Starting chemo Dec 2007
Comments
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Hi all. Laura, Happy very late birthday.
So far I've found radiation easier than chemo. I have more energy, too. The only bad thing is I get so tired so early because I get up so early. I sleep good when I'm sleeping, but because our bedroom is directly next to the living room and my husband likes to watch tv until almost midnight or after, I'm only getting between 4 and 6 hours of sleep every night. I wish I could sleep with the tv on, but even if the volume is off all that flashing drives me batty.
Anyone else still having hot flashes with radiation? I am.
Cindy, The pictures are so cool! My daughter and I walked a mile and thought about you.
Suz, sorry to hear about your test results. Your in my prayers! :O)
Amy, I hear you with the battling the house. I am so glad to have energy to work some. I can't believe how bad things have gotten in the "dust" area.
Everyone, I'm so glad the journey is getting closer to the end for everyone! Good to hear so many good things happening. I still have a swollen lumpy thingy, but the redness is fading. The radiation onc says we'll just not worry about it til after radiation. Pray it's nothing and even better that it disappears.
((HUGS)) to you all
Kate
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swollen lumpy thingy??? Kate, do you mean in your breast?
Laura, in case I missed it, ( I think I posted @ it), hope you had a very happy birthday!
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Evening all! I've been away too long!!
Laura, Happy belated Birthday! I hope it was wonderful!
Suz, Sorry about your results but like Amy said, getting hit by the bus at 98 is totally do-able at this point!! LOL You are in my thoughts and prayers!!
So, I was halfway thru rads after yesterdays session and after today I've got 14 more to go! I am starting to get a bit red and itchy only at my collarbone. I got a script for the Biafine now and am also using the cortisone cream. I did color my hair with "Grey Solutions" by Clairol and it turned out great! A little too dark at first but after a few washes it looks good. I have to say it really colored the greys better than anything else I've ever used and did it in 25 minutes. With other hair colors they will say you can leave it on for up to 45 minutes for color resistant grey and I always had to but not with this stuff!! I'm quite happy with the progress my hair is making....it would even be kind of cute if I just had more bangs!! My eyebrows are about ready for a waxing also! I'm really feeling quite back to my old self and of course, getting very excited about Vegas!! This coming Monday I'll be at the "6 more weeks" countdown!
Cindy, loved the picture from your walk! That was really great! I walked about 2 miles that day also and thought of all of us!!
Hope all the rest of you are doing well (WIW, Kate, Kimbly, Sal, Amy, Jeannie and everyone else!) Hang in there everyone...every day that passes gets better and better!!
Big Hugs, Lori
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cortisone cream? Did they tell you to use that? I'm surprised if they did, b/c that thins the skin and most times, they say to stay 'out of the sun' while using it even the 1% stuff. It's one of those photosensitives or what ever they call it. You can burn easily with it. Are you using it where you are getting rads?
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Thanks Everyone, I appreciate all your thoughts and prayers{{hugs}} Don't know what Id do without all your support. I'm ok with all of this now and am getting more informed so I can deal with this as just another bump in the road.
So it was #3 of 20 today (16+4 boosts so I'll just call it 20). I got an extra tattoo today so I'm up to three dots now
. I was sore after the first two treatments but with lots of aloe & cream its feeling much better today. My biggest issue now is how to keep the radiated area out of the sun... they have zapped the left side of my neck almost to the jaw line. I was told no sunscreen until after all radiation & boosts are done. It was beautiful outside today so I tried to fashion a lightweight scarf kind of draped around my neck, but it kept slipping. Any ideas or suggestions would be most welcome?
Kate, How many treatments will you be getting? I'm still having hot flashes but they have slowed down a bit in the last two weeks. I get the feeling that because of my age menopause might be here to stay. The chemo onc said something about it being a few years before they would know if it was permanent (I think).
Lori, whoo hoo.. over the halfway point without a burn is fantastic. Hope the collarbone doesn't get too bad. I just don't get it.... how do you manage to have enough hair to color??? (ok I get it but am really jealous) Lucky you!
