Starting chemo January 2009?
Comments
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I hope everyone has enjoyed the long weekend!!! Tonight I will eat sushi!!!! I have done without it for so long.....At this point it can't kill me right? Wish me luck!!!
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Hi Jewels: I loved racing around to all those sporting and music events. I am with you Kim.. I don't miss it at all -- I do miss all us parents who endured the routine together though. We sure had fun.
Warm here in Northern WI -- got most of my pots planted and gardens tuned up. I have a little left to do. I scaled way back this year, with work and radiation and all, it seemed prudent to not overextend - could become my new "normal".
My port site is still a bit sore, but nothing to complain about. Nice to have it gone! That side bugged me more than my other bc side.... which is now nicely tanned after 12 rads. I just put four coats of nail polish on to cover the ugliest nails on earth -- the top third are yellowish brown and not attached to the nailbed -- thank you taxotere!! At least they don't hurt and I don't think they will fall out.
This week we have Relay for Life activities - a plant sale and a community wide open house for cancer survivors - I think that is were I get my (our) survivor T-shirt - the one that will have all the Jan Jewels names on it.... And I came up with an idea to do a 50/50 raffle at work as a fundraiser - bought tickets at Walmart today -- will see how many I sell.
Hang in there Patti and Phyliss....
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Hi all. I am doing OK other than alot of fatigue. I am not sleeping well. Friday night I was up from 2am to 6am. Saturday I took an atavan at bed time and slept through, but woke up feeling as tired as when I went to bed. Sunday night I just woke up repeated during the night but not so much awake that I got out of bed. We had a fairly busy weekend. Saturday we visited with a friend who had some plants he needed to thin out and which we could use to fill in. Then Saturday night we visited with other friends for the first grilled meal of the season. They have a son a little younger than mine and the boys are finally starting to really enjoy each other company. The age gap is narrowing. Today we got up and planted the new plants before driving to RI to visit with my ILs who just got back from wintering in FL. It was a nice visit. Tomorrow I have to get up and out because DS has a dentist appoint and then I need to get him to school in time for gradutation rehersal.
I am starting to think that some of the weird numbness and aching in my feet and maybe hands, arms and legs, maybe from some water retention. I am not sure but I looked at my feet today and I think they look a sort of puffy, not enough to be sure. I still have ankle and all, but I think I used to be able to see the bone on the top of my feet and I don't see them now. And my arms feel thicker around than I remember. But it is hard to be sure when you don't have anything to compare to and the swelling is not so extreme that it is obvious. My belly certainly looks way bigger than ever, but that could of course just be fat. I weight 15 pound more than when I started this journey.
Wednsday makers then end of treatment in my mind. Thats the day I don't go back for another infusion. We still don't know what we are doing to celebrate. I want to celebrate as a family, but I don't want to spend my time entertaining my son at what ever we do. That is not a celebration for me.
I need to run. Hope you all had a good weekend and took a moment to say a thank you to all those men and woman through our history who have chosen to be of service to our way of life and given their lives though that service. That debt can never be paid off.
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Alo 123 - Where are you stationed? My son is also in Hawaii right now. He is on the Pasedna. My husband will be retired with 30 years on June 1. How time flies when you are having fun. Will try to let you know about insurance differences. My DH bought a supplement so he tells me to stop worrying about the $ because he does not think we will notice much difference in coverage.
Took some pain killers this weekend so spent most of the weekend sleeping. Better than being in pain I guess. I am up early today and I am hoping to get through the last week of school. Maybe the kids will take my mind off the pain. In any event, I am going in and I'll see what happens.
Love to you all.
Patti
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Hi everyone. I hope you all had a good holiday weekend. There was no parade here either but I remember going to them as a kid.
Catherine - congratulations of finishing rads!!!!!
Thanks everyone for the info. about gene testing. I have many female cousins, most of whom have kids and I have a sister. I hope I will be able to have the test for their sakes at least. If I am positive then I'll likely have the ovaries removed.
