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I hope you don't mind but in reading all the post about how you found out

about your or your loved ones CF I have been trying to decide if it would

help me to share. I think I had decided it will help me. Sorry to be so

selfish and boring!

Christian was a hard child to have, after my daughter was born the doctor's

told me that due to certain problems I would never be able to have another

child. I was young and didn't really think too much about it at that time.

Time passes and as my biological clock started clicking louder and louder my

husband and I said why not try? It wasn't really hard to get pregnant, just

really hard to keep the child. I had pretty much decided not to try again

when I lost a baby 5 days before Christmas 1990. It was too difficult and

the pain of loosing another child was something I didn't think I could

handle. When I went back to the doctors for my 6 week check up, I was

pregnant! The pregnancy went great and after 36 hours of labor, Christian

was born via c-section. The first clue that there was something wrong was

his AGAR score was a 2. After a week in ICU, he came home. He is such a

beautiful boy, big brown eyes and light brown hair but from the start he

always had a nasty cough. Doctor's told us to raise one end of the crib

mattress so he didn't lie flat. At the time of his diagnoses he slept sitting

up with 7 pillows behind his back or he couldn't breathe. So for the next 9

1/2 years he continued to cough, at 9 1/2 he only weight 52 lb. and still was

wearing 4T clothes. Doctor's told us " not to worry to look at his feet he

will grow into them sooner or later. " After listening to me question them

they started questioning me. They actually asked me if I was giving him

stuff to make him cough. Are you feeding him on a regular schedule, what are

you giving him, etc. I felt that everytime I called them they were writing

down that I was doing something to him to make him sick. They finally gave

us two referrals to Nemoirs Childrens hospital, only two visits cause they

thought it was all in my head. Within 15 minutes of being with Dr. Schaffer

he asked if he could do a sweat test on Christian, just to " rule out " cf. Did

the test and he said they would call me back with the results that it takes 4

hours to determine the level in the sweat, we left the office at 11:40.

, Christian, and I left the doctor's office and went to have lunch at

Roadhouse Grill, it was a Tuesday and kids eat free! After lunch we got home

and there was a message on our answering machine from Dr. Schaffer himself to

please call him as soon as I could. It was now 2:20. I figured it was to

say that they would be changing Christian inhalers and whatnots, but when I

called and the nurse that answered the phone asked me to hold on I kinda got

to feeling sickly. Dr. Schaffer himself came back on the phone and said that

Christian's test was overwhelmingly positive he has CF and the culture that

he coughed up had already started growing Pseudamonas, and we really needed

to get him into the hospital as soon as possible. One hour later we were

being admitted to Wolfson's Children's hospital. I really don't remember

much but I remember when Christian went to sleep that night I went out in the

hallway and read all the information the doctor's had given me....I cried so

hard and so long, still do. They tell me that he wouldn't have the permeant

lung damage he has if he had been diagnosed earlier, I should have pushed

them sooner to get him to Nemoirs maybe it wouldn't be that bad. I feel that

I failed him in that respect, if only I had made them send him sooner. We

have been fighting the Pseudamonas since October now, he was in the hospital

in December and home IVs for 2 weeks and still he can't get rid of it. They

say that if he still has it in May that he will have to be admitted for 2

weeks possibly. He is such a beautiful child, he is truly a gift from God.

My husband named him Christian because his name is and my name is Tina.

He gave him the middle name of after his sister . He is a little

bit of all of us. Mostly though the name Christian is very fitting because

of the meaning of his name. We are very fortunate that he doesn't have much

of the digestive problems, he mainly has the lung stuff. He has gained

weight he now weight 65 lb. and has actually gotten onto the 25% of his age

group, that in itself is a miracle. Someday are better than others, some are

worse. He asked me the other day when we were talking about the Great

Strides walk that he hopes they find a cure before he goes. I asked him what

he meant and where was he going. He said " you know before I die from it. "

It isn't fair. Right now we have been up since 3 am, he is sick coughing,

vomiting, sneezing, and there isn't anything I can do.

Well, sorry to have dragged on and on. Christian is sleeping on the couch

right now, good thing cause I wouldn't want him to see me crying; again!