Gotta run, take care all you lovely ladies and have a great Friday. Much love & hugs, Suz
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{{{Suz}}} hope things improve with the rads
So sorry you're having problems. As for the sun, be very careful. I heard you can actually get a sunburn through cloth, so be really careful dear! Maybe call a derm office and ask what they recommend for keeping it covered and free of sun exposure? Not sure what they would say, but I know there is a material that's better than others for keeping you safe from the rays. Good luck and let us know what you find out!
Everyone else, have a great Mothers day weekend! Hoping to see my mother this weekend sometime!
Enjoy the warmer weather too!
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Wish-No, well, it's where my breast used to be on the side opposite of the side that had the cancer. It's at the surgery site. My port is directly above it and they think the taxol was attracted to the space and caused a problem. Of course, the hardness bothers the doc, but I'm not going to worry about it yet. One thing at a time.
Suz- I have to get 33 treatments. I've had five. So far so good. Not to bad. I haven't had any skin problems yet. That's a good thing. Tuesdays and Thursdays, they give it a boost. The worst thing so far has been the 25 minute ride every day. ick. But, I guess it could be much worse. I have to put aloe on every day and some aquaphor cream every night. I forgot to ask if I needed to do that on the weekend.
Well, it's been a really busy day. I hope you all have a wonderful mother's day tomorrow!
Kate
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WIW, Yes, the hydrocortisone cream (Cortaid) was recommended by the oncologist...it is the 1% stuff. Interesting...looks like I need to do a search and see if anyone else is using it!! It really helps the itching anyway! LOL
Isn't today beautiful? It was warmer here than first forecasted.
Hope everyone has a great Mother's Day tomorrow!! Lori
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WIW,
OK, did my search and looks like lots of others have been using it as recommended by their doctors as well. Glad to hear because the itching can be terrible at times! Lori
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Well, just be careful. They say with cortizone you are more apt to sunburn. I was using on my head when I had that rash after the 1st 3 chemo's each time and my derm said not too. It thins the skin. I have 5% for my hands for that rash from chemo after the 4th on the palms. I pokes literal holes in my palm reaching in the d/w to put away forks the the other day! I mean, it bled even. I use my hands a lot for everything (not a painted lady at all), so I was surprised at how easy it was to open the skin with a light poke of a fork no less.
Just be careful, b/c you will be a higher risk of sunburn there.
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Kate, I'm praying that your swollen area turns out to be something simple.
You ladies going thru radiation sure sound brave. I'm sure it isn't easy, but you all sound like you're cruising through it. You're amazing!
Wanted to thank everyone for "listening" to my whining this week. I do seriously think the Tamoxifen is giving me mood swings, so I'll blame it on the drugs.
I saw my onc and was pleased with the visit... he didn't poo-poo my problems, which I half expected. We're gonna do an MRI to rule out (or find) any disc problem that is causing the pains; if that doesn't work, we'll try the osteopathy.
He also gave me a prescrip for Effexor. It's an anti-depressant (wondering if it is the one Amy used?) which is supposed to have the SE of reducing hot flashes. I sure hope so, since now I'm getting chills too
So I run the gammit of sweating/normal/shivering/normal/sweating... etc etc. all night. Whodda thought there'd be more ways to keep me awake? Oh well, since I've been moody too, perhaps an "anti-depressant/hot flash reliever" is just the ticket.
Happy Mother's Day, by the way, to all you moms out there. My cat usually gives me a card, but he (aka my hubby) forgot this year. It's been a rough few months for us all, so I'll let it slide.
And speaking of a few months, I was seeing how far I've come...
It has been almost 2 months since my last chemo tx.
5 months since my first chemo tx.
6 months since my surgery.
7 months since I was diagnosed.
8 months since I found the lump.
I'm not sure looking at that makes me feel better or worse, but I know that I've made it through the worst. My new realistic goal is to feel like my life is back under control-- pain issues resolved, reconstruction completed, etc.-- in 4 more months (1 year after finding the lump).
Gonna go enjoy the day. Hope you ladies do the same!!!
Hugs, Sal
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Happy Mothers Day!!!
