March 2009 Rads Group?
Comments
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ROFL mfgibby!!!!!!
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Hi ladies--haven't posted in a bit...Partly a good thing because I have been busy, starting to get back into life, feeling physically good, but also partly because I have also felt a bit depressed.
I spent much of Saturday at a small church conference/meeting (not many people, 50 or so) and my ex was also there--taught one of the workshops I went to, actually. We're adjusting to being friends--slowly--so that wasn't too bad in and of itself, it was just a long day (7:30 am - 10:30 pm), and I got worn out. So in the evening, I misinterpreted something my ex did (arm around someone during the service), and thought for a bit she was already seeing someone else, and just had a meltdown (thank God I work in that church and knew where to hide for my cry!). But I calmed down eventually and realized I was misinterpreting--for many reasons (it's too soon, she's not any more ready than I am; it was someone who goes to that congregation and she was clergy there, so it's a no-no; she wouldn't be public about a new relationship without letting me know; she's a touchy-feely sort of person, etc.). I had a good conversation with her Sunday night and we're OK again...THis learning to be friends instead of partners is a rough road (for both of us), but ultimately worth it.
ANYWAY, what I mean is that I realized I'm still recovering and still tire easily. A year ago a day like that--breakfast, workshop, lunch, workshop, dinner, worship--would have made me a little weary, but I could have done it for three or four days in a row. Now, one day of it reduces me to a worn out frazzled emotional mess prone to emotional firestorms!
I didn't really feel myself until today. Sunday I was just exhausted, Monday I was spacey, yesterday I was tired, today I'm back to whatever you want to call normal.
Sigh. I know I'll have to get used to a "new normal" but I'd like to know what the new normal is...
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Hello ladies! Sorry for the long delay in answering, I haven't been on! Just really pooped out after completion of Rads.
bluedasher: Boy, I am glad I am done with Rads! Those Kaiser ad's took on new meaning for me after my diagnosis! "When I grow up I want to be an old woman...." is my mantra these days!!!! Just keep putting my future out, you know what I mean!
ReneeS: I know what you mean now about how people respond to radiation! I look like I have 3rd degree burns, raw, blistered and oozing flesh. Putting that Silver Sulfadiazine on it twice a day, which is yucky sticky! Nothing like waking up to a wet sticky shirt to start one's day!
Ahhh, the joys, HA!
It REALLY is good to be done with Radiation, started exercising again. I decided I want to start working at creating my life again, albeit a new different one! Weightloss and exercise are on my horizon!
Hugs to all!
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I noticed something today: My last rad treatment was April 15th, and the area that was radiated is still HOT! I saw my oncologist on May 4th, and he touched it and mentioned it was still warm from the radiation. Well. . . it's STILL warm!!!! It made me think that I should keep on using the cream, etc., as I noticed that it was a little flakey again. Have any of you noticed this????
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May 6, 2009 08:32 am nelia48 wrote: Hi Nelia! For your friend who said "get over it!" I say in advance this must be the AI's (aromasin to be precise) talking mind you! She should also have a good swift "boot kick", I cannot believe anyone would be that thoughtless and callous! One of the Chemo nurses where I go was recently diagnosed with breast cancer, when I found out I gave her a big hug knowing what lay ahead for her. Do you know what she said: "I had no idea what horrible things you guys go thu, .........This is the heardest thing I have EVER experienced! I had no idea!" She sees this every day but there is a completely different reality when you go thru this, fatigue means something different, nausea - different, rad burns -different..... New understanding!
Nelia, don't listen to people like this friend, they are clueless (and in her case thoughtless!) Hugs to you!
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Hey all. I've been meaning to post, but have been hit with fatigue this week. Napping helps for a bit, but it doesn't take much for me to enter that fogged zone.