Thank you all for being here, this list has really helped me in a lot of

ways. Sorry to be grabbing at ya'll while I wallow in my self pity! Just

thought it might make a difference, I feel kinda like an intruder reading all

of your posts and not sharing my son's and my own. I think that since we are

home sick today I am going to try to get a picture of Christian to post so

you all can see how handsome he is! thank you again

Tina Mom of Christian 10 yowcf and 18 yowocf

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Tina,

I am so glad you shared that with us and don't feel bad about not diagnosing

him sooner. My oldest wasn't diagnosed until she was 6 and I have felt that

same guilt but on the other hand I am also mad that the doctors didn't see

it. I asked all the right questions about her stools looking funny and about

her complaining her stomach hurt and all they would say is oh maybe it was

the juice she was drinking or she has a stomach virus. They always had and

excuse. Some doctors are just to busy to listen to all of the symptoms so

they take the easy way out and call it a virus that they don't do have

anything to treat a virus. Well, thanks again for sharing and you are a GOOD

MOM! Deb A

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Tina,

I am so glad you shared that with us and don't feel bad about not diagnosing

him sooner. My oldest wasn't diagnosed until she was 6 and I have felt that

same guilt but on the other hand I am also mad that the doctors didn't see

it. I asked all the right questions about her stools looking funny and about

her complaining her stomach hurt and all they would say is oh maybe it was

the juice she was drinking or she has a stomach virus. They always had and

excuse. Some doctors are just to busy to listen to all of the symptoms so

they take the easy way out and call it a virus that they don't do have

anything to treat a virus. Well, thanks again for sharing and you are a GOOD

MOM! Deb A

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Tina,

I am so glad you shared that with us and don't feel bad about not diagnosing

him sooner. My oldest wasn't diagnosed until she was 6 and I have felt that

same guilt but on the other hand I am also mad that the doctors didn't see

it. I asked all the right questions about her stools looking funny and about

her complaining her stomach hurt and all they would say is oh maybe it was

the juice she was drinking or she has a stomach virus. They always had and

excuse. Some doctors are just to busy to listen to all of the symptoms so

they take the easy way out and call it a virus that they don't do have

anything to treat a virus. Well, thanks again for sharing and you are a GOOD

MOM! Deb A

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Chad just got over that, ask your Dr. if Coly-Mycin is an option for your

baby? Its expensive to say the least, and you will also need to rent

nebulizer (for the masks ask the hospital, they gave me some for Chad before

we went home) The Coly-mycin is inhaled and goes straight to the lungs to

stop the problem instead of other meds that get broken up over the whole

body, this one goes right where it's needed. If you don't have insurance,

remember to keep all medical reciepts for tax time.

Hope this helps.

April Dewell29 nocf mom of

Chad H.10wcf

and Terry H.8nocf

When we found out about Christian

> I hope you don't mind but in reading all the post about how you found out

> about your or your loved ones CF I have been trying to decide if it would

> help me to share. I think I had decided it will help me. Sorry to be so

> selfish and boring!

>

> Christian was a hard child to have, after my daughter was born the

doctor's

> told me that due to certain problems I would never be able to have another

> child. I was young and didn't really think too much about it at that

time.

> Time passes and as my biological clock started clicking louder and louder

my

> husband and I said why not try? It wasn't really hard to get pregnant,

just

> really hard to keep the child. I had pretty much decided not to try again

> when I lost a baby 5 days before Christmas 1990. It was too difficult and

> the pain of loosing another child was something I didn't think I could

> handle. When I went back to the doctors for my 6 week check up, I was

> pregnant! The pregnancy went great and after 36 hours of labor, Christian

> was born via c-section. The first clue that there was something wrong was

> his AGAR score was a 2. After a week in ICU, he came home. He is such a

> beautiful boy, big brown eyes and light brown hair but from the start he

> always had a nasty cough. Doctor's told us to raise one end of the crib

> mattress so he didn't lie flat. At the time of his diagnoses he slept

sitting

> up with 7 pillows behind his back or he couldn't breathe. So for the next

9

> 1/2 years he continued to cough, at 9 1/2 he only weight 52 lb. and still

was

> wearing 4T clothes. Doctor's told us " not to worry to look at his feet he

> will grow into them sooner or later. " After listening to me question them

> they started questioning me. They actually asked me if I was giving him

> stuff to make him cough. Are you feeding him on a regular schedule, what

are

> you giving him, etc. I felt that everytime I called them they were writing

> down that I was doing something to him to make him sick. They finally

gave

> us two referrals to Nemoirs Childrens hospital, only two visits cause they

> thought it was all in my head. Within 15 minutes of being with Dr.

