lookingforward
DIS Veteran
- Joined
- Mar 23, 2001
- Messages
- 3,065
Sorry if I'm blurting in - but need to get this off my chest. Get it?![]()
sorry about the wait. This is a long week.
On Monday I went to the PS dude, asking if surgery will rid of pain, could not get an answer, but all this info about tissue expanders and return visits to the PS for expansion. Uh? I want no pain not really need new b**b. I asked him about cording - no clue, he has been a PS for years, how does he not know about cording? He suggest a second opinion from his co-PS, sure! another idea would be good. I & DH go back in the afternoon, this PS doesn't even listen to my question on pain, but says the tissue expander would not work, but maybe the dorsel flap would. Proceeds to tell me if then limits movement of the right arm, leaves oozing hole for a couple weeks and requires drains in back and front. uh?Then it would be three surgeries, one for expander under flap, then those visits, then the surgery for the insert, and then the third surgery for reduction on the left. uh? Where is the part where you tell me the about the pain? Well, there is no guaranty that the pain will be gone. So, rather than listen to me - I think he was listening to cha-ching. I did ask how many procedures like this had he done - he had assisted in 80. How many have you done? None. and you want me to be your guinea pig? And the pain might stay?
Told them on Weds - no thanks. Then the Main PS wanted to talk to me - try and talk me into this - had his assistant call me. Still no thanks!![]()
I saw the pain Dr on Weds (after whining whining whining) and got a cortisone shot for the elbow pain (ain't working as of this moment) and a NEW drug to try. I've got a pain patch on the elbow. Use of the computer - makes it worse. Ergo the lack of posting.
I know I know- see another Dr. in a bigger city.
GAGWTA! You are all in my thoughts!
Oh my goodness! I finally found you all. I am so confused about the proper thread but I think this is it. Forgive me for being out of touch and for not having the time to read all six pages!
I am having my third chemo tomorrow, 2/14. I am on the steroids and can't sleep. Its been a rocky road with my blood clot and the blood thinners.
I wanted to write about my ongoing reconstruction. I have the tissue expander and its really not painful. It was after the orignial mastectomy surgery but I am used to it now. My surgeon has done hundreds and I have "seen" his work at my support group. The final outcome is amazing. He is very uber cautious and quite the perfectionist. I adore him, he is kind, optimistic and professional. I wanted to say that reconstruction is a super personal decision.
I will have to endure only one more surgery when he puts the implant in and then he will also do the reduction to match both sides. Then an outpatient nipple job, so to speak. I can't wait for it to be done but he is adament that I wait at least 3 months following radiation. I figure by October I will be done with everything (and I might even have some hair!). It is so important that you find an experienced surgeon no matter what method you choose.
As for pain, well, I am having chronic pain from my blood clot in my arm and from the chemo (not from the expander) and am on pain killers (they don't really "KILL" the pain, they soften it

Good luck in whatever you choose and in managing the pain that comes along.
