Kellogg cancer center
hello everyone. I am just newly diagnosed as grade 3 invasive ductal cancer. I meet with a surgeon Monday. I will be cared for at the Kellogg cancer center in Evanston IL. Does anyone have experience with this center? Am I in good hands? My surgeon is Dr. Winchester. All i hear about is how great northwestern is but they don't accept my insurance. Should i still get a second opinion there? I'm just so scared and anxious now as I am sure all can relate. I have 9 month twins and a 3 year old and just turned 39. Anyways, any input is appreciated.
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I was diagnosed with IDC stage IIA back in May. My PCP is over at St. Francis, and I ended up getting a lumpectomy there. There is one surgeon there, Dr. Hyser who has a wonderful bedside manner, who does almost all of the breast cancer surgeries there, and he even did my biopsy. I also had an anal polyp that was causing my lots of rectal bleeding that I had to have surgically removed anyway, and so while I was seeing him about that, I asked him if he could examine a lump I had in one of my breasts. He immediately decided that the breast lump needed to be investigated first, and he sent me for a diagnostic mammogram and an ultrasound, where they found a lump. The only complaint I had about St. Francis, is that it took me 11 days to get an appointment for a mammogram and ultrasound, and then it took me three weeks to get the biopsy. I saw him the end of May, and I did not have the lumpectomy until the end of May. Kellogg is much quicker. St. Francis is trying to compete with Kellogg though. They hired two well known MO to join their staff, and they opened up a place to do chemo and I believe radiation across from Old Orchard. I decided I wanted to go to see a MO at Kellogg though, because you get lots of attention there that you don't at St. Francis. The first chemo session I had over at Kellogg in Evanston, I was also visited by a pharmacist, and a social worker. The social worker was fantastic, and visited me at all four chemo sessions. Dr. Winchester is supposed to have a good reputation, and his Father practiced there for years. I have heard many good things about Dr, Yeh too.
My MO is Dr. Merkel. People either love him or hate him. He is really shy, and it takes him a few visits to warm up to you. The people that seem to hate him, only go to him once, and say never again. I have two friends that go to him and love him, and there are people with stage IV breast cancer that say that he is the only reason they are still alive. He only treats breast cancer, and he knows everything there is to know about it. There are a few MO's that are female there, that also only treat BC. The thing I like about Kellogg is that all the MO's have nurses that work with them, and if you have a question or a problem you can leave a message, and the nurse will get back to you usually the same day. The nurse also does a chemo 101 session before you start chemo. Dr Merkel's nurse Bonnie is fantastic. Dr. Merkel is only at Evanston three days a week though, and he is at Glenbrook and HP the other days, and so I always try to call up one of the days he is there. I think it is the same with the other MO's.. We have a breast cancer support group that meets once a month at 1000 Central in the professional building across from the hospital. You might also try posting this in the Illinois woman facing BC group too. You would get a better response there Sorry you have to be here, but you will get good care at Kellogg. Hope this helps.
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Another satisfied Kellogg patient here (and part of Peaches’ support group). When I got my biopsy diagnosis, I had heard a lot of good things about Dr. Winchester, but he was not available on the timetable I needed (i.e., ASAP). He is extremely in demand. The nurse-navigator and my GYN said his colleague Dr. Yao is also excellent and available in the next week. I saw her and she was fantastic. She laid out all my options and was supportive of my choice of lumpectomy + radiation. One week later she did my surgery. I did see Dr. Winchester on an emergency basis when the weight of my breast pulled my sentinel node biopsy incision open, and he sutured it closed. My MO is Dr. Law and she is also great, as was my RO Dr. Shah (unlike your ongoing relationship with your surgeon & MO, you no longer see your RO once your radiation treatments are over and you’ve healed from them). I like that Kellogg integrates its care with the adjoining Evanston Hospital, whose Center for Breast Health is where I began my “journey” with my annual routine screening mammogram. (I don’t like that its parking isn’t free, but it is relatively cheap). The staff is wonderful, there are integrative programs (qi gong and mindfulness classes) and Evanston has the preeminent lymphedema specialist in the Midwest, if not the whole country, with a terrific PT department.
Northwestern (where I had my first knee replacement) is a pain in the butt to get to, inconvenient to public transit (Evanston/Kellogg is 1-2 blks from Central Street on the CTA Purple Line), with much costlier parking with narrow spaces which fill up quickly. My insurance at the time covered both hospital systems; three months later I went on Medicare so coverage was no longer a question. Interestingly, the NorthShore system of which Kellogg is a part used to be affiliated with Northwestern; it’s now affiliated with U. of C. and Mayo.
Speaking of St. Francis, it’s where my husband had both his colon surgery to repair a problem caused by a colonoscopy botched by an outpatient facility on the other side of Chicagoland (can’t get more specific than that), and his hernia repair—same general surgery group to which Peaches’ surgeon belongs. He likes it because of his faith-based vibe (he’s Catholic and his three hospitals are Catholic—one was recently acquired by Mt. Sinai, so “my people” are now part of the team--& Protestant) and it’s closer to us. My PCP is at St. Joseph, part of the Presence group along with St. Francis. But my PCP prefers to refer his patients who need specialists, especially surgical, to NorthShore hospitals.
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Thank you peaches and chisandy. I appreciate your input. I will also check out the support group!
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We meet the second Wed. of each month. (I won’t be there for April, because I’ll be in London).
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