TRIPLE POSITIVE GROUP

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  • jumbledbamboo
    jumbledbamboo Member Posts: 158
    edited September 2015

    KateB your DX is so similar to mine. I had mixed tumors however I was grade III in the DCIS tumors. You are in my thoughts Special K I wish you were here to read my reports!


  • twiggyOR
    twiggyOR Member Posts: 270
    edited September 2015

    I'm looking for sources of nutritional information. What foods should I avoid and what foods are particularly good to eat? Does anyone have any good resources to point me to?

  • momwriter
    momwriter Member Posts: 310
    edited September 2015

    SpecialK-

    Congratulations on 5 years!!! That's just great.

    Thanks for sharing your experience. I hope your next surgery is your last for a very long time!

    My MO yesterday said that because I have to see her every 6 months for the clinical trial followup protocol,I don't need to see the BS or the RO, (unless something comes up of course). She also recommended I stay on tamoxifen given my age (50) and the outside chance the period could come back- she also sees Herceptin (and perjeta) as the silver bullet for Her2 people.

    Thanks again for helping navigate it all.


  • SpecialK
    SpecialK Member Posts: 16,486
    edited September 2015

    momwriter - thanks! Unfortunately, the next surgery will not be my last as my PS will hopefully be able to place another expander - I will have to go through the expansion process again and then exchange for an implant if all goes well. Because things are such a mess on the left side I think it will require some more fat grafting after exchange to make things look presentable. Glad you can pare the doc appts down to a manageable level.

    jumbled - thanks for the good thoughts, but I am not having any surgery yet, probably not until the end of the year. You can PM anytime if you want me to look at any of your report info.

    twiggy - there doesn't seem to be much hard and fast food info. A lot of people like David Servan-Schreiber's book, Anti-Cancer, A New Way of Life. There are also some threads on BCO, here are a couple:

    https://community.breastcancer.org/forum/79/topic/...

    https://community.breastcancer.org/forum/78/topic/...

    Here is another site some people use. Also, just Google breast cancer diet and you get a bunch of info:

    http://foodforbreastcancer.com/

  • lago
    lago Member Posts: 17,186
    edited September 2015

    Congrats SpecialK. I can't believe you are still dealing with recon 5 years later! I feel I've been with you the entire time

  • KateB79
    KateB79 Member Posts: 747
    edited September 2015

    Well, it's time for the next echo (in two weeks). Fingers crossed that the old ticker is strong enough to keep going with Herceptin/Perjeta! No reason to think it isn't, but I'm developing test anxiety. . . .

    twiggyOR, check out a cookbook called the *The Cancer-Fighting Kitchen.* Fantastic recipes and tips.


  • Moonflwr912
    Moonflwr912 Member Posts: 6,856
    edited September 2015

    Specialk congrats on 5 years! In December it will be 4 for me. My regimen is close to yours, but my B'S quit so no B'S visit. However, my PS took over as hes VERY familiar with my implants! LOL My MO sees me very 3 months yet because of my low magnesium issues still. Also I've never had a scan and my Dexa was still this side of osteoporosis. As usual, every MO is different. Actually just saw my PS this month for some scar tissue along the incision line. Thank goodness that's what it was. And y PCP saw me very 3 months during cancer tx and now back to 6 months because of my diabetes.

    I don't need rads as i had a BMX with clear margins. But as my tumor was Her2+ Definitely chemo.

    Much love to all

  • lago
    lago Member Posts: 17,186
    edited September 2015

    Moonflwr912 I was osteopenic before even chemo. After chemopause I took a big drop but still osteopenic. My MO does dexta scans every year when you are on the AIs and not being treated for osteoperosis. Now that I have osteoperosis and it's being treated she only scans every 2 years.

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited September 2015

    Congrats, Special K! Hope you get your reconstruction finished soon.

    I'm on Zoladex to suppress my ovaries so I can take Aromasin. It means getting a shot at MO's once a month. If I get an ooph, I can get off of Zoladex. Has anyone had difficulties convincing their insurance companies to pay for an ooph? How much recovery time is involved? Thanks!

