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hazer

HealingWell Forum
>
Member Profile
Display Name
hazer
Profile Created
7/16/2008 3:24 PM
Last Seen
3/30/2011 5:34 PM
Total Posts
33

Last 50 Posts

lookin 4 info

im considering bring my daughter to canada for 3 months this summer.but when i was in america last i couldnt work her nebulizer as they run on different power. what should i do? has any1 had the same...

3/30/2011 6:31 AM

Cystic Fibrosis
hi Darkies Gem

your not going to believe this! last friday i was talking to a friend of mine about the hospital in mullingar the one i was telling you about, when they messed up with taking out gypsys long line and...

12/1/2008 11:12 AM

Cystic Fibrosis
hi Darkies Gem

gypsy's on tobi at the moment aswell. shes been on and off it now 4 about 6 months or more. but she seems to be doing well with it. i nearly had a heart attack when we got to america her nebulizer...

11/24/2008 5:44 AM

Cystic Fibrosis
hi Darkies Gem

hi gemma,hazel here havent been on the site in a while now. have been quite busy was over to /community/emoticons/cool.gif disney world with gypsy it was brill :) was sad to be comin home we had such...

11/23/2008 9:58 AM

Cystic Fibrosis
Hazer-Re: Health costs in the USA

Has anyone seen the movie Sicko, i watched it the other day. Its a bad time when a country can load money into a war on the other side of the world from them, thats going no where, when there own...

11/23/2008 9:32 AM

Cystic Fibrosis
daily routine

Hi jessie. my name is hazel I dont have cf ,my six year old daughter has so i'll give you a quick run down of her day . IN the morning she takes her nebs thats ventolin then she has an accapella...

8/27/2008 4:41 AM

Cystic Fibrosis
The cf gene

Thats strange james my boy friend got tested , it came back clear but they told me 1 in 1000 chance he could still be a carrier. and i far as i know in Ireland cf testing is not encluded in the heal...

8/27/2008 4:22 AM

Cystic Fibrosis
The cf gene

Just found out that my boyfriend does not carry the cf gene from what they have tested him on but there is still a 7.2% chance that he could still carry a more rare shrain of the gene. Dose anyone...

8/26/2008 8:32 AM

Cystic Fibrosis
i feel so alone

I keep my fingers crossed for a cure . hopefully a miracle will come soon . untill that day comes we just have to try and be as strong for our kids as we can . i wish it was me that got it and not...

8/12/2008 3:58 AM

Cystic Fibrosis
New in Chicago

hi raisen, i was just wondering i,m from ireland and here in my situation i have all my healthcare paid for, my question is if you have cf in america is your medical care all paid for, by the...

8/9/2008 11:44 AM

Cystic Fibrosis
i feel so alone

jesus i havent a clue about computers just gettin the hang of this, a bit. where are you planing to go on holidays ? i probably already told you but were heading to disney world in september i cant...

8/9/2008 11:28 AM

Cystic Fibrosis
i feel so alone

forgot to ask did you get your tatoo done yet ?...

8/9/2008 9:59 AM

Cystic Fibrosis
i feel so alone

do you realy want to know sad i realy am :) me and my boyfriend watched the first two movies of "the lord of the rings " and i stopped through the 3rd 1. I think my brain has serously melted a bit :)...

8/9/2008 9:58 AM

Cystic Fibrosis
i feel so alone

Eastenders, cornation street and emmerdale im hooked cause thats when i do gypsys nebs and accapella. such a battle :) shes gas the hole time im watchin it im counting then 3 huffs and on again its...

8/8/2008 3:45 PM

Cystic Fibrosis
i feel so alone

Keep the chin up wont you ! I had that with gypsy aswell they wouldnt let her into a playschool, i gave out stink so she rang me back a few days later and said that gypsy could share a day with a boy...

8/8/2008 8:08 AM

Cystic Fibrosis
i feel so alone

hi jessy thanks for the comment but 1 thing i want to know,you are 23 and gypsy is on the same medication as you and shes only 6 does that mean that she is really sick with it? (Darkies gem can u...

8/7/2008 9:07 AM

Cystic Fibrosis
i feel so alone

Thank you so much 4 that xx. i know. i walk down the street and gypsy will start coughing and people will stare at me and say things like you need to bring that child to the doctuir i used to answer...

8/6/2008 2:53 AM

Cystic Fibrosis
im new im Andrew

well andrew im hazel im new to this aswell.i'm old ,24. i dont have cf,my daughter has shes 6. any crack with u? how r u gettin on?tell me all about yourself i'd b glad of some 1 to chat to x...

8/3/2008 6:22 AM

Cystic Fibrosis
i feel so alone

im finding it so hard to cope i need some help,nobody around here understands whats going on. i think im on the furge of a brake down. what will i do?gypsy is well takin care of but im in depression...

8/2/2008 10:23 PM

Cystic Fibrosis
marrying someone with cf and insurance issues

i have planed 2 bring my daughter to disney world in september and i couldnt believe it when the insurance company rang me back and said they wouldnt cover her. for god sake its only 4 two weeks, i...

7/29/2008 4:34 AM

Cystic Fibrosis
bubble gum club in ireland

thanks a mill, no where from the midlands in ireland. havent been on the internet 4 a few days it was broke im going to look up about them now....

7/29/2008 10:18 AM

Cystic Fibrosis
bubble gum club in ireland

my daughter is 6 with cf i want to get her involved with the bubble gum club or some sort of organisation like that 1 i think she would realy enjoy it.if any1 knows anything about it please let me...

7/17/2008 2:00 PM

Cystic Fibrosis
Two small children with CF

i might just copy your tatoo idea but i think i'd get the number 65(if anything it would b cheaper /community/emoticons/tongue.gif )gypsys canulas dont last long the last time she was in hospital...

7/17/2008 4:20 AM

Cystic Fibrosis
Two small children with CF

i just turned 24 i had my baby when i was 17,GYPSY.when we were sent 2 crumlin i was callin it statistic fibrosis i had'nt a clue. (i still dont have a clue) i thought it was the end of my world,it...

7/16/2008 4:26 PM

Cystic Fibrosis
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