Starting Chemo June 2013!?!?!
Comments
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When do you start the Brian Joseph? I'm on just finished my second chemo.
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Chemo treatment today, scalp infection, and period, all at the same time! Life can be so funny at times. I guess it could be worse, just gonna smile and get through it.
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Tasharka, I started Brian Joseph's a few days into my 1st round of chemo. I still have my brows and eyelashes after 2 rounds. I do have thick eyebrows to start with however.
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Day 12 (late) and my hair is starting to shed.... very lightly but for sure it started. Have a buzz cut scheduled for Thursday. My sweet hairdresser told me she won't charge me til Im cancer free. This will be my second cut !! Feeling good but blood counts are down a bit. 2nd treatment AC on Monday,really hope I'll do better... 5 days puking wasn't fun.... Where can I get the brow stuff and is it too late??
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Has any one else's port moved? I think my doctor put mine too deep
Because it takes a 1 1/2 inch needle and the nurse said it should only need a 1 inch usually. It takes several different nurses taking turns about 45 minutes (of pain) to access it. It has moved I believe at least one inch towards my arm from first treatment to the second. -
This is the Brian Joseph web site http://brianjosephs.com/cgi-bin/Agora/agora.cgi?cart_id=&product=PersonalCare I started a week before my 1st infusion and every day since. I have a girl friend that had used it a year or two before to make her eyelashes longer and thicker. It worked for her. I was telling her what I was doing and that is when she told me she had used it.
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I made it out to play with the horses today. I got pictures of me with Comet. He's been there 9 days and I'll bet he's gained 20 or 30 pounds! He's on the fast track! There are several people working with him so he should be fat and sassy in a couple months.
Today I felt good. I'm bald and I'm tired but at least I felt good. Hoping for a good week before Round 3 on Tuesday. ugh, I can see why it get's harder. What's harder is keeping your chin up.
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Kati,
Chin up girl, we're here with you. If you ever need someone to have a cup of coffee with or a shoulder to cry on, I'm 20 mins away! -
Hello all been very trying lately. Round three postponed till next week going g to gastroentorologist Thursday Onc said no more chemo until they find out what is causing the rectal bleeding g I'm having. Well gee maybe Bc chemo burns your entire intestinal tract. Probably need a colonoscopy oh yippy cant wait to drank something that is going g to make me go more.
Ocean are you taking clariton it really works for me. Aaoaao your amazing with all you do. And as for shaving your heads I think I did to soon but I just have to own it like we all do. Good luck to all today. What doesn't kill us makes us stronger and Stronger we will be. -
Tasharka, my port hasn't moved so I can't tell from experience. I do know that the needle to access my post is very small and is always finished after one poke. It is also relatively painless. Unless others here have the same experience as you and it is normal, I don't think so, I'd call your surgeon and have it checked. If you've noticed that it moved it may have. These things can happen, one of my breast expanders moved after implantation. It fell to the side towards my arm, made for one funny looking breast. I hope all works out for you, keep in touch.
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I see some of you able to keep your hair? I was a cueball after day 14!!!!! And still am!!!! It starts growing a little before next infusion and then out it comes after. When I say growing, I mean a little fuzz. Haven't shaved under my arms or legs for weeks. (That is nice) Envy those of your with hair!
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I had my first chemo two weeks ago. I was going to do my second one yesterday but it was canceled because of low white cell count. They called me asking if I had a shot after my chemo. I said never heard about shot. I think they forgot to give me a shot after my first chemo. And told me "sorry you couldn't understanad". I looked my appointment list they gave it to me nowhere it was mentioned. Has anyone experienced something like that? I don't know who forgot about it but can't wait to talk to my onc next week. Nurse was so mean on the phone. But first chemo was not that bad as I thought it would be.
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Laka,
If you are doing does dense treatments, meaning every two weeks, you're supposed to be getting a Nuelasta shot on Day 2 after every treatment to boost your production of red blood cells. Obviously they didn't explain your treatment plan to you very well. There's no reason for rude nurses, that really drives me nuts. I'd give my onc a call and let her know what happened and ask for clarification. Like dealing with chemo isn't enough, we have to deal with poor care on top of it! -
Laka you should never have a nurse be mean to you report her after all hour going through they shouldnt treat you like that. Where do u live. The treatment alone is so barbaric at least the nurses should be nice. I would flip if anyone was mean to me. Enjoy yourday tomorrow is another day..:)
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Thank you ladies. Nobody mentioned or scheduled me for any shots after chemo. How would I know yes I am going to talk to my onc. dlm425 I live in Atl Ga.
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Melrosemeir, I will be curious to hear more about your experiment (:,please keep us posted.... I was expecting my hair to begin falling out today, but it started two days ago- not in clumps, but strands- I purchased my 'cranial prosthesis' last week- and a few scarves.. still feel like someone on the outside looking in at all this.....
My head is really sore, all over. Anyone else experiencing this?
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Just curious. Has anyone tried Brian Joseph's on their head? Just occurred to me that if it worked on brows and lashes might it not protect hair follicles?