Well, all of you Michigan Gals ... my son is on his way to Grand Rapids Michigan as we speak...it is about a 12-13 hour drive... he has been promoted to play baseball (minor league) for the West Michigan Whitecaps... He is scheduled to pitch his first game on Tuesday in Fort Wayne. (not sure the name of the Fort Wayne team).... I talked to him a little bit ago and he said it has been raining and cool all day driving up. When he left home this morning it was sunny, humid and 80 degrees.. Talk about a Shock to his system... He is excited though, and will be staying with a Host Family in Grand Rapids...So that is how I've spent my mothers day (worrying about the son, he's 19)...
How have all of you been? Hope everyone is feeling better and stronger w/ each passing day... I know I am!!!
I hope everyone has a WONDERFUL Mothers Day!!!
Love and Blessings,
Jeannie
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Jeannie! Tell Ds congrats! You must be proud that he's on the road, even though it's a worry. Honey, my dd is in town here and even though, she travels 20 miles to work and then back again to work at a bar/restaurant and takes classes too, so she's on the road always
Hate it, but....at least she's close. Sometimes I think it makes me worry more b/c I know her schedule.
Hope your dson does wonderful. It's not been hot, but warm during the day. Evenings are cool though! Brrrr
Sal, hope the pain gets some relief very soon. Will the MRI show problems that the osteo would deal with then? Hope it's something a realignment will help and no more surgery or serious stuff sweetie!
Kate, keeping you in good thoughts and prayers!
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Hello ladies, it seems like forever since I've even had time to read, let alone post! I've been very busy with work and house projects - starting to fill holes and paint walls.
And a belated Happy Mothers Day to all of us moms!
Sal, I am glad to hear that you had a good visit with the oncologist and that something will be done to investigate the pain. There is so much that you have had to deal with, it's no wonder your moods might be swinging. Don't you worry about whining - that's what we're here for!
Amy, I can totally identify with the house struggles. I am battling a house full of junk and have managed to get rid of some of it. On my birthday my son and his buddies took some old sofas that weren't even saleable and the old dishwasher, an old microwave, toaster oven, easy chair, to the dump. It was SO good to get rid of that stuff! But I STILL have tons of stuff to get rid of. Does this stuff multiply in the dark in the basement, or what????
Suz, I am sorry to hear about the positive genetic result. I know you are strong and can deal with this as you have with everything else. I wish I could come up with a solution for sun protection!
Kimbly, very happy to hear about node negative - I remember when I was just waking up from surgery and that was all I cared about - it was SUCH a relief when the surgeon came by and told me the nodes were negative! Congratulations!
Kate, glad you are doing well with rads. It is such a relief not to feel completely run over like with chemo!
Loriann - Glad the cortisone helped with the itching! I've seen quite a few ladies getting that and it is very effective. The grey hair! I, too, will need to do something about this grey when my hair gets a bit longer. I had started colouring my hair about 8 years ago, as soon as just a few greys started showing up, so I had no idea actually how much grey there was in my hair. Well, now I can see it is quite a lot and I'll have to do something about that. It is only about ½" long so I'll hang on a bit longer.
WIW - I cracked up reading your laundry suggestion on the "I can't get my act together and don't know why" thread! It sounds like a great idea!
Jeaniebell - glad to hear you are doing well, and the news of your son's big move!
I want to thank all you ladies for the birthday wishes - it was fun but exhausting. I keep trying to do too much and that fatigue thing happens. At first when chemo finished, after about a month I found my energy levels were really getting good. This continued, but with radiation finally last week the fatigue from the radiation started to hit me. It is ok if I am working from home and can be physically fairly relaxed, but if I go to the office and then the hospital, on the bus/train hauling my heaving backpack with my laptop in it, I feel pretty wiped out by the time I get home. Regardless, my general sense of well-being is hugely improved since chemo ended, and I am feeling quite good.
