Hi, I’m a genetic counseling student who is interested in learning more about what childhood and adult life is like for people with achondroplasia. I am hoping to be a prenatal genetic counselor, and though I have not yet met parents expecting a child with achondroplasia, I want to be able to help them as much as possible when the day comes. Any thoughts you could provide, such as what good and/or negative experiences, challenges, joys, etc. you have had would be greatly appreciated!
