The Chemosabe March Cruise
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Isn't it simply wonderful to hear everyone finishing up?!? Big hugs and congratulations to you all! Welcome to the dance floor!
Dawn - thanks so much for checking in! Hope the time off helps your body adjust. The swelling in your feet/legs may very well be the Taxotere, not lymphedema (hope, hope!). Mine are all puffed despite a diuretic, but my friend on Taxol has it even worse.
Rosebud - just love the way your eyebrows are coming in!
I, too have been eating fresh fruits and veggies all along. Salads make up a huge portion of my diet and I couldn't have done without them (still managed to pack on 14 pounds since Feb ). I was advised not to go to a salad bar, to have all of my eating-out food cooked. Fortunately, I seldom eat out, and self-prepared foods were fine by my MD. Also, I get all of my fruits and veggies at a certified organic Farmer's Market or grow 'em myself.
I've also been okay to swim - both ocean and pool, since my 'port hole' closed up. I haven't had the energy to do laps or anything, but the salt water immersion and the full-body massage of the waves always is invigorating to me.
MissS - so are you taking off for a vacation tomorrow? I was hoping to be able to get away, too - but have ended up with three days w/ appointments next week. Thursday is my bone scan - which I am not looking forward to. If they can only give me at least an initial reading before the weekend so I don't go looney waitng on results! They say they cannot use my port and have to establish a peripheral IV in my good arm - not an easy task. They can't even use my hand, so this is going to be a real challenge. On the positive side, I have a consult with another plastic surgeon about DIEPs, in Los Angeles on . . . drumroll. . . Friday the 13th. This guy is within my HMO, so I am very hopeful.
My BIL is still in the ICU, poor guy. Thank you all for your good wishes. Continued prayers for recovery are appreciated.
Lisa -
Hi Max! <waving> We were posting at the same time! Glad to hear your body is remembering how to grow hair, even if it is on your legs.
Where is Terri (playwriter), anyway?!?
Lisa -
Lisa eluded to this - but, for those having problems with weight gain and swelling - ask your onc about a diuretic. Lisa - prayers for a great scan and, at least, an initial report! Prayers, too, for your BIL.
Teri is posting regularly on her blog, so I know she is doing well. She has been busy scrapbooking, so she probably just hasn't taken time to check in.
Dawn - you have had quite a time of it. Hang in there - things really will get better! -
Hiya Gals,
I'm still here. Going away for the week just didn't work out. I'm sure it's for the best because I am just so tired all the time. I went to a little party tonight with some work friends and after two hours (it was hot there), I felt really heavy and tired. It's pretty normal for me to last about two hours.
Anyway, I am trying to arrange for two girlfriends and me to go to a spa for two nights. I would have to put my rads off a week because they can't do it THIS week, but the rad onc wanted me to wait three weeks after my last chemo anyway. We'll see. I totally can't afford it, but ka-ching... I'll do it anyway.
Rosebud , loved your pic... I need some of those glasses! I used to have some.
So good to hear from you, Dawn . Sorry to hear you're having so much trouble right to the end, but you made it and that is what matters! My feet are swelling too and my dumb PCP said I had lymphedema. I need a new doctor. I am happy to hear Taxol causes the swelling. My feet are so fat and I have neuropathy in my feet and fingers.
A few of us here are also posting on the rads July 07 board if anyone else would like to join us, please do.
Angel , thanks for checking in. I hope you'll recover quickly and be able to take off the weight. I didn't gain during chemo, but I was gigantically fat to start with, so I am anxious to get into exercising again and lose some serious weight.
Max , glad to see you're getting hair. Mine is growing on my head, but not a lot! It's white! I'm also growing these atrocious, ugly age spots all over my face and head. Let's see how ugly I can get!
Lisa , good luck with your bone scan and your other appointments, as well. Hopefully, you'll get the results quickly. I hate waiting for news like that... it's so stressful. My PCP got me an appointment with an orthopedic doc so he can order an MRI for my knee which I injured last summer. I am hoping it can be fixed without surgery and I want to work on it while I get rads. If I got back to work and can't stand up after they have held my job all this time, it won't bode well for me.
Still thinking of your family and praying for your dear BIL.
I envy you the luxury of the ocean nearby. I lived at the beach for nine years and drug my kids to the beach constantly. I just feel so close to God there. I guess because the ocean is such a great example of His mighty work. I always stand and look out over the horizon and sing, "On Jordan's Stormy Banks." I also used to find a spot without many people around. The more deserted the better!
