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    ….how can you help others with this terrible disease, if you don't know how truly devistating it is?”

    That is what my long awaited answer was…. some 2+ years ago. You can read my story here: although it is mainly just like everyone elses…

    Whew, try and find someone to treat you for it here in Illinois. NOT! I have to travel out of state to see a LLMD.

    Finally, diagnosed with “a lyme-like illness”(my LLMD will NOT call it Lyme) it is a Borellia infection and RMSF(Rocky Mt. Spotted Fever) after 3 years or so, p[/size] this terrible spirochetal brain infection unknowing it was there.

    I have learned so much since my journey began.

    I would like to share it with all of you, and maybe it will shed some light on all of this.

    I can not wait to get to know you all and share some thoughts and good times.




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