Low Risk IDC w/ Baseline Multiple Painful Conditions

Posted by krisrwalters @krisrwalters, Mar 29 1:47pm

I'm wondering what others might do in my situation and would appreciate your thoughts. I'm 65 and have Gr 1, St 1c IDC, 2 tumors: one 10 mm and the other 15, hence the St 1c, brca-, high percentage E+, P+, HER -, had lumpectomy of right breast 4 weeks ago w/ 7 nodes, all negative. Was told by my surgeon that I would probably be offered whole breast rad tx as well as estrogen suppressing meds. I went cold turkey stopping my bio-identical est, prog, test creams (big mistake, what was I thinking??), now I'm slowly weaning them. I'm awaiting Oncotype results and visits with the oncologist and rad onc to hear about recommendations. I have Ehlers-Danlos syndrome (a collagen defect that causes skin to be fragile among many other problems) and chronic inflammation of my spinal meninges (adhesive arachnoiditis). I cannot sit, stand or walk without moderate- severe pain. That leaves the recliner at just the right angle to take all pressure off of the affected areas of the spine, but I refuse to stay there all the time. Some activities are worth the pain. I am currently taking on line classes from the recliner with adaptive equipment for medical coding to supplement my disability. I do not have pain meds because of the opioid crisis. I do have suboxone, which is all that the doctor would prescribe for the pain, and it does help a little bit. I have osteoporosis and diabetes from chronic steroid therapy. My other diagnoses aren't pertinent to the discussion. My quality of life is not very good due to the pain and limited mobility (I use a cane and a walker and can't walk very far due to leg weakness and pain). I have 2 grown sons and older grandchildren and wonderful, caring friends that I do have a lot of joy with. I am not seeking sympathy..I just want to share all this as it will certainly impact my decisions.
When I stopped my hormones, I was unable to get out of bed and walk without intolerable pain. I could not think straight, nausea, etc, etc. I am down to one dose of hormones every 3 days but increased pain won't let me get beyond that. I'm trying but unless this gets better, I can't live in a bedbound state. Then the meds? I don't see how at this point. I do not make collagen appropriately. Estrogen helps collagen production. Logic tells me that my pain and quality will worsen. I could take tamoxifen due to its ability to help osteoporosis; however, things would deteriorate on the med. Logic also tells me that radiation could put me at risk for serious skin complications, (as well as the diabetes) due to the Ehlers-Danlos. This seems like an impossible situation to me. I need to research what the chances are of recurrance that doing nothing would bring. I don't think I would tolerate chemo for obvious reasons. Each therapy could cause long term problems, compounding my poor baseline. What a train wreck, right? I feel blessed to have the low risk cancer that I do have and respect all of the experts abilities to help us. I'm just not sure what true "help" would look like for me. This was probably premature without Oncotype and recommendations. I will report back. Thank you for reading all of this. I feel somewhat relieved in just getting it all out there. Wishing all of you the very best on your personal journeys.

Interested in more discussions like this? Go to the Breast Cancer Support Group.

It seems like a priority to get off hormones, sorry. That is my lay person's view but with high estrogen scores, the hormones are feeding any stray cancer cells- if there are any.

If anyone continued low dose hormone replacement in the context of a hormonal cancer, I hope they will chime in.

It does sound like tamoxifen would be better than an aromatase inhibitor for you!

This is a complicated situation, one that requires your doctors to talk with one another. You could see a second opinion on the radiation. Was a mastectomy out of the question for you? That is how I avoided radiation.

