Sweat Test Results are in!

Munkeesmama

New member
I kinda figured I should push for testing. I just didn't want to seem crazy and alone in my thinking when I go back to her doc and tell them i'm not satisfied. I called a cf accredited place today and think I want to have her sweat test re-done through them, as well as called ambry for the full genetic testing kit.

Her Diagnosis and symptoms so far:

VERY foul smelling poops, off and on chronic diarrhea/loose stools (sometimes orange and floaty)

Was eating over 2,000 cals and did not gain any weight (although did gain height)

Failure to thrive

Reflux

Malabsorption (but doc doesn't see a need for enzymes since her fecal elastace was in the normal rage).

Get sicks alot, alot of "colds", tons of mucous, gets sick quick and lingers forever. Needs breathing treatments to bring her o2 sats up and to function while sick.

She's 2 1/2 and has had pnuemonia 3 times, and has been diagnosed as having lung damage (could be caused by prematurity though)

Delayed gastric emptying.

She's had tons and tons of tests donek, an odd lab here or there, but nothing substantial which would lead the docs to a diagnosis, allergies, celiac, chron's, they've all been ruled out. It seems like CF or mitochondrial disease are the last two avenues to pursue. It's just frustrating. While I hope she doesn't have CF, the unknown seems a bit scarier at this point.
 

Munkeesmama

New member
I kinda figured I should push for testing. I just didn't want to seem crazy and alone in my thinking when I go back to her doc and tell them i'm not satisfied. I called a cf accredited place today and think I want to have her sweat test re-done through them, as well as called ambry for the full genetic testing kit.

Her Diagnosis and symptoms so far:

VERY foul smelling poops, off and on chronic diarrhea/loose stools (sometimes orange and floaty)

Was eating over 2,000 cals and did not gain any weight (although did gain height)

Failure to thrive

Reflux

Malabsorption (but doc doesn't see a need for enzymes since her fecal elastace was in the normal rage).

Get sicks alot, alot of "colds", tons of mucous, gets sick quick and lingers forever. Needs breathing treatments to bring her o2 sats up and to function while sick.

She's 2 1/2 and has had pnuemonia 3 times, and has been diagnosed as having lung damage (could be caused by prematurity though)

Delayed gastric emptying.

She's had tons and tons of tests donek, an odd lab here or there, but nothing substantial which would lead the docs to a diagnosis, allergies, celiac, chron's, they've all been ruled out. It seems like CF or mitochondrial disease are the last two avenues to pursue. It's just frustrating. While I hope she doesn't have CF, the unknown seems a bit scarier at this point.
 

Munkeesmama

New member
I kinda figured I should push for testing. I just didn't want to seem crazy and alone in my thinking when I go back to her doc and tell them i'm not satisfied. I called a cf accredited place today and think I want to have her sweat test re-done through them, as well as called ambry for the full genetic testing kit.

Her Diagnosis and symptoms so far:

VERY foul smelling poops, off and on chronic diarrhea/loose stools (sometimes orange and floaty)

Was eating over 2,000 cals and did not gain any weight (although did gain height)

Failure to thrive

Reflux

Malabsorption (but doc doesn't see a need for enzymes since her fecal elastace was in the normal rage).

Get sicks alot, alot of "colds", tons of mucous, gets sick quick and lingers forever. Needs breathing treatments to bring her o2 sats up and to function while sick.

She's 2 1/2 and has had pnuemonia 3 times, and has been diagnosed as having lung damage (could be caused by prematurity though)

Delayed gastric emptying.

She's had tons and tons of tests donek, an odd lab here or there, but nothing substantial which would lead the docs to a diagnosis, allergies, celiac, chron's, they've all been ruled out. It seems like CF or mitochondrial disease are the last two avenues to pursue. It's just frustrating. While I hope she doesn't have CF, the unknown seems a bit scarier at this point.
 

Munkeesmama

New member
I kinda figured I should push for testing. I just didn't want to seem crazy and alone in my thinking when I go back to her doc and tell them i'm not satisfied. I called a cf accredited place today and think I want to have her sweat test re-done through them, as well as called ambry for the full genetic testing kit.

Her Diagnosis and symptoms so far:

VERY foul smelling poops, off and on chronic diarrhea/loose stools (sometimes orange and floaty)

Was eating over 2,000 cals and did not gain any weight (although did gain height)

Failure to thrive

Reflux

Malabsorption (but doc doesn't see a need for enzymes since her fecal elastace was in the normal rage).