One thing that has happened to me the last few weeks is that I have developed this pain in my hip/back. I had a similar pain a couple of years ago in one hip and it was the beginning of arthritis in the sacro-iliac joint. I had taken glucosamine faithfully and after a year or so that pain was completely gone. So I don't know if this is arthritis or what, but it is....well...a pain. Also, I think I now have arthritis in my hands. I didn't get any of the chemo that usually causes bone/joint pain (no taxol/taxane and I am not on tamoxifen), but when I wake up in the morning all the joints in my hands ache and they are stiff. I am just generally feeling all of a sudden....old! My grandmother had terrible arthritis and my mom also suffers a lot with it. Anyway, I'm not too worried about these aches and pains as they are not stopping me from doing anything yet. I will definitely start back with the glucosamine after rads finish.
I have also had trouble sleeping - I have no idea why, but some nights I drift off to sleep then wake up after an hour, and then I'm up until 4 or 5 am. This is hugely frustrating, but the last few days I've exhausted myself so much during the day with all the stuff I'm doing that I have been sleeping through the night. Maybe that's the answer! lol
I am in my LAST WEEK of rads! Friday will be my last day and I will definitely be drawing a happy face on my boob to give the nurses a laugh. They have been great! Rads has been a breeze after chemo. I have been fortunate to have no burning, just a bit of a tan and the nipple is tender and a couple of small itchy spots. Tomorrow thru Friday are the boosts to the scar area, so I'm not anticipating any significant reaction at this point. What a relief! I've used calendula cream (when I've got around to it) and castor oil a couple of times, and aloe vera a couple of times. I just try to make sure I give the boob lots of air as that seems to help.
Hubby is waiting for his papers to exit Cuba and busy wrapping up loose ends, which will take some time, so I think it will be June when he gets here. I still can't believe it. That will be the best thing to happen this year!
Well, I need to get some sleep. Big hugs to all you wonderful ladies, and I hope the positive results keep rolling in, and the aches and pains and SE and hot flashes keep going away!
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First things first! So glad you are getting closer to having your dh at home with you! YEAH!!!!!!!!
Then, I'm sorry you having so many problems with your hips/lower back. Been there and dealing with it. What a pain, as is said too often!
Hope it gets straightened out as well as with your hands. Hope you can find something to alleviate without more 'pills'!
Are you on any of the anti-hormones things yet? Perhaps they are aggravating the stuff? I don't have the hand problems, but hear so many that do after some of the chemo's and while doing the Hormone tx. Are you post meno? I'm thinking a lot of my hip stuff might be that. Hoping it's something that will get better, not worse
All in all, you should like you are looking forward to getting over the tx and moving on with dh! Hope that's true!
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Hope everyone enjoyed their Mother's Day. We didn't do anything much as here in SE Michigan it was rainy and just plain old miserable. Mostly I played Mario Cart with my kids on our new Wii and read. My mom was on holiday and my mil lives in Florida so no commitments that way this year.
Laurita glad to hear your radiation is almost complete!!!! I hear you about the hair. My hair is growing in thickish but so much gray UGH. As soon as it covers my scalp and is maybe an inch long I will probably color it. It is about 1/2 or so now with a few longer strands that drive me bonkers and I trim to make even LOL. Sorry about the pain you are experiencing. No fun at all! I am on tamox. and herceptin right now and nothing so far so keeping my fingers crossed. I know you said you don't have these meds so though. Congrats on your dh's progress with leaving Cuba! that will be nice finally!
Jeannie, Yes Michigan has been cool and rainy a few days. Grand Rapids is about 3 hours west of me. Good luck to your son! My kids are 16 and 13. I have one more year before my son goes off to college. I keep telling him he doesn't 'have' to go away to school if he doesn't want to. I think I handle my cancer better than the thought of him leaving home!
Well wishes to those I didn't mention...
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Hey all--still playing catch-up with messages, and not enough time to write a whole message, but--
Sal--you should do a little research about Effexor...when I was deciding to do an antidepressant I read some stuff about them, and I remember that Effexor can be very difficult to stop taking. I'm so sorry to complicate your life more. You really need some relief, and maybe it is a good choice--I just don't want you to get stuck with something that gives you problems later...
this is my fav. website for this stuff:
Sorry, for some reason it won't let me make a live link. look up effexor on it and see what you think.
love--and let us know what you decide
A
here's an excerpt--there's more if you look at it:
Effexor's Pros: There are two last resorts among the modern meds to cure the deepest, blackest depression when your doctor is just switching you from one horsie to another on the med-go-round: Effexor XR (venlafaxine hydrochloride) and Remeron (mirtazapine). Either in combination with an antipsychotic would really get you out of that hole of despair, but first you should throw away every mirror and scale in your house and buy expandable clothing. But for deep, despairing clinical depression that needs to respond to the standard tweaking of the three most popular neurotransmitters, Effexor XR (venlafaxine hydrochloride) often pulls people out of the abyss.
