Calling all TNs
Comments
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TIFJ- yes it is rare but it can change. I've been praying for a mutation too. When I developed the skin mets that can be a sign that the FC has changed to her positive, but no such luck. The chances are small. I hope you had a good day.
OBXK- our brunch was so much fun. We are going to try and do that more often. I hope you had a good day too. -
Thanks for the info Laurajane! Having a lazy day at home with the family. Husband is messing around in the garage and kids are playing with Legos. I am sitting on my butt playing games on my Kindle Fire. Glad you had a nice brunch! Have a great evening!
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I found my lump around Christmastime. 2009. I hit my breast on a chair and it hurt. Then I found a lump. Pigeon egg sized. It throbbed! Due to my husband then being laid off work. I didn't go in. NO money! A Cafemom friend had the same symptoms.. Sounded like me. So when I made my apt. for my mammogram. One where you go to a clinic and they take you out back to the Van! I said I had a lump. she goes, then I can't do you! So I had to wait and go to another city. I didn't have a safe car. So my newly jobless Daughter decided to take care of me! It was always she driving, her Dad & I!! Mammograms, Biopsies.. And having a morning Friday hurting test. Took until 3:17pm on Monday March 1st. A Scheduled Fun Day! Well the phone cracked the girl's voice cracked and I heard I have Breast Cancer!! Everything changed then!! I had some tests, sentinel biopsy Etc.. A bad DR. that couldn't do anything Right! A Surgeon that did my first surgery and installed my Not Good Chemo port. Then she decided to close her practice and run for politics! So I had to find a New surgeon. I did 4 rounds of Adriamycin/Cytoxan every other Monday with a neulasta shot on Tuesdays. The did 7 weeks, every Monday of Taxol. It was disabling me. So I couldn't do the 12. I had a lumpectomy scheduled on my 50th Birthday but she changed it to 2 days before my Birthday. I ended up with 35 days of Radiation including a boost. I'm still tanned, swollen and hurting!! My husband is still jobless. So we have no income! I never recovered from all of this! I'm in pain from head to toe. But we still have each other and Love!! That dear husband whom I met one Christmas eve 1976. Begged me to live to stay with him. I did. I feel helpless and hopeless. But am still alive to live to love another day.. Nothing in this was easy. Whatever could go wrong did! But I got through it! Thinking back on my life.. This wasn't even the worst part of it!! I guess "Triple Negative" anything can't be Good!? I hope that we can find any common denominator and see what it is.. Do we fit into any profile? I'm a 32 year Migraine sufferer and was told migraine sufferers are less likely to get breast Cancer. They've never stopped!! I hope to live to see Prevention and The cure to all Cancers!! When I was 19 & pregnant. We found my Bio mom. Whom I was taken away from by the RN in my birth hospital. So When we found her in time. She was dying from Breast Cancer. She never shared if I had a Dad or family. I never shared she'd be a mother. not that she lived. We had a short emotional visit. She was 46. My poor dear husband got to see her dying look on my face! It was so hard to see his broken heart looks on his face. He felt so helpless but tried to encourage me! I do have married daughters and grand babies. I always wanted a big family I never had! I now have it. Its all you Cancer fighters right with me! Thank you! Nice to know you! Strangers are friends I've yet to meet!
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LJ..give Mary a hug from me too...good thing about the er positive..I hope this helps! and have fun shopping at Zappos..I wear a size 8..lol.
Welcome Angelinda!..so you are more than 3 years out? Thats a good thing!
Today is my 29th wedding anniversary and my husband left for a business trip...wow..I'm lonely...it's good for him to go...I think he would have declined a couple of years ago..I sent him a pic of our toothbrush holder..with only one toothbrush in it...
I miss him...Tomorrow is 35 months out from my surgery...sometimes I just can't believe it...
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Titan - ((hugs)) to you with your husband out of town, and celebrating not one but TWO important milestones. I'll be thinking of you tonight and tomorrow.
