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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.

Thursday, February 2, 2012

From tears to smile

I seldom have a headache but today I felt bad with bang head and a light virtigo. It was going for migraine and on my way home from office I had tears running down my cheeks. Not just because of pain, not really - but because of general weakness, general bad feeling. I did not even know exactly why tears were falling. Was like an all over resignation.
Anyway, that little pain killer did its job (I really try to avoid meds, this time I allowed myself to take one pill as this would be better than crash with a sick headache for 24 hours). Now I am back on line, on life - smiling. Off pain.

See, those Borrelias are dancing with me. Sometimes changing within a few hours. I should not forget this when it comes to pain next time.





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