Effexor's Cons: For many people Effexor XR has the absolute worst discontinuation syndrome of an antidepressant. Effexor (venlafaxine hydrochloride) is a medication people utterly loathe to have taken. It is not uncommon for someone to fire doctors during or immediately after they quit taking Effexor XR(venlafaxine hydrochloride).
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Hey Amy... thanks for the link. I went right over to it. I wish they would explain what they mean by "discontinuation syndrome".... I know that the literature that the pharmacy gave with the medication did heavily emphasize that you can't just wake up one day and stop taking it, but I wonder if there is more to it than that. Blah. Now I'm wonderin'. Egads.
Well I've been on it for a week now. The multiple hot flashes have simmered down to occasional warm flashes with only one or two hot ones a day, so I'm pleased about that... except for having trouble staying asleep for a long chunk of time, I am getting some sleep now. I was a little freaked out about the "don't just stop the meds" literature, though, and asked my doctor if I could stay on this lower dosage... I was supposed to start taking a larger dose tomorrow... I figured that since the flashes have simmered down a bit, the low dose is all I need. The only thing I need to figure out now is how I know when to ask my dr about going off of it... a couple months, a year? But one thing at a time.
Laura, sorry to hear about your pain issues, but very glad that your last rad tx is THIS WEEK!! Congratulations!!
Jeannie, great news about your son. Wow-- he's gonna be famous I'll bet!!!
Wishiwere, I'm on Tamoxifen. So far it hasn't been bad. Just the hot flashes. But I did read quite a bit about ladies that have had pain problems while on it. I guess I beat 'em to the punch and got my pain problems early
I'm having a pretty good week so far. Aches not going away, but I am getting used to them and can ignore them better (if that makes sense). The hair is slowly starting to get thicker, but is sure taking it's time growing longer, he he he. I bought a box of hair coloring and it is standing at-the-ready on my bed stand... probably will have to wait another month, realistically. But I'm in no big rush.
Gotta scoot. Hope everyone has a marvelous day.
-Sal
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Hey Sal--
I wish I could link you to the "discontinuation syndrome" page, but all I get when I copy/paste is the top page...anyway, if you poke around there you'll find it. I think that site is a little skewed, but probably a good source of stuff the docs actually don't seem to know. I've been going off my SSRI (Celexa) very slowly. The thing that happens when I wait too long to take it is that I get what people call the "zaps", which is this weird little shiver in my brain. It's unpleasant, but I guess, overall, not as bad as the hot flashes at their worst. I don't know what else happens to people. My husband went off Prozac, cold-turkey, years ago, and didn't sleep at all for two weeks; hasn't really slept properly since. But he's a whole other can o worms.
Anyway. Good that it seems to be helping with the hot flashes. Mine are definitely much more manageable--much fewer, and less intense. Waiting on my period...supposedly should come back soon. Every time I get really grouchy I think that might be it.
so. now for the really important topic--I bought product for my hair today, cause it was getting unruly! How cool is that!? I am totally going to stick with the grey for a while...I think it suits me, and I've really hated coloring it all these years. Maybe down the road I'll decide to color again, but I'm kinda psyched about the grey, weirdly. It was there anyway, now I'm not fighting it.
Suz--hope your back problems are better...
more later--
A
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oh, sal, you should absolutely stick with a lower dosage if it works--especially since you're small and seem to react pretty intensely to medicines...
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Good morning all! After catching up on the posts it sounds like most of us are settling back into some new form of "normal".
Sal, I hope you can get your flashes under control and that you can finally get your back/hip pain corrected easily!
Laura, June is almost here! You won't be waiting much longer to have that hubby of yours close at hand!! You must be so excited! Hope your arthritis calms itsself down also!
