Starting Chemo May 2008
Comments
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As promised.
I hope I covered everything.
Skin care 101
Step 1 Exfoliation 2-3 times a week your skin must be exfoliated. If you do not exfoliate you are wasting your money on lotions and balms. Lotions etc simply will not penetrate dead skin.
That said, exfoliating has to be done with some caution.
There are 2 kinds of ways to exfoliate: Physical and Chemical. Physical means using salt, sugar, pumice etc or tools like loofah, and other scrubby devices. Personally I have always preferred scrubby gloves for my regular exfoliation head to toe. I use salt and sugar scrubs for occasional exfoliation times.
Chemical exfoliants use ingredients like alpha hydroxy acid, fruit acids, glycolic acids etc.Face and décolleté should be exfoliated gently with sugar, chemical or finer grit scrubby devices.
Do not exfoliate broken skin, or open sores. On keratosis, psoriasis and excema use extreme caution and when using product only use unscented, natural and sugar based exfoliants.
I do not shower everyday, so I exfoliate whenever I shower.Step 2 Moisturization
The best times to moisturize are directly after bathing, or before bed.
Body and Hands- when skin is still wet from bathing or showering slather on a rich lotion or balm, or body butter onto wet skin, then wrap in a towel or robe for a few minutes. If your skin is oily then use lotion sparingly in those areas. On keratosis, psoriasis and excema use rich unscented products like Shea Butter.Face- when skin is still wet from toning ( yes toner is an important step for facial skin for those over 25, or with acne issues) add moisturizer in morning, and at night or whenever face is washed.
Step 3 Maintenance - If you follow steps 1 and 2 regularly you will see a huge change in your skin within a few days. To Maintain it you can skip the occasional day here and there, but skipping more than a week without these steps will make your skin go back to rough, and dry.
As you know, I sell products for all these things.
I don't want to be known as the girl trying to sell things on this site. If you do want to know more about my products PM me. I am working on a chemo skn kit for my website, and would happily make things cheaper for you guys if you want to be my guinea pigs.
I am racing to the post office to get a letter to my kid at camp who bawled his eyes out when i dropped him off.....
Cheers, N
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Eddie , Sable are you packed for our trip to the Swiss Alps tomorrow! My avatar is a sunset in the Alps, so how about enjoying a little wine and cheese overlooking that view? P.S. don't forget your lederhosen and Sable bring your happy face!
Good luck Gracie and Roxi today and congrats roxi on last Taxol !!
I've been full of mixed emotions today, excitement of tomorrow being the last and and a little nervous, don't know why and just emotional. Heard a song on the radio in the car and had weepy eyes, watching little house on the prairie and crying ( yes ok .....when nothing else is on I do watch it once in awhile
) I'm just not used to the ups and downs I'm experiencing today. I have had my first dose of steroids so i will blame it on that!!
I'm afraid pole dancing is not in my genes so I will do a happy dance instead tomorrow , i will consider myself done with chemo when the SE have passed !
Hope everyone has a great day ! ......
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Thank you Noelle!
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Just got back from the Swiss Alps, they were amazing. What a fantastic feeling to be done with chemo!!!!! I shaved my head completly last night to make sure and not miss the slighest sprouting of new hair. I've heard it could be as soon as two weeks after your last teatment. I lost my bottom eyelashes last week but the tops and eyebrows hung on. I baked mini cheescakes for the celebration today. The Onc nurses blew bubbles and presented me with a Certificate of Completion and Appreciation. My camera snapped one picture and died. Luckily in the room next to me was a newly diagnosed BC patient taking photos for her scrapbook. She took some photos of the celebration and the pole dance. She said she'll email them to me later. As soon as I get them I'll post. Nothing too exciting compared to all you other hotties.Radiation- The Dr. suggested I get a second opinion. He explained that I would raise the risk of lymphadema with radiation. This is really a hard decision to make.Genetic testing-found out my insurance doesn't cover the consult and they would have to fight for the test to be covered. They are reviewing my paperwork to see if I am a candidate. Both parents (are/were) only children so no first generation cases, only second (Great Aunt and second cousin). Argh. My girls just may have to be watched more closely I guess. Wait and see, lovely. More to come...Otter, I have been getting occasional pain in my abdomen and my onc told me it could be because my body still wants to ovulate even though my cycle left in April. It may return, who knows. Hoping it doesn't. Fingers crossed.Ellenoire, thanks for the skin care book camp. I need to amp up the whole body and face thang.Angels, yeah for tomorrow. You'll be done. I too was a bit worried when me onc said I'll see you in 3 weeks, then 6 after that. Every little pain and swelling freaks me out. Do I have lymphoma, cramps ? uterus cancer. Heck, we just can't think about it. I'm so thankful to have completed my treatment of chemo, and have such wonderful friends to get me through all this. This has been the toughest challenge God has tested me and I truly feel so different, uplifted and positive and I have all of you to thank.Pole dance later. Love you all.
