Starting Chemo April 2009
Comments
-
Amy, good to hear your results ..... I think we all relate to the vulnerability. Once you've had bc, I think you carry a sense of fragility.
I'm still feeling sad a lot. But I go to work. I'm getting ready for the wedding. Only 3 weeks to go. It's difficult spending time getting ready to look "good" when nothing I do will make me look good at this time. I want my kids to be happy and I don't want to do anything that will take away from their happiness. So I don't say anything and I'm doing my best.
Thanks everyone. It helps to know I have your support.
-
Hard Head = Sore Shoulder!
Ok, in my quest for all things "New Normal" I admit I've been happily neglectful of some of the things I should have been doing on a regular basis (*ahem* exercises 3 times a day) to ensure I would not end up BACK in Restorative Therapy for my arm on my mastectomy side.I hate those exercises! And so, I didn't do them. For months. And now, I'm back to having really limited range of motion, a SUPER-SORE Shoulder, and my neck isn't feeling so hot either!
So back to therapy, 2x a week I go. Therapy is a kind word for what actually occurs. Torture is more like it. Therapeutic Torture.
*sigh* There are days I wonder if I will ever be DONE with this? The answer makes me sad, a little mad, and then I try to think about something else.
On a happier note, I had a WONDERFUL Memorial Day Weekend! 3 cookouts in 3 days! Whirlwind eating fest! Love it!
I'm looking forward to a fun summer, culminated by my reconstructive surgery on August 25th! My new ta-ta's are on their way, and while the surgery is a BEAR (10-14 hours) and the recovery is a BEAST (4-6 weeks), I'm am SO ready! I have to think of something creative to do with my 4 pound brown prosthetic...LOL!!!
Anywhoo...pray for me beloveds (for discipline)! Continue to pray for my parents, they are both doing well, appreciably better than before, and for that I am grateful.
So the formula for pain relief is 2 liters of water daily, and arm exercises 3x a day; and for now, physical therapy 2x per week.
Question of the Week ~ How do YOU do things you really don't WANT to do, but SHOULD do?
In Love & Pain, Alaina
-
Amy ~ I'm so happy to hear your good results! Hang in there!
Alaina
-
Amy - I am so pleased that everything was normal! I completely relate to you being all shaky, it is perfectly normal - take time to get yourself together again. You must be so relieved. I wonder if we will ever be able to undergo tests again without it throwing us all off balance.
Alaina - loved reading your post and hope that you are feeling ok. You always find a positve spin on things and as I have said so many times, you are an inspiration.
Geri - I am counting down those treatments with you and hope that your pain eases up.
Helen - you are showing great strength in thinking about your kids happiness and I really hope that you enjoy the wedding.
Titan - I am crazy busy with family and don't know what to do first! I am enjoying it though.
Hugs to you all and take good care, Judy xxx
-
Feeling SO MUCH BETTER today. I just needed a good night's sleep to put the anxiety behind me. I woke up today detemined to go forward as the new, healthy, POST-TREATMENT me.
Got a really short haircut today in preparation for the wedding. I LOVE IT. (photo to follow) My hair was so thick and bushy it was like a THATCHED ROOF. It was hard to get it wet all the way through in the shower. The poor hairdresser was afraid to cut too much (she has been with me through everything) and I kept saying "Cut more off, I mean it." So she did. And I love it.
Went to Macy's and got a wonderful makeup lady to help me find the right shade of dermablend to cover my scar (in the dress I am wearing to the wedding, it will show). She also helped me pick out jewelry to go with my dress. It was like having a personal shopper - she kept saying "You deserve this!" It was super fun and I felt very pampered. So now I have the scar makeup and jewelry (and of course the dress/shoes) and I am READY. Well, I do have to color the grey in my hair this weekend, but THEN I will be all ready!
So I made it through the test and came out the other side. Whew.
Thank you again everyone. I will return the favor when it is someone else's turn.