Amy, Cindy, Kate, Suz, Kimbly, WIW, Jeannie....Hope all of you are doing well!!
I'm down to 3 more regular rad's then the 5 boosts. My collarbone will be VERY happy after Wednesdays tx since it is the reddest area...actually it's even gone thru and causing red, itchy's on my back! It really hasn't been too bad all things considered! So I'll be all done on the 29th (since they are closed on Memorial Day ) and at that point I will be 24 days away from Vegas!! I am so ready for that trip....I picture myself breaking down on the plane...You know, telling myself all thru this entire BC thing that I would still make this trip, but not really knowing that in the beginning, and to finally be on that plane!! We made our reservations in October and then I found my lymph node lump about 2 weeks later! I've already dragged my suitcase up from the basement, pulled out my "Vegas" purse...small with a long strap to wear over the shoulder and my collection of player's cards. Bought a few new clothes and I am just ready to go!!
Hope you all have a great weekend! Lori
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Loriann - enjoy your holiday! I have never been to Vegas but it is one of my preferred destinations post cancer! I am not a gambler but have heard even if you aren't it is a wonderful place to visit.
How is everyone's hair coming? I am so impatient!! It is coming but slower than I thought it might.
How is everyone's new normal? I am having a hard time with it, waivering between old normal and new .. ugh.. I will get there though.
I am 2.5 weeks post surgery and doing well. Had one fill last week and will have another tomorrow. 100cc at a time. It wasn't so terribly painful just felt really wierd. My PS is wonderful. I saw him in the grocery store yesterday and he hugged me! He is just such a nice man, so caring etc.. In fact all my doctors have been this way. I feel blessed in this department for sure.
For those of you with kids.. how did they deal with your cancer? Did they talk to you about it much ? My kids are 16 and 13 so not little but never really ask me alot of questions. It is probably because they have none as we are so open with them. I do notice alot more attention paid to me as far as "mom are you alright' though.
I am so glad Spring is finally here and gardening time has begun.
Well wishes to all !!!!
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My KID is 24, so can't help there, although she is starting to at least be open for discussion, b4 she wasn't. VERY helpful to my situation but would NOT discuss her risks and such till lately. It's hard on them all.
My BS is a super guy, but the onco I may do without. HE's good for absolutely nothing really. He's answer few questions, only time he checks anything was when he papers to draw blood or listens to my heart on my back! I think he's afraid of women, to be honest! He's just got a bad way about him. Not to mention he's from another country, so the discussions are difficult at best
So glad you healing is progressing well! IT's hard to deal with all this 'new' stuff, but it does get better! HAS to, right?
Hair? It can never grow too fast, can it? Mine is about 3/4 inch maybe? NOT enough for certain! Still feel like a young boy with it! Scary!
Gardening and pulling weeds is a GODsend for me! It's the best therapy one can ask for!
TIll that night of and day after and I feel muscles that are asking for relief! :O
Have a great day all, off to the yard again!
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Hi all!
Lori, hang in there for Vegas--it's gonna be a blast. Not only can you celebrate being DONE, but you'll be feeling better! Not much longer!
Kimbly, I'm having some trouble with my "new normal" too. I feel very "carved up" and kinda sorry for myself and unhappy when I look in the mirror at the new me. It doesn't help that (possible TMI alert, sorry) I haven't had sex in nearly 7 months. My husband has been very supportive in every other way, but he hasn't really helped me to feel better about my body. Granted, I'm only now starting to feel like I'd even want to try...sigh. Anybody else in that situation?
My kids are little (5 and 9), and didn't really have any understanding of what cancer is (except the baldness!). So they have been ok--we told them everything very matter-of-factly. My older one is very uncommunicative, and has little spells of feeling sad, but he never says it has anything to do with the cancer, so who knows.
My hair is now over an inch long, and definitely covering my whole head. I started going "topless" about two weeks ago. The hardest part is how you have to talk to everybody about it. I think I've had the "you look great" conversation with almsot everybody now, though--hopefully we can all just talk about something else now! (Not US, here, I mean all the people in the world who feel obliged to say something to me!)