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Noelle,
I will try to exfolliate sometime soon.... thanks. I will need lots of help in this area.
Angels, packed and ready. You get to be done. Am so pleased for you. Sable and I will be bringing up the rear. A happy dance will work as well as a pole dance...you are weepy because you had a battle plan and it is ending and you are thrilled to be done, but wondering what is next. I think everyone gets weepy. My pal, Dottie, cried for five hours straight after chemo and for days on and off after...it's normal. We support you.
Graci, hope taxol went well.
Roxi, WOOOOOOOO HOOOOOOOOOO!!!! Waiting for the pole dance.
Jean, so nice to hear about your mom.
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I'm here.
Noelle-so sorry to hear about your friend's son. That's a tough one, and it breaks my heart that anyone has to go through it.
Roxi--whoo hooo you are done! Congratulations! Anxiously awaiting pole dancing pics!
FEC #5 completed (finally), so I am now to the half way point! Got there at 9:10am, nurse flushed my port-good-couldn't get any blood return-not good. Drew labs from hand. Counts good. Start pre meds-good-still can;t get a blood return-not good-can't give the epirubicin without a blood return. So, after numerous flushes (and a total of 2 hours later), decide I need to go to the hospital for floroscopy on port, can't so it for an hour & a half --nurse says, go eat-so I left, went and got something to eat and went shopping (looking for shows forclass reunion). Go to hosp., there stands my DH (Did I tell you that he had to go to Atlanta last night? Sorry-chemo brain) Wasn;'t expecting to see him. He was freaked because I wasn;t at the onc office, he wanted me to know that he had gotten in early.
Test done-everything is in place-but there is a fibrin clot at the tip. Port usable, still no blood return. Sent me back to onc, borrowed a med from the hosp and dessolved the clot, finally got treatment, left office at 4:45pm. At one point they ahd been talking about-port may need to be removed & replaced--I don't think so----then onc said that may consider putting in a PICC line for last 2 FEC treatment (this was before clot dissolved), I don;t think so--Was very thankful that they finally got blood return.
So, that has been my day------long.
Went with DD yesterday to take new baby to pediatric urologist yesterday. Little fellow had to have another ultrasound of his kidneys (no one can seem to get a good shot). He has a perfectly developed left kidney, but no right kidney. Looks like it had tried at one time, but just couldn;t do it. Left kidney is great and fully functional. (We knew that this was a possibility when DD was 5 months pregnant, but at that time there were several possibilities) A person can live a very long, healthy life with one kidney--I know this, but it breaks my heart because we can't fix it. This little guy is my little angel, Nana is supposed to be able to fix it. DD is trying to be strong, but I can tell it is bothering her, but at the same time, we now know. She is one tough Mama and all will be fine soon.
Can you tell I got steroids today????????
Hope that all is well with all of you--my friends!
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Gracie,
My husbands best friend was born with only one functioning kidney and didn't find out about it until he was in his 30's. His good kidney needed a transplant and he had 5 siblings that matched. His sister donated a kidney 12 years ago and he's doing great. I can't imagine how scared your daughter probably is but please know that your grandson will be just fine. Our friend never knew about his kidney and did just fine. Your grandson will be monitored and well taken care of.
