Jan 2008--Ain't it Great?
Comments
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good morning and happy Valentines Day Jewels....may the se's leave our chocolate fix alone today!!!
had to take the sendokot S last night..sighs... time to take the advice here and start a day before tx. Well, last night I joined the baldacious babe club, still stubble....but I'll try to get hubby to take a pic later today...
Now to see how many guys from work will hold their end of the bargain...shave their heads too, to support me.
Off to work...tootles
Kris
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Quick shout out to Sherry, Julie and Donna, what a heck of a Valentines treat. You go get um today at the chemotini bar, we'll be thinking of you all.
Kinda a restless night, between the "roids" winding me up, drinking like a fish, so you got it up to pee 4 times and a funky stomach at about 2:00am, toast and peanut butter took care of that, it was a topsy turby kinda night. Into the shower now and off to work, we'll see how long I last. Its a bummer morning of no caffiene for me, I may have to sneak a sip or two.
Carol
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Good Morning Jewels, Had round #2 A/C yesterday went smoothly no se yet. I'm trying a new anti nausua med this time called ondansetron I will take it after the steriods wear off thats when my awareness starts. Gotta go get my nuelasta this after. Next tx 2/27 @7am yuk way to early. My rbc is low hopefully I won't need a transfusion.
Joined the bald club Tues eve dh and ds gave me the buzz they were trembling so bad they scared me luckily I came out with both ears and no blood shed (whew).
SIS Kimberly, I'M doing a clinical for Avastin its already in use for colon, rectal and some lung cancers. Its supposed help with blood fed cancers there is a little info in the bc.org site. It is being tried for triple neg breast cancer to help stop reoccurance since there is no preventative meds on the market for us yet after treatment is finished. My Onc wants me to do Taxol weekly X12 after my A/C is finished since my cancer is blood fed and they not sure if there a cells floating around so she is being proactive. Thanks for asking.
Carol, I'll get out a check to you, hopefully I have my shirt in time for my next tx.
D1, Bio looks good I have a port also if you wanna through it in the mix. Thanks
Have a nice Valantines Day all!
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Wendy, got your PM, no problemo!!! As for the Ondansetron, I believe it always has the name Zofran, I faithfully take one pill every morning while I'm taking my oral cytoxan. It has worked like a charm and it doesn't make you loopy. Good Luck with it!!
I'll be sneaking a peak from work throughout the day, Carol
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Good Morning Jewels-
So, I got my new fridge, and washer and dryer. Oh, they’re so pretty…I know…it doesn’t take much to make me happy eh?
So, my eyes have been watering a lot. My tears are feeling like they’re burning my skin, so the skin around my eyes are a bit red. Also puffy under my eyes. This is not exactly the look I was going for tonight. I’ll be serving a lovely dinner to my dh in my new red wig and watery red puffy eyes…not the sexy siren I was hoping to be. Sigh!!!!
Denise- You know, I don’t know if this is called blogging either…but whatever it is, it’s really great!!!! I just noticed you’re from the San Diego area…I’m in Northern, Ca in Lincoln about 30 miles North of Sacramento. San Diego is a nice area. And you put out some great d words to put in front of the h…just know as Carol said…lower case is positive and upper case means there’s trouble in paradise.
Carol- Well…glad you got the 4th FUBC-er MF out of the way. :-) and that your Mirilax kicked in…oh, the simple pleasures we delight in, girls. Wow, the dh commutes part way to work on bike…impressive. Is he biking to a bus or the ferry for the remainder of his commute? Does he pack his clothes and then shower and change when he gets to work? What does he do for a living? Sorry you had a rough night…hope your sip or two of caffeine helps you stay alert driving those trucks.
D1- Wow, I’m not sure if I want those drugs you’re having or not…not recalling conversations could be a good thing or a bad thing depending upon the topic. Your gf is probably so thrilled to help out…so often friends and family don’t know what to do for us…so anything they can do no matter how small makes them feel good…but I know what you mean about how you thank everyone who had been there for you.
