Continue to work full time?

N

NoExcuses

New member
you're having all of these symptoms, and you haven't explored every option 100% to ensure that you don't have CF?

come on now.... you're smarter than that. i know you are.

not every single person who is jewish with CF has typical jewish CF genes as I'm sure they explained to you.

it's time to get the test. as nicole said, it will make your life so much easier in the end.

here's their phone #. 866-262-7943 Toll Free


<b> No excuses, now. </b> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
N

NoExcuses

New member
you're having all of these symptoms, and you haven't explored every option 100% to ensure that you don't have CF?

come on now.... you're smarter than that. i know you are.

not every single person who is jewish with CF has typical jewish CF genes as I'm sure they explained to you.

it's time to get the test. as nicole said, it will make your life so much easier in the end.

here's their phone #. 866-262-7943 Toll Free


<b> No excuses, now. </b> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
N

NoExcuses

New member
you're having all of these symptoms, and you haven't explored every option 100% to ensure that you don't have CF?

come on now.... you're smarter than that. i know you are.

not every single person who is jewish with CF has typical jewish CF genes as I'm sure they explained to you.

it's time to get the test. as nicole said, it will make your life so much easier in the end.

here's their phone #. 866-262-7943 Toll Free


<b> No excuses, now. </b> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
N

NoExcuses

New member
you're having all of these symptoms, and you haven't explored every option 100% to ensure that you don't have CF?

come on now.... you're smarter than that. i know you are.

not every single person who is jewish with CF has typical jewish CF genes as I'm sure they explained to you.

it's time to get the test. as nicole said, it will make your life so much easier in the end.

here's their phone #. 866-262-7943 Toll Free


<b> No excuses, now. </b> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
N

NoExcuses

New member
you're having all of these symptoms, and you haven't explored every option 100% to ensure that you don't have CF?
<br />
<br />come on now.... you're smarter than that. i know you are.
<br />
<br />not every single person who is jewish with CF has typical jewish CF genes as I'm sure they explained to you.
<br />
<br />it's time to get the test. as nicole said, it will make your life so much easier in the end.
<br />
<br />here's their phone #. 866-262-7943 Toll Free
<br />
<br />
<br /><b> No excuses, now. </b> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0"> <img src="i/expressions/face-icon-small-smile.gif" border="0">
<br />
 
M

moosemom

New member
Hey nervous,

I get it. I was in a similar situation a few years back. I kept working reduced it to part time, no real diagnosis until I went to National Jewish In Denver. They were sure it was CF and they dug till they found the gene. I continued working against their advise for several years until I just couldn't do it anymore. The work, the stress, the germs... I wasn't any good for anyone, not at work and not at home.

I was never the primary bread winner but we counted on the money... It was tough, probably toughest on me for emotional reasons but we all worked through it. I now get disability and we do what we have to. For me it was worth it... It has taken a while to get to this place...

Do what you need to and remember we get it... Good luck
 
M

moosemom

New member
Hey nervous,

I get it. I was in a similar situation a few years back. I kept working reduced it to part time, no real diagnosis until I went to National Jewish In Denver. They were sure it was CF and they dug till they found the gene. I continued working against their advise for several years until I just couldn't do it anymore. The work, the stress, the germs... I wasn't any good for anyone, not at work and not at home.

I was never the primary bread winner but we counted on the money... It was tough, probably toughest on me for emotional reasons but we all worked through it. I now get disability and we do what we have to. For me it was worth it... It has taken a while to get to this place...

Do what you need to and remember we get it... Good luck
 
M

moosemom

New member
Hey nervous,

I get it. I was in a similar situation a few years back. I kept working reduced it to part time, no real diagnosis until I went to National Jewish In Denver. They were sure it was CF and they dug till they found the gene. I continued working against their advise for several years until I just couldn't do it anymore. The work, the stress, the germs... I wasn't any good for anyone, not at work and not at home.

I was never the primary bread winner but we counted on the money... It was tough, probably toughest on me for emotional reasons but we all worked through it. I now get disability and we do what we have to. For me it was worth it... It has taken a while to get to this place...

Do what you need to and remember we get it... Good luck
 
M

moosemom

New member
Hey nervous,

I get it. I was in a similar situation a few years back. I kept working reduced it to part time, no real diagnosis until I went to National Jewish In Denver. They were sure it was CF and they dug till they found the gene. I continued working against their advise for several years until I just couldn't do it anymore. The work, the stress, the germs... I wasn't any good for anyone, not at work and not at home.

I was never the primary bread winner but we counted on the money... It was tough, probably toughest on me for emotional reasons but we all worked through it. I now get disability and we do what we have to. For me it was worth it... It has taken a while to get to this place...