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Had second chemo last wed. Was doing great till Monday. Now pain is almost unbearable Onc gave pain meds not doing much. Any advice?
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sarajaneevans-I'm 11 months PFC and my hair is a little wavy and about 3 1/2- 4 inches long. I haven't cut it since early May 2012 right before my second round of chemo. My last hair cut was a pixie cut that I started myself. My short bob hair started to aggravate me once it started to leave so I made some little ponytails and snipped away. I'm sorry you are experiencing the scalp soreness. Your little hair follicles are letting you know that the hair will be leaving. I felt the most relief during that time when I took a shower and had that water running down my head. The hair does start coming out in strands at first and then the hair fallout may accelerate. If you have cut your hair very short or buzzed it, you may notice that there are hair stubs. I slept on a polyester satin pillow case when my hair was short and coming out because it didn't seem to get "stuck" or caught on my cotton pillowcase. Just remember, there are no written rules about hair---- you keep it as long as you like for as long as you want. I never buzzed and just let my hair do its thing. I know that how I handled the hair situation isn't for everyone. Some of my mighty hair held on until after I finished 6 rounds of Cytoxan/Taxotere chemo. My eyebrows became more sparse towards the last few rounds of chemo and only my bottom eyelashes fell out. I occasionally used some $8 Rimmel Eyebrow/Eyelash Serum that I got from Target. Do I think it worked.... who knows. On this particular chemo regimen, one can lose their eyebrows and eyelashes after finishing chemo and can also lose them several times during the next year post chemo. The growth cycle of eyebrows and eyelashes is different from the head hair. If you have any questions about this chemo regimen, please don't hesistate to private message me. Always willing to help anyone here.
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Jorman,
What type of chemo are you getting? I've heard some here take Claritin 24 on the day they get Nuelasta and for 7 days after. Are you talking bone / joint pain? I've also heard Glutamine helps but I've never taken it. Give a call to your onc and let them know you are suffering! Hope that helps... -
I feel pretty human today. But ... I have a sore throat. Don't know if that's chemo or if I'm getting sick. Frustrating. Do NOT want to get sick and drag this chemo thing out any longer than I have to. I want to get through it and be done.
Thanks Dyvgrl! It might be nice to meet up and compare notes!
Hang in there Dim425. I've had some rectal bleeding but it feel like fissures or hemorrhoids. It's minimal. Hope yours is just an internal hemorrhoid (they're not too hard to take care of) and not something serious.
Going to bed early - my husband snores and keeps me awake. TIRED.
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Tasharka--my port hasn't moved, but it can only be accessed if I am reclining or lying down! I won't know till I go for chemo today if that means I will have to be in a reclining position for all of the infusion or what.
Sherry--good luck with chemo today
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KatiAK,
Sore throat is most likely from the chemo.
It has happened to me each of my four transfusions...thankfully not as bad as some people get it.
Rinse after each meal...use Biotene or try 1/4 tsp salt, 1/4 tsp baking soda and 1/2 c. Warm water. Keeps those food sugars out of your mouth.
It could also be from heartburn.(yes, who would thinkit goes into the throat! But I never had heartburn before!)...so you might want to try using Prilosec.
I keep my "bowl of goodies" (medicines) on my kitchen table and make sure to take them first thing in the am. Claritan for the Nuelasta shot, , Prilosec for the heartburn, stool softener to avoid constipation, vitamin D (mine became low), Miralax to mix into my water. It makes me look like I am a sick person! Lol (keeping the sense of humor).
In my pocketbook i keep an old pill bottle with a few Tums in it, (for the heartburn that comes out of nowhere even though I took the Prilosec!) and a few anti-Nausea meds. If I am out running I don't have to worry about not having my pills.
Pat
(Katie, I haven't forgotten you, I am in the "sleepy" post chemo days and will get to the Post Office soon) -
I have just started having tingling in my hands, this is after my third treatment. I hope it does not get any worse.
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Brooksy - my onc told me to call right away if I had any tingling or numbness. Maybe you should call them. Best wishes!
Jorman - NEVER be in pain. Call your Onc night or day, someone is there to help. Best wishes for a better tomorrow.
Kmurphy - I did fine. Out in record timing. I hope yours went well.
aaoaao - love your humor! I'm right there with you!
Tasharka - my port hasn't moved, but I would definitely report that. Best wishes and prayers.
KatiAk - I hope your throat feels better and no colds!
Laka - after reading your post and several others, I vented below! I pray you have better nurses on the phone, and hoping that nurse doesn't have any more "bad" days!
Pat - I have come to LOVE my bowl of goodies...I hope they LOVE me back! I love reading your helpful posts!
Sarajaneevans - my sore head (bad pain) gave me a headache for 4 days until almost all my hair was gone. I send you lots of hugs for less soreness. Everyone is different, but I call myself "Sherry Seven Hairs". I think it helps get my family through it with the humor.
Dyvgrl - you are awesome with your quick responses! You make me smile.