So sorry to hear about your port. They have a hard time pulling my blood too. They tip me back and I have to do deep breathing exercises.
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HELLO!!!!! Just popping in, have to work early, I will catch up this weekend. I am taking off early Friday for an echocardiogram. One piece of good news--some of you may remember my son taking off for Pittsburgh to attend college, and taking his greyhound and miniature husky with him. His Dad and I knew it would be difficult having the dogs in an apartment, but went along with him. Well, he called tonight and asked if they could come home. He said it's just too much, and they are having to spend too much time in their crate. When he left I told him if he changed his mind about having them with him I would come and get them and wouldn't say, "I told you so." So, I'm not saying it. But "my" babies are coming home!!! My husband and I will fly to Pittsburgh later this month and get them!!! I am so happy!!
A greyhound named Lois who is lovely and a miniature husky with ice-blue eyes and the disposition of an angry Latina.
I can't wait.
Hope everyone has a great rest of the week with few to no se's.......congrats to those finishing up this week....pictures, please!!
Love,
Sue
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Eddie! with us being last we had better beat the other gals pics... what you think??? LOL
I have a late start tomorrow for mine... be there at 1140.... I'll be there all flippin day :O( Took my steriods today and popped out in hives again. Its in the same exact spots each time. I wonder if I am allergic to them. And to top things off I have put on 7 pounds this week... I'm sure it is all the swelling in my ankles and chest. I'm so bummed about it too. After dropping 16 the first half of this I was hoping to keep it off. Hubs told me that if I come out in the end even then count myself as lucky. I guess he is right.... still like to not gain it back. There was alot of no eating in there for 4 tx's.
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OK...heard this tonight. One of my favorite songs
Dream Weaver
I've just closed my eyes again
Climbed aboard the dream weaver train
Driver take away my worries of today
And leave tomorrow behind
Ooooh, dream weaver
I believe you can get me through the night
Ooooh, dream weaver
I believe we can reach the morning light
Fly me high through the starry skies
Maybe to an astral plane
Cross the highways of fantasy
Help me to forget todays pain
Ooooh, dream weaver
I believe you can get me through the night
Ooooh, dream weaver
I believe we can reach the morning light
Though the dawn may be coming soon
There still may be some time
Fly me away to the bright side of the moon
And meet me on the other side
Ooooh, dream weaver
I believe you can get me through the night
Ooooh, dream weaver
I believe we can reach the morning light
Dream weaver
Dream weaverI just know that you all now have this song stuck in your heads! My gift for today.
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Damn Gracie...what a day! I'm glad you finally got your tx. When I read what you typed about your DH being there...I felt for him. Seriously, our significant others are put through so much. How cool that he was early and his first thought was to be with you. And the grandbaby...wow! I know your daughter is freaking. I don't know what to say other than breathe.
Sue..I remember when your son left. I think there is a reason why those babies are coming home to you. A very good reason. Enjoy them. They are lucky to have YOU.
Eddie and Sable...thinking of you tomorrow! Sable..I've lost or maintained during my tx but this week I've been enjoying my ice cream in the evening...BIG bowls (even tho it is fat free....it is delish!). I feel my first gain in 10 months coming on! We'll see............
BTW...Sable, I love the avatar. I laugh when I see it. It reminds me that DH has these stickers that he got at the surgeons office. Parts of MR. Potato Head. He threatened to put them on my head when I sleep. He hasn't had the nerve...lol Smart man.
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Randie - Love that letter, especially since Aunt Flo is visiting me this week! And, btw, had to go check my Always. I don't see anything there, so maybe they got the message?! And I have to correct myself (chemobrain!!), it was not Kahlua (although that's good too), but Bailey's Irish Cream. Yuuuuummm. Can't have any tonight because of the PET scan tomorrow. Drat. I wll have to find the raspberry wine at Trader Joe's. That sounds like it might be more up my alley.
Roxi - Yay for you!!! We await your pictures!
Gracie - What a day. Wow - I'm tired just reading it! Good thoughts going out about your gs...
