get it all cleared by the insurance company before the end of the year so it'll go on this year's coverage and we won't have a huge deductible to pay in one lump sum in January or February. Our insurance has already told me that they do cover it 100%, but I'm betting that the paperwork will take a little while. As for the cost, the docs at the hospital when Triana got dx'd a couple of months ago said it runs about $15,000 or so. I about fell out of my seat on that one! Holy cow! On the upside, it's got a lifetime guarantee on it, and getting bigger vest sizes as your kid grows is included in the price tag, so there's no extra cost for those later on down the line. Hope this helps some... Shanna mom of Triana, age 2 wcf other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 Get your Pulmo doc to write a prescription for The Vest Airway Clearance System. He'll have to send some sort of info to the company that makes them...he should know how to do this. The company that makes them will probably call you for info (they called me anyhow, to find out about our insurance and my daughter's symptoms, etc...), and then they'll write a letter to your Pulmdoc, and have him write them a letter about the medical necessity. Then, after they get that, they're fully armed to talk to your insurance company about how it's Durable Medical Equipment and is medically necessary for your child's continued wellbeing, etc. Also, they have a deal where even if they haven't gotten approval from your insurance by 60 days, they'll still send one to you and they have other avenues like payment plans and a Vest Foundation that helps people who can't afford to pay for one. They say it can take up to 60 days to get the vest to you after they get the letter of medical necessity from the Pulmdoc. Reason I know all this is because I just talked to the lady from the company yesterday and got further into the process of getting Triana's vest...we're hoping to get it all cleared by the insurance company before the end of the year so it'll go on this year's coverage and we won't have a huge deductible to pay in one lump sum in January or February. Our insurance has already told me that they do cover it 100%, but I'm betting that the paperwork will take a little while. As for the cost, the docs at the hospital when Triana got dx'd a couple of months ago said it runs about $15,000 or so. I about fell out of my seat on that one! Holy cow! On the upside, it's got a lifetime guarantee on it, and getting bigger vest sizes as your kid grows is included in the price tag, so there's no extra cost for those later on down the line. Hope this helps some... Shanna mom of Triana, age 2 wcf other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 My daughter is 2.5 years old, and she's getting it as soon as it goes through all the paperwork. They told me it's the size of the chest that matters...has to be at least 21 inches. Shanna mom of Triana, age 2 wcf Re: other cf lists jeannie, My daughter has a therapy vest she's had it for about 5 or 6 years and at that time it was $17,000 - $18,000, my insurance company paid for it. I think they start children on it when they're 5. Good Luck mom to 14 w/cf, Cody 11wocf, Zoey 3 wocf, Evan 11 wks w/cf Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 My daughter is 2.5 years old, and she's getting it as soon as it goes through all the paperwork. They told me it's the size of the chest that matters...has to be at least 21 inches. Shanna mom of Triana, age 2 wcf Re: other cf lists jeannie, My daughter has a therapy vest she's had it for about 5 or 6 years and at that time it was $17,000 - $18,000, my insurance company paid for it. I think they start children on it when they're 5. Good Luck mom to 14 w/cf, Cody 11wocf, Zoey 3 wocf, Evan 11 wks w/cf Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 My daughter is 2.5 years old, and she's getting it as soon as it goes through all the paperwork. They told me it's the size of the chest that matters...has to be at least 21 inches. Shanna mom of Triana, age 2 wcf Re: other cf lists jeannie, My daughter has a therapy vest she's had it for about 5 or 6 years and at that time it was $17,000 - $18,000, my insurance company paid for it. I think they start children on it when they're 5. Good Luck mom to 14 w/cf, Cody 11wocf, Zoey 3 wocf, Evan 11 wks w/cf Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 Hi Jeannie, I'm Randy with Advanced Respiratory, the Vest Company. I monitor cfparents and Cystic-L as a resource person for families with the Vest and for those considering the Vest. I am not here to do a sales job...anyone on either of these lists would be able to verify that for you. I am here to answer questions and help where I can. To get a Vest, your MD must write a prescription for it. Once that happens, we contact you to get your consent to obtain information so that we can get you the right size Vest. We work directly with your insurance company. We submit all of the necessary paperwork and handle all appeals if your insurance denies it. If all efforts fail with your insurance company (this process can take up to 2 years), we check to see if there is anyway possible you can afford the device. It has been our experience that most families are just trying to stay above water and put food on the table. There is no way they can afford the cost of a machine. We understand that and we have a foundation that can cover part or all of the cost of the Vest. The most important thing you need to remember is that we want people to get the Vest based of medical necessity, not financial availability. Now you are probably thinking, " I have to wait 2 years to get one of these machines??? " No. We try to work with your insurance company for up to 60 days from the time the MD signs all of the necessary paperwork. If we cannot get a clear answer from your insurance company by then, we automatically send the Vest to you. You start using it while we move forward with the process. We frequently get asked, " Well, what if my insurance company refuses to cover it and I can't afford it. Does that mean you are going to take it away from me? " Again, no. Once a device is placed in the home, the only way it is removed is if you request it to be removed or the MD orders it to be discontinued. We will not come knocking on your door, harass you, give you grief, etc. That is not the way we do business. If you are interested, let me know where you live and who you doctor with. I can help you get things started if you would like. In the meantime, visit our website at www.thevest.com. There is a bunch of information there that will answer many of your questions. This list as well as Cystic-L are also very valuable because so many people and families here use the Vest. They can give you insight about the Vest and many other CF topics. I hope this helps. Let me know if I can do anything else. Randy other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 Hi