Starting chemo Sept 05
Comments
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Welcome Candi and PSA. So sorry that you needed to find us, but this is a wonderful group of people!
As to hair, as you will read, we have all had surprising ways to deal with the short hair loss. Vacuuming, cat hair removers, cat clippers, and electric razors. Personally, I think the vacuum idea is the most creative.
I am on Day 3 of my third A/C round, and fatigue and low grade nausea are an issue this time around. Plus, my anticipated decadron energy rush isn't kicking in. I had so many magazines to organize and my pantry needs attention. This was the only good thing about breast cancer... getting my house organized. And now, I am not even getting that side benefit!
But enough kvetching, my daughter is home for her October break and this time she brought her roommate with her. Too bad they are seeing me during the 'down' week, but they have a bunch of things to see and do. Her roommate is from Alaska, so Boston is a totally new and different place. She is enjoying the exploration.
Hope everyone else is doing well.
*susan*
a decadron-inspired posting -
OMG...gone for three days and 85 posts to read...
What a week....I just spent three days in the hospital because I started running a fever Tuesday morning...My counts are back up now due to way to many shots/antibiotics ect....I sure hope I don't have to do that again! Quarantine in the hosptial sucks!
Talk to you all tomorrow...
Tina -
Hi all, Sorry have not been on here for a while, am tring to deal with my elderly father. Took him to nephrologist for second time yesterday.
He has Multiple Myeloma and now the Dr says his kidney function is only 10%! That is off the charts low. It is either dialysis or death in 2-3 months, the Dr laid the truth out to him in a good way. The Dr also said if it was his dad, he would not send him to dialysis, the problem is that the Mult Myeloma cells will continue to make toxic proteins to clog his kidneys as well as cause other problems so all that dialysis might buy him some time but who knows how much time. Maybe a year at the most.
So my dad has to make a decision. A hard one. I drove back home yesterday crying though I know I can handle ANYTHING after this hard chemo. Dad is 81 and I would not blame him either way he decided, hospice or dialysis.
Everything seems to hit me at once. But today i know i can get thru it all. God always helps me and I have no doubt HE will be with me helping me again. It is just sad. -
Hey, I'm Glenda, new to the discussion board. Diagnosed in early july, double mast in mid July, taking AC as of 9/19 and jsut finished #2. I wonder if any of you have had the reaction to AC that is pain in the heart on injection with subsequent pain (squeezing, sharp pain) on rest for days after? My onc seemed puzzled, nurses never heard of it or blow me off. I'm concerned -- your thoughts? g. Also, I'm using my partner's log in (elleen) hence the name change in case that's confusing.
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Pat,
My answer to the hair removal issue (what was not being handled by the chgemo) was to get a good friend to do the electric razor shave. I hope you found someone to help you. -
Bubbles,
I am so sorry about your Dad! This is so hard!..chemo or not!....
Pegk,
thanks for the chuckle...
Welcome to all the new ladies on board!!
Looks like the candy of the day for me is now TUMS of all things. I had to fast yesterday for my PET scan and that was horrible, I had such heartburn, I didn't know what to do and it sticks to me now...yuck
I don't know any results yet but thank you for thinking of me. Hanging and waiting and praying!
Looks like my appetite for hardy food has weaned, I am actually sick of eating (never thought I'd say that ) but I need to eat anyway. I just made a "spice cake" by Duncan Hines (I hate that stuff actually) but it looked so good on the shelf. Chemo has my brain morphed....I just noticed that all the bills that I paid at the end of Sept. where dated at for the end of October, I am so embarrassed, I hope the checks will be cashed..aarrgghh...what's next?
Monday (day before treatment # 2)I will get my long hair cut and buzzed by a friend. Her financee is bald and we have a contest who will be prettier I hope I "win"....She will be using 'his' clippers to get me bald, ha!
Hope everybody is continue to do great!
God Bless -
Ellen,
I noticed palpitations and occassional chest pain, I was a little worried that AC could cause this so early (I had only one chemo so far).
God Bless -
Tina,
oh my goodness! What a trial you have been through! Quarantine is awful, and well, so isolating! :-)
Clearly your plan to stay close to home is your best plan. Any word on your disability yet?
Take care... and let us know if there is anything more we can do for you.
*susan*
a decadron-inspired posting -
Dear Barb,
A virtual hug to you {{{{{{{{{{{{{{}}}}}}}}}}}}}}}. I know how hard it was for you to give up the daily care of your Dad. And now this setback.