I did want to mention to everyone to go to Lifetime.com and sign the petition about legislation pending about mastectomy and hospital stays. They are trying to pass a bil making a mastectomy an outpatient procedure. That seems crazy to me. I had a lumpectomy, so I can see that being outpatient, but with ports and LE issues, this bill seems ridiclulous to me. I believe the petition is to require a mandatory 2 day hosptital stay covered by health insurance.
Also, thanks for the response about my cat. He had an infection and 3 of his liver enzymes were off the chart. So, like me, he's on medication for a month. I'm just lucky that he didn't try to make me take my meds the same way I have to give him his.
I've got two more boosts and then I'm done. I was hoping to end this part of the ride as quietly as possible, but both mornings are now filled with errands and favors for people. If I can just get through the morning before the rads, then I'll be fine...exhausted, but fine. Last night I took an ambien and still couldn't get to sleep until 4am. What's up with that?
Okay, gotta take a neighbor to the airport early tomorrow, so I'm going to head out.
Catherine
Pass the word around on this one!
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Three months post chemo TC x 6
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No eye lashes but I can see a few eyebrows coming in.
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I know what you mean about tiring easily. I am not sure if it is adjusting to the tamoxifen, the se of rads or the Effexor. It could even be that summer is almost here and I am counting down the days to the end of school, only 16, then I am off all summer.
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Susie- sure is nice to see you again! Yeah, I got back on the elliptical trainer, and trying to lose weight... I should be on there now actually
... that's wild about the chemo nurse. And sad.
Martha- I can't tell if my tiredness is some usual thing or radiation-related. Its high allergy season and I am not having bad allergies, the weather is a bit warm but lovely, my sleep is a bit screwy but more in the usual way it always was screwy... and the kicker is that my kid is just as sleepy. Today he slept until like 1030, and just chilled out in his crib. I gave him uh.. brunch... and he went back to sleep for a nap until like 630! Then I gave him dinner and sent him to bed at 9ish. The kid is only 15 months old! I think seeing your ex like that is emotionally draining- on any day. But I can't even tell for myself so...?
nelia- i hadn't noticed but yes, my radiated boob is hotter especially on the boost area! oh that is weird!
catherine- i am trying to imagine what the deal is with dosing your cat... and how it could be worse than chemo? yes... the weird insomnia...
renee- woohoo on the pics!!!! and I keep thinking... wow... she's a natural blonde... no roots!
mary- yeah! same here on not knowing what the tiredness is about. OK, getting on the trainer now...
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One click donates a mammogram... and 9 days left to reach a goal of 250...
http://www.thebreastcancersite.com/click -
Does anyone here know if it is ok to get a tattoo on the radiated boob, or should I wait for the first mammogram? I did not go to my rads 2 week check up, so I could not ask my rads onc.
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Heya guys! So, I finshed rads yesterday (clap clap), but boy am I tired! And the rad nurse tells me that it will be like this for about a week or two before I start to notice my energy levels come up. Ugh. I remember having this type of fatigue after chemo and before rads where I didn't feel like eating, went to dark places mentally...but I think that was mostly exacerbated by the fact that I wasn't eating as much as I should. So, I'm trying to keep on top of that.
Okay, this is OT, but I'm hoping that maybe a pet owner might have some familliarity with this. Last week I took my cat in. Xrays were clear with no tumors(can't tell ya what a rellief to hear that was...on a bunch of levels), but some liver enzymes were really high. So, my cat has been on antibiotis and liver pills for the next month. But I noticed a bump that has formed on the side of his rib cage. It's not causing him any pain, but it sort of formed out of nowhere. Because of the holiday weekend, I can't take him the the vet until Tuesday. And he has really improved since the antibiotics...but this bump is...weird.
Renee--Love the pics! I'm glad that your hair is bouncing back so quickly! I wish it would grow faster because I love the shot with you and your friend, and I love your hair in it. Preaching to the choir, I know. I don't know about you, but I refer to myself right now as the fuzzy monkey. You can't see my scalp anymore...and it feels really soft like a plush-toy monkey. I brush it now with a soft bristle brush and can actually see the hair change direction in how it lays...but I mostly do it to stimulate the scalp.