I am having a bad time with SEs....I'm very achy, have no energy and there is numbness. I am so glad though that this is the LAST round. Thanks for the head's up BKim. I'll try not to get too excited but I am still so happy that I'm not getting a fresh dose this Friday.
Take care everyone,
Nancy
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hi ladies! finished #3! I had a really good weekend. DH and I bought some more flowers to plant. We just had a deck put in the front of our home and it was finished last Wed. Its really nice, now we can go from the backyard deck to the front when the sun moves. I didn't feel too good yesterday. Sat outside most of the day. Had a couple of people over for a cookout but I had no sleep this weekend. I'm really feeling like crap today. My body aches and I have a headache that just won't go away. I was going to run some errands but It will have to wait. no energy. Hope all of you have a good week.
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Sorry to hear that Plutz. Only now when I'm sleeping better do I understand how much not sleeping well during chemotherapy contributed to how lousy I felt
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I am in Kailua. Which is probabyl the other side of the island from where your son is stationed. He must be at Pearl Harbor. We are Navy...but stationed at Marine Corp Base Kaneohe. My hisband is an avaiator.....they fly from the MC base.
I can't wait to here about the health care....I hope it goes seemlessly!
I hope everyone is rested up enough to take on a new week!
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Year of the Hat---I hope you feel better soon. I am still having trouble with my aching knees. I so wish it would go away. Oncologist said exercise would help, but that hasn't been the case with me. Congratulations on being done!!!!!!!!!!!!!!!!!! I always do a mini celebration dance when Thursday comes by for me.
I can't wait to get my port out. Has anybody read about getting yours flushed every four weeks?
Renrel--i have been wondering how you were doing. I am sorry your hands and feet feel numb. I hope that is resolved quickly.
Kathy-- I bet you are glad to get the port out...That side has bugged me as well. It feels so tight and bulky. glad it did what it was meant to do, and I hope I'll never need it again!!!!!!
Patti--Hope the pain goea away quickly.
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Renrel: Good to hear from you. I started a diuretic, lasix 10 mg daily, to get rid of the excess fluid. I take it early and pee like a race horse til noon. Fluid still builds up by evening, esp after I sit in the car for 3-4 hours but it is better. My onc says it will get better over time - the lasix is just to help it along.
Jess: I was told I'd need to have the port flushed every four weeks if I left it in.
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I still have my port; i'm keeping it till all my sugeries are done (ovaries removed; phase 2 of my reconstruction).
I was told to have my port flushed every 6 weeks. I had if flushed today, in fact. It took less than 5 minutes. no biggie at all!
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Jess - OUCH to your toe injury! For me, the numbness has a way of feeling like the nail is separating from the nail bed, although I don't think they are related. I'll relax more when my neuropathy is gone.
Holtbolt - I'll be damned if I know how to keep false eyelashes on. I know the waterproof adhesives work better. I wore them one day and they were really obvious and kind of messy looking. They started falling off and I pulled them off by Noon. I would invest in an applicator tool to place them in a smooth curve, except that they always seem to fall off anyway. Has anyone tried NUBrow? Now that I'm done with chemo I probably won't bother with fake facial hair but maybe. I suppose pulling at your skin with adhesives could delay hair growth but I am tired of being so blank looking, without hair I mean.
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renrel- I also have the numbness in my hands and feet. I was just getting it on the tips, but today its the whole thing. I can barely pick up anything. My legs are still achy and of course I'm very tired. I slept fairly well last night but woke up at 3am and was awake for awhile and managed to get a little more sleep. was planning on running some errands but I really don't want my legs giving out on me so I'll stay home and get some stuff done. Hope your feeling better
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Phyllis - #3 finished for you. How many more? The achiness in my legs seems to be taking over my entire body. Feels like arthritis is everywhere or what I think it would feel like to have it everywhere. Finally got new painkiller from Dr. so hopefully that will help. I try not to take painkillers if I really don't need them but I am at the point where pain is getting me really down so I will take them today as "prescribed" instead of when I can't stand the pain anymore and see if they work better that way DUH!