Jacque , my PCP said I shouldn't take diuretics for my swelling! I'm gonna ask my onc for a refill on mine. Thanks for the update on Terri. I'll have to pop over and check her site.
I hope everyone has a great Sunday and I look forward to reading all of your posts!
Love you,
Miss S -
Hey there Dawn - so sorry to hear of the rough time for the last chemo...the same thing happened with me and the ONLY thing that got me through was knowing it was the last. Now - 3 weeks post chemo I feel great! I mean - high energy, great appetite...sleeping well...you will TOO!
I start rads soon and go back to work...am a bit worried about all that but nothing like the chemo nightmares...
Hang in there.
Hugs from Holly -
Dawn you've had such a hard time of it, we all have but..no more chemo. Even with the stupid SE, everyday does get better. If you're like me you just can't wait so it seems like it dragged. But, it will be better soon..Huggs rosebud
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Wow -- we've slowed down. Did we hit the Bermuda Triangle?
Had my first rad tx today -- you can read the details of my nervous breakdown on the July rads thread if you like. Got my big girl panties on now...I think.
Lisa: How did the bone scan go? Glad to hear you've got the DIEPs appointment lined up -- that only took forever, didn't it? How is your BIL doing?
Jacque: Thanks for the news about Teri. Hope she still checks in.
MissS: How is your leg swelling doing? I had some with the last two Taxols. The first time scared me to death, because the onc ordered that second MUGA scan when I had swelling during the AC, but then I put my feet up and the swelling went down. And once I was more careful about putting my feet up at work, too, I didn't have any more problems with it. Taxol ending probably helped too.
More gifts from chemo. You call them age spots; I call them freckles.
Holly: You've really roared back to live. Wonderful that you are feeling so much better.
rosebud: I forget -- are you doing rads? -
Hi girls,
Just returned from a great weekend in Spokane! It was sooo hot! And I was "flashing" like crazy as well.
I'm so excited to hear about everyone being done, and de-ported!
How wonderful! Love the hair pic and yes, too bad about the nose hair. . .
I'm back to reality now and will start my 35 minutes a day of exercise again tomorrow. I really dislike it, but I think it's what is going to help with{{everything}} in the future.
And Taurie, my hair is pretty white and feels sorta soft like a baby's. The white part was kinda shocking since everyone told me it would be dark and curly. Oh well, it's hair!
Hope everyone continues to be well as they dock!
Christine -
I am soooooo darn jealous of some of you. I had my last TAC two weeks ago and am waiting to see just one little itsy bitsy hair show up somewhere on this ole body of mine. That will be my sign from above that this nightmare is OVER!!!...hehe I am looking sooooo forward to Christmas just to think I'll have a head of hair again. Not long but at least hair again. I'd be happy with white, grey or anything at this point but I know it will show up sooner or later.
As far as the weight gain I'm jealous of some of you with that as well. I wish I only gained 14lbs since chemo started. I gained..........get this......drum roll please............a whopping 54lbs. I already feel like a ooompa loompa as Dawn says...lol But you have to remember that I have had the hardest time with sleep over this ordeal only averaging about 6-10 hours per week....so I not only have been eating all day but all night too and havn't been able to get around well with the knees and hips going.
Hey can someone post the link to the rads thread so we can just click on it and bookmark it? Even though I'm not going to do rads I still want to keep up with you all.
My infection doesn't seem to be getting any better. I guess I'm going to have to break down and make another appt with the surgeon; although he said last time something about removing sweat glands if necessary and I cringed. He's not coming after this arm again with his switch blade again the little demon!!! We're gonna knock this thing in the butt one way or the other or I'll have his head on a platter before it's over with....lol
Hope everyone's se's are starting to be over and done with finally and the title waves within our stomaches and bad taste in our mouthes gone. Hey btw I actually went back to regular toothpaste yesterday. It tasted so weird and strong to use it again instead of the Biotene. I actually felt like my mouth was clean for a change.
Love,
Angel -
hi guys!
