Possible Move to Raleigh/Durham

catboogie

New member
Allie,

Thanks for letting me know about the concert. I think it's great you guys are continuing to do fund raisers for the CF foundation.

How is your daughter doing?

As you know, it's not a good idea for cystics to congregate... I'm not sure how many cystics might be at this show. But these days I'm reluctant to go somewhere public because of the possibility of cross-contamination.

Thank you for thinking of me, though. <img src="i/expressions/face-icon-small-smile.gif" border="0"> And I hope the show is a big success!
 

catboogie

New member
Allie,

Thanks for letting me know about the concert. I think it's great you guys are continuing to do fund raisers for the CF foundation.

How is your daughter doing?

As you know, it's not a good idea for cystics to congregate... I'm not sure how many cystics might be at this show. But these days I'm reluctant to go somewhere public because of the possibility of cross-contamination.

Thank you for thinking of me, though. <img src="i/expressions/face-icon-small-smile.gif" border="0"> And I hope the show is a big success!
 

catboogie

New member
Allie,

Thanks for letting me know about the concert. I think it's great you guys are continuing to do fund raisers for the CF foundation.

How is your daughter doing?

As you know, it's not a good idea for cystics to congregate... I'm not sure how many cystics might be at this show. But these days I'm reluctant to go somewhere public because of the possibility of cross-contamination.

Thank you for thinking of me, though. <img src="i/expressions/face-icon-small-smile.gif" border="0"> And I hope the show is a big success!
 

catboogie

New member
Allie,

Thanks for letting me know about the concert. I think it's great you guys are continuing to do fund raisers for the CF foundation.

How is your daughter doing?

As you know, it's not a good idea for cystics to congregate... I'm not sure how many cystics might be at this show. But these days I'm reluctant to go somewhere public because of the possibility of cross-contamination.

Thank you for thinking of me, though. <img src="i/expressions/face-icon-small-smile.gif" border="0"> And I hope the show is a big success!
 

catboogie

New member
Allie,
<br />
<br />Thanks for letting me know about the concert. I think it's great you guys are continuing to do fund raisers for the CF foundation.
<br />
<br />How is your daughter doing?
<br />
<br />As you know, it's not a good idea for cystics to congregate... I'm not sure how many cystics might be at this show. But these days I'm reluctant to go somewhere public because of the possibility of cross-contamination.
<br />
<br />Thank you for thinking of me, though. <img src="i/expressions/face-icon-small-smile.gif" border="0"> And I hope the show is a big success!
 

allie5

New member
Hey Catboogie:

The only CF person that I know will be there is someone that has received a lung transplant. She is actually the author of "Sick Girk Speaks" Have you heard of her or her book? I know none of us CF families are taking our children with CF (even though I am taking Allie to sound check since it might be her only time to see her dad's band play)

I totally understand your hesistance.

Allie is currently doing well. Only one round of TOBI was needed this past year <img src="i/expressions/face-icon-small-smile.gif" border="0"> How are you doing??? My email is amyplymale@gmail.com if you want to email me sometime!

Thanks, Amy
 

allie5

New member
Hey Catboogie:

The only CF person that I know will be there is someone that has received a lung transplant. She is actually the author of "Sick Girk Speaks" Have you heard of her or her book? I know none of us CF families are taking our children with CF (even though I am taking Allie to sound check since it might be her only time to see her dad's band play)

I totally understand your hesistance.

Allie is currently doing well. Only one round of TOBI was needed this past year <img src="i/expressions/face-icon-small-smile.gif" border="0"> How are you doing??? My email is amyplymale@gmail.com if you want to email me sometime!

Thanks, Amy
 

allie5

New member
Hey Catboogie:

The only CF person that I know will be there is someone that has received a lung transplant. She is actually the author of "Sick Girk Speaks" Have you heard of her or her book? I know none of us CF families are taking our children with CF (even though I am taking Allie to sound check since it might be her only time to see her dad's band play)

I totally understand your hesistance.

Allie is currently doing well. Only one round of TOBI was needed this past year <img src="i/expressions/face-icon-small-smile.gif" border="0"> How are you doing??? My email is amyplymale@gmail.com if you want to email me sometime!

Thanks, Amy
 

allie5

New member
Hey Catboogie:

The only CF person that I know will be there is someone that has received a lung transplant. She is actually the author of "Sick Girk Speaks" Have you heard of her or her book? I know none of us CF families are taking our children with CF (even though I am taking Allie to sound check since it might be her only time to see her dad's band play)

I totally understand your hesistance.

Allie is currently doing well. Only one round of TOBI was needed this past year <img src="i/expressions/face-icon-small-smile.gif" border="0"> How are you doing??? My email is amyplymale@gmail.com if you want to email me sometime!

Thanks, Amy
 

allie5

New member
Hey Catboogie:
<br />
<br />The only CF person that I know will be there is someone that has received a lung transplant. She is actually the author of "Sick Girk Speaks" Have you heard of her or her book? I know none of us CF families are taking our children with CF (even though I am taking Allie to sound check since it might be her only time to see her dad's band play)
<br />
<br />I totally understand your hesistance.
<br />
<br />Allie is currently doing well. Only one round of TOBI was needed this past year <img src="i/expressions/face-icon-small-smile.gif" border="0"> How are you doing??? My email is amyplymale@gmail.com if you want to email me sometime!
<br />
<br />Thanks, Amy
 
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