Tx again tomorrow. ALREADY. Seems like tx comes really fast when you do it once a week doesn't it. Oh well at least it seems to be getting done faster even though it's not. 4 more to go including tomorrow.
Only three more days with my studentds. Took my hat off at school yesterday because I was really hot and the kids were like WOW. Out of the mouth of babes... I said it would grow back and a little guy sitting next to me said "My uncle has no hair but his isn't going to grow back." Reminded me to be grateful that my hair thing is only temporary.
My daughter and her new husband have decided to move to Maryland. I am so excited. They will be moving into my basement for awhile around the end of June. I am hoping they will both be going back to school. This of course means my new grandbaby will be here 24/7. I am very happy about it and hoping it works out okay for all of us. My two children still here 15 and 13 are really excited about it too. They really miss the older sibs and the house always seems empty since they left so it will be full again. I try not to think about reoccurrence and spreading cancer, but every now and then (like yesterday) I get a real feeling of dread and think I am going to die from this because it spreads...that's what cancer does...Well anyway I am glad I will have time to get to know and be with my grandbaby just in case!!! It will also be nice to have DD home again. I think???? lol
Gonna go try to get something done before school. Hope you all are feeling good and starting to feel like you are moving on. I am inching to the finish line. We can do it PHYLLIS....who else is still getting tx. I can not keep track anymore even though there are only a few of us.
Patti
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Good luck Patti and Phyllis!!! You ladies are bring up the rear with grace!
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Woo Hoo Patti and Phyllis!!!!! Of all the January Jewels...you guys are the Jeweliest! What? Are you the chemo overachievers or what? Just had to make the rest of us look like wimps for finsihing our chemo sooner, but not you guys. Noooooooo, had to show us all up by still making the rounds, huh. Well, you know what? You're time is coming, and it's sooner than you think.
Can't wait for you both, and anyone else who started in January, to end this leg of the journey.
Catherine
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Very good Catherine and so true. come one Patti and Phyllis....We are rooting you on! A toast!
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Hang in there Patti and Phyllis!! Chemo over-achievers.. lol. We are all waiting to see you both cross the finish line!
YearoftheHat... these false eyelashes are ridiculous but sometimes I put them on anyway.. I am so over looking sick, I'll try anything!!
I made a PS consultation appointment for 6/22 to see what the good doctor can do with my ironingboard.... shopping for a swimsuit for my trip really made me think I might go down the recon road.... who knows... we'll see what he says...
Peace everyone!! My birthday is this Saturday (the 30th).. normally I don't celebrate but this one seems like something to celebrate... now who wants to giftwrap some boobs, hair, eyelashes and eyebrows and send them to me? LOL
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LOL Holt! PM me your address!!!!!! Let's toast!!!!
I'll send you something...what do you want?
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Go Patti and Phyllis! You'll both be crossing that finish line before you know it.
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Holtbolt: If I had 'em I'd share LOL!! Have great birthday!
Patti: Thinking about you tomorrow and 3 more Thursdays to follow. Then your baby will be there --- that is wonderful news.
Phyllis: what's your chemo schedule? Want to be sending positive vibes on your days too.
Take Care Jewels
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LOL KT57!!!!!!
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Patti and Phyllis, I'll echo the other's we're still here and rooting for you.
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Hi ladies. Thanks for hanging in there for me when I finish. I have 1 more on June 12th. These treatments have been rough on me, but I made it through this week without being dehydrated. I'm just very fatigued and a little weak. Went to the grocery store this morning and was winded when I got home. Had to take a break before I could put the stuff away. But I am feeling better. Going out to dinner tonight. Don't know what I'll eat without the tastebuds. We're going cuz a 14 yr. old student thats in one of my daughters classes has cancer in her spine and has been going through treatments and the restaurant is donating 20% to help with costs. So if all of you could pray for her. Her name is Kelsey. Such a young age to get cancer. I thought all of us were too young to get it. I hope all of you are doing well. I should be back to almost normal by the weekend. Have a good one.