Love
Amy
-
Uh..Amy..now that you have your hair cut...and you know I'm just kidding when I say this..please don't be mad..but I think one of those peace signs with a silver chain would have looked good with your hair..I'm sorry...just my first impression....please don't hate me..you can cut on my avatar if you want to.. I have ALWAYS had curly frizzy hair and I hated it...now I have what my dd calls "more defined" curls...I kinda like them..but my mom and dad are so weird about it..they don't like me being a blonde..I don't know..I think it is the cancer thing that bothers them.
And Amy I'm thrilled about your good results...scary stuff...we go through way too much...
Alaina..maybe you could use that prothesis as a weight when you exercise.
Geri..way too many treatments....it will definitely be a celebration when you are done!
Everyone have a great weekend! I had better go to bed b-4 I get in more trouble.
-
Wishing you all a great weekend! Amy, so pleased to hear that you are feeling more upbeat!
Titan - my hair is so curly, I find it very hard to manage : )
I will try and write over the weekend.
Hugs to you all, Judy xxx
-
Have a good weekend everyone
Geri
-
Hi, everyone. Sorry for not checking in sooner - I have been busier than I thought I would be with this job search - I am spending 75% of my time "working" on looking for jobs - and I'm branching out from marketing to all kinds of different fields - executive assistant, etc. It's brutal out there - so many people applying for the same jobs - half the time I don't hear back from the employer at all! Went on a couple of interviews, one of them was for something I would like, but it's 45 min. away (I've never had to commute more than 20-25 min., so it would take some getting used to), but if the money is right, I'll take it. Keeping a spreadsheet of everything I've applied for with details, and trying not to be depressed, which is harder as the weeks go on (one month now!). Very different job market than before, where if you wanted a job, you could pretty much get it. I know I am stressed over this, been having to take my heart medication (for an irregular heartbeat, only need to take it usually occasionally, now, every day) and am breaking out in hives. Trying to remain upbeat and energetic, and am losing my mind staying home!!! I am such a go-go-go person that one month home, even though I have been busy with the search and all, is not for me. I don't want to get too involved in any big projects, because if I start working then everything is hanging. It's nuts!
Geri, I would love to help you plan your Hereceptini party!! I love to organize events!
Got the official mammo results - said there were no huge changes from last year, nothing to be alarmed about. That's good, and the onc's office was pleased, so I guess that is good. They haven't mentioned to me about going on any more AIs, so maybe I'm done. I should have a 3 month follow up coming soon, at least I need to get one more in before the insurance goes away in September, unless I am on a new plan by then. Waiting for the paperwork to come in for COBRA and I guess I'll see what the premiums are on that. I hear it's expensive.
Helen, how are you? Amy, whew, I'm relieved it's just a cyst. I had many of those over the years when I had my ovaries - too much estrogen bubbling over! Your super curly hair looked like mine before I had it trimmed a few weeks ago. I'm going to get mine relaxed a little next week - with the incredible heat and humidity that arrived here in south Florida a few weeks ago, even though I painstakingly blowdry and flatiron my hair into a cute little short hairstyle, spending just FIVE minutes outside turns it into a curly mess. I tried to work the curly hair last weekend, just to see and it looked JUST like Rizzo from Grease. Just not me - I think it makes me look too old. If I wanted to 'fro it up, it would be a super fro. We could all go as '70s girls with our "natural" hair, tie dye and peace signs. Lena, hope you're doing okay on Aromasin. Femara was terrible for me too and isn't it amazing at how quickly you feel better (normal) when you stop taking it?? Titan, I agree - the "cancer" subject can make some family members very uptight - my sister still won't really talk about mine, my treatment or anything. Just glazes right over it, like if she doesn't think about it, it never happened.
I don't have any photos yet, but I was chosen as one of the calendar girls for the group I volunteer with, Pink Tie Friends (www.pinktiefriends.org) for their 2011 calendar. We did my shoot at the beach, at my old bosses (not the one who laid me off, this was a previous employer) beach house - I wore my typical outfit - t-shirt and jeans, bare feet (or flipflops) and we took a few different shots. I'm nervous - I don't photograph well, I get too stiff and weird in the pictures, I like being BEHIND the camera. When I have a chance to get some of the shots, I'll post them.
Have a great weekend, ladies. Everyone relax, enjoy and smile.
-
Count me in with the 70's look! The fro anyway...all my friends had super straight hair, parted in the middle and long..not ME...fro girl the whole way.
Anyway..now that my hair is short (and new)...I put all kinds of junk on it...gel, anti friz cream and this kind of spike stuff that actually makes it kind of "hard"...but it doesn't frizz anymore even in the rain and we have had tons of that in Ohio...I just use a flat iron on my bangs. I like it.
Really, did anyone expect 14 months ago that we would be totally different people than we were before? I'm definitely not the person I was before BC. What a change...going through all the surgeries, chemo, rads etc., gaining weight, losing hair, growing new hair. ..just different relationships with my husband and kids and other friends in general.....what a life change!
And of course..meeting people like you guys....
-
Thank God I'm not the only one struggling with my hair still. I've kept mine short...but it's so curly on top and straight on the sides, I wake up every morning looking like Lyle Lovett....Eee gads! I may have to try a flat iron. If it works for the nut, it may work for a duck.
Amy, I am so glad to hear your good news. Although, just a warning if your cyst ruptures it's VERY PAINFUL. Hope you have some pain meds on hand. I'm glad you felt pampered on your shopping trip...plus it sounds like you got a little bling bling for the wedding. Good for you!
I saw a women tonight when walking with a shaved head. Wow...what a flood of memories.
I had a set back this week. Didn't have time to go to the gym much and my red hot momma returned. I called for an appointment with my PT and she reassured me that everything is ok. She said the more I exercise the better my lymph fluid flows and it's normal to have occasional set backs now and again. I'm starting to think my new normal is going to be a constant battle keeping the lymph fluid from building up in my breast. Oh well, I guess it could be worse.
Judy - Happy Birthday! I had chemo on my birthday last year. This year is so much better isn't it? I read an article about it this past week and thought of you. It was about almonds and how quickly they help with heartburn. I thought you might want to give it a try the next time you have a bout.
Geri - Love your posts. What night is are next martini night? What's the count down number? Maybe by the end of this I might have a better appreciation for martini's.
-
Hey Betsy - Every night can be a martini night - however, officially I have crowned next Saturday, June 12th, as Herceptini night, as the countdown will be 5 to go.
After that, every Saturday night you all must have some type of "ini" - alcoholic or not - to join me in my countdown to finish the (hopefully) last of the infusions of Herceptin, due to complete July 13th. That day #52 will have been completed, and when I think back I have been getting some kind of drug intravenously for this cancer thingy for 15 months! Hard to believe the end of that part is near...and thanks in great part to all of you, my handholding buddies!
Have a good weekend
Geri
-
Hi all, it was great to read all of your posts this morning, although I don't have much time to write today. Some of our family leaves today and some are staying for another couple of weeks.
Betsy - hope you are feeling better soon. Amy - hope you are still enjoying your good news! Chelev - good luck with the job search! Can you tell me which product you used to relax your hair. I cannot find one that is suitable for me and I do not like the curls on me at all.
Titan - You are so right! We are so different now, I hardly recongnize myself sometimes, both inside and out. Having all of you has been such a life line for me.
Helen - how are you doing and how are all your wedding plans going?
Lena - how's things? Geri - counting down the days with you!
I had a lovely birthday and it was certainly much more fun than last year. I have found the weekend so exhausting though, I am worn out.
Hugs to you all, have a good weekend, Judy xxx
-
Hiya all,
Well I guess it was nice while it lasted, however brief it was, but I'm getting tired and having horrible mood swings again..naturally, this didn't start back up again until AFTER I'd been to the oncologist and told him I was actually thinking the Aromasin MIGHT be a little better than the Femara, too. I mean I still had the joint aching/feet hurting, but I thought I was a little less tired and moody on the Aromasin than I'd been on Femara. But no. My last couple walks in the park that I go on for exercise, felt like death marches, and even though I went to my friend Kym's yesterday (and stayed the night), I have still managed to have four cry fests this weekend. So I guess it all comes down to this, and no, I'm not surprised, this is why I didn't want to go on any of the AIs to begin with:
I SIMPLY CANNOT TAKE ANY HORMONAL MEDICATION WITHOUT GETTING THOROUGHLY FUCKED UP FROM IT.