Sue - Yay for you and for doggies!!! And for holding your tongue with your son...lol...
Noelle - Thanks for the tips. I will start using my body scrub more often. I empathize with your little guy. My 9 y.o. dd had the opportunity to go to gymnastics camp this summer but declined because it was too far away and she would have been gone for "a whole week? No way!" (her quote, not mine).
Sable - You are a crack-up! Chemooooo to you and Eddie and Angels - Yay! Last One!!!!
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Just dropping in with a note- I am out of town for a few days!
Hot Springs, Arkansas
Hot tub and strawberry margarita to celebrate the end of chemo- PRICELESS!!!!
Kristy
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good morning and chemooooo to y'all!
Sue, I know how much you missed those doggies.
Eddie and Jen and Angels, have a peaceful trip to the alps.
The construction workers on my street seem to have half buried my ar in gravel, it will be an annoying morning.
I am off to a long day: A perfume blend in the AM, a funeral home visit and an afternoon with an old friend who has come in from Vermont. I chose to drive into the city (Toronto, about an hour's drive) to see him and meet the BF for drinks and dinner.
Cheers!
N
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ugh steroids suck. was wide awake till about 230-3 last nite then tossed and turned till about 4-5....still got up at 930.. I am hoping that i nap thru treatment again today. makes it go oh so much better.
I gots my lederhosen and my bug honkin beer ready to go.
edit: I just found a new hair growing in!...... bad side... it was on my lip damn it!
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Roxi - Congraaaaaaats on making it to the other side of the river!! I will meet you there next week! Looking forward to seeing the pictures.
Eddie, Jen & Angels - Thinking of you and wishing you minimum SEs.
Gracie - I could not believe what I was reading . . . glad that you were able to still take treatment despite the long day.
Have to run for now, off to lymphedema PT. Jean
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Hi, all--
Roxi, I know what you mean about the post-tx doctor visits. My first re-check with my onco was this week, 2-1/2 months after my last chemo infusion; but she said she doesn't need to see me again until 6 months from now. She doesn't do any scans (PET, CT, etc.) on asymptomatic, stage I patients; so you're right about the aches and pains and twinges being spooky. I think once the doc visits are farther apart, we'll be able to forget about BC most of the time. OTOH, that means the re-check visits and mammograms will be even scarier, 'cause it will bring it all back to us. (More about those memories in a minute...)
Angels, I felt really strange for the first few wks after my last chemo. I was so accustomed to building up my courage for each round of TC that I felt like something was missing when it wasn't happening. And, yes, I felt weepy off-and-on during chemo, and for the first few wks after I was through. It was like PMS--weepy and sad for no reason.
Gracie, that darn port! I sometimes wondered if I should have asked for one, but in the end I'm glad I didn't have to fool with it (just 4 infusions). My grandpa only had one kidney, and he did just fine. A lot of times we have anatomical problems that aren't even discovered until we're adults, and then they're found incidentally.
Sue, I'm glad you're glad your 4-legged kids get to come home. How is work going? Still wanting to retire? Still thinking of relocating some day?
Sable, I recognized you in your avatar (ha ha). You look just like me. Cristine, Kahluha and Bailey's are my two favorite "comfort" drinks. Either one will do. Hi to Adrienne, Jean, Noelle (sorry about not exfoliating...), Kristy, Eddie, ... where's Rock? Who else am I missing?
Those of you who are just finishing up this week--swim hard for shore, the current is strong but you can make it. We're all over here waiting for you on the "safe" side. (Maybe the Swiss Alps would be a better fantasy after all...).
BTW, Roxi, you said there was a newly dx'd BC patient in the room next to yours, who was "taking photos for her scrapbook." You mean some women really have the courage and presence of mind to do that? I was too overwhelmed and afraid to consider documenting everything. Even now, all these months later, I am not sure it would have been a good idea for me. Although there are some aspects of this experience that I want to remember (like y'all), most of it I want to put in a box, lock up with a padlock, and bury in a deep hole in the back yard. It's part of my life now, but I can't imagine looking back at it in a scrapbook 5 or 10 yrs from now. Maybe I'm still too close to the emotions... or too afraid of a recurrence or new primary. I wonder if that fear ever dulls....
otter
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Ok, I am kicking ass all over the boards today. I started with the losing weight board and now I am onto you guys.
TRY? TRY? to exfoliate?
Hallo???
Get a face cloth and a bar of soap and rub yourself down head to toe... exfoliation done.
How hard is that? Want great skin? Just do it.
Ok, ranting over.
I am done making the perfume... I am off to the funeral home and then to Toronto for my first city jaunt since this BC crap started. I plan to spend money on myself even though I cannot afford to!!!
chemooo to everyone, you are with me at every turn.
xoN
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I'm here. Trying to clean my apartment.
Thinking about Gracie's DD. Debating on whether or not to say this for fear it will be misinterpreted. Will go ahead and hope for best: Gracie, I do hope your daughter is not blaming herself for her baby's missing kidney. Like bc, so many, many many factors go into producing a baby. We put so much pressure on pregnant women to do everything "right." The reality is, as with bc, women can do everything "right" and get less-than-ideal outcomes, or do everything "wrong" and have everything come out fine.
Also, Gracie, I really hand it to you for not unravelling over the port. I am really strong, but that scenario (as with repeated "sticks") is the sort of thing that makes me kind of bonkers. Because there is seemingly no end to it.
Mary: Congratulations. You know how happy I am for you, right?
Jen -- Leiderhosen. As with Sue and "fedora" the very word makes me smile. Lovely.
Sue -- Dogs, son, all good. All very good and better than scans.
Otter -- I haven't said "hey" in a while and I wish I could come up with something more creative than "hey."
Everyone: Enjoying your posts as always, just need to get a move on rather than wile away hours at computer. Will be away next week for the road trip. Doing a lot of fun stuff the next few days with friends, Hedwig play, Patti Smith, movie in the Park. I'd rather pretend my fatigue is from too many late nights out rather than after effects of chemo or anemia.
Dreeeeeam weaver... (Yeah, THANKS Adrienne!)
Trying to gear up for moving out of country in January. LOTS to do. But I'm starting to allow myself to get excited. Have decided am going to try to go even if State Department doesn't medically clear me. It's been a lifelong dream of mine to live out of the US. If not now... you know?
Smooches.
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Hey all,
First, Gracie, sorry about the port. When I started treatment, I was told that a port was the only way to go because it was foolproof...hah! Turns out like everything else, they tend to leave the bad points out. What's the grandbaby's name? Told my kds and they want to say a special prayer for him, but Sam says he needs a name! I am so jealous that you get to hold him, mine is due in 8 weeks and al I will get are pictures of her til the summer.
Rock, move out of the US? Wahhhh, make sure you have high speed internet where ever you go!
Sue, Dogs, yeah! Our 21 yo ds and his wife bought a ferret in Germany and with the baby coming, they need to get rid of it. If there was a way to ship it here, i am sure it would be a part of our menagerie! Right, now 16 yo dscat is starting to have seizures, she's 16 and is looking a little scraggy, hope she holds out until I am in the clear, because that would be too much for him to handle this year.
Otter (more creative then Rock , I am) Hey THERE!
Noelle, I have always used a washcloth in the shower, so that means I am an exfoliater-yeahhhhhh chemmooooo. I keep trying to tell my son that a bar of soap does not wash away body smell, you need to rub them dead cells off, maybe now he will listen!
Okay, this is for everyone, put on your white coats and stethoscopes, hands o chin, GOOOO
Last week the chemo onc told me that she was worried that I had weird numbing in my first 3 left fingers after the 1st taxol.They just feelas if I was either playing the guitar or the Wii too long and te pads are sore-ish. She thought that I was reacting too quickly and wanted to slow me to evry 3 weeks. She said that if I got any worsening symptoms after the 2nd tx to call and she would hold off the next one. Here's my dilemma, I have those same weird feelings, not as strong on the sole of my left foot. It feels like I was walking too long in the sand, not irritating, just kind of on the edge of my awareness. My friends tells me that I should call her up and tell her so that she can postpone the next treatment so I won;t get worse. I don;t want to, i want to be done wih the last 2 tx on 9/11. What should do? I really don't want to stretch this out. I was thinking of telling her to cancel the last 2 taxol tx since she said the tumor was gone.Whatcha all think????
randie
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Oh, randie, HEY THERE!