Susan -
angellinda - thanks for sharing with us. All I can say is that you are one heck of a strong woman and some one up there seems to be taking care of you. Life can get very challenging sometimes, but just hang in there. After every dark night comes a bright beautiful sunny morning. I didn't see your diagnosis at the bottom of your post. If your add that to your profile, then it will appear under your post. Do your know your stage?
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My heart breaks to hear about MBJ. How, when did this all happen? My God! I just cannot believe how one day someone is well, getting better, and then it is back. I know that MBJ was taking all kinds of precautions. I am glad she will be able to take tamoxifen now. My body could not take aridimex for the very small percentage of positivity. I am so scared, my core needle biopsy is scheduled for Tuesday afternoon. I had my Cervical spine MRI on Friday and the results are not out yet. When the surgeon calls me at work next week to give me my results, I swear to God, I will have a heart attack before I can hear it. Can anyone please give me any advice as to how to hear your results. To me this is the single most difficult thing in the world. Shall I have her call my son who can tell me easily later? I swear I don't know how to handle this. I am sure I will pass out, as my heart will come out of my chest. I am so scared of another cancer diagnosis. What shall I do, ladies. Does anyone know what percentage of TN's have a local recurrence? What percentage have a distant mets?
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Lovelyface,
I wish there was a way I could take away your anxiety. I hate scans and waiting for scan results. It makes me so anxious. Just know we are all thinking of you and hoping the best. Sending you a hug through cyberspace.
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Titan, Congratulations on 29 years!! That is a great accomplishment. And 35 months is awesome, too - you are almost to the big milestone for us!
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Another good day today. Managed to get a heap of work done. I am a medical typist so probably read too much and know so little. Tomorrow I go for a bone scan and whilst I am in Hamilton will see the Wig Lady. I have told her I would like long, beautiful, wavy, shiny locks that will make me look like Julia Roberts (yea right). Have noticed my head is itching like mad at times but it isn't even a week until tomorrow. Honestly haven't got nits!!
Laurajane - yes been drinking heaps of water. At least 2 litres per day so that might be why I am also so puffy. In the middle of the night sometimes I feel like I won't stop peeing.Will talk to my Onc as you suggest though so hope its not kidneys.
OBXK - Yes having another upswing day. Have taken a stool softener and not working much but didn't take it right from the start. So will take it as soon as I start the next chemo this time. Hopefully I will come right as I am eating lots of veges.
Mccrimmon324 - I have found that putting my feet up for half hour during the day helps though haven't been getting the exercise that everone talks about. Gotta make an effort.
BernieEllen - your Pet Moneky joke was excellent. Keep them coming.
Lovelyface - I pray that your scan will be ok. I know how you feel waiting for results, absolutely nerve racking. They will ring you and say I hope you are sitting down cause we have some good news.
Can anyone help me with thrush in the mouth and to the sides of my mouth. Very uncomfortable when I am eating. Not a major just irritating me.
Can anyone tell me if they have had a CT scan where you take a contrast drink first and what it was like. Will be having that next.
Keep your chin up ladies. You are all so positive I take my hat off to you all.
Annie ooxxoo
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Annie, I got thrush twice, and both times, the doc wrote for me to take Nystatin, an oral anti-fungal. It's a sweet liquid you swish and swallow four times a day. Some don't like the taste, but I thought it tasted like candy, so I never forgot to take it!
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Titan - Congrats on your anniversary!! So sorry that your alone, the single toothbrush makes me sad but its only a business trip and he'll be home in no time.
Lovelyface, I am so sorry your having such anxiety, I really wish there was something we could do or say that would make it better. My only suggestion is to start taking your xanax or your anti-axiety meds on a regular basis. Practice your deep breathing and maybe let your doctor's know that your extremely anxious and would like the results ASAP. Keep posting, maybe just talking about it will release some of it. We're all her with you.
