Bone Mets Thread
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Good morning all,
Rachel - congrats on TMs and good luck with echo!
Suems - good luck with the antihistamine. I agree with Lindalou that you should report those SEs. I remember the first 3 to 4 infusions were hard and got easier with time. Hoping the same for you.
Cristina - good luck with brain MRI!
Dee - wouldn't that be the irony! Let's hope not. Will be thinking of you tomorrow!
Lindalou - happy teaching!
Last but not least, Lalady a warm welcome to you on this thread. I find the combo ibuprofen and Tylenol very good as well. I also take a long lasting narco (hydromorph contin) with that combo. You have to find what is best for you, don't hesitate to talk to your MO or a pain specialist. Keep us updated!
Wishing us all a good day!
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Dee what about an open MRI? Some places offer it. good luck
Rachel happy dance! it's so good to hear these things actually work
Terre fascinating and scary, I put it on my bookmarks to review
Deanna glad that you are doing what you like and telling the pain to shove it...
Besides dear Pearlady I got no responses on the triple+ w mets using Ibrance. I wonder if i have to post it in a dif matter to get responses, Pearlady said prob not too many ppl in the same status taking Ibrance, one of the reasons would be approval from Ins for a not dedicated drug to Her2+
Lindae thx for the bump on the site...
Myra haven't heard from you...
Aurora how are you coming along with the walking...
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welcome lalady, sorry you are here but I know you will find wisdom and support. I am struggling with pain in the last few weeks and try to use a well planned nap (when my son is at school), and heat to supplement the pain meds. Wishing you find the best answers for you.
Lindalou good luck with the trial and let us know how it goes. Your students are lucky to have such a compassionate teacher.
Momallthetime I would not be surprised that Dani was trail blazing because you are such a strong advocate. I am wishing the combo brings her some good news.
Christina you have been on my mind. I am sending positive thoughts for your mri.
Happy Thursday to all
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did someone from Australia send me a birthday card? I'm so bad w names and I got a birthday card from a Megan in Australia?
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Hello all,
Just wanted to share my good news with you all.
For the first time since I was dx with MBC, my TM's (which are always indicative of what's going on for me) went down! I'm so relieved and happy. They went down 14 points-the Xeloda is working for me! My hope is that everyone here experiences similar results on whatever they're on.
Babs
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Woohoo, Babs!!!
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Thrilled for your news, Babs!!!!
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That's great news Babs happy for you.🎉🎉🎉🎉
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Babs: thanks for sharing your great news. Congratulations!
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Wonderful to read about your TM's Babs! Thank you for sharing your good news. Cheers, Dee
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Happy day Babs! That's great news.
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Thank you all for your good wishes. It's so good to share good things with you!!
Bab
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Babs.Congratulations on those TMs! It is good news. Time for my happy dance for you.. Woohoo! I hope you continue to get good news after good news.
Lynne
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Babs, congrats! Love reading this!
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I didn't receive a response to the PM that I sent to Kendrasue. Hopefully, she is okay and just needs to take a break from the boards.
Lynn
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Lynn and Linda
Thank you. My DH was so cute last night. He was crying with joy and refused to let me make dinner- took me out. My dtr called from Paris crying too
I am so blessed to have all of my family friends and my BC sisters supporting me
Bab
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Great news Babs! Enjoy the lower stress that comes with a good report :-)
Welcome Lalady! This is a great group with helpful advice.
Sending good wishes to all. I'm off to Florida tomorrow for a week of thawing out. Hope everyone has a pain free weekend!
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Congrats Babs! Mine are trending downwards as well, not such a huge jump and still abnormal but a little lower.
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I have an open MRI Tuesday afternoon for my brain. Hoping it's just headaches, nothing more. I wasn't really thinking much of the headaches but onc wants the MRI.
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Cristina, I am sending you good vibes for Tuesday and hoping that nothing bad is found on your brain MRI. It is best to have the testing done even if it just rules things out. At least you will be able to relax a bit if the headaches are just headaches.
Lynne
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I had a terrible reaction to Zometa as well (102 and above fever for 10 days). Tylenol and Advil did NOTHING. Then, the tenth day, it magically disappeared.
The doc changed me to Xgeva.
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Yay!!!! I'm so happy for you!!
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Ladies, I have a question for you - I am on Ibrance right now, but was on Abraxane before this. It worked (until the side effects became really really toxic). Now I can't feel my toes (it's like there's cardboard in them), I have trouble sitting on the floor or getting up, and my two middle toes (after the big toe) no longer touch the floor.
It's nerve damage for sure. Umm.. has anyone had these problems? Is it reversible?
The neurologist I saw said if it didn't go away by Dec 2015, it would be permanent...
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Im on Abraxane as well and the ball on the sole of my feet are numb. I've accepted it as long as the Abraxane works.
Aurora
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Babs great news !!! So happy for you!
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Hi Cristina,
Hope the MRI goes well. I have headaches every morning when I get up, but they usually dissipate during the day. They scanned for brain mets, but there was nothing...just random headaches. Hoping the same for you!. So glad it's an open MRI to help with the claustrophobia...
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Congrats Babs! Thank you GG27 and LindaE54 for suggesting tylenol/ibuprofen combo. I need non-narcotics to work at a computer (mostly) at my job plus commute 39 miles each way in LA traffic. ugh 3-16-2011 I will try some heat relief. Just microwaved a lavender sachet pillow to see how that works - at least it smells good. Ibrance is causing some nose bleeds and gum bleeding, I hope that can ease up. On the plus side, I have less neck pain than before. Wishing all a pain free evening. We are expecting a big rain on Sunday.
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Thanks Cristina and Kathryn. Christina I hope your test results show nothing of concern
Babs
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I have a question about tumor markers and XGeva. My tumor markers (CA27-29 and CEA) both went down drastically with chemo. After my last chemo in Sept both were within normal ranges. I started the Femara right then but I had a wound from the failed reconstruction so had to wait to take the IBrance. I started XGeva four months ago. With each XGeva shot my markers have done different things the CA27-29 rose slightly with each shot while the CEA dropped. This last blood test two days ago showed my CA27-29 is now at 43 (normal for this lab is below 38). The CEA dropped yet again to just over 3. I am wondering if the XGeva can cause a rise in CA27-29? I have read that some treatments do but can't find anything that says that happens with XGeva. I was sent for a scan of my chest yesterday (no results yet) because of some congestion in my lungs. I know tumor markers can jump around and can indicate other things but of course, because it is above normal again I am concerned. When I began my journey it was nearly 480 with the CEA over 50. I am supposed to start the IBrance but until they know what is going on in my lungs for certain they don't want me to start it. I am going to be taking a round of antibiotics since I am coughing more. Has anyone had a rise in their tumor markers with XGeva?
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Babs - congrats!!
Sqrlady - no experience with Xgeva, but wishing you good luck and good answers soon!
Cristina - sending hugs for your MRI.
LALady - I feel for you with the commute. I do the train now and it's lovely. People here in NZ generally don't commute, but I'm so used to it taking an hour to go 10 miles, that an hour on the train is no problem at all.
Sorry to hear about numb feet and toes. Not fun.
Just got home from a day of driving and kitty cuddling. Picked up a mom and 2 kittens to take to Kitten Inn, loaded up the car with stuff for the market tomorrow (kind of like a flea market) to sell on behalf of KI. We'll see how it goes. I think it's going to be a long day. I am taking a chair!
Here's a few of the babies I got to cuddle today...
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