Don't mess with neuropathy. It might get worse with each treatment. This was your first taxol, and you're already getting numbness and tingly feelings in your fingers and foot. That is sort of quick, and maybe you're right--maybe it's not an SE of chemo.
As much as you want to be done with chemo, don't let it cause more damage than necessary. If slowing your schedule would reduce the risk of nerve damage, I think that's what you ought to do. At least try it for the next treatment, to see if it makes a difference.
The neuropathy caused by Taxol and Taxotere is very serious. It occurs when the chemo drug damages the sheath surrounding the "axons" of our nerves. Once the nerve sheaths are damaged, nerve impulses aren't transmitted effectively. The damage is most likely to be noticed on the sensory nerves that lead from our fingers and toes to our spinal cord. That's where we get symptoms, because those sensory axons are really long.
Neuropathy was the one SE my onco talked about at length before I started Taxotere/Cytoxan. She said I needed to let her know if my fingers felt tingly, or if I started having trouble buttoning a shirt or, heaven forbid, walking. Neuropathy is one justification for reducing the dose of the chemo drugs or for stopping chemo entirely.
Please call your onco about it and see what she says.
otter
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Randie -- I had virtually the same symptoms (except it was the last 3 fingers of my left hand). They had started to appear at the end of AC and then got much worse after I started Taxol. (I also had those horrible foot blisters and the burning feet feeling that was a function of my jumping rope smashing open my capillaries and letting A/C leak into the soles of my feet. And I still wonder if my finger problems were brought about by playing guitar while I was on AC.)
After 1 DD Taxol, I was backed off to weekly Taxols (w/ lighter dose) for 2 weeks.
At the same time as I switched to Taxol, I started taking 50 mgs of B6, only exposing my skin to cool or lukewarm water, moisturizing my hands and feet a lot (but NOT massaging), keeping my feet up at night, swapping walking and jumping rope as exercise for a stationary bike, protecting my hand, and wearing Crocs 24/7 (well, except to bed, of course!). Now my hand has completely healed and my feet are in pretty good shape. Most importantly to me, I was able to resume DD Taxol and finish on schedule. My podiatrist also gave me some ointment that fortunately, I did not have to use: Voltaren Gel.
I don't know what to recommend to you, Randie, other than some measures I took that helped alleviate the symptoms or at least, prevented them from getting worse while I was on Taxol.
If it were ME (and it is not, so feel free to ignore this!), I'd probably try stuff to reduce or halt the worsening of the symptoms and not say anything to the doctor in hopes that I could finish on schedule. If it were ME, I would not cancel any treatment.
Them's my two cents. I support whatever you decide to do.
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Hey, Rock!
I know the feeling of wanting to get back to life as usual. If you do disappear from here, please know that we will miss you terribly. I would certainly like it if you dropped in from time-to-time, just to say "hi". (You don't need to read all the posts you will have missed.)
And, as for that overseas adventure you're planning: we want postcards. You'll be busy, but not all the time. And, since you'll be associated with an academic institution (right?), you should have an internet connection... So, let us know sometimes, how things are going.
I wish there was a smooth way to transition from being "BC sisters" to being friends.
otter
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Randie - did the numbing lesson as you got farther out from treatment? Say week 2?
I ask because I responded to the Taxol that way. It wasn't ever bad, just every once in a while the fingers would feel weird/tingly/numby. It wasn't constant and it did diminish as time went on. Each tx it was a little bit more of that feeling...but again would diminish with time. I would feel weirdness like that in my fingers and toes and, oddly enough the skin over my ribs. Even once on the left side of my face...that was kind of creepy. Today is day 9 followng my last tx and I still get a little bit of the numbies (I'm sure that isn't a word but you know what I mean) on the fingers and toes. It has started to diminish and hope it will be completely gone soon!
