Guest guest Posted April 29, 2003 Report Share Posted April 29, 2003 In a message dated 4/29/2003 1:36:19 AM Central Daylight Time, bethmcd70@... writes: > Ok, I have some questions about testing and such. My nephew (10 > months old) had a sweat test and they said it was negative, but they > weren't completly sure. At least that's what his mother told me. > She said the next appointment for him isn't until May 28th and they > are going to do more tests. Why would they wait that long? I mean > how hard it is to draw some bloods and do the DNA test? At least if > they did that now, by May 28th they might have some results! This > all may be a non issue anyway because my husband and I might be > getting custody of our nephew anyway. And believe me, if he comes to > us the first thing I'll be doing is getting him to a CF specialist > and getting the damn DNA test. Enough with this already. We need to > know if he has it or not so we can move to the next step. > > Anyway, just wanted to know if anyone had any thoughts or ideas for > me. Thanks, > > -Beth There is know reason why they could do a DNA test. It is so easy to do!! And you are right by the time May 28 would come around you would have the results it takes and where from 2 to 4 weeks to get results. Good luck!! Deb A Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2003 Report Share Posted April 29, 2003 with the sweat test, anything below 40 is normal, anything above 60 is considered positive for CF. So, Maybe his test is between 40 and 60 and considered borderline. Usually they do the sweat test again before they do any other tests. I don't know why they would wait to draw blood to do a DNA test. Is he being seen by a CF clinic and was he tested at a CF center? If you do get custody, as a guardian you should be able to find out why they are waiting on all this. Could it be your sister not insisting on it being done right away or putting it off? I hope not but if he is being seen by a CF center they are usually pretty anxious to get a diagnosis too, so they can begin to treat the child. I'm back....more questions Ok, I have some questions about testing and such. My nephew (10 months old) had a sweat test and they said it was negative, but they weren't completly sure. At least that's what his mother told me. She said the next appointment for him isn't until May 28th and they are going to do more tests. Why would they wait that long? I mean how hard it is to draw some bloods and do the DNA test? At least if they did that now, by May 28th they might have some results! This all may be a non issue anyway because my husband and I might be getting custody of our nephew anyway. And believe me, if he comes to us the first thing I'll be doing is getting him to a CF specialist and getting the damn DNA test. Enough with this already. We need to know if he has it or not so we can move to the next step. Anyway, just wanted to know if anyone had any thoughts or ideas for me. Thanks, -Beth Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2003 Report Share Posted April 29, 2003 Unfortunately I don't know what the number actually was for the sweat test. I do believe that is somehow (even unconsiously?) delaying these tests and such. I am almost positive that he has only been to a pediatric pulmonologist. Not a CF specialist and not at a CF clinic. She has been taking him to somewhere in Syracuse (NY), I'm guessing a big hospital there. She isn't very telling with actual details and such. We are waiting to find out if we may get custody of him because she is being investigated by CPS for various reasons, medical neglect is in that list of reasons. We are keeping our fingers crossed. Even the child's father wants us to have custody (he is my husbands brother), because he knows she is not caring for him correctly and he unfortuntely doesn't have the resources to take care of the child either. Hopefully by the end of the week I'll know something. Does anyone know of a CF clinic in NY? We are 90 miles west of NYC. Any info would be great. -Beth > with the sweat test, anything below 40 is normal, anything above 60 is considered positive for CF. So, Maybe his test is between 40 and 60 and considered borderline. Usually they do the sweat test again before they do any other tests. I don't know why they would wait to draw blood to do a DNA test. Is he being seen by a CF clinic and was he tested at a CF center? If you do get custody, as a guardian you should be able to find out why they are waiting on all this. Could it be your sister not insisting on it being done right away or putting it off? I hope not but if he is being seen by a CF center they are usually pretty anxious to get a diagnosis too, so they can begin to treat the child. > > I'm back....more questions > > > Ok, I have some questions about testing and such. My nephew (10 > months old) had a sweat test and they said it was negative, but they > weren't completly sure. At least that's what his mother told me. > She said the next appointment for him isn't until May 28th and they > are going to do more tests. Why would they wait that long? I mean > how hard it is to draw some bloods and do the DNA test? At least if > they did that now, by May 28th they might have some results! This > all may be a non issue anyway because my husband and I might be > getting custody of our nephew anyway. And believe me, if he comes to > us the first thing I'll be doing is getting him to a CF specialist > and getting the damn DNA test. Enough with this already. We need to > know if he has it or not so we can move to the next step. > > Anyway, just wanted to know if anyone had any thoughts or ideas for > me. Thanks, > > -Beth > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 30, 2003 Report Share Posted April 30, 2003 There are more than one cf clinic in NY .I take my kids to SUNY Health and science center in Syracuse the head doctor is Dr. Swender he only sees new patients and a few older ones.Dr.Anbar is the usual doctor for pediatric pulmonology.This is the clinic we have used for 19 years and they are aggresive at cf treatment.BeckyB. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 30, 2003 Report Share Posted April 30, 2003 My very special thoughts & good wishes are out there for you in all these situations & what is best for this precious wee one LOVE & HUGS, grandmomBEV Re: I'm back....more questions Unfortunately I don't know what the number actually was for the sweat test. I do believe that is somehow (even unconsiously?) delaying these tests and such. I am almost positive that he has only been to a pediatric pulmonologist. Not a CF specialist and not at a CF clinic. She has been taking him to somewhere in Syracuse (NY), I'm guessing a big hospital there. She isn't very telling with actual details and such. We are waiting to find out if we may get custody of him because she is being investigated by CPS for various reasons, medical neglect is in that list of reasons. We are keeping our fingers crossed. Even the child's father wants us to have custody (he is my husbands brother), because he knows she is not caring for him correctly and he unfortuntely doesn't have the resources to take care of the child either. Hopefully by the end of the week I'll know something. Does anyone know of a CF clinic in NY? We are 90 miles west of NYC. Any info would be great. -Beth > with the sweat test, anything below 40 is normal, anything above 60 is considered positive for CF. So, Maybe his test is between 40 and 60 and considered borderline. Usually they do the sweat test again before they do any other tests. I don't know why they would wait to draw blood to do a DNA test. Is he being seen by a CF clinic and was he tested at a CF center? If you do get custody, as a guardian you should be able to find out why they are waiting on all this. Could it be your sister not insisting on it being done right away or putting it off? I hope not but if he is being seen by a CF center they are usually pretty anxious to get a diagnosis too, so they can begin to treat the child. > > I'm back....more questions > > > Ok, I have some questions about testing and such. My nephew (10 > months old) had a sweat test and they said it was negative, but they > weren't completly sure. At least that's what his mother told me. > She said the next appointment for him isn't until May 28th and they > are going to do more tests. Why would they wait that long? I mean > how hard it is to draw some bloods and do the DNA test? At least if > they did that now, by May 28th they might have some results! This > all may be a non issue anyway because my husband and I might be > getting custody of our nephew anyway. And believe me, if he comes to > us the first thing I'll be doing is getting him to a CF specialist > and getting the damn DNA test. Enough with this already. We need to > know if he has it or not so we can move to the next step. > > Anyway, just wanted to know if anyone had any thoughts or ideas for > me. Thanks, > > -Beth > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 30, 2003 Report Share Posted April 30, 2003 YES, this clinic has a nationwide GREAT reputation. Best wishes if you good there LOVE & HUGS, grandmomBEV Re: Re: I'm back....more questions There are more than one cf clinic in NY .I take my kids to SUNY Health and science center in Syracuse the head doctor is Dr. Swender he only sees new patients and a few older ones.Dr.Anbar is the usual doctor for pediatric pulmonology.This is the clinic we have used for 19 years and they are aggresive at cf treatment.BeckyB. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
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.