May you and your Dad find the strength to make the decision that makes you both comfortable. Either way, know that we are all sending you whatever extra strength, thoughts and prayers we can.
Take care of yourself too.
*susan*
a decadron-inspired posting -
Welcome Glenda,
I have not had this side effect, though certainly the A in the A/C is hard on the heart. Did you have a MUGA before beginning treatment? Basically, I would not like being blown off in any way.
Not sure if I have any advice to offer... just keep demanding the best care you can find.
Take care,
*susan*
a decadron-inspired posting -
Hi all
hope every one is well.
My friend has been coming over to see me and she told me yesterday that she has got the measles,now im worried im gunna get them too.
On the countdown for a/c #3 and getting nervous,trying not to think about it.
With the hair mine has come to a stand still too,I have a thick patch right on top of my head looks funny,with the vacume cleaner thing I didtn do my hair with it but after i seen it i thought i would do the cat shes a ragdoll and its spring here now so its all over the house,she didnt like it so guess i gotta do it the normal way oh well thats what i get for trying too cheat.
love to all
carol -
Bubbles
I am so sorry to hear about your dad. My mom had to go on dialysis because of renal failure and I can only imagine what you are going through. She also had conjestive heart failure which she did die from not the renal failure. When she found out about the renal failure she refused to go on dialysis (probably spelled wrong) and I had a horrible time conviencing her to take it. It wasn't a really big deal....kinda like us on chemo. Hang in there and I'll keep you and your dad in my thoughts....when it rains it pours doesn't it? After loosing my husband last year, 2 hurricanes and now this cancer I can relate to what your going though.....
Cheryl -
Good morning ladies! 3rd day after my 2nd treatment Thursday & I really feel pretty good! I'm starting to wonder if this chemo is working or not (ha ha). No headaches, no nausea (so far) and NO HAIR!!! I had an appt yesterday with my onc and to get my neulasta shot. I talked to her about my tooth problem and she said if it needs to be pulled out I should have it done 1 week before my next chemo treatment because thats when your WBC is the highest. I'm going to call my dentist Monday and talk to him. Well the veins in my left arm are gone. They tried taking blood yesterday in 3 spots and couldn't get it. They had to call another nurse in to take it from my port (2 pokes within 2 days). Boy am I glad I had that port put in!!! I asked my doctor if I was going to get anything else with the Taxotere for my last 4 treatments and she said that was all I was getting. She also said the Epirubicin, Cytoxan & Taxotere are the 3 strongest chemo drugs they use. I didn't know that. I guess my decatron is working pretty good today because I've been awake since 2am. Looking forward to my "nap".
My daughter is getting a bit bored sitting around this dinky town so she joined a gym. I didn't even think Okeechobee had a gym but they have 3!!!!
Susan - My daughter made the best smoothie for me yesterday! Bananas, pears, vanilla yogurt and frozen vanilla yogurt. She also put some kind of protein powder in it. IT WAS SUPER!!!!
Cheryl -
Hi everyone
To all the new ladies, I'm glad you found this thread, these ladies are terrific!!!
Well today is day 5 of second FEC and I feel good... tired, but good.
Sandra, I am eating for the British Isles at the moment and i'm loving it, loving it, loving it!!!
Normally, I have a small appetite, and I have always been underweight, so this increased appetite is wonderful.
Looking at the way my clothes fit me, I don't think i've put on any weight yet, but you never know, I might get up to an acceptable weight! before chemo I weighed 100lb,(7stone 2lb)
Tina,
So sorry to hear you have been to hell and back again.
hospital sucks....
Bubbles
I'm so sorry about your dad...I dont know what else to say except we are here for you.
Have a restful weekend ladies, speak to you all soon
Maxine -
HI Pat I had trouble getting anyone to buzz my hair. It was hurting just to be out in the wind and I was drowning in it every morning. Finally I took the clippers, sat in a chair, and bent forward and clipped my own hair. It took a couple retries until I got it all but boy did I feel better. Welcome to boards. Don't you love that all the smily face Icons are bald too!!!
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Tina so sorry to hear you had such a bad time. One of my fears is having to go to hospital for chemo related problems. Where was the infection? I am avoiding places where there are a lot of people, between school starting and the fall weather everyone is sniffling and coughing around here.
