Bottle o Tamoxifen
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You know I love my oncologist but she never told me what not to mix with tamoxifen. I gave her a list of my 15 vitamins and supplements and she never said don't take this or that nor did she mention juices, etc. I like the fact that I don't have to change anything but it makes me kinda wonder. And I've never gone on that drugs.com list to look anything up.
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Gee you gals were busy last night and today.
Jules sorry about your other pains, hope you can get some relief
sgreenarch--yeah for your swin that is incredible, sorry about the lump, will be praying for B9 on that. Interesting that you post about arthritis I will post my Dr visit recap on my next posting.
Whack- jo I got you when you were not looking. so there.0 -
Ok so here is my recap from the pain Dr visit
He said that since the Elavil is working for the most part he wants me to continue to use it. He also gave me a compounded cream to use topically. I used it after lunch and it works. He felt that this course was better than using a nerve block which I am fine with. I also talked to him about my sore hips and shoulder area. He was very good at explaining that radiation does cause more problems. He said it is very good at doing it's job killing cancer but that there are SE's that come up and you have to deal with. He said that even though our breast got radiated that there is no way for them to miss our bones in that area. He said the radiation can cause a molecular change in our bone marrow and can cause osteoarthritis and osteoporosis in other parts of our body. He said expecially if you were maybe prone to it and it can cause you to have an earlier onset of it. He feels that mine is osteoarthritis. He said since the Celebrex helped along with the private yoga lesson that I had last night that really stretched my hips and shoulders he felt was the best way to deal with it for now and we will continue to monitor it. He feels like the nerve damage was caused more from radiation than my surgery. Although my BS says it was from both. I talked to him about my surgeon wanting to do the MX. He said if it was only for the nerves he would not recommend it but because I have some other issues he felt that it was a good choice and then she can deal with my nerves from there. Although my BS told me and he told me there is no guarantee that it will completly go away but they both said that she can make it much better where I can probably get off the Elavil and if I need to keep the topical I can. So it was a very good office visit and he was supper nice and informative. Oh also because I broke my neck in 1995 and already had nerve damage on my left side he said that did not help my situation any. He felt that with the fact that I already had nerve damage on the same side I was radiated that it left me more vunerable to more nerve damage. He did say that joint stiffness is a SE from tamox but with what I was explaining to him he felt mine was more from radiation. Like Jo says who really knows seems no one can agree on things. But the good part is I really like him, he listens and seems to want to really help. My DH went for his neauropathy and his case is much more complicated than mine and he was great with him as well and going to try some different things to get him some relief.
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Found this great place for a party. Getting it set up for tonight.
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Sherry - Now I know you had a good visit with the pain doctor today - that is great news and you are pain free - guess I can really give you a good WHACK WHACK - bet you did not see that one coming hehehe
Chabba - Here is our waiter for the evening. Maybe Sherry can come up with some other boy toys.
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Hello!!!! Sheesh ..sorry I have not been on in a week...5 days in Ottawa and then three days catching up....spent five days talking and walking and drinking wine!...Went to a lymphodema massage therapist today....wow!!! She spent the entire hour massaging my lymph system and talking about how it all works etc...guess I have a few other things going on (who else slumps/ed a bit because of large breasts!) but I feel better and we are both thinking I may have caught this before it is the no turning back scenario...she thinks she can help and get me back into my favrouite underwire bra...and take down the swelling...wheeeehhhaaaa!!!!
How are the rest of youladies faring??
WHACK!
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Forget the drinks Ill take him!!!!
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Sherry, glad you got to see the pain dr! I was referred to our local "pain and symptom management" clinic, but got ticked off when they required a drug screen prior to even being seen by any of the providers, before I even decided I wanted to actually BE their patient, so am pretty frustrated with the whole neuropathy thing. Can you tell me (PM if you want) where you are and a little more about how you go about getting taken care of? I am SOOO frustrated with quality of life these days.
Surfette, I did read somewhere about melatonin decreasing the invasiveness of breast cancer in some animal models in the basic science literature, but there have not been any human applications or stuides yet that I know of. But my PCP said it would be fine to take it, most people need to start with 3 mg, some need as much as 9 mg for sleep. I got a bottle that I am going to try soon, just having a hard time deciding when I want to risk any SEs from THAT one! My understanding is there aren't all that many, maybe just some mild GI stuff that resolves over short time??
Holy moly, Jo and Sherry, those guys are GORGEOUS!!!! Sorry I will not be able to join the party tonight (again) - have old people's early bird dinner date with DH, then leaving to visit family for the weekend. Have a great Memorial Day weekend, all (and try not to get into too much trouble, esp. Jo and Tink....)!
So here are a couple of WHACK WHACK WHACK AND I AM OUTA HERE!!!
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Oh tammi sistas we were talking about weight lose and gain the other day. Well at the Dr office today I weighed in at a woping 111 lbs. Hubby was right next to me as we had appts together. When we got out he said you really need to gain weight. I told him you see how I eat I don't know what else I can do. His answer was eat more. I rolled my eyes at him and said I eat till I am stuffed I will be miserable if I eat more. Maybe I need to try more ice cream at night I do love that and it is full of calories. I really thought I had leveled off of this weight loss but guess not.
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Sherry- would having a protein mix in yourmilk shake help? My ex used to add whey powder to shakes and smoothies every day when he was trying to gain weight....