Now for my venting: I love my chemo nurses. They are so nice! I hope everyone gets treated nice or better.....like a Queen! I read horror stories about nurses with attitudes, nurses not listening, etc., please make sure you have nice nurses and caregivers, or report them. You should feel good when you leave your team after treatment. It's crappy with all you are dealing with, do not take less-than from anyone! Peace be with all of you, and I pray for sleep-filled nights and beautiful days! {{{{{{Group Hugs}}}}}} Sherry -
I just saw the cutest web site. I really liked it. Maybe it will help someone else. http://www.godvine.com/Father-Sings-a-Sweet-Song-for-His-Daughter-With-Cancer-When-I-Get-Bald-3612.html?utm_source=newsletter&utm_medium=email&utm_campaign=7-11-2013
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My chemo also went good. Did not feel as in a fog as I did last time, but I had a lot more going on the first time. Both physically and emotionally.
As far as my port, for whatever reason, I have to be in a reclining position for anything that requires its use. So I didn't get things done that I was going to, but I did watch tv and get a mini nap so that wasn't bad!
No one should have mean nurses or doctors. Along the way, I have been touched at how wonderful every doctor, nurse, volunteer, etc has been. They listen to everything I have to say and have given me gentle, reassuring hand squeezes along the way. They definitely have helped to make this process easier. Report anyone who is out of line. No one needs this process to be harder.
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Netter that was a cute song. Thank you for sharing.
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Netter,
That video was great. Puts it into perspective. -
I just FINISHED chemo in June. Please feel free to message me to share fears' complaints and questions! Don't go through it alone!
Soteria205 gave FANTASTIC tips! Only lasting effect seems to be that I have numb toes from taxotere but its tolerable.
I got a port because I am HER2/neu positive meaning I need to get Herceptin infusions for a full year and did not want my veins used each time.
The unknown is awful. It was better when I knew what to expect. Here's how it went for me:
I had my lumpectomy Feb. 1st...had my port put in Feb 18th and first chemo tx Feb. 20th. I had weekly infusion of Herceptin and every three weeks I had Taxotere, Carboplatin and Herceptin (TCH). I had a total of six tx of TCH and the H will continue through February 2014. My radiation starts next week.
I had long hair but cut it short a couple days after my first treatment. It started really falling out 18 days after my first treatment...that's when I had my husband shave it off. I was fine wearing hats only...it was winter in Ohio so I found cute hats and scarves! I went to a wig store and bought two sleeping hats that I still use. TLC catalog from Amerian cancer society has them also. I bought a wig just for a family reunion and photo we planned for summer...but that's all I have worn it, once. Feels itchy and hot but I guess there's a head cover you can put
First couple of treatments were actually not too bad. I was given the usual steroids during treatment to help offset side effects (SEs) I had very little nausea and no vomiting at all. I had treatment on Thursday and worked Friday in the OR. I had some back pain over the weekend that kept me from sleeping well but over the course of that first week I felt progressively better. After the second treatment I took extra steroids in a dose pack so back pain was not bad. I did this for every treatment after that.
Small collateral issues started to arise. I had heartburn for the first time in my life so I had to sleep raised up on a couple pillows. I had numbness from the taxotere off and on mostly my feet but also fingers.
By my second treatment I had low white blood cell count so I began NULASTA...that's a shot given the day after treatment. It kicked my butt!! I hurts so bad...all I could do is try to sleep that weekend. I relied on Tylenol PM to get me to sleep. Food did not taste good and smells got to me too...so I drank chocolate whey shakes. Was nauseous but not throwing up. I simply hurt all over...my sternum especially...my spine and pelvis too...thats where the white blood cells are made and sure enough...for my 3rd treatment my wbc count was minimum but MO said I had to continue with Nulasta following all my treatments.
The third treatment I asked for pain pills to deal with nulasta. And a new symptom came up, anxiety prior to treatment.
By now I started having fatigue and was short of breath. At work (yes, was still working) I would only have one good week where I felt OK. The first two weeks following treatment were riddled with the collateral damage of chemo. Toes hurt, nausea, pain,fatigue, swollen ankles, runny nose (no hair in my nose) smell trigger, anxiety, diahrrhia,fingernails were like paper and all grooved.
Summer brought the need to drink more than I had been drinking...you can't hydrate too much!
I had a chance to go to Aruba for a week ... The week of my last tx...so I went...flying was difficult. I needed compression hose...still swelled a lot! A woman came up to me and my bald head to say she admired me...as she slid her wig back she said she is not that brave.
I was careful everywhere about germs!! Just careful! Still I did catch a cold...that was miserable. Additionally, my platelets are low so I bleed easily.
Radiation starts next week! I've had a mammogram and an MRI that shoe I am cancer free! YAY! I just had to keep telling myself I am worth it and this is just hat has to be done...no choice really...
Drinking Water and short walks outside...saving grace. I worked until I couldn't...I left right before my 4th tx because I knew it was getting harder...the SEs are cumulative so number 4,5,&6 were so very hard.
Its been a month since my last tx and I am still not working...hurray for those who can...not me...just don't go through it by yourself...talk to someone who has done it and follow Soteria205 advise!
I will be wishing you well!
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