So…baldacious babe gets one freaked out and bolted…and one can I check your ID…so is this clerk flirting with a bald woman or does being bald peel off the years? I’d say you’ve scored even for the day. Loved the Haiku…
Vettegal- I’m so sorry the diarrea is back. I’m thinking the se’s last the whole time in varying degrees. This time for me, the energy is up and down this third week. The eyes are watering more as mentioned earlier this third week. I don’t get a bag of each of those…I have large syringes of Aloxi and other se preventatives (no pepcid). I also get my Adriamycin in a big syringe. Hope your onc can give you some advice on the digestive issues.
LJ13- So glad that your #4 went so well. Whew, done with that!!!! Hopefully the Herceptin doesn’t have se’s that are too bad especially cause you’re doing it for a year.
Your partner sounds like she’s a doll. How sweet to wear a mask, sleep in another room, and be so worried about passing the germs. Isn’t it amazing the things our loved ones will endure to show us they love us? Hope the MUGA goes well.
CHJ- Let’s hope if the truck comes, it’s not a semi and only runs over you once if it has no choice than to hit you.
Jenn- I so loved hearing about what you and the dh do…how wonderful that you work for a family owned business and they you two really are like family to the owners. Everyone should feel so supported. Glad you were up to going in last night and today.
Paula- Glad to hear your cold is only a night nuisance and that you’re able to be there for your students as they prepare for the competition.
Suz- I’m so glad to hear that sense of humor at the end…whew, you’re going to be fine. 5 years out all ready?
I just reread your first post…duh, you said you were diagnosed 5 years ago. So you can give up tips!!!! Are you taking Tamoxifin or an AI? If so, what has your experience been?
About meds. It sometimes takes awhile to find the right anti-depressant and the right dosage. I PM’d you not knowing all this info, so some of what I said won’t apply now.
Anyway, yeah, the shock of the family history and worrying about your daughters can be overwhelming, but the good news like I said is knowing so your daughters can be vigilant.
How are your family members doing?
Take care, sweetie.
Kris- Welcome to the club!!!! You’ve got to get a pic with all the guys at work that live up to their end of the bargain. And…it sounds like the dh is being supportive and helpful.
Wendy- Thanks for giving me the info on your Avastin and Taxotere x12. Interesting…hope the study bears out positive results. And welcome to you to the club…glad you still have your ears and didn’t lose any blood…not good on the blood count numbers. :-) How sweet that the dh and the ds did the honors…and were shaking ‘cause they didn’t want to cut you…I’d be a little nervous,too…but it all turned out well. Whew!!!!!
Well, gotta run to the oncologists…I’ll check in later…
HAPPY VALENTINES DAY, JEWELS.
SIS Kimberly -
Kimberly, my eyes have been watering like buggers since I started chemo. Every morning they are all crusty. Yet during the day they seem dry and burning. What's up with that? The skin around them and eyelids are very tender also.
Nose runs in the morning a lot too, and gets a bit bloody (just some clots when I blow it, never nosebleed-type activity).
I'm hoping these are from the AC and with the Taxol/Herceptin it goes away.
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Happy Valentine's Day!!!
Welcome to the baldicious babes club, Kris and Wendy. Pictures, please.
SIS Kimberly and LJ13--I've had the watery eyes, too, but it comes and goes for me. Seems to be one of the later se's to hit, usually shortly before I go in for the next tx. I just gave up on my contacts while I do the chemo thing! Also, LJ13's description of the nose thing is dead on for me, too. Although I can tell the insides of my nostrils are dry if I don't swab A+D ointment in there a few times a day on a Q-tip. I still have the bloody clots, but my schnoz is more comfortable. As for sexy siren, SIS Kim--you got that down, girl! The watery eyes won't take away a thing!
Carol--for the first two tx I went off coffee the day before tx and stayed away till about a week later. I was having awful headaches. This time I didn't imbibe the day before or day of (didn't want to mess with my hydration schedule), but I've had an 8oz cup every day since. Headaches were non-existent. Allow yourself.
Note to self: stop preening when you sleep well. Last night I don't think I slept a wink. And then there's been all that talk of being PG around here, that I had a dream that I was PG. Dream ended and I'm abruptly VERY alert when I deliver this monster baby!!! I have GOT to stop reading the posts right before bed!
