Post-Appointment Thoughts

Lance2020x

New member
Well I'm pretty depressed right now. I created a new topic because this one isn't about my appointment, it's about what happens to us (at least me) after an appointment.

All in all the appointment went well, I was very pleased with the results. My brother (James) has basically maintained stable stats, and I actually improved a bit in weight and lung functions.

The highlight of the day though was when I struck up a conversation with another patient I had seen around, taking the chance that she too was a CF patient. She was indeed, and it was the first time that my brother and I had met ANYONE in person (other than ourselves) who also had CF. It was very interesting, very touching, and very good for James and myself.


Now, I'll back up a bit to say that, until I joined this website, I had never heard of cepecia, and had never even THOUGHT about the fact that CF patients should STRONGLY avoid being in close proximity with each other (seeing as how I grew up with a brother with CF, I never thought about it).
Ever since I learned these things on this site (me being Obsessive Compulsive as it is) I've been completely freaked out when ever I'm around my brother, constantly washing my hands, trying not to get to close, etc.


So here we are, the three of us CF patients, standing in a hospital making a little triangle trying to keep a good safe space between each of us, having a wonderful conversation.
An hour later James and I are driving home, and as we're driving, though moments before we were joyful and happy, (as we always are with our wonderful doctors and nurses) the psychological depression that always rears it's ugly head after an appointment starts to surface.
We arrive at my place, and James starts to pack things into his car to drive the rest of the drive to his place, a couple towns over.
I give my best friend in the whole world; my brother, a very awkward, "safe" half hug, avoiding close contact due to our differences in health status, he leaves, and I go switch out all the hand towels he used last night and this morning while he was over.

After all this that I have seen and felt today, all I can say is this:
What a fucked up way to live.



If you feel like responding to this message, that is fine, I'm not seeking advice or help, I just need to voice my feelings at this moment to a crowd that I believe can comprehend at least part of what I'm feeling right now.

Tomorrow I will wake up, push all of these feelings back down to my feet, and I will continue to walk.

But right now, in this moment, the fact that you are reading this.... It helps.
 

Lance2020x

New member
Well I'm pretty depressed right now. I created a new topic because this one isn't about my appointment, it's about what happens to us (at least me) after an appointment.

All in all the appointment went well, I was very pleased with the results. My brother (James) has basically maintained stable stats, and I actually improved a bit in weight and lung functions.

The highlight of the day though was when I struck up a conversation with another patient I had seen around, taking the chance that she too was a CF patient. She was indeed, and it was the first time that my brother and I had met ANYONE in person (other than ourselves) who also had CF. It was very interesting, very touching, and very good for James and myself.


Now, I'll back up a bit to say that, until I joined this website, I had never heard of cepecia, and had never even THOUGHT about the fact that CF patients should STRONGLY avoid being in close proximity with each other (seeing as how I grew up with a brother with CF, I never thought about it).
Ever since I learned these things on this site (me being Obsessive Compulsive as it is) I've been completely freaked out when ever I'm around my brother, constantly washing my hands, trying not to get to close, etc.


So here we are, the three of us CF patients, standing in a hospital making a little triangle trying to keep a good safe space between each of us, having a wonderful conversation.
An hour later James and I are driving home, and as we're driving, though moments before we were joyful and happy, (as we always are with our wonderful doctors and nurses) the psychological depression that always rears it's ugly head after an appointment starts to surface.
We arrive at my place, and James starts to pack things into his car to drive the rest of the drive to his place, a couple towns over.
I give my best friend in the whole world; my brother, a very awkward, "safe" half hug, avoiding close contact due to our differences in health status, he leaves, and I go switch out all the hand towels he used last night and this morning while he was over.

After all this that I have seen and felt today, all I can say is this:
What a fucked up way to live.



If you feel like responding to this message, that is fine, I'm not seeking advice or help, I just need to voice my feelings at this moment to a crowd that I believe can comprehend at least part of what I'm feeling right now.

Tomorrow I will wake up, push all of these feelings back down to my feet, and I will continue to walk.

But right now, in this moment, the fact that you are reading this.... It helps.
 

Lance2020x

New member
Well I'm pretty depressed right now. I created a new topic because this one isn't about my appointment, it's about what happens to us (at least me) after an appointment.

All in all the appointment went well, I was very pleased with the results. My brother (James) has basically maintained stable stats, and I actually improved a bit in weight and lung functions.

The highlight of the day though was when I struck up a conversation with another patient I had seen around, taking the chance that she too was a CF patient. She was indeed, and it was the first time that my brother and I had met ANYONE in person (other than ourselves) who also had CF. It was very interesting, very touching, and very good for James and myself.


Now, I'll back up a bit to say that, until I joined this website, I had never heard of cepecia, and had never even THOUGHT about the fact that CF patients should STRONGLY avoid being in close proximity with each other (seeing as how I grew up with a brother with CF, I never thought about it).
Ever since I learned these things on this site (me being Obsessive Compulsive as it is) I've been completely freaked out when ever I'm around my brother, constantly washing my hands, trying not to get to close, etc.


