How Many Are We?
Comments
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Good morning -- My primary diagonosis was StageIIb, but it has now metastized to my liver and some lymphs. I understand I will always be "counted" as stage IIB -- but I'm now a IV.
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hi, I was diagnosed stage lV March 17, 2014 mets to hip and rib. Yikes glad I found you!
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Nice to meet you Spelin! Good look to you. How did you update your diagnoxix? I was not able to do that without my first dx going away?
Surpised that no one else has responded to the question on how we are counted as StageIV -- already having a primary diagnosis.
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Hi JourneyOn, I'm pretty new to this as I just joined April 2014 and am still trying to navigate my way through. On this question there are 18 pages before us that have signed in with stage 4. And on my home page I listed my first diognose and then listed my new diognose but still haven't figure out how to list all of my treatments of chemo, radiation.... etc etc.
So nice to meet you! This has helped me so much in the feeling that I am not alone and any question I have I am able to fine or ask.
Always lynette
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i am new to posting, but am also a stage iv comrade...
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Count me in too. Used this site a lot when going through treatment the first time around and then after popped in once in awhile. I know this site helped so much the first time around and I love that we get the support we do here. Also have tried to keep up with the latest treatment options or new discoveries.
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Metastatic breast cancer, throat and voice box, femara for 2 and a half years.
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Hi All! DX stage 4, Aug 2013, 15 years after original dx, stage IIb. Mets to both hips, almost all spine, ribs, neck, skull and lung. On A/A ever since w/Zometa. Tried xgeva, it has sorbitol in it, and I'm allergic. I'm blogging about it all at http://earthandskylotus.wordpress.com
Is there a "blogger" thread?
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Hi skylotus!
As far as we know, there isn't a "blogger" thread here but, if you want, feel free to start a new one under the Recommend Your Resources forum.
Best,
The Mods
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Might be too late, but you can count me also.
I was diagnosed with pretty much stage nothing breast cancer in 2011, but in April 2014 we learned it had metastasized to my spine, left hip, liver and left adrenal gland.
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I was diagnosed stage IV Breast HER+ , ER+, PR+ with bone mets in hips, spine and ribs Oct 2012. I had Aridia and 7 rounds of taxol. In May 2013 had nod for 9 blissful months.
Tumor markers spiked in March of this year ... back with Bone in scull, neck, spine, hips and ribs
and Liver mets and being treated with Kadclya and Zometa .
My side affects are a little less with Zometa in place of the Aridia. However i am not sure if the steady weight loss, random stabbing pains, tiredness, headaches and
nausea is due to my Kadclya or the Liver cancer. Had my third treatment today and markers are spiked even higher...with LDH at 3088 and all others in the 100's.
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Dx'd w/diffuse bone mets in January of this year -- a month shy of my 6 year mark. Subsequently dx'd in March w/pathological fractures to my femur and pelvis that necessitated a total hip replacement, which may have been a blessing in disguise, hopefully removing any mets in that area. Most recent CA27-29 showed TM's down significantly. On Anastrazole. Very grateful for the support on the Bone Mets thread these days!
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Hi
My name is Rozann and I am Stage IV BC. I was diagnosed Stage IV last summer. I was on Faslodex, but have just been changed to A/A. I can't remember how to put my treatments on here.
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me too
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new to the forum.....stage four from the get go.
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Hello... My name is Raymonde. I learned I had stage IV IDC, mets to a lung and to liver, last October.
:-D
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Hi Rozann - to update your treatments, click on Profile at the top of this page and then on the appropriate tab. :-)
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Hi Okimie... This is to let you know that I have mets to liver, diagnosed last fall. I have never suffered any of the symptoms you describe.
However, we are all different from one another; this is just my experience.
Best wishes..
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dear ladies, stage iv, dx 3 weeks ago.mets to liver.
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Hello. Mets to spine getting more under control since I started the Affinitor/Aromisin meds. Plus continuing Xgeva monthly injection. Tumor on left adrenal gland DX 2013. Not responding as quickly as Onc would like so March 31 finished 8 Stereotactical Radiation Surgery treatments followed by PET scan. Tumor reduced by 2/3.
At age 73 I just keep rolling along these 21 years of breast cancer with renal cell carcinoma meaning right nephrectomy 7 years ago.
All of you give me encouragement to do what needs to be done.
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Diagnosed first time around stage 2b in August 2011. Diagnosed stage IV in April 2014 with two small mets in the liver only. These were found incidentally on a CT scan that was ordered by a urologist for something totally unrelated. Talk about a surprise! Oncologist said I probably wouldn't have had symptoms for another 6-12 months! Had a resection of one lesion in May and SBRT of the other in June. -
Add me as of 7/24/14....single lung met. Three times with cancer in last 7 years. Still trying to decide exactly what to do. Ugh.
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Hello Everybody! This is Jabid from Fiji. I mom was diagnosed with lung mets in February this year. Had 5 rounds of chemo in India and is now on oral chemo, Endoxan (50mg) AND levesam. is anyone here on the same medications especially endoxan? I would like to know what the side effects are as my mom gets nausea too often and does not feel like eating most of the time.
Thanks
Jabid
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Sorry kinda late with the post. I was diagnosed with metastatic breast cancer about a year and a half ago. "Lucky me" I went from being healthy, hardly ever even getting a cold, to being told I have stage 4 cancer. Its been one heck of a year and a half, but I refuse to let chemo, radiation, or cancer stop me.
Kara
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Jabid
Endoxan is a name for cyclophosphamide which is a common chemo drug. I don't remember the side effects but the doctors ought to be able to prescribe something for nausea. I think I was given domperidome for anti nausea but you need to speak to your mum's oncologist.
The other drug is anti-seizure medication I think.
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You can add me to the list. Found out I have bone mets 2-2014. I'm currently taking arimidex.
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Also a member of the club. Diagnosed Stage 4, triple positive, straight off the bat in May, with spread to lymph nodes, sternum, left pelvic bone, and possibly lungs (could also just be nodes). Doing weekly Taxol (just finished round 12) with herceptin and perjeta every 3 weeks.
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Add me to the list as well. Stage IV in May 2014. Dee (GG27)
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I'm stage 4 as of last Tuesday... to the bones (spine)
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