Nelia--that is weird that the area on your boob is still hot after, what...six weeks? My rad nurse told me that I should still moisterize for at least a month afterwards and keep the area clear of the sun as well. But you're past that timeframe...hmmm.
Rachel, thanks again for the link...I say again, since I also responded to it on the Tatas forum.
I am so over this fatigue thing...again! It's one thing to feel tired, but the mental drain of everything is such a pain. I have to keep reminding myself to not give anything too much thought because of the mental fatigue. But I can already tell that's it going to be one of those weeks where getting the mail or having to get groceries is going to feel like a Herculean effort. And I just got the official date of my termite tenting, June 3-5. Can't even think about that right now because I know it'll overwhelm me.
But aside from that (LOL), it's the holiday weekend, and I hope everyone has some nice way to spend it. I'm guessing that there will be grilling involved! OMG...just realized that that term no longer applies to me! What do you know?
Catherine
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Hey Catherine, I think I got the link from you because I lost it too!
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I had a total of 37 radiation treatments. 25 to the whole side and 12 boosters to the tumor site and some surrounding tissue. I am done almost 3 weeks now and I am still pink on the booster site. Is this normal? And, where I peeled on my areola..it is so pale. Anyone else have this? Damn..I hate radiation!!!!!!!!!!!!!!!! Who invented this barbaric treatment?
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Jeanne D--I think the skin discoloration is normal and takes a while for it to go completely away. I think my rad nurse mentioned several months. I equate the time it would take for a really strong summer tan line to fade. Also consider you skin tone. If you're normally pale, then it might take longer than someone whose skin in the area has previously been exposed to the sun. And even though your last tx was 3 weeks ago, the affects of the radiation continue for 7-10 days afterwards. As long as you are starting to see an improvement in the skin itself, then you're doing fine. How have your energy levels been since your last tx? I had my last of 5 boosts this last Friday, and the weekend has had me pooped. The rad nurse says that the 7-10 day rule also applies to energy levels as well. Also, I was counseled to continue moisterizing 2ce a day for the next month.
Rachel...I'm pretty sure I got my link fom you.
I had posted a link previously about a potential bill legislation and hosptial stays. But your link was for a site that had other causes linked as well, like animal rescue. In short, your link was much more useful and varied.
Okay, feeeling the ambien start to kick in and gardeners are coming early tomorrow to start tree clearance for our upcoming termite tenting. Oh this year has afforded so many opportunites for glamorous living...yeah...right...
I hope everyone can find a momemt, public or private to pay some homage to our armed forces tomorrow, esecially the little guys who don't set the policy, but carry it out because of their faith in our nation. Now more than ever, they need to be returned home, treated with the best medical care available and reassimilated back into society. Just my 2 cents.
Catherine
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Hey Catherine, I missed that you were done! Well done, and not medium rare!!!!
One of the nicest things about being done RADS and also now two weeks out is having my MIND clear. I can remember things. And today, May 25, is the FIRST day I woke up normally. It's been a bit of a bumpy mess these last 2 weeks, not knowing if I was going to be Perky Penny all day or Crash Test Dummy Mommy made of sand.
It's the continuing I-can't-keep-a-commitment thing. I think that's got to be another thing cancer patients have going on in our heads. We are mostly the kind of people who make and keep commitments, and it really sucks big time having to be someone else.
Again, well said about the analogy of when a really strong summer tan fades. Maybe I should have kept using calendula, because although my skin and boob are basically back to where they were, the skin itself is kinda not so nice in texture. I hope that changes.
Ah, you are right about the links. I don't remember then who it was who posted and re-reminded me about the breast cancer site... free mammos and stuff. hard to believe its so easy.
I am extremely proud to say that I do a lot of work for the troops in Iraq and Afghanistan, as well as the FDNY firefighters. It makes me feel good on a day like today.