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Glenda and calico, The palpatations could be from the steroid Decadron. I found I was having heart palps right after my treatments and for the next few days while I was taking decadron at home. One other thing to consider is the pain in your chest could actually be heartburn. However you should definitely be questioning the heart issues. I had a MUGA test before I started and another one after my second treatment. I will find out monday if my heart function is dropping. I started at 84% heart function so it is a concern for me.
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Husband thinks he'll be able to suck it up today and get the clipping job done. I'll admit here because you all can't smell me that I haven't showered since Wed., afraid of the feeling of all my hair going down the drain. But the hair is EVERYWHERE, worse than a shedding dog. So I'm hoping today's the day.
It's interesting how my focus changes as this thing moves along: I hardly notice that my breast is gone any more. This week it's all about my hair. -
Hi y'all. My Dad is still trying to decide about dialysis, i told him today that i would take him to the center to see what they do if he wanted to to help make the decision. I have come to accept either way he wants to go on it. If he does do the dialysis, the Myeloma could end his life in a worse way then if he did not do the dialysis. He has to decide, what a hard decision.
About my hair though, like Susan said there were some longer strange strands hanging to the mother ship! But i looked like a radiation accident victim because of that hanging hair!
I got the nerve up last nite to ask my husband to use the "pet" clippers and clip it about 1/2 or 1/4 inch all over! Wow i feel much better and my scalp does not pull or hurt anymore. I slid my wig on really easily without the hair in the way.
I feel like i have "arrived" like most of you! The hair thing takes a while to accept to say the least but once we accept it, wow. He was proud to clip me (i was surprized) and vacumed up the "remainder" on the bathroom floor.
Then he told me he got me a gift, the magazine, MAMM, all about breast issues, etc. I sure appreciate him.
So i hope all of you are doing great today. Just one day at a time! And we will be thru our trials before we know it.
I am taking it easy because my back spasms started coming back again and this time i popped a bunch of Valium to head them off. Think i caught it in time....Will be resting today. Funny the spasms are the same day as the last chemo session, DAY 10. But then i remembered i carried stuff out of the truck like I did the last session around this time. So it is no surprise.
I have to remember to be careful for my back when taking those neupogen shots since I read they aggravate any inflammation you already have in your body. You be careful too, you all!
Teeth, my teeth seem more sensitive and harder to get dental floss thru than before. I am sure chemo is hard on our teeth, just look at heroin addicts or meth head's teeth. I am counting the days until my chemo is over! -
PSA...I went to the hair salon and told the woman that I wanted my hair cut short because I was fighting breast cancer and it was due to fall out soon...next thing I know I'm hearing about all these other women who have battled cancer that she knew or was related to...it truly is a small world. I am hoping to be strong enough to share this other people to help them get screened...I was at WalMart today and couldn't believe the amount of PinkStuff...t-shirts, sweatshirts, bandanas, hats, umbrellas, bags, etc...I bought a t-shirt, sweatshirt, bag, bandanas and hats...tonight I'm going out to a dinner with other horse owners and I'm wearing my pink t-shirt with jeans and my pink cowboy hat (I do still have my hair, even though it's short...I'm at day 16 from my first chemo, so I know I don't have long...and I have a pair of buzzers just waiting for me!)
Bubbles...I'm sorry to hear about your dad. My father-in-law was on dialysis for ELEVEN years...they never thought he would live that long and he lived and enjoyed life! He eventually passed away due to other problems. You might want to suggest to your father that he try it...he can always stop if it's too hard on him. I think we can all empathize with how hard it is to deal with these things...but that doesn't make it any easier.
Sandra...if the decadron helps...then use it. I think it's good to have an excuse to eat as much as we want without feeling guilty during certain times in our lives...we deserve it! Even with the decadron, I didn't have much of an appetite as nothing tasted very good for about 10 days...but I ate anyways, primarily due to the way my stomach felt.
Have a good one everyone! Janet -
I am almost looking forward to the hair cut partially because I can't stand the smell of shampoo anymore. I just ditched my old one, bought another one (did smell test at store) and washed my hair, OMG, I could run from myself...
Chemo sure does a turn on the nose...I ditched the dish soap too, my husband is NOT allowed to eat garlic, even though I loved garlic until chemo day (he said I was a hound dog in my former life ). I am at wits end with the smells, I even add lemon to my water to make the water (which is filtered and good by the way) smell better....
Sure glad when this "side effect" is over
God Bless -
My hair has stopped falling out for the most part...I actually have quite a bit left...(kind of like the very thin 80 year old..LOL)
cali- that smell thing...omg it has gotten to me tooo!
