Son just diagnosed with CF

T

txlimo

New member
My 11 y.o. son was diagnosed about 2-1/2 months ago that he has CF. His sweat test came back normal but the genetic test came back with 2 mutations. School started last week and we are already in the hospital. I hope this isn't sign of things to come!!

It started Sunday with a fever between 100-104 that wouldn't break. Called the pulmonary dr. on call and they said to take him to emergency room. They ended up admitting him and were talking like he might be able to go home later today (Tuesday) or tomorrow. Well, we just got word that they are going to keep him probably all week. This is not a good way to start the school year!!
 
T

txlimo

New member
My 11 y.o. son was diagnosed about 2-1/2 months ago that he has CF. His sweat test came back normal but the genetic test came back with 2 mutations. School started last week and we are already in the hospital. I hope this isn't sign of things to come!!

It started Sunday with a fever between 100-104 that wouldn't break. Called the pulmonary dr. on call and they said to take him to emergency room. They ended up admitting him and were talking like he might be able to go home later today (Tuesday) or tomorrow. Well, we just got word that they are going to keep him probably all week. This is not a good way to start the school year!!
 
T

txlimo

New member
My 11 y.o. son was diagnosed about 2-1/2 months ago that he has CF. His sweat test came back normal but the genetic test came back with 2 mutations. School started last week and we are already in the hospital. I hope this isn't sign of things to come!!

It started Sunday with a fever between 100-104 that wouldn't break. Called the pulmonary dr. on call and they said to take him to emergency room. They ended up admitting him and were talking like he might be able to go home later today (Tuesday) or tomorrow. Well, we just got word that they are going to keep him probably all week. This is not a good way to start the school year!!
 
T

txlimo

New member
My 11 y.o. son was diagnosed about 2-1/2 months ago that he has CF. His sweat test came back normal but the genetic test came back with 2 mutations. School started last week and we are already in the hospital. I hope this isn't sign of things to come!!

It started Sunday with a fever between 100-104 that wouldn't break. Called the pulmonary dr. on call and they said to take him to emergency room. They ended up admitting him and were talking like he might be able to go home later today (Tuesday) or tomorrow. Well, we just got word that they are going to keep him probably all week. This is not a good way to start the school year!!
 
T

txlimo

New member
My 11 y.o. son was diagnosed about 2-1/2 months ago that he has CF. His sweat test came back normal but the genetic test came back with 2 mutations. School started last week and we are already in the hospital. I hope this isn't sign of things to come!!
<br />
<br />It started Sunday with a fever between 100-104 that wouldn't break. Called the pulmonary dr. on call and they said to take him to emergency room. They ended up admitting him and were talking like he might be able to go home later today (Tuesday) or tomorrow. Well, we just got word that they are going to keep him probably all week. This is not a good way to start the school year!!
 
M

Mommafirst

Guest
ugh -- I'm so sorry, that certainly doesn't sound like a good start at all. Hopefully they will get him healthy, and maybe do a tuneup and he will have a great rest of the year. hang in there, I hope the stay goes quickly and you can get home soon.
 
M

Mommafirst

Guest
ugh -- I'm so sorry, that certainly doesn't sound like a good start at all. Hopefully they will get him healthy, and maybe do a tuneup and he will have a great rest of the year. hang in there, I hope the stay goes quickly and you can get home soon.
 
M

Mommafirst

Guest
ugh -- I'm so sorry, that certainly doesn't sound like a good start at all. Hopefully they will get him healthy, and maybe do a tuneup and he will have a great rest of the year. hang in there, I hope the stay goes quickly and you can get home soon.
 
M

Mommafirst

Guest
ugh -- I'm so sorry, that certainly doesn't sound like a good start at all. Hopefully they will get him healthy, and maybe do a tuneup and he will have a great rest of the year. hang in there, I hope the stay goes quickly and you can get home soon.
 
M

Mommafirst

Guest
ugh -- I'm so sorry, that certainly doesn't sound like a good start at all. Hopefully they will get him healthy, and maybe do a tuneup and he will have a great rest of the year. hang in there, I hope the stay goes quickly and you can get home soon.
 
A

amityvsvenom

New member
Keep your head up! Its that time of year for all of us parents with CF children. We are all going to be trying to dodge the hospital stays but we can't always control everything. I am also sorry to hear that he has been diagnosed. I can't imagine finding out so late in his life. If you ever need any emotional support or just want to talk Im hear to talk to.
 
A

amityvsvenom

New member
Keep your head up! Its that time of year for all of us parents with CF children. We are all going to be trying to dodge the hospital stays but we can't always control everything. I am also sorry to hear that he has been diagnosed. I can't imagine finding out so late in his life. If you ever need any emotional support or just want to talk Im hear to talk to.
 
A

amityvsvenom

New member
Keep your head up! Its that time of year for all of us parents with CF children. We are all going to be trying to dodge the hospital stays but we can't always control everything. I am also sorry to hear that he has been diagnosed. I can't imagine finding out so late in his life. If you ever need any emotional support or just want to talk Im hear to talk to.
 
A

amityvsvenom

New member
Keep your head up! Its that time of year for all of us parents with CF children. We are all going to be trying to dodge the hospital stays but we can't always control everything. I am also sorry to hear that he has been diagnosed. I can't imagine finding out so late in his life. If you ever need any emotional support or just want to talk Im hear to talk to.
 
A

amityvsvenom

New member
Keep your head up! Its that time of year for all of us parents with CF children. We are all going to be trying to dodge the hospital stays but we can't always control everything. I am also sorry to hear that he has been diagnosed. I can't imagine finding out so late in his life. If you ever need any emotional support or just want to talk Im hear to talk to.
 
You must log in or register to reply here.
Top