Question about secondary bone cancer
Kathy
Comments
-
I have secondary bone
I have secondary bone cancer. They did a bone scan on me and then a Pet/Ct scan and it lit up on the pet scan. It is in my lumber, T10 bone. I completed my chemo and I go every month for a drug called Zometa which is given through my port but it does not make you sick, although it does have side effects. I was diagnosed 1 1/2 years ago. The zometa is supposed to strengthn your bones. I do have a little back pain, but it is not too bad. My last pet scan in October came back stable, so right now they just watch it very closely. I understand what you are saying about the tests, it is just so scary, but you do need to stay strong. I hope all goes well for you, please let me know what happens with the MRI. Take Care0 -
Hi Kathy ☻
I haven't had this happen to me. I am so sorry that you even have to go thru any more tests. I am praying that everything will go fine with your test and that it is something that is easily treated and not cancer. I know that your mind will take you to that, but, try to stay positive. I will be waiting to see you post your news. Take care!
Love, Jeanne ♥0 -
I will be praying for goodJeanne D said:Hi Kathy ☻
I haven't had this happen to me. I am so sorry that you even have to go thru any more tests. I am praying that everything will go fine with your test and that it is something that is easily treated and not cancer. I know that your mind will take you to that, but, try to stay positive. I will be waiting to see you post your news. Take care!
Love, Jeanne ♥
I will be praying for good news Kathy.
Hugs!0 -
thank youmeena1 said:I have secondary bone
I have secondary bone cancer. They did a bone scan on me and then a Pet/Ct scan and it lit up on the pet scan. It is in my lumber, T10 bone. I completed my chemo and I go every month for a drug called Zometa which is given through my port but it does not make you sick, although it does have side effects. I was diagnosed 1 1/2 years ago. The zometa is supposed to strengthn your bones. I do have a little back pain, but it is not too bad. My last pet scan in October came back stable, so right now they just watch it very closely. I understand what you are saying about the tests, it is just so scary, but you do need to stay strong. I hope all goes well for you, please let me know what happens with the MRI. Take Care
Thank you so much for your reply. It helps to know it's not the end of the worldand that it is manageable. I am so glad your last scan was stable. Hopefully I will reach that same point. Did the chemo for the bone cancer make you lose your hair? I am really hoping to keep mine this time around, since it just came back 4 months ago. Unfortunately I happened on a website that said for primary bone cancer, the 5 year survival rate is 65%. Being a math teacher, that statistic freaked me out. I do know that this is not primary bone cancer, and I should stay away from anything other than this website until I speak to my doctor. It just freaked me out because my bloodwork and scans all through the chemo, bilateral surgery, and radiations were fine, until October. I finished the radiations on Oct. 20. I will let you know how everything goes. Thank you again for all of your help and support. This board and all the "sisters" have been a lifesaver for me.
Kathy0 -
Don't believe statistics!kathyDDD said:thank you
Thank you so much for your reply. It helps to know it's not the end of the worldand that it is manageable. I am so glad your last scan was stable. Hopefully I will reach that same point. Did the chemo for the bone cancer make you lose your hair? I am really hoping to keep mine this time around, since it just came back 4 months ago. Unfortunately I happened on a website that said for primary bone cancer, the 5 year survival rate is 65%. Being a math teacher, that statistic freaked me out. I do know that this is not primary bone cancer, and I should stay away from anything other than this website until I speak to my doctor. It just freaked me out because my bloodwork and scans all through the chemo, bilateral surgery, and radiations were fine, until October. I finished the radiations on Oct. 20. I will let you know how everything goes. Thank you again for all of your help and support. This board and all the "sisters" have been a lifesaver for me.
Kathy
Please Kathy. There is so much misinformation out there on the internet that it is best to stay on a site like this or another reputable site to get more info. I am glad that someone could help you with some answers. Sending you positive thoughts!
