Emily65Roses
New member
I third these ladies. Genetic blood test is an essential move.
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Emily65Roses
New member
I third these ladies. Genetic blood test is an essential move.
Emily65Roses
New member
I third these ladies. Genetic blood test is an essential move.
Emily65Roses
New member
I third these ladies. Genetic blood test is an essential move.
Well, that is one step down but to be completely safe the full ambry genetic test is the way to go. Take it from me who has tested in the 30 range when I was in my teens and because of that I was told I did not have Cystic Fibrosis. I wish they had the genetic testing back then to prove otherwise. I would have received proper treatment so much earlier.
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
Well, that is one step down but to be completely safe the full ambry genetic test is the way to go. Take it from me who has tested in the 30 range when I was in my teens and because of that I was told I did not have Cystic Fibrosis. I wish they had the genetic testing back then to prove otherwise. I would have received proper treatment so much earlier.
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
Well, that is one step down but to be completely safe the full ambry genetic test is the way to go. Take it from me who has tested in the 30 range when I was in my teens and because of that I was told I did not have Cystic Fibrosis. I wish they had the genetic testing back then to prove otherwise. I would have received proper treatment so much earlier.
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
Well, that is one step down but to be completely safe the full ambry genetic test is the way to go. Take it from me who has tested in the 30 range when I was in my teens and because of that I was told I did not have Cystic Fibrosis. I wish they had the genetic testing back then to prove otherwise. I would have received proper treatment so much earlier.
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
Well, that is one step down but to be completely safe the full ambry genetic test is the way to go. Take it from me who has tested in the 30 range when I was in my teens and because of that I was told I did not have Cystic Fibrosis. I wish they had the genetic testing back then to prove otherwise. I would have received proper treatment so much earlier.
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
Well, that is one step down but to be completely safe the full ambry genetic test is the way to go. Take it from me who has tested in the 30 range when I was in my teens and because of that I was told I did not have Cystic Fibrosis. I wish they had the genetic testing back then to prove otherwise. I would have received proper treatment so much earlier.
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
I am not complaining but since we have the medical technology to use more than one test to confirm CF we should avail ourselves of it when warranted and your son's situation warrants a more accurate diagnosis. I hope his correct diagnosis, whatever it turns out to be, is found soon so that he can get all the medical treatments needed to be the healthiest he can me.
Keeping you and Aiden in prayer.<img src="i/expressions/heart.gif" border="0">
A
Aidenmurphy
Guest
Well Aiden is doing well. They put him on an inhaler w/ a stronger medicine and his nose isn't running as much but he's coughing a little but not a daily or even a monthly thing. The Ear Nose Throat dr has him on a high dosage of anitbiotics for the strep he has in his ear??????
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">
A
Aidenmurphy
Guest
Well Aiden is doing well. They put him on an inhaler w/ a stronger medicine and his nose isn't running as much but he's coughing a little but not a daily or even a monthly thing. The Ear Nose Throat dr has him on a high dosage of anitbiotics for the strep he has in his ear??????
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">
A
Aidenmurphy
Guest
Well Aiden is doing well. They put him on an inhaler w/ a stronger medicine and his nose isn't running as much but he's coughing a little but not a daily or even a monthly thing. The Ear Nose Throat dr has him on a high dosage of anitbiotics for the strep he has in his ear??????
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">
A
Aidenmurphy
Guest
Well Aiden is doing well. They put him on an inhaler w/ a stronger medicine and his nose isn't running as much but he's coughing a little but not a daily or even a monthly thing. The Ear Nose Throat dr has him on a high dosage of anitbiotics for the strep he has in his ear??????
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">
Would be a smart move for me to be tested as a carrier first and see i am even a carrier?<img src="i/expressions/face-icon-small-confused.gif" border="0">