I don't know if that helps but thought I'd share my experience. I know others have completely different experiences.
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Hey, randie--
Rock does have a point. Your numbness could be an early stage of "hand-foot syndrome", instead of neuropathy. The early signs are similar, I think. Hand-foot syndrome eventually hurts (as Rock will attest), but the redness and blistering will heal with time.
If what you have is early HFS, it's not so bad to go ahead with your next chemo and see what happens. The oncos sort of leave it up to us to decide whether we can tolerate the burning and peeling.
Neuropathy is more serious, though. I don't know how to tell which it is, from here.
otter
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ranD--gs name is Landon. Thank you for the prayers. Your kids sound terrific.
DD is doing better now. I think it's more the getting over the initial shock. I have to go tomorrow to get my neulasta shot, and I thilnk that I am going to get her to meet me and go shopping. She needs a little papmering--4 kids, husband who works a full time job and is a preacher, so they are always busy.
So far, SE's not bad. I am hoping they aren't too bad this time round. Hoping this for all my sisters getting treatments this week.
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eddie~ if my hair is coming from deeper in my body does that make me thick skulled?? har har
Randie~ I had that pain in my feet the first taxol hurt like hell to walk! #2 it was in the first 3 fingers on my left hand. I found that the more I moved that hand andslight lighty brushed those fingers with my other hand it made the pain go away or become lesser. I asked the doc about it today and she said that was a good thing. Just keep an eye on it
rock~ I knew I spelt that wrong... My excuse is that it was late at nite and I was on steroids lol. You had BETTER plan on coming in to visit us in here if you move. I'm not ready to let go of you just yet!!
Just got home from taxol #3 OMG I more to go!!!!!!!!!!!!! I'm so excited. It went very smoothly again for me today.. so relieved. I even got in another nap and the machine I was hooked to woke me up with its beeping.Then I get home to find $150 check from the insurance company yay! We were scraping the bottom of the barrel again.
lovebugs! Jen
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LOL Jen! Your post just made me chuckle. YAY! on one more to go.
OK...panic attack...uh Rock...yoohoo...did I miss something? Will we be seeing less of you? I know, I know...the road trip and your sisters visit....totally cool for you and I hope you have a blast! But you'll be back right?
Kind of on the same subject...at the end of my last tx, the nurses gave me a book called After Breast Cancer...Answers to the Questions You're Afraid to Ask. Has anyone else seen this book? I hadn't thought much about it until today (1 week later). I started reading it this afternoon and so far I recommend it for all of us. Even more, it pounds home how very much we'll continue to need each other as we continue to move past this chapter in our lives. That while others in our lives think "ok, she's done. Its time to move on with normal lives"...it just doesn't work that way. I've found it very comforting so far.
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Hello to everyone - I've been off this site for so long that it's going to take a while to catch up. I've been traveling - partly for work, partly for my dad's heart surgery (he's doing great, will be going home tomorrow), and partly for a long-planned and much needed vacation - and haven't had much internet time. So this will be a quick post, just to announce that I had my LAST CHEMO this afternoon. No weird reactions this time, other than a sudden urge to pole dance at the end (pix to follow, but probably not until this weekend). I collected a hokey-but-nice "congratulations" certificate signed by all the nurses and skedaddled out of there as fast as I could.
Now I just need to ride out the side effects and see what being on the other side is like for me.
Love to all of you,
Linda
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Hey All did manage to get in my first Rad treatment today... After all the problems on Monday with arm falling asleep and being heavy and dead. My Rad onco told me to take 2mg of my Adtivan. Well I did and it worked. Drugs don't usually affect me but this is feeling good. Going to take it one step further and have a beer with it. This is so great, haven't felt like this for a long time. You have to excuse me because ever since last T/C infusion it has been like post partum depression and am so sick of crying for no reason. Feel like partying now just have to be careful I don't fall, lol.
Enjoy the day, Karin
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