  • SpecialK
    SpecialK Member Posts: 16,486
    edited September 2015

    Thanks all for the congrats! Seems like a lot of time has passed, but it also seems like yesterday!

    lago - I know, right? Seems endless, but I did have a couple of years with no issues, then when I had the allograft repair last year everything went to hell in a handbasket. That surgery spawned four more, with at least another two coming - and that is if everything goes perfectly - what are the chances of that happening? Lol!

    elainetherese - I have a BRCA1+ friend who had a robotic ooph after her BMX with recon and was back to work in a relatively physical job, on her feet a lot, within two weeks. Her insurance didn't hesitate to pay, even though she was TN, but I would guess that was because of her BRCA status. I would think if your onc is recommending it you could get a pre-auth so you would know for sure.

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited September 2015

    Special K: Yes, a pre-auth would seem to be in order. I'm seeing my OB-GYN this week, and his website brags that he is an expert in daVinci robotic assisted surgery. I never paid much attention to that before because the only time he has ever operated on me was to give me a C-section. I will ask him about how much recovery time his patients typically need.

    Re: reconstruction, I don't know if there is a record for number of recon surgeries, but you may very well hold it. Here's hoping the next two do go perfectly!

  • SpecialK
    SpecialK Member Posts: 16,486
    edited September 2015

    elainetherese - I would also think with being pre-meno and ER+ would be an easy approval for ooph. My friend did bmx with TE, fat grafting and exchange and the ooph was easiest by far. And, yes, it seems like I should contact the Guiness Book with my number of surgeries - lol! I actually know someone who has had 18, I'm hoping to stop short of that, but I may not, as that is only four away

  • Musosgirl
    Musosgirl Member Posts: 387
    edited September 2015
    I have had some tingling in the tumor area and always thought "great!" the chemo is working, those cells are dying! But the last 24 hours it has ITCHED. It is driving me crazy. Anyone else have that SE?
  • Mommato3
    Mommato3 Member Posts: 633
    edited September 2015

    Elaine, I had a laparoscopic ooph/salpingo yesterday morning. I've felt pretty good. No running down the street though! I went to my DS two baseball games today. The incision at my belly button is a little sore but the other two don't bother me at all. I was told two weeks for recovery although I could get back to most normal things within a few days.

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited September 2015

    Thanks for your sharing your experience, Mommato3! Glad to hear it went so well for you. If an ooph is that low impact, I'll definitely consider it.

  • Jerseygirl927
    Jerseygirl927 Member Posts: 438
    edited September 2015

    specials you really explain thing so we can understand all. Had my 8th round of herceptin , have 9 more to go per my MO. He definitely wants me to get flu shot and pneumonia shot. And consider shingle. I am not fond of vaccines, so I will get pneumonia and Prolia shot, but slightly considering flu, and no shingles. With immune system being almost killed with these chemicals he thought it a good idea. I feel about 2/3 close to almost 100% but not there yet, fatigue is pretty compelling some times. Just hate to put anything else in my body. So just gonna take it slow for now. I only did 4 rounds of tcph b cause of side effects and other factors my MO felt I did enough to satisfy protical . Your MO is your guide in these matters..

  • lago
    lago Member Posts: 17,186
    edited September 2015

    Jerseygirl927 I did get the flu shot. Was not offered a shingles shot. 6 weeks after my final chemo I got the worst case of shingles. I was still doing Herceptin but my reconstruction/exchange surgery was delayed another month… trust me you don't want shingles.

    I never took any pain meds, didn't use the pain pump or even a tylenol after my BMAX with nodes removed on both sides. I did try to take narcotics for the shingles but they made me nauseous. Trust me you do not want shingles!

  • zjrosenthal
    zjrosenthal Member Posts: 2,026
    edited September 2015

    Anyone here have muscle and joint pain and/or spasms subside after finishing herceptin / perjeta? Love, Jean

  • KateB79
    KateB79 Member Posts: 747
    edited September 2015

    Anyone have gum recession or tooth pain on TCHP?

    I swear I have my first cavity....

