My daughter Kealy needs help.

My daughter has a rare form of atypical HUS. This is her 3rd bout with it. We have been through this with no answers. This time it's seems there might be hope for some answers. This form of HUS never goes away the best we can hope for is a regiment that can keep it at bay. At this point she is still touch and go. Kealy is a fighter and I'm proud to be her dad. For a 7 year old she amazes me everyday. If you could help in any way you can we would very much appreciate. I love my daughter with all my heart. Thanks for taking the time.