infant starting to cough

TobysMom

New member
My son was diagnosed with CF through his newborn screening and after he had part of his bowel removed from a meconium ileus.

He has been affected by the pancreatic deficiency and has been on enzymes and vitamins and zantac for his AR and we have been doing his nebulizer 2-3x a day for preventative measures.

This past weekend, we were in Orlando visiting my family and my niece and nephew both at some point said they werent feeling well, but when I told them they couldn't be around the baby if they werent feeling well, they almost immediately (or within 10 minutes) said they were feeling fine. I confronted their mother and she agreed they were fine, which I am not so sure about. They are 7 and 5, so they really dont understand the dangers of getting "baby toby" sick. We tried to explain to them it could put him in the hospital, but still, they said they were okay.

Since I was staying with them, I couldnt really keep them completely away from the baby but i tried to keep them as far as possible just in case.

Well, yesterday morning, he woke up with a cough. Hes never really had MUCH of a cough, nor CF affecting his lungs. The last time I noticed him starting to have a cough, Clinic said I could increase his neb to 3x to every 4 hours if necessary. Every 4 hours is virtually impossible with this child as he must be sleeping to get his nebulizer or will scream bloody murder and push it away and turn his head and thrash it back and forth. Well, anyway, I doubt anyone here could really answer this for me, but I am wondering what I should do... should I continue giving him the neb 3-4x a day and see if it helps over the next few days and pick up an infant cough medicine? We have appointments with both CF and his pedi for 6 month checkup on monday, so i am thinking i should just wait it out unless it gets severely worse or his temp goes up. (it was low grade earlier today)

Any suggestions? Should I just treat it as though its a cold and not progression of CF to affecting his lungs? I think clinic would just tell me the same thing- to increase his nebulizer, so i dont think i should even bother with them for this cold or whatever it is. <img src="i/expressions/face-icon-small-sad.gif" border="0">
 

TobysMom

New member
My son was diagnosed with CF through his newborn screening and after he had part of his bowel removed from a meconium ileus.

He has been affected by the pancreatic deficiency and has been on enzymes and vitamins and zantac for his AR and we have been doing his nebulizer 2-3x a day for preventative measures.

This past weekend, we were in Orlando visiting my family and my niece and nephew both at some point said they werent feeling well, but when I told them they couldn't be around the baby if they werent feeling well, they almost immediately (or within 10 minutes) said they were feeling fine. I confronted their mother and she agreed they were fine, which I am not so sure about. They are 7 and 5, so they really dont understand the dangers of getting "baby toby" sick. We tried to explain to them it could put him in the hospital, but still, they said they were okay.

Since I was staying with them, I couldnt really keep them completely away from the baby but i tried to keep them as far as possible just in case.

Well, yesterday morning, he woke up with a cough. Hes never really had MUCH of a cough, nor CF affecting his lungs. The last time I noticed him starting to have a cough, Clinic said I could increase his neb to 3x to every 4 hours if necessary. Every 4 hours is virtually impossible with this child as he must be sleeping to get his nebulizer or will scream bloody murder and push it away and turn his head and thrash it back and forth. Well, anyway, I doubt anyone here could really answer this for me, but I am wondering what I should do... should I continue giving him the neb 3-4x a day and see if it helps over the next few days and pick up an infant cough medicine? We have appointments with both CF and his pedi for 6 month checkup on monday, so i am thinking i should just wait it out unless it gets severely worse or his temp goes up. (it was low grade earlier today)

Any suggestions? Should I just treat it as though its a cold and not progression of CF to affecting his lungs? I think clinic would just tell me the same thing- to increase his nebulizer, so i dont think i should even bother with them for this cold or whatever it is. <img src="i/expressions/face-icon-small-sad.gif" border="0">
 

TobysMom

New member
My son was diagnosed with CF through his newborn screening and after he had part of his bowel removed from a meconium ileus.

He has been affected by the pancreatic deficiency and has been on enzymes and vitamins and zantac for his AR and we have been doing his nebulizer 2-3x a day for preventative measures.

This past weekend, we were in Orlando visiting my family and my niece and nephew both at some point said they werent feeling well, but when I told them they couldn't be around the baby if they werent feeling well, they almost immediately (or within 10 minutes) said they were feeling fine. I confronted their mother and she agreed they were fine, which I am not so sure about. They are 7 and 5, so they really dont understand the dangers of getting "baby toby" sick. We tried to explain to them it could put him in the hospital, but still, they said they were okay.

Since I was staying with them, I couldnt really keep them completely away from the baby but i tried to keep them as far as possible just in case.

