We will have things on my time. That in itself is relaxing and less stress.
Hehehe so yes i can do things when I want, after I ask permission. Hahahaha
I am less stressed. So thats great 👍
No one wants to feel like they are being used.
All week I have been with people who just want to help others. They are important. At least to me they are.
They have to get me back up and working on recovery before they Can stop.
They had me going 24 hrs a day . Then hard cord steroids . We had to stop the cancer from hitting ad destroying the nerves. They thought I had a stroke. Whole right side was gone. Made no sense to them. Until the tumor came beach on the CT. My oncologist also called and had contacted them. To make things short they have to get you stable.
I do nderstand the results of brain lesions and nerve damage. I am glad they were able to quickly figure out what was going on with you and start a course of action.
That is great that you understand the lesions. They are deep in the brain.
Well the ER has to follow their protocol. They see stroke. When the oncologist called and said they wanted a CT of the brain they had to comply . The oncologist radiation is from there hospital .
This was one of the plan that you hope you don’t have to use. Better prepared then to just react.
It helps that you are activily involved and understand the treatments. I'm pretty sure that is not the case with most patients that the oncologist works with.
I am going home. Checked out of Wesley now at VA ER. Getting meds to last for tuesday Apointment.
Been two hours and was just told
That is great news!
Its even greater sitting here in my chair, watching my TV hahahaha I could go on and on .
It is nice being home. Better
Good. Hope today is relaxing and you can spend it doing things when you want to do them, not when it fits into a hospital schedule!
We will have things on my time. That in itself is relaxing and less stress.
Hehehe so yes i can do things when I want, after I ask permission. Hahahaha
I am less stressed. So thats great 👍
Asking permission is essential in making the person who is doing all the caretaking work feel important!
No one wants to feel like they are being used.
All week I have been with people who just want to help others. They are important. At least to me they are.
And you too
Just got all pills and testing equipment
Checking out
Yay! That makes me so happy!
I am home. Gong to sleep great tonight
I hope you do. A good nights rest has to be healing! I don't know why hospitals haven't figured that out!
They have to get me back up and working on recovery before they Can stop.
They had me going 24 hrs a day . Then hard cord steroids . We had to stop the cancer from hitting ad destroying the nerves. They thought I had a stroke. Whole right side was gone. Made no sense to them. Until the tumor came beach on the CT. My oncologist also called and had contacted them. To make things short they have to get you stable.
I do nderstand the results of brain lesions and nerve damage. I am glad they were able to quickly figure out what was going on with you and start a course of action.
That is great that you understand the lesions. They are deep in the brain.
Well the ER has to follow their protocol. They see stroke. When the oncologist called and said they wanted a CT of the brain they had to comply . The oncologist radiation is from there hospital .
This was one of the plan that you hope you don’t have to use. Better prepared then to just react.
It helps that you are activily involved and understand the treatments. I'm pretty sure that is not the case with most patients that the oncologist works with.