Schaffer

> he asked if he could do a sweat test on Christian, just to " rule out " cf.

Did

> the test and he said they would call me back with the results that it

takes 4

> hours to determine the level in the sweat, we left the office at 11:40.

> , Christian, and I left the doctor's office and went to have lunch at

> Roadhouse Grill, it was a Tuesday and kids eat free! After lunch we got

home

> and there was a message on our answering machine from Dr. Schaffer himself

to

> please call him as soon as I could. It was now 2:20. I figured it was to

> say that they would be changing Christian inhalers and whatnots, but when

I

> called and the nurse that answered the phone asked me to hold on I kinda

got

> to feeling sickly. Dr. Schaffer himself came back on the phone and said

that

> Christian's test was overwhelmingly positive he has CF and the culture

that

> he coughed up had already started growing Pseudamonas, and we really

needed

> to get him into the hospital as soon as possible. One hour later we were

> being admitted to Wolfson's Children's hospital. I really don't remember

> much but I remember when Christian went to sleep that night I went out in

the

> hallway and read all the information the doctor's had given me....I cried

so

> hard and so long, still do. They tell me that he wouldn't have the

permeant

> lung damage he has if he had been diagnosed earlier, I should have pushed

> them sooner to get him to Nemoirs maybe it wouldn't be that bad. I feel

that

> I failed him in that respect, if only I had made them send him sooner. We

> have been fighting the Pseudamonas since October now, he was in the

hospital

> in December and home IVs for 2 weeks and still he can't get rid of it.

They

> say that if he still has it in May that he will have to be admitted for 2

> weeks possibly. He is such a beautiful child, he is truly a gift from

God.

> My husband named him Christian because his name is and my name is

Tina.

> He gave him the middle name of after his sister . He is a

little

> bit of all of us. Mostly though the name Christian is very fitting

because

> of the meaning of his name. We are very fortunate that he doesn't have

much

> of the digestive problems, he mainly has the lung stuff. He has gained

> weight he now weight 65 lb. and has actually gotten onto the 25% of his

age

> group, that in itself is a miracle. Someday are better than others, some

are

> worse. He asked me the other day when we were talking about the Great

> Strides walk that he hopes they find a cure before he goes. I asked him

what

> he meant and where was he going. He said " you know before I die from it. "

> It isn't fair. Right now we have been up since 3 am, he is sick coughing,

> vomiting, sneezing, and there isn't anything I can do.

>

> Well, sorry to have dragged on and on. Christian is sleeping on the couch

> right now, good thing cause I wouldn't want him to see me crying; again!

> Thank you all for being here, this list has really helped me in a lot of

> ways. Sorry to be grabbing at ya'll while I wallow in my self pity! Just

> thought it might make a difference, I feel kinda like an intruder reading

all

> of your posts and not sharing my son's and my own. I think that since we

are

> home sick today I am going to try to get a picture of Christian to post so

> you all can see how handsome he is! thank you again

>

> Tina Mom of Christian 10 yowcf and 18 yowocf

>

>

> PLEASE do not post religious emails to the list.

>

>

> -------------------------------------------

>

>

> 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.

>

> --------------------------------------------------

>

>

>

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Chad just got over that, ask your Dr. if Coly-Mycin is an option for your

baby? Its expensive to say the least, and you will also need to rent

nebulizer (for the masks ask the hospital, they gave me some for Chad before

we went home) The Coly-mycin is inhaled and goes straight to the lungs to

stop the problem instead of other meds that get broken up over the whole

body, this one goes right where it's needed. If you don't have insurance,

remember to keep all medical reciepts for tax time.

Hope this helps.

April Dewell29 nocf mom of

Chad H.10wcf

and Terry H.8nocf

When we found out about Christian

> I hope you don't mind but in reading all the post about how you found out

> about your or your loved ones CF I have been trying to decide if it would

> help me to share. I think I had decided it will help me. Sorry to be so

> selfish and boring!

>

> Christian was a hard child to have, after my daughter was born the

doctor's

> told me that due to certain problems I would never be able to have another

> child. I was young and didn't really think too much about it at that

time.

