Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Hi Ella and everyone, My story is much the same as Ellas. I found out 2 months ago that my son (who's nine) has cystic fibrosis. He was also treated for asthma for years. He's already improved and looks good - I still feel a bit raw at times (usually when he's not around) but on the whole I'm doing okay. I still feel really angry about him not being diagnosed any sooner. why don't they give people with asthma and bowel problems a sweat test as a matter of course - they can't be that expensive. Christy if you would like me to give you my address for Wyatt to write to I would be happy to - you can e-mail me personally. Perhaps they can moan about their little brothers (Ours is Jake and he turned 2 in July) That's it for now - hope you're all doing okay Sx Hello from Ireland Hello Everybody, A friend of mine in work sought out this website, cfparents, for me so I only just signed on yesterday. I have been reading some of your stories and they are all so interesting and some very funny about the eating or over eating should I say!! I have three beautiful girls, 10, 8 and 5. My eldest girl always suffered with asthma and chest infections and was always really weak and I was always coaxing her to eat etc. etc. Last year after years of bringing her to our local doctors, I finally got to see an asthma specialist, well the rest is history. At 9 years of age, he told me she had what was called Cystic Fibrosis. Needless to say my world just fell apart and is slowly coming back on line. It's been a year of learning and trying to understand the illness and all that goes with it. At least I know now what's been wrong with her all these years. With the right antiobiotics and enzymes she looks better than she ever looked in her life. My other two girls were tested and are fine. It's great to be talking to other parents. I feel so isolated sometimes, like I'm the only CF parent in Ireland and I've so much I want to talk about. I'll go for now. Hope you all have a nice weekend. Ella. For more information on the C&C Group visit http://www.candcgroupplc.com ********************************************************************** Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Hi Ella and everyone, My story is much the same as Ellas. I found out 2 months ago that my son (who's nine) has cystic fibrosis. He was also treated for asthma for years. He's already improved and looks good - I still feel a bit raw at times (usually when he's not around) but on the whole I'm doing okay. I still feel really angry about him not being diagnosed any sooner. why don't they give people with asthma and bowel problems a sweat test as a matter of course - they can't be that expensive. Christy if you would like me to give you my address for Wyatt to write to I would be happy to - you can e-mail me personally. Perhaps they can moan about their little brothers (Ours is Jake and he turned 2 in July) That's it for now - hope you're all doing okay Sx Hello from Ireland Hello Everybody, A friend of mine in work sought out this website, cfparents, for me so I only just signed on yesterday. I have been reading some of your stories and they are all so interesting and some very funny about the eating or over eating should I say!! I have three beautiful girls, 10, 8 and 5. My eldest girl always suffered with asthma and chest infections and was always really weak and I was always coaxing her to eat etc. etc. Last year after years of bringing her to our local doctors, I finally got to see an asthma specialist, well the rest is history. At 9 years of age, he told me she had what was called Cystic Fibrosis. Needless to say my world just fell apart and is slowly coming back on line. It's been a year of learning and trying to understand the illness and all that goes with it. At least I know now what's been wrong with her all these years. With the right antiobiotics and enzymes she looks better than she ever looked in her life. My other two girls were tested and are fine. It's great to be talking to other parents. I feel so isolated sometimes, like I'm the only CF parent in Ireland and I've so much I want to talk about. I'll go for now. Hope you all have a nice weekend. Ella. For more information on the C&C Group visit http://www.candcgroupplc.com ********************************************************************** Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Hi Ella, welcome to the list! I've been in contact with other parents from Ireland in the past, but they are incommunicado for years now. But we have members from the UK here and others have " the Luck of the Irish " . We have named our daughter Fiona because we looked for a name that is pronounced the same in english and german. I am sure you'll like it here and find lots of parents to talk to. Peace Torsten, dad of Fiona 5wcf > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Hi Ella, welcome to the list! I've been in contact with other parents from Ireland in the past, but they are incommunicado for years now. But we have members from the UK here and others have " the Luck of the Irish " . We have named our daughter Fiona because we looked for a name that is pronounced the same in english and german. I am sure you'll like it here and find lots of parents to talk to. Peace Torsten, dad of Fiona 5wcf > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Hi Ella, welcome to the list! I've been in contact with other parents from Ireland in the past, but they are incommunicado for years now. But we have members from the UK here and others have " the Luck of the Irish " . We have named our daughter Fiona because we looked for a name that is pronounced the same in english and german. I am sure you'll like it here and find lots of parents to talk to. Peace Torsten, dad of Fiona 5wcf > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Ella, We both shared exactly the same feeling of isolation & being lonely in the CF world before we found this list. Now it is really a great support. My only daugher Sharada is diagnosed very early i.e. at 5 days of age. In CF the earlier you know is better. I hope now your daugher will be fine after proper medication Warm Regards SHRIKANT Father of Sharada 5 yowcf Abu Dhabi, United Arab Emirates Hello from Ireland Hello Everybody, A friend of mine in work sought out this website, cfparents, for me so I only just signed on yesterday. I have been reading some of your stories and they are all so interesting and some very funny about the eating or over eating should I say!! I have three beautiful girls, 10, 8 and 5. My eldest girl always suffered with asthma and chest infections and was always really weak and I was always coaxing her to eat etc. etc. Last year after years of bringing her to our local doctors, I finally got to see an asthma specialist, well the rest is history. At 9 years of age, he told me she had what was called Cystic Fibrosis. Needless to say my world just fell apart and is slowly coming back on line. It's been a year of learning and trying to understand the illness and all that goes with it. At least I know now what's been wrong with her all these years. With the right antiobiotics and enzymes she looks better than she ever looked in her life. My other two girls were tested and are fine. It's great to be talking to other parents. I feel so isolated sometimes, like I'm the only CF parent in Ireland and I've so much I want to talk about. I'll go for now. Hope you all have a nice weekend. Ella. For more information on the C&C Group visit http://www.candcgroupplc.com ********************************************************************** Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Ella, We both shared exactly the same feeling of isolation & being lonely in the CF world before we found this list. Now it is really a great support. My only daugher Sharada is diagnosed very early i.e. at 5 days of age. In CF the earlier you know is better. I hope now your daugher will be fine after proper medication Warm Regards SHRIKANT Father of Sharada 5 yowcf Abu Dhabi, United Arab Emirates Hello from Ireland Hello Everybody, A friend of mine in work sought out this website, cfparents, for me so I only just signed on yesterday. I have been reading some of your stories and they are all so interesting and some very funny about the eating or over eating should I say!! I have three beautiful girls, 10, 8 and 5. My eldest girl always suffered with asthma and chest infections and was always really weak and I was always coaxing her to eat etc. etc. Last year after years of bringing her to our local doctors, I finally got to see an asthma specialist, well the rest is history. At 9 years of age, he told me she had what was called Cystic Fibrosis. Needless to say my world just fell apart and is slowly coming back on line. It's been a year of learning and trying to understand the illness and all that goes with it. At least I know now what's been wrong with her all these years. With the right antiobiotics and enzymes she looks better than she ever looked in her life. My other two girls were tested and are fine. It's great to be talking to other parents. I feel so isolated sometimes, like I'm the only CF parent in Ireland and I've so much I want to talk about. I'll go for now. Hope you all have a nice weekend. Ella. For more information on the C&C Group visit http://www.candcgroupplc.com ********************************************************************** Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 In a message dated 10/18/2002 7:45:45 AM Central Daylight Time, ella.rafter@... writes: > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > Ella, I have 3 girls also 10,8, and 5. My oldest and youngest has CF and my middle one is fine. They were diagnosed when my oldest was 6 years old. I know what you mean about the roller coaster ride you go thought the first year. It just seems like yesterday when we were diagnosed. This is a great support group and I know you will meet a lot of neat people. I am in Iowa. Deb A Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Sheila, That would be great to have Wyatt and talk. I don't see your email address on here. Mine is seabeewife2@... I can't imagine what it's like for those of you who learn about the CF so much later in life. My nephew was having bowel and weight problems last year and I immediately told them to test him for CF. Thank the Lord his does not have it but it was such a scary time for me as well as my brother and sister in law. Christy mom of Wyatt 7wcf and Hunter 2wocf > > Hi Ella and everyone, > > My story is much the same as Ellas. I found out 2 months ago that my son > (who's nine) has cystic fibrosis. He was also treated for asthma > for years. He's already improved and looks good - I still feel a bit raw at > times (usually when he's not around) but on the whole I'm doing okay. > > I still feel really angry about him not being diagnosed any sooner. why > don't they give people with asthma and bowel problems a sweat test as a > matter of course - they can't be that expensive. > > Christy if you would like me to give you my address for Wyatt to write to > I would be happy to - you can e-mail me personally. Perhaps they > can moan about their little brothers (Ours is Jake and he turned 2 in July) > > That's it for now - hope you're all doing okay > > > > Sx > Hello from Ireland > > > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Sheila, That would be great to have Wyatt and talk. I don't see your email address on here. Mine is seabeewife2@... I can't imagine what it's like for those of you who learn about the CF so much later in life. My nephew was having bowel and weight problems