Jun 7, 2014 10:50AM Adnerb wrote:
SW, Mame, and Maureen,
Wow! I am so happy to hear good news and great responses from treatment!
That really makes my day. Thanks for sharing, fellow-metsters!
Brenda
Posted on: Jan 6, 2012 11:53AM - edited Oct 12, 2013 10:32AM by bhd1
Posted on: Jan 6, 2012 11:53AM - edited Oct 12, 2013 10:32AM by bhd1
bhd1 wrote:
hello. i got scan rusults yesterday. looks like abraxane is not working, since cancer is spreading. i am going on navelbine now. any words of encouragement? thanks. i am new to the boards, happy to find you all
barb
Jun 7, 2014 10:50AM Adnerb wrote:
SW, Mame, and Maureen,
Wow! I am so happy to hear good news and great responses from treatment!
That really makes my day. Thanks for sharing, fellow-metsters!
Brenda
Jun 7, 2014 02:21PM carolsue63 wrote:
So happy to hear all the good news! Keep it coming!
Jun 7, 2014 02:39PM - edited Jun 7, 2014 02:43PM by tryn2staycalm
Great news ladies! Do you ladies get the bad taste like tin with the Taxol? Another question. I did Tamoxifen for 2 years and it was holding my "spots" (unknown if it was cancer or not at that time) stable. However I had extreme s/e of being hot and severe hot flashes with it. I will be getting Letrozole in this drug study and hopefully the trial drug (66% chance) rather than Letrozole and placebo. My onco did say it can also cause hot flashes. Did anyone have bad hot flashes or sweats from it?
Brenda:
Not sure if I have to drink anything for the scans or not. I can not have anything to eat or drink after midnight on Sunday other than clear fluids. I will have to drink some apple juice so sugars stay stable.
Cathy
Jun 7, 2014 03:13PM Maureen813 wrote:
I get the taste from the heparin flush I try to have a piece of hard candy in my mouth to mask that taste.
Jun 7, 2014 10:02PM Adnerb wrote:
Cathy, I did have hot flashes from letrozole, but not severe. I only took it for 3 months because it did not work. There is a femara thread: Letrozole is generic for femara.
https://community.breastcancer.org/forum/78/topic/...
There's a myriad of side effects, but not everyone gets them. I hope you are one of the lucky ones.
Brenda
Jun 9, 2014 02:49PM tryn2staycalm wrote:
Thanks Brenda will look into it!
Jun 11, 2014 10:38PM tarheelmichelle wrote:
Hello Skylotus, welcome! It's fine to say you feel crappy. So many of us do, and like you, we just keep pushing on.I've learned so much from the Stage IV ladies, and I'm proud to be here. You're at home here.
I'm glad to read that I'm not the only one who takes breaks of a week or two, and then has to take awhile to catch up reading all the posts, and gets kind of lost. lol
Glenna, I wanted to just add "Wow" to the beautiful wedding photo. What a lovely couple and YOU WERE THERE!!! Whooppeeee!!! :-D .... You had asked about morphine and my reconstruction. I finally had fat grafting reconstruction to fill in my left breast, which had a partial mastectomy in 2008. But I am on morphine for the cancer pain. My bones and lungs hurt. I don't think the lung has nerves, so it's my pleura or something. I can't be off pain meds for longer than an hour or two or it's unbearable. It is getting better though. I no longer have bone pain that wakes me up out of a deep sleep if I sleep too hard against my ribs. Thank God.
Adnerb, yes, I can drive on morphine, but only short distances (30 minutes or less) and I have to be very cautious. I've been on 3 painkillers, Fentanyl, OxyContin and Morphine. Morphine definitely has the least side effects when it wears off, so that's a blessing and I wish I had tried it sooner. But the memory loss ... not sure if it's the morphine or the Tamox, but it seems to be getting worse, not leveling off. I am trying every trick I can think of. I shun phone calls, because I can't remember what people tell me. I communicate with friends primarily by text and email, so I can refer back to what they have told me. I can't be honest with my husband about how much I don't remember. Only with you ladies can I share how frightening and sad it is not to remember meeting people, or eating at restaurants, or even more important things. I've stopped locking my car door because I'm afraid I'm going to lock the keys in the car (which I've done 3 times already) Sometimes my speech or handwriting is jumbled.
My son gets his driver license in two weeks, he is a very good, careful driver. He will be happy to drive me around, I think. Adnerb, you also asked about the Tamoxifen. It has slowed down the tumor growth, though not as substantially as Aromasin (which I couldn't tolerate, the bone pain was excruciating). So, while the Tamox is keeping the tumors at bay, I still have to deal with the tumors that are there, and the pain they cause. I hope that over time Tamoxifen may help reduce those tumors, so I can reduce my dependence on pain meds. I'm back at Sloan-Kettering for my 3-month scans in a couple weeks. I am feeling good and expect the scans to show tumor stability. A little regression would be nice!
Someone mentioned hot flashes, Here's something that helped mine. It's kind of embarrassing because it took me a while to realize I was causing them! I bought a down comforter about a year ago, for the first time, something I have wanted my whole life. Even though it was a lightweight down, it was doing a superior job of trapping the heat, and almost every night I would wake up covered with sweat, have to change out of my pajamas, or grab a towel and sleep on it, etc. My husband suggested we take off the down duvet, and sure enough, my nighttime hot flashes disappeared. Admittedly, once or twice a week I wake up a little warm, and I keep cornstarch on my bedside table, and apply that. It's not that down/feathers are "bad" -- it's just that my body can't regulate its temperature properly, and I can't cool myself down when the down heats me u[. Now, whenever my husband and I travel, I have to find something to sleep under besides the down comforters that most hotels are using these days. I hope this helps someone else stay cool.
Wishing all of you ladies lots of energy and happy moments with your family. I think my son may have landed his first job at 16. He had an interview today that went well, with the restaurant manager, "putting stars beside my name and work hours on the piece of paper he was writing on while he interviewed me."
Jun 11, 2014 11:51PM Adnerb wrote:
Ronda,
I am keeping my fingers crossed and hoping that your next scans show regression! Thank you for updating us. There is so much that we can learn from each other!
Brenda
Jun 12, 2014 12:17AM susaninsf wrote:
My unbelievably wonderful MO e-mailed me after midnight last night to give me my scan results: "Nodes much better. Lung mass stable but much less active. Overall improved!". Got the written report today and it did sound very good. Everything is either better or stable with the exception of my eye tumor which I already knew was thicker from my photos done in Ocular Oncology. My first scan since diagnosis two months ago. Feeling relieved!!!
Jun 12, 2014 01:05AM susan3 wrote:
hello ladies..I am new to this thread. Just wanted to pop . I had my recurrence almost 3 yrs ago now. Many many nodes in neck, clavicle, alongside neck by jugular , lung, rib, spine..think that's where Waldo has been showing up. I stay on chemos for about 4 months then we have to change cause Waldo starts to move around again...always need to find him. Can't to targeted treatment anymore cause I became hormone refractory . Waldo eats up those treatments like food and spreads even faster. So general chemo for me. This last one I started December 13 th, havelan.....and I am still on it. And with good reports. The only node detectable is one in my jawline on left side, but it is smaller than it was in December. Best news I have had in 3 years. Maybe this one will,work for a nice long time. Se are very very doable. I have been having a blast since February, and will continue to do so :) , for as long as I can!
Hope we can all get on something that gives us great relief for quit a fee months so we can live fully and maybe for a moment, maybe, just forget we have this......hugs to all