Sorry i haven't posted in a while. my last chemo is in a few hours! i just went to a midnight showing of the Harry Potter movie, and drank a large coke, so now i'm not sleepy.
have been doing well for the past week, except for some swelling in my feet, and the everpresent fatigue and hot flashes, tho i did find a cooling rag at a sporting goods store that has helped.
my last chemo is, of course, at the ofc 30 min away, instead of the one 5 min away. onc's ofc called me to switch it over. the lady didn't know why, she was just the messenger. ok.
ins co has quit paying for the decadron, as they want me to go on a mail order hoohah. and the decadron? costs $10.99 w/o insurance. so, thanks but no thanks, insurance co! since my copay is $10 anyway, I'll just pay the extra dollar and forego sending in the script and waiting 2 weeks to get my medicine.
anyway, i am very excited that i am long last going to be done with chemo. i'm not starting rads until mid-august, and i'm going to see if i can do that accelerated partial breast radiation. -
Yes, I've been doing rads. I'm on my 20 tx out of 33, almost done, It's a walk in the park for me. I love the place and the techs and the Doc. Everybody is great there and the se I can manage. I've had some skin issues but they have everything under the sun to help.
I started walking again due to my weight gain.....20lbs. I can't believe that I gained that much since everything tasted like dirty sweat socks! lol...rosebud -
Hey ladies! Remember, as you end your chemo and start to feel better, that a lot of your weight gain is probably fluids. I look back at my pictures from four years ago and am amazed at how puffy I looked! Now, this doesn't mean you don't have to watch what you eat and exercise, but hopefully some of the weight should come off easy -especially if you watch your sodium intake!
One thing about my present chemo is it hasn't made me gain weight (even though I had plenty to start with!). I also have water pills because of my heart issues that I use if my weight fluctuates too much.
I, too, am jealous of all of you sprouting hair! It will be a long time before I get to see what mine will look like, but that's OK as long as the chemo is kicking cancer's butt. -
Last chemo was today! I am doing the nomochemo dance! long day as usual. got there at 9:15, didn't get home till 3. but still.
has anyone investigated the accelerated rads? -
Hi chemo ladies,
It's good to see some posting over here. I get all sad when I come and look and see no updates. I am way too addicted to you guys!
Max,
My swelling goes down when I put my legs up, too. I sleep with them propped on three pillows and try to put them up when I can. I went to an orthopedic doctor yesterday and he did xrays. He said I have arthritis in my knee and my ankle. He gave me a cortisone shot in the knee and will give me one in the ankle if it's not better with Aleve in three weeks. My knee feels a bit funky, but it may take a few days. We'll see.
Angel, I am so sorry to hear your infection is not clearing up. I sure hope you don't have to go through more surgery. My mouth seems to be all better now, too. I'm left with a whole bottle of that expensive mouthwash now.
Keenie,
Glad you got away for a fun weekend of flashing. I need to get on an exersize regimen, too. Thirty minutes a day sounds doable. My hair is coming in white, too. What tiny bit of it there is anyway.
Terri,
Good to hear from you. I can't believe your insurance just quit paying for decadron. That is just so crazy to me. What is up with that anyway. Glad it turned out you end up paying just about the same amount anyway.
It's good to hear you're getting out and about and having fun. I am still so tired, but beginning to feel normal again.
Congrats on finishing chemo! *Dancing with you* I have actually found it kind of weird to be finished. My life has been so wrapped around chemo, and now poof-- over.
Jacque,
I know I look puffy, especially in the eyes. People keep asking me what's wrong! Of course, the no eyelash jungle animal look doesn't help. I do need to be more careful with my salt intake.
You keep on kicking the big C's butt and stay with us.
I need to get to bed!
Love you guys!
Miss S -
WTG Terri!!! Everyday you'll feel a litle better. I can tell we all do. Congrads Everyone! Rosebud
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Congrats, Teri!
I am with you, Miss S, I am sad when there aren't any posts. So, here is just some chatty news about me.....
Went to see the new Harry Potter last night and was not dissapointed! I think I am going to have to reread book 6 so I can remember the plot so when book 7 comes out I won't be lost.
Friends are coming over tonight (one friend is from Pennsylvania and we only get to see her every few years, if that). Early tomorrow morning my DH, two other couples and I leave for Minneapolis. Our son, Matt, will ride along as his fiance will be up there for an interview. We are going to see a Dave Koz concert (Jazz musician), shop and eat good food. On Sunday we will go over to St. Paul - which is right next to Minneapolis (they call the area 'the twin cities') to see where Matt will live when he starts law school and visit his campus. It should be fun!
I plan on taking my laptop with me, but don't know if I will have time to check in or not - so I hope everyone has a great weekend!
