Tuesday, July 31, 2012

spirochetes This means war!!!!!


spirochetes This means war!!!!!I started the doxycycline yesterday around 1pm - 100 mgs. taking my next dose around 12am - 100 mgs. I already have hives on one of my feet. It Burns and itches.  Hurts to touch.  woke up this morning and took another dose and now I feel really crappy. nausea, vomiting, tingling in random parts of my body. dizziness, dry itchy eyes.  but I do have to say that there is little head pain to report today. herxing is the worst.  I think I was in the middle of Lyme Flare and the spirochetes and whatever other bacteria that maybe in there are really pissed off. I feel as though my whole body is under attack and I can not control it.  I just want to be better. 
I wanted to talk a little about psychosomatic.  and what exactly that means.  if someone is experiencing symptoms that one does not understand or has never heard of or experienced then that makes one crazy. the thought that one would psychosomaticly give themselves hives, headaches, vomiting, etc. is way beyond my capabilities of comprehension. why in anyone's name would one make this shit up. really why. which brings me back to a previous post that I never posted.
the edited version would be "Duck you" Duck You to all the people that ever doubted you. Duck you to anyone that ever said it was all in your head.

spirochetes are real and anyone who has ever shared a space with them know that the real. why is this a topic that is so controversial. why is it again that big business rules all... Including the quality of healthcare which one receives. why are there not more doctors llmds. why is it there are not more regular physician's that test for Lyme and Co infections. why must one go undiagnosed for so long only to be told that what they are feeling is not real.  does the world really believe that as many people that suffer from this illnesses are faking it.  Really

As I mentioned in a recent post, my bacteria have set up camp in my head.  hence all the neurological problems that I have. Besides the autoimmune blood clotting disorder.  Which could take a blog on all by itself. there is limited resources and information on the topic.

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