Description
This breast cancer support group is open to individuals diagnosed with stage 0 – stage 3 breast cancer. The group meets via Zoom every Monday from 7:00 to 8:00 PM CT (find your time zone). Mayo Clinic and non-Mayo Clinic patients are welcome.
This is a compassionate virtual space to connect with others who can relate to the physical and emotional impacts of breast cancer. The support group is community-based led by two breast cancer survivors who facilitate the meetings enhanced by their personal experiences. Regularly, providers from Mayo Clinic's Breast Cancer care team join the group to offer support and share their breast cancer expertise.
To register and get the Zoom invite, contact: Lisa Halverson 507-254-4141 lisahalver@gmail.com
I' 63 years old. And i had my fouble mastectomy two weeks ago withouth reconstruction. I has breast cancer 3 times and during my quimio my onco tested with genetic and i'm brca2 +. So that was my decision to take them.out. i don't know what is going next.i'm afraid but on the other hand in peace with my mind.
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In 2020, I had a lumpectomy and 30 days of radiation . I have a mammogram and ultrasound ( dense breasts) every year. My radiation oncologist wants to see me for 5 years for an annual breast exam. I see my oncologist/ hematologist every 3 months ( I also have essential thrombocythemia)and she does a breast exam about every other visit.
I don’t like the radiation doctor and I don’t see the necessity of continuing to see him .
I would like to know other’s opinions.
Thank you!
Hi, I am 54 and was told that I have dense breasts, as well. I have a mammogram every year because [breast and other] cancers run in my family. I know that seeing your doctors, especially when you have had specific issues is vitally important. I have not been diagnosed with any issues with my breasts, other than being told that they are dense, but due to a motorcycle accident years ago I have had a lot of experience with doctors and other therapists over the become a believer that if you don't feel good about one [or more!] of your doctors or therapists, there is usually a good reason for this. It might be that they don't know as much as they would have you believe, maybe they have made a false call about something and ae trying to cover-up their mistake, or they simply don't know what they are doing.
It is important to have a good working relationship with your health care team. Once every five years probably doesnt provide any useful data, especially since your oncologist is doing one every six months. Talk to your oncologist about your concern. Should it be necessary for you to undergo more radiation, (unlikely), I'm sure another radiation doctor can be found.
If you have dense breasts you need an ultrasound as well as the mamagram .
Thank you for your helpful comment, I will certainly do that.
I am having a masectomy soon as I have now got lobular cancer after a lupectomy fpr DICS==about a year laterllobular cancer was told to me after urging my consultant/surgeon over the phone---im afraid iam still in limbo and have had to deal with this alone and im77years----I got no explanation as to what or where i am with this type of cancer and feel have been treated with indifference.. and she gives me the impression she is either going through some form of crisis herself or simply cant relate to people shes quite young with 3 of a family---so im grateful for any kind of information available.
I am so sorry to hear that you are still in limbo and not feeling support from the surgeon; contact the American Cancer Society and see if they have any "navigators" who can support/ educate/ prepare you for your ongoing treatment plan. Sometimes you can even find a navigator through your doctor or hospital. The navigators are often RN's or other medical personnel who understand and have experience in the field. It is important that you find somebody with whom you have a good rapport, as this is so important to have a team you trust and can confide in.
Good luck to ya!!
absolutely,my friend your spot on all the videos I have watched and what they say is of course invaluable -Ihadnt fully realised that Mayo is an American company -I do relate to Macmillan a large organisation in England and they too are very helpful -though my progress would have been A1if it hadnt been that theres definitely no openness nor actual communication -im seriously thinking about putting it on hold but have no knowledge of what they the medical team know even the fact that I suffer GAD-and stress --and my consultant did not allay my fear when i asked if I could take a 2mg diazapam -im left in limbo!! So thanks everso much for that info much appreciated..