hello everyone

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emerenta18

Guest
god its great being here,i was diagnosed with cf at 14 and have never met another person with cf,this site made me realise that there is other people here who went through what i went through,the illness,the misdiagnosis,the operations,the bullying by people who didnt understand,feeling like you dont have 'real' cf because you arent on loadsa meds,reading the posts here has made me feel a lot better,i still dont know lots of things about cf,and now i have been diagnosed for 5 yrs,my cf clinic isnt very forthcoming,and i have no idea about things like what i culture or my mutations,but im going to take a closer interest now <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
god its great being here,i was diagnosed with cf at 14 and have never met another person with cf,this site made me realise that there is other people here who went through what i went through,the illness,the misdiagnosis,the operations,the bullying by people who didnt understand,feeling like you dont have 'real' cf because you arent on loadsa meds,reading the posts here has made me feel a lot better,i still dont know lots of things about cf,and now i have been diagnosed for 5 yrs,my cf clinic isnt very forthcoming,and i have no idea about things like what i culture or my mutations,but im going to take a closer interest now <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
god its great being here,i was diagnosed with cf at 14 and have never met another person with cf,this site made me realise that there is other people here who went through what i went through,the illness,the misdiagnosis,the operations,the bullying by people who didnt understand,feeling like you dont have 'real' cf because you arent on loadsa meds,reading the posts here has made me feel a lot better,i still dont know lots of things about cf,and now i have been diagnosed for 5 yrs,my cf clinic isnt very forthcoming,and i have no idea about things like what i culture or my mutations,but im going to take a closer interest now <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
god its great being here,i was diagnosed with cf at 14 and have never met another person with cf,this site made me realise that there is other people here who went through what i went through,the illness,the misdiagnosis,the operations,the bullying by people who didnt understand,feeling like you dont have 'real' cf because you arent on loadsa meds,reading the posts here has made me feel a lot better,i still dont know lots of things about cf,and now i have been diagnosed for 5 yrs,my cf clinic isnt very forthcoming,and i have no idea about things like what i culture or my mutations,but im going to take a closer interest now <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
god its great being here,i was diagnosed with cf at 14 and have never met another person with cf,this site made me realise that there is other people here who went through what i went through,the illness,the misdiagnosis,the operations,the bullying by people who didnt understand,feeling like you dont have 'real' cf because you arent on loadsa meds,reading the posts here has made me feel a lot better,i still dont know lots of things about cf,and now i have been diagnosed for 5 yrs,my cf clinic isnt very forthcoming,and i have no idea about things like what i culture or my mutations,but im going to take a closer interest now <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
A

albino15

New member
Welcome!!!
Sounds like we have some things in common.
Sometimes I also feel like I don't have real CF because I'm not sick all the time or have to take alot of meds.
I have had a few surgeries to remove polyp from my nose and that's a pain.
glad you found the site.

Hannah 15 with CF
diagnosed at a month old.
 
A

albino15

New member
Welcome!!!
Sounds like we have some things in common.
Sometimes I also feel like I don't have real CF because I'm not sick all the time or have to take alot of meds.
I have had a few surgeries to remove polyp from my nose and that's a pain.
glad you found the site.

Hannah 15 with CF
diagnosed at a month old.
 
A

albino15

New member
Welcome!!!
Sounds like we have some things in common.
Sometimes I also feel like I don't have real CF because I'm not sick all the time or have to take alot of meds.
I have had a few surgeries to remove polyp from my nose and that's a pain.
glad you found the site.

Hannah 15 with CF
diagnosed at a month old.
 
A

albino15

New member
Welcome!!!
Sounds like we have some things in common.
Sometimes I also feel like I don't have real CF because I'm not sick all the time or have to take alot of meds.
I have had a few surgeries to remove polyp from my nose and that's a pain.
glad you found the site.

Hannah 15 with CF
diagnosed at a month old.
 
A

albino15

New member
Welcome!!!
Sounds like we have some things in common.
Sometimes I also feel like I don't have real CF because I'm not sick all the time or have to take alot of meds.
I have had a few surgeries to remove polyp from my nose and that's a pain.
glad you found the site.

Hannah 15 with CF
diagnosed at a month old.
 
S

Steve

New member
Hi i'm steve and i'm 16 years old with CF and i'm glad to be here as well if you need anyone to talk to just ask. I was diagnosed at 2 months old. Don't worry you will be ok CF can be very unusual but you just gotta keep going and no matter what there are people who will always understand you for you.
 
S

Steve

New member
Hi i'm steve and i'm 16 years old with CF and i'm glad to be here as well if you need anyone to talk to just ask. I was diagnosed at 2 months old. Don't worry you will be ok CF can be very unusual but you just gotta keep going and no matter what there are people who will always understand you for you.
 
S

Steve

New member
Hi i'm steve and i'm 16 years old with CF and i'm glad to be here as well if you need anyone to talk to just ask. I was diagnosed at 2 months old. Don't worry you will be ok CF can be very unusual but you just gotta keep going and no matter what there are people who will always understand you for you.
 
S

Steve

New member
Hi i'm steve and i'm 16 years old with CF and i'm glad to be here as well if you need anyone to talk to just ask. I was diagnosed at 2 months old. Don't worry you will be ok CF can be very unusual but you just gotta keep going and no matter what there are people who will always understand you for you.
 
S

Steve

New member
Hi i'm steve and i'm 16 years old with CF and i'm glad to be here as well if you need anyone to talk to just ask. I was diagnosed at 2 months old. Don't worry you will be ok CF can be very unusual but you just gotta keep going and no matter what there are people who will always understand you for you.
 
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emerenta18

Guest
hey steve and hannah!! everyone is really nice and understanding here,thanks for the replies and its nice to have people to talk to <img src="i/expressions/face-icon-small-smile.gif" border="0"> yes i guess cf is different for everyone,if you wana chat im here anyway even though i dont know a lot about cf <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
hey steve and hannah!! everyone is really nice and understanding here,thanks for the replies and its nice to have people to talk to <img src="i/expressions/face-icon-small-smile.gif" border="0"> yes i guess cf is different for everyone,if you wana chat im here anyway even though i dont know a lot about cf <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
hey steve and hannah!! everyone is really nice and understanding here,thanks for the replies and its nice to have people to talk to <img src="i/expressions/face-icon-small-smile.gif" border="0"> yes i guess cf is different for everyone,if you wana chat im here anyway even though i dont know a lot about cf <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
hey steve and hannah!! everyone is really nice and understanding here,thanks for the replies and its nice to have people to talk to <img src="i/expressions/face-icon-small-smile.gif" border="0"> yes i guess cf is different for everyone,if you wana chat im here anyway even though i dont know a lot about cf <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
E

emerenta18

Guest
hey steve and hannah!! everyone is really nice and understanding here,thanks for the replies and its nice to have people to talk to <img src="i/expressions/face-icon-small-smile.gif" border="0"> yes i guess cf is different for everyone,if you wana chat im here anyway even though i dont know a lot about cf <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
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