PreciousJewel
New member
i have been told by my doctors that something is in the offering in relation to CF...I have been told that they are looking at large clinical Trails where by Cf'ers will have to use a nebuliser maybe 4 times a year which will put the corrected gene into the lungs..My doc says its like money in the bank saving for a rainy when it comes to looking after your child....I am feeling rather down at the mo as i am scared for the future. What do you all think???/ Have your Docotrs been saying any of this....
I need to know that there is hope out there
I need to know that there is hope out there