WIW, I am right there with you in the garden. So therapeutic in so many ways. This is the first year since we bought our house (3 years ago) that I've felt like things are growing the way I want them to, and I have a handle on how to treat the perennials, etc. It's gorgeous, it smells wonderful (lilacs right now), the sun feels marvelous, even the aches and pains are gratifying. It's what I dreamed of all winter. aaahhh....
Hope all are well--suz, how's your back? Sal? Laura, are you counting the days?
love to all--
A
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Hi ladies,
Was supposed to have an MRI today to look for cause of my aches. However, my Plastic Surgeon neglected to tell me that the tissue expanders (temporary implants) he put in have metal in them. Grumble grumble. The minute they put me in the machine I felt pressure on my chest, but I had no idea what was causing it. Well, no harm done... they figured it out after the first run and sent me home. I'm kinda po'd at my PS for never mentioning something like this... in this day and age of security checks and metal detectors, you kinda need to know if there is something metal inside ya... I'd really like to smack the guy. I just better not get charged for the MRI.
The good news is that as the days go by, I'm getting more "used" to the aches and they don't bother me as much. I can kinda overlook them for most of the day now, unless I have a particularly achey day. No, I don't intend to live like this, but at least I can bear it better until we do find a solution. The new Indiana Jones movie comes out this week, and I'm a HUGE fan, so no stupid butt pain is gonna keep me from sitting in the theater for 2 hours this weekend!
Wishiwere, bummer about your onc. He sounds pretty useless. He must have gone to the same medical school that my PS went to.
Kimbly, it sounds like you are recovering from your surgery very well. That's is wonderful! Good luck with the fills. Sounds like you're doing great so far.
Amy, I have to admit I'm right there with ya in regards to the sex. I think it's a combination of my still coming to terms with my new look-- I might have 2 objects that have the general shape of my old breasts, but they certainly don't look or feel anything like them-- and my being pre-occupied with other icky things-- like aches/pains, lack of hair, lack of energy, etc. My husband has been very patient and has made every effort to make me feel loved, so I can only blame myself... I'm just not ready yet. I'm trying to cut myself some slack and just let that part of my life "get back to normal" in its own good time like everything else.
Speaking of normal, someone asked about our "new normal"s. I'm glad to report that over the weekend I noticed a slight change: I seem to be getting back into a relatively normal sleeping routine. Now that the hot flashes seem to be under control, and I've learned to sleep on my stomach/expanders, I've been able to get some normal sleep. Believe it or not, but that simple thing has made me start to feel like my old self.
Hair check... my hair seems to have stopped growing length-wise but is filling in thicker. And it's starting to look a bit ruffled, so I think it will come back curly like it used to be... I'm glad about that. It does feel like it's taking foreeeeevvvveeerrrrrr... at this rate, I don't think I'll have a decent short hairdoo until mid-July.
For therapy, I've been rather enjoying my daily walks. Today I did 5 miles. I've been feeling less stress lately, and I attibute it to the exercise I'm getting. I used to exercise once a week, so it's weird to see myself exercising every day now. I only hope that I will keep it up and not let it pass once I get the aches under control.
I've yakked your ears off long enough. Hope everyone is coming along nicely. Anyone doing anything exciting for the upcoming long weekend? All I have planned is the Indiana Jones movie. Welcome to my boring life
Big hugs, Sal
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ugh....just lost my post, first time I didn't take my own advice and put it in Word first
Sal, I'm glad you are getting some relief from the hot flashes and that sleep is stabilizing for you. It's amazing what a difference that makes. When will you get the expanders out? Your poor little bod has gone through SO MUCH! I sincerely hope things continue to work their way back to normal. You too, Amy!
Loriann, good to know things are on track for finishing rads soon. Those boosts can be quite a bit stronger and it was only after them that I noticed any changes to my skin. Make sure you keep using that cream! You will be in great shape for Vegas and that will be a great celebration of getting your life back.
Kimbly, glad to know you're getting filled up and have a great PS - this makes the world of difference. My kids are 20 and 22 and they have been ok with things as I've been pretty strong and open with them and they seem to have taken things in stride.