And of course, when "my" troops and firefighters found out about my breast cancer, they were all worried about ME. Sheesh.
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Thanks for the reply Eadsla. I will be 3 weeks done this Wednesday and I am still exhausted. I can't seem to get my energy back yet. I feel like I could sleep all day, but, when I lay down, I have trouble sleeping. I see my radiation oncologist this Thursday...I will ask them when I can expect some energy to return. I just am getting really down about this..tired of feeling tired.
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Congrats to all who have finished radiation!!!!!! I just caught up on all the posts ---- whoever said that rads were barbaric is right on!!!!!! You might as well have put me on a stick and turned me on the rotisseri for a nice, slow cooked, crispy burnt piece of meat.
I must say, though, that in a way, I'm aggrivated that I don't have anything to show now for all my misery. It's all healed and cleared up nicely. When I complain about radiation and someone wants to see it, they just don't understand. Maybe we will all forget over time, I don't know.
This is also off topic, but I'm a little worried. My rads were on the left side, but I'm having some pain on my right side, right where my liver would be. I'm having headaches, too. I know I'm paranoid about all this!!!!! How long do I give it until I call my oncologist???? I hate to run in there for every ache and pain that comes up. I don't have an appointment until August! I just feel overall crappy!!!! Anyone feel like this?
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nelia, I have to get you to come up to NYC so I can give you proper bitching lessons. After all you went through already and already learned the lesson to stand up for yourself and BITCH... maybe you need to drive a taxi here for a shift to get used to the up-in-their-face stuff.
As much as I think the pains are probably nothing, I'd say call your onc or your GP, the GP that was so nice and said you should have called them before.
here's a tip: don't wait another 8 years, OK?
repeat after me: I am not paranoid, my concerns are valid, I deserve attention
for crying out loud, it would be more strange if you DIDN'T feel like crap after all you have been through!
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Nelia--Gotta second Rachel on this one. The one thing that is sort of keeping me in check about my feeling like a slug is that I have to remind myself that since Jan 2nd of this year, my body has had to deal with something toxic in it. Of course that's why I'm tired, why I'm mentally sluggish, why I'm feeling things physically that are different. If you think there's something off in your liver, have it checked out. Our livers have been working overtime. You can't tell me that after all of this we haven't earned the right to be a bit paranoid. I'm dreading the next time I catch a serious cold or flu. Finishing treatment is one thing, but there isn't a whole lot they can offer for what we are going to go through mentally for the next few months...except therapy. And you know your body more than anyone. If you feel like something is wrong...make someone check it out.
And yeah I feel a bit of a hypocrite, because I should heed my own advice more often than I do. In the back of my mind, I think: "Okay I just finished all the treatments for bc...can't I just take a pass on anything that could be serious...just for a while...couple of months...?" Funnily enough, my onc turned out to be sympathetic to this as well. When I went for my recent one month follow-up post chemo, he finally mentioned my taking tamoxifen, but he was going to hold on prescribing it until next month. He thought that I could use the break after rads...and also wanted to see about giving my ovaries some extra time to kick back into gear. That's what slaps me mentally sometimes--when I realize that I injected my body with something that shut down my ovaries. So the time it takes for us "bounce back"...? Yeah, it's going to be a while. We're not the doctor. We don't know what is something that shouldn't be alarming or what is still the effects of chemo or rads. If you don't know who to consult...consult everyone and see who calls back first!
Nelia--just reread your post. Yeah, I know what you mean by crappy. Before bc i would ascribe how I feel to being in a "blue funk." Not a whole lot of energy and even less motivation to do something about it. Just sort of...eh...blah... I wonder if it could be likened to post partem depression? The situations aren't completely dissimillar when you think about it. Hmmm...time to google...