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Phyllis, I am glad you were able to get around some. Doing simple things becomes such a project with chemo. Just keep conserving your energy to take care of yourself and try be comfortable. I had my last Taxol last Friday and I have been really tired, with very swollen legs and achy feet and hands. I've had moderate and continuous neuropathy also. I can't taste almost anything except maybe sweet stuff, like strawberries.
It should feel good for you to go out for a cancer cause. I give so much credit to those non-adults who manage through chemo. It's great that Kelsey is getting some public support.
Patti - I am still taking painkillers too. I was taking them as prescribed for some of last week but will try to taper off and use Tylenol instead. I am hoping my aches will subside since this is my first week without chemo in 3 months. I too had aches everywhere which I suppose is what arthritis feels like. I kept saying I imagine that's what ninety year old women feel like. I am still limping around from foot pain. I hope next week that will be more mild.
I'm thinking of you both. You are both doing great!
Nancy
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Nancy--- I have had a horrible time with inflmmation of the knees. I can hardly walk up and down stairs without pain and exhaustion. I talked to a nurse today who said the taxanes do a number on the joints. I just feel like cursing up a blue streak and having a major temper tantrum. She said time will go by and the pain will lessen. I hope so because I really am tired of being angry.
Nancy, Phyllis and Patti- I have taken fewer pills this week and I don't want to have to take anymore atavan, but that has really helped me sleep at night. Plus, I don't get the "hangover" feel from it. Hugs to all of you.
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Just got back from Open House, which was really nice. Bittersweet for me since my job and program are being eliminated. I'll be placed somewhere else, but I'm hoping I can get the resource specialist job at the same school--although the current resource teacher has lots of seniority and a doctorate and has told me she wants to stay. I think I can get my teachers to write me letters of support.
My legs are SO SORE. It's not my joints so much as my quads.Maybe I've been overdoing the walks, but nurse and accupunturist/onc say it's typical taxol. My feet are more numb than during treatments, but getting a bit better,. Hands improving.
One lash left on one eye, and brows have scraggly hairs here and there.
Patti--Great news about your daughter moving closer to home!! And grandbaby nearby. My students haven't seen me wigless yet--maybe I'll surprise them last day of school. Another treatment down!!!! You're getting so close to the end.
Phyllis--glad you're feeling better. It is so sad when young people get cancer. One of my sister's bf's 13 yr. old daughter just finished chemo for Hodgkins' lymphoma and is now getting radiation. They also had a fundraiser dinner. It's so nice when the community comes together. It's just so hard for the family too.
I still have taste buds--too many I think. I just want to eat and eat and eat.
HoltBolt--HAPPY BIRTHDAY. Wish I had some extra hair to send. But the stuff I do have you wouldn't want. Curly frizzy white stuff.
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Berkeley Kim--I am sorry about your job position. Gosh, just another stressor to add to the list, huh? We have graduation and everything this Sunday. I will be very happy when that is said and done for the year. This group of seniors has been a handful.
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ALO123 - "Bringing up the rear with grace" what a nice thing to say especially coming from someone who has walked the walk. I put on a happy face for most of the world, but you guys have seen the real me and I will be the first to admit I have not always been doing this gracefully.
CATHERINE - Thanks for the laugh out loud start to my day. Chemo Overacheivers. That's hoot, especially to those who know me well. I am kind of a perfectionistica overacheivers in a lot of ways. My DH thought that was a riot, he said "Boy did she peg you!" Seriously though I would rather be done. All the delays due to illness, hopital stays and bad SEs from the taxotere still make me angry when I realize I COULD BE DONE!
