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Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

Trypsinogen...n sent me a message about it (Thanks n!), and my mom

told the docs to check for it. I'm pretty certain it's not automatically done

here, or they would have caught my daughter when she was born instead of at 2.5

years. It's unlikely he'll have it, but better safe than sorry.

Little Gideon Lamont Donaho (we call him Giddy, his daddy's side calls him

Monty) was born around 7:25am, and weighed in at 5lbs 3oz, so has just set the

record as the smallest full-term baby in our family so far. He's rather tiny,

and VERY hairy...his whole back is a fur rug, and he's got a full head of hair.

We had to go buy him some preemie clothes, since he's too small to wear the

newborn ones. We told my sister to get some preemie clothes just in case

because tiny babies run in the family, and she didn't listen to us. But he's

got a few outfits now.

My mom wanted me to bring Triana up there to see him. I was like " Are you out

of your mind? " Hospitals aren't that fond of kids under 12 or so anyhow, but

I'm also thinking about Triana. The two places the docs told us to avoid unless

it was necessary were doctors' offices and hospitals because of all the sick

people. My mom just thought that was silly.

Anyhow, I'm an aunt now...yay...a kid that I can see and spoil, and give back to

his mama!

Shanna

mom of Triana, age 2 wcf

Re: Newborn testing

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

Trypsinogen...n sent me a message about it (Thanks n!), and my mom

told the docs to check for it. I'm pretty certain it's not automatically done

here, or they would have caught my daughter when she was born instead of at 2.5

years. It's unlikely he'll have it, but better safe than sorry.

Little Gideon Lamont Donaho (we call him Giddy, his daddy's side calls him

Monty) was born around 7:25am, and weighed in at 5lbs 3oz, so has just set the

record as the smallest full-term baby in our family so far. He's rather tiny,

and VERY hairy...his whole back is a fur rug, and he's got a full head of hair.

We had to go buy him some preemie clothes, since he's too small to wear the

newborn ones. We told my sister to get some preemie clothes just in case

because tiny babies run in the family, and she didn't listen to us. But he's

got a few outfits now.

My mom wanted me to bring Triana up there to see him. I was like " Are you out

of your mind? " Hospitals aren't that fond of kids under 12 or so anyhow, but

I'm also thinking about Triana. The two places the docs told us to avoid unless

it was necessary were doctors' offices and hospitals because of all the sick

people. My mom just thought that was silly.

Anyhow, I'm an aunt now...yay...a kid that I can see and spoil, and give back to

his mama!

Shanna

mom of Triana, age 2 wcf

Re: Newborn testing

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

Trypsinogen...n sent me a message about it (Thanks n!), and my mom

told the docs to check for it. I'm pretty certain it's not automatically done

here, or they would have caught my daughter when she was born instead of at 2.5

years. It's unlikely he'll have it, but better safe than sorry.

Little Gideon Lamont Donaho (we call him Giddy, his daddy's side calls him

Monty) was born around 7:25am, and weighed in at 5lbs 3oz, so has just set the

record as the smallest full-term baby in our family so far. He's rather tiny,

and VERY hairy...his whole back is a fur rug, and he's got a full head of hair.

We had to go buy him some preemie clothes, since he's too small to wear the

newborn ones. We told my sister to get some preemie clothes just in case

because tiny babies run in the family, and she didn't listen to us. But he's

got a few outfits now.

My mom wanted me to bring Triana up there to see him. I was like " Are you out

of your mind? " Hospitals aren't that fond of kids under 12 or so anyhow, but

I'm also thinking about Triana. The two places the docs told us to avoid unless

it was necessary were doctors' offices and hospitals because of all the sick

people. My mom just thought that was silly.

Anyhow, I'm an aunt now...yay...a kid that I can see and spoil, and give back to

his mama!