> Time passes and as my biological clock started clicking louder and louder

my

> husband and I said why not try? It wasn't really hard to get pregnant,

just

> really hard to keep the child. I had pretty much decided not to try again

> when I lost a baby 5 days before Christmas 1990. It was too difficult and

> the pain of loosing another child was something I didn't think I could

> handle. When I went back to the doctors for my 6 week check up, I was

> pregnant! The pregnancy went great and after 36 hours of labor, Christian

> was born via c-section. The first clue that there was something wrong was

> his AGAR score was a 2. After a week in ICU, he came home. He is such a

> beautiful boy, big brown eyes and light brown hair but from the start he

> always had a nasty cough. Doctor's told us to raise one end of the crib

> mattress so he didn't lie flat. At the time of his diagnoses he slept

sitting

> up with 7 pillows behind his back or he couldn't breathe. So for the next

9

> 1/2 years he continued to cough, at 9 1/2 he only weight 52 lb. and still

was

> wearing 4T clothes. Doctor's told us " not to worry to look at his feet he

> will grow into them sooner or later. " After listening to me question them

> they started questioning me. They actually asked me if I was giving him

> stuff to make him cough. Are you feeding him on a regular schedule, what

are

> you giving him, etc. I felt that everytime I called them they were writing

> down that I was doing something to him to make him sick. They finally

gave

> us two referrals to Nemoirs Childrens hospital, only two visits cause they

> thought it was all in my head. Within 15 minutes of being with Dr.

Schaffer

> he asked if he could do a sweat test on Christian, just to " rule out " cf.

Did

> the test and he said they would call me back with the results that it

takes 4

> hours to determine the level in the sweat, we left the office at 11:40.

> , Christian, and I left the doctor's office and went to have lunch at

> Roadhouse Grill, it was a Tuesday and kids eat free! After lunch we got

home

> and there was a message on our answering machine from Dr. Schaffer himself

to

> please call him as soon as I could. It was now 2:20. I figured it was to

> say that they would be changing Christian inhalers and whatnots, but when

I

> called and the nurse that answered the phone asked me to hold on I kinda

got

> to feeling sickly. Dr. Schaffer himself came back on the phone and said

that

> Christian's test was overwhelmingly positive he has CF and the culture

that

> he coughed up had already started growing Pseudamonas, and we really

needed

> to get him into the hospital as soon as possible. One hour later we were

> being admitted to Wolfson's Children's hospital. I really don't remember

> much but I remember when Christian went to sleep that night I went out in

the

> hallway and read all the information the doctor's had given me....I cried

so

> hard and so long, still do. They tell me that he wouldn't have the

permeant

> lung damage he has if he had been diagnosed earlier, I should have pushed

> them sooner to get him to Nemoirs maybe it wouldn't be that bad. I feel

that

> I failed him in that respect, if only I had made them send him sooner. We

> have been fighting the Pseudamonas since October now, he was in the

hospital

> in December and home IVs for 2 weeks and still he can't get rid of it.

They

> say that if he still has it in May that he will have to be admitted for 2

> weeks possibly. He is such a beautiful child, he is truly a gift from

God.

> My husband named him Christian because his name is and my name is

Tina.

> He gave him the middle name of after his sister . He is a

little

> bit of all of us. Mostly though the name Christian is very fitting

because

> of the meaning of his name. We are very fortunate that he doesn't have

much

> of the digestive problems, he mainly has the lung stuff. He has gained

> weight he now weight 65 lb. and has actually gotten onto the 25% of his

age

> group, that in itself is a miracle. Someday are better than others, some

are

> worse. He asked me the other day when we were talking about the Great

> Strides walk that he hopes they find a cure before he goes. I asked him

what

> he meant and where was he going. He said " you know before I die from it. "

> It isn't fair. Right now we have been up since 3 am, he is sick coughing,

> vomiting, sneezing, and there isn't anything I can do.

>

> Well, sorry to have dragged on and on. Christian is sleeping on the couch

> right now, good thing cause I wouldn't want him to see me crying; again!

> Thank you all for being here, this list has really helped me in a lot of

> ways. Sorry to be grabbing at ya'll while I wallow in my self pity! Just

> thought it might make a difference, I feel kinda like an intruder reading

all

> of your posts and not sharing my son's and my own. I think that since we

are

> home sick today I am going to try to get a picture of Christian to post so

> you all can see how handsome he is! thank you again

>

> Tina Mom of Christian 10 yowcf and 18 yowocf

>

>

> PLEASE do not post religious emails to the list.