Take aim, Cupid!!!!
D1
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Hey, gang, I have a question. As I recall, there are a few of us experiencing back spasms as a se. If you are one of those people, will you please describe your spasms and try to pinpoint on what day they appear (giving both the day expressed after infusion and neulasta shot).
For example, mine are a tightening in my lower back, right on top of my butt. They kinda ripple and when they're really bad, I have them in waves to the beat of my heart and will travel up my spine, across my shoulder blades. They seem to be aggravated by activity and then come on strong when I sit back down. They appear on Day 8 after infusion, Day 6 after neulasta shot. I manage them by laying around and using the heating pad.
I'd like to see if we have some sort of trend here. My onc claims this cannot possibly be a se associated with anything I'm taking, but I've never had this before tx and they appear on exactly the same day every time. I'm suspecting they're linked to the neulasta shot, but if we see a different pattern, I'm willing to be proved wrong.
Thank you for participating in my empirical study.
D1 (mad scientist)
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Hi Jewels -- just checking in before I head off to tx #3 -- HALF WAY -- Woo hooooo!! I'll catch up with everything later.
Happy Valentine's Day, Jewels! Hope you all have an se-free day!!
{{{HUGS}}} to everyone!
Julie
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Hi All,
I have been just lurking lately, too. Been feeling fine. I have enjoyed looking at everyones pictures - you are all looking great!
Good luck Julie hope third time is a charm and you have much fewer se's!
D1 I get some sharp pains from the neulasta. I guess you could call them spasms. They are very severe, but last for only seconds. I usually get them when I go from sitting to standing or from standing too long. I get my shot on Monday afternoon. I get the spasms starting on Thursday afternoon. They start with my hips and thighs. The next day they are my spine and my ribs. I get a lot of them right at the base of my spine and they travel up a bit sometimes. After #2 I was getting them at the top of the spine right at the base of my head and that was very bizarre feeling. Not sure if that is the same is what you are experiencing.
golfer - are you avoiding coffee because of the dehydrating effect? I have had coffee throughout this journey and haven't had a problems. One thing I am just not willing to give up I guess!
Kimberly - loved your supergirl pic!
Hope everyone is hanging in there well.
Cheers!
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Helloooo and Happy V-Day Jewels! No, I have not been lurking.. my d*mn internet router died yesterday, so I've been without internet until now. I was gonna freak on the Verizon guy if he didn't fix it today! So, I've been feeling good-- the neu-nasty must be doing it's thing b/c this was when I ended up in the hospital last time. Whew! I'm still being a major cleaning/handwashing germ freak though. I think I have another cold (how can I possibly ever avoid it with 2 preschoolers unless I wrap them in bubbles... or me)-- I've been congested all week, as has the dh and my littlest one. I'll take it though over some GI illness and the flu, which I know are also going around. Ok, my shout outs... I'll add some "nursing pearls" to them, too (hope you guys don't mind.. I have no one to take care of but me, the Jewels, and my kids since I'm not working these days)...
Note about Miralax: if you need a "starter boost" (cuz nothing's happened in a few days), you can take 1 1/2 - 2 capfuls instead of the usual one.
Vettegal: Fruit has lots of fiber, so it can cause diarrhea. Pectin (a fruit sugar) is another culprit also, so avoid juice especially if you have diarrhea. Bananas are the exception, they can constipate. Apples can go either way. Applesauce has lots of pectin so it usually causes diarrhea. I agree with Paula: my onc said to avoid fresh fruits when counts are low unless they can be washed very well b/c of the bacteria potential. And my "cocktail" includes: Aloxi, saline, bendryl and decadron (added after my reaction), Taxotere, Cytoxan, and Herceptin. I'm there about 5-6 hrs.
LJ13: Good luck with your MUGA! I thought this was the easiest test so far. And I hear herceptin is easy (v. little SEs). I can't really tell what SE is from that b/c right now I get it with everything else. But I hear the biggest SE is "flu-like sx" the day after infusion. I don't experience any of that right now. I'll be curious to see what if anything I notice when I'm just doing herceptin alone (by April).
