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Austria
In August 2011 the puzzle of my randomising symptoms finally got a name: chronic persistant lyme and neuroborreliosis. I created this blog to find and provide sharing. I guess you must be lymean to understand. ******************************** Im August 2011 bekamen all die diversen Symptome, Schmerzen, Probleme und Problemchen einen gemeinsamen Titel: chronische persistierende Lyme Neuroborreliose. Ich habe diesen Blog eröffnet, um Erfahrungen teilen zu können. Borreliose macht einsam, vielleicht muss man Borreliose haben, um das zu verstehen.

Sunday, January 29, 2012

Better dance than fight - so let's bolero

Doing my usual hot - hot! - shower to relieve pain and feel free, with the water stream new thoughts and ideas seem to stream into me too. So this is what I got today:

To fight against someone/something, you need to have the will, to be strong enough and to know much about the enemy. Many believe that life itself means fighting against all odds. Even birth can be a fight, not to talk about the end of life. Is it what I was looking for?  

What is the message of my lyme disease? I do not know enough about them borrelias, I have no chance to kill them all, I am not strong enough for it - not physically nor in my mind. So the message to me is... if I cannot fight I need to look for co-operation. Dance with them if you cannot kill them. I will try to learn more about them and listen.

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