Shanna

mom of Triana, age 2 wcf

Re: Newborn testing

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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In Colorado, they do newborn screening on all newborns, based on the

idea that if you catch cf earlier, you can avoid most of the

malnutrition assoicated with pancreatic insufficency. That is how we

found out our daughter, Maya, has cf. She is now 18mo, and though I

didn't want to hear it at the time, I am now glad because she has

thrived and is now in the 50th percentile for weight! I believe New

York and California are adding the testing soon. States don't want

to generally because the test costs about $10 per newborn, and there

is no cure for cf.

,

mom to Maya 18mo old with cf and chd

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In Colorado, they do newborn screening on all newborns, based on the

idea that if you catch cf earlier, you can avoid most of the

malnutrition assoicated with pancreatic insufficency. That is how we

found out our daughter, Maya, has cf. She is now 18mo, and though I

didn't want to hear it at the time, I am now glad because she has

thrived and is now in the 50th percentile for weight! I believe New

York and California are adding the testing soon. States don't want

to generally because the test costs about $10 per newborn, and there

is no cure for cf.

,

mom to Maya 18mo old with cf and chd

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Share on other sites

In Colorado, they do newborn screening on all newborns, based on the

idea that if you catch cf earlier, you can avoid most of the

malnutrition assoicated with pancreatic insufficency. That is how we

found out our daughter, Maya, has cf. She is now 18mo, and though I

didn't want to hear it at the time, I am now glad because she has

thrived and is now in the 50th percentile for weight! I believe New

York and California are adding the testing soon. States don't want

to generally because the test costs about $10 per newborn, and there

is no cure for cf.

,

mom to Maya 18mo old with cf and chd

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Dear Chaos,

How very wonderful all is well.You sure sound like a proud auntie:):)

Your right to follow the docs instructions on this one.Don't ask /look

for any infections.there will be plenty of time for them to be together

soon.

How long before they will let you all know about the test--------? Did

they do the heal prick test?? I sure hope all is clear, but as you

said, Knowing early is best for the wee one though. Keep us posted:):)

LOVE & HUGS,

GrandmomBEV

Re: Newborn testing

Trypsinogen...n sent me a message about it (Thanks n!), and my

mom told the docs to check for it. I'm pretty certain it's not

automatically done here, or they would have caught my daughter when she

was born instead of at 2.5 years. It's unlikely he'll have it, but

better safe than sorry.

Little Gideon Lamont Donaho (we call him Giddy, his daddy's side calls

him Monty) was born around 7:25am, and weighed in at 5lbs 3oz, so has

just set the record as the smallest full-term baby in our family so far.

He's rather tiny, and VERY hairy...his whole back is a fur rug, and he's

got a full head of hair. We had to go buy him some preemie clothes,

since he's too small to wear the newborn ones. We told my sister to get

some preemie clothes just in case because tiny babies run in the family,

and she didn't listen to us. But he's got a few outfits now.

My mom wanted me to bring Triana up there to see him. I was like " Are

you out of your mind? " Hospitals aren't that fond of kids under 12 or

so anyhow, but I'm also thinking about Triana. The two places the docs

told us to avoid unless it was necessary were doctors' offices and

hospitals because of all the sick people. My mom just thought that was

silly.

Anyhow, I'm an aunt now...yay...a kid that I can see and spoil, and give

back to his mama!

Shanna

mom of Triana, age 2 wcf

Re: Newborn testing

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

Dear Chaos,

How very wonderful all is well.You sure sound like a proud auntie:):)

Your right to follow the docs instructions on this one.Don't ask /look

for any infections.there will be plenty of time for them to be together

soon.

How long before they will let you all know about the test--------? Did

they do the heal prick test?? I sure hope all is clear, but as you

said, Knowing early is best for the wee one though. Keep us posted:):)

LOVE & HUGS,

GrandmomBEV

Re: Newborn testing

Trypsinogen...n sent me a message about it (Thanks n!), and my

mom told the docs to check for it. I'm pretty certain it's not

automatically done here, or they would have caught my daughter when she

was born instead of at 2.5 years. It's unlikely he'll have it, but

better safe than sorry.

