- Post starter
- #13
J
just me here
Thanks for keeping me grounded everyone. It is as I suspected, my T is required to cut and paste EVERYTHING into my health record where all can see it. BUT, she has been editing it down to an acceptable level of anger or cursing or whatever it was I was guilty of at the time, and even then only moving the stuff that was directly related to my diagnosis or when I asked her to forward info to other docs.
The rule came after I was using the email to talk to her, so she didn't apply it to my situation, or tell me about the new rule.
All is Okay, I am still in a trustworthy caregivers office and will be there for the foreseeable future.
A story about trust as it applies to Dr./ Patient confidentiality:
I was diagnosed with Hepatitis C and beat it in 2005.
My job required me to work with razor sharp tools all the time, I was constantly exposed to sharps, I was constantly in danger of getting cut and contaminating very expensive cutting tools. And I was looking at a treatment that could limit my ability to work for up to a year.
The first place I went was to my companies Human Resources department and I told the head of the department all I knew about my situation. I thought they should know, it was the right thing to do.
Our HR head was on the board of directors of our local hospital, so after talking to me he called the hospital to get more information. He was put in touch with a Dr. that explained the risks, methods of transfer etc. Our HR head evidently asked some pretty specific questions, and after their discusion the Dr. evidently knew that there was a Hep C case at my company and he knew what department it was in.
He talked about it with a nurse whose husband worked there, warning her to tell her husband to be careful at work.
He and his wife were both good friends of mine. We had fished together, eaten dinner at each others homes, gone camping on our vacations together. When he got home that night, she told him about the Hep C case, and what department it was in. The next day, less than 24 hours after I had talked to human resources, my friend stood in front of me and warned me that there was Hep C about, and it was in my department.
I could have destroyed the careers of several people, one of wich would definitely have been my friends wife. Another might have been my friend, and another might have been mine, although I probably would have been moved to a job picked to make me quit on my own rather than be fired. They aint smart, but they are far from stupid in HR.
So, that experience and others like it make me very protective about who I tell anything about my health, and to even think for the past 48 hours that I might be seeing my personal info getting into the hands of nurses and clerks was enough to trigger me to a repeat of the anger and stress of the previous experiences.
My emails to my T included my thoughts of suicide, the depth of my disgust with the prescription trail I have been on for sooo long, my difficulty in maintaining the diets and restrictions I face due to my liver and medications.
This isn't stuff I want sitting on the desk of someone someday that is trying to decide if I get a liver transplant or not. I have always been led to beleive that the only thing on my general record from the mental health department would be diagnosis and prognosis of disorders, nothing more. Now I know that ANY communications are supposed to be put in, and that some of mine have been, but I feel I can trust my T to have only put in very little, non harmful stuff.
Today I thanked her for her discretion, warned her that I am not worth risking her career over, and offered to stop sending her anything via email, official or not.
Thanks for the support, thanks for caring enough to post, thanks for helping me through this. This forum has been the best part of my PTSD diagnosis by far. Thanks.
Picture me sitting by a stoked woodstove watching the snow fall and feeling cared about by some really wonderful people on the PTSD forum. Thats my plan for tonite, thanks again.
The rule came after I was using the email to talk to her, so she didn't apply it to my situation, or tell me about the new rule.
All is Okay, I am still in a trustworthy caregivers office and will be there for the foreseeable future.
A story about trust as it applies to Dr./ Patient confidentiality:
I was diagnosed with Hepatitis C and beat it in 2005.
My job required me to work with razor sharp tools all the time, I was constantly exposed to sharps, I was constantly in danger of getting cut and contaminating very expensive cutting tools. And I was looking at a treatment that could limit my ability to work for up to a year.
The first place I went was to my companies Human Resources department and I told the head of the department all I knew about my situation. I thought they should know, it was the right thing to do.
Our HR head was on the board of directors of our local hospital, so after talking to me he called the hospital to get more information. He was put in touch with a Dr. that explained the risks, methods of transfer etc. Our HR head evidently asked some pretty specific questions, and after their discusion the Dr. evidently knew that there was a Hep C case at my company and he knew what department it was in.
He talked about it with a nurse whose husband worked there, warning her to tell her husband to be careful at work.
He and his wife were both good friends of mine. We had fished together, eaten dinner at each others homes, gone camping on our vacations together. When he got home that night, she told him about the Hep C case, and what department it was in. The next day, less than 24 hours after I had talked to human resources, my friend stood in front of me and warned me that there was Hep C about, and it was in my department.
I could have destroyed the careers of several people, one of wich would definitely have been my friends wife. Another might have been my friend, and another might have been mine, although I probably would have been moved to a job picked to make me quit on my own rather than be fired. They aint smart, but they are far from stupid in HR.
So, that experience and others like it make me very protective about who I tell anything about my health, and to even think for the past 48 hours that I might be seeing my personal info getting into the hands of nurses and clerks was enough to trigger me to a repeat of the anger and stress of the previous experiences.
My emails to my T included my thoughts of suicide, the depth of my disgust with the prescription trail I have been on for sooo long, my difficulty in maintaining the diets and restrictions I face due to my liver and medications.
This isn't stuff I want sitting on the desk of someone someday that is trying to decide if I get a liver transplant or not. I have always been led to beleive that the only thing on my general record from the mental health department would be diagnosis and prognosis of disorders, nothing more. Now I know that ANY communications are supposed to be put in, and that some of mine have been, but I feel I can trust my T to have only put in very little, non harmful stuff.
Today I thanked her for her discretion, warned her that I am not worth risking her career over, and offered to stop sending her anything via email, official or not.
Thanks for the support, thanks for caring enough to post, thanks for helping me through this. This forum has been the best part of my PTSD diagnosis by far. Thanks.
Picture me sitting by a stoked woodstove watching the snow fall and feeling cared about by some really wonderful people on the PTSD forum. Thats my plan for tonite, thanks again.