New to Group today--metastatic breast cancer
Comments
-
Hi sockmonkey! Just want toCR1954 said:sockmonkey......
Like Kat, I don't have the answers either. But I too wanted to welcome you to the board and let you know that I will keep you in my prayers.
Hopefully, someone here will have answers for you....
Hugs,
CR
Hi sockmonkey! Just want to welcome you also to a great support group. I will be praying for you!0 -
Sockmonkey, you are one STRONG woman!~!~~~lizzie17 said:sorry
I am sorry you are going through so much, and over a long period of time.
My prayers are with you, and welcome to this group. Lots of support here.
I'm amazed at all you've been through and BEATEN!! You can do this again! Keep the faith and keep fighting! It sounds like you are in good hands.0 -
HI Sockmonkey and welcome to
HI Sockmonkey and welcome to this site! Like Mama G said, sounds like your a true warrior, you have gone through a lot, mine was in my left breast all lymph nodes, inner mammery node and left supraclavicular, I'm good so far, but I have not had it in my bones, I know many women on here have and I'm sure you will be getting some good feedback soon. Again welcome an keep the faith.
Cyber Hugs,
~Kari0 -
Welcome, Sockmonkey. You
Welcome, Sockmonkey. You are an inspiration and have certainly had your fair share. I can't believe that you have to go through this an additional time. I have been through a lumpectomy, chemo, rads and am on my 5-year plan of Arimidex. We are a very strong board with informative, supportive, caring and loving members. We'll be with you through your treatments so please keep us posted. Sending (((hugs))) your way!!!0 -
Have metastatic bc
Hi sockmonkey, I found out about 2months ago I have bone met I had 10 round of radiation and once a month I take zometa infusion to strength my bones. I will go see a neruo surgeon to see how they can fix my T6 in my back. Good Luck on your treatments I hope I have answer your question.
Barb0 -
welcome, sorry you are here,bjmom1 said:Have metastatic bc
Hi sockmonkey, I found out about 2months ago I have bone met I had 10 round of radiation and once a month I take zometa infusion to strength my bones. I will go see a neruo surgeon to see how they can fix my T6 in my back. Good Luck on your treatments I hope I have answer your question.
Barb
welcome, sorry you are here, but its agreat site with lots of wonderful people. I just finished treatment and am going on a bone med every months IV to help prevent bone mets. I guess in studies in europe it has shown to decrease bone mets by 30 plus percent. I am also starting tamoxifen. hope they get rid of the cancer. hugs0 -
Thank youKat11 said:Welcome Sockmonkey
I am sorry for the reason your here, but I am glad you found this site. I don't have the answers to your questions, but I am sure someone here might. I just wanted to welcome you and let you know there is someone here for you anytime.
Kat 11--Thank you for welcoming me...sometimes I find everything overwhelming & I need the support!0 -
Thank youbjmom1 said:Have metastatic bc
Hi sockmonkey, I found out about 2months ago I have bone met I had 10 round of radiation and once a month I take zometa infusion to strength my bones. I will go see a neruo surgeon to see how they can fix my T6 in my back. Good Luck on your treatments I hope I have answer your question.
Barb
Thanks for letting me know about your bone met treatments. Yesterday I went to the oncologist & he changed my meds to Xeloda (oral chemo) & I will start zometa infusions once a month too after I get the surgery done to my leg. Do you have any side effects? Good luck to you too!0 -
Thank youCR1954 said:sockmonkey......
Like Kat, I don't have the answers either. But I too wanted to welcome you to the board and let you know that I will keep you in my prayers.
Hopefully, someone here will have answers for you....
Hugs,
CR
CR: Thank you for your prayers & hugs. I have already gotten responses from others who have some answers for me. Thanks again for the support!0 -
Welcome Sockmonkey
I am so sorry to hear what you are going through. I will keep you in my prayers. You are in the right place to talk, vent, find answers, and make friends. We are all with you every step of the way. Keep us posted. Do you know when Surgery is yet? You are a Strong lady and the cancer don't have a chance.0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 122K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 398 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 673 Leukemia
- 795 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 239 Multiple Myeloma
- 7.2K Ovarian Cancer
- 65 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 543 Sarcoma
- 737 Skin Cancer
- 658 Stomach Cancer
- 192 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards