February 2011 chemo pals
Comments
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Hi Mel!
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Hi to all my cancer sisters
hope you're all doing well. It's been too long since I've checked in but I think of our little group of fighters often.
I had my ovaries removed beginning of May. My onc wants me in menopause and there's no question I'm fully in it now! WOW! Plus Ontario is in a heat wave right now so it's already 33 degrees here, add the humidity it's 40 degrees and add my hot flashes it around 100 degrees. But I'm managing. I'm supossed to switch to AI in October. Until then all my dr's told me I'm taking the summer off! So, I'm excited to be off and feeling well. I still have my days and somedays I'm pretty stiff and sore but I've managed to plant two beautiful flower gardens and got my veggies in as well. I'm happy to spend the summer with my 4 year old, although that could change after a week of her being home! Lol.
Well, I just wanted to say hi and send a big hug to my very special friends who were are me on this journey. Happy Summer Everyone! xoxoxo -
Hey ruff - glad you are enjoying - I have been on a mini-vacation from my AI. I had enough pain from Femara that my MO switched me to Arimidex. Wanted to be certain which SE were from which so I took 3 weeks off from Femara, will start Arimidex tonight. It was nice to not be so achy and I am hopeful the new drug will be easier - but not feeling too confident! I have to take one of them, I know that for sure at 96% ER+, but...
Also, have enrolled in a vaccine trial for Her2+ in Washington, DC. Start mid-July - will go there once a month for 6 months - wish me luck in getting the vaccine instead of the placebo alone - it is a Neulasta-like drug, so boosts immune system, a nice consolation prize, but I want the vaccine. It is showing great promise for reducing recurrence.
Hope you all are doing well! How about a roll-call?
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Hi SpecialK I am still here. Doing physical therapy and making a little headway in the walking department.. Wow I hope you get the vaccine too. I am on generic Arimidex and have been since last August 1st. Hard for me to tell if some of the things I feel are SE's or just what I would have with my feet problems anyway but I do know that it effects my knees... There are mornings when I wake up and it hurts like heck to just move my knees. Other mornings I don't feel it at all... I have hot flashes but had those before BC..
Cindy -
Hey Special K, Good luck with the trial.
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Good luck K! I hope you get the good stuff too!
I'm coming up on 1 year PFC (July 7). Dreamed I'd have more hair by now. Oh well ...
Arimidex has my bones hurting, but I'm alive to tell about it!
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Hi ladies - I too am willing to put up with some aching if it means I get to be alive to whine about it! Small price to pay. I had lots of hot flashes before the AI too, so that is not new. We all probably wish we had more hair - too bad it falls out so fast and grows back so slow!!
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Hi Everyone,
I'm still here and checking in to see how everyone is.
Cindy- have you tried glucosamine? I had random joint pains in different parts of my body for the first six months, especially one of my knees, but with glucosamine it subsided. I'm now trying to just take it every other day and that seems to be enough. Ruff- Sorry to hear about hot flashes, especially in the heat of the summer! welcome to menopause.
This is what I've been up to: I talked myself into signing up for an adventure race to raise funds ($1500 is my goal) for Miles of Hope Breast Cancer Foundation, which provides financial assistance and other support for women with BC. I'm going to run the SOS Triathlon - an 8 stage race --for Miles of Hope and have about $1130 left to raise. Here's the link for tax-deductible contributions. www.imathlete.com/donate/LauraWongPan.
I hope it's okay to post that here. Have a good night, stay cool.
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Thanks for the suggestion Mamo. I have not Glucasomine.
Cindy -
I have just made the switch from Femara to Arimidex - I am curious about whether I will have as much joint pain. I will try the Glucosamine if I do - but I did want to throw this out there - my DH was taking it (Glucosamine and Condroitin supplement) because he is a long-distance runner (and over 50!) and had to have a routine liver panel done for a prescription med he was to take short-term. His liver numbers were off the chart! So high that the doc called our house and his office to make sure he had not started the prescription. Turned out that the Glucosamine and Condroitin was the culprit! He is a rare person who reacts to it - but I don't want that to happen to someone here and then they automatically think liver mets!
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Thanks for that info too SpecialK... Scary isnt it...... I am not going to start using unless mine gets worse or is happening all the time. Mine is not every morning but maybe a couple times a week..
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Yes, thanks for that info, Specialk! I remember reading one of your posts about the high liver numbers. Something else I need to monitor. Did you husband go off the supplements?
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mamaoftwo - yes, he did go off. He has had a couple more liver panels (for the prescription he has taken intermittently) and never had elevated numbers again. My MO does quarterly CMP testing so I will know about the liver numbers if I decide I need to take Glucosamine/Condroitin. I have been on Arimidex for a week and not too bad so far, but it usually takes me a couple of weeks to reach full achiness, lol! We will see!
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Checking in

Lets see....I found another lump but we're pretty sure its nothing. I am off of all the meds that messed with me! Two fills in and my range of motion has fallen below 50%...lost strength in the same. Recon in October or so...still pretty messed up from the chemo and rads....bought a trike and ride the hell outta it: ) spending time with my lovely family and Baby....breathing deep and loving everything I can....fixing my nugget a bit at a time. Wrecked my ankle but getting geared up to start jogging again!
Who's next? What cha doin'?
Checking out haircuts again...or color...or both! -
Hey all!! Strange question...
