Once Christine was diagnosed, I made an appointment for my mammogram. I had been putting it off, but I know I won’t do that anymore! Now I am due for my next one and I won’t delay.
I hate needles! During treatment there are so many blood tests and IV drips. When I found someone who was very good at drawing blood, I asked for them. I had a nurse who failed after 4 tries. I demanded the best person in staff to draw my blood. They were glad to know this nurse needed more training and after wards they were careful to find someone skilled to put the IV in. Yesterday I didn’t even feel a pinch!
My mother cried daily during my treatment. She found solace in going to daily mass. I ended up caring for her, which helped me feel useful. Sometimes this is more difficult on family members.
I found that the easiest way to keep my family informed was an email letter written right after my appointment. Some people use sharing website, but for some reason I didn’t like that arrangement. I was able to get the facts straight, tell everyone the same thing — nothing like people sharing information and getting it mixed up — and get it done quickly.
sending...
Once you have been diagnosed, bring a tape recorder to your doctor visits to reference as you may feel overwhelmed by the information.
Once Christine was diagnosed, I made an appointment for my mammogram. I had been putting it off, but I know I won’t do that anymore! Now I am due for my next one and I won’t delay.
When sitting in the waiting room, I texted friends on my cell phone. Their comments often made me giggle and passed the time. I felt loved.
I hate needles! During treatment there are so many blood tests and IV drips. When I found someone who was very good at drawing blood, I asked for them. I had a nurse who failed after 4 tries. I demanded the best person in staff to draw my blood. They were glad to know this nurse needed more training and after wards they were careful to find someone skilled to put the IV in. Yesterday I didn’t even feel a pinch!
My mother cried daily during my treatment. She found solace in going to daily mass. I ended up caring for her, which helped me feel useful. Sometimes this is more difficult on family members.
Cards! I loved all the cards people sent. I still have them.
I found that the easiest way to keep my family informed was an email letter written right after my appointment. Some people use sharing website, but for some reason I didn’t like that arrangement. I was able to get the facts straight, tell everyone the same thing — nothing like people sharing information and getting it mixed up — and get it done quickly.