Jump to content
RemedySpot.com

Re: Sweat test scheduled, what do I expect?

Rate this topic


Guest guest

Recommended Posts

I'm not sure why anyone has to wait so long for the results they are ready in

2 to 3 hours. Maybe we have had so many kids tested they don't want us

hanging around so they tell us as soon as they have the answer? The sweat

test is a solution is swabbed on the skin and a tiny electrical impulse is

given the sweat glands (to make them sweat) the sweat is collected in a

plastic disc that is covered in plastic (helps to sweat) the test is really

quick my 8th baby has been tested 3 times 3 ways (he is a carrier) He had the

cheek brush test, the blood DNA test, and the sweat test (he was

FTT,reflux,preemie)My best to you and yours. BeckyB.

Link to comment
Share on other sites

In a message dated 10/30/00 1:58:34 PM Pacific Standard Time, Mmloft@...

writes:

<< cfparentsegroups >>

We (and our child) found out right away; they just stimulate electronically a

tiny area

of the arm, usually, put gauze on it, and weigh and measure and analyze the

chloride, usually sodium, sometimes potassium, too of the chloride and give

you

a resulting figure in relation to average; for example many people test

around 23-26;

our CFer hit 102; one of my cousing hit 68, and I came out at 175! There has

not

been found to date any connection between high sweat chloride excretion amount

or mineral content and severity of disease, only to dehydration and rare,

seizures

when extremely dehydrated (not the same as epileptic condition). That's the

best

I can do at this time of the evening; I hope it helps. There are rare cases

of double

DeltaF508 gene copies who are very ill at diagnosis, often with meconium

ileus, but

not always where the sweat chloride excretion level is about 33; in these

cases, the

child clearly has cf, and is jost not losing much more than the average

amount of

sodium chloride. Good luck with the test, and if you don't keep us posted,

we will

all be short of breath! n Rojas wcf, mom of 3, 1 wcf--kids grown and

fine, mom

a bit off kilter lately--too many doctor appointments!

Link to comment
Share on other sites

Meredith -

My daughter had the test at 13 months old. A solution was put on her arm, and

then her arm was wrapped and plastic was put on top of that. She had to stay

that way for about half and hour, but it didn't seem to cause her much

discomfort (although my older children who had it said it burned and itched a

little). It took us 1 to 2 weeks to get the results, but I think our doctor

was out of town for part of the time, and we didn't call because we had no

reason to worry that the results might be positive (oops!).

Hang in there. I think the waiting is worse than anything . . .

, mom of Syd, 2 w/cf

>

> OK, we finally got one scheduled for Wed. Nov 1 at 10 am (EST). Is

> there anything I can expect? Dylan is almsot 11 months. Can you

> tell me what is involved? Will they be able to tell immediatley?

> Will I? How soon did you all find out?

> Thank you all so much...

> Meredith

>

>

>

> ***********************

> This is a secular list.

> ***********************

>

>

> 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.

>

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

>

>

> Our webpage is at http://www.eohio.net/malbright/cfparents.htm

>

> _________________________________________________

> Post message: cfparentsegroups

> Subscribe: cfparents-subscribeegroups

> Unsubscribe: cfparents-unsubscribeegroups

> List owner: cfparents-owneregroups

> _________________________________________________

>

> WE HAVE A CHAT PAGE!!!

> /chat/cfparents

> _________________________________________________

>

>

>

>

Link to comment
Share on other sites

My daughter has cf but my son was sweat tested at 3. They put white stuff on

his arm then covered it in plastic for about 1 hour. We knew in a couple of

days. This was only a precaution as he was tested at birth with the Guthrie

test (heel prick) as that is done before any babies leave the hsp. straight

after their birth in Australia and all these tests are free.

Bye

RE: Sweat test scheduled, what do I expect?

Meredith -

My daughter had the test at 13 months old. A solution was put on her arm, and

then her arm was wrapped and plastic was put on top of that. She had to stay

that way for about half and hour, but it didn't seem to cause her much

discomfort (although my older children who had it said it burned and itched a

little). It took us 1 to 2 weeks to get the results, but I think our doctor

was out of town for part of the time, and we didn't call because we had no

reason to worry that the results might be positive (oops!).

Hang in there. I think the waiting is worse than anything . . .

, mom of Syd, 2 w/cf

>

> OK, we finally got one scheduled for Wed. Nov 1 at 10 am (EST). Is

> there anything I can expect? Dylan is almsot 11 months. Can you

> tell me what is involved? Will they be able to tell immediatley?

> Will I? How soon did you all find out?

> Thank you all so much...

> Meredith

>

>

>

> ***********************

> This is a secular list.

> ***********************

>

>

> 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.

>

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

>

>

> Our webpage is at http://www.eohio.net/malbright/cfparents.htm

>

> _________________________________________________

> Post message: cfparentsegroups

> Subscribe: cfparents-subscribeegroups

> Unsubscribe: cfparents-unsubscribeegroups

> List owner: cfparents-owneregroups

> _________________________________________________

>

> WE HAVE A CHAT PAGE!!!

> /chat/cfparents

> _________________________________________________

>

>

>

>

eGroups Sponsor

***********************

This is a secular list.

***********************

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.