Jacque -
I'm drinking water like crazy this morning, hoping to be extra hydrated when they try to find a vein this morning for my bone scan. I still don't understand why they can't use my port - they say they can't even use my hand for it - so this will be an ordeal. Wearing long sleeves to keep the area warm - everything they suggested to help make an IV possible in an arm that has few and then previously damaged veins. Yes, I'm pretty cranky about this. I should be finished by noon and then the wait begins to get the "All Clear" that I hope to hear. I rescheduled my consultation with the Plastic Surgeon because I simply don't have the stamina to drive to LA and back. Certainly not in that horrendous traffic. I should be better up to it on the 24th.
Terri - CONGRATS on your last chemo! WTG!
Jacque - Have a great trip. Lots of excitement planned - you will enjoy Dave Koz, I am sure.
Gotta go feed the dog and then get myself down to the hospital. I am so ready to be done with tests and procedures and it is just not happening!
Lisa -
Lisa, i hope and pray everything goes smoothly for your bone scan. i've been told the my port is for chemo only, they don't take blood from it or anything.
jacque -- i went to see the HP movie at the mightnight showing! i liked it, too. MUCH better than the 4th one. hope u have a fabulous time in MSP. are you going to the Mall of the Americas?
rosebud -- funny pic! made me smile.
angel and taurie -- hope everything is going better for you guys. -
Hey girls,
I, too, love to read the posts - usually checking in twice a day. Now, I must admit I've been posting a bit on the other boards, but my chemo brain is so bad, I can't remember which ones I've been too! So, I spend a lot of time reading about other people I've never met and finding out stuff about hormones and radiation . . . Such a loser!!
I'm not a big HP fan, so I'm not sure which summer blockbuster we'll attend. Maybe Ratatouille? Maybe Transformers? Maybe just catch up on some reading - and hopefully remember what I've read!
Have a great time shopping - I love the shopping experience in the USA. And our dollar is so much closer to USD now, it's terribly enticing. Glad to hear that everyone is enjoying the week and if you're recovering, hang on, we're praying for you!
Christine -
Good luck Lisa on the bone scan. I hope it doesn't cause you much discomfort and you pass with flying colors! rosebud
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I made it! So far no hospital on this last chemo but my temp is going up a bit today so my fingers are crossed. My blood pressure has been so low and the bone pain has been terrible, but it is my last one so I can grin and bare it.
Melissa -
It is so awesome to see everyone getting to the end of this part of the bc journey. I actually washed some hair today. I look like a newborn baby. I wish the hair on my upper lip wasn't growing. But I also noticed that I have a few eyebrows that are looking ragged. Wow, all the hair we don't want is the first to grow in!!!! How lucky is that?
I am so proud of all of us. We are truly survivors.
Dear Heavenly Father, Thank you for sending Your Son, Jesus, to die for our sins so that we might have eternal life. I am grateful to be Your child. I thank You for purifying me from the things that are not like You. Lord, I cannot cleanse myself, but I know when I ask You to remove the things in my life that are wicked, You will come and do it. Keep me this day from temptation and fill me with Your love and help me to become more and more like You. I asked this in the name of Your precious Son, Jesus. Amen -
I am proud of all of us too! We are survivors...many of us are on the July Rads board too...Thank goodness this portion of our journey is complete...or nearly so for everyone....
Hugs from Holly -
I've tried to stick to a low fat diet for the past couple of weeks, but I've been having such a rough week emotionally that for lunch today I went to Baskin-Robbins and had a scoop of pralines and cream on a sugar cone. Ahhhhhhhh!
Keenie: Great that you got your weekend away. Too funny about posting on other threads and losing track of where you've been. LOL
Angel: Sorry your infection is still acting up. I had to laugh at the mental picture of the demon with the switch blade coming after you. Keep that demon away!
I've been afraid to try my regular toothpaste because I tried a little of the blue Listerine one day and OWWW! But I'm looking forward to that clean mouth feeling too!
Teri: Congrats on getting through that last tx. Doing a round of the happy dance for you!
A friend of mine looked into the accelerated radiation for herself and found a rad onc that would do it, but then the insurance company wouldn't cover it.
rosebud: It's amazing how much we can eat, trying to find something that doesn't taste like dirty sweat socks. LOL
MissS: Wow -- you really do elevate your feet at night! I hope your knee and ankle settle down and quit aggravating you.
Jacque Sounds like you have a fun weekend planned -- and it was fun reading non-BC news, too.
Lisa: I hope the prep for the bone scan wasn't as bad as you feared. Weird that they couldn't put it in your hand.
Melissa: Holding good thoughts that you can stay out of the hospital this time and the BP comes back up. -
Hey Girls!!!
Terri, Congratulations on your last chemo....doing the nomochemo dance with you!!!
