
Katie Bailey
im 19 and was diagnosed with cf at 3 after my sister....my annual review monday and had a lung function of 97% :D (touch wood it stays that way!) never really tell people i have cf as i dnt want people to treat me carefully as im as fit as themselves...i live everyday to the full as you never know what is around the corner!!
lets hope i stay strong for another 19yrs

Chloe i' ve got cf xx

Joanne 'Rigby' Brayshaw Hi - Has anyone out there experienced discrimation when trying to get there CF affected child into primary school? Any comments/advice/experience sharing welcomed.........

Elaine Butler
Hi, I am after some advice if anyone can help - my husband has CF and our 2 year old daughter has just been diagnosed with Swine flu. We are concerned that my husband may catch it and our CF consultant has advised that he should have the swine flu immunisation however our GP has said that they immunisations are not ava...ilable until December. Does anyone know if this is true? The GP has a sign up in their surgery saying that they wuill have the vaccination from October and we now dont know what to do. ThanksRead More

StrongThunderbird April big props to this trust my niece has CF.

Cystic Fibrosis Trust We are looking for someone to take part in article who had life saving treatment in time for Christmas (e.g. a transplant), or whose partner/child had life saving treatment in time for Christmas. Please contact gfoy@cftrust.org.uk with some more info about yourself if you are interested.

Simon Parker i am just wonderin if there are any lads or girls out there that are in the same boat as me. i am in a relationship with someone who suffers with cf. and just wants too know how other couples where one person has it how the other one finds it copin and stuff

Jaynee Harsum
thank you for this page it has made me smile laught and cry ... from a mother of 3 beautiful daughter ...leanne passed away age 10 weeks of CF... charlotte 20 has CF and is getting married in wow 10 weeks ...and lily who is a carrier ... sometimes the tears we have shed as a family could fill every ocean. but the me...mories that we have made as a family are lite by every star that glows in a beautiful clear summer sky love you my beautiful daughters x x xRead More

Cystic Fibrosis Trust Christmas is coming! Buy your CF Trust Christmas cards today and help raise vital funds http://www.cftrust.org.uk/cfshop/
Source: www.cftrust.org.uk
Registered Charity No. (England and Wales) 1079049 Registered Charity No. (Scotland) SC40196Registered Company No. 3880213

David McGow I am nearly 43 years old and still doing quite well and my next achievement would be to reach my 50th!!

Cystic Fibrosis Trust 's feed: CF Trust Blog
YOUNG SINGER SONGWRITERS TEAM UP TO SEE OFF CF
A charity single and album are set to raise vital funds for the Cystic Fibrosis Trust. The project has been masterminded by manager and promoter Lee Robson from Rochdale, who wanted to do something for the charity after meeting one of its young ambassadors who has Cystic Fibrosis, Kelli Gallache...
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A charity single and album are set to raise vital funds for the Cystic Fibrosis Trust. The project has been masterminded by manager and promoter Lee Robson from Rochdale, who wanted to do something for the charity after meeting one of its young ambassadors who has Cystic Fibrosis, Kelli Gallache...
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Karen Ratcliffe
Halloween Ball in Tadcaster raised £800 for Cystic Fibrosis on Saturday. Check out the photos at http://www.wallworksphotography.co.uk/HA LOWEENBALL.aspx

Cystic Fibrosis Trust A charity album featuring young talented singer-songwriters will raise vital funds for the CF Trust. Find out more http://tiny.cc/a3gRc
Source: tiny.cc

Lorraine Barnes
GET IT OFF YOUR CHEST t-shirts, hoodies and tote bags on sale NOW. Ideal Christmas presents. Log on to http://www.mrblippy.co.uk for more details.
http://www.onetruemedia.com/shared?p=867 e97d547f20a2a20203d&skin_id=601&utm_sour ce=otm&utm_medium=text_url









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