Cystic Fibrosis

I lived: One republic raising awareness for Cystic Fibrosis

I was just reading the From A to Pink blog which you can see here which is written by a lady called Katherine who was diagnosed with a "mild" form of cystic Fibrosis at the age of 16, when I came across this video which she encouraged her readers to watch: http://www.youtube.com/watch?v=z0rxydSolwU I personally have not… Continue reading I lived: One republic raising awareness for Cystic Fibrosis

Advertisements
Cystic Fibrosis, Family, Photos

Living in the moment- coping with your child’s diagnosis

Even though I have known about Joseph's cystic Fibrosis for 15 months I still struggle to cope with the idea that my child has an incurable, life shortening illness and I probably always will. Some days when he is well, which luckily for us at the moment is more often than not, I still imagine… Continue reading Living in the moment- coping with your child’s diagnosis

Photos

Tonsillitis

Joe had a trip to the hospital recently, but is now nearly fully recovered. We went out to buy him a paddling pool and play in granny and grandpa's garden in the sunshine but all our best intentions were thwarted as Joe was very lethargic and grumpy and wouldn't go anywhere near the paddling pool.… Continue reading Tonsillitis