Bottle o Tamoxifen
Comments
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Shari - My story is very similar to yours. My tumor was found on a routine mammogram and verified on a compression mammo and US. Like you I was medically boring. Now, it is a nightmare of doctors appts and testing. So sick of it. I have many more appts this month and will be so glad to see July come.
I do alot of research on the internet and somtimes think I shouldn't as I don't always like what I am reading. But, as they say, knowledge is power and we do have to be our own advocates. Case in point, my gyn was talking about doing a transvaginal US maybe next year since I am on Tamoxifen and I asked to one on my visit last week to establish a baseline. He did agree and it turned out I needed a biopsy for a 1.5 cm fibroid and very thick uterine lining. So glad I asked. Had a hysteroscopy D & C done on Saturday and will get the results next Tues.
Hope all you TammiBabes are having a good day.
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Not sure if this has been posted before or not, but I came across it on another site and thought it was interesting, although I wonder how accurate some of this research is. I was taking fish oil, but I stopped a while ago...I'll have to talk to my MO about it next time I see him. Hope everyone is having a good day
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My DIL from Seattle sent me an email last night and her mom now has DCIS. I just hate cancer. Anyway she wanted to let me know and to tell me she had given her mom all my numbers and email in case her mom wanted someone to talk to. She said she knew I wouldn't mind but wanted to fill me in on what is going on. So I sent her an email back with probably more info than she wanted but I wanted her to really understand about her Mom's cancer. So she emailed me back this morning and was thankful because I was able to tell her alot more than her mom did. It is all so new her Mom probably does not know all this yet either. Heck I've been searching for months now for info. Anyway I think my DIL felt better with the info I gave her. I hope her mom gives me a call.
In the last ten days I have only had one night that I had one hotflash. I really do think they are gone. wooooohooooooooooo
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Sherry - Finally no hot flashes - now that is something to celebrate. So sorry to hear your DIL's mom has to join the rest of us in the BC journey. Soundss like you provided them with lots of good information that I'm sure will be a tremendous help. This whole thing can be so overwhelming. Wish I had known more in the beginning. Oh well - hindsight is 20/20.
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Jo I am like you and wished I had known more in the beginning.
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Sherry so sorry to hear about your DIL mom. I agree lasies wish i was better informed int he beginning and to shell shocked to research right then and there... but better llate than never and especially if it helps someone else who has to go through all this...
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Tink - What far away places have you been flying off to? Haven't seen you in days. Hope you are not tired from all the flying. hehehe0
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Can I hear a whoopwhhoopp!!!??? Cancer free and lymphodema free!!!!!! got mymammogram results at noon just as I was leaving for my meeting with the physiotherapists at the lymphodema clinic....was told in the end that they believe I have tendonitis in the left shoulder which has caused swelling and pain....so it is back on the routine mammogram train for me....my god....my relief is palpable!
Sherry- sorry to hear about your DIL's mom...having you there to pave the way is a gift for her.
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JO..HEHE Never tired of flying ... just flying around too much!.. Alis sched has been all over the place with finals and catching up with appts and lots of end of school year lets get together before summer starts stuff... and trying to get ready for vacation. ... leaving MOnday...
How are you feeling????... hugs!!!!!!!!!!!!!!!!!
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Sandee - Congrats on the negative mammo and not having lymphedema - that is so exciting and the good news we all like to hear.
Tink - Vacation? Where are you going and for how long? Wherever it is, I hope you have a wonderful time - you certainly deserve it.
I am doing really good. Still have a bit of a sore throat from the breathing tube but that will go away in the next couple of days. I have a follow up appt with the pain specialist in the morning. I am going to see if he will let my MO do the follow ups and refills on the medicine. Trying to get everything down to two doctors - MO & GP.
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Sandee~~
Congratulations on your good news. I just got my 2 year mammo and cancer free also.
We can both do The Happy Dance.
CatbirdC0 -
CatbirdC - Doing the Happy Dance with you. Congrats on the 2 year cancer free.
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Yahoo Jo, Sandee, and, CatbirdC!!! Doing the happy dance for ya. YAHOO!!!!
Tink getting ready for a vaca, luckey girl! I am green with envy, lol. My vaca this year was spent recliner side at hotel Paula recovering from my BMX. Atleast I had a HOT HOT waiter who waited on me hand and foot.
