Second Opinons
Comments
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I live in a fairly rural area. I like my team so far, but I feel as if I should get a second opinion from a major cancer center. Has anyone had a second opinion from MD Anderson in Texas? If so how does the process work and how did you feel about it? Thank you for your help.
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Are you closer to Houston or Dallas? UT Southwestern in Dallas is an NCI designated Comprehensive Cancer Center and gives great care
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A second Opinion is a good Idea...But it often leads to a Third Opinion...You have to be careful that the Second Opinion is Valid...and not something you just want to hear...meaning that Both First and Second should be the same...a lot of people just go and take second because that is what they want to hear....if you have two different then you may need a Third Opinion....MD Andersen is a good Start and also a NCI Cancer Center....Liz
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Hi there. IMO getting a second opinion at a major university teaching hospital is essential. Good luck and keep us posted...
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Thank you for all of the advice. I am so new to this. I think that I am going to find the nearest NCI Cancer Center and then go from there. Thanks again
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I went to MDA for my 2nd opinion. I called and they set up easily. Had appts in week/two in about 10 minutes. They are a machine when it comes to this. I believe they got all the records after I told them where to go. They re-ran pathology -- which I was happy to have done. This may be fairly typical process for a 2nd O.
Everyone was really helpful and nice. They keep you moving through appts and I found it a very organized process.
Good luck.
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I just found out today I have breast cancer. I think I’m going to call MD Anderson and set up app for them also. I have been going to the VA hospital but I don’t feel very comfortable with them. The doc who called me today to tell me just told me I have Ductal cancer. I ask for more info and she said she wasn’t a specialist. Now i have to wait till Tuesday to go pick up my path report to find out myself exactly what they found. I’m not a happy camper right now and in shock and scared
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Oh Quiltingnut, I am so sorry. That is just plain cruel to call you and then give you zero information. I won't tell you don't worry because that's what everyone keeps telling me and it does not help. I am a newcomer here and no expert, but ductal cancer can mean different things and those things are very treatable. I am wishing you all the best. Please let us know what happens
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I'm so sorry for anyone newly diagnosed and joining us here. But glad you found this site. I could not have made it through the past year without it. Ask any and all questions, as I say on post after post. Someone will have advice or an experience to share. And vent if you need to. We get it.
I will also say that the initial time after diagnosis but before you have all information and a plan in place is the WORST time. It does, believe it or not, get better. I promise this.
Big virtual hug to you guys!!!!
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Oh, so sorry QultingNut. Dealing with this over the holidays is just wretched. I would highly recommend MD Anderson, since they are very good, efficient, and also have cutting-edge clinical trials. I've email consulted with Ben Smith, a radiologist who went to school with a doctor on my team, and he seems really knowledgeable + very caring. Best of luck and do let us know when you get your biopsy report.
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I went to MD Anderson for a second opinion, and it was really helpful for me. My MO was glad I did that too. If you can't make it to MD Anderson, there are many NCI facilities to choose from.
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I went to MD Anderson for a second opinion on type of treatment and later for surgery and reconstruction. I was satisfied with both opinions and found them to be easy to work with.
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I had 2nd O and later surgery at MDA as well. They were in-network with my insurance and I had such confidence in everyone there.
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