Calling all TNs
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Good Evening Ladies
Not so good today. I think that darn taxol is catching up with me. Aching joints, headaches, numbness in the side of my hand and general fatigue, mouth ulcers as big as rocks, furred up tongue and blocked and runny nose. So ugh. On top of that I woke up with a boil or cyst lump of some sort on a very private part so a trip to the doc's was in order. The only trouble was our doctors were on duty and none of those doc's there have ever seen my anatomy before. Anyway I grabbed my daughter to come with me cause old fellar was out (probably buying brazil nuts) and off we went. Needn't have worried, so professional, and had a good laugh with the nurses and staff as a bonus. But I am on antibiotics now so hopefully they will go with the other crap I am taking. Even took a nap this afternoon cause I didn't feel right. Anyone ever had a boil before and can advise the best way to treat one?. It's certainly uncomfortable when I sit down. Oh my God am I in a bad way or what. But thinking of you all and our dear Karen who also has troubles. Hopefully things will be better for us tomorrow. Big hugs ladies. Annie
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Christina - interesting article and I hope they find something that works soon! I hate not being able to have a "maintenance drug" or something that makes me feel a recurrence is less likely.
CS - you are hilarious! I've always said laughter is the best medicine and you truly are a comedian! I sure appreciate your positive outlook!!
I can't keep up with this thread...it is very active and I'm not on the computer that much. I do go back through the posts occasionally and wanted to let you know I'm thinking of you ladies and hope everything is going well.
Yesterday was my last day of work for the summer and for the first time in 12 years I will have a summer off (I recently got a job in a school district). Woohoo! Yesterday was also 1 year from my diagnosis so I'm going to relax and enjoy myself this summer instead of going through treatments like last summer.
For all of you going through treatments...hang in there! I didn't think I would ever get through them but I'm living proof that it can be done and a year later I'm very happy and healthy
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CS - I too had a boil under my arm and it was painful. This was about a year and a half ago and we had quite a discussion on this thread about home remedies, black oil, etc. I wasn't alone. I ended up on antibiotics and used boiled water with epson salt compresses. The big bandages taped under my arm were a lovely site when I went to a work formal gala (wore a shawl to cover it). Hang in there...
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That sucks CS.... hope you feel better really soon. And still you made me laugh

Positive vibes and hugs to all of you, whether you be feeling OK or crappy - thoughts with you all.
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live-laugh- I too just got a job (March) with the local elementary school as a paraprofessional in the special ed-life skills classroom. So, I have the summer off too! This is the first time I have had a job in 10 years! I have been a stay at home Mom for all that time. Although, I guess it really isn't time off because I have my 2 kids 24/7!!
Tazzy- Woo Hoo for finishing chemo!!
Happy Saturday ladies!!
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Thanks for your love and support. I am going to live on round the clock ativan for a couple of days.
Annie - so sorry about your boil! I hope the compress help or maybe a sitz bath?
Poor DH is so concerned about me. I hate what I put him through. He is my rock.
Wishing everyone a good weekend. -
Cocker - when I mention SE from Taxol, I completely forgot about those damn boils! All mine were in my lady bits and the nether regions. A bit hard to stick bandages there!!!! Warm compresses are the most common treatment. Warm Tea bags also work well (they are often used for sty's in the eyelid. It's an old-fashioned remedy, but they actually found out the tannic acid in tea helps, but I've forgotten why). There is another old time remedy that works well, but it's hard to find and you usually have have a pharmacist make it up for you. It is called Icthamol. It's a combination of petroleum jelly and coal tar. You put it on the boil, and cover it with an occlusive dressing (fancy word for a gauze dressing with plastic over it) . The plastic keeps heat in the area to help bring circulation to the area. This stuff is old school, but works really well. Rest up my little friend, and I hope you feel better soon. (sorry, I'm also laughing here because I'm remebering having to bend over and spread em, for my first round of boils)
L-L-L Nice to see you, enjoy your vacation
Tifj - * thumps TIFJ on the head*. You've been working all along!!!!
