my son is just out of hospital

katie4byz

New member
Hi Bill am in the UK so things work different here but I am not going to give up untill I have the answers that we need, what I mean by moving hospital and making things worse is that the other hospital may be worse than the one he is at then what do I do?
Thanks Becca's mom, no my son not had a sinus CT I could ask for one? Also yes the nebulizer is working brilliant hes clearing out everyday with it.
 

katie4byz

New member
Hi Bill am in the UK so things work different here but I am not going to give up untill I have the answers that we need, what I mean by moving hospital and making things worse is that the other hospital may be worse than the one he is at then what do I do?
Thanks Becca's mom, no my son not had a sinus CT I could ask for one? Also yes the nebulizer is working brilliant hes clearing out everyday with it.
 

Printer

Active member
There has to be a CYSTIC FIBROSIS FOUNDATION or something like it in the UK.

There are patients on here from the UK.

Post a question: WHERE IS THERE A GOOD CF CLINIC NEAR _________.

Bill
 

Printer

Active member
There has to be a CYSTIC FIBROSIS FOUNDATION or something like it in the UK.

There are patients on here from the UK.

Post a question: WHERE IS THERE A GOOD CF CLINIC NEAR _________.

Bill
 

albino15

New member
The UKs version of the CFF is called the cystic fibrosis trust, the web address is cftrust.org, they have a link to a list of CF centers in the UK

Just click on the "about cf" link then click on "CF care" you should see "UK specialist CF centres" hope this helps.
 

albino15

New member
The UKs version of the CFF is called the cystic fibrosis trust, the web address is cftrust.org, they have a link to a list of CF centers in the UK

Just click on the "about cf" link then click on "CF care" you should see "UK specialist CF centres" hope this helps.
 

CrisDopher

New member
The UK has the CF Trust, I believe. I have seen their lime-green jerseys while running the NYC marathon. (Them running, not me. Though I did that once, too.)
 

CrisDopher

New member
The UK has the CF Trust, I believe. I have seen their lime-green jerseys while running the NYC marathon. (Them running, not me. Though I did that once, too.)
 

katie4byz

New member
Hi yes done that and where my son is being seen is our local one, I would prefer my son not to have CF but if he has I want to know properly and get the Diagnosis. I just don't understand from what I am reading that people have a Diagnosis with one gene yet my son is'nt. I just don't know how to make sure my son is getting the best!
 

katie4byz

New member
Hi yes done that and where my son is being seen is our local one, I would prefer my son not to have CF but if he has I want to know properly and get the Diagnosis. I just don't understand from what I am reading that people have a Diagnosis with one gene yet my son is'nt. I just don't know how to make sure my son is getting the best!
 
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