Newly Dignosed...Postive Sweat Test

Emily65Roses

New member
Every case of CF is very very different. There's not really different kinds of CF "strands." I cannot stress this enough, each CF is SO VERY different. There's no real way to tell how "severe" he'll be until you watch him grow. If a doctor tells you he's got "mild" CF, don't listen. I know you'll want to listen and hang onto it, but try to understand this: CF is <u>progressive</u>. If your nephew is "mild" now, it doesn't mean anything for his life. He can be mild for another year and then go straight down hill. Not saying he will. He's young, he'll probably be relatively healthy for a while.

But I HATE when doctors tell new parents (who are still learning!!!) that their kid has a "mild, moderate, or severe" form of CF. Because none of that stays true. It's not like with cancer where there's one type worse than another, and one type is easier than another to beat. You cannot "beat" CF, and there really is no "one type" better or worse than another. CF is what it is, and it is progressive. So do yourself and everyone around you a favor, and ignore anyone who says anything about "mild" CF or anything like it. There's no point hanging onto "nice" words like that because it won't do anyone any good.

Having said that... CF is a lot better now than it was years ago. I was born in 84, before they had even discovered which gene caused CF. I was 5 when they discovered the CF gene in 89. There weren't even any good nebs to go on until I was 9. And despite that, I'm almost 23, with 70% of my lung function. That's pretty d*mn good. Your nephew will be doing even better. He's going to get proper health care right from the beginning (nebs, among other things), and he's going to keep his lung function for a long time. The life expectancy average goes up every year. When I was born, my parents were told not to expect to see me reach 18. I'm now 23, and the average is something like 35. By the time your nephew reaches that 35 mark, I imagine it'll be even higher.

The only piece or two of advice I have for new CF relatives is this: Don't treat the kid like a freak. Not saying you'd go out of your way to do that, but let me enlighten you a bit. There's a certain type of bacteria that CFers get called pseudomonas. It likes to live in wet areas, particularly baths, showers, pools, hot tubs, etc. A lot of new parents, as a result, like to shelter their kids. Don't let them go to pool parties, things like that. That's a useless way to handle it. Pseudomonas is EVERYWHERE. Sorry to have to tell you, but it is. And one way or another, your nephew will more than likely get a strand somewhere down the road. So why deprive him of things that every normal kid likes to do? Anyway, pseudomonas doesn't mean the end of the world. I've had 2 or 3 different strands now for almost 7 years, and I'm still here. I'm a college student, I go out, I have fun. I'm not some useless sick lump. I also have a worse bacteria called MRSA and I'm still functioning and doing well.

The other thing I would advise is not to be "germaphobes." A lot of new parents take this route too. And here's my two cents on that: Again, the kid already has a difficult life, do you really want to make him weirder by home-schooling him simply for the purpose of keeping him away from sick kids? Everyone needs an immune system. EVERYONE, and that includes CFers. I went to nursery school, I went to kindergarten, I went to public school my whole life, and I'm relatively healthy for someone my age born as far back as I was. I played in the back yard with dirt and worms and frogs. I had sleepovers. So not only is it unfair to wrap the kid in a bubble, but it doesn't help anything. He needs to build an immune system, same as any "normal" child.

So really... let him be a kid. Give him the meds he needs, make him see the doctor, but let him be a kid. Let him play with other kids, and get his hands dirty, and go swimming, and make mistakes, and learn lessons like any other kid. In other words: work the CF around his life.... don't work his life around the CF. <img src="i/expressions/face-icon-small-smile.gif" border="0">

Feel free to come back and ask any other questions you like. If you ever want to contact me personally, feel free to do that. You can use the private message feature here (the little head with the talking bubble at the top right corner of every post), or you can email me. Emily65Roses@yahoo.com.
 

JennifersHope

New member
I am sorry for your dx... I feel like it is better to be dx and start treatments than not know.... I personally do have a mild a typical form of CF.

I am 34 and my lung function is near normal.. I do need to take enzymes when I eat... etc but so far.. so good...

I was much sicker before I was dx with CF.. I was dx late in life at the age of 29... Once I started treatments I am much better.

I agree with Emily that you really can't tell or ever know what course CF is going to take.. A perfect example of not being able to tell is I know identical twins with the same gene (obviously) One is very sick and awaiting transplant. The other is pretty healthy, not usually sick and a very good body weight.

Proof is you just can't tell, and no one will know... I have heard of kids being real sick as babies then having pretty good teenage years... etc.

I am glad your sister has you to be a support to her.. Please keep us updated.
 

JennifersHope

New member
I am sorry for your dx... I feel like it is better to be dx and start treatments than not know.... I personally do have a mild a typical form of CF.

I am 34 and my lung function is near normal.. I do need to take enzymes when I eat... etc but so far.. so good...

I was much sicker before I was dx with CF.. I was dx late in life at the age of 29... Once I started treatments I am much better.

I agree with Emily that you really can't tell or ever know what course CF is going to take.. A perfect example of not being able to tell is I know identical twins with the same gene (obviously) One is very sick and awaiting transplant. The other is pretty healthy, not usually sick and a very good body weight.