Get sicks alot, alot of "colds", tons of mucous, gets sick quick and lingers forever. Needs breathing treatments to bring her o2 sats up and to function while sick.

She's 2 1/2 and has had pnuemonia 3 times, and has been diagnosed as having lung damage (could be caused by prematurity though)

Delayed gastric emptying.

She's had tons and tons of tests donek, an odd lab here or there, but nothing substantial which would lead the docs to a diagnosis, allergies, celiac, chron's, they've all been ruled out. It seems like CF or mitochondrial disease are the last two avenues to pursue. It's just frustrating. While I hope she doesn't have CF, the unknown seems a bit scarier at this point.
 

Munkeesmama

New member
I kinda figured I should push for testing. I just didn't want to seem crazy and alone in my thinking when I go back to her doc and tell them i'm not satisfied. I called a cf accredited place today and think I want to have her sweat test re-done through them, as well as called ambry for the full genetic testing kit.
<br />
<br />Her Diagnosis and symptoms so far:
<br />
<br />VERY foul smelling poops, off and on chronic diarrhea/loose stools (sometimes orange and floaty)
<br />
<br />Was eating over 2,000 cals and did not gain any weight (although did gain height)
<br />
<br />Failure to thrive
<br />
<br />Reflux
<br />
<br />Malabsorption (but doc doesn't see a need for enzymes since her fecal elastace was in the normal rage).
<br />
<br />Get sicks alot, alot of "colds", tons of mucous, gets sick quick and lingers forever. Needs breathing treatments to bring her o2 sats up and to function while sick.
<br />
<br />She's 2 1/2 and has had pnuemonia 3 times, and has been diagnosed as having lung damage (could be caused by prematurity though)
<br />
<br />Delayed gastric emptying.
<br />
<br />She's had tons and tons of tests donek, an odd lab here or there, but nothing substantial which would lead the docs to a diagnosis, allergies, celiac, chron's, they've all been ruled out. It seems like CF or mitochondrial disease are the last two avenues to pursue. It's just frustrating. While I hope she doesn't have CF, the unknown seems a bit scarier at this point.
 

amyr

New member
I was in the same boat. All three of my kids were just recently dx. Sweats were 24,25,49. All of our tests were in the grey area.
 

amyr

New member
I was in the same boat. All three of my kids were just recently dx. Sweats were 24,25,49. All of our tests were in the grey area.
 

amyr

New member
I was in the same boat. All three of my kids were just recently dx. Sweats were 24,25,49. All of our tests were in the grey area.
 

amyr

New member
I was in the same boat. All three of my kids were just recently dx. Sweats were 24,25,49. All of our tests were in the grey area.
 

amyr

New member
I was in the same boat. All three of my kids were just recently dx. Sweats were 24,25,49. All of our tests were in the grey area.
 

thefrogprincess

New member
100 genes is not enough in my book. I would also throw the sweat test out the window, there are numerous people on these forums who had "normal" sweat tests but have CF. That's just my opinion.
 

thefrogprincess

New member
100 genes is not enough in my book. I would also throw the sweat test out the window, there are numerous people on these forums who had "normal" sweat tests but have CF. That's just my opinion.
 

thefrogprincess

New member
100 genes is not enough in my book. I would also throw the sweat test out the window, there are numerous people on these forums who had "normal" sweat tests but have CF. That's just my opinion.
 

thefrogprincess

New member
100 genes is not enough in my book. I would also throw the sweat test out the window, there are numerous people on these forums who had "normal" sweat tests but have CF. That's just my opinion.
 

thefrogprincess

New member
100 genes is not enough in my book. I would also throw the sweat test out the window, there are numerous people on these forums who had "normal" sweat tests but have CF. That's just my opinion.
 

BabyBeauty

New member
If it were me, I would push for the full panel. But that is just me. I would want to rule it out 100% and move on to the next possibility.
 

BabyBeauty

New member
If it were me, I would push for the full panel. But that is just me. I would want to rule it out 100% and move on to the next possibility.
 

BabyBeauty

New member
If it were me, I would push for the full panel. But that is just me. I would want to rule it out 100% and move on to the next possibility.
 

BabyBeauty

New member
If it were me, I would push for the full panel. But that is just me. I would want to rule it out 100% and move on to the next possibility.
 

BabyBeauty

New member
If it were me, I would push for the full panel. But that is just me. I would want to rule it out 100% and move on to the next possibility.
 
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