Bad Dr Appt Today

jamie6girl

New member
I haven't really felt very good the last few weeks, and I knew that I would probably need to get back on IV's or something to get me back to my usual self. <br><br>
Please keep in mind that I've only done IV's twice in my life, the second time was last Oct, the first time was back when I was like 14 or 15, so the concept of Picc Lines still scares me right now.<br><br>
I called the doc today and they said they could get me in today, so I went up there and of course my lung function dropped again.<br><br>
He scheduled me for a picc line tomorrow and said that after that I would want to look into getting a port. The thought of a port scares the living crap out of me, and it turns my stomach thinking about it. I think about how sore my arm is when I got the picc, and the thought of a port makes me sick to my stomach. <br><br>
He also said that since my lung function tests have been consistently low for so long, that this is usually the time that people go on the transplant list. To actually hear him say this - I can't even put into words what this did to me. He said that this doesn't mean I need one now, but this is where people would do this for the future.<br><br>
He said that I could get a port on a Friday and go back to work on Monday. Is this true? I thought I'd have to take a week off or something. When I got a picc in Oct, my boss let me work from home. I guess I am going to have to "man up" and come to work and do my daily things with a stupid cord hanging out of my arm. I know that everyone else does this, but how does one work a full time 40 hours a week and have all this going on? I am going to have to just accept that I will be on IV's a lot now, and just learn how to live my life and this will be "normal" for me. <br><br>
Any suggestions on how to deal with all this and still function as a human being? I came back to work after my doc appt when really all I want to do is go home and curl up on the couch and cry.<br><Br>
Also, I want to add, that it doesn't help that I work with a bunch of work-a-holics that will continue to work even when their kids are sick at school or will rather go without eating just to knock out a few extra emails. <img src="i/expressions/face-icon-small-disgusted.gif" border="0">
Thanks for any advice that you can give me.
 

jamie6girl

New member
I haven't really felt very good the last few weeks, and I knew that I would probably need to get back on IV's or something to get me back to my usual self. <br><br>
Please keep in mind that I've only done IV's twice in my life, the second time was last Oct, the first time was back when I was like 14 or 15, so the concept of Picc Lines still scares me right now.<br><br>
I called the doc today and they said they could get me in today, so I went up there and of course my lung function dropped again.<br><br>
He scheduled me for a picc line tomorrow and said that after that I would want to look into getting a port. The thought of a port scares the living crap out of me, and it turns my stomach thinking about it. I think about how sore my arm is when I got the picc, and the thought of a port makes me sick to my stomach. <br><br>
He also said that since my lung function tests have been consistently low for so long, that this is usually the time that people go on the transplant list. To actually hear him say this - I can't even put into words what this did to me. He said that this doesn't mean I need one now, but this is where people would do this for the future.<br><br>
He said that I could get a port on a Friday and go back to work on Monday. Is this true? I thought I'd have to take a week off or something. When I got a picc in Oct, my boss let me work from home. I guess I am going to have to "man up" and come to work and do my daily things with a stupid cord hanging out of my arm. I know that everyone else does this, but how does one work a full time 40 hours a week and have all this going on? I am going to have to just accept that I will be on IV's a lot now, and just learn how to live my life and this will be "normal" for me. <br><br>
Any suggestions on how to deal with all this and still function as a human being? I came back to work after my doc appt when really all I want to do is go home and curl up on the couch and cry.<br><Br>
Also, I want to add, that it doesn't help that I work with a bunch of work-a-holics that will continue to work even when their kids are sick at school or will rather go without eating just to knock out a few extra emails. <img src="i/expressions/face-icon-small-disgusted.gif" border="0">
Thanks for any advice that you can give me.
 

jamie6girl

New member
I haven't really felt very good the last few weeks, and I knew that I would probably need to get back on IV's or something to get me back to my usual self. <br><br>
Please keep in mind that I've only done IV's twice in my life, the second time was last Oct, the first time was back when I was like 14 or 15, so the concept of Picc Lines still scares me right now.<br><br>
I called the doc today and they said they could get me in today, so I went up there and of course my lung function dropped again.<br><br>
He scheduled me for a picc line tomorrow and said that after that I would want to look into getting a port. The thought of a port scares the living crap out of me, and it turns my stomach thinking about it. I think about how sore my arm is when I got the picc, and the thought of a port makes me sick to my stomach. <br><br>
He also said that since my lung function tests have been consistently low for so long, that this is usually the time that people go on the transplant list. To actually hear him say this - I can't even put into words what this did to me. He said that this doesn't mean I need one now, but this is where people would do this for the future.<br><br>
He said that I could get a port on a Friday and go back to work on Monday. Is this true? I thought I'd have to take a week off or something. When I got a picc in Oct, my boss let me work from home. I guess I am going to have to "man up" and come to work and do my daily things with a stupid cord hanging out of my arm. I know that everyone else does this, but how does one work a full time 40 hours a week and have all this going on? I am going to have to just accept that I will be on IV's a lot now, and just learn how to live my life and this will be "normal" for me. <br><br>
Any suggestions on how to deal with all this and still function as a human being? I came back to work after my doc appt when really all I want to do is go home and curl up on the couch and cry.<br><Br>
Also, I want to add, that it doesn't help that I work with a bunch of work-a-holics that will continue to work even when their kids are sick at school or will rather go without eating just to knock out a few extra emails. <img src="i/expressions/face-icon-small-disgusted.gif" border="0">
Thanks for any advice that you can give me.
 

