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April 2, 2011


My first infusion in the Infusion Center.
I have been diagnosed with Lyme Disease since November 9, 2010...approximately four months.  My life has been twisted upside-down with this diagnosis.  Really early on in my treatment I was encouraged to write a journal, keep a diary, log my symptoms and none of these were appealing to me...until now.  I think I am finally at a point where I can share where I am at with all this disease has to offer.  Give insight to my friends and family on how I am handling all these changes in my life.  I have never really been much of a reader nor a writer and it is even worse with my "lyme brain" or as I call it "brain fog".

This blog is going to be very challenging for me to expose myself to the world and be okay with showing my unclear thinking patterns and poor word choice because it is a process of me not trying to impress you or anyone else reading this, but really to track my progress and push myself to get better.


  1. Yay! I'm so glad you finally started a blog!!
    I think it will be beneficial for you, but also for all of us who love you and many other people who are new to Lymes disease!
    Love you!

  2. Love it. So glad to be reading your blog!!