OBXK - sending hugs and good thoughts. -
OBXK- I'm so sorry your having a rough time. I am keeping my fingers, toes, evrything crossed that the high calcium is nothing.
Kathyrnn- You and I know (well, all women) know this, but trying to convince a man is another thing!! My husband was excited I got a job, but now wonders why the house isn't always perfectly clean and why dinner is just thrown together each night. Men are kind of dumb!!
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Tifj - Amen!!!!
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I totally lost track of this thread. Just wanted to jump in here as I'm at the beginning of my journey. Starting ACT on June 19th and getting my port on Monday. Think I'd like to camp out here on this thread for the duration. Nice mixture of conversation going on here. Hope to get to know you all a bit.
Sally
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Good Morning Ladies
Well I'm still here complete with boil. When I found the lump in the middle of the night my eyes were instantly wide open. I must have looked like a possum in headlights. Panic panic, sweat sweat. I nudged the old fellar awake (very hard). He said wot, wot wotsamater. I said I've got cancer down there! he said down where, so I said you know down there, he said tell me about it in the morning. Fat lot of good he was. Hell this could have been life threatening and he wants to know in the morning!!. I'm thinking of trading him in for two 30 yr olds.
Well the doc gave me some magnesium sulfate paste to put on it but like Kathrynn says its hard to get a bandage down there and it keeps coming off and I feel like I am walking funny so everyone will know!! lol.
I feel better today but I'm not sure I will make the 12 taxol cause me fingers feel funny and numb.
Sugar - boils may only be little but they pack quite a painful punch. That would have been sore under your arm and I have to sit down very gingerly.
Kathrynn - what do you mean ALL of yours were in your "lady Bits" (just love that). Panic panic, how many of the friggin things do we get.
OBXK - your dear hubby will understand what you are going through and "your Rock' will be there for you every step of the way as you would him and just as we will be for you. We are all as one through this battle, through the good and bad days and the tears. That is the only thing that is good about cancer it brings people together in so many ways just when we need a helping hand or a sympathetic ear even though we have never met. Your hubby and your dear son's will help you through this time and hopefully tomorrow may be brighter for you. Just hang in there you can get through these horrible days. Thinking of you heaps and sending lots of love.
Tifj - I have just heard my dear feller turn on the vaccuum cleaner. Wonders will never cease to happen. Just tell your dear fellar that you work, he works, so you are both responsible for cleaning and that he can throw together something for dinner just as well as you can. Remind him that marriage is a partnership so he'd better do his share or you will get Annie on to him.
Clowngirl - welcome back. We have been wondering where you were. Hope everything is going ok for you. We would just love it if you camp out on here with us, wouldn't have it any other way.
Oh well girls, what did I say about marriage being a partnership, better go and make sure the old fellar is making a good job of the vaccumming. (You thought I was going to say help him didn't you lol).
Have a good day. Thinking of you all and sending lots of love. Annie.
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Annie hope that boil gets better - sounds painful!
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And of course she just had to add a bit more!
I have just gone to have my shower and I found out that the dear fellar had left the hard backing bit of the plaster on as well as the plaster. No friggin wonder I can't pee properly or sit down. I told him and he had this funny (woops) look on his face then he said, well I didn't know did I. duh!. Some mothers do have em. I'm sure he was dropped on his head as a baby. Whenever he leaves sugar out of my coffee by mistake I always accuse him of trying to kill me. Oh well ladies keep laughing. Annie
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CS- Hope you feel better soon. I had numbness in my fingers and toes during Taxol but it all went away soon after the last one.
Well…. Went to the doctor today because of an itchy rash that started on my shoulder (cancer side) and now spreading. Immediately thought "skin mets", googled a bit on it so of course I was in panic mode this morning
. Turns out I have shingles. So 7 days of antiviral and anti-itch cream.Wishing everyone a good weekend! Hugs.