My SE have kicked up abit. I had extreme bone pain from the taxol, so I can handle this. It is abit uncomftable, I can do this though.
Sherry Im so to hear about your DIL mother. Im glad to see she has you to guide her thru this. Its like you said on the searching, theres so much to try and find. Let alone a site you can trust.
It so nice out here in my part on the woods. Its raining, but atleast its not 100 degrees out. Enjoy it while I can.
Have any of you gals been BRAC tested? If you have tested positive and have kids, how do you deal with it mentally? Im still having bad days with it, and could use alittle advice on how you handle it. I know that just because I tested positive that doesnt mean my kids are either. My family history with BC is very strong so with me being positive really does a number on me some days. Thanks for any suggestions.
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Jo/Ctbird/paula/catbird c - Thank you for the kind thoughts - feels good to write somehing positive down hnnmm? fear has left the building for now! wheeeha!!
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Good news is always celebration time.
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Sandee woohoooooooooooo. Doing the happy dance for a clear mammo and no lyphedema
Catbirt congrats on 2 years. I'll be so happy when I can say that.
Paula I am sure someone can help out here. I was negative and have all boys so not sure how I would handle it but know that it would bother me like it is bothering you.
OK gals I will wear some pockets tomorrow as I have my first appt with the PS. Kinda nervous cause I don't really know what to expect but I have lots of questions. Kinda weird thinking about taking a body part off and rebuilding it. hum I never use to think of myself as vain but I guess I need to admit I do have some vanity. I'll be in the city all day so I will check in tomorrow night
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Dear sandee and catbird, so happy to read of your good news. You should know that it inspires all of us. Good to know that test results can come back ok. I wish all of us year after year of boring, normal test results. My mom had lung ca two years ago ( shes fine now) and i remember her saying that her new favorite word was 'normal.'
Jo, glad you are feeling better and thanks for your supportive words. I have a scan scheduled for weds and am following your 24 hr rule strictly.
Tink, where are you flying to? I am set to visit my family in a few wks in the US which means an international flight for me with a stopover so plenty of ops for Security snafus. I flew in january and decided not to wear my prosthesis (wore bulky clothes) to avoid any weird situations. Nothing happened. I had also been nervous about potential blood clots due to the long flight but i got compression stockings and walked a lot and it was ok. So many new, wacky things to worry about.
Paula, i feel for you re talking to your family about the gene. Not easy. I guess they are wondering about it anyway and maybe you could present it as a good thing in the sense that they can be watched very closely and if anything, it would be caught early. Of course no one wants the gene but if they have it (which they wont know they do unless theyre tested) at least they shpuld be treated well by the system and have sympathetic docs and fewer insurance hassles. Here in israel, where unfortunately the Ashkenazi Jewish gene is prevalent, there are accepted protocols if you have the gene. Yearly MRI, etc. Maybe the same there. Not easy news but once they are over the shock (should they choose to get tested, and test +) they can at least use the info to make choices such as perhaps doing prophylactic mx. I know quite a few women here with the gene who havent been dxed with BC. Most havent done prophylactic mxs but have done oopherectomies (after they had kids) and are watched very closely. There is also a website FORCE something, that deals well with these issues. Good luck.
SherryC, sorry about your DILs mom. Sounds like they are both lucky to have you. I would imagine that theyll have good resources in Seattle. Nice for them to be able to talk to you.
Well, good day to everyone!
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Paula, please forgive me. Forgot to add that so far all the women that i know who have the gene and are being watched closely, are fine, and living very normal lives.
Shari0 -
Sandee/Catbird congrats on the clear mammos and good news... so happy for you ladies!!!!
Paula. I had the BRCA test done but mine was negative. I do have a daughter and what they told me with her was that if I was positive they would do a test on her when she was out of her teens to test her for the gene since i was negative they told me she should get a mammogram ten years earlier then she normally would so i would imagine she would have to start at 30. There is not a strong family history but me fear is I have started that strong family hostory if you kknow what i mean... as the future unfolds my hope andprayer is that it stops with me.
Jo/Shari.. my FIL has a house n Myrtle beach so we are headed down there to stay for 10days. They have a laptop down there, there is know way i will be able to not check in for ten days lol!!!!
Sherry...my wings are ready to go for tomorrow what time we leaving????? good luck tomorrow please let us know how it goes..