Well, yesterday morning, he woke up with a cough. Hes never really had MUCH of a cough, nor CF affecting his lungs. The last time I noticed him starting to have a cough, Clinic said I could increase his neb to 3x to every 4 hours if necessary. Every 4 hours is virtually impossible with this child as he must be sleeping to get his nebulizer or will scream bloody murder and push it away and turn his head and thrash it back and forth. Well, anyway, I doubt anyone here could really answer this for me, but I am wondering what I should do... should I continue giving him the neb 3-4x a day and see if it helps over the next few days and pick up an infant cough medicine? We have appointments with both CF and his pedi for 6 month checkup on monday, so i am thinking i should just wait it out unless it gets severely worse or his temp goes up. (it was low grade earlier today)

Any suggestions? Should I just treat it as though its a cold and not progression of CF to affecting his lungs? I think clinic would just tell me the same thing- to increase his nebulizer, so i dont think i should even bother with them for this cold or whatever it is. <img src="i/expressions/face-icon-small-sad.gif" border="0">
 

TobysMom

New member
My son was diagnosed with CF through his newborn screening and after he had part of his bowel removed from a meconium ileus.

He has been affected by the pancreatic deficiency and has been on enzymes and vitamins and zantac for his AR and we have been doing his nebulizer 2-3x a day for preventative measures.

This past weekend, we were in Orlando visiting my family and my niece and nephew both at some point said they werent feeling well, but when I told them they couldn't be around the baby if they werent feeling well, they almost immediately (or within 10 minutes) said they were feeling fine. I confronted their mother and she agreed they were fine, which I am not so sure about. They are 7 and 5, so they really dont understand the dangers of getting "baby toby" sick. We tried to explain to them it could put him in the hospital, but still, they said they were okay.

Since I was staying with them, I couldnt really keep them completely away from the baby but i tried to keep them as far as possible just in case.

Well, yesterday morning, he woke up with a cough. Hes never really had MUCH of a cough, nor CF affecting his lungs. The last time I noticed him starting to have a cough, Clinic said I could increase his neb to 3x to every 4 hours if necessary. Every 4 hours is virtually impossible with this child as he must be sleeping to get his nebulizer or will scream bloody murder and push it away and turn his head and thrash it back and forth. Well, anyway, I doubt anyone here could really answer this for me, but I am wondering what I should do... should I continue giving him the neb 3-4x a day and see if it helps over the next few days and pick up an infant cough medicine? We have appointments with both CF and his pedi for 6 month checkup on monday, so i am thinking i should just wait it out unless it gets severely worse or his temp goes up. (it was low grade earlier today)

Any suggestions? Should I just treat it as though its a cold and not progression of CF to affecting his lungs? I think clinic would just tell me the same thing- to increase his nebulizer, so i dont think i should even bother with them for this cold or whatever it is. <img src="i/expressions/face-icon-small-sad.gif" border="0">
 

TobysMom

New member
My son was diagnosed with CF through his newborn screening and after he had part of his bowel removed from a meconium ileus.
<br />
<br />He has been affected by the pancreatic deficiency and has been on enzymes and vitamins and zantac for his AR and we have been doing his nebulizer 2-3x a day for preventative measures.
<br />
<br />This past weekend, we were in Orlando visiting my family and my niece and nephew both at some point said they werent feeling well, but when I told them they couldn't be around the baby if they werent feeling well, they almost immediately (or within 10 minutes) said they were feeling fine. I confronted their mother and she agreed they were fine, which I am not so sure about. They are 7 and 5, so they really dont understand the dangers of getting "baby toby" sick. We tried to explain to them it could put him in the hospital, but still, they said they were okay.
<br />
<br />Since I was staying with them, I couldnt really keep them completely away from the baby but i tried to keep them as far as possible just in case.
<br />
<br />Well, yesterday morning, he woke up with a cough. Hes never really had MUCH of a cough, nor CF affecting his lungs. The last time I noticed him starting to have a cough, Clinic said I could increase his neb to 3x to every 4 hours if necessary. Every 4 hours is virtually impossible with this child as he must be sleeping to get his nebulizer or will scream bloody murder and push it away and turn his head and thrash it back and forth. Well, anyway, I doubt anyone here could really answer this for me, but I am wondering what I should do... should I continue giving him the neb 3-4x a day and see if it helps over the next few days and pick up an infant cough medicine? We have appointments with both CF and his pedi for 6 month checkup on monday, so i am thinking i should just wait it out unless it gets severely worse or his temp goes up. (it was low grade earlier today)
<br />
<br />Any suggestions? Should I just treat it as though its a cold and not progression of CF to affecting his lungs? I think clinic would just tell me the same thing- to increase his nebulizer, so i dont think i should even bother with them for this cold or whatever it is. <img src="i/expressions/face-icon-small-sad.gif" border="0">
<br />
<br />
<br />
 

SARAHSARAH253

New member
Hi there,

This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck

Sarah
 

SARAHSARAH253

New member
Hi there,

This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck

Sarah
 

SARAHSARAH253

New member
Hi there,

This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck

Sarah
 

SARAHSARAH253

New member
Hi there,

This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck

Sarah
 

SARAHSARAH253

New member
Hi there,
<br />
<br />This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck
<br />
<br />Sarah
<br />
 

TobysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>SARAHSARAH253</b></i>

Hi there,



This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck



Sarah</end quote></div>


Hmmm, they never told me that i couldnt give him anything for a cough, but I guess I shall call them in the morning. The last time they asked if there was any discharge from his nose. I had to suck out some boogies this morning when he woke up and once after that. Maybe this time they'll call in an RX for antibiotics. Im not totally sure why they didnt last time, but it seemed his cough went away after a few days just increasing his nebulizer. Thats why I hoped increasing would help, but his cough sounds a LOT worse this time around than it did last time. I figure clinic probably would call in the appropriate RX for a cf baby than his pedi would...

