Kiara’s CCAM Lung Operation

My daughter Kiara was born with a really rare condition called CCAM.  

Her left lung grew mainly as a cyst rather than a full healthy lung, this pushed her heart over to the right hand side and she only has the function of her right lung which is now under pressure from her bad lung and her heart.

When this was diagnosed at 20 weeks during the pregnancy Kiara was given little to no chance of survival but she has defied all the odds and she really is a true miracle baby and a true CCAM warrior.

Those that know Kiara have all said how much of a fighter she is and you couldn’t meet a happier baby even though she can’t fully do everything a healthy baby can do and due to only having 1 lung is constantly living with pneumonia. We have been waiting for Kiara to have an operation to remove 80% of her left lung for a year now and the time has finally arrived, our little girl will be going in for her lobectomy operation in a couple weeks and we all pray it will start her on her long path to recovery and allow her to live her life fully.

I’m raising money to help with the costs associated with the operation and to hopefully treat Kiara to something amazing to look forward to when she has fully recovered and is CCAM free.

Thank you so much for taking the time to read about my precious little girl.