August 2013 Chemo Sisters
Comments
-
Lisa, wear a mask, theaters for filthy!
-
ForMG, that was great. I claim that for myself, since you so kindly included all of us.
I just wanted to say that it is no coincidence that God led all of us to this particular site. Why else would every member be in tune with God's will for our lives. Why else would I have clicked on chemo, before, during, and after? It was not a coincidence. It was for me to be able to talk about my God in a forum in which others are of the same mind. How great is that. We're all going to beat this. Take care. I'll try not to hog the boards today. I'm good at that, but just wait until I have my next round of steroids!!! I'll type your ears off. I'm not cleaning house today because I know that every three weeks, after my steroids, I'll spring clean every last inch of it. God bless those doing chemo today and those with side effects that are unpleasant.
-
Hello Ladies,
I am heading out in an hour for my second infusion of TC. As many of you know I had every SE possible. I am going in positive that this chemo treatment will be different with fewer side effects. I have done a few things different for myself this time to see if that helps. Like I will be floating into chemo. I drank so much water this time. I hope it doesn't make me sick. I am going to take pre meds before things start to hit to see if I can be ahead of the curve. It seems like for me it is hard to play catchup. I had three different nausea meds until we found one that worked. I can do this and will do it!! Hugs to everyone!! -
Sharon - my thoughts exactly about all of you and this board being a gift from God. I've had such incredible love and support from all my friends at church - it's just a double blessing to find the same love, support and recognition of God's power here, too!
How's this for a verse for today: God has said, Never will I leave you; never will I forsake you. So we say with confidence, the Lord is my helper. I will not be afraid. Heb. 13:5-6.
(By the way, after I read your post about steroids and cleaning house to my husband, he said I should see if I can get a double dose....)
-
Julie: The blog I visited at Caring Bridge at the address you gave is the one from 2011. Is there a more current one?
Ok so much for no SEs; the bad mouth taste came back. What helps me with this is sugarless gum and sugarless candy. At least last time it went away about 6 days before the next infusion. Bleh. -
Saltjack, Tell your husband he sounds like mine. Tell him to go play golf.
Good Luck today, togetherness. I don't think the water will make you sick. I think you'd be sicker without it. I felt normal after my infusion Monday until I ate some fat. DO NOT EAT FAT for a few days.
QUESTION: My MO said that I shouldn't sub the first week after chemo, but what about the immune system being at its lowest from days 7-10? I will ask when I go in, but I'm scheduled to sub next Thursday, which is my 10th day. What are your MOs saying? Also, a biggie. My 50th class reunion is 5 days after my 3rd infusion. Would I be able to go with a mask or something and just not eat the buffet? I haven't seen some of these people for probably 50 years. I hate to miss it altogether.
-
Sharonanne: About subbing and your reunion, follow your MOs advice because he knows you, your treatment plan and your overall health status better than we do. Ask him every single exacting question you can think of, that's what he gets the big bucks for! Also ask the onco nurses because they will know and if not will ask the doc. Just guessing here but I expect a lot would depend on your cell counts whenever you want to do something.
-
Lisa, that sounds like good advice. I will see what my counts are on the Monday before. I have to go this coming Monday for bloodwork. Hope everything is coming back up. I feel like the bloodcount will be back up, at least somewhat, since I feel so good today. I wonder how effective a mask is on the 5th day from chemo. I would hate to have to wear it, but will if my MO says I can go that way. I definitely will heed his advice.
-
Saltyjack, great verse for today! I have not been a religious person most of my life, but I am spiritual in my own way. However I have had so many signs since the day of my biopsy (too many to list and explain, but I definitely believe they are signs), that it tells me it's time to make some changes. I have two local churches that I am going to check out, my only challenge is timing. We are away this weekend, next weekend will be likely SE from first round of chemo, following weekend = neutropenia, so probably looking at 9/22 at the earliest. And then the cycle starts again.
I am reading everyone's posts, too many to keep up with! Welcome to the newest joiners, we are sorry to have you need to join us but we welcome you with open arms!
