Tuesday, June 14, 2011

The Mayo Clinic!

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!

3 comments:

  1. I can guess that you will be super excited to go to the Mayo clinic. It would be great to get some answers about your NF.
    I will be looking forward to following this journey.

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  2. Courtney,

    I'm excited at what you are starting Rochester Minnesota. I will do my best to visit here often. Please send me a email if you know of a way I can be a help to you. I would be very happy to help where needed. Make it a tremendous day. Reggie

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  3. Well, I am having fun. Don't know if the first msg went through so I am trying again Glad to hear your flight went well and you have met some nice people so far.... Talk to you later. Luv Auntie Di

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