Which means I have a decision to make: Do I want to live longer and be miserable (stay on this horrible med for as long as the doctor wants me to take it), or do I want to be happy and die soon (go off 'em and say totally screw it to any more doctors and treatments and crap)?
Amy -- whew! Glad nothing serious was actually going on with that cyst business!
Geri -- If memory serves me correctly, wouldn't you be just over the Tappan Zee Bridge? Just curious is all (though personally I find the idea of you showing up at my doorstep to be much better IMO than the idea of anybody expecting me to drive to Maryland or ever get on an airplane!). Glad you're almost done with your herceptin...but you're probably not going to believe this -- I've never had a martini! It's true! Really!
Judy and Titan -- both of you are clean-and-tidy freaks? Hahahaha, warning, if you decide to gang up on me here, don't forget to put on your Hazmat suits first! I am a Sewer Rat, remember? LOL
Titan and Betsy -- I still totally hate my way-too-short hair. That "70s hair" of long and parted to the center -- was my hairstyle then and forever until this stinking cancer/chemo/hair loss/hormonal therapy/weight gain shit destroyed what was left of my looks. Dammit, there's nothing I can do about it but...well, no, there's just nothing I can do about it period, and I hate it, and I hate being damaged goods.
Chelev... dunno what to say, the job market has totally sucked since before the economy ate my last job (May 2008). :-( Hope you find something, and yes, COBRA is expensive. I was not able to afford it when I got laid off.
Alaina -- I hate exercise too, and I'm sorry you had to go back to the torture chamber. :-(
Helen -- all I can do is hug you, hope you don't mind...{{{{{HELEN}}}}}
Judy -- I'm glad you had a good birthday. :-D
Oh, no, I have no idea when the next Pack Rat visit will be. This is the "between visits limbo" where I have no idea when we'll get together again. I NEVER know when I'm going to hear from him, and half the time when I call him he's not reachable -- it's just "somehow" that we manage to speak on the phone a couple times a week and occasionally plan our visits. Yes, I've been putting up with this for 7 years. I can't decide if I'm too tolerant or too desperate, or if he's just soo incredibly good in bed I'm willing to overlook a lot of things no one else I ever knew would put up with from their boyfriend or girlfriend. But, I do love him. Oh yeah.....I gotta find that computer program thingie that compares boyfriends and husbands to operating systems...maybe in my next post...
~Lena.
-
Lena - good to hear from you! Sorry that you are not feeling so great again. I had a great birthday, thanks! So much better than last year.
Take care all you ladies,
Hugs to all, Judy xxx
-
Hi all
Lena, I'll echo Judy's sentiments - sorry that you are again feeling the bad effects that the hormones have on your body. I hope there is an answer for you between pain and not taking them at all. You hang in there with Pack Rat - you love him and it has worked for you two for seven years, so something keeps you two going.
Very sad news last night - I got a call from a good friend who is also a nurse. We both worked for hospice (she still does) years ago, but lost touch until I saw her recently. She knew I had cancer, but wasn't sure of the location. She called me late last night and asked if she could ask me where my cancer was. I told her, and she said, "oh, I wasn't sure - I just got diagnosed last week with lung cancer and I thought maybe I could ask you some questions". My heart broke for her. We spoke for an hour, and I shared much of what I learned here about coping, having a strong support network, not trying to be brave for everyone else, etc. etc.
Sometimes you just have to wonder! Still very affected by this today - talk about something bringing you back - as soon as she said she was diagnosed with cancer, I flew back to over a year ago when I heard those words and didn't realize that life would change forever - some change good, some not so good. Anyway, as always, thanks for letting me get this off my shoulders, and please say a little prayer for Bonnie.
Geri
-
Geri - I am so sorry to hear about your friend's diagnosis. I will definitely say a prayer for her. She has a good friend and support in you - I can say that from experience. It will obviously bring it all back to you, as do so many things, and you can always come here to get things off your shoulders. That is what we are all here for - good times and not so good times.