Bubbles- that is a rough decision your dad is going to have to make. I know that going through your own stuff was more then enough to deal with....you two will be in my thoughts and prayers.
***************''
Things I have learned I will be more carful with on round three....stay as far away from crowds next time...wash hands 100 times a day...LOL...even if I feel half ways ok my counts are probably in the toilet so STAY HOME>>>>>
this has been such a crazy week...even though my counts were so low..I only got a bit tired (the fever was a killer though....)
Have a great evening everyone.
Tina -
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Good morning Aussie! I've been awake since 12:30am (EST) thanks to that darn decatron. Boy that is quite the movie! I'm sitting here in tears now. We are sure STRONG aren't we?
Cheryl -
Good morning Cheryl!
It is actually about 6:30 pm EST Australia.
I hope the tears are bitter sweet (smiles through the tears = rainbows) -
Yes they are...boy sometimes I just so depressed. Friday when I was at the cancer institute I just want to cry when I see all the YOUNG people there. I'm 54 and seem like the oldest one there. I think its because we're so much more aware of these cancer things now than years ago. My daughters 35 and I'm going to be on her case BIG TIME about getting mammograms etc as soon as she gets a job when she gets back to Texas & has insurance. Cancer is such a shock when you realize you have it.
Cheryl -
Tina- Sorry to hear there have been complications--I've been looking for you on this site for 3 weeks now I think I have hit the jackpot!! We worked together for Camino Real MHMR-Please tell me I am correct!!Sent you a PM let me know how you are
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Morning All,
I am finding my third round of A/C more wearing. It isn't that I have new or worst side-effects, I am just getting tired of having to manage them. This must be the fatigue my doctor warned me about! For the first time, I find myself saying "I am going to let them do this again????"
Of course I will. I have no choice, but doesn't mean that I have to like it does it?
Tina, my hair loss has definately slowed as well. I still sit with the lint brush, but the number of hairs that stick to this tool gets less with each day.
Cheryl, keep up your spirits any way you can. I am not the right person to tell you how to do that right now though. But I can pretend! :-)
AussieMom, I haven't made it through that movie yet. I have been trying to for about 3 months, but can't get past the MRI. Isn't that odd? I have an easier time dealing with my own stuff, than watching others do it.
I feel that I haven't kept up with so many of you lately, and am sorry for that. I can only hope that my energy and optimism will return tomorrow.
One of my former employees, a wonderful young woman, is coming to visit in a bit, so I should go prepare. I origianlly hired her right out of college. She is now finishing a double master program at Indiana University, and still comes to see me when she is in town for mentoring. How wonderful is that?
Take care all....
*susan* -
Hi everyone
1 more day till a/c #3,Im starting to taste it,going to buy lollipops today to suck while im having it 1 more a/c to go after tommorrow woohoo,then on to the tax wonder what the side affects wil be from that.To top it off I got my periods right on time again Im as regular as clock work.
Hi to all the new ladies here.
Hope everyone is going ok with the hair thing,mine had come to a stand still till last night when i started losing the rest of what hair I had down below the head hair is very itchy and my eyebrows are falling out now,was hoping to keep them because Im not a makeup person and I cant draw a straight line to put eyebrows on.I was thinking about going and gettin a henna tattoo to replace them they usually last for a few weeks longer if I dont wash my face.the pubic hair doesnt seem to be worrying my partner,what is it with men and no hair below.Well at least I wont have to get a bikini wax this year,but Im worried about summer I live in a small holiday town on the coast I dont want to go swimming without a boob I know you can get them to go into swimmers but what if your swimming and your boob floats out or i cant go under the water because my boob will float like a life jacket Im a e cup in a bra so alot of bouyency there, well its a bummer because if theres a spunky life guard there I wont need him to help me if I drown.
I read every post and feel for the ones that are having problems with the chemo or with sick family members I think this teaches us that life goes on even though we are all going through hell and back,but at least we can all still joke and laugh about our situations.
well enough of me rambling on
love to all
carol -
I would wait and check on that tatooing...I read that cosmetic tatoo's prevent you from having MRI's...it might have been only one color (having some metal particles in it), can't remember where I read the article (I hate my brain currently.... ) but I definetly would check maybe with a Radiologist/Imaging....
I will ask the PS about that (don't know yet if I want nipples or tatoo's)if I ever get to that point.
Anybody heard about this too?
God Bless
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