Does everyone or anyone still have their port in? I'm not sure how long it can stay in there...I get it flushed every 30-45 days and it works fine....just wondering who all has one still... -
Hey! I still have my port. Seeing my MO every 3 months and keeping it for the labs. I go every 6 weeks for the flush, then have it flushed at my 3 month MO visits. When the visits are every 6 months, will probably get it out.
Still on Arimidex which is ok though definitely feel it some days.
Enjoyed a beach trip for the 4th and thankful to be a year out. Last year had my recon right after July 4th.
Think of you all often. Hope all is well. Fuzzy hope all turns out ok.
My hair is still short and wildy curly. Not the shine it used to have but thankful to have it.
Love my sisters here.
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LisaGH - Hey! How are you? I still have my port too - just doing the same as Fuzzy, getting the 6 week flush. My MO would like a PET scan before I remove it, but honestly, it doesn't bother me and nobody can see it, even though it is in clear view all the time, because it is so small. I would almost rather keep it and not have another scar. I had a PET scheduled for the day prior to exchange but they couldn't get my insurance ducks in a row in time to order the nuke meds the night before so I cancelled it. I don't want another one set up until it has been at least six months since exchange because all the surgical area light up and we don't get a clear look. I have switched from Femara to Arimidex - I seem to be tolerating it better. I have a trigger thumb from Femara but it seems to be less painful - hopefully it will resolve.
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I got my port out yesterday! It's sooo sore! But I've been icing and taking tylenol.

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Congrats Mel!!!!!!!!
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Hi February girls
just wanted to check in and say hi and hope everyone has a great weekend.
Special k, how is the arimidex going? I'm supossed to switch from tamoxifen to AI in October. I still get no sleep, not sure if it's from the tamoxifen, I take it at bedtime as I take my other meds in the morning, I might try to switch them around. I had my ovaries out and menopause is tough! Especially during this heatwave we're having. Otherwise everything is going ok. I'm still off work, trying to take it easy and figure out what's in store for me next
Hope you're all feeling good
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mel - yay for the port out! I still have mine for the forseeable future - just had it flushed yesterday, no problems.
ruff - hey! How are things, this thread has been quiet! I am liking Arimidex better than Femara. On Femara I had more joint aching and I developed a trigger thumb - super painful and it is my dominant hand. Also cound not lose those 10 chemo pounds no matter what I did. I went off Femara for about 3 weeks, then switched to Arimidex. Less aching, sleeping better, lost the weight, thumb is better - so all good stuff. Not SE free, but I'll take it! Yes, menopause is a not a fun time - had a total hyst/ooph 11 years ago, still having hot flashes multiple times a day! Going to a BCO ladies lunch tomorrow - should be fun!
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Gotta say hey! I love seeing when you all stop in and update!
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Hi fuzz!
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Hello S.K.!!! I've been "stalking" You a little.....LOL....just keeping up with ya really 'cause you know how much I wuv ya....
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Fuzzy - you can stalk me any time! How are things? What is new? Love you right back!
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Hi everyone! I know we have all moved on. I do miss the folks on this thread alot. It's been a tough week- I worked at a hospital system & our beloved CEO died Monday of complications of cancer (Not exactly sure of the type). He was diagnosed just about 2 months ago.
We are warriors & thankful for each day the breast cancer beast is not a part of my life. I have been sad all week. I realize that every day is great!
I am doing pretty well. My hair still is crazy- the curls are now longer so my hair sticks out all over- I am trying to let it grow this time & deal w/ it b/c when I cut it I get mad that it's too short. Then I think back to one year ago- I had just stubble at this point!!!
I don't love Arimidex but I am dealing w/ it. I feel I have gained about 5 pounds & do not eat more at all. I still have my port. I might get it out sometime but w/ MO visits every 3 months- those lab draws wouldn't be easy w/ my terrible veins, so maybe I'll keep it 6 more months or so.
Hope you are all great. Love my BC sisters on here- Think of you all often.
Lisa
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Hi Lisa. So sorry that your week has been such a sad one... ((((Lisa)))) thought maybe you could use one of those!!!!
Cindy -
((((Hugs))))
Special....whew....didn't want ya calling the po-po on me: )
I'm hanging in and hanging on... I Should be getting this lump removed on the 18th so I'm happy about that! Just got back from the Michigan UP and Sleeping Bear Dunes....it was amazing!! I would have loved to go to FL to see ya but we toured all the way around Lake Michigan.. -
LisaGH - Hey! Good to see you but sorry that you have had a week of loss - it is so hard when one is so sensitized to it from our perspective, right?
fuzzy - come to FL anytime - but especially in the winter since you live in a cold place! FL in the summer - not that nice, lol! It is hot as a freakin' oven down here! Michigan is beautiful, glad you enjoyed it!
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Hi everyone
hope you're all doing well. I have a question and just wondering if any of you can relate? I've been on tamoxifen since last October and had my ovaries out in May. So I'm in menopause -not a ton of fun, but my feet are so achy and I'm nauseated and fatiqued usually every afternoon
I'm walking every morning once I get my daughter in the bus, 45-50 minutes with my dogs - but by 2:30 I'm exhausted. I'm not back at work yet, using my benefits as long as I can but honestly don't know if I could work as I'm that tired
do you think it's the tamoxifen? Or menopause? Chemo side effects? All of the above?
Anyways, just wanted to reach out to my feb girls - happy Fall, I hope everyone is doing well xo
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