Jenn51: Hee hee hee-- can't imagine being bald as a SE of PG! I DID have some hair thinning though at the top of my forehead after I delivered my son . My OB (and hairdresser) said it was from the drop in hormones.
Kris60 and Wing: Welcome to the bald babes club!
Wing: That "o" drug is Zofran. I love it, as I can't take compazine (allergic), but it IS very constipating (go figure!). How low are your RBCs? And what's your H/H (hemoglobin/hematocrit)? Sometimes the oncs will give Procrit (a shot given once) to boost them and/or iron (pills taken daily for "a while"). I may be able to give you an idea. PM me if you want.
SIS Kimberly: Glad you got your appliances! It's kinda like having a new car: all shiny, and with the "new" smell! I had a woman who's stage 4 tell me about the runny eyes and nose thing at my last infusion (our oncs are the same, and she said he told her about it). Evidently it is from chemo, usually the taxanes. They cause watery eyes. The runny nose is actually the tears from your eyes coming out your nose. Makes sense as they are connected at the tear duct area. And I've noticed my runny nose IS very watery, not like usual "thicker" snot. Sorry to be gross... but I found it very interesting. I thick our bodies contain levels of the chemo drugs in our secretions for quite some time after tx, so the mucus membranes and anything the "tears" touch are affected--probably it's why your surrounding skin gets red, too I would think. Maybe you can protect your skin with Vaseline or Aquaphor?
So good to be back online! Hope everyone has a great rest of the day.
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vettegal - I get all the same drugs as you, except I think my aloxi is in a shot that they push through? I go for number 3 tomorrow so I will try to pay attention. I do know I get the pepcid - thankfully cause the acid stomach I get is awful. Mine takes about 4 hours.
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KathyL, I agree with you that apples can go either way with your lower GI system, but I'm pretty sure that pectin is a good thing as regards diarrhea. Applesauce is part of the famous "BRAT" recommendation for diet while suffering with the runs. Fruits like blueberries are very soothing to cantankerous intestines because of their high pectin content. (Pectin gives its name in part to Kaopectate.)
Maybe you were mixing up pectin and sorbitol, which occurs naturally in some fruits too (apples, peaches, nectarines) and which is very much a baddie when it comes to diarrhea.
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HAPPY VALENTINES DAY
I received a card in the mail from my real estate lady..we where looking for a house but, since the bc my health came first..anyway i want to share with you all!
No one said it would be easy
to lose your hair
But knowing you,
you'll find a way
to turn this situation around
and use it
as a badge of honor,
a sign to the world
you treatments are working.
And when this is all behind you
and you grow your hair back,
you'll be able to say with assurance
that every day is a good hair day.
I thought it was great..she wrote in the inside..Your courage is inspiring!!
Remember, no storm can last forever. The sun will shine again! When you get through this you are going to be a better, stronger you! Be gentle with yourself, don't rush things, enjoy the small things in life,and remember, I am only a phone call away if you need anything.
Just thought I would share this on Valentines Day to all the wonderful Jewels that have helped me through this bc.
Will post tomorrow with photo of me with balditude and my t-shirt I am wearing to round 2..got the gloves on ready to take it down..DING!
Lets also pray for those kids that got shot at that collage in Illinois, so many young people hurt and died. Those poor families.
To the other Jewels going in tomorrow..LETS ROCK!
hugs to all
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LJ: Maybe I am befuddled with the chemo-brain... all I know is when we prescribe BRAT at our practice we always say "apples" not applesauce b/c the sugars in the "sauce" can go the other way. And blueberries surely give me the runs
hee hee!
Vettegal: I like the card you got.
Night night gems! Good luck to everyone doing chemo-tinis tomorrow!