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Clown - we'll be here, holding your hand.
Annie - your poor old dear! Pestering him in the middle of the night, complaining about his plaster job - and then he runs the sweeper! Sounds like a keeper! Glad your feeling better.
Babs - how horrible! I hope they run their course quickly.
Gave the 5 pound pooch a trim and bath - still have all my fingers! -
Annie, with you posting, we will always be laughing. Never had a boil but they sound really painful. Have you tried sitting on a rubber ring so that the actual boil is not touching anything? Just a thought !?
I also have numbness and tingling on Taxotere - pleased to hear it goes soon after last treatment.
Babs... hope you get better soon too.
Peace and Love to you all xx
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Annie- I may complain about my "dear fellar", but I do have a great one so I shouldn't complain too much and he does help out when I ask, but i do have to ask. Hope your friend "down there" goes away soon!!
Tazzy- My numbness stopped not too long after the last taxotere, but I do still have an occasional tingle on the soles of my feet, on the left side of my tongue and mouth and on the palms of my hands. Nothing painful, just a little tingle that lasts a very short time.
Babs-sorry to hear about the shingles, but I'd take that over skin mets any day!! I wish you a speedy recovery!
Clowngirl- we are here to help- stick around!!
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Clowngirl - welcome back. We were starting to worry about you.
Cocker - I had about 6 of the wee bastards, but I thought it was related to the fact that I had cystular acne until my 30's. (had cystular acne, cyst on my ovary and fibrocystic breasts. I'm sensing a theme here). I can say one good thing for chemo. About 5 years ago I started developing syringomas all around my eyes (yes, they are a form of lumpy cyst, lol). When I started to look like a Klingon, I went to a plastic surgeon, but nothing they could do. They are still there after the chemo, but they are much flatter and less noticeable. Yay chemo, for at least one good thing!!
Babs - take care of yourself and get plenty of rest. Shingles can be nasty.
Tazzy - may all SE disappear quickly!
OBXK - don't worry, pooch is busy plotting revenge. -
Hi!
I was just wondering out loud today while I was at work how the H*** did I make it through chemo, surgery, infections, radiation, (boils!)? Thinking of all that are in treatment. It is such a whirlwind that seems like it won't end, and I am so thankful mine did end(hopefully for awhile at least, a long while), and so sad that it has been non ending for many. Y'all probably don't even remember me! This thread moves so fast. Remember, I am the crazy one who posted very long posts while doing chemo in the hospital!
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I remember you Bak94 because I remember the goats but you haven't posted for a while. Good to see you are back. I think I must be the crazy one because I'm not in the hospital and I do long posts, at least you had a good excuse. Hopefully your whirlwind will stay away from you for a long long time never to return. Hope you will stay with us this time. Annie.
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Hi can I jump in? Realizing we were probably on very similar meds and stuff, so probably similar lingering side effects too? I have an extreme photo sensitivity since chemo. My hands are very sensitive to hot water as well....weird?
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Hi Gina welcome. You don't say what treatment you are having but I am on taxol but if you aren't on that the other ladies on this thread will be along soon to welcome you and they may be able to help. Don't go away they won't be long. Annie
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Welcome Gina!
Bak...nice to see you "bak" on the thread.
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BAK - Good to see you. I hope you've beaten back the beast for good!
Kathy - LOL
For those of you on taxanes - if the numbness and pins and needles get too bad, see if they will put you on Neurotin. It helped me with the zingers! I never fully recovered feeling on the last three toes on my left foot. Boy you don't realize how important those piggies are to balance, until they are numb. But my brain learned. I still have numbness from treatment a year ago and sometimes it feels like someone is pouring ice cold water down my legs.
There is some kind of hand and foot syndrome that can happen, they get very red and start peeling. Try using your elbow to test temps, to avoid hurting your self.
Annie - do you have a donut to sit on? I know it must be horribly uncomfortable. Speedy recovery wishes.