jamie6girl

New member
I haven't really felt very good the last few weeks, and I knew that I would probably need to get back on IV's or something to get me back to my usual self. <br><br>
Please keep in mind that I've only done IV's twice in my life, the second time was last Oct, the first time was back when I was like 14 or 15, so the concept of Picc Lines still scares me right now.<br><br>
I called the doc today and they said they could get me in today, so I went up there and of course my lung function dropped again.<br><br>
He scheduled me for a picc line tomorrow and said that after that I would want to look into getting a port. The thought of a port scares the living crap out of me, and it turns my stomach thinking about it. I think about how sore my arm is when I got the picc, and the thought of a port makes me sick to my stomach. <br><br>
He also said that since my lung function tests have been consistently low for so long, that this is usually the time that people go on the transplant list. To actually hear him say this - I can't even put into words what this did to me. He said that this doesn't mean I need one now, but this is where people would do this for the future.<br><br>
He said that I could get a port on a Friday and go back to work on Monday. Is this true? I thought I'd have to take a week off or something. When I got a picc in Oct, my boss let me work from home. I guess I am going to have to "man up" and come to work and do my daily things with a stupid cord hanging out of my arm. I know that everyone else does this, but how does one work a full time 40 hours a week and have all this going on? I am going to have to just accept that I will be on IV's a lot now, and just learn how to live my life and this will be "normal" for me. <br><br>
Any suggestions on how to deal with all this and still function as a human being? I came back to work after my doc appt when really all I want to do is go home and curl up on the couch and cry.<br><Br>
Also, I want to add, that it doesn't help that I work with a bunch of work-a-holics that will continue to work even when their kids are sick at school or will rather go without eating just to knock out a few extra emails. <img src="i/expressions/face-icon-small-disgusted.gif" border="0">
Thanks for any advice that you can give me.
 

jamie6girl

New member
I haven't really felt very good the last few weeks, and I knew that I would probably need to get back on IV's or something to get me back to my usual self. <br><br>
Please keep in mind that I've only done IV's twice in my life, the second time was last Oct, the first time was back when I was like 14 or 15, so the concept of Picc Lines still scares me right now.<br><br>
I called the doc today and they said they could get me in today, so I went up there and of course my lung function dropped again.<br><br>
He scheduled me for a picc line tomorrow and said that after that I would want to look into getting a port. The thought of a port scares the living crap out of me, and it turns my stomach thinking about it. I think about how sore my arm is when I got the picc, and the thought of a port makes me sick to my stomach. <br><br>
He also said that since my lung function tests have been consistently low for so long, that this is usually the time that people go on the transplant list. To actually hear him say this - I can't even put into words what this did to me. He said that this doesn't mean I need one now, but this is where people would do this for the future.<br><br>
He said that I could get a port on a Friday and go back to work on Monday. Is this true? I thought I'd have to take a week off or something. When I got a picc in Oct, my boss let me work from home. I guess I am going to have to "man up" and come to work and do my daily things with a stupid cord hanging out of my arm. I know that everyone else does this, but how does one work a full time 40 hours a week and have all this going on? I am going to have to just accept that I will be on IV's a lot now, and just learn how to live my life and this will be "normal" for me. <br><br>
Any suggestions on how to deal with all this and still function as a human being? I came back to work after my doc appt when really all I want to do is go home and curl up on the couch and cry.<br><Br>
Also, I want to add, that it doesn't help that I work with a bunch of work-a-holics that will continue to work even when their kids are sick at school or will rather go without eating just to knock out a few extra emails. <img src="i/expressions/face-icon-small-disgusted.gif" border="0">
Thanks for any advice that you can give me.
 

purplemartin

New member
You will LOVE the port! I know children bounce back a little quicker than adults do, but the port placement didn't seem to have any effect on Briceton afterwards! Not to mention the port being soooo much eaier when IV infusions are in need!

Hope the IV's get you to felling a bit more like yourself, and I'm sending good vibes your way for a great increase in lung funtion soon!!!!!!!

Sherry
 

purplemartin

New member
You will LOVE the port! I know children bounce back a little quicker than adults do, but the port placement didn't seem to have any effect on Briceton afterwards! Not to mention the port being soooo much eaier when IV infusions are in need!

Hope the IV's get you to felling a bit more like yourself, and I'm sending good vibes your way for a great increase in lung funtion soon!!!!!!!

