Moving out of 'home'

theLostMiler

New member
I took a long time to write back, because for now, I am out of ideas... you are definitely in a tight spot and I wish I knew a better way to help you out.
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<br />Again, I would totally ask your doctors about what they think about a port.
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<br />And as for CFRD, I am sometimes borderline (if I am sick, the inflammation really boosts my numbers) but I havent really changed anything in my diet yet.
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<br />That is something that is pretty confusing for me at least, I have a CF friend in Maine that has it and she seems to do okay with it, but I do believe there is a bit of a learning curve once you are diagnosed. I saw you answered that your sister has it, so you probably know more about it than I.
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<br />If I think of any ideas or you have any updates please post them <img src="i/expressions/face-icon-small-smile.gif" border="0"> I hope you can find a way to get all the stuff done that we need done, it is always a struggle especially by yourself.
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b12bc

New member
Again, thanks. I guess I'll just have to do some adjusting and try to use willpower to combat laziness. I'd love to hear from anybody else as well who has dealt with this.


May I ask where your friend in ME is? I used to live there <img src="i/expressions/face-icon-small-smile.gif" border="0"> My sister did have CFRD but she passed several years ago and I honestly didn't pay much attention to the finer details of it. I just remember her keeping a food log and having the pump, but I never really thought too much about it at that point.
 

b12bc

New member
Again, thanks. I guess I'll just have to do some adjusting and try to use willpower to combat laziness. I'd love to hear from anybody else as well who has dealt with this.


May I ask where your friend in ME is? I used to live there <img src="i/expressions/face-icon-small-smile.gif" border="0"> My sister did have CFRD but she passed several years ago and I honestly didn't pay much attention to the finer details of it. I just remember her keeping a food log and having the pump, but I never really thought too much about it at that point.
 

b12bc

New member
Again, thanks. I guess I'll just have to do some adjusting and try to use willpower to combat laziness. I'd love to hear from anybody else as well who has dealt with this.
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<br />
<br />May I ask where your friend in ME is? I used to live there <img src="i/expressions/face-icon-small-smile.gif" border="0"> My sister did have CFRD but she passed several years ago and I honestly didn't pay much attention to the finer details of it. I just remember her keeping a food log and having the pump, but I never really thought too much about it at that point.
 

theLostMiler

New member
She lives in Saco, ME, she is 19/20 age. I am sorry to hear about your sister. You sure dont have it easy at all.

Hoping someone else can answer this too <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

theLostMiler

New member
She lives in Saco, ME, she is 19/20 age. I am sorry to hear about your sister. You sure dont have it easy at all.

Hoping someone else can answer this too <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

theLostMiler

New member
She lives in Saco, ME, she is 19/20 age. I am sorry to hear about your sister. You sure dont have it easy at all.
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<br />Hoping someone else can answer this too <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

b12bc

New member
Wow! Saco is maybe 20 minutes from where I lived. I'm a little more than 2 hours from there now.

Thank you for your condolences. No part of CF is easy or fun, and losing loved ones is among the most difficult parts, but we have to just keep going.
 

b12bc

New member
Wow! Saco is maybe 20 minutes from where I lived. I'm a little more than 2 hours from there now.

Thank you for your condolences. No part of CF is easy or fun, and losing loved ones is among the most difficult parts, but we have to just keep going.
 

b12bc

New member
Wow! Saco is maybe 20 minutes from where I lived. I'm a little more than 2 hours from there now.
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<br />Thank you for your condolences. No part of CF is easy or fun, and losing loved ones is among the most difficult parts, but we have to just keep going.
 
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