I am happy to report I am feeling better this morning! Thanks for the good thoughts and wishes - they worked!
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Bak - so nice to see you!
Sugar - *gigglesnort*.
Welcome Gina, jump right in, tis a lovely group. Neuropathy show in many different ways, so I would guess the problem with hot water is one of the variations.
OBXK - I'm on Neurontin also. Hasn't solved the problem, but it at least as toned it down. (there was a point during treatment where my feet felt like I was walking on hot, broken glass)
Off to install two new ceiling fans with roomie. I'm starting to love that man, lol -
Cocker - this is especially for you. I'm still laughing from your line, "You thought I was going to say help him didn't you lol).". I think I have told the other ladies this before, but your comment made me think of it.
In many ways I was a horrible wife, lol. When we first got married, we had a big debate about how toilet paper should be hung. (I'm an over the top, hubby was insistent it was from the bottom). I thought about it for a few minutes, and then told hubby, "I've got a deal for you, whoever changes the roll, gets to have it the way they want". (knew hubby had some control issues, lol). I swear, I didn't have to change the roll more than 10 times in 20 years, heheheheheheeh. Probably cost me some money (would hear him furiously using up the end of the roll), but I never once had to plop my butt on the toilet, and find an empty roll. Bad wife.....very bad wife!!!!! *big old evil grin* -
Been out of the loop for a few days while I went to my consult in NC w/Dr Carey.
All in all it was worth the trip. She is wonderful, UNC is a great facility. However, she had no real earth shattering news for me about what I should do about my TNBC and this local recurrance. She said absolutely surgery, which I've done, absolutely radiation, which I'm starting hopefully next week, and she also suggested an anti hormonal since this recurrence is 1% ER+ as opposed to last time's 0%. She says any positive is a positive. And then her last thought - more chemo.She recommended FCM and/or TC, but said there is no data to prove it would help in my situation, a local recurrance after having done AC/Taxol. She said the AC/Taxol could have partially worked, no way to tell, but it is the strongest chemo out there and I can't do it again. So basically the decision to do more chemo is up to me because there's no data to help me out either way.
Great. If she would have said for sure it would help I'd consider it, but putting myself through 3-6 months of more hell for something that might not help and is sure to make me feel worse... I am thinking not.
She did stress that this does look pretty local, and if it would have metastisized she'd expect it to be on a similar schedule as the breast lump and should have shown up in the PET. So we are cautiously optimistic about that.
Metformin - she says the jury's still out, but if I want to take it, fine.
Last thing - Flying and the TSA. I did NOT want to go through the scanner since I'm about to get 35 doses of radiation and now have only half a breast. I told them I didn't want to go through so they gave me a pat down. While I was being patted down I told her I'd just had surgery, be careful, and she said next time just tell them I want to opt out because I had surgery and couldn't lift my arm. Which is only half true. But on the way back I tried it, and sure enough, they just had me go through the metal detector instead, no pat down, that was it! So keep that one in your back pocket next time you fly.
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Minxie - I wish you had been given better news. I hate to have things put into my hands. I don't think I could do more chemo, unless they really wanted me to have it. Thanks for the TSA tip, I'm sure it will be of use to some here.
Kathy - when my neuropathy was causing me foot pain, they added an old antidepressant - I think it was nortriptoline (sp?) but it made me horribly depressed.
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Morning Ladies,
Man this thread moves fast!! I'm sure I'll forget somebody.
Welcome back BAK - was starting to worry about you.
Karen - I'm so sorry, big hugs
Babs - hoping your singles clears up ASAP
CS - hoping the same for your boils. I too, developed a lovely one in my girly bits too. As if the entire situation isn't bad enough Chemo has to throw that one at us too. I know we've moved on from the Physic conversation but wanted add my two cents. I'm not for finding out my future anymore but after my mom died I REALLY wanted to find a reputable phyic to "contact" my mom. I needed closure. I still do, but I think I'll always be on the fence as to whether or not its real.
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