Little Gideon Lamont Donaho (we call him Giddy, his daddy's side calls

him Monty) was born around 7:25am, and weighed in at 5lbs 3oz, so has

just set the record as the smallest full-term baby in our family so far.

He's rather tiny, and VERY hairy...his whole back is a fur rug, and he's

got a full head of hair. We had to go buy him some preemie clothes,

since he's too small to wear the newborn ones. We told my sister to get

some preemie clothes just in case because tiny babies run in the family,

and she didn't listen to us. But he's got a few outfits now.

My mom wanted me to bring Triana up there to see him. I was like " Are

you out of your mind? " Hospitals aren't that fond of kids under 12 or

so anyhow, but I'm also thinking about Triana. The two places the docs

told us to avoid unless it was necessary were doctors' offices and

hospitals because of all the sick people. My mom just thought that was

silly.

Anyhow, I'm an aunt now...yay...a kid that I can see and spoil, and give

back to his mama!

Shanna

mom of Triana, age 2 wcf

Re: Newborn testing

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

Dear Chaos,

How very wonderful all is well.You sure sound like a proud auntie:):)

Your right to follow the docs instructions on this one.Don't ask /look

for any infections.there will be plenty of time for them to be together

soon.

How long before they will let you all know about the test--------? Did

they do the heal prick test?? I sure hope all is clear, but as you

said, Knowing early is best for the wee one though. Keep us posted:):)

LOVE & HUGS,

GrandmomBEV

Re: Newborn testing

Trypsinogen...n sent me a message about it (Thanks n!), and my

mom told the docs to check for it. I'm pretty certain it's not

automatically done here, or they would have caught my daughter when she

was born instead of at 2.5 years. It's unlikely he'll have it, but

better safe than sorry.

Little Gideon Lamont Donaho (we call him Giddy, his daddy's side calls

him Monty) was born around 7:25am, and weighed in at 5lbs 3oz, so has

just set the record as the smallest full-term baby in our family so far.

He's rather tiny, and VERY hairy...his whole back is a fur rug, and he's

got a full head of hair. We had to go buy him some preemie clothes,

since he's too small to wear the newborn ones. We told my sister to get

some preemie clothes just in case because tiny babies run in the family,

and she didn't listen to us. But he's got a few outfits now.

My mom wanted me to bring Triana up there to see him. I was like " Are

you out of your mind? " Hospitals aren't that fond of kids under 12 or

so anyhow, but I'm also thinking about Triana. The two places the docs

told us to avoid unless it was necessary were doctors' offices and

hospitals because of all the sick people. My mom just thought that was

silly.

Anyhow, I'm an aunt now...yay...a kid that I can see and spoil, and give

back to his mama!

Shanna

mom of Triana, age 2 wcf

Re: Newborn testing

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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They told my mom they would do the test. I know they took blood from his heel,

but I had not heard how long it would be before the results came back. I don't

think my sister and her husband know they tested for it yet...my mom will

probably tell them after my sister isn't drugged out of her mind. She had to

have a C-section because the cord had wrapped itself around his body, and every

time she'd have even a mild contraction his heart rate went down.

I'm hoping, and expecting, that he'll be clear. He may end up a carrier, but

his chances of having CF are low, about a 2.5% chance. (I'm figuring 10% chance

that my brother-in-law is a carrier, since they said he's 90% sure not to be

one...and a 1/4 or 25% chance that if he is, they'll have one with CF...so 25%

of 10% is 2.5%. Erk...math...bleh...always did hate it, even though I made good

grades in it.)

Everything is going pretty good for us. We took Triana shopping with us today,

and she had a ball (up until she got so wet she drenched yet another outfit...30

oz of Gatorade will do that to ya.) We were sitting in the line at the

lay-a-way in Wal-Mart to pick up the stuff I had put in in October (like 3 days

before she was dx'd with the CF)...and my child is yelling " Help me! Help me!