♠♣ Christmas Susie ♠♣0 -
You are in my prayers Kathy.survivorbc09 said:I will be praying for good
I will be praying for good news Kathy.
Hugs!
You are in my prayers Kathy.0 -
I had the chemo for breastkathyDDD said:thank you
Thank you so much for your reply. It helps to know it's not the end of the worldand that it is manageable. I am so glad your last scan was stable. Hopefully I will reach that same point. Did the chemo for the bone cancer make you lose your hair? I am really hoping to keep mine this time around, since it just came back 4 months ago. Unfortunately I happened on a website that said for primary bone cancer, the 5 year survival rate is 65%. Being a math teacher, that statistic freaked me out. I do know that this is not primary bone cancer, and I should stay away from anything other than this website until I speak to my doctor. It just freaked me out because my bloodwork and scans all through the chemo, bilateral surgery, and radiations were fine, until October. I finished the radiations on Oct. 20. I will let you know how everything goes. Thank you again for all of your help and support. This board and all the "sisters" have been a lifesaver for me.
Kathy
I had the chemo for breast cancer, and yes i did lose my hair. As far as I know, you will lose your hair for all chemo. Anyway, i believe that you may not need chemo for the bone mets, they may just need to do radiation, but you should wait to see what your doctor says. I have seen worst stats than 65% on the internet, so i try not to look at them and my doctor has never told me a survival rate. I know several woman who are doing well with bone mets (that is what secondary bone cancer is called), and living normal lives for years. There is hope. Take care and remember to let me know how you are0 -
KathyMoopy23 said:Failing Tests
I know how you feel about tests, Kathy. I will be hoping for no cancer results and wishing you only good thoughts as you wait for the Friday MRI.
I am getting a monthly infusion of Zometa for mets to bone, and I take a daily dose of Femara. Both are considered chemotherapy. However neither of these drugs has caused hair loss or even thinning...at least not so far. I've been in this treatment program since September. I hope and pray your tests go well. Hugs to you. Gracie0 -
Sending you lots of prayersm_azingrace said:Kathy
I am getting a monthly infusion of Zometa for mets to bone, and I take a daily dose of Femara. Both are considered chemotherapy. However neither of these drugs has caused hair loss or even thinning...at least not so far. I've been in this treatment program since September. I hope and pray your tests go well. Hugs to you. Gracie
Sending you lots of prayers Kathy!
KYLEZ ♥0 -
Aw, Kathy.....kathyDDD said:thank you
Thank you so much for your reply. It helps to know it's not the end of the worldand that it is manageable. I am so glad your last scan was stable. Hopefully I will reach that same point. Did the chemo for the bone cancer make you lose your hair? I am really hoping to keep mine this time around, since it just came back 4 months ago. Unfortunately I happened on a website that said for primary bone cancer, the 5 year survival rate is 65%. Being a math teacher, that statistic freaked me out. I do know that this is not primary bone cancer, and I should stay away from anything other than this website until I speak to my doctor. It just freaked me out because my bloodwork and scans all through the chemo, bilateral surgery, and radiations were fine, until October. I finished the radiations on Oct. 20. I will let you know how everything goes. Thank you again for all of your help and support. This board and all the "sisters" have been a lifesaver for me.
Kathy
I was given a 5 year survival rate of 37%, with a 6 months average survival time. Granted, this was for my first cancer...rectal...but I just made up my mind that I was one of the 37% and, well...it's 5 years for me now....
I take Actonel to strengthen my bones. There is a study that says that this also cuts down on the reocurrance rate, although not as well as the Zometa...
Hang in there, dearheart...and remember that statistics on this stuff are usually calculated on 3 to 5 year old data...
Hugs, Kathi0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.9K 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
- 794 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 238 Multiple Myeloma
- 7.2K Ovarian Cancer
- 63 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 540 Sarcoma
- 735 Skin Cancer
- 655 Stomach Cancer
- 192 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards