A place for those managing the ups & downs of a Stage IV/metastatic breast cancer diagnosis. Please respect that this forum is for Stage IV members only. There is a separate forum For Family and Caregivers of People with a STAGE IV Diagnosis.
Posted on: Feb 14, 2008 03:47AM
Here is a quick background of my case. I was diagnosed with bone mets on Jan.18th. My original bc was June 2007, Mastectomy in July then Chemo which ended in December. I am ER/PR+ and currently taking tamoxifen, clondorate and hydromorphone and tylenol 3 for pain management. I have an appointment for consult with a radiation oncologist at the end of this month.
I just went this morning for an ultrasound of my thyroid, which was a follow up from a CT scan. The Doctor radiologist told me that there is abnormalities and it looks like it might be related to my breast cancer. Has anyone have mets to their thyroid and if so what is the treatment and prognosis.
Thank you for your support,
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Posts 1 - 27 (27 total)
Feb 14, 2008 04:19AM katie11 wrote:
Sorry to hear you are dealing with progression. I don't have mets to the thyroid so can't offer any good advice, but just wanted to let you know I am thinking of you.
Feb 14, 2008 06:52AM Jellydonut wrote:
Sorry you're having to deal with this.
My thyroid experience: Last year I had a CT scan and the report read, "metastatic foci 2.2 cm on thyroid". Needless to say, my doctor was alarmed and so was I!!! Anywho, I had a biopsy (five needle sticks because the nice doc wanted to ensure he got enough tissue) and it was benign! Wishing you have the same result.
What I've learned through this cancer experience is that most of us have "growths" in our bodies that are harmless, but because we have cancer and have scans, these things are detected and cause us needless worry. A growth also showed on my liver and I thought I was as good as dead, but that's nothing either .
Good luck to you and let us know the outcome.
Feb 14, 2008 08:20AM Danie wrote:
Thank you for your positive support. I'm sure hoping it is B9 aswell. Having been diagnosed with bone mets is enough for one month. I'm hoping that the spread to other organs will take a bit longer then this.
Feb 14, 2008 09:41AM NYCarol wrote:
I had a thyroid scan on Monday because nodules showed up in my thyroid on a chest CT scan I had done in January. I missed a call from my doctor today as I was out when she called, but in my experience, the fact that she called so fast does not bode well. I suppose a biopsy is next. The worry never ends does it?
I hope both of our thyroids turn out to be benign!
Feb 14, 2008 10:23PM Maya1 wrote:
I had a benign tumour removed from my thyroid about 10 years ago. It is very difficult to do a biopsy on the thyroid as there are so many blood vessels in the area. They tried 4 times to get a good sample from me but each contained too much blood to be useful.
When I first found the lump on my neck my doc told me that the likelihood that it was cancer was slim, then if it was ca the chances it was malignant were slimmer still. And even if it was malignant the prognosis was extremely good. She said if you're going to have cancer then thyroid is the kind to get.
I have not heard of anyone having bc spread to the thyroid but it's possible, I guess. Most likely the lump is unrelated.
I wish you well with whatever treatment they decide.
Feb 15, 2008 05:35AM TripleNeg wrote:
Praying for B9. Regardless of the results, God is able, Stephanie
Feb 15, 2008 10:06AM PuppyFive wrote:
I too am having a problem with my thyroid!
I had tests and a nodule was found, but doctors did nothing!
Not really concerned! way over a year ago!!!
So now I am waiting on them to read my CAT scan, so they can
figure out what to do! they will take the thyroid out, but I dont know yet about the DX! will let You know!
I will keep You in My thoughts and Prayer!
Feb 16, 2008 10:08PM morgansmom wrote:
Just wanted to add my two cents worth as someone else who has had thyroid and bc problems. Actually my thryoid problems were found before the bc but what I learned is that an amazing number of women have thyroid nodules and much like breast lumps a vast majority of them are b9. That still is not much comfort when it is your body that we are talking about. I hope they can get a biopsy of that for you and set your mind at ease with good results.
I do not know about bc mets to the thyroid but I did have thyroid cancer. Actually, it was found two years before I was diagnosed with bc & mets. My thyroid cancer was diagnosed by a needle biopsy and then removal of the thyroid. It is one of the most treatable forms of cancer and nearly 100% curable with surgery and a radioactive iodine treatment. I had just had a thyroid scan last winter and received a NED diagnosis six weeks before I found a lump in my breast that turned out to be bc that had mets to bones.
I am sending you wishes for good results! If you have any questions about thyroid stuff that I can answer feel free to post them or pm me. I will be happy to share anything I have learned.
Feb 16, 2008 10:23PM susan320 wrote:
A friend of mine had thyroid cancer from her bc. If I remember correctly, she did a special type of radiation treatments. They made her tired, otherwise she did quite well with her treatment and has been bc free for about four years. I have heard thyroid cancer is very treatable, with good prognosis. Still hoping for benign results for you!
Feb 16, 2008 10:31PM - edited Feb 16, 2008 10:32PM by susan320
Feb 17, 2008 02:24AM Danie wrote:
I went to see my doctor yesterday for the ultrasound results and he mentioned that there were some nodules in the thyroid which were not of concern. They also found a mass behind the thyroid which is of concern. He said it is not part of the thyroid, but it looks like it is next to it or attached to it. Thus, he is scheduling me for a biopsy. Has anyone had a biopsy for this before and if so how was it. I would just like to know what to expect. I'm still hoping for B9.