So here we are, the three of us CF patients, standing in a hospital making a little triangle trying to keep a good safe space between each of us, having a wonderful conversation.
An hour later James and I are driving home, and as we're driving, though moments before we were joyful and happy, (as we always are with our wonderful doctors and nurses) the psychological depression that always rears it's ugly head after an appointment starts to surface.
We arrive at my place, and James starts to pack things into his car to drive the rest of the drive to his place, a couple towns over.
I give my best friend in the whole world; my brother, a very awkward, "safe" half hug, avoiding close contact due to our differences in health status, he leaves, and I go switch out all the hand towels he used last night and this morning while he was over.

After all this that I have seen and felt today, all I can say is this:
What a fucked up way to live.



If you feel like responding to this message, that is fine, I'm not seeking advice or help, I just need to voice my feelings at this moment to a crowd that I believe can comprehend at least part of what I'm feeling right now.

Tomorrow I will wake up, push all of these feelings back down to my feet, and I will continue to walk.

But right now, in this moment, the fact that you are reading this.... It helps.
 

littledebbie

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Lance2020x</b></i>

After all this that I have seen and felt today, all I can say is this:

What a fucked up way to live.

</end quote></div>

You know sometimes I know they censor the language around here and I can sort of see their point...but sometimes there is no more eloquent way of expressing the truth. Well said!
 

littledebbie

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Lance2020x</b></i>

After all this that I have seen and felt today, all I can say is this:

What a fucked up way to live.

</end quote></div>

You know sometimes I know they censor the language around here and I can sort of see their point...but sometimes there is no more eloquent way of expressing the truth. Well said!
 

littledebbie

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Lance2020x</b></i>

After all this that I have seen and felt today, all I can say is this:

What a fucked up way to live.

</end quote></div>

You know sometimes I know they censor the language around here and I can sort of see their point...but sometimes there is no more eloquent way of expressing the truth. Well said!
 

Diane

New member
I have to agree with Debbie, There really isnt a better way to put it. Life with cf is hard enough, but having a brother ( or any family member) with cf also, and having to be "careful" Just makes it downright worse.
 

Diane

New member
I have to agree with Debbie, There really isnt a better way to put it. Life with cf is hard enough, but having a brother ( or any family member) with cf also, and having to be "careful" Just makes it downright worse.
 

Diane

New member
I have to agree with Debbie, There really isnt a better way to put it. Life with cf is hard enough, but having a brother ( or any family member) with cf also, and having to be "careful" Just makes it downright worse.
 

Breezy

New member
I completely understand, as i do the same thing when people have been to my place, with regards to washing hand towels and everything. It IS fucked up and sometimes it really sucks when there's nothing you can do about it. We should talk sometime. PM me and i'll give you my MSN or AOL addy if you've got either.
 

Breezy

New member
I completely understand, as i do the same thing when people have been to my place, with regards to washing hand towels and everything. It IS fucked up and sometimes it really sucks when there's nothing you can do about it. We should talk sometime. PM me and i'll give you my MSN or AOL addy if you've got either.
 

Breezy

New member
I completely understand, as i do the same thing when people have been to my place, with regards to washing hand towels and everything. It IS fucked up and sometimes it really sucks when there's nothing you can do about it. We should talk sometime. PM me and i'll give you my MSN or AOL addy if you've got either.
 
Blake,

Well said. There isn't anything quite like being able to talk to another CFer face to face. Did anyone ever attend a "CF Camp" when they were younger. Obviously they stopped doing that upon the cepecia discovery. But it was nice to be around others that could truly understand what was going on to a degree.
 
Blake,

Well said. There isn't anything quite like being able to talk to another CFer face to face. Did anyone ever attend a "CF Camp" when they were younger. Obviously they stopped doing that upon the cepecia discovery. But it was nice to be around others that could truly understand what was going on to a degree.
 
Blake,

Well said. There isn't anything quite like being able to talk to another CFer face to face. Did anyone ever attend a "CF Camp" when they were younger. Obviously they stopped doing that upon the cepecia discovery. But it was nice to be around others that could truly understand what was going on to a degree.
 

Jane

Digital opinion leader
The loneliness my kids feel is one thing that makes me sad about their disease. They do have each other, but its not the same as relating to person outside the family. They have never talked to another person about their medicines, their g-tubes or their various therapies. That is a huge burden to carry around!

My boys grow mostly the same bugs so we have not tried to keep them separate (although we are cautious). I can't bear to think about a time that they have to keep apart. It will break their hearts and their spirit.

Blake, you have described it so well.
 

Jane

Digital opinion leader
The loneliness my kids feel is one thing that makes me sad about their disease. They do have each other, but its not the same as relating to person outside the family. They have never talked to another person about their medicines, their g-tubes or their various therapies. That is a huge burden to carry around!

My boys grow mostly the same bugs so we have not tried to keep them separate (although we are cautious). I can't bear to think about a time that they have to keep apart. It will break their hearts and their spirit.

Blake, you have described it so well.
 
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