Help me Daddy! " We haven't been able to make her understand yet that " Help me! "

and " I need help with this " are two totally different sentiments. There were

some other parents there who thought it was highly amusing, though.

I was quite happy that we've managed to get all of her toys from us (for

Solstice) and Santa (for Christmas), and to get Christmas gifts for her young

cousins (including the new one). Although she really wanted the semi truck that

we got for one of her cousins. (They're all boys, the ones ages newborn-7,

except her.) And we've figured out what we're getting most of the family (gift

certificates are wonderful things...people get what they want, and we don't have

to try and find something we know they'll like...especially the teenage

girls...eeek! All the kids ages 14-17 are girls.)

Triana's congestion is better. The Gatorade is a hit. At least she likes the

stuff...I never have. She calls the orange flavor " orange juice " . And she'll

guzzle the stuff at an incredible rate. So all is well and good on that front.

We'll talk to you later...I need to answer the rest of my mail, and then go make

yet another batch of cookie dough.

Shanna

mom of Triana, age 2 wcf

Re: Newborn testing

Yes, it is a heel prick, which tests for a high level of

Tryp-something. Sorry, I can't recall.

What state do you live in?

It might be done automatically.

Let me know. I'll get you the details.

Lenora

>Didn't I read something about some sort of newborn testing they

>could do for CF that involved levels of something in the blood? (As

>opposed to the DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell

>the docs to test for it, without scaring the heck out of my sister.

>Her husband tested negative for carrier status with the 25 most

>common mutations, but that still leaves a 10% chance that he could

>be a carrier, and we'd none of us rather take the chance of catching

>it late if little " Giddy " ends up having CF. (Although it's

>unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it,

>I'd appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

They do it in Nebraska. We found out that PJ's was high a few days? after

he was born. Back in 99 the didn't do it in FL and I do believe that AK

still doesn't screen for it at birth. The doc told us that it could come

back high with the baby just being a carrier. Good luck and let us know how

everything goes.

Jen A. mom to ALex 4, Yolanda 3 and Phynix 7 months all w/cf. Baby Orion

due in April we're keeping our fingers crossed.

>

>Reply-To: cfparents

>To: CF Parents cfparents >

>Subject: Newborn testing

>Date: Wed, 11 Dec 2002 23:30:55 -0600

>

>Didn't I read something about some sort of newborn testing they could do

>for CF that involved levels of something in the blood? (As opposed to the

>DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell the docs

>to test for it, without scaring the heck out of my sister. Her husband

>tested negative for carrier status with the 25 most common mutations, but

>that still leaves a 10% chance that he could be a carrier, and we'd none of

>us rather take the chance of catching it late if little " Giddy " ends up

>having CF. (Although it's unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it, I'd

>appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Share on other sites

They do it in Nebraska. We found out that PJ's was high a few days? after

he was born. Back in 99 the didn't do it in FL and I do believe that AK

still doesn't screen for it at birth. The doc told us that it could come

back high with the baby just being a carrier. Good luck and let us know how

everything goes.

Jen A. mom to ALex 4, Yolanda 3 and Phynix 7 months all w/cf. Baby Orion

due in April we're keeping our fingers crossed.

>

>Reply-To: cfparents

>To: CF Parents cfparents >

>Subject: Newborn testing

>Date: Wed, 11 Dec 2002 23:30:55 -0600

>

>Didn't I read something about some sort of newborn testing they could do

>for CF that involved levels of something in the blood? (As opposed to the

>DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell the docs

>to test for it, without scaring the heck out of my sister. Her husband

>tested negative for carrier status with the 25 most common mutations, but

>that still leaves a 10% chance that he could be a carrier, and we'd none of

>us rather take the chance of catching it late if little " Giddy " ends up

>having CF. (Although it's unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it, I'd

>appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

Link to comment
Share on other sites

They do it in Nebraska. We found out that PJ's was high a few days? after

he was born. Back in 99 the didn't do it in FL and I do believe that AK

still doesn't screen for it at birth. The doc told us that it could come

back high with the baby just being a carrier. Good luck and let us know how

everything goes.