Proof is you just can't tell, and no one will know... I have heard of kids being real sick as babies then having pretty good teenage years... etc.

I am glad your sister has you to be a support to her.. Please keep us updated.
 

JennifersHope

New member
I am sorry for your dx... I feel like it is better to be dx and start treatments than not know.... I personally do have a mild a typical form of CF.

I am 34 and my lung function is near normal.. I do need to take enzymes when I eat... etc but so far.. so good...

I was much sicker before I was dx with CF.. I was dx late in life at the age of 29... Once I started treatments I am much better.

I agree with Emily that you really can't tell or ever know what course CF is going to take.. A perfect example of not being able to tell is I know identical twins with the same gene (obviously) One is very sick and awaiting transplant. The other is pretty healthy, not usually sick and a very good body weight.

Proof is you just can't tell, and no one will know... I have heard of kids being real sick as babies then having pretty good teenage years... etc.

I am glad your sister has you to be a support to her.. Please keep us updated.
 
M

Mommafirst

Guest
I am so sorry that you didn't get better news. But while it may not be consoling to you now, it is great that he has been diagnosed so young and will get all the important preventative care. It is all pretty overwhelming in the beginning, just know that it won't always feel like a little black cloud sitting over your family. Life will go on, and he will be a normal boy but he'll have a pretty regimented preventative care schedule that will hopefully help him live a long life!! Don't try to absorb everything at once, it will all make sense and come together over time!!!
 
M

Mommafirst

Guest
I am so sorry that you didn't get better news. But while it may not be consoling to you now, it is great that he has been diagnosed so young and will get all the important preventative care. It is all pretty overwhelming in the beginning, just know that it won't always feel like a little black cloud sitting over your family. Life will go on, and he will be a normal boy but he'll have a pretty regimented preventative care schedule that will hopefully help him live a long life!! Don't try to absorb everything at once, it will all make sense and come together over time!!!
 
M

Mommafirst

Guest
I am so sorry that you didn't get better news. But while it may not be consoling to you now, it is great that he has been diagnosed so young and will get all the important preventative care. It is all pretty overwhelming in the beginning, just know that it won't always feel like a little black cloud sitting over your family. Life will go on, and he will be a normal boy but he'll have a pretty regimented preventative care schedule that will hopefully help him live a long life!! Don't try to absorb everything at once, it will all make sense and come together over time!!!
 

Augustmom0003

New member
I'm so sorry to hear of his diagnosis. I know the pain you and your family are feeling right now and I wouldn't wish it on my worst enemy. BUT...It will get better (emotionally) eventually. Please know my thoughts and prayers are with you all.

Ethan was diagnosed by sweat test. He had his second (and final) sweat test while he was in the hospital with RSV. They then did a DNA test (and asked me all kinds of questions that I had NO answer for regarding my decendents) and showed me how to give him enzymes and do chest therapy. The only change in his diet that was made was that they had me add extra formula to his bottles to make them more fattening and add a little salt to each. He also had to do breathing treatments every four hours until the RSV was gone. It was quite a shock but let me tell you something good about his diagnosis. From the moment he was born...he was skinny (my daughter was big, chubby, and dark complected and he the polar opposite and this led me to know something was wrong), he ate and ate and it passed through RIGHT AWAY! He cried and cried unless he was held and just didn't seem to be very happy (or maybe he just wasn't ever comfortable). From the moment of his diagnosis, he was a brand new baby. Like "You figured it out! You figured it out! Yaaaay!" Honestly. He went from the 10-15 percentile to OFF THE CHARTS! This baby got B I G! It was crazy! He was so, so happy!!

If you or anyone in your family would like to talk, vent, ask questions, etc...please feel free to email me: amanda_roberts76@sbcglobal.net

Again, thinking of you...
 

Augustmom0003

New member
I'm so sorry to hear of his diagnosis. I know the pain you and your family are feeling right now and I wouldn't wish it on my worst enemy. BUT...It will get better (emotionally) eventually. Please know my thoughts and prayers are with you all.

Ethan was diagnosed by sweat test. He had his second (and final) sweat test while he was in the hospital with RSV. They then did a DNA test (and asked me all kinds of questions that I had NO answer for regarding my decendents) and showed me how to give him enzymes and do chest therapy. The only change in his diet that was made was that they had me add extra formula to his bottles to make them more fattening and add a little salt to each. He also had to do breathing treatments every four hours until the RSV was gone. It was quite a shock but let me tell you something good about his diagnosis. From the moment he was born...he was skinny (my daughter was big, chubby, and dark complected and he the polar opposite and this led me to know something was wrong), he ate and ate and it passed through RIGHT AWAY! He cried and cried unless he was held and just didn't seem to be very happy (or maybe he just wasn't ever comfortable). From the moment of his diagnosis, he was a brand new baby. Like "You figured it out! You figured it out! Yaaaay!" Honestly. He went from the 10-15 percentile to OFF THE CHARTS! This baby got B I G! It was crazy! He was so, so happy!!

