I am trying to go as long as possible on absolutely no medications in order to gain clarity on my problems. I am only using estrogen cream right now externally twice a week. My identical twin sister uses the exact cream for a few years with no problem so it's nothing to do with that. That also goes for no cortisone injections. I want to definitely know I do not have a late infection before complicating things with the injection. I am managing my walking just fine for now.
I heard a doctor on public television say that the secret to a long life was making good decisions. I guess I did not make good decisions. I have forgiven myself. I trusted my GP, OS, and dentist to guide me and they all said that they did not see any reason for me not having this hip replacement. Endo said he saw nothing and dentist said ,I don't know what to tell you."
I wish someone had said "run don't walk away from this surgery."
Now that I have been able to stay off all antibiotics for 4 months, I wish I could get another blood test for C reactive and sed rate.
I feel better now that I am off of everything. I was hoping that the itching and stinging of my skin, the bladder pain, anal rectal pain and stomach pain would go away. But they haven't. I know these are chronic life long conditions now.
If I could get rid of that, I would live with the limitations of my hip. I can walk. Just not for long. I have to limit my walking. For instance do one errand a day. Not all day on my feet or all day lying down.
Traveling seems like a distant dream. Last night I chatted on the phone with my daughter. She is so lovely. When I hung up the phone I buried my head in my lap and began wailing, I could not tell her that I have gastroparesis now. I always looked forward to dancing at her wedding one day and lots of wonderful times.
I will be honest. When I dreamed if how I would be after this surgery I had high hopes. I am left dealing with a tragedy and an uncertain future.