Written on
May 26, 2011 by
Kelli in
Chronic Fatigue Syndrome/ME,
Depression and Mental Health,
Endometriosis,
Exercise,
Fatigue,
Fibromyalgia,
Limitations,
Medications & Treatments,
Original Post,
Pain,
Sleep,
Support,
Vent
The other day one of the trending topics was #50thingsIhate. One of the people I follow, @FibroWarriors, decided to list of her 50 things that she hates.. about fibro.. I figured I’d do that today myself for Fibro & CFS.. The most obvious, Pain.. no matter where it is, no matter how bad it is,…
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My last GP/PCP, Dr Caroline Newman, decided that because I am to high maintenance which requires additional work from both herself and her staff, so that I was no longer wanted in her practice. I was given a letter stating that she would continue to serve me as a patient for another 60 daysto give…
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Have I ever mentioned how much I hate my body?? If not, it’s official. I hate my body & not even from the Fibro this time. Between the CFS screwing with my sleep schedule, the IBS helping the CFS out with it’s erratic movements, and then adding my TMJ to the situation keeping me awake…
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There are the things I would like you to understand before you judge me… Please know that being sick doesn’t mean I’m not human. I may spend most of my day flat on my back and I might not seem like great company, but I’m still me stuck inside this body. I worry about school,…
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What would you do? How would you react? If you got told by the person that has been your primary support person for the last 3 + years.. That he/she doesn’t believe you’re sick? Doesn’t believe you’re really *that* tired? Doesn’t believe you’re in *that* much pain? And thinks it’s all in your head. I…
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I don’t think I’ve mentioned it.. but I Hate stupidity.. & ignorance.. People who think they have the right in everything. Yesterday, I was walking to the doctor’s office (she’s 3 blocks away) and I was standing to wait to cross the street.. now the intersection is a little odd.. one street runs E/W, the…
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