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vettegal - what a great message, i enjoyed that. i am constantly being told by friends and coworkers how strong i am and how well i am handling this, especially now with the baldness proclaiming my circumstances. being bald is so symbolic of 'chemo patient' and i'm just not stressing about it. everyone else seems to be more worried about how i feel, which i have come to decide is, in part, their own fear manifesting itself. an old friend and coworker couldn't keep the tears out of her eyes when we were talking about my baldness and i just had to keep reassuring her that it's okay, I'M okay. I actually feel very blessed at this point that things aren't worse because they easily could have been. my feeling is that people are watching me (us) and seeing us get through it and be okay. statistically, breast cancer IS going to happen to another one of my coworkers and/or friends. when it does and if they have to go through chemo, i hope they can look back and think, "i watched 'sista2' go through this and she made it in to work and she did it" and somehow they can gain something from that.
having said all of that, i've only had two tx and still have six to go. we'll see how strong i am a month from now. lol. ugh.
D1 - my back trama happened day 8 after neulasta shot, 9 after treatment and was in my lower back right above the butt. the pain was intense but would come and go. it was only for a day but was a kind of pain i haven't had before. had my counts done the day prior and they were low so i know it hadn't kicked in before day 8. i'm convinced it was that shot, it was just so unusual. had my counts done today and they were low. tomorrow will be day 8 after the shot again so i guess i will see if the pain returns on a schedule.
Happy Valentine's Day Jewels! i hope everyone can enjoy some chocolate or whatever their pleasure may be today.
omg, i just read about the illinois university killings. here we are fighting for our lives and some bast*** can just come in a take away those young lives in an instant. it makes no sense.
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Happy Valentine Day,
To Sherry, Julie and Donna lets hope your V-day at the chemo lounge was uneventful and your feeling alright this evening.
PALady, looks like your knocking down another txt tomorrow, one step closer to the end of the tunnel! In regards to the caffiene, it is "recommended" to avoid it while I'm taking the oral cytoxan. Couldn't tell you why, but I'm trying to do everything I can to not rock the boat. Albeit, I did have a little sipper of coffee this morning and god it tasted good!
Kathy, yeah for the internet guys ... I think I'd have a meltdown if ours pooped out.
I took note on your heated blanket, I've been using the heating pad (in fact its behind my back right now), and then putting it in the bed to keep my feet warm. I think my circulation is worse now than its ever been, the poor guys in my shop at work...I walk in and crank the heat, the "big" guys are roasting and I'm freezing. They put up with it pretty good, I guess its one of the perks of being the "gimpy" one.
I'm still having a tough time regulating my Miralax, I hate to say it but remember your cinder block comment a few weeks ago, I think my cinder block messed up the ol' hole! Too much Miralax is kinda scary if you get my drift! This is so sad I'm sharing this, would not in a million years think I'd be discussing bowels on a regular basis.
sista2, what a cool gesture of your dh to shave his head as well. I think I would be scared to see my dh's head shaved. Hopefully you get your nausea meds figured out so they are more productive for you. I always say that any se is tolerable as long as I'm not puking!
chj, yeah for feeling good, is something wrong with you!!!! Its great to hear somebody is having a tolerable txt.
D1, loved your story about Dave at the grocery store ... the poor guy! It had to be pretty embarassing for him. Glad you got some use of your "boobies" hat!
Vettegal, what a great card, must be a very personable real estate office. Go get um tomorrow, I'll look forward to your pic proudly displaying your FUBC shirt. I've printed out the pics of those that have shared and keep them in my "notebook" with all my "C" stuff. I've had fun sharing as I talk with the dh, mom-in-law, friends, it really adds alot to a conversation when there is a face to the story.
LJ, hope your scan you had today has good results, hopefully your friend is feeling better soon and you escape the wrath of it.
Paula, hopefully your nights sleep are extending past a few hours at a time. Nothing worse than that tickle cough at night. Looks like its your turn to belly up to the bar tomorrow, we'll be sending positive vibes your way for a smooth txt.
Kimberly, have you peaked at the "more ooph questions?" posting, there are a few new post there.
The dh commute goes drive 15 min to park and ride lot, get on bicycle, ride 10 min to ferry, 30 min ferry boat ride to Seattle, then about 30 bike ride to work. He has changes of clothes and a shower at work. He has been driving this week, we just bought a new car over the weekend (Accord) and it doesn't have a bike rack. I'm not too crazy about one of those hang off the trunk styles and I'm not sure if you can get the hitch type that doesn't show. I would be the picky bitch when it comes to the vehicles.