Jen A. mom to ALex 4, Yolanda 3 and Phynix 7 months all w/cf. Baby Orion

due in April we're keeping our fingers crossed.

>

>Reply-To: cfparents

>To: CF Parents cfparents >

>Subject: Newborn testing

>Date: Wed, 11 Dec 2002 23:30:55 -0600

>

>Didn't I read something about some sort of newborn testing they could do

>for CF that involved levels of something in the blood? (As opposed to the

>DNA testing.)

>

>My sister is getting induced tomorrow, and we want to quietly tell the docs

>to test for it, without scaring the heck out of my sister. Her husband

>tested negative for carrier status with the 25 most common mutations, but

>that still leaves a 10% chance that he could be a carrier, and we'd none of

>us rather take the chance of catching it late if little " Giddy " ends up

>having CF. (Although it's unlikely, it's still possible.)

>

>If someone could tell me what it was or if I was just imagining it, I'd

>appreciate it.

>

>Thanks,

>Shanna

>mom of Triana, age 2 wcf

>

>

>

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Congratulations on your new baby nephew! " Gideon " is a great

name. AND... You were so SMART not to take Triana to the

hospital. Triana will see Gideon soon enough and in a much safer

environment.

Sounds like your family is ready for some very happy holidays!

Gale

> Trypsinogen...n sent me a message about it (Thanks n!),

and my mom told the docs to check for it. I'm pretty certain it's

not automatically done here, or they would have caught my daughter

when she was born instead of at 2.5 years. It's unlikely he'll have

it, but better safe than sorry.

>

> Little Gideon Lamont Donaho (we call him Giddy, his daddy's side

calls him Monty) was born around 7:25am, and weighed in at 5lbs 3oz,

so has just set the record as the smallest full-term baby in our

family so far. He's rather tiny, and VERY hairy...his whole back is

a fur rug, and he's got a full head of hair. We had to go buy him

some preemie clothes, since he's too small to wear the newborn ones.

We told my sister to get some preemie clothes just in case because

tiny babies run in the family, and she didn't listen to us. But he's

got a few outfits now.

>

> My mom wanted me to bring Triana up there to see him. I was

like " Are you out of your mind? " Hospitals aren't that fond of kids

under 12 or so anyhow, but I'm also thinking about Triana. The two

places the docs told us to avoid unless it was necessary were

doctors' offices and hospitals because of all the sick people. My

mom just thought that was silly.

>

> Anyhow, I'm an aunt now...yay...a kid that I can see and spoil, and

give back to his mama!

>

>

> Shanna

> mom of Triana, age 2 wcf

>

> Re: Newborn testing

>

>

> Yes, it is a heel prick, which tests for a high level of

> Tryp-something. Sorry, I can't recall.

> What state do you live in?

> It might be done automatically.

> Let me know. I'll get you the details.

> Lenora

>

> >Didn't I read something about some sort of newborn testing they

> >could do for CF that involved levels of something in the blood?

(As

> >opposed to the DNA testing.)

> >

> >My sister is getting induced tomorrow, and we want to quietly

tell

> >the docs to test for it, without scaring the heck out of my

sister.

> >Her husband tested negative for carrier status with the 25 most

> >common mutations, but that still leaves a 10% chance that he

could

> >be a carrier, and we'd none of us rather take the chance of

catching

> >it late if little " Giddy " ends up having CF. (Although it's

> >unlikely, it's still possible.)

> >

> >If someone could tell me what it was or if I was just imagining

it,

> >I'd appreciate it.

> >

> >Thanks,

> >Shanna

> >mom of Triana, age 2 wcf

> >

> >

> >

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