>

>

> -------------------------------------------

>

>

> 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.

>

> --------------------------------------------------

>

>

>

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Share on other sites

Guest guest

Chad just got over that, ask your Dr. if Coly-Mycin is an option for your

baby? Its expensive to say the least, and you will also need to rent

nebulizer (for the masks ask the hospital, they gave me some for Chad before

we went home) The Coly-mycin is inhaled and goes straight to the lungs to

stop the problem instead of other meds that get broken up over the whole

body, this one goes right where it's needed. If you don't have insurance,

remember to keep all medical reciepts for tax time.

Hope this helps.

April Dewell29 nocf mom of

Chad H.10wcf

and Terry H.8nocf

When we found out about Christian

> I hope you don't mind but in reading all the post about how you found out

> about your or your loved ones CF I have been trying to decide if it would

> help me to share. I think I had decided it will help me. Sorry to be so

> selfish and boring!

>

> Christian was a hard child to have, after my daughter was born the

doctor's

> told me that due to certain problems I would never be able to have another

> child. I was young and didn't really think too much about it at that

time.

> Time passes and as my biological clock started clicking louder and louder

my

> husband and I said why not try? It wasn't really hard to get pregnant,

just

> really hard to keep the child. I had pretty much decided not to try again

> when I lost a baby 5 days before Christmas 1990. It was too difficult and

> the pain of loosing another child was something I didn't think I could

> handle. When I went back to the doctors for my 6 week check up, I was

> pregnant! The pregnancy went great and after 36 hours of labor, Christian

> was born via c-section. The first clue that there was something wrong was

> his AGAR score was a 2. After a week in ICU, he came home. He is such a

> beautiful boy, big brown eyes and light brown hair but from the start he

> always had a nasty cough. Doctor's told us to raise one end of the crib

> mattress so he didn't lie flat. At the time of his diagnoses he slept

sitting

> up with 7 pillows behind his back or he couldn't breathe. So for the next

9

> 1/2 years he continued to cough, at 9 1/2 he only weight 52 lb. and still

was

> wearing 4T clothes. Doctor's told us " not to worry to look at his feet he

> will grow into them sooner or later. " After listening to me question them

> they started questioning me. They actually asked me if I was giving him

> stuff to make him cough. Are you feeding him on a regular schedule, what

are

> you giving him, etc. I felt that everytime I called them they were writing

> down that I was doing something to him to make him sick. They finally

gave

> us two referrals to Nemoirs Childrens hospital, only two visits cause they

> thought it was all in my head. Within 15 minutes of being with Dr.

Schaffer

> he asked if he could do a sweat test on Christian, just to " rule out " cf.

Did

> the test and he said they would call me back with the results that it

takes 4

> hours to determine the level in the sweat, we left the office at 11:40.

> , Christian, and I left the doctor's office and went to have lunch at

> Roadhouse Grill, it was a Tuesday and kids eat free! After lunch we got

home

> and there was a message on our answering machine from Dr. Schaffer himself

to

> please call him as soon as I could. It was now 2:20. I figured it was to

> say that they would be changing Christian inhalers and whatnots, but when

I

> called and the nurse that answered the phone asked me to hold on I kinda

got

> to feeling sickly. Dr. Schaffer himself came back on the phone and said

that

> Christian's test was overwhelmingly positive he has CF and the culture

that

> he coughed up had already started growing Pseudamonas, and we really

needed

> to get him into the hospital as soon as possible. One hour later we were

> being admitted to Wolfson's Children's hospital. I really don't remember

> much but I remember when Christian went to sleep that night I went out in

the

> hallway and read all the information the doctor's had given me....I cried

so

> hard and so long, still do. They tell me that he wouldn't have the

permeant

> lung damage he has if he had been diagnosed earlier, I should have pushed

> them sooner to get him to Nemoirs maybe it wouldn't be that bad. I feel

that

> I failed him in that respect, if only I had made them send him sooner. We

> have been fighting the Pseudamonas since October now, he was in the

hospital

> in December and home IVs for 2 weeks and still he can't get rid of it.

They

> say that if he still has it in May that he will have to be admitted for 2

> weeks possibly. He is such a beautiful child, he is truly a gift from

God.

> My husband named him Christian because his name is and my name is

Tina.