How is everyone else doing? Helen? The wedding is getting close now - you must all be very excited. Lena - I agree with Geri, if things between you and PR work, then "if it ain't broke...." Always thinking about you.
Chelev - how are you doing? Any joy on the job front?
Amy - hope you are once again enjoying getting back to some "normality". Titan - where are you? Betsy - how are things?
If anyone knows of a mild hair relaxer, could you give me the details? I am soooo fed up of the curls!
Hope you all have a wonderful day! Hugs to you all,
Judy xxx
-
Hi all, I am new to this group...and to writing on a forum in general. I was diagnosed April 9 and started chemo April 21 of this year. I just finished my last dose of AC yesterday and start Taxol in a week and a half. I am nervous about the new drug. I am a nurse and work on a pediatric Hem/Onc unit but we don't really give Taxol. I felt prepared for the side effects of the Adriamycin and Cytoxan, but I am a little anxious about the Taxol. Any tips would be welcome. (For those interested, surgery after Taxol then 6 weeks of radiation).
Also curious to know if anyone else in the forum has young children and if you are doing anything regarding fertility? I discovered the tumor myself because I was still breastfeeding my 11 month old. We had plans to have more children and hopefully still have that option with the monthly Lupron shots I am taking.
Thanks for letting me join.
Meredith
-
Meredith -
Of course you are welcome to join our thread. However, this particular one is for women who started chemo in April of LAST YEAR, 2009! So we are all done and a year past everything and our situations may not be as relevant to you as a thread for women who are going through chemo with you now.
Maybe someone here will be able to chime in re the Taxol. I didn't have it, so can't offer any advice. Also my kids are grown so no help there either.
Just wanted to say welcome and possibly steer you to a more current group.Best wishes for you to get through all this. It really is a challenge but you can do it. We all did!
Amy
-
Meredith- The things I recall most about Taxol were that my fingers and toes hurt a lot and the neuropathy. I did AC first also...then followed up with six weeks rads. What worked for me re: neuropathy...even though I was very resistant at first, was Glutamine (dietary supplement). I was encouraged to take it by my onc nurses. I tried to get at least two tablespoons down per day. The only thing that worked getting it down was ginger ale. Good thing I like ginger ale. At least it stayed suspended in it, otherwise it's like drinking chalk. It did help. Good luck to you and like Amy said...seek out the April 2010 thread. If it's like this group...the friends you meet on the thread will help you get through the lowest of lows and become the best support you could ever imagine.
Geri - so sorry to hear about your friend. I will keep her in my prayers.
Amy- where are those pics of your new hairdo? I'm going in next week for another cut..I may go super short based on what you wrote.
Titan- Are you out there?? Hopefully you didn't get blown away in the weekend storms in Ohio. Very sad indeed.
Judy - I'm doing better. My manual lymph drainage seems to do the trick so it was just an minor set back. I have my onc appointment in two weeks. I'm already nervous about the blood draw. My veins are so bad these days. I need to remember to hydrate before the appt.
I'm also nervous about my onc appt. because based on the chemical menopause they've put me into I think I will be classified as post menopausal in the next round of testing...which means I need to make a decision on whether to take the next round of drugs or not. A year ago, when they put me on tamox. I told them I would most likely not take the drugs they were pushing a year out. When I read through the SE's they had a lot of bone and joint pain associated with them. I do not want to go there again. I'm going to see if they will keep me on tamox., I've read it's slightly less effective but better than nothing. Lena you might discuss it as an option to Aromasin? Not sure that it won't mess with your hormones but maybe your body would be able to handle it. Just an idea.
-
Judy, I had my hair relaxed with a mini keratin treatment that they did at the salon. It was $65, but worth EVERY penny. I had it done yesterday, and they did a pre-treatment of something that relaxed it even more. She hit it with a flatiron and I am not to wash it for another couple of days. It should last about 2 months, because I don't wash every day. OMG, it made my hair so soft and non-curly. We'll have to see what it looks like after I wash and style it. I need to do a color touch up too, because it lightened my hair some, but it is straight, straight straight.