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Sherry - Wow! You did good girlfriend! They are gorgeous - ride em cowgirls. Go ahead, enjoy the ice cream at night if it helps put on a few pounds. You certainly deserve it and hubby is encouraging it - so go for it. You still will get a good WHACK! Let's get this party started.
Tink - Where are you? We are getting a bad rap already and the night is still young.
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Sherry, I think I am gaining your weight. Grr
OK, we have the tent, cabana boy and I will bring the Lychee Martini's which I spent all of last night perfecting. I know, I'm a perfectionist. It's a cross I have to bear LOL
See you all later xxxxxxxxxxxxx
Jules
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Wow I wish tamox made me lose weight but I've gained 15 pounds! I saw my radiation onc yesterday and he said that for SOME people (me apparently) it slows the metabolism. I already exercise 2 hours a day, can't do much more than that.
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I whipped up a little appetizer - who can resist this.
Somehow I am able to maintain my weight. Guess I am lucky there.
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When I was on tamox, I went to the gym and worked out with a trainer....I lost 2.5 inches in BMI but only two pounds...I figure Imay only have lost two but it likely prevented me from gaining 10 more!
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Paula.thanks so much for that info.. that is good to know as every morning I have aglass with my tamoxifen yikes. wont be doing that anymore..thank you!!!
OH MY GOODNESS!!!! They look like they are dessert wow wow wow!!! nice work!
thoose strawberries look great Jo!
and hoep i am not too late tonight but WHACCCCCCCCCCCCKKKKKKKKKKKK!!!!
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Sherry I understand how you feel I am down to 113 I know stress was a big part of it, i do get hungry thats not the issue but I get full very quuickly and if I push it i feel sick too... i would like to put just 5 pounds back on and I woul d be happy with another surgery coming up in July I dont think that is going to happen....
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HOLD on .....Did I just go back and read " TINK BEAHVE????""... lol... thats not fair look at them and my closet is empty....whats a Tink to do???? lol
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oh man I think I partying alone tonight!!!! come on guys in the closet you gooo!!!!!!!!!!!!!!!
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WHACK, WHACK, gotcha tink!
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surfette - my naturopathic oncologist had me on 20 mg of melatonin for 3 months. Then my skin got icky, tissue paper like and dry, so she took me off of that. But it is supposed to help prevent recurrence.
Girls thank you for the eye candy! haha!
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Tink - Looks like the party was a bust last night. Too bad the boys had to go home. I think we must have scared the girls off. I don't know how we got such a bad reputation. I was so ready with my pillow and those strawberries - I did have to eat those myself - oh well, you snooze you lose.
As a 20 year Air Force veteran, I would like to ask everyone to send up prayers and good thoughts to all our troops. Let's honor them all this Memorial Day Weekend.
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Sending up prayers and thanking you for your service JO!!! THANK YOU
Who said the boys went home???? I told them to get in the closet...hahahaha I thought it was just me and them had to do something hehehe
HOPE everyone has a wonderful day. Our pool is opening today and my DH is HOA pres so he has volunteered us to serve food for the opening!!!!

Hugs to all!
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jo1955......
Glad to hear the Elavil gave you a good night's rest. It's a medication that has been around for a long time. Don't get too stressed about your annual, mine went fine a month ago as did the mammo, but the bone density was not good.
I haven't heard any talk about "fried bologna sandwiches" in a long time but since chemo and the estrogen inhibitors I can't afford to treat myself to any so eat a couple for me !!! I thought that was a midwest thingy.
You'll do fine.........just focus on the fact you have enough rads in you to fight an army !!
Norma Jean
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Tink - You could share the boy toys. I don't think you can handle them all by yourself. They looked pretty frisky to me. LOL!
NormaJean - Thanks fior those words of encouragement. It is just the thought of getting squeezed - never did look forward to this time of year. Rads and their nasty SEs - who would have known? I chalk this us as a learning experience and once is enough for me - Thank You every much.
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Well jo1955...........chemo isn't any better, at least not the kind you get for BC. Now, Hubby was treated a few months ago for Hairy Cell Leukemia. His chemo was one chemo for ONE week, 24/7 via a pump he wore. Looked like a fanny pack. No Fair !!!
Hope everyone has a great Memorial Day weekend & be thankful for those who keep us free.
Norma Jean
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Getting a little stressed and anxious the last few days. Wed. was a year since DX. First mamo on 6/3 and for the last week I've been getting those shooting pains in the breast. At least I'll be seeing my BS. He is a fantastic surgeon, wonderful doctor, a kind caring person and even has a great sense of humor. I love him.
I also have an appointment scheduled for July with me MO--But I don't intend to see him. Ours is a satalite clinic. Each day a different Dr comes here from the main clinic. Since my MO never explains things and dosen't like questions I'm changing my appointment day. I find I'm unable to continue with the day I've been going. I'ld rather try a different MO at a clinic 25 miles away than have to go 90 miles.
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Chabba - It looks like we both have our first mammo since dx. Mine is also on June 3rd - first thing in the morning. That is good - I can go and get it over with. The shooting pains could be the same as Sherry & I had. It is nerve damage from radiaiton - go figure - another SE we were not told about. Both of us are taking Elavil and it does work. I am finally pain free and full of energy. Sleeping great since starting the medicine. Both our pain doctors said the same thing about nerve damage so there really does have to be some truth in it. You may want to ask your onc about this and see what he recommends. It would be interesting to hear what your doctor has to say.
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Jo - I plan to ask my new onc, but first I will ask my BS, I already have faith in him!
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