Sherry
 

purplemartin

New member
You will LOVE the port! I know children bounce back a little quicker than adults do, but the port placement didn't seem to have any effect on Briceton afterwards! Not to mention the port being soooo much eaier when IV infusions are in need!

Hope the IV's get you to felling a bit more like yourself, and I'm sending good vibes your way for a great increase in lung funtion soon!!!!!!!

Sherry
 

purplemartin

New member
You will LOVE the port! I know children bounce back a little quicker than adults do, but the port placement didn't seem to have any effect on Briceton afterwards! Not to mention the port being soooo much eaier when IV infusions are in need!

Hope the IV's get you to felling a bit more like yourself, and I'm sending good vibes your way for a great increase in lung funtion soon!!!!!!!

Sherry
 

purplemartin

New member
You will LOVE the port! I know children bounce back a little quicker than adults do, but the port placement didn't seem to have any effect on Briceton afterwards! Not to mention the port being soooo much eaier when IV infusions are in need!

Hope the IV's get you to felling a bit more like yourself, and I'm sending good vibes your way for a great increase in lung funtion soon!!!!!!!

Sherry
 

NoExcuses

New member
Just as a quick question - if your lung function is so poor, how is it that you've only been on IV's twice in your life?
 

NoExcuses

New member
Just as a quick question - if your lung function is so poor, how is it that you've only been on IV's twice in your life?
 

NoExcuses

New member
Just as a quick question - if your lung function is so poor, how is it that you've only been on IV's twice in your life?
 

NoExcuses

New member
Just as a quick question - if your lung function is so poor, how is it that you've only been on IV's twice in your life?
 

NoExcuses

New member
Just as a quick question - if your lung function is so poor, how is it that you've only been on IV's twice in your life?
 

Skye

New member
Jennifer,

My heart goes out to you. I know the crushing feeling of those words transplant. It can be overwhelming. If you can take one piece of it at a time and deal with it as your questions arise, it is easier. Don't try to swallow the whole big picture. Your doctor just doesn't want you to be in a position that you are not well enough to even think about a transplant. It is much easier to go to the appointments and get your questions answered when you are well and clear-headed. Just because they want you to connect with a tx center doesn't mean you are ready for a transplant. It is just with the unpredictability of CF, they want to be safe. I was evaluated over a year ago and I am still doing well and enjoying every minute of my life. Sending hugs your way!!
 

Skye

New member
Jennifer,

My heart goes out to you. I know the crushing feeling of those words transplant. It can be overwhelming. If you can take one piece of it at a time and deal with it as your questions arise, it is easier. Don't try to swallow the whole big picture. Your doctor just doesn't want you to be in a position that you are not well enough to even think about a transplant. It is much easier to go to the appointments and get your questions answered when you are well and clear-headed. Just because they want you to connect with a tx center doesn't mean you are ready for a transplant. It is just with the unpredictability of CF, they want to be safe. I was evaluated over a year ago and I am still doing well and enjoying every minute of my life. Sending hugs your way!!
 

Skye

New member
Jennifer,

My heart goes out to you. I know the crushing feeling of those words transplant. It can be overwhelming. If you can take one piece of it at a time and deal with it as your questions arise, it is easier. Don't try to swallow the whole big picture. Your doctor just doesn't want you to be in a position that you are not well enough to even think about a transplant. It is much easier to go to the appointments and get your questions answered when you are well and clear-headed. Just because they want you to connect with a tx center doesn't mean you are ready for a transplant. It is just with the unpredictability of CF, they want to be safe. I was evaluated over a year ago and I am still doing well and enjoying every minute of my life. Sending hugs your way!!
 

Skye

New member
Jennifer,

My heart goes out to you. I know the crushing feeling of those words transplant. It can be overwhelming. If you can take one piece of it at a time and deal with it as your questions arise, it is easier. Don't try to swallow the whole big picture. Your doctor just doesn't want you to be in a position that you are not well enough to even think about a transplant. It is much easier to go to the appointments and get your questions answered when you are well and clear-headed. Just because they want you to connect with a tx center doesn't mean you are ready for a transplant. It is just with the unpredictability of CF, they want to be safe. I was evaluated over a year ago and I am still doing well and enjoying every minute of my life. Sending hugs your way!!
 

Skye

New member
Jennifer,

My heart goes out to you. I know the crushing feeling of those words transplant. It can be overwhelming. If you can take one piece of it at a time and deal with it as your questions arise, it is easier. Don't try to swallow the whole big picture. Your doctor just doesn't want you to be in a position that you are not well enough to even think about a transplant. It is much easier to go to the appointments and get your questions answered when you are well and clear-headed. Just because they want you to connect with a tx center doesn't mean you are ready for a transplant. It is just with the unpredictability of CF, they want to be safe. I was evaluated over a year ago and I am still doing well and enjoying every minute of my life. Sending hugs your way!!
 
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