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@krisrwalters You might want to talk more about tamoxifen with your oncologist. For us post-menopause, tamoxifen only blocks estrogen in the breast, but has estrogen-like effect in most of the rest of the body including bone, heart, skin, and brain. I do not believe it damages collagen.
I have been amazed at the estrogen effect I’ve seen in my body: a reverse of GSM (vaginal atrophy, dryness, etc), and better skin elasticity. It seems to be dose dependent. At 20 mg I had better estrogen like affects - but also came with moodiness and headaches. I did not have hot flashes, but it did seem to take longer for my body to cool off if I got overheated in a hot car, or after hike in the sun. At 5 mg, I still had good GSM response, less moodiness. The jury is still out on whether the headache I now have after 3 months on this dose is actually from tamoxifen or other causes. At closer to 2.5 mg, I lost the benefit of the estrogen-like boost and again had moderate GSM. (Yep, I’ve tried them all working through which dose is best, with a drug holiday between 20 mg and 5 mg).

Here is a case of someone with hypermobile Ehler Danlos. I realize there are different forms of the condition, so this may not apply to you. My cousin has Ehlers Danlos and had major major multiple surgeries to his legs and knees at a young age.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514306/

Wishing you the best!

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@windyshores

It seems like a priority to get off hormones, sorry. That is my lay person's view but with high estrogen scores, the hormones are feeding any stray cancer cells- if there are any.

If anyone continued low dose hormone replacement in the context of a hormonal cancer, I hope they will chime in.

It does sound like tamoxifen would be better than an aromatase inhibitor for you!

This is a complicated situation, one that requires your doctors to talk with one another. You could see a second opinion on the radiation. Was a mastectomy out of the question for you? That is how I avoided radiation.

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@windyshores I appreciate your thoughts. I explained my situation to my surgeon after her offer of a lumpectomy and asked her if, knowing my conditions and concerns, a mastectomy would be better in order to avoid radiation. She told me that breast conserving surgery with radiation would still be better on the whole for me than a mastectomy and no radiation. I still question that and wish i had asked for a second opinion. Yesterday was 3 days without hormones, so I'm making progress. I'll make it 4 today. I would very much like to hear if others have continued bioidentical hormones. Thank you!

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@krisrwalters

@windyshores I appreciate your thoughts. I explained my situation to my surgeon after her offer of a lumpectomy and asked her if, knowing my conditions and concerns, a mastectomy would be better in order to avoid radiation. She told me that breast conserving surgery with radiation would still be better on the whole for me than a mastectomy and no radiation. I still question that and wish i had asked for a second opinion. Yesterday was 3 days without hormones, so I'm making progress. I'll make it 4 today. I would very much like to hear if others have continued bioidentical hormones. Thank you!

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@krisrwalters is the oncology surgeon refusing to do a mastectomy? My docs were concerned about my ability to handle that surgery so they did one at a time. I did fine. They were more concerned about radiation for me given my lupus diagnosis, not sure why.

What happens if you tell your current doctor that mastectomy is what you want? You do have a right to that choice, I would think.

I hope day 4 without hormones goes okay!

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@krisrwalters

@windyshores I appreciate your thoughts. I explained my situation to my surgeon after her offer of a lumpectomy and asked her if, knowing my conditions and concerns, a mastectomy would be better in order to avoid radiation. She told me that breast conserving surgery with radiation would still be better on the whole for me than a mastectomy and no radiation. I still question that and wish i had asked for a second opinion. Yesterday was 3 days without hormones, so I'm making progress. I'll make it 4 today. I would very much like to hear if others have continued bioidentical hormones. Thank you!

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@krisrwalters I thought I read that with Ehlers Danlos that skin does not heal well after surgery. That it can lead to sutured areas that don’t mend quickly leaving them open to infection- which would then cause damage to the fragile skin and more problems. I believe it is because connective tissue is altered in Ehlers Danlos.
It could be the surgeon was trying to limit the size of the open wound on your chest?
Going forward, I’d suggest discussing the Ehlers Danlos with the radiologist. Lower doses of radiation might help limit skin damage? Maybe even ask if it’s possible to do half the radiation sessions and take a break to see how it’s affecting your skin before continuing with the rest. I realize their protocol is to give radiation doses in consecutive weeks, but maybe it could be adjusted for you. I don’t know if/how it would affect the effectiveness of the radiation.