Have a wine for you to try, Marietta Old Vine Red (California), our neighbor has been buying it for years, starting at one of the first Lots. Its now at Lot #44. He shares a bottle of two with us quite often, I mow the lawn that adjoins our lots and thats my thankyou in return.
We should be getting a call later this evening from my step daughter, her boyfriend is proposing tonight, he had my dh mom's wedding ring spruced up and is giving it to her tonight. She will be overjoyed with the sentimental value of the ring, she was soooo close with her grandma.
Well, the dh called asked if I would like to go out to dinner, I said not really, hate to say it but a bowl of Cream of Wheat is calling my name! So much for say Lobster and a glass of wine! But the good news is there will be many more V-Day's in the very near future.
Carol
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Happy Valentine's Evening, Jewels! Hope you've all had a nice day and have been se-free!! I completed tx #3 today -- uneventful, thankfully!! It definitely feels good to know that I'm half-way done!!! Yay!!!! I'm REALLY hoping this one will go much better than my first two.
Okay - my sister took me today and took my pic donning my FUBC shirt! It's below........
My husband and I went to my primary doctor today to meet with him about my disability application and fill him in on everything that's happened since the last time I was in - about 6 months ago. Anyway, my husband was telling him about this website and how much it's helped me to have the connection with other women going through the same thing and then he says, "Tell him about the shirts your chemo group made!" So, I told him our motto "FUBC" and just let him take that in for a second or two -- he busted out laughing and laughed for quite some time. He loved it!!
I'll catch up when I have time and post more later. Hopefully I'll be okay the next couple days at least. To all those who took part in chemotini's with me today -- hope your tx went well and you have minimal se's!!
Here's to a good Valentine evening!!
Julie
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Okay, I am sooo ready for tomorrow and I've got plenty of Jewels to accompany me on the Magic Chemo Ride. I believe WVGirl, PALady, Deb1023, Vettegal, Jenny and Peg1212 are riding with me. I'll be wearing my Jewel tee!
Julie- love your picture! I won't be looking as snazzy in my layers, but maybe I can shed them for a photo!
D1- I hate that you are still having such problems with your back. Your description of the spasms is identical to my experience after round 1. Mine first occurred 7 days after first Neulasta injection. Worse with movement--esp. when I first sat down, starting around my tailbone, rippling out and around to my hipbones and take-your-breath-away intensity. They would last about 10 minutes if I was settled, but recurred every time I changed position. I had them for 2 days and then they disappeared. I haven't had any with this round. Go in for shot #3 Saturday, so we'll see how it goes this time. I've never had any back problems before either.
Sista- keep us posted on your back. Here's hoping you don't have any problems!
LJ- how's your partner? Wishing you both good health!
Vettegal- what a nice card! What time is your tx tomorrow? Mine is 12:30p.
Carol- I hear you on the Cream of Wheat! I'm all about comfort foods. I love my coffee, but I don't even want it for the first week after chemo. I replace it with tea to get my caffeine fix. I've been living on hot tea and Hall's cough drops for the past week. Now there's an aphrodisiac for you!
I hope everyone has had a nice VDay. I know there won't be as much "activity" around here as usual, but we'll make up for it later. I forgot to mention that my dh's first response to seeing my bald head was "I've never 'done it' with a bald woman..." Well, I was already sick with this cold when I got sheared so he STILL hasn't....
I'm working half-day tomorrow. Will check in b4 or after chemo (probably both--I love you all!)
Nite all, Paula
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Happy Valentine's Day Sister Jewels - warrior women! I continue to be so inspired by you all.
I've been pretty miserable the last two days.
My Tx # 2 a week ago today brought very few se's or so I thought, until the past couple of days when the neuropathy has become almost intolerable. It's all over my hands which is unsightly but at least manageable. In addition though I have a patch of it on the heel of my right foot. The entire heel is red, tingling and becoming more and more numb each day. Yet even putting a shoe on it or any pressure walking is excruciating. I've been taking the L.Carnatine & B6 that was suggesed. I picked up some Capsacian roll on lotion that I read helps and it did- for about 10 minutes.
