Any May 2009 Chemo Starters?
Comments
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My 10 year old grandson is very concern about my hair loss and his mom and I have been going back and forth on how to deal with it so is not so scary for him and his 2 other younger brothers. I think what I am going to do if have her cut my hair shorter by the end of next week ( 12 days after chemo) so they get used to the idea of seen me with less hair and then when it starts to fall out I want to ask them to help cut it. She already has the clippers since she cuts their hair and I am hoping that our plan will work for all of us.
TexasRose-I am trying to look at the loss of hair as part of the recovery process and not as a bad side effect. I know is going to be hard but we can do it like many before us have. Deal with the situation in a way that you are comfortable with and that will reduce the stress of the moment.
To all stay strong even through the darkest hours! Have a great day and a good night! Diana
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Texas Rose, We purchased the clippers and did the buzzing at home. My stylist cried when I told her what was going on-- she said she would buzz my hair in the salon in a heart beat, but like you, I wanted to to this in private. We (hubby, girls and girlfriend) cut my hair really short first (my teenage girls helped with this part) then we started with the longer clip and finnished with the shortest setting. (I still have stubble despite the duct tape trick). I was happy to do it at home. I cried when I first looked in the mirror--as you do look like you are sick--which we are, so it's OK. A week later, I am at peace with my baldness--like many of you guys, my wig looks really good, but it is not comfortable due to remaining stubble. My wig lady siad to wash the wig a few times to soften in up. Might give that a go today. Also, my oncology nurse said that they do questionaires at the hospital post-chemo, and the #1 most stressful thing mentioned by women is the hair loss. You will be fine-- you are so strong. Also, call the ACS and ask them to send you a kit for the look good feel better. I cannot imagine they would not do that for you.
Tylenol arthritis did not work for the neupogen pain so I am back on Aleve and under a moist heating pad (for arthritis--works a treat) My Doc did say that thin, long boned people do worse on bone pain (one of you guys had also mentioned this to me), so that explains some of it I guess. Although I feel more like a bloated, long-boned person at the moment!
I also went to FL right after my first chemo--my husband wanted to get me in a good place before all the SE 's set in . PLEASE use lots of sunscreen and wear a big hat. I was on the beach on a cloudy day and still got a bit burned. The water is the absolute best---the salt in it must do something, so be sure to bathe as much as you can! Enjoy every minute.
Hope that everyone has as good of a day as they possibly can. You are all amazing to me.
Helen
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Thanks for the advice on the hair everybody. I know my hairdresser would come to my house if I asked her or she would do it after hours. I just don't want her to. I love her dearly. We've been together a long time. But this is intensely private to me when it comes time to actually shave it. I want to do it at home privately. Thanks Becky and NYmom60 for telling me what kind of razor to buy.
ladbham- I'm sorry that you aren't getting the support you need from your hubby. Can you sit him down and explain to him what you need from him? Mine has been great. Honestly much better than I expected him to be. But the other day he did say to me that he can't read my mind. If I need something from him, I have to tell him exactly what I need. And I know he's right. I think it's hard for men because they want to fix things and they can't fix this. Tell him how you feel. And you can tell him from me- I had my second AC Tuesday. It's a week. It's not one tired day. It's one yucky week- minimum. And throw in losing your hair. What I hate the most about round 2 is now I know what to expect. I'm glad you can sleep on your tummy again though! Hey, we take our victories where we can!!
Becky- I've never been a germaphobe either, but now I'm avoiding crowded places and people who sound even remotely sick send me running the other direction. I used to walk through the lobby of the hospital to get to the cancer center. Now I slip in the cancer center side door where I can avoid as many people as possible. Would you consider wearing a mask on the plane? I know it would suck. I don't know if I would either. But that is a confined space. I would say take a Xanax or an Antivan since it's too early for cocktails, but you will have your son with you? I forget how old he is. Old enough to take care of a stoned Momma? LOL Xanax makes everything better for me right now. I don't take it often, but I do take it on chemo day and I wouldn't hesitate to take it for anything else that was stressing me out. And I hear ya on the patience and the chemo brain.
NYmom60- I have several wigs and I really love two of them. I wish my own hair could look like them but never in a million years would it! I'm emotional about losing the hair but I like my wigs so that makes it a little easier.
sherrilynne- Good to see you again! I don't know how you ladies do it who work. Good luck today! I'll be thinking of you and hoping all goes well. Get some rest when you get home! I hope you have the rest of the week off.
Hug to everybody!
Mary
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Sorry I split up my replys, but I can't remember things from both pages anymore! Damn chemo brain!
Diana- That sounds like a great plan you have with your grandsons! I agree we have to deal with each situation in the way that is most comfortable for us and it sounds like yours will work perfectly for you and your family. And you are right too- we will get through this like so many others before us.
Helen- I totally understand the wanting to shave at home. It's just private to me. My hair is so thick that I still have quite a bit. I'm not sure anybody besides me or my family would even notice I was missing some. But it's a mess on the floor and my head hurts. So I guess I will buy the shaver and be ready for when I can't stand it anymore. Once it's done and I cry about it, I'll be fine. Just another thing to get used to and it's temporary. I hope you gt some relief from the Aleve.