Martha
-
There seems to be more ILC gals here than I thought the debate about alcohol and aggressivness here is a link about it.
http://www.cap.org/apps/docs/reference/myBiopsy/BreastInvasiveLobularCarcinoma.pdf
Formygranddaughter: My mom doesn't know why i am having a BMX either and I've told her the same thing that because its that sneaky I'm not leaving any breast tissue on me. -
Martha, I believe our walk with the Lord is individual and in its time. I have been a believer since age 9, but a spiritual worshiper since my late 20's. I was fortunate enough to have a grandmother who dragged me to every church service, revival, Girl's Auxiliary meeting, Sunday school, and Bible School in our community. She was a great roll model. On the day I had the biopsy, I walked out of the hospital along with a younger woman (everyone is younger than I am). We began to talk. She asked me if I were visiting and I told her I had just had a biopsy for breast cancer. She threw up her hands and said that she was a two time cancer survivor-ovarian and breast. She was still in treatment. She told me the names of her surgeon and MO and sang their praises. We connected in a spiritual way and left one another that day with phone numbers. The next day, while searching for things to make hats in Walmart, a woman came around the end of an aisle who had a cap on. I said, "Are you wearing that cap because you have cancer?" She and I talked for about 20 minutes, talking about how she was doing well and how we both thought God had literally bumped me into her. She told me her surgeon and MO, who were identical to the ones the other woman had told me about. I already had the name of the same two doctors from a friend who had them. The third time a confirmation that I was making the right choice was when my best life friend's mother, who asked me who I had chosen. When I told her, she screamed into the phone that they were the very best and that she was so glad I was having them. There were others who had had the same doctors, but after three, I figured I was in the right place. Then, as I was being sedated for surgery, my MO bent over my bed and said, "God bless you." I knew right then that I was in the hands of God and could be in no better place. I am blessed. I believe the Bible where it says that if we seek, we will find. Seek his face daily and he will acknowledge you and guide your way. I'm not telling anyone on this thread anything new. Just reconfirming my convictions.
-
welcome to you Salty Jack. I just joined a few days ago so I think you are the only after me...but wow how do you all do such a great job of keeping up with all the new members?! Salty my in-laws live in Conroe right by the woodlands. I have been down your way many times! My father-in-law is getting chemo down there for kidney cancer. He was diagnosed about a month before me. I still think God used his situation to cause me to think about this weird lump I noticed. I have never been one to self examine for lumps and for some reason the night they told us he had cancer I found this weird lump. I think I wouldn't have given it a second thought except for the fact that they had just told us he had cancer.
Cutiekool- I can relate to your germ fear. Anyone ever watch the tv show Monk...boy do I feel like him! Especially now that I was told my white blood counts are so low. I am hoping they are coming up but unfortunately because of the holiday I can't find out until Tuesday if they are.
Sharon-loved your comment about the steroids and going to be online all the time. When is your next chemo? I am guessing I will be going crazy when I get on the steroids so after I am done cleaning the house and garage we'll have to hog the board together. :-)
Rayna-that was a good question about how to clean our bald heads. I see some have already answered and look forward to seeing what others have to say.
Formygranddaughter and Togetherness. I will be praying for you today and anyone else who I missed that is geting chemo today.
Martha-I would encourage you to seek a church. I believe God allows things into our lives to call us to him.
I can't remember who wrote the "verse for today" but I do love hearing God's word so thanks for posting that.
-
Togetherness: Good luck with chemo today. I think if you have drank as much water as you say and are ahead of the game with the meds you may find this time around alot better than the first. The second was better for me than the first.
Love, Rayna -
Hi all,
I'm having a major side effect that no one else seems to have. I just had my second treatment, and by day three for each of them I start getting these full torso charliehorses, like a giant cramp on the outside of my ribs, sometimes one side or sometimes both. My MO asked if I thought it had to do with the Compazine and I said I didn't think so, because I've been taking that since Tuesday and the cramps didn't start til Thursday, plus I hadn't taken one yet today when the cramp hit. I know from last time that I need to nip it in the bud medicinally because otherwise I'll be totally clenched and cramping all day otherwise and it hurts like hell.
I took a muscle relaxant and then sent an email to my Dr.s office about it, saying it's the same as last time and then the headache from hell hit. It doesn't seem related to taking anything, but could it be related to one of the meds from the infusion wearing off? That's more what it seems like with the timing. I haven't heard back from him, I'm hoping someone has a clue what this is. When it's not cramping up it feels like it's about to, like a huge dragon's claw around my torso, poised to start squeezing.