This morning I called my doc's office and he called in a script for Lyrica which of course my insurance co. wouldn't approve. (My new group insurance carrier is horrible, IMO)
Finally they approved Gabapentin which I am praying will kick in soon. I had to go to work with my shoe half off looking like I was drunk probably; and then walk around the office on tiptoes in my socks - between that and my wig slightly askew, I was a vision of loveliness!
I'm so sorry to be so whiney, but this hurts like hell!
Wah! Wah! Wah!!
Even nausea is better this.
Take good care dear jewels... and thanks for letting me vent.
ps. oh, i have the runny nose too!
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A quick shout-out to all the girls partaking in chemotini's tomorrow -- WVGirl, PALady, Deb, Paula, and Vettegal! (and anyone else I missed!!) Go kick some BCA, girls!! I'll be thinking about you!
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Oh, CarolC - I'm so sorry you're having such a hard time with the neuropathy! That sounds awful! I'm hoping the medicine your dr prescribed will give you some relief soon. {{{{{BIG HUGS}}}}} for you!! Take care of yourself.
SIS Julie
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hello everyone
It's day 15 from my first chemo and I finally feel good. well not exactly great but no nausea like week one and my bowels seem to be back to normal from weeks one and 2. now i have the sore scalp and falling hair of the third week.
I had my wig styled today and i've been wearing it all day. Yesterday i had my hairdresser cut my hair half an inch long all over. I thought it would fall out from there and I'd be OK with that but my scalp hurts when my hair gets bent and it was bent all day in the wig. My hairdresser said she would come to my house anytime and shave the hair off for me. She wouldn't take any payment for making it short yesterday then today she wouldn't take any payment for cutting the wig because she'd never done one before and said she wanted to do something for me. It feels good to know she cares. now i hate to ask her to come to the house for free. I think i could get it all off with a lint roller but it would take a long time (just kidding) anybody try using the vauum cleaner to get it off?
D1- Happy belated birthday. Hope you could feel the love.
vettigal- thanks for sharing your card with us.
Those getting chemo tomorrow- i wish you an uneventful time and low side effects.
I hope everyone has a good restful sleep
Goodnite
Judy
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Good morning Jewels
Been up since 4am. Getting a little anxious round 2. My infusion is at 10:30am..dr appt is at 9am. He is always late..
dh is up making breakfast, gotta take those steroids this morning...they make me hyper. will be wearing my t-shirt today PROUDLY
Todays chemo ladies....Lets go get em and we will all chat later!!
HUgs....xxxoo
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Good morning to everyone! Vettegal looks like im right with you today on this one, have to be there at 800am for round 2. Good luck to you, and to anyone else needing some good luck today.
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WVGirl, PALady, Deb, Paula, peg1212 and Vettegal - wishing you a gentle day as you partake of your chemotini's today.
As for me - I think the pain meds are kicking in and the neuropathy on the bottom of my foot is starting to feel better. At least I can walk without ouching with every step.
Have a good day Sisters -so glad it's almost the weekend!
Carol
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Good morning Jewels! Had to say hi and good luck to today's gems doing tx before I go eat something. Hope everyone has an easy day and all the SEs stay away (hey, that rhymes).
Carol: so cool to hear about the stepdaughter's engagement. It's nice to hear some good news. And now there will be a wedding for you to look forward to
Speaking of good news... I forgot to tell you guys I'm an aunt! My stepbrother and his wife had a little girl on Wednesday and are doing great! My dd is so excited b/c she said it would be a girl and the baby was born on the 13th and that's also her b-day (hers is Nov. 13).
Julie: great pic in your shirt! I have got to get the dh on helping me mine this weekend...
I'm concerned about all you Jewels with these back spasms. How can the docs deny something's going on here? It definitely sounds like it could be the Neulasta since you're all on it. Any other common meds? Hope you all find some relief.