People keep asking me if they do tests/scans to ensure the beast is completely gone from your body. Do they do this? Have any of you had this done? I didn't and basically the plan is just to get back into regular checkups/mammograms afterwards and hope for the best. I think because my cancer was not anywhere else other than the tumor they assume it is gone after the lumpectomy, chemo and rads. I wish people would stop asking me this stuff.
Rads finished last Friday. Yesterday I had a very small amount of superficial skin breakdown in the fold under the breast. I also look tanned and spotty, which is pretty much normal for rads. Other than that it all went very well and I'm glad to have it done.
Hair - shaved my legs on the weekend for the first time, as I was out in a sundress and realized there was quite a crop going on, lol. My eyebrows now need plucking as well. The head hair continues to fill in nice and salt and pepper
but better than none!
I am super fatigued this week, more than ever. It's like the rads have had a delayed reaction. I wake up feeling tired. I am really looking forward to recuperating from this and having energy back, as I'm trying to tackle projects around the house and it's hard getting much done at this pace.
My hands are really bad. I'm going to have to see the dr. about this in case it's rheumatoid, because for that you need more than just pain relief. I can live with the pain, but some things are just really hard to do and once the pain gets to a certain level (as it is in my thumb joints) you basically can't force them to work. Between this and the fatigue I am feeling like a very old woman. Whine.......
We just had our long weekend here. The weather was super fabulous and it was great to feel the sun shine on my balditude. I, too, have been enjoying garden therapy with my mom. The cherries and apples are blooming, the tulips etc. are just finishing, and the lilacs will be out very soon. I got my garage cleaned out (it was FILTHY!!!). I'm trying to get some stuff out of the way so when hubby gets here it's not all hard work and we can have some R&R together.
I hope you all enjoy your long weekend! Vanquish those aches and pains and sleep well and enjoy life! Hugs to all!
Laura
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Cheese for you whine dear? You've earned it! That and a chunk of good chocolate! Remember to not over do it. It will take time to get over that run down feeling from rads. Remember that is your body saying, I need to rest!
Soory to hear about your hands! Dang it's always something for each of us, isn't it! WILL there be a day we don't feel something from treatments I wonder?
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Hi gals !
Hair check, thick and very wavy in back, length about the same. Used second box of color this week, now back to blond with white hight lights. I too am having to shave once again, everywhere! My face/side burn area is super peach fuzzy! And, you know who came back....you got it, I am once again buying tampax! I was really hoping that my period was over, but I am just "going with the flow" , so to speak! No way to predict what is around the corner on our road to complete recovery. I should have known something was up when my hot flashes started becoming less frequent !Laurita, I am not scheduled for a PET scan, but have an MRI scheduled for August, only cause I pushed onc for one. Pretty much for piece of mind. Mammos scheduled for September 08, one year after original shit hit the fan. BTW, I was dxed with Rheumatoid Arthritis three years ago, and take meds for it, and it is pretty much under control. Started in my thumbs like you mentioned. Going to see Mom and Bro this weekend in Rehoboth Beach Delaware. Wishing you all the GLORIOUS weekend. xo cld
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Have fun! I'm going to Cleveland with my mom and should be a long haul, but hope it's nice weather and not raining for everyone!
Hair....seems like the same length as the last 3 weeks, but more of it maybe? It's wavy, but not curly I wouldn't say. The sides above my ear are almost completely straight! UGH! And yes, the peachfussy sidesburns are killer
Best be doing something soon, or I'll be doing it! At least it's light and only those up close and personal can see it! At least that's what I tell myself!
Sorry about the flow
Win some, lose some. I've spotted here and there but no flow to speak of, which is nice! I'd send you my tampax, but I'm keeping them only b/c both dh and I feel if I got rid fo them, she'd rear her ugly head again!
So there is one in the car (in case) in the purse, and suitcases. I've left them there as susperstitious stuff to ward it off so to speak!
Have a great one this weekend!
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WiW- I should have done the witchcraft trick, but I GLADLY ( at the time ) gave my vast supply away! Good thinkin on your part! Its kinda like when you give all your pregnancy clothes away, that's when you are unexpectedly expecting! LOL ! Safe travels to all!
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