> He gave him the middle name of after his sister . He is a

little

> bit of all of us. Mostly though the name Christian is very fitting

because

> of the meaning of his name. We are very fortunate that he doesn't have

much

> of the digestive problems, he mainly has the lung stuff. He has gained

> weight he now weight 65 lb. and has actually gotten onto the 25% of his

age

> group, that in itself is a miracle. Someday are better than others, some

are

> worse. He asked me the other day when we were talking about the Great

> Strides walk that he hopes they find a cure before he goes. I asked him

what

> he meant and where was he going. He said " you know before I die from it. "

> It isn't fair. Right now we have been up since 3 am, he is sick coughing,

> vomiting, sneezing, and there isn't anything I can do.

>

> Well, sorry to have dragged on and on. Christian is sleeping on the couch

> right now, good thing cause I wouldn't want him to see me crying; again!

> Thank you all for being here, this list has really helped me in a lot of

> ways. Sorry to be grabbing at ya'll while I wallow in my self pity! Just

> thought it might make a difference, I feel kinda like an intruder reading

all

> of your posts and not sharing my son's and my own. I think that since we

are

> home sick today I am going to try to get a picture of Christian to post so

> you all can see how handsome he is! thank you again

>

> Tina Mom of Christian 10 yowcf and 18 yowocf

>

>

> PLEASE do not post religious emails to the list.

>

>

> -------------------------------------------

>

>

> 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.

>

> --------------------------------------------------

>

>

>

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In a message dated 4/15/2002 8:18:31 AM Eastern Daylight Time,

TBug1964@... writes:

<< They tell me that he wouldn't have the permeant

lung damage he has if he had been diagnosed earlier, I should have pushed

them sooner to get him to Nemoirs maybe it wouldn't be that bad. I feel

that

I failed him in that respect, if only I had made them send him sooner. >>

Don't blame yourself! My daughter wasn't diagnosed til age 6 - also with

damage to lungs but we took her to specialist etc. - she was negative w/

sweat test and will always be negative. We did everything you could. So

many parents of kids undiagnosed are considered to have Munchheysers by proxy

(Boy did I spell it wrong)....disease where Mom makes child sick...

I enjoyed/liked your hearing your story.

Rosemary in New York with three children with CF - they are 11, 9, 5.......

I coined the phrase " BREATHE DAMMIT "

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In a message dated 4/15/2002 8:18:31 AM Eastern Daylight Time,

TBug1964@... writes:

<< They tell me that he wouldn't have the permeant

lung damage he has if he had been diagnosed earlier, I should have pushed

them sooner to get him to Nemoirs maybe it wouldn't be that bad. I feel

that

I failed him in that respect, if only I had made them send him sooner. >>

Don't blame yourself! My daughter wasn't diagnosed til age 6 - also with

damage to lungs but we took her to specialist etc. - she was negative w/

sweat test and will always be negative. We did everything you could. So

many parents of kids undiagnosed are considered to have Munchheysers by proxy

(Boy did I spell it wrong)....disease where Mom makes child sick...

I enjoyed/liked your hearing your story.

Rosemary in New York with three children with CF - they are 11, 9, 5.......

I coined the phrase " BREATHE DAMMIT "

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In a message dated 4/15/2002 8:18:31 AM Eastern Daylight Time,

TBug1964@... writes:

<< They tell me that he wouldn't have the permeant

lung damage he has if he had been diagnosed earlier, I should have pushed

them sooner to get him to Nemoirs maybe it wouldn't be that bad. I feel

that

I failed him in that respect, if only I had made them send him sooner. >>

Don't blame yourself! My daughter wasn't diagnosed til age 6 - also with

damage to lungs but we took her to specialist etc. - she was negative w/

sweat test and will always be negative. We did everything you could. So

many parents of kids undiagnosed are considered to have Munchheysers by proxy

(Boy did I spell it wrong)....disease where Mom makes child sick...

I enjoyed/liked your hearing your story.

Rosemary in New York with three children with CF - they are 11, 9, 5.......

I coined the phrase " BREATHE DAMMIT "

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We are having my six year old tested this week he was tested when he was a

baby and tested neg, his twin died from cf . Now we are having so many probs

have for awhile and today doc said Sidney has awful prob in lungs says lungs

look hardened !! I am so horrifyed !!! If he has cf I don't think I wiil be

able to cope ! I have a n 8yr old w CF. I am feeling so overwhelmed and

scared right now. What if he does ? I will be overcome with guilt I don't

think I will be able to handle it ! I feel like I have let him down how

could I not know ?Keep us in your prayers. Crystal, Mom of Ty 8yrs W CF and

Siney 6 yrs soon to be 7 yrs w or w/o CF ?