Rachel--looking forward to the mind clarity. I think I need to do a detox cleanse, but need to have at least a week where I can be home and close to the bathroom since you end up urinating a lot. And I 'm a little tired of the little "projects" that I would like to get done, like weaning myself off of ambien, weaning myself off megestrol before starting tamoxifen, getting my cat through his month of liver meds. Jeez, I just started whining. I know the rads are making me feel funky because I know in this company, I should be/am extremely grateful that my rads experience was a cake walk. And while I know it sucks that others are feeling this energy...malaise, if you will...it's sort of comforting to know that you guys are feeling it too. Because honestly, I'll catch up on posts and sometimes I'll think: "How are they doing that?" I'm a slug.
Oh, and the commitments isssue. Yeah, I've had to cancel on so many things this year, which came with it's own set of mental disappointments. And it's been really hard to hear of fun things going on with friends or having to decline invites because I knew I wasn't going to be able to make it, or thought that I would, but on the day having to cancel. That's another transition to work on...being able to make commitments and feel like I can keep them. But I know that will happen. It's just going to take time. Hell it took me 6 months to get to this point, the least I can do is give myself 6 months to get back to where I was.
And lastly...I know today is a holiday, and an important one that I truly respect, but today just felt like another day. Not a Monday in particular...just another day. Hmmm, see what I mean about the apathy? I know that's the fatigue talking...and ugh...now I'm pissing myself off, because that sounded so pathetic...argggggghhhh! Just last night I went to a concert where I literally laughed nonstop for two and a half hours...and today I'm sounding so...tragic...! What is UP with THAT!
Catherine
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Catherine, since I am on one of my UP days, even woke up early like I used to today, I have this probably resistable urge to pick on you, since you are just out of RADS and probably have the energy of say... a doorstop. From the other thread where I was bitching at Jazzy to get in bed and stay there today, I said I'd sit on her, but then I saw your post and thought, probably better to put Catherine on Jazzy, like a paperweight.
Girl, you not only did chemo and have all that dental shit plus RADS (and not drinking water) you just gotta be a big old sandbag- and problems with your cat... the cat thing alone on a normal day for a normal person would be emotionally and physically draining.
Love how you say "make someone check it out". That's right, that's exactly right. Nelia MAKE SOMEONE CHECK IT OUT. The part where we get used to the blood and pus makes us a bit dangerous.
Jeez Nelia, you were the one who put that on the list for RADS patients. Speak up!
Catherine, I like your onc. Sounds like mine. One thing at a time, let you sort out what's you and what's the drugs. I have been a busy girl researching Tamoxifen, and also Zometa. When you are ready, and if you want, lemme know and i will send. It's all good news.
I can tell you are having the fatigue, I could tell from your posts. Its a real challenge, and frustrating. I thought it couldn't be radiation making me have like "radiation brain" because that's a chemo thing, but I have been reading more posts and yes, there is radiation brain. Felt like I had to cut through thick cobwebs to remember anything, a word I wanted to use, someone's birthday, where I put my dinner... I wouldn't do a detox cleanse, then again I wouldn't do one anyway. You gotta do what makes you comfy but my suggestion would be GOOF OFF! Take a freakin break. Curl up with the kitty (is the kitty with you?) and take back your TIME. I'd be all peppy one day and the next day I couldn't move. Yesterday I had all this great stuff planned and I just sat down on the bed for like 5 minutes... and 5 hours later I woke up. Yesterday. My last RADS were May 8. You know already that the RADS delay is like 5 days, and we've done the scene where they killed off Spock every day for 6 weeks man... the changes in our boobs continue for months and years... not to mention the chemo ... hellooooooooo....
I'd say instead of cleansing your body and having to pee every other minute, I'd like to see you floating on a lotus leaf on a clear pond of warm water being showered with fragrant blossoms while shirtless buff men walk by the pond admiring you. Or a nap. A nap is nice, you can dream about floating on a lotus leaf... you get the idea.
