I am super excited to be going to the Mayo Clinic this summer in Rochester Minnesota. There, I will be seeing 7 specialists about various problems I have encountered with NF. My family and I are all hoping that there is something that the doctors down there can do to help me. There is no cure for NF, but there are various treatments that can be used to treat any problems associated with NF.
This blog is intened to keep family and friends informed about what is going on while I am in the USA, and I hope that people find it useful in keeping them updated!
