Kaethe, I read dasjdmum as saying her son had been pancreatic insufficient since he was 5 months old! Maybe she can tell us which she meant. However, I have heard from other people that they had to continue taking enzymes while on the new medicine since the pancreas was already damaged.
Nedda, I do think there is chance it will work on other Class III mutations. I don't know where you live but if I am not mistaken I thought I read there would be trials on other Class III mutations in the U.S. Also I thought I read that Europe was CONSIDERING making it available to other Class III mutations when approved. I am writing this from memory so I hope I am not steering you wrong. You should probably call the Vertex medical line and ask your questions if your doctor cannot tell you more.
Nedda, I do think there is chance it will work on other Class III mutations. I don't know where you live but if I am not mistaken I thought I read there would be trials on other Class III mutations in the U.S. Also I thought I read that Europe was CONSIDERING making it available to other Class III mutations when approved. I am writing this from memory so I hope I am not steering you wrong. You should probably call the Vertex medical line and ask your questions if your doctor cannot tell you more.