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We are having my six year old tested this week he was tested when he was a

baby and tested neg, his twin died from cf . Now we are having so many probs

have for awhile and today doc said Sidney has awful prob in lungs says lungs

look hardened !! I am so horrifyed !!! If he has cf I don't think I wiil be

able to cope ! I have a n 8yr old w CF. I am feeling so overwhelmed and

scared right now. What if he does ? I will be overcome with guilt I don't

think I will be able to handle it ! I feel like I have let him down how

could I not know ?Keep us in your prayers. Crystal, Mom of Ty 8yrs W CF and

Siney 6 yrs soon to be 7 yrs w or w/o CF ?

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We are having my six year old tested this week he was tested when he was a

baby and tested neg, his twin died from cf . Now we are having so many probs

have for awhile and today doc said Sidney has awful prob in lungs says lungs

look hardened !! I am so horrifyed !!! If he has cf I don't think I wiil be

able to cope ! I have a n 8yr old w CF. I am feeling so overwhelmed and

scared right now. What if he does ? I will be overcome with guilt I don't

think I will be able to handle it ! I feel like I have let him down how

could I not know ?Keep us in your prayers. Crystal, Mom of Ty 8yrs W CF and

Siney 6 yrs soon to be 7 yrs w or w/o CF ?

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Crystal,

You and your family are in my thoughts and prayers I hope everything turns

out for the best. It is hard to question you doctor if the test was negative

there is nothing you could have done. I think I would be pointing the finger

at the doctor that said he was negative. I hope they are wrong about his

lungs but please keep us posted. We really care. Deb A

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Crystal,

You and your family are in my thoughts and prayers I hope everything turns

out for the best. It is hard to question you doctor if the test was negative

there is nothing you could have done. I think I would be pointing the finger

at the doctor that said he was negative. I hope they are wrong about his

lungs but please keep us posted. We really care. Deb A

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Crystal,

You and your family are in my thoughts and prayers I hope everything turns

out for the best. It is hard to question you doctor if the test was negative

there is nothing you could have done. I think I would be pointing the finger

at the doctor that said he was negative. I hope they are wrong about his

lungs but please keep us posted. We really care. Deb A

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hi this is lisa with daughter heather 16 w/cf just wanted to let you know

that might be gone for acouple of days she has been fighting this infection

for a week on oral antibiotics called her cf doctor he wants her there

tomorrow and to be prepared to stay in hospital i have to go 2 and ahalf

hours but it is worth it and she feels very much at home in john hopkins so

just wanted to touch base

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hi this is lisa with daughter heather 16 w/cf just wanted to let you know

that might be gone for acouple of days she has been fighting this infection

for a week on oral antibiotics called her cf doctor he wants her there

tomorrow and to be prepared to stay in hospital i have to go 2 and ahalf

hours but it is worth it and she feels very much at home in john hopkins so

just wanted to touch base

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Just a quick note to everyone who thinks they aren't happy with their

Drs..Piper started out going to a Ped that everyone in my

husbands family had used for their kids. I had started out breastfeeding

Piper and saw a lactation consultant three..yes THREE times a week for her

first month because she was gaining slowly. The first time we went to see

this Dr the first thing he did was look at me and tell me something was wrong

with my body and to stop breastfeeding immediately..he even insinuated he

would call children's svcs if I didn't. Needless to say we switched Drs...the

second Dr we took her to told me

that it was perfectly normal that she was coughing so much & so

congested and that more than likely she would be that way all winter

...when I took her back the next week her Dr was out of

the office and we saw a CNP...she took Pipers sat level and it was 82!!! Part

of her lung had collapsed. Anyway..needless to say we switched again. My

point is by no means stay with a Ped you aren't

comfortable with..I think a lot of us have a habit of trusting Drs because

they are a Dr..but on the same token would you trust any hairstylist just

because they had gone to beauty school? Just some food for thought. As I

know they are for everyone Piper is more important to me than what anyone may

think about how critical I am of her Drs or her care....

Manda & Piper..10 mths w/cf..and on her 3rd Pediatrician

Always remember that beginnings are always scary, endings are usually sad,

but it's the middle that really counts....

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