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Old 06-23-2008, 04:58 PM   #1
dberg
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Join Date: Sep 2005
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after 4 years...then what?

My onc doesn't seem to be all that interested in me. I'm doing fine, with no problems, which may be the problem! He seems to pooh-pooh any questions I have about recent developments.

I'm wondering if you all have had regular mammos or if you've gone to digital for your remaining breast. Are they worth it? I'm supposed to have a mammo followed up by a MRI. I'm now 49, used to have dense breasts, but don't know what they are considered now since I've gone through chemopause. What are the "interested" docs saying now?

Yes, I'm searching for a new onc!
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Old 06-23-2008, 05:30 PM   #2
Carolyns
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That is a GREAT question. I can't wait to hear the answers. I am 19 years out from my first diagnosis (in my early 30's) and had a second primary and now I have mets. I had to insist that my doctors follow me and I am convinced that they never took it seriously...perhaps because they don't believe that an early diagnosis of mets extends life.

Anyway, I was followed by a diagnostic mammogram on my remaining breast (while I had one) and tumor markers. The mammogram uncovered my second primary 10 years after the first. My tumor markers spiked when I had mets but unfortunately they were drawing the blood and no one was reviewing the results. I presented with two lumps and was still told it was "nothing". I insisted on an ultra sound which proved it was not nothing. My Onc. was SO sorry that she ignored my concerns and then I found out that no one was reading my marker results which had spiked prior to the lumps appearing. It seems that they were just humoring me with visits.

In my opinion this is a huge issue. I hope that there has been progress made in this area.

Thanks for asking the question.

Carolyn
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Old 06-24-2008, 03:35 PM   #3
CLTann
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I can't believe my eyes while reading your post. This is malpractice. If the tumor is in the doctor's body, I bet he or she will take more than notice. Consult an attorney and sue the guilty person.
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Ann

Stage 1 dx Sept 05
ER/PR positive HER2 +++ Grade 3
Invasive carcinoma 1 cm, no node involvement
Mastec Sept 05
Annual scans all negative, Oct 06
Postmenopause. Arimidex only since Sept 06, bone or muscle ache after 3 month
Off Arimidex, change to Femara 1/12-07, ache stopped
Sept 07 all tests negative, pass 2 year mark
Feb 08 continue doing well.
Sep 09 four year NED still on Femara.
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Old 06-24-2008, 05:55 PM   #4
Carolyns
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Ann,

It is very discouraging to be treated this way. I tried to sue the first doctor who delayed my diagnosis 19 years ago. He said that I was too young for a mammogram at 32 when I told him that I felt a lump. He told me to visit every 3 months to monitor the lump and seemed very attentive. All the while in my chart he was writing that I was "obsessed" with a fear of beast disease. I found this out after reading my chart in the lawyers office. I changed doctors and got a mammogram which found cancer the first time. Anyway, I learned it is not so easy to sue a doctor and it is very time consuming.

Anyway, that experience made me understand that I am not up to suing anyone. It also made me wonder - What is the proper follow-up for long time survivors. I wish that someone could gain from my experience.

I think that the excellent question raised by dberg. In my case markers would have been a sign. I also had bone pain but mistakenly thought that the bone density test would show activity in the bones but I was wrong on that. So a bone scan would have also helped me discover the cancer sooner.

Carolyn
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Old 06-24-2008, 08:05 PM   #5
Becky
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In alittle more than 2 months, I will be 4 yrs out. In Sept (when I am at 4 yrs) I will see my onc for the last every 4 month appointment and will move to every 6 months. I asked if at 5 yrs if I would move to once a year but he said "we'll see". I get a digital mammo every year (I still have both breasts) but want to also start getting a Dilon or MRI at the opposite 6 months. My onc does the tumor marker and blood work every time but I get a copy too and review it with him (I go to the cancer center a week before my appointment for blood work). My onc is the best but anyone can forget to look so I make a point to look myself. However, any test or bloodwork done by others I have a copy sent to my onc. He always, always emails me to say they are normal or what things mean (even if I already know). I am also carefully watched by my PCP and radiation onc who both see me every 6 months (opposite of each other). I see my surgeon once a year. I call them Mr. March, Ms June, Mr September and Mr December. I see my gyn in July but they don't care and I am looking for a new practice. The more people you get involved with your care, the more you are cared about.
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Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
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Old 06-24-2008, 10:25 PM   #6
ElaineM
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after 4 years..........then what?

I follow my doc around if he ignores my concerns. I would also get a second opinion. I have been there and done that. Recently I got a third opinion which helped to move things along. I remind my doc when it is time for tests like cat scans, mammograms, Pet scans, MRIs, ultra sounds, blood tests etc. I keep those things on my list and remind him the next time I see him if he doesn't respond the first time. Doctors are human beings. They forget things. They get overwhelmed or stressed out by work just like we do some times. I tell mine that I am helping him to help me when I remind him about things.
It pays to be as proactive and assertive as we can be.
Keep going !! Follow your intuition. If you think you need help, please find ways to get it.
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Peace,
ElaineM
12 years and counting
http://her2support.org/vbulletin/showthread.php?t=48247
Lucky 13 !! I hope so !!!!!!
http://her2support.org/vbulletin/showthread.php?t=52807
14 Year Survivor
http://her2support.org/vbulletin/showthread.php?t=57053
"You never know how strong you are until being strong is the only choice you have." author unknown
Shared by a multiple myeloma survivor.
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