If you or anyone in your family would like to talk, vent, ask questions, etc...please feel free to email me: amanda_roberts76@sbcglobal.net

Again, thinking of you...
 

Augustmom0003

New member
I'm so sorry to hear of his diagnosis. I know the pain you and your family are feeling right now and I wouldn't wish it on my worst enemy. BUT...It will get better (emotionally) eventually. Please know my thoughts and prayers are with you all.

Ethan was diagnosed by sweat test. He had his second (and final) sweat test while he was in the hospital with RSV. They then did a DNA test (and asked me all kinds of questions that I had NO answer for regarding my decendents) and showed me how to give him enzymes and do chest therapy. The only change in his diet that was made was that they had me add extra formula to his bottles to make them more fattening and add a little salt to each. He also had to do breathing treatments every four hours until the RSV was gone. It was quite a shock but let me tell you something good about his diagnosis. From the moment he was born...he was skinny (my daughter was big, chubby, and dark complected and he the polar opposite and this led me to know something was wrong), he ate and ate and it passed through RIGHT AWAY! He cried and cried unless he was held and just didn't seem to be very happy (or maybe he just wasn't ever comfortable). From the moment of his diagnosis, he was a brand new baby. Like "You figured it out! You figured it out! Yaaaay!" Honestly. He went from the 10-15 percentile to OFF THE CHARTS! This baby got B I G! It was crazy! He was so, so happy!!

If you or anyone in your family would like to talk, vent, ask questions, etc...please feel free to email me: amanda_roberts76@sbcglobal.net

Again, thinking of you...
 
S

sdelorenzo

Guest
Sorry to hear about the diagnosis. We were in a similar situation when my daughter was diagnosed five years ago. She was born at 6lbs 9 ounces and was 6lbs 10 ounces when she was diagnosed at five weeks of age. She gained a pound that first week on enzymes. What a blessing! The diagnosis was very hard, but we were joyful that something could be done to help her. She did not have any respiratory problems but they still started her on chest physical therapy as a preventative measure.

My son also was born with cf. Try to encourage your sister to treat him as normal as possible. Both of my kids have double delta 508 (which is thought to be one of the more progressive genes) although it does differ from person to person. Plenty of people with this genetic make-up do great. They have been in all sorts of activites, swimming, mothers-day-out, gymnastics, play group, etc and have done great. They maybe get 1 or 2 colds a year and get over them easily. Occassionally (maybe one time per year) my kids will need to go on an oral antibotic to help clear up the cold. I know it is an overwhelming time for your family. You, your nephew, and family will be in my prayers. Feel free to e-mail me with any questions
sdelorenzo@sbcglobal.net
Sharon, mom of Sophia, 5 and Jack, 3 both with cf
 
S

sdelorenzo

Guest
Sorry to hear about the diagnosis. We were in a similar situation when my daughter was diagnosed five years ago. She was born at 6lbs 9 ounces and was 6lbs 10 ounces when she was diagnosed at five weeks of age. She gained a pound that first week on enzymes. What a blessing! The diagnosis was very hard, but we were joyful that something could be done to help her. She did not have any respiratory problems but they still started her on chest physical therapy as a preventative measure.

My son also was born with cf. Try to encourage your sister to treat him as normal as possible. Both of my kids have double delta 508 (which is thought to be one of the more progressive genes) although it does differ from person to person. Plenty of people with this genetic make-up do great. They have been in all sorts of activites, swimming, mothers-day-out, gymnastics, play group, etc and have done great. They maybe get 1 or 2 colds a year and get over them easily. Occassionally (maybe one time per year) my kids will need to go on an oral antibotic to help clear up the cold. I know it is an overwhelming time for your family. You, your nephew, and family will be in my prayers. Feel free to e-mail me with any questions
sdelorenzo@sbcglobal.net
Sharon, mom of Sophia, 5 and Jack, 3 both with cf
 
S

sdelorenzo

Guest
Sorry to hear about the diagnosis. We were in a similar situation when my daughter was diagnosed five years ago. She was born at 6lbs 9 ounces and was 6lbs 10 ounces when she was diagnosed at five weeks of age. She gained a pound that first week on enzymes. What a blessing! The diagnosis was very hard, but we were joyful that something could be done to help her. She did not have any respiratory problems but they still started her on chest physical therapy as a preventative measure.

My son also was born with cf. Try to encourage your sister to treat him as normal as possible. Both of my kids have double delta 508 (which is thought to be one of the more progressive genes) although it does differ from person to person. Plenty of people with this genetic make-up do great. They have been in all sorts of activites, swimming, mothers-day-out, gymnastics, play group, etc and have done great. They maybe get 1 or 2 colds a year and get over them easily. Occassionally (maybe one time per year) my kids will need to go on an oral antibotic to help clear up the cold. I know it is an overwhelming time for your family. You, your nephew, and family will be in my prayers. Feel free to e-mail me with any questions
sdelorenzo@sbcglobal.net
Sharon, mom of Sophia, 5 and Jack, 3 both with cf
 
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