Does anyone else have this SE?
-
Beeve - that's an interesting SE! I have a similar one.. I have restless legs syndrome (mostly at night), and as soon a my infusion started, my legs went nuts! It was all I could do to sit still. They were still bad when I was home on th couch. Not sure what the deal is.
-
Beeve Does it feel like your throat is swelling too? That happened to me and I think it was an allergic reaction to the antibiotic I was on. I haven't had what you are describing but its a good thing you have got a message to your doctor, it sounds horrible, I'm so sorry you are having to deal with this. I hope you get some answers soon.
Love, Rayna -
Mankatostate, When I had those steroids the day before my first infusion Monday, I hogged the boards to the point of embarrassment. I cleaned everything in sight, cooked, typed, you name it. I didn't feel like I was hyper, but when my DH came in, he just laughed at that statement. He said I didn't stop talking for 4 days. I have over 2 weeks before I take it again, so maybe others will have a chance to talk before the day we hog the boards. I'm going to look up sites on youtube to see how to tie headscarves. I look like a dork when I put one on, so I need help if I don't intend to wear my wig every day.
-
Hello girls !! I have been reading a lot of this group, you help a lot really !!
Today is my first chemo TC x 4 and i am really freaked out !!! i have been drinking a lot of water but nothing else apart from that !
Should i buy icecream ? i live in chile and some of your words i do not understand, what is popsicle ? should i paint my nails ?
Thanksssss !!!
-
Wow! We are a chatty lot...I couldn't believe how many pages have gone by since I last looked.
ForMyGD- I'm a bit like you. I'm very reluctant to take drugs I don't need to. I don't seem to have been given any where near the amount that most of you US women are getting. I had steroids for 3 days - no high energy rush. Anti vomiting medication for 3 days and then one to take if I needed to. I did feel nauseous but coped without taking it. I have not been offered Neulasta but maybe that will be for the T side of my FEC-T treatment which I'm not up to yet.
No one told me to take anything for constipation but I did take Coloxyl (senna) from day one gradually increasing then reducing it after the Big Relief.
My big problem I have now has been to do with the port I think. It was excruciatingly painful for at least 5 days and is still painful. I took only panadol for it as for some reason, I'd been told no ibuprofen, which no one has been able to give me the reason for. What has happened is because I didn't want to pull the tissue around the port with every step I take , I hunched over and often had my arm up supporting my breast ( this is with a bra on too). I now have done something to a muscle in my neck/ shoulder area which is very painful. Constant burning. Again I can't take ibuprofen . Have tried topical cream which is ok but limited. Scared about putting my liver to the extra work of lots of panadol. Last night I cried from the pain, it's starting to wear me down . My husband was furious with me for not going to the GP about it, but the effort of that just seemed too much so now I'll have to wait till Monday.
On a positive note - my kiwi cut isn't quite as kiwi as I thought it would be, because the poor girl was really reluctant to do it. I think she tought I'd complain if I was unhappy about the cut, no matter that I said it will probably all be gone by next Friday anyway. So I have a Miley Cyrus style cut. A number 8 at sides and back , and longish on top. At the sides and back it's my natural grayish and on top there is still some blonde from last color . So it actually looks pretty trendy, although very short. Went straight to the supermarket afterwards without a hat on and was looked at a little bit but largely ignored...so very ok with it. My daughter came with me and she thought it was a hoot. Pity it probably won't last the week. I'm not sure if I'll over it for school next week. I don't want to absentmindedly scratch my head and for it to come out in front of the kids.
Next week, we are having people from the Muslim and Jewish communities coming to speak to the kids...it will be funny if all 3 of us are in head scarves : ) -
Welcome Floruchag!
Where I come from a Popsicle is frozen ice on a stick, usually fruit or lemonade flavored. High in sugar but less fatty and more watery than ice cream. Good for fluids and sore mouths.
Yes paint your nails! Nothing to lose by doing it. And it is fun. You've reminded me to go shopping for some nail varnish today.
Don't be afraid ! The advice to drink is really good. The only thing for me was I was up and down to the toilet 4 x during chemo.
Carol, how are doing? Hope all is well! -
P.S. in case you are wondering, there is nothing in Miley Cyrus' more recent activity that I would care to imitate...well, with a 50 year old, balding, not exactly pert, woman, the effect might be quite different! Where is that girl's dignity?.............at the bank, I guess.