Nothing new on the job front - I'm broadening the search even wider, and may start looking at retail (ugh, thought I was over that part of my life), but only jobs that offer insurance. Lena, yeah, I just got the paperwork on COBRA, and good thing I was laid off before May 10 of this year, because they are providing a subsidy discount where the gov't picks up 65% of the cost, putting my portion at around $350 a month for health, dental and vision. Hopefully we'll be able to swing it.
I've been doing manual lymphatic drainage on myself - I have a lot of congestion in the breast still, and a very tender nipple area with discharge. I see my surgeon in August and will ask him about it then. The MLD helps, as does wearing my sleeve occasionally. Otherwise, feeling pretty good. I've been in a slump where I haven't been working out the last month (gee, wonder why) but got out at 6:15 this morning for a walk/jog (okay, more walk than jog) and it felt sooooo good, I need to pick up and start again. If for nothing else, then to just bolster my self esteem and well being. Trying really hard not to start in with junk food and eat all day. Eating as healthy as I can, lots of fruit and veg, limiting bread, etc. Its so easy to fall back into the bad zone. Have any of you tried the Jello dark chocolate mousse?? 60 calories and it is incredible!!!! 1 large glass of vino each night, right now it is too hot for red, unless it is the light beujolais I had last night, otherwise, chardonnay, pinot grigio, etc. are my summer staples.
Lena, Betsy has a good point. I also cannot at all tolerate the hormone stuff, but I did really well on tamox (except for developing an allergy to it) - it is a natural vag lubricant too, so the benefits there were pretty darn good, but there was NO bone pain, NO fatigue, nothing like Femara or Aromasin. There is also another alternative to tamox, can't remember the name of it, but it begins with an "f" - I tried that too but had the hive issue. Try that, if your onc is game, because the se's are minimal.
Good wishes to everyone - have a great day.
-
Hi Meredith and welcome....I just wanted you to know that there are forums for young women w/bc on this board...also forums for triple negative on this board too (I'm tn too)...lots of place you can go to find out your info.
I did take taxol also...ac and taxol....it was "different" than AC..but still chemo...it took longer than AC but you don't have to take all those anti naseua drugs!
I'm still here! .....I have been soo busy...this summer is going to fly by!
The Ohio storms were not near us..thankfully....
-
Hi Meredith and welcome....I just wanted you to know that there are forums for young women w/bc on this board...also forums for triple negative on this board too (I'm tn too)...lots of place you can go to find out your info.
I did take taxol also...ac and taxol....it was "different" than AC..but still chemo...it took longer than AC but you don't have to take all those anti naseua drugs!
I'm still here! .....I have been soo busy...this summer is going to fly by!
The Ohio storms were not near us..thankfully....
-
Hi all,
I'm still really bummed about my friend's diagnosis of lung cancer - she was seeing the oncologist this afternoon and had her pet-ct scan yesterday. I don't imagine I will hear frome her for a day or two, as we all know the time it takes just to absorb information, deal with telling family, etc.
And a "hi" here also Meridith - I also did Taxol. Had AC first, and as Titan said, taxol was different than ac, and had it's own side effects, but I did weekly for 12 weeks and got through it.
Da da....5 MORE HERCEPTIN TO GO...break out the Herceptini glasses for Saturday night's countdown toast! - Chelev in charge of invitations and decorations ; - well, you voluntered
Lena - we will introduce you to the blessed martini - Betsy also was a "tini" virgin, but she's almost a pro now, and by the time this Herceptin is done for me, we should all be sucking olives like champs! (oh oh - I know I just gave Lena an opening). And yes Lena, I am about 30 miles north of the Tappan Zee bridge - so where are you in NJ?
I know I should take more time to ask all of you individually how you are doing, but I know you'll forgive me if tonight I'm just going to wish you all ((((hugs))), like Judy!
Geri
-
Hiya again.
It's my birthday today and all I can think is how I wish I had never been born. Why do people celebrate birthdays anyway? (Never mind, don't answer, it's just a rhetorical question...)
