Part 2: Capsular Contracture at 4 Months Post Op- Houston, TX
You can read Part 1 of my journey here. Hello...
You can read Part 1 of my journey here.
Hello Ladies!
It's been almost 3 weeks since I started my ultrasound appointments. The therapy is done for 10 minutes at 2.0 (Kwh?), although yesterday she did it at 2.5.
My hubby and I are thinking that it has softened the CC boob up some. We are gauging by feel and also when I lay flat on the floor it no longer feels like such a big ball on the left side. It is by no means gone, but maybe some improvement. The big question is will it stay this way once treatments are done or get worse again??
I think the size difference is still there, the left one has not dropped back down.
I checked another doctor and he basically quoted me $5K to do a capsulectomy compared to my docs $3,300. Interestingly enough, he actually did not think I had CC and thought my pocket needed to be dropped instead and would do a capsulotomy for $3,100.
Ooops, I accidentally put my official post int he...
I am reposting it. Sorry!
So I am making an official post since I havent been able to in a while b/c I talk waaaayy too much! Yup, me and Breasto broke the word limit! LOL~ Well I have 1.5 weeks left of ultrasound (US) treatment. That is a total of 6 more visits totaling 6 weeks of 3x's a week. I think I could really feel a hardness difference at 4 weeks. When I massage with my hand, for the most part can still feel the hard capsule still it's just not as hard. But when I lay flat on the floor, I no longer feel the hard ball that was once present on my left side. They feel the same now withonly a tightness on the sides if I roll to the left or right. As a side note, I am concerned I might be grade II on my right side and the doc just hasnt caught it. I go in for an appointment on the 15th, my PS is going to evaluate my progress. I am going to ask him if the hardness may come back after I stop US treatments. I am worried about that. At this point I am on hold for doing anything. Options I have been considering are 1) Capsulectomy 2) Capsulectomy w/Strattice 3) Pocket Protector by Dr. Berman 4) Explant (remove em!) 5) Or live with them as they are for as long as I can stand it. At this point, everything is on hold. I am not going to jump the gun, and in the meantime I have been doing as much research as I can trying to figure out what to do. I am looking to see how many people have had a straight capsulectomy and have not had a recurrence. I have found a few people who have been so lucky. Makes me consider trying it.
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