Thanks! <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

TobysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>SARAHSARAH253</b></i>

Hi there,



This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck



Sarah</end quote></div>


Hmmm, they never told me that i couldnt give him anything for a cough, but I guess I shall call them in the morning. The last time they asked if there was any discharge from his nose. I had to suck out some boogies this morning when he woke up and once after that. Maybe this time they'll call in an RX for antibiotics. Im not totally sure why they didnt last time, but it seemed his cough went away after a few days just increasing his nebulizer. Thats why I hoped increasing would help, but his cough sounds a LOT worse this time around than it did last time. I figure clinic probably would call in the appropriate RX for a cf baby than his pedi would...

Thanks! <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

TobysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>SARAHSARAH253</b></i>

Hi there,



This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck



Sarah</end quote></div>


Hmmm, they never told me that i couldnt give him anything for a cough, but I guess I shall call them in the morning. The last time they asked if there was any discharge from his nose. I had to suck out some boogies this morning when he woke up and once after that. Maybe this time they'll call in an RX for antibiotics. Im not totally sure why they didnt last time, but it seemed his cough went away after a few days just increasing his nebulizer. Thats why I hoped increasing would help, but his cough sounds a LOT worse this time around than it did last time. I figure clinic probably would call in the appropriate RX for a cf baby than his pedi would...

Thanks! <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

TobysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>SARAHSARAH253</b></i>

Hi there,



This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck



Sarah</end quote>


Hmmm, they never told me that i couldnt give him anything for a cough, but I guess I shall call them in the morning. The last time they asked if there was any discharge from his nose. I had to suck out some boogies this morning when he woke up and once after that. Maybe this time they'll call in an RX for antibiotics. Im not totally sure why they didnt last time, but it seemed his cough went away after a few days just increasing his nebulizer. Thats why I hoped increasing would help, but his cough sounds a LOT worse this time around than it did last time. I figure clinic probably would call in the appropriate RX for a cf baby than his pedi would...

Thanks! <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

TobysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>SARAHSARAH253</b></i>
<br />
<br />Hi there,
<br />
<br />
<br />
<br />This is tricky isn't it...My son started a cough a few weeks, and the clinic told me to watch it for a couple days. If it didn't seem to go away they would call in RX of antibotics. Well, his cough continued so they called in the presciption. My son was also around older kids, so I thought it be better safe than sorry. I would just watch it, and if it doesn't clear up..Call your clinic..I may be wrong but i don't think children or adults with CF can take cough meds..Because they want them to get the yucky stuff up..Good Luck
<br />
<br />
<br />
<br />Sarah</end quote>
<br />
<br />
<br />Hmmm, they never told me that i couldnt give him anything for a cough, but I guess I shall call them in the morning. The last time they asked if there was any discharge from his nose. I had to suck out some boogies this morning when he woke up and once after that. Maybe this time they'll call in an RX for antibiotics. Im not totally sure why they didnt last time, but it seemed his cough went away after a few days just increasing his nebulizer. Thats why I hoped increasing would help, but his cough sounds a LOT worse this time around than it did last time. I figure clinic probably would call in the appropriate RX for a cf baby than his pedi would...
<br />
<br />Thanks! <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

ehtansky21

New member
No cough meds, it can dry out everything, which with CF would most likely double the production of mucus.
Whenever the kids are not feeling well, I give them Ibuprofen. It can decrease inflamation and help with stuffy noses and congested cough.
Blessings,
Missa
 

ehtansky21

New member
No cough meds, it can dry out everything, which with CF would most likely double the production of mucus.
Whenever the kids are not feeling well, I give them Ibuprofen. It can decrease inflamation and help with stuffy noses and congested cough.
Blessings,
Missa
 

ehtansky21

New member
No cough meds, it can dry out everything, which with CF would most likely double the production of mucus.
Whenever the kids are not feeling well, I give them Ibuprofen. It can decrease inflamation and help with stuffy noses and congested cough.
Blessings,
Missa
 

ehtansky21

New member
No cough meds, it can dry out everything, which with CF would most likely double the production of mucus.
Whenever the kids are not feeling well, I give them Ibuprofen. It can decrease inflamation and help with stuffy noses and congested cough.
Blessings,
Missa
 

ehtansky21

New member
No cough meds, it can dry out everything, which with CF would most likely double the production of mucus.
<br />Whenever the kids are not feeling well, I give them Ibuprofen. It can decrease inflamation and help with stuffy noses and congested cough.
<br />Blessings,
<br />Missa
 
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