Um well, OK, moving right along...
Geri, I'm so sorry to hear about your friend Bonnie being diagnosed with lung cancer. :-(
Judy -- what's going on in your world? You keep replying to the rest of us but don't say anything about you -- or am I just still chemo-brained and not noticing?
Helen -- I hope you're feeling OK. {{{{{Helen}}}}}
Meredith -- hi there, sure it's OK if you're here, but you'd probably relate more with the April 2010 chemo group. I did AC, but my T was taxotere, not taxol, and I did it WITH the AC. Someone on the Stage IV board calls it "taxoterrible" and I have to agree. No worries about kids or fertility for me either -- I hate kids and got spayed years ago (15 years before breast cancer) to make sure I wouldn't have any -- by far and away, that was the smartest decision I ever made in my entire life!
Titan -- glad the storms didn't get you!
Chelev and Betsy: I would LOVE to go back on Tamoxifen, certainly compared to this aromatase inhibitor crap. I WAS on Tamoxifen with ALMOST no SEs from 7.30.09 (the week after my last chemo) until February of this year. However, the SE I got was that deep vein thrombosis in my splenic portal vein, and THAT's why my oncologist took me off the Tamoxifen, ordered me to get all those horrible Lovenox injections/transitioned me onto Coumadin, which I'm STILL taking because my platelets are STILL too low (meaning, I still have the clot even though I stopped Tamoxifen and have been treated/am still taking medication for it. I have my next series of scans next week (PET, CT and Bone) so it'll be interesting to find out how the clot situation reads from THERE..So since the chemotherapy pushed me the rest of the way into menopause (it's official, I'm now postmenopausal: my last period was 4.22.09) and I can't take Tamoxifen because of the clot issue, that's why my oncologist put me on AIs. Now if I wasn't a Stage IV and hormonal treatment was simply a matter of reducing the risk of RECURRENCE if I took it, I would have said no I'm not going anywhere near that stuff (AIs anyway: Tamox didn't initially scare me like AIs did/do, so THAT I'd have at least agreed to try anyway), based on my nasty reaction to birth control pills when I was younger. But not only is my cancer not all gone, I'm nowhere near remission -- even though it's much smaller, I do still have a palpable tumor in my right breast, and the bone met too. Which means I have to take this crap to control my cancer.
BUT...(ooh, my Pack Rat just called me, squeeeeek!) ... we were talking the other day (he actually called me from work in the middle of the day on Monday!) and now tonight too and with our respective web researches, think we "hit on it" so I gotta call the psychiatrist and schedule an appointment with him to discuss it. My problem being dopamine deficiency brought on by first the chemo killing my estrogen, then the anti-cancer hormonal therapy killing my estrogen -- my entire list of physical, emotional and cognitive complaints/side effects is also on the list of dopamine deficiency symptoms, and estrogen deprivation messes up dopamine! So maybe there's a way I can up my dopamine to compensate and still be able to take the AIs to control my cancer.
So I'll give the shrink a call tomorrow when I get back from having the car inspected.
Oh, one more thing....2 pounds down, 28 to go. Too bad by the time I lose 'em and would look decent again, I'll have to be all bundled up for freezing weather!~Lena.
-
Happy Birthday, Lena
-
Chelev - Thanks for the hair tips! Oh to be straight again, my hair that is. LOL
Have you tried any compression garments for the truncal LE? MLD helps tremendously but so do the garments. The best is the Jovi...yes it squashes your boob with waffle iron imprints but it doesn't hurt. I wear it every night. On my bad days I wear a smaller pad that fits under the compression bra during the day. I use a Wear Ease compression bra. It looks like an exercise bra. Exercise is good, at least that's what my PT keeps telling me. She says it gets the lymph fluids flowing through the diagram correctly. Good luck.
Sounds like you are approaching your job situation the best you can. We are all rooting for you on the job front.
Titan -glad to hear you are ok. It's been miserable weather here lately. Cold, rainy and it has not let up but no tornado's TG. I'm ready for summer...or at least a little heat like something in the 60's or 70's would be nice. They are forecasting a good weekend but we are headed to eastern OR for a Board meeting and the good weather is not suppose to hit there until Sunday (the day we leave).