Oh for crying out loud, nelia thinks she's "paranoid" and you think you're "whining". I'm going to poke you in your frikin booster spot if you don't snap out of it! Sheesh. Another thing I am feeling is the fog lifting, a fog of judgments, and misjudgments. Just try to go easy on yourself, you are trying too hard to be better too soon too fast and beating yourself up for it. I did the same. You shoulda seen me at Da Silvano- you read Cancer Vixen, right? The after RADS ended I dragged myself out for the bake sale, I only made it at like 3pm, it ended at 4pm, I thought I was going to be there from the beginning for set up... anyway, so I hustle to the fire station (she drew it int he book) across from Da Silvano and also to Da Silvano and its a humid day as well, plus of course I have the petrolum bandage and the bacitracin leeching out onto my dark t shirt, so I am sweaty and pale and sorta wild-eyed and have this dark blob of mystery goo coming out from my t shirt and I the first words out of my mouth to the elegant host are "I have breast cancer" and of course he thought I was a panhandler... so I was like... no, no, I dont want money I came to tell you abotu this bake sale, I am just a little out of it from the treatments, and he understood, because of her. Remember how she was always trying to drag her ass out of bed to be there ... to be there. A combination of not wanting to let cancer have one second more of your life than it already took plus mind fog and physical exhaustion and guilt because we think we haven't been keeping our commitments...
Just think Catherine... tomorrow you do not have to go to RADS. You can do anything you want with your day. And the next one too. And the one after that. You can look at your calendar now and actually make some plans. If you can just cut yourself some slack, relax and enjoy the recuperation, give your body a chance to heal and repair.
On the commitments... I just opened my birthday cards... from May 14. And this weekend was my family reunion in Vermont. Hell, i didn't even make it out to meet friends yesterday, I didn't get OUTSIDE yesterday or today and it was totally gorgeous, I didn't take my son outside. I slept all of yesterday and today I spent doing 2 months of bills. Tomorrow I will go outside. I am always thinking about how I only did lumpectomy and RADS and i am this wiped out, that's not even chemo. It wont take you 6 months to recover. But it will take longer than a weekend!
No, you don't sound even a little pathetic, and it makes perfect sense to me that today feels like another day. My son's 1st birthday, Passover (my favorite holiday, lots of family), Easter (very important to my step mom and her family) Mother's Day, my niece, my birthday, I could not give a shit about any of them. I got the mammo on the anniversary of my mother's death and the cancer confirmed on her birthday, I saw my surgeon first time on my brother's birthday, had surgery on my sister's birthday, found out my margins were clear and the sentinel node was clear on Valentines day, heard about my FISH test results on my son's birthday- and none of those days meant anything but cancer shit. Next year, they can all go back to being holidays and birthdays and days of remembrance. Its like I fell asleep on January 25, the last day before the mammo, and I just woke up. The only thing I battled to stay aware of was my son's progress in life, and i missed his first steps. I saw his second steps though, and I took good care of his Mom too, so every day forward I can celebrate.
And I celebrated every day before cancer too.
What's UP with that? I will tell you, its the frikin RADS baby. Friday may 8 was last RADS and I was 10 feet tall, my doorman said I looked like a rock star. Saturday I couldn't get out of bed for the bake sale until 3pm, I was good for about 3 hours but it was hard. Sunday I felt like my whole body was made of sand bags. I couldn't even type. I made it out to a mother's day meal in time for coffee, it was about 4 blocks from here, I got there about 7 and was home by 8. Monday I was out and about and shopping and Little Miss Energy. Tuesday I could not wake up, that's the day my idiot friend (who is still not speaking to me) called me every 45 minutes until I told him to stop in what was left of my voice. Wednesday I dont remember, Thursday was my birthday and I slept through that too. I had an appointment for my son this wednesday, we didn't make that either.
So no dear, you are not whining, pathetic or tragic. You're just recovering from RADS and we all know exactly how you feel. You are a slug. A doorstop. A paperweight. A sand bag. Do something self indulgent. Oh this is a GREAT time to hang otu with your cat! My cat and i did so much napping together! Poor cat, I haven't had the energy or time to play with him for months- and dont even ask about the litter box!