last year and I immediately told them to test him for CF. Thank the Lord his does not have it but it was such a scary time for me as well as my brother and sister in law. Christy mom of Wyatt 7wcf and Hunter 2wocf > > Hi Ella and everyone, > > My story is much the same as Ellas. I found out 2 months ago that my son > (who's nine) has cystic fibrosis. He was also treated for asthma > for years. He's already improved and looks good - I still feel a bit raw at > times (usually when he's not around) but on the whole I'm doing okay. > > I still feel really angry about him not being diagnosed any sooner. why > don't they give people with asthma and bowel problems a sweat test as a > matter of course - they can't be that expensive. > > Christy if you would like me to give you my address for Wyatt to write to > I would be happy to - you can e-mail me personally. Perhaps they > can moan about their little brothers (Ours is Jake and he turned 2 in July) > > That's it for now - hope you're all doing okay > > > > Sx > Hello from Ireland > > > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Sheila, That would be great to have Wyatt and talk. I don't see your email address on here. Mine is seabeewife2@... I can't imagine what it's like for those of you who learn about the CF so much later in life. My nephew was having bowel and weight problems last year and I immediately told them to test him for CF. Thank the Lord his does not have it but it was such a scary time for me as well as my brother and sister in law. Christy mom of Wyatt 7wcf and Hunter 2wocf > > Hi Ella and everyone, > > My story is much the same as Ellas. I found out 2 months ago that my son > (who's nine) has cystic fibrosis. He was also treated for asthma > for years. He's already improved and looks good - I still feel a bit raw at > times (usually when he's not around) but on the whole I'm doing okay. > > I still feel really angry about him not being diagnosed any sooner. why > don't they give people with asthma and bowel problems a sweat test as a > matter of course - they can't be that expensive. > > Christy if you would like me to give you my address for Wyatt to write to > I would be happy to - you can e-mail me personally. Perhaps they > can moan about their little brothers (Ours is Jake and he turned 2 in July) > > That's it for now - hope you're all doing okay > > > > Sx > Hello from Ireland > > > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Ella, Welcome to the group. I hope that you enjoy the friendship that you find here. The people on this list can relate to the emotions that go along with the diagnosis and the ordeals that pwcf live daily. I hope that you find great comfort in being a part of this group. Welcome, Gale - Ohio, USA > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2002 Report Share Posted October 18, 2002 Ella, Welcome to the group. I hope that you enjoy the friendship that you find here. The people on this list can relate to the emotions that go along with the diagnosis and the ordeals that pwcf live daily. I hope that you find great comfort in being a part of this group. Welcome, Gale - Ohio, USA > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > > > > For more information on the C&C Group visit http://www.candcgroupplc.com > > ********************************************************************** > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 20, 2002 Report Share Posted October 20, 2002 Ella, I know what you mean about the first year also, it is like a dream, so much to learn, things you dont want to learn, dna, deltaWHAT,??? and all the other bizarre things they throw at us. Then here I am 12 years later wondering where did those years go, they went by so fast, I wish i had them back. He is growing up getting ready for college and still the unknown. Enjoy, Love and never forget to Laugh, Laugh Laugh, I wish you well with your daughters . Keep Your Spirits Up and remember CF stands for Cure Found. Re: Hello from Ireland In a message dated 10/18/2002 7:45:45 AM Central Daylight Time, ella.rafter@... writes: > Hello Everybody, > > A friend of mine in work sought out this website, cfparents, for > me so I only just signed on yesterday. > > I have been reading some of your stories and they are all so > interesting and some very funny about the eating or over eating > should I say!! > > I have three beautiful girls, 10, 8 and 5. > > My eldest girl always suffered with asthma and chest infections > and was always really weak and I was always coaxing her to eat > etc. etc. Last year after years of bringing her to our local > doctors, I finally got to see an asthma specialist, well the rest > is history. At 9 years of age, he told me she had what was > called Cystic Fibrosis. Needless to say my world just fell apart > and is slowly coming back on line. It's been a year of learning > and trying to understand the illness and all that goes with it. > > At least I know now what's been wrong with her all these years. > With the right antiobiotics and enzymes she looks better than she > ever looked in her life. > > My other two girls were tested and are fine. > > It's great to be talking to other parents. I feel so isolated > sometimes, like I'm the only CF parent in Ireland and I've so > much I want to talk about. > > I'll go for now. Hope you all have a nice weekend. > > > Ella. > Ella, I have 3 girls also 10,8, and 5. My oldest and youngest has CF and my middle one is fine. They were diagnosed when my oldest was 6 years old. I know what you mean about the roller coaster ride you go thought the first year. It just seems like yesterday when we were diagnosed. This is a great support group and I know you will meet a lot of neat people. I am in Iowa. Deb A Quote Link to comment Share on other sites More sharing options...
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