Jacque, hope you enjoy the Twin Cities...we lived there for 11 years....sure am happy that you're visiting in the summer and not the winter.
Lisa...will be praying for an easy time with your bone scan and for good results.
Melissa....prayers that you are feeling much better real soon!
I've been running a fever for the past couple of days and just feel pretty wiped out. Not the way I was planning on spending this time. Scheduled to start Herceptin 7/24 and Arimidex on 7/23.
Hope everyone has a blessed weekend!
Nancy -
doing ok today. tummy hurts a bit.
just stepped on a brad that was sticking out from a piece of quarter round that had come off in the kitchen, so now i'm freaking out that i might get tetanus. (i tend to be a bit of a hypochondriac). -
Hi All - I had 4 weeks between chemo and rads. I get my first radiation tx on Monday. When I had my second planning session today I had 3 rad therapists working on my the whole time. It was strange to be pulled, poked and pushed (albeit gently) by 3 folks - 2 gals and a guy. The rad onc changed her mind again and now says that I will be getting 25 tx and then 6 boots....I should finish toward the end of Aug. They printed out a schedule...my appt time is 3:36!! Can't belive they plan it down tot he minute!!
They said to only use Tom's of Maine deodorant and Aloe Vera gel for skin issues.
Also had 1 month follow-up with med onc (whom I have a major crush on!!) who said I'm doing great. He will see me every 3 months for 2 years and then every 6 months for 5 years. He mentioned the possibility of mets and recurrences which I just tried not to listen to (wanted to put my fingers in my ears and sing la-la-la-la) but stopped myself. He looked at the moles on my head which I didn't know I had before getting bald and said definiteively they were NOT melanoma...which of course, was where my mind went first.
Will we ever feel strong and healthy again?? -
pmarsh,
Weird thing is I never lost any eyebrows or eyelashes and kept all the hair on my arms. Lost it everywhere else so found it kind of weird all that didn't go as well. My eyebrows are so blonde though you never could see them and many people always thought I shaved them off....weird!
Jacque,
Awwww an attorney in the family huh? No wonder he's getting married soon (if that's the same son)....hehe The fiance probably not only saw someone good looking but a goal and money at the end of the tunnel as well.....lol Aw just kidding ya. Keep posting your personal news because I too enjoy hearing what others are up to besides BC all the time.
It's always fun to get away with friends and have a good time. Personally we do a lot of home entertaining and sit by the fire outside at night a lot with some good talks.
Holly,
I'm laughing at your appt. time 3:36......like it will matter. Have you ever had an appt. anywhere where they had you on the table and the Dr. in front of you at your scheduled appt. time.............NOT!!!!
playwriter,
Glad you're done with the chemo thingy as well now and can get on with your life like the rest of us. It's great knowing that phase is over with.
Lisa,
I'm done with chemo and still havn't had my bone scan yet. They sent off for approval right after my surgery and somehow it got shoved by the wayside and never sent. Then when they realized it they sent it right away only to code it wrong and have it denied. They resent it about 4-5 weeks ago and I still havn't heard anything as yet. Gotta love how people do their jobs these days.
Ok just some unimportant news around here. Since the first of the year I havn't been putting away the groceries or anything after we shop other than breaking down pkgs of meat for the freezer etc. Everytime I tell someone to go get something they tell me it's not there. Ok so yesterday I started cleaning out all of the cabinets of food, washed the inside of all the cabinets and took out half of what was there and didn't belong. Then today I started on the hallway closet of food (we do food storage enough for a year). Our hall closet is shelves from top to bottom and that's where all the extras go from Sams etc.
Well I could barely open the door for all the crap everyone's been shoving in there over the past few months. No wonder they couldn't find anything. Now it's all organized again and everything can be seen when you open the door. It was a long job but the hubby helped hand stuff back and forth to me so it wasn't that bad.
The hubby bought me a baby grand piano last year for my Birthday. Since the mastectomy and problems with the underarm I don't think I'm going to be able to ever learn to play it now. We've been trying to decide wether or not to sell it. God we'd take such a loss on it and it's so beautiful and I do love it. But if I'm not going to be able to sit and play it what's the point.