Hang in there Catherine... you will soon be your normal peppy self. And as much as I don't wish you any more trouble I think it will be a hoot to do the Tamoxifen thing with you. But... later.
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Are you all going to take Tamoxifen? I haven't decided yet if I will or not. I am so sick of dealing with cancer and all of the side effects that I just want a break from all of it. Is that normal?
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Thank you, all of you, for your kind words and I will see the doc about how I feel. It hasn't gone away. I do wonder about the side affects of the Arimidex, though. The list is so long. I'm not used to having anything wrong with me and never saw doctors before the BC thing. So aches and pains are all new to me. The Arimidex causes so many things, and I'm already dealing with the bone pain from it and the high BP, the mood swings, etc. Since all of that is controllable, I thought I would stick it out for a while, as my oncologist said that the Arimidex would be my lifeline to survival through this. The way he put it, I'm paranoid about missing a day!!!!!
About the Tamoxofin: I would really sit down with your dr. and discuss that since you are ER+. Not an easy decision to make there.
I liked the comparison to feeling like a sandbag!!!!!! Aint that the ever livin' truth!!!!!
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Okay, I'm just on my way to the vets, so I will come back and post later, but I had to LOL at the the thought of Rachel putting me on Jazzy as a paperweight.
My first thought was of an old Far Side cartoon that depicted a a farm with all of these chickens just sprawled about everywhere, over fences, on rocks, on the roof and in the dirt.
The caption was "Boneless Chicken Farm."
That is exactly what I feel like lately.
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I think gals with radiation fatigue make great paperweights or doorstops. If you get us during radiation or soon after you could use us as irons.
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OT- anyone got a recommendation for a good book for kids to help understand their mom's breast cancer? My pal is diagnosed with DCIS, she is planning a double mast, her daughters are like 5 and 9 years old. Many thanks for post or PMs with good books. Thanks!
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Hi all! As I have written, I am about 3 weeks out of 37 rad treatments. But, I still have some bruising and redness on my breast. Is this normal? And, my areola is still so pale. It did peel, so, maybe it is just the new skin? And, it will tan when I tan possibly next year? I see the radiation oncologist tomorrow, so, I will ask him. But, you all know more than the doctors do, in my opinion. Thanks! p.s. oh, and does anyone else still have pain? I had my lumpectomy Jan. 26, 2009. But, I still have pain.
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Hey all! Doorstep/sandbag checking in. On the plus side, I've already noticed the "Tanned square" of radiation is starting to fade. My big project today was bringing the cat home from the vet. He has this 5" by 7" bald patch on his side. I looked at him when we got home and thought: "Well, now we both have to regrow our hair, huh?"
Nelia...I hear ya on all of these health things being new. That's what has made this whole experience so overwhelming for me. Going from one day where the most medication I ever took as alleve for cramps to all of this other stuff. from easily sleeping 10-11 hours if I wanted to to not being able to sleep unless I take ambien cr, and then it's 7 hours on the dot. And now being on tamox for five years...yeah, your life gets altered. Right now, the thought of change in any form strikes this pang of fear that just hits all the wrong nerves. But the mental fatigue spares me a bit from mulling over it too much. At night, it's a whole other story.
Funny thing, Rachel. Today was the first day it hit me that I wasn't doing rads anymore. Also, your post rads daily account mirrors my own, only two weeks later, in so many ways it's freaky. Even down to the birthday. Yours was on the 14th, mine is on the 28th. I'm not planning on doing anything on the day, but friends of mine set up a b-day brunch for me on Sunday. I really appreciate it, but it's going to take a lot of energy. And it's not like I could cancel at the last minute on this one.
Okay, gonna try for a nap, but will robably end up watching some show online and vegging out. I know, there are worse ways to get through the day.
Catherine
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- 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