Do what you need to and remember we get it... Good luck
 
M

moosemom

New member
Hey nervous,
<br />
<br />I get it. I was in a similar situation a few years back. I kept working reduced it to part time, no real diagnosis until I went to National Jewish In Denver. They were sure it was CF and they dug till they found the gene. I continued working against their advise for several years until I just couldn't do it anymore. The work, the stress, the germs... I wasn't any good for anyone, not at work and not at home.
<br />
<br />I was never the primary bread winner but we counted on the money... It was tough, probably toughest on me for emotional reasons but we all worked through it. I now get disability and we do what we have to. For me it was worth it... It has taken a while to get to this place...
<br />
<br />Do what you need to and remember we get it... Good luck
<br />
 
N

Nervous1

New member
Thanks to all of you. I have spoken to two geneticists and who knows how many doctors, and everyone has told me that it would be a waste of money to do the Ambry full panel. Maybe you are all right though, and I should do it. I don't know. Maybe I will call the phone number you gave me and see what Ambry says.

For four years I have been desparately trying to get a diagnosis. The stress involved in searching for a diagnosis was taking its toll though, so over the past half a year or so I have more or less given up searching for answers and tried to live my life as best I can. The support on this site has been invaluable to say the least.

For those of you who are working, does your employer know about your illness? Do they take your limitations into consideration? One thing I'm debating is whether to tell my employer about my condition, and request to limit the amount of traveling requested of me. It would obviously impact my chances for advancement, but that seems unimportant at this point. Looking to learn from your experience ...
 
N

Nervous1

New member
Thanks to all of you. I have spoken to two geneticists and who knows how many doctors, and everyone has told me that it would be a waste of money to do the Ambry full panel. Maybe you are all right though, and I should do it. I don't know. Maybe I will call the phone number you gave me and see what Ambry says.

For four years I have been desparately trying to get a diagnosis. The stress involved in searching for a diagnosis was taking its toll though, so over the past half a year or so I have more or less given up searching for answers and tried to live my life as best I can. The support on this site has been invaluable to say the least.

For those of you who are working, does your employer know about your illness? Do they take your limitations into consideration? One thing I'm debating is whether to tell my employer about my condition, and request to limit the amount of traveling requested of me. It would obviously impact my chances for advancement, but that seems unimportant at this point. Looking to learn from your experience ...
 
N

Nervous1

New member
Thanks to all of you. I have spoken to two geneticists and who knows how many doctors, and everyone has told me that it would be a waste of money to do the Ambry full panel. Maybe you are all right though, and I should do it. I don't know. Maybe I will call the phone number you gave me and see what Ambry says.

For four years I have been desparately trying to get a diagnosis. The stress involved in searching for a diagnosis was taking its toll though, so over the past half a year or so I have more or less given up searching for answers and tried to live my life as best I can. The support on this site has been invaluable to say the least.

For those of you who are working, does your employer know about your illness? Do they take your limitations into consideration? One thing I'm debating is whether to tell my employer about my condition, and request to limit the amount of traveling requested of me. It would obviously impact my chances for advancement, but that seems unimportant at this point. Looking to learn from your experience ...
 
N

Nervous1

New member
Thanks to all of you. I have spoken to two geneticists and who knows how many doctors, and everyone has told me that it would be a waste of money to do the Ambry full panel. Maybe you are all right though, and I should do it. I don't know. Maybe I will call the phone number you gave me and see what Ambry says.

For four years I have been desparately trying to get a diagnosis. The stress involved in searching for a diagnosis was taking its toll though, so over the past half a year or so I have more or less given up searching for answers and tried to live my life as best I can. The support on this site has been invaluable to say the least.

For those of you who are working, does your employer know about your illness? Do they take your limitations into consideration? One thing I'm debating is whether to tell my employer about my condition, and request to limit the amount of traveling requested of me. It would obviously impact my chances for advancement, but that seems unimportant at this point. Looking to learn from your experience ...
 
N

Nervous1

New member
Thanks to all of you. I have spoken to two geneticists and who knows how many doctors, and everyone has told me that it would be a waste of money to do the Ambry full panel. Maybe you are all right though, and I should do it. I don't know. Maybe I will call the phone number you gave me and see what Ambry says.
<br />
<br />For four years I have been desparately trying to get a diagnosis. The stress involved in searching for a diagnosis was taking its toll though, so over the past half a year or so I have more or less given up searching for answers and tried to live my life as best I can. The support on this site has been invaluable to say the least.
<br />
<br />For those of you who are working, does your employer know about your illness? Do they take your limitations into consideration? One thing I'm debating is whether to tell my employer about my condition, and request to limit the amount of traveling requested of me. It would obviously impact my chances for advancement, but that seems unimportant at this point. Looking to learn from your experience ...
 
You must log in or register to reply here.
Top