BCNA Online Network
Urgent Removal of tissue expander
edited February 7
just curious as to know if anyone had to get the tissue expander/s removed due to pain, severe pectoral spasms and body basically rejecting it?
I certainly was in a great deal of discomfort until about 5.5 weeks...I was thinking I would need mine out. Then suddenly it wasn't an issue.
Even after changeover it is a different feeling and it takes some getting used to.
I have had mine in for 11 months now doing chemo and radiotherapy which I wasn't expecting. will be glad to get it out in Sept (after birth of grand-daughter). It's uncomfortable and I didn't have the full amount injected to expand, stopped after my second chemo session it was all too much for me. I think I will be glad to have done it but the past 10 months have been tight and uncomfortable.
I chose to have mine out and go flat, because it was SO uncomfortable and often painful. The mesh (inserted to support the implant) also dug into me. I had it in for 18 months because I had to wait until after chemo then radiation then wait for post-radiation healing, then availability of surgeon. I was so glad to see (feel!) it gone!
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