I have collected Dept 56 Christmas villages for years now. I have the complete Christmas in the City collection as well as the Snow Village. We had to buy a huge shed in the backyard just to house it all. I've decided to get rid of it all as soon as summer is over. Going to sell it all off on Ebay. Been trying to collect cardboard boxes so I can ship this stuff off and have been having a hard time finding them. Everyone here nowadays seems to crush them all. I only have collected about 40-50 boxes so far and need hundreds of them. Any suggestions? The priority boxes from the post office aren't big enough. Each piece does have it's original box but they all have to be bubble wrapped and shipped in a larger box to protect them.
Havn't been anywhere fun other than Disneyland a couple of weeks ago but just been hanging around here. Seems like I'm tired constantly and just can't sleep at night. The ambien was working for a while but then stopped again. You notice it's 2:53am right now and here I am again. The infection is still there but getting a bit better. Just the constant nagging dull pain all the time is a nuisance. I don't think it helps that I try to do everything with that arm I did before the surgery.....lol
Well I'm off to try the bed thing again.
Love,
Angel -
Hey there ladies!
Patti - I hope you are still improving steadily from your last tx. and are staying out of the hospital.
Max - My daughter took me for Pralines & Cream on the way home from my final infusion. I do think P&C is very therapeutic for chemo mouth. Hope it helped with your tough week.
Nancy is your fever gone yet? Have you called your oncologist? Our blood levels stay suppressed for weeks, so take it seriously, hon.
Holly - glad that your hottie med. onc. said you are doing well and was able to reassure you about the moles on your noggin. Is your 3:36 appointment time going to fit in with your plans to return to work?
Angel - again, I am impressed with the energy you find to tackle big domestic tasks. It must feel great to have your cabinets and pantry organized your way again. Hope the shed full of Christmas stuff sells easily - I know it's a popular line.
THANK YOU to all of you for your good thoughts about my bone scan. My appointment was at 8am to establish the IV line, then I was to be in Nuc. Med. at 845. Well, sure enough, after 45 minutes and 3 different RNs attempting umpteen sites, they gave up and called Nuc. Med. and said an IV was impossible, they needed to use my port (which is PRECISELY what I had told them when I first scheduled this). So they went after my port. First nurse had no success, even after digging around. Second nurse (the most experienced on the floor) had no success. But he didn't give up and got it on the third try. Did I mention that because I was told my port could NOT be used that I hadn't put any EMLA numbing cream on it? I felt like I had been beat up. Three infiltrated veins in my left arm bruising about 5" already and my port is one big hematoma.
Don't you just love doctors and procedures? I know *I* do.
The scan tech says it usually takes a week for results to be transmitted to the referring MD. So I asked for something, even preliminary, to help me make it through the weekend.. The radiologist did a very preliminary review said it "appears CLEAR" at first glance.
YAY!
Now, it's back to the waiting to get the final reading. But I am encouraged. Also had some bloodwork done - as long as they had my port going, why not? Alkaline phosphotase was within range. I have chemo-induced Macrocytic non-Megaloblastic Anemia (oh, fun!) and the new tumor markers should be in next week, about the same time as the scan results.
I've got out-of-town guests due in this afternoon (including four teenagers!). One of those times it's GOOD to have a small house - they'll be staying in a condo a few minutes from here. Weather is great and ocean water temp is up - so perfect timing for a vacation in San Diego.
I hope I am able to join them frequently - I enjoy vacationing in my own town!
Lisa -
One week of rads down, 5 to go, and the weather is beautiful.
I've started sprouting longer hairs in various places. There's one about an inch long on my front hairline, and there finally seems to be more action beyond the stubble on the rest of my head.
Today my sister nicely took me shopping for a mother of the groom dress -- she's a born shopper. Five stores down, more to go, and I have to get it before the rads fatigue sets in! I only needed an hour and a half nap when we got back. LOL Tonight we're going to a retirement party for one of DH's colleagues and tomorrow I'm going to my niece's baby shower.
Lisa: Wonderful, wonderful to get that preliminary all clear! Sorry to hear the IV line was as much trouble as you feared it would be -- gee, if they had listened to you...
Is the kind of anemia you have the only kind that is brought on by chemo, or does it come in a variety of flavors? I haven't had any blood work since chemo, but wondered whether my anemia had resolved itself. I feel a lot better but my heart rate is still fast.
Have fun with your friends!
Angel: Impressive work on your food storage!
Holly: Great mental pic of you with your fingers in your ears, going lalalala, to avoid negative news. LOL Some days you just don't need to hear it.
playwright: Hope you're feeling better. I didn't consider chemo really over until 2 weeks had passed.
Nancy: How's your fever? That's too bad that your time "off" is being ruined by this. Hope you recover and get some time with your energy back.
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- 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