I know exactly where your coming from, I just need to know. After my last biopsy they said again that it is an acute, chronic granulomatis mastitis, which means that the infection has been there for a long time and the tissue has developed granulomas. My surgeon has reassured me that it isn't granulomas mastitis. It sure sounds it to me. But even after the 2nd biopsy still don't feel 100% with the diagnosis. I am being sent to an infectious disease Dr. who has never delt with this type of infection, then in 2 weeks I get to go to one of the top guys at the Avon Breast Center at Mass General Hospital in Boston for a 2nd opinion. After all this I hope to finally have the answers and will feel confident in the Dr.s in Boston. I hope for you that you find the answers soon. Let me know how things go.
~Blessings,
Mijeva
hi mijeva, i really feel for you. i have had concerns about ibc for 5 months now and all docs say don't worry--well now there is a 2cm axillary node they say should come out and i want to say i told you there was a problem--but i hope it is a more minor problem. i have been going crazy with this as well. i have a 2 year old and i can't bear the thought . . . i want to know what is wrong with my breast, and i simply don't trust the explanations i get. been on 5 types of antibiotics continuously, node just growing, pain, thickening. will probably fly to large center soon for more expertise. hang in there, good luck to you and be well.
wondering1719
Thank you for your response....I am at a loss and feel very alone. I have asked my surgeon about GM but she said that this is defiantly not it. I will wait till I get the results on Tues and then decide from there if I keep my appt. in Boston. I have a friend who keeps telling me not to borrow trouble but I just really need to know, I'm a single parent with 3 kids and I really don't have a support system.
Well, since there was some fluid expressed I would tend to go with the infectuous process. Has Granulomatous Mastitis ever been mentioned ??? This is often referred to as being rare but I certainly see a lot of posts here regarding this condition. Everything you say seems to fit and it is VERY hard to cure .... may last for months and even longer. Perhaps the recent tests will reveal something definite. I'm not sure if I'd go for a second opinion because all I can see as a result there is more of the same testing procedures. If it does turn out to be G.M. then you may be dealing with it for some time to come. Regards ....,