    Thanks

  • momwriter
    momwriter Member Posts: 310
    edited September 2015

    Hi zj, my muscle and joint pain did lessen after I finished Herceptin (and possibly Perjeta- was on double blind study so don't know if I got it). I still have some on tamox, but it definitely made a difference for me finishing up- I also felt my energy was better. It's also possible that it improved because I was further out from chemo- taxol definitely was rough on my joints. Tamox still is but nothing as bad as taxol/herceptin was for me.

  • SusanHG123
    SusanHG123 Member Posts: 414
    edited September 2015

    Kate.

    Yep. Actually had fillings drop out--yes. Drop out.

  • SusanHG123
    SusanHG123 Member Posts: 414
    edited September 2015

    Thursday begins another year of Pinktober or *%&#tober. Or your designation of choice.

    Today, the eggs I purchased were stamped with pink ribbons. If the company had spent the money on research instead of stamping pink ribbons--oh my. I have said this during my three years of membership-and will again. I do NOT enjoy *$&%tober. In my prior life I was thrilled to purchase food items with a pink ribbon-I was certain so much money was going to research. Now just let me have my eggs and sweet potato and spend the money elsewhere.

    This month I will have my first appointment with my new MO as mine moved to Wisconsin. Anyone living in or near Appleton PM me-he is the best ever. As a nurse, I don't like the new guy. But have said I will give it one appointment. I have an appointment for a bone density. Am thinking my bones are hollow by now and I will be classified as a bird---if you see an odd looking flying object in your yard--might be me. Have an appointment to meet with yet another GI guy. And more labs in hopes there is just a tad of iron in my blood. I used to say I wanted a salt lick (still do) but maybe should add an iron lick of some sort. And eat a placenta.

    But, I did use a hair dryer today for the FIRST time since my hair fell out--the first of three times. Not saying I enjoyed it. Will probably have chemo curls again tomorrow. Am clueless as to why I still have chemo curls. Never had a curl in my life before the great adventure.

    Blood moon tonight. For the nurses and other medical persons among us. Yikes.

    Much love.

  • lago
    lago Member Posts: 17,186
    edited September 2015

    In defense of Pinktober. Before Susan Komen Charity no one ever talked about the disease. People were embarrassed. Finding information was hard for those diagnosed.

    Now I agree some of the "Save the boobies" is offensive since we know it's about saving lives but we can't put this back in the closet. Women are dying from mets and/or treatment. You would be surprised how many people believe if you have been diagnosed with early stage and treated that you are free and clear after 5 years!

    My recommendation is choose your charity wisely.

  • ang7894
    ang7894 Member Posts: 540
    edited September 2015

    Well said Lago

    ThumbsUp

  • Suladog
    Suladog Member Posts: 952
    edited September 2015

    yes, that's the catch with the pink... My MO told me 25 yrs ago that I needed to think of bc as a chronic disease... Hopefully you stay clear and never have any more problems but the get out of jail free card just doesn't seem to be there for this on

  • BlownOffCourse
    BlownOffCourse Member Posts: 37
    edited September 2015

    I guess I'm in the minority, but I not only don't have a problem with Pinktober but I actually appreciate the efforts that go into it. I know not every product/package/t-shirt/whatever is putting every single penny to BC research or awareness and the like, but if it has contributed, even in a very small way, to the life saving treatments and support that I've benefited from over the past 18 months or so I'm all for it.

  • Jerseygirl927
    Jerseygirl927 Member Posts: 438
    edited September 2015

    agree choose your charity wisely, as some are not what they seem. I was appalled to find out one of the major BC groups contribute heavily to planned parenthood who make it their business to kill babies.

  • wabals
    wabals Member Posts: 242
    edited September 2015

    Jersey girl which group contributes to planned parenthood?

  • lago
    lago Member Posts: 17,186
    edited September 2015

    Planned Parenthood doesn't kill babies. And yes Komen does give them some funds.

  • ashla
    ashla Member Posts: 1,581
    edited September 2015

    Jersergirl Planned Parenthood does not "make it their business to kill babies."

    They are funded by organizations like Komen to provide breast examinations to nearly half a million mostly poor women many of whom would go untreated each year.

    Educate yourself. This from the New England Journal of Medicine....Doctors and scientists...the ones who find cures for the deadly disease which we all share..


    http://www.nejm.org/doi/full/10.1056/NEJMe1510281

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