Jeannie, I'm Randy with Advanced Respiratory, the Vest Company. I monitor cfparents and Cystic-L as a resource person for families with the Vest and for those considering the Vest. I am not here to do a sales job...anyone on either of these lists would be able to verify that for you. I am here to answer questions and help where I can. To get a Vest, your MD must write a prescription for it. Once that happens, we contact you to get your consent to obtain information so that we can get you the right size Vest. We work directly with your insurance company. We submit all of the necessary paperwork and handle all appeals if your insurance denies it. If all efforts fail with your insurance company (this process can take up to 2 years), we check to see if there is anyway possible you can afford the device. It has been our experience that most families are just trying to stay above water and put food on the table. There is no way they can afford the cost of a machine. We understand that and we have a foundation that can cover part or all of the cost of the Vest. The most important thing you need to remember is that we want people to get the Vest based of medical necessity, not financial availability. Now you are probably thinking, " I have to wait 2 years to get one of these machines??? " No. We try to work with your insurance company for up to 60 days from the time the MD signs all of the necessary paperwork. If we cannot get a clear answer from your insurance company by then, we automatically send the Vest to you. You start using it while we move forward with the process. We frequently get asked, " Well, what if my insurance company refuses to cover it and I can't afford it. Does that mean you are going to take it away from me? " Again, no. Once a device is placed in the home, the only way it is removed is if you request it to be removed or the MD orders it to be discontinued. We will not come knocking on your door, harass you, give you grief, etc. That is not the way we do business. If you are interested, let me know where you live and who you doctor with. I can help you get things started if you would like. In the meantime, visit our website at www.thevest.com. There is a bunch of information there that will answer many of your questions. This list as well as Cystic-L are also very valuable because so many people and families here use the Vest. They can give you insight about the Vest and many other CF topics. I hope this helps. Let me know if I can do anything else. Randy other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2002 Report Share Posted December 3, 2002 Hi Jeannie, I'm Randy with Advanced Respiratory, the Vest Company. I monitor cfparents and Cystic-L as a resource person for families with the Vest and for those considering the Vest. I am not here to do a sales job...anyone on either of these lists would be able to verify that for you. I am here to answer questions and help where I can. To get a Vest, your MD must write a prescription for it. Once that happens, we contact you to get your consent to obtain information so that we can get you the right size Vest. We work directly with your insurance company. We submit all of the necessary paperwork and handle all appeals if your insurance denies it. If all efforts fail with your insurance company (this process can take up to 2 years), we check to see if there is anyway possible you can afford the device. It has been our experience that most families are just trying to stay above water and put food on the table. There is no way they can afford the cost of a machine. We understand that and we have a foundation that can cover part or all of the cost of the Vest. The most important thing you need to remember is that we want people to get the Vest based of medical necessity, not financial availability. Now you are probably thinking, " I have to wait 2 years to get one of these machines??? " No. We try to work with your insurance company for up to 60 days from the time the MD signs all of the necessary paperwork. If we cannot get a clear answer from your insurance company by then, we automatically send the Vest to you. You start using it while we move forward with the process. We frequently get asked, " Well, what if my insurance company refuses to cover it and I can't afford it. Does that mean you are going to take it away from me? " Again, no. Once a device is placed in the home, the only way it is removed is if you request it to be removed or the MD orders it to be discontinued. We will not come knocking on your door, harass you, give you grief, etc. That is not the way we do business. If you are interested, let me know where you live and who you doctor with. I can help you get things started if you would like. In the meantime, visit our website at www.thevest.com. There is a bunch of information there that will answer many of your questions. This list as well as Cystic-L are also very valuable because so many people and families here use the Vest. They can give you insight about the Vest and many other CF topics. I hope this helps. Let me know if I can do anything else. Randy other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2002 Report Share Posted December 4, 2002 RANDY, I just had to jump in & tell you how great it is your on line & how really super the company is . I knew them when they first decided to buy it & That have been wonderful to all since then too. Give Eldon & Rod , & all the road-gang(haha) my love & great thanks. LOVE & HUGS, grandmomBEV other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2002 Report Share Posted December 4, 2002 RANDY, I just had to jump in & tell you how great it is your on line & how really super the company is . I knew them when they first decided to buy it & That have been wonderful to all since then too. Give Eldon & Rod , & all the road-gang(haha) my love & great thanks. LOVE & HUGS, grandmomBEV other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2002 Report Share Posted December 4, 2002 RANDY, I just had to jump in & tell you how great it is your on line & how really super the company is . I knew them when they first decided to buy it & That have been wonderful to all since then too. Give Eldon & Rod , & all the road-gang(haha) my love & great thanks. LOVE & HUGS, grandmomBEV other cf lists hi can someone please send me some of the other list adresses of sites like this and cystic-l please i like to read these as i can see how others are and there kids are so far williams only had gi probs and asthma and thursday we will find out if his sinuses are causing him to pause in his breathing at night he will be in the hosp thurs night for a aleep study.. now can someone please tell me how to get a vest for him and how much it costs im sure there expensive so if i can ill get a loan if ins dont cover it thanks jeannie mom to william 5yowcf &hannah 101/2mosnocf ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
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