--------------------------------------------------

Our webpage is at http://www.eohio.net/malbright/cfparents.htm

_________________________________________________

Post message: cfparentsegroups

Subscribe: cfparents-subscribeegroups

Unsubscribe: cfparents-unsubscribeegroups

List owner: cfparents-owneregroups

_________________________________________________

WE HAVE A CHAT PAGE!!!

/chat/cfparents

_________________________________________________

Link to comment
Share on other sites

My son was sweat tested at 4 months when he was in the hospital for

dehydration and low salt levels. We had the results in a couple of hours.

(We had to wait all weekend for the test as noone in the lab on the weekend

knew how to do the test.) They also did a sweat test at the CF clinic. I

think the results from that one took a little longer but we already had

positive results from the first so I don't really remember. They each did

the test a little different but neither seemed to cause any discomfort to

JC.

Angie in Florida (mom to JC 7 months wcf)

>

>

>

> >

> > OK, we finally got one scheduled for Wed. Nov 1 at 10 am (EST). Is

> > there anything I can expect? Dylan is almsot 11 months. Can you

> > tell me what is involved? Will they be able to tell immediatley?

> > Will I? How soon did you all find out?

> > Thank you all so much...

> > Meredith

> >

> >

> >

> > ***********************

> > This is a secular list.

> > ***********************

> >

> >

> > 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.

> >

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

> >

> >

> > Our webpage is at http://www.eohio.net/malbright/cfparents.htm

> >

> > _________________________________________________

> > Post message: cfparentsegroups

> > Subscribe: cfparents-subscribeegroups

> > Unsubscribe: cfparents-unsubscribeegroups

> > List owner: cfparents-owneregroups

> > _________________________________________________

> >

> > WE HAVE A CHAT PAGE!!!

> > /chat/cfparents

> > _________________________________________________

> >

> >

> >

> >

>

>

>

> eGroups Sponsor

>

>

> ***********************

> This is a secular list.

> ***********************

>

>

> 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.

>

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

>

>

> Our webpage is at http://www.eohio.net/malbright/cfparents.htm

>

> _________________________________________________

> Post message: cfparentsegroups

> Subscribe: cfparents-subscribeegroups

> Unsubscribe: cfparents-unsubscribeegroups

> List owner: cfparents-owneregroups

> _________________________________________________

>

> WE HAVE A CHAT PAGE!!!

> /chat/cfparents

> _________________________________________________

>

>

>

>

>

>

Link to comment
Share on other sites

<< My daughter had the test at 13 months old. A solution was put on her arm,

and

then her arm was wrapped and plastic was put on top of that. She had to stay

that way for about half and hour, but it didn't seem to cause her much

discomfort (although my older children who had it said it burned and itched a

little). It took us 1 to 2 weeks to get the results, but I think our doctor

was out of town for part of the time, and we didn't call because we had no

reason to worry that the results might be positive (oops!).

>>

Hey, there is a little box style machine, too....that delivers electrial

current that only tingles, does not hurt, to stimulate sweat along with the

solution....at least thats what most centers do, I think. Anyway, so there

will be some wires, but nothing at all invasive....the plastic stuff is kind

of a para film of some sort (kind of waxy feeling)

We got results the same day....usually at the end of the day...each lab does

it differently, some do them in batches...but the technician should be able

to tell you how long that lab takes. At ours, we noticed on the report later

on there is a time that the results are phoned to the doc (I think they only

call the doc if positive? at least at our hospital anyway, other wise, they

prob wait for the doc to pull all test results down that day) Its probably

not so much how long it takes for the lab to do the test, but how long it

takes for the doc to call you!

Good luck, I know you are worried.....we will be hoping for a negative!

Jen

Link to comment
Share on other sites

The sweat test is no big deal. Scout had it done at 7 months of age. It

isn't at all painful, they just have to cooperate a little - which can be a

somewhat tough, but of all the tests we went through the sweat test was by

far the easiest.

We had our results mere hours later. Did the test in the morning and had

results that afternoon. We were admitted into the hospital that night for

" CF education " and to make sure Scout started gaining on the enzymes. We

stayed three nights and then were released as soon as she showed a weight

gain.

Good Luck. We are certainly a group that knows what you are going through

right now. CF is not the end of the world. You can handle it. It is tough

sometimes, but it is better than not knowing what is wrong and seeing your

baby suffer.

We'll be thinking of you.

Lori

mom to Scout 2 wCF

Sweat test scheduled, what do I expect?

> OK, we finally got one scheduled for Wed. Nov 1 at 10 am (EST). Is

> there anything I can expect? Dylan is almsot 11 months. Can you

> tell me what is involved? Will they be able to tell immediatley?

> Will I? How soon did you all find out?

> Thank you all so much...

> Meredith

>

>

>

> ***********************

> This is a secular list.

> ***********************

>

>

> 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.

>

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

>

>

> Our webpage is at http://www.eohio.net/malbright/cfparents.htm

>

> _________________________________________________

> Post message: cfparentsegroups

> Subscribe: cfparents-subscribeegroups

> Unsubscribe: cfparents-unsubscribeegroups

> List owner: cfparents-owneregroups

> _________________________________________________

>

> WE HAVE A CHAT PAGE!!!

> /chat/cfparents

> _________________________________________________

>

>

>

>

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...