Cystic Fibrosis

my son

george had cf and we all miss him like crazy 26/03/1986 to 07/07/2007 xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx

Maggie Jones September 6, 2008

Remembering my daughter leanne...

A message to say im remembering my daughter leanne eccles(23/5/80) who sadly passed away on jan 5th 2007 of this awful illness....
To all the families out there who have lost people to this illness i would like to say you are not alone there are so many babies children any young adults who have sadly passed away and their families all feel the same way....... its too late for a cure for our children and young adults but lets not forget those being born everyday with cf and their families..
god bless all of those who have passed and may they stay safe and pain free with the angels now...
my heart goes out to all who are bereaved by this illness....
love to you all
carol eccles x

Carol Eccles May 20, 2008

Rhona, Stephen @ John Garry have all died of cystic fibrosis. My big brother was only 4, I was 2. I have a few precious memories of his short life, like visiting him in hospital and after he just vanished from my life, visiting his grave. A few years later When I was 6 my baby brother John Garry was born but only lived for the first 6 weeks, C F also claimed his life. I remember helping mum and dad to feed and change him when he got home from hospital for a few days. And then On the 14th July 1982 when I was 17 my beautiful baby sister Rhona came into the world, she departed from this world on the 21st November 2007, she was 25 years old, I am now 42. I don't know any other life other than a life that is consumed with cystic fibrosis and the resulting devastation that it brings to all the family's that have to endure the pain and grief of a loved one taken too soon. I'm trying really hard to look forward but its so painful, I cry every day and my mind is constantly filled with thoughts of my brothers and sister. I cherish the time that i was able to spend with my sister in the last 10 months of her life, staying over in hospital with her, just being there for her. We shared so much, laughter, love and of course many tears because we new what lay ahead. I was able to tell her how much I loved her and how proud I was to be her big sister. She is the bravest person i have ever known, she battled with courage and dignity until she drew her last breath, She was an inspiration to all who were blessed to know her. My heart aches for all who have lost loved ones to C F and to the ones who continue to have to watch them suffer.. God Bless you all..

Karen Fraser (Sister) March 18, 2008

hi everyone my name is kerry blackmore my daughter chloe aged 9 months died of this terrible disease on 31st may 05
i am going to raise some money for the cf trust and alderhey
the first day will be a sponsered run and the 2 day will be a concert my aim is to raise at least £700

Kerry Blackmore February 29, 2008

when I had this very beutiful little girl they told me she was perfect then on her 1st birthday she started being ill they told me she had hooping cough then she had some test it broke my heart when they told me that this little girl had cf I didn't know or had ever heard of this decease then they told mne she wouldn't be four but we fought for ever but sadly kimberley could not take any more and died at the age of six my whole world fell apart. I had not only lost my daughter but my best friend that was 20yrs ago and I still miss her more ever day this is a horrible thing for a child to go through because no mum should loose the little one. we must fight on to find a cure

Martha Davies (Mother) February 29, 2008

in this counrty there are so many people suffering from this illness, with all the fund raising people do for CF we must be nearer a cure, if not a cure an least to mek it easier to live with, Im planning to do the great north run to try an raise some more to send to them! im keeping everything crossed so that we dont have to keep loosing people we all love so much from this disease!!

love to everyone xx xx

Fay Calvert November 19, 2007

Lorraine...

Lorraine, if you would like your loved ones remembrance dates added to our list please contact me through the link with the dates. So sorry to hear of your loss.

Our thoughts and prayers are with you xxx

Gill November 16, 2007

my cousin craig was the first born to my cousin debbie who then knew nothing about cf, then came liam a good few years later by then craig had already been diagnosed with cf, it was then liam was also diagnosed.
sadly liam only lived until he was four years old the illness took over alot quicker with him and he just couldnt fight anymore.
it was only three years ago that craig passed at the age of 22 he fought so hard but towards the end it just got too much for him i miss them both very much and i just wish craig and i had made our peace before he passed. i will always be thinking of both of you. forever missed by everyone who knew them. all my love lorraine xxxxx

Lorraine (Cousin) November 14, 2007

my baby girl chloe marie blackmore died of this disease 31st may 2005 aged just 9 months 2 days before my 22nd birthday
she was diagnosed with this illness at 10 weeks
and sadly died through this illness
up untill my daughter had this illness i had never heard of cystic ffibrosis.then i did all the research my daughter chloe is also featured on this site chloemarieblackmore this is her page i miss you baby forever in my heart

Kerry Blackmore (chloes mummy) November 13, 2007

Breathe Easy

My daughter died at the age of 15 from this terrible disease in 2006. She is featured on this site. Her name was Lauren. We need to raise much more awareness of this disease and raise funds to help find a cure. I think a lot of people forget that there are still a lot of young people dying out there from CF. May they all breathe easy Now.

Ssss Sssss November 12, 2007