So with that said, what do you do with all that "stuff" in your head.
I have tried every thing I could to deal with the stress and fears of living with Crohn's disease.
- Denial - only lasts so long when you gut hurts
- Anger - keeps coming back no matter how I work on it
- Stifling - probably what makes my gut hurt more
- Isolation - the pity party that says "nobody understands"
- Negotiating - trying to find someone who cares and can give me hope. "God please let me get well and I will ________(fill in the blank) or I will do yoga three times a week, not take out my frustration on my loved ones if only _______ (fill in the blank)
- Acceptance - well it's really more like resignation that this is my reality after dealing with it for 25+ years. And I am still here!
- Hoping for Hope - searching for a new medication, trial, doctor, break through, anything
- Hope - being well enough to think and function again
Sound familiar?
So, I am now starting a phase of Hope - Yeah for me. The brain fog is lifting; my anemia/blood work is back to normal; my muscle fatigue doesn't show up until 15-30 minutes after doing housework; and lots and lots of rest.
Okay, okay, so I am a work in progress.....
Next post - I am hopeful about an acupressure technique called EFT, Emotional Freedom Therapy.
Sounds good doesn't it!
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