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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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Golly, that sounds like a very busy time for all -----but fun:):) I am so

happy she like the gator ade. It can be a big help..(& flusher

outer ---hahahehe)Your family sounds as large as mine. I love gift

certificates too. I give them all a check in a small gift.There are a few

exceptions, but that is how most are handled. the ones out of town, I do

pick out a few things from home they like too.

Have a great week & I hope your sister, her baby & all the family are well.

LOVE & HUGS, grandmomBEV

Re: Newborn testing

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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Golly, that sounds like a very busy time for all -----but fun:):) I am so

happy she like the gator ade. It can be a big help..(& flusher

outer ---hahahehe)Your family sounds as large as mine. I love gift

certificates too. I give them all a check in a small gift.There are a few

exceptions, but that is how most are handled. the ones out of town, I do

pick out a few things from home they like too.

Have a great week & I hope your sister, her baby & all the family are well.

LOVE & HUGS, grandmomBEV

Re: Newborn testing

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

Golly, that sounds like a very busy time for all -----but fun:):) I am so

happy she like the gator ade. It can be a big help..(& flusher

outer ---hahahehe)Your family sounds as large as mine. I love gift

certificates too. I give them all a check in a small gift.There are a few

exceptions, but that is how most are handled. the ones out of town, I do

pick out a few things from home they like too.

Have a great week & I hope your sister, her baby & all the family are well.

LOVE & HUGS, grandmomBEV

Re: Newborn testing

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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