Geri - Congrats...your down to FIVE!!! The end is near, I bet you can't wait!
-
Hi everyone.
Geri, sorry about your friend....I'm sending PV's
Chelev...good luck with the job search. I'm sure something good will turn up for you.
Judy, how are you?
Lena, thanks for the (((hugs))) - felt good. I had a similar relationship with a man for several years. Difference is, even though he promised to stick with me, he abandoned me.
Betsy & Titan .... glad that things are progressing positively
Wedding is in 2 weeks. I'm going to try a different hairdresser this weekend to see what he can do. This is the guy who is going to do the bride's hair - might as well try - nothing to lose. It would be great if he could some extensions for me. Keep your fingers crossed. I'm going topless because I just didn't want to wear a hat in the heat and I have too much hair for the wig. I'm still using the minoxidil two times a day. I think it helped a little. But my hair is still very thin and very fine. I used to have the thickest hair ... very, very curly....but with thick hair, I could do a lot with my hair. Now I have "old man" hair ..... really ugly. I'm still carrying 50 - 60 pounds too much. I've put on about 40 since the bc dx ... chemo, etc. and then the Arimidex makes it impossible to lose. I have a dress. It's nice. Too bad I look crappy in it. But I am excited for the kids and want them to have a special day. My biggest worry is this stupid G20 that's happening. Bad enough our government is spending 2 billion on security and various things - a waste of money. But the security zone starts 20 steps away from our wedding venue. There's lots of protesters in town so I'm worried that they might be rabble rousing in front of the hotel. My son works in the middle of the financial district, which is in the security zone...fortunately, he's going on his honeymoon but the bank is moving people out for the week because of the potential danger. I bet none of you had to worry about the G20 disrupting your child's wedding .... wish us luck.
-
Lena - Happy Birthday and I hope you get some good news from your call with the psychiatrist. Sometimes it really does feel like it's up to US (not the docs) to figure out/solve our own problems. Frustrating when we are medical outsiders......
Helen - good luck w the hairdresser. Crazy about the G20! All I am worrying about for my daughter's wedding on the 19th is the WEATHER - not any protesters! I hope it all goes well and they STAY AWAY from your joyous occasion.
Everyone else - keep on trucking. We are so much better off than we were at this time last year when we were all beaten down by chemo and struggling to get through. Even with our extra weight, various aches/pains and problems, I'm still glad it is 2010, not 2009!
-
Lena - Happy Birthday!!! Thanks for asking after me. I am doing ok. I have actually just been out of town with my husband and we had such a great time. Just one night, but it was good to have a break. I am generally feeling ok, but still get very tired. My hair is coming in crazy curly (thanks Chelev! for the info on the relaxer). On the whole, I get by. I have started therapy and hope that one day I will come to terms with what I have been through and how I can live my new life now. I need Alaina for some inspiration. But thank you for asking.
Helen - two weeks to go and very exciting. I completely understand that this is a challenging time for you, but I am so sure that your family are just so happy that you are all sharing this together. Enjoy! Even with the G20...
Geri - You can always lean on us. I am sure that you are taking the news of your friend badly and we are all here for you.
Chelev - I am convinced that your persistence and postive attitude will help you find a new job.
Amy, Titan, Betsy - always good to hear from you and sending you all (((HUGS)))!
Meredith - good to hear from you and good luck! I finished chemo in July 2009 and I did 4 AC and 4 Taxol. I found the taxol quite unpleasant. I think the fact that it was unpredictable is what made it so hard for me. I found the AC hard, but I always knew where I was in the cycle. The worst se for me was the aches in my muscles. I had very little numbness in my fingers and toes.
We are all very happy to help you out with any questions you have, but you may find it more relevant to speak to the April 2010 group. I wish you the best of luck and we are all living proof that it will pass and life will continue after this. Sending you (((HUGS))).
We have done quite a bit of driving over the last couple of days and I am sooo tired, so I am going to have an early night.
Take care all of you and sending you all hugs. Judy xxx
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team