While I'm devasted over MBJ's reocurrance I have to admit that I am very happy to hear it switched to ER+, so glad to know she's got some other treatment options now.
LJ - Have fun shopping!! I could use a shopping trip. Vacation is 4 weeks away!!
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CockerSpaniel,
I have had two CTs with contrast - the test itself is not scary - I didn't like the breast MRI even though supposedly it is somewhat "open", I found it very claustrophobic. But the CT scan IS open and relatively quick. Make sure you put the contrast in the fridge the night before so it is cold. It tastes better that way. I have had the cappuchino (yuk) and berry (less yuk) flavors of contrast. They told me berry was the most popular. Both times it took at least a day or two to get my results. I was so anxious I went to the nurse's station and got a copy of mine because I hadn't heard from the doctor yet. Sending you my best for a clean scan!
Pretty day here in Tennessee. I am just now getting up; my days and nights are all mixed up due to chemo. Feels weird to be finished after a year of active treatment. I am going to be on tamoxifen for the 5-10% ER receptors but won't start for a couple weeks. Hope everyone has a great day! I'm headed into my office once I can get moving.
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Annie - just a word of warning about the CT contrast. A few hours after getting home afte the CT I had a sudden urge to get to the bathroom. Though I rushed, didn't make it in time.
The first time I pooped my pants in a long time!!!! This happened to a couple of other ladies on my chemo thread - but nobody had warned us about the possibility. I was lucky, only 10 minutes from the hospital. Where are you - England? Just some of the things you say makes me think that. -
Happy Anniversary Titan!! Make sure you use the guilt factor when he gets home- always leads to a nice gift or evening out!! HA!!
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Good afternoon ladies. I hope you are having a good day so far.
Angellinda- congratulations on being almost 3 yrs out. I'm curious as to what stage you were diagnosed at too! Any lymph nodes? We are all here for you. I hope you have a good day today. Do something nice for yourself.
Titan- happy anniversary! 29yrs is amazing. I hope you both can celebrate when he comes back from his business trip. I think your photo of the single toothbrush is priceless. It should be on a Hallmark card or something. 35 months since surgery is cause for celebration too! I'll toast you tonight with a glass of wine.
Lovelyface- I'm saddened you are having to go through this anxiety. I wish I could think of words to help you through this. I'm hoping with all my might that everything is going to be ok. I'll be
thinking of you tomorrow when you get your biopsy. I hope it is pain free and again everything is fine. I also hope someone is going with you. Breath in breath out and concentrate on each breath.
Pop a Xanax, I hope you have some. Please let us know as soon as you can.
Cocker spaniel- I had thrush real bad and could hardly swallow, but the Nystatin helped me also as it did Riley. As far as your CT scan, they had a new flavor, vanilla, didn't seem as bad as so many of the others I've
had, chill it, drank with a straw, pretend it's a milkshake, helped it go down faster for me.
I spoke with my onc's primary nurse today and my onc wants to see me tomorrow instead of next Tuesday. Im trying to not let myself get worried. I'll get the results from my MRI and she wants some extra X-rays done. Hoping I can share good news with all of you about my appointment with her
tomorrow. It is beautiful here today in the high 40's and sunny. Im feeling happy to be here. I'm going to go out and play a little in my greenhouse and maybe work on my painting some more. I'm working on an abstract landscape which I've never done before. I've always done figurative paintings. It's kind of fun to challenge myself. wishing you all smiles and sending hugs. -
Laurajane- we will all be with you in spirit tomorrow- praying for good, no great results!! have fun in the greenhouse today!
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LauraJane, praying for fantastic results, have fun today!
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Hey
I havnt got my hormone report yet and am scared tht am TN my bioposy shows am grade 2 Can TN occurs in grade2? I find that all of you are in grade3 tht s y I ask thank u
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Rosa - Most Triple Negatives are Grade 3 but there are a few of us who are grade 2 - I am a grade 2.