JESS AND KMMD-Thanks for the cheers and the toast. It is really nice and I am extremely grateful to know that you are still here.
HOLTBOLT - Celebrate big time! I agree with you the first birthday after dx does seem like something special. HAPPY BIRTHDAY tomorrow and many more. I love your gift list and I too would share if I had any of that stuff left....
KATHY - Thanks for thinking of me yesterday. One more down and 3 to go!!!
PHYLLIS - So how does it feel to be bringing up the rear with grace? Glad to hear this tx was a little better. June 12th is your last one right? Really sad to hear about 14 yr. old with cancer. Did you guys hear about the 8 year old with BC on the news recently? I have a 4 year old student whose sister had brain cancer last year at 6 and a little boy in the 3 year old class across the hall from me has been doing chemo most of this school year right along with me. I am beginning to think there has to be something in the environment causing all this cancer. Have also had other young children in our church who we have been praying for with cancer. What kind of research is being one on that? Think I will look it up. A cure would be great but I cause would be nice too don't ya think.
NANCY - How far out are you from your last tx? Just trying to prepare myself for when all the SEs do NOT go away immediately after last tx. I had tx #4 yesterday. Worked from 8:30 to 1:30 went for tx until 5 came home and crashed until 8 and woke up in horrible pain from the waist down. I did take one of the new painkillers he gave me and it worked great. When I finally got back to sleep I slept all night without waking up once from the pain and I am still pain free this a.m. Not sure whether to take another one before my afternoon class as I am afraid of driving and other things like...functioning lol. Maybe I will wait until I get home unless the paid in unbearable before I leave the house...Sorry thinking through my fingers now.
Yesterday was my last tx while still in school so maybe my legs won't feel so bad after the next three since I would be standing on my feet all day before tx. I can hope at least. That little glimmer of hope will help me go to tx next week without having to be pushed from behind. My sister is coming from New Hampshire to go to my next tx since DH will be finally working at his new job and will not be able to go. My sister has been such a source of support through this whole thing. I get cards in the mail from her three times a week. She is an oncology nurse and I think my dx hit her as hard as it did me (even though she is older than me and has escaped the breast so far). I think even though she has not walked in our shoes, she understands more than most what we are going through.
KIM - So sorry to hear your job is being eliminated. That is just not fair. You should not have to deal with that right now. When things come up like they will I think Oh come on I have CANCER isn't that enough..PLEASE do not give me anymore to handle right now...How long have you been in your present job? I will put you on the hope you find a new and better position for next year prayer list. Good luck.
KT57 - Thanks for thinking of me yesterday. 6 down 3 to go!! Next 3 are gonna costs me some $ as my insurance changes the first of June. Anyone know what a chemo tx costs? I have no idea as thank the lord all mine have been fully covered up until now.
Well time to crawl up stairs to the shower and get ready for my LAST DAY OF SCHOOL -
and
...I have mixed emotions.
Take care. Love you all.
Patti
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Holtbolt- HAPPY BIRTHDAY! sorry, don't have any hair or lashes to spare. LOL I have like 3 hairs on my brows. No lashes. I hope you have a great day.
BerkleyKim- I'm also sorry to hear about your job loss. Its tough finding employment anywhere. Our employment in Ohio is over 10%. My brother is losing his job in the next couple of months.
jrgolomb- I hope your legs are feeling better. My legs actually didn't bother me this time around. I wonder if it was because my dose was lowered. One less thing I had to worry about this week. The fatigue is really getting to me.I'm just not sleeping well.
eadsla- I don't know about being a chemo achiever, but thanks for saying that. It made me laugh. The taxoteres been very rough on me. I wish i didn't have to have the 4th one but I will get through it.
KT57- Are you on taxotere? It costs $11,000 for each treatment, but thank God my insurance has covered it. My bill through all this is at least $200,000. I can't imagine having to come up with the money just to get well. hang in there. There will be help out there for you.
everyone have a great weekend.
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