Thanks for your good info and support. It is much appreciated.
Feb 17, 2008 02:30AM Danie wrote:
Me again. My doctor also mentioned that it might be a lymph node that is next to the thyroid. Thus, meaning that it might be mets to lymph which is located behind the thyroid. What would this mean? I have bone mets, thus if it is in the lymph nodes, would this mean that it is mets to the soft tissue now.
Feb 17, 2008 12:02PM sallyk wrote:
I have a large 3.7cm complex cyst on the thyroid. I was told with the size and how fast it grew there was concern. I had it biopsy and was told it was benign. My doctor said the thyroid on that side needs to come out. I do not want to go through more surgery so we will biopsy and us again in 6 months.
Mar 20, 2008 12:47AM FloridaLady wrote:
I was just searching this yesterday, for another lady on this site. Do a Internet search of Thyroid Cancer and BC connection. There is a lot of info out there. I was looking for a article that I had seen that said daughter's who's mom's had bc are more liking to get thyroid cancer. I know two ladies this happen too.
You will see there is some connection to rads but they are not sure how strong. But in this information you will read a lot about your thyroid health could show you are at a higher risk for bc.
Living in Hope
Mar 20, 2008 07:50AM Danie wrote:
Once again, thank you so much for your concern and information. I will have to look into web search.
Sorry, I haven't been posting much. I have been sleeping lots and having very bad bone pains. I have been reading and following everything that is happening on the site. I try to go on the site every couple of days. We have been having a very hard time lately with everything going on with the sisters. It makes me so sad and a feeling of no control over this disease. I have been praying for everybody and hoping that things ease.
I have been having lots of bone pain and also sleeping lots. I'm doing not to bad, as best as I can. I'm going for a PET scan for my thyroid in April and an MRI of my head for my lazy eye next week and having another bone scan at the beginning of April. It feels like it is test after test and not much break. I should know more about my thyroid and if there is progression at the end of April.
My pain has been really bad for the last few weeks. I changed oncologist two weeks ago and he gave me zoladex which has put me into instant menopause. I read on the side effects and it says that the first month on zoladex makes your tumours and bone cancer flare, thus giving more pain. I am on hydromorphone which is not really working, but that is what I have for now. I'm waiting till mid April, then I will call my onc. if it doesn't get better. I am currently taking a long lasting morphone of 6 mg every 12 hours and a quick release morphone that is 2 mg every 2hours and also take zopiclone for a good night sleep which is probably 4 good hours in a row(pretty good). I also take clondronate for my bones. I have been sleeping lots and always dozzy, which I hate. Hopefully the pain subsides, so I can take less med's and be more alerte.
My prayers are with you all,
Mar 20, 2008 08:37AM LuAnnH wrote:
Diane, call your onc and ask for help with pain management. You shouldn't be so drugged that you are sleeping all the time and you also shouldn't be in lots of pain. There are lots of different types of pain meds to use and we all react differently to them. You may have to try different meds to find the ones that work the best for you that gives you the best QOL. So don't wait til April, make that call and get your pain meds fixed.
Mar 20, 2008 12:27PM Danie wrote:
Thank you LuAnn. I might just take your advise. I just thought, having this pain was normal with the zoladex.
Hope I can do something before next week. We are leaving for holidays, next Wednesday to Mexico for a week. I just can't wait. I think it is going to be so relaxing. I do need a break from all this. My life has been a rollercoaster since last June, when I originally got diagnosed. I'm sure we all have the same ride.
Take good care,
Mar 27, 2008 02:17AM kimf wrote:
I am so sorry for what you are going through. I was dx'd stage III IDC in 12/04. During tx, a routine scan picked up a large goiter on my thyroid. I had it biopsied and was told negative. Due to its size, upon completion of chemo & herceptin, I had a thyroidectomy. As it turns out, the goiter was malignant, but was not mets, but a brand new thyroid cancer. It was dx'd papillary carcinoma, follicular variant. The treatment was having it removed, which I already did, and completing a single radioactive iodine treatment. At first it floored me to have another cancer, but I found out that the type of thyroid cancer that I had was really mild and curable. I hope that you find out that yours is similar and not more mets.
I'm sorry for all the pain you have been experiencing. Here's hoping that you adjust to the new meds quickly and the bone pain eases up.
Mar 27, 2008 02:45AM Mazy1959 wrote:
I have bone mets that are in remission right now but I do still have pain. I have been on Oxycontin 20mg, twice daily and 2 Oxycodone/Tyl, 5/523, as needed for break thru pain every 6 hrs for more than a year now. It works really well for me but I do have to eat a sandwich or something with it. It doesn't make me near as tired as hydromorphone did and it doesnt make me sick. We had to switch my pain meds alot until we found something that was tolerable. Maybe your onc would consider trying different combinations too. They thought I had thyroid cancer too but it ended up being goiter and they just removed the left half so I dont have to take meds for it. The biopsy was no big deal at all. I take Aromasin and that is what shrunk my tumor. I also take zometa iv once monthly. Bone tumors take longer to shrink and its a slow process but it can be controlled in many cases. Which bones are your mets in? Mine is on the 5th lumbar on the spine. Hugs, Mazy
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