Welcome Valarie!

@Vhopper

Welcome to Ben’s Friends, Valarie.

If you take a look at many of the posts in this forum, there’s alot of frustrated people that are in the same boat as your daughter, Emily. They have all of the symptoms and have done lots of tests, but they still can’t seem to get the diagnosis.

Since you are here on her behalf, I encourage you to get involved in the community, ask questions and start discussions. This place is for you to learn more about Chiari, understand other patient’s experiences and relate them to Emily’s experiences so far. She is young, so I can imagine that this is very difficult for her.

Once again, welcome to Ben’s Friends, Valarie.