Paula: your dh sounds like mine... any excuse to "do it"! They are so funny. (by the way, mine hasn't had the opportunity yet either, despite the fact that I've been bald for 2 weeks now
)
CarolC: Glad to hear the Gabapentin seems to be working. You seem to have been hit really hard with the neuropathy SE-- big hugs to you!
Judy (sheebas): nice to hear from you. That scalp/hair pain is so weird, huh? I found that the shorter my hair is (or when it's gone), the better. LOL about the vacuum... my dh actually vacuums our dog and he loves it (the dog, not the dh)-- maybe it would work...
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A QUICK HELLO AM AT WORK UNTIL 10 GOING FOR CHEMO AT 11
GOOD LUCK TO ALL GETTING THERE DOSE TODAY
WILL CHECK BACK IN LATER YEA WILL HAVE A 3 DAY WEEKEND COULD NOT COME AT A BETTER TIME AFTER GETTING TREATMENT TODAY
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Good morning Jewels!
I have to be quick. Been forgetting to share with you guys that college girl is coming home this weekend and I'm supposed to leave in 3 mins (!!!) to start the drive and I haven't even showered, yet! Yikes! (Oh, but if I'm a little MIA this weekend, you'll know I'm basking in the love of having my family all under one roof again.)
Vettegal--loved the valentine! Thinking of you right now--bet you're still with your doc...
Sista2/PALady/Paula--thanks for sharing your back stories. I'm going to arm myself with all of our experiences the next time I see my onc because he needs to acknowledge this is something real. If there's anyone else, please pile on (I hope there isn't). If you all will keep me updated if your bad days change/don't exist, I'd appreciate it. For me, the spasms are on Day 6 after neulasta (shot day is day 1) like clockwork. That's too much coincidence for me not to think there isn't a link.
Hey Carol, by the time you figure out the Miralax you'll be done!! hehe. That's such exciting news about your stepdaughter. I "awwed" out loud (is that aol? naw, that's something else, now, isn't it?) when I read it.
Julie, girl, you rock the FUBC shirt. And look at you all up in your chemo chair with a pink doo-rag! Minimal se's, minimal se's...
CarolC--Oh man, I hear you on the neuropathy issues. Mine have only affected my hands so far--can't imagine the feet! Hope those drugs help. I also laughed at your askew wig comment. Last night I was at dd's basketball game talking to a parent from the other team (my kid went to AAU Nationals with her dd when they were 10 years old, so we have lots to catch up on when our high schools play each other. Oh, and I'll brag--that year her team came in 4th in the Nation!!!). Anyway, I'm chatting away and for some reason patted the top of my head--only to discover that my wig had ridden up and was actually perched on my beanhead! My bangs came down about an inch when I did it! (And this mom didn't know about my bc!) The dh saw it happen and laughed and said, "Nice hair." We all lol and then I told the mom. Guess I should wear that tape they gave me, but I HATE the whole wig thing so much, I think it's my protest not to wear it properly!
Sheebas--Good to hear from you. Sorry the past 2 weeks haven't been so great. Try to enjoy your good days. Vacuuming is an idea. I kept toying with getting those cold wax strips and waxing the hair off!
Congrats to Auntie KathyL!!! February is a GREAT birthday month!
You will NOT believe (I'm still in shock) what my dh gave me for valentine's day! A gift certificate for a massage!!! He said he thought I'd want one when I'm done with all of this. How extravagant! I'm psyched!
oh man, g2g!!!
Good luck today Vettegal, Peg1212, Jenny, PALady, Paula, Deb and WVgirl. Have it shaken, not stirred! FUBC!!!!!!!
D1
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Good morning Jewels! Happy Friday! Hope everyone has a great weekend, even though I gotta work Sat and Sun night depending on my se's which havn't been bad for me luckily.
D1, I had the back spasms and pain breathing but I thought I strained my back I'll have to see if it comes back again I got my nuelasta shot yesterday! I guess its just more icing on the cake of BC.
Carol, Congrats on the upcoming nuptials for your family!
Kathyl, Great to hear your an auntie!
Good luck to all going for chemo-tini's today!
Carol C, Hope you feeling better today, just wear fluffy slippers to work!
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