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Happy 29th wedding anniversary Titan!
Loverlyface- Sending you calming vibes. I know waiting for result is hard.Deep breaths.....(((Hugs)))
CS- My onc prescribed what was called "magic mouthwash" for mouth sores. I had to use it once on AC and it worked wonders. Ask your onc for it.
LJ- Wishing you good results tomorrow.
MBJ- Hope you are feeling better and that the fact that your BC switched to + will open up new treatments for you. Fight on!!! We are all with you. (((Big Hugs)))
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LJ praying for good results tomorrow.
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LJ..you WILL hear good news tomorrow..I know it...know it know it know it...
Thanks for the anniversary wishes (both BC and wedding)..god he irritates the hell out of me sometimes but I miss him when he is not here...he was my rock during surgery/chemo/rads..very patient with me..while I was climbing the freaking walls...my daughter said he cried when the BS told them that they had "got it all" and that there was no lymph node involvement (not that I knew what that was at the time..duh)...he still won't admit that he cried..but I remember..oh yeah..I remember..
Mary..thinking about you all the time..remember...we are planning to get together since we are now neighbors!!
Lovelyface..thinking of you as well...praying for good results...I know you are freaking right now...its so dang hard to go through all these tests...hoping for benign
Cocker..hang in there ok? se's will happen...just take it easy..rest when you need to..eat when you want too...I still say that going for a little walk or just going out somewhere helps alot....don't cage yourself in your house...
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Oh yeah Rosa..tn can be Grade 2...that's a good thing...
I don't worry too much about being Grade 3...it is what it is...
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LJ - hoping tests come out good for you.
Saw onc today, will be calling hospice tomorrow. Even though the Halaven is working at keeping me stable, I still seem to be headed downhill. My appetite is nil, I'm not keeping much down, I'm using a wheelchair constantly, and am on oxygen most of the time. All I want to do is sleep. There are some chemo options I may be be willing to try as long as SEs aren't too bad. They are simply palliative so not a problem with hospice. My MO is consulting with Dana Farber also, but we aren't holding out much hope.
My doctor can't give me a definite timeframe. From one week to five months, but likely somewhere in between. I physically don't feel great, so my guess is three months.
I won't be posting much, but when the time comes, my best friend will be sure to let everyone know so there aren't any questions.
This board has meant more to me than words can ever say. I am okay, and am going to take these next weeks really trying to feel well.
I love you all,
Susan -
Susan, what a courageous thing you have done. As much as this board has meant to you, there are hundreds of us on here whom have been inspired, and educated, and helped by you! I lurk a lot but have checked back often to check up on, well, you, and a few others, and am heart broken, and inspired.
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CockerSpaniel, I got a mild thrush just after my second round. I didn't want to take any more drugs (cripes, we had enuf huh?) so I, in the days coming down from steroid high and before SEs kicked in, found a yogurt I liked (lemon meringue yum) and ate a few of those a day. Protein was good. And it got rid of the thrush, which was, uh, gross. I was on taxotere, which I blame for this nice SE. I also had neulasta shots the day after. The claritin thing sounds kinda kooky, but I didn't take it the first time, and I had horrible leg and body aches. And took claritin the second time, and still felt crappy the fourth day out, but no aching - so go figure. So for whatever it's worth...
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It seems like only days since I met you here on the boards. You always have the right words to calm me. I am wishing only the best for you, pain free days and much time to spend with your beautiful family. I think of you always and will be happy for the days you decide to post to us.
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Susan - I have no words except..........tears, tears, tears, and a very broken heart. I still want to believe in miracles. Please don't say goodbye. You have helped me so much on this board, so my heartfelt sincere thanks for all your help and guidance. I hope your kids are doing okay. May God bless you and your family, my friend.
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To suze35 (Susan),
I cannot find the words to express the sadness I feel about what is happening to you. You have been such an inspiration to all of us on the TN threads.
Thinking of you,
Sylvia.
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