-
Beeve, that sounds like a serious side effect that should be dealt with pretty quickly. I'd be at the doctor's office insisting that they figure out what is going on. Is it just on the outside of your ribs or does it feel internal as well e.g. Heart?
-
Hi ladies, doing really good after 2nd infusion yesterday, sitting in MO office to get my Neulasta shot and head out for our 3 hour drive home, I hope the shot agrees better with me tis time. Welcome to our new ladies and I will read all the info later, a little hard when on the road. I am praying for minimal SE'S for all of us having or had Tx this week.
Hug's Shary🇺🇸 -
Beeve I wonder if I had something simular? I had a cramping in my left rib area. It would cramp for a few minutes on and off. It was the worst during day 3-5 and mostly when I was lying down. I am on compazine and for some reason (idk why) I wondered if that might be the cause. Haven't had that issue for days now.
-
Beeve: Can you call the doc's office? Maybe it's a carboplatin SE since it seems like a lot of us are on Taxotere/Cytoxan or an Adriamycin combo. Seems like you should talk to the MO or the staff immediately!
Gashgold: Please tell your MO about your port right away! That is serious sounding and please talk to an MD! And wow that Miley Cyrus is totally crazy, isn't she? I cannot believe how trashy she is, it even shocked her peers at the VMAs. Ugh Gashgold hope your fellow New Zealanders don't judge all us Yanks by her behavior.
Welcome to our group Floruchag! Yup Popsicles are flavored ice on a stick. We're here all the time so any question you have ask away! -
Welcome Floruchag...I find it fun that we have women from all over the world here in our group! I wish it was ice cream...I love ice cream but maybe would ice water be better words??? I am afraid to try ice cream right now and get sick. While I was pregnant I had one two many dairy queen blizzards and now can't stand the sight of one. So my goal is to avoid ice cream to no make a negative association with it. I will then reward my self with some when this is all over.
-
Gashgold, I agree with Lisa. I don't have a port, but I've read that you need to report any pain that is like that. I'll be praying for you more tonight and so will others. That sounds serious.
In order to keep up with everyone, I put tabs on a notbook with everyone's name so I can flip to it. Now that's serious business, isn't it?
-
I just returned from my 2nd infusion. My blood count was excellent + the treatment flowed easily without complications.
I removed nail polish this morning. I noticed that 4 of my nails are getting dark near the cuticles. I spoke to the nurse, she said it's a side effect of chemo and the dark nails will eventually grow off as the nail grows. She said I could use nail polish. I also noticed that a few of my veins are becoming "chemo veins" and are also getting darker; this they say, too, will return to normal after chemo ends.
My friend + I had a good time during treatment. We did not open The Four Agreements book nor did we write any poetry. We just sat, talked, laughed then talked and laughed some more. She fell asleep on me so I let her nap for about 45 minutes.
beeve, did you have a Neulasta shot? If so, could that be the source of the charlie horse?
I'm going to sit in the recliner, watch a little TV and hopefully fall asleep.
Peace + blessings to everyone!
-
Hello, August Ladies! I am from the January group just stopping in to wish you all well...reading your posts reminds me of all that I went through with my 'chemo sisters' and I'm happy to say we have all made it through chemo! I finished radiation (EASY) in May and just had my implant exchange (EASY, too!) and am just happy living life now with all of this behind me. Before you know it, it will seem like a distant memory to you as well...I just wanted to say hang in there, you've got this, and you will soon be on the 'other side'. Hugs to you all!
-
Hello Ladies,
Returned from my second treatment. The tweaks we made to the drip did not help with the migraine that I get during the infusion and for the seven days afterwards. Which in return causes naseau. They gave me two scripts for pain meds that I willingly took this time because of the migrane. I can only be so strong and do not need to suffer. I will go in the hospital this time for fluids for dehydration as well if they recommend it like they did last time. Instead of going in everyday to the center for fluids. The pain meds knocked me out so I maybe sleeping for the next three weeks until next treatment .... Lol. That might not be a bad thing. One new SE that I am having that I didn't have last time is it feels like they did a tonsilectomy on me. I have a sore throat. Any recommendations to alieve that would be greatly appreciated. Hugs to you all!!
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team