Shari.. glad all went well for your travels. I know what you mean though the simple things like driving flying that we really didnt give a thought to before is all so different now, everything kinda has to readjusted. I have not flown yet and it is about a 6-61/2 hr drive down to Myrtle beach from here and this is our first trip since all this started last summer was spent recoup from a bilat.with reconstr. As excited as I am to go away i am also a little nervous too.. when i get back a few weeks later i will have another revision surgery yet that doesnt scare me....too much.... wow how life has changed lol!
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Will be so glad when this month is over, Still have several appts to get through - all follow ups. I am off this morning to the pain specialist. Hope this is the last time I have to see him. This is one doctor I do not like - his is so arrogant but good at what he does so at least there is a positive in seeing him
Have a Great Day TammiBabes!
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Sandee, congrats on your results. I have my own MRI coming up in August and a little worried.
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surfette - Thinking positive thoughts for B9 results on your MRI (((HUGS)))
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surfette...good luck! hugs coming your way!
I know JO it seems like it never ends... I have 2 6 month check ups on Thursday BUT the some vacation then when I get back pre ops and surgery... but I will enjoy the break and be happy for it, this time last year I was preparing for the "big" surgery 13 hours worth after that all the others have felt like a breeze so to speak...
have a great day Ladies.
hugs to you all!!!!!!
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Tink - I will be thinking about you on Thurs. Hope you have big pockets because I am ging to jump in one of them so I can be with you.
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I'll be there too Tink
edited to add--Hope the pocket is deep, I'm 5'10"!
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Hello ladies I am missing you all like crazy here!!!
Year end School stuff along with many nieces graduating and parties galore that I have not had any time to chat......I am 6 pages behind, so please forgive me for not being able to catch up.
Sandeee and Catbird what fantastic news to have clean and clear results!!! PARTY!!!
Alicia hoping you are out of your funk and the pills are really helping you!!!
Tink- Vacation, how nice and much needed for you my friend!! My vacation is not schedules until 3rd week of July and boy I cannot wait!!!
Been doing Physical Therapy 2 times a week with my busy schedule for my armpit (Lymphodema) Who would have thought that I would get that without having any nodes taken out. She told me it is very common with women who underwent more than one surgery and Radiation.....fun fun!
Other than that I am doing really well and really miss chatting with each and everyone of you......hope you are all well and know that I think about you gals daily!! Hugs and kisses!
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My pocket is big enough for all you wonderful ladies!!!! hop aboard!!!!
JUne so glad you are doing better... you going away for vacation?? hugs!
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June - Sure miss you. Glad you are doing good.
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Sandee and Catbird CONGRATULATIONS on the good news !!!!
Jo ~ Glad to hear you are doing okay, good luck with your appt today.
Today I see a new therapist and next Thursday is my breast surgeon appointment. I hope she doesn't feel anything. I am feeling a little better. But definately not completely out of the funk. It's tough but I will get there !!!
Hugs girls !
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Good morning all, so much to read today! sgreenarch ~ I'm trying to get approval to have the facial still, waiting for a return call, what a thing to have to bother a Dr about, sigh. Also wanted to tell you that my naturopathic onc told me to get up and walk every hour on a longer plane ride, up and down the aisle 3 or 4 times, at least, and she also has given me a supplement to take called, Nattokinase 50mg, 2 capsules, twice daily for 2 days before and 4 days after flights to help prevent blood clots. I think I'm going to "overlook" that ? if I ever attempt a facial anyplace. How are the cells on my face going interacting with my tatas exactly? - thanks Surfette.
Schipmom, thanks for the link, I'm on 1500 mg/day and good to know it's helping me in more ways than one.
Sherryc, sorry to hear about another cancer story, but your experience and knowledge can help another and that is something very good. Yay for zero heat!!
Sandee and Catbird, Hooray for Happy News!! Thanks for sharing, it is good for my heart to hear!
I'm going to have surgery on 1 July to repair a cystocele the tamox has worsened to the point where it is now just ridiculous. My breast surgeon told me to stop the tamox but to check with the chemo doc to see for how long. The chemo doc said don't stop taking it, called the breast surgeon back with that news and was told to stop taking it 4 days ahead of surgery. And I like both my Docs, they are both great, knowledgeable and skilled people. Just thought I'd share that with all of you for future reference. I'm taking my surgeon's advice. She's the one that slices and dices and that's who I want to hear from on this issue.
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