This is a sample guest message. Register a free account today to become a member! Once signed in, you'll be able to participate on this site by adding your own topics and posts, as well as connect with other members through your own private inbox!
Ok I figured it out. You hae to go down to the bottom and do a search. There are 162 of me in the database. This is good an bad. They know nothing about me and really can't help. They are guessing.
You may actually be part of the data base; I think most of us are.
At some point your CF Center probably gave you a form to sign which allowed them to share some of your data anonymously (without using you name) with other organizations. That is where the genetic data base complied at CFTR2.org comes from.
You may actually be part of the data base; I think most of us are.
At some point your CF Center probably gave you a form to sign which allowed them to share some of your data anonymously (without using you name) with other organizations. That is where the genetic data base complied at CFTR2.org comes from.
Yes I am. There are only 162 of me in the world. They know little to nothing about my mutations. Makes it very hard for me to get appropriate treatment.
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.