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@triciaot

@krisrwalters I thought I read that with Ehlers Danlos that skin does not heal well after surgery. That it can lead to sutured areas that don’t mend quickly leaving them open to infection- which would then cause damage to the fragile skin and more problems. I believe it is because connective tissue is altered in Ehlers Danlos.
It could be the surgeon was trying to limit the size of the open wound on your chest?
Going forward, I’d suggest discussing the Ehlers Danlos with the radiologist. Lower doses of radiation might help limit skin damage? Maybe even ask if it’s possible to do half the radiation sessions and take a break to see how it’s affecting your skin before continuing with the rest. I realize their protocol is to give radiation doses in consecutive weeks, but maybe it could be adjusted for you. I don’t know if/how it would affect the effectiveness of the radiation.

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Yes, poor skin healing is part of the equation and she may very well have been thinking of that. Seems rad tx would be more concerning in terms of skin healing in the big picture but her perspective would be primarily surgical I suppose. I'll have to remember that it may be only me that's keeping the big picture in mind going forward. I really like your ideas to negotiate on the radiation and will definately discuss with the rad oncologist. Thank you for caring enough to understand my situation and respond. Means a lot to me. Big hugs!!

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@windyshores

@krisrwalters is the oncology surgeon refusing to do a mastectomy? My docs were concerned about my ability to handle that surgery so they did one at a time. I did fine. They were more concerned about radiation for me given my lupus diagnosis, not sure why.

What happens if you tell your current doctor that mastectomy is what you want? You do have a right to that choice, I would think.

I hope day 4 without hormones goes okay!

Jump to this post

Oh no, the surgeon didnt refuse but strongly pushed for the lumpectomy and I went along with that. I'm 4 weeks out now. How did you do with your surgery given the lupus?

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@triciaot

@krisrwalters You might want to talk more about tamoxifen with your oncologist. For us post-menopause, tamoxifen only blocks estrogen in the breast, but has estrogen-like effect in most of the rest of the body including bone, heart, skin, and brain. I do not believe it damages collagen.
I have been amazed at the estrogen effect I’ve seen in my body: a reverse of GSM (vaginal atrophy, dryness, etc), and better skin elasticity. It seems to be dose dependent. At 20 mg I had better estrogen like affects - but also came with moodiness and headaches. I did not have hot flashes, but it did seem to take longer for my body to cool off if I got overheated in a hot car, or after hike in the sun. At 5 mg, I still had good GSM response, less moodiness. The jury is still out on whether the headache I now have after 3 months on this dose is actually from tamoxifen or other causes. At closer to 2.5 mg, I lost the benefit of the estrogen-like boost and again had moderate GSM. (Yep, I’ve tried them all working through which dose is best, with a drug holiday between 20 mg and 5 mg).

Here is a case of someone with hypermobile Ehler Danlos. I realize there are different forms of the condition, so this may not apply to you. My cousin has Ehlers Danlos and had major major multiple surgeries to his legs and knees at a young age.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514306/

Wishing you the best!

Jump to this post

Excellent article,
thank you!! Wow, you've been through it with the tamoxifen! I'm glad to know about the action of it. Hopeful! I'll be talking to my oncologist about that for sure. My former spine doctor diagnosed EDS but didn' mention a type. I'd need to see a geneticist to determine that. Unfortunately, estrogen is involved in collagen formation but I'm charging ahead. I appreciate all of your good info and wish you all the best!

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@krisrwalters

Oh no, the surgeon didnt refuse but strongly pushed for the lumpectomy and I went along with that. I'm 4 weeks out now. How did you do with your surgery given the lupus?

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@krisrwalters I did fine with the first mastectomy so they agreed to do the second shortly after the first. I went flat so it was easy. I didn't know you had already had surgery so my comments aren't relevant!

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I’m new to this, so I am extremely grateful to everybody sharing the best/worst experiences they’ve had and the extremes of information covered.
One of the very best sites for feedback I have come across.

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