My oncologist gave me an Rx yesterday for two mastectomy bras and a prosthethis. I had told the clinical trial nurse I needed a boob! So I guess I get to go boob shopping now. The fun just never stops does it?!
Hugs to all doing treatment today or getting over the last one or getting ready for the next one.
Mary
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Good morning May Marvels. I'm doing fine three days out from chemo. A little nausea this time but the Emend and the zofran are working. I didn't need the zofran the last two chemo rounds. I didn't drink water this round and I'm wondering if that's why I have some nausea. I'm trying to drink more now but it's not going down as easier as before.
Texas Rose - my hubby is is Dallas for work this week (of course - second time he's been away the week of my chemo). He texted messaged my daughter and told her there were two "touchdowns" last night. My daughter was confused. I told her I don't think he's talking about football! Hope the weather clears up down there. Also, I understand about the hair issue. It is an emotional thing to go through. I felt a lot better after it was off. I think a lot of it is the anticipation about what it'll be like. It also make this whole thing more real.
Sherryilyne - glad to have you back in the loop here!
ladbham - Men can be funny about these things (not in a ha, ha way). I've had some other medical problems over the years and my hubby's reaction has been "interesting". I think a lot of times they just want things to be ok and if things aren't then they want to fix them. Obviously, they can't "fix" this so they pull away or pretend that everything is ok. when in fact things aren't. I think it's their way of "dealing" with it. Doesn't make it right though. Texasrose is right about telling him what you thinking and what you need. They should be able to read minds but they can't!
Wish I could talk to all of you but I have to run. Got a lunch date. Hope my stomach can handle it. love to all.
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TexasRose - I hope you enjoy getting your bras and your new "boob" ... I've had mine this week and they look great and have made me feel much more "whole". I shaved my head at home with two friends, as well. I've read a couple of times that losing your hair can be one of the hardest things to deal with and I have to agree. I am having fun wearing different scarves every day, though (I'm still not brave enough to go out in public with my wig on yet ... I'm working on it though) ... Here's a web site I found that has some good instructions on how to die scarves different ways, in case you're interested:
http://www.tznius.com/cgi-bin/tying.pl
I'm going to make some big scarves out of some fabric I have around the house to see if I can get some to look cute like these do.
Have a great day everyone!
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ladbham- I think you must be married to the clone of my ex! Sorry I can't provide any suggestions except perhaps as Mary suggests to sit him down and have a talk. If he isn't the type, would it help to write him a letter? Or maybe show him this forum!
Mary - and anyone else needing new boobs. This is a link to the pattern my daughter used to knit me new ones (only need one, but I have a selection) http://knitty.com/ISSUEfall05/PATTbits.html I noticed that on the site, she refers to this site. Even if you don't know a knitter, the pattern is fun to read! I prefer the knitted ones to the store bought one.
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Hi May Marvels. I'm on Day 3 after 2nd treatment. First day was not as bad as the first treatment but did have nausea and vomiting only once. The dr. did change the nausea medication in the IV prior to receiving chemo plus benadryl. On 2nd day, I felt wonderful!!! A little tired but that was all. I received my neulasta shot. Today I am experiencing some minor bone pain even though I am taking Claritan and Tylenol. I am taking the Tylenol every 8 hours. My nurse said I wouldn't experiece pain until 3 days after shot but I am having it the first day after. I also feel blah and fatigue. However, it is better than my first treatment.
I went to a wig shop yesterday to find a new wig as I don't really like the wig I have. I found one but was hoping to get insurance to pay for it's expensive but I can't seem to get the right code from the store. What a disappointment. Oh, well...will check on line now that I know more about wigs and what looks good on me. I love the duct tape story--I still have some stubbles too on my head but I just rub it good after I shower. It doesn't bother me. I noticed that I lost the air under my arm and legs-- no more shaving.
Hope everyone is having a better day and hanging in there. We will make it through!!!!
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Today at work, I got realy frustrated with my computer. It just would not perform correctly. Once I was upset, I started having heart palpatations. The more frustrated and upset I got, the worse the palpatations got. Has anyone else experienced this?
Kelly - try aleve with the claritin instead of tylenol. I have not had any pain with my neulasta shots. Someone on here said that tall, thin people usually have the pain. Well, I am tall 5'9" but I haven't been called thin for a few years.
I am not wearing my wig to work, I bought lots of scarves because I knew the wig would be hot. Hubby has started calling me "pirate mom" He said he was going to get me a Harley do rag so that I can be a biker bitch.
One of the doctors I work for told me today that I am an inspiration. Why don't I feel like an inspiration. I'm just doing whatever anyone in my position would be doing. I mean, what choice do I have? I do what I have to do. My will to live is stronger than my will to give up.
Hope everyone is feeling better today.
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TexasRose - I am glad you were able to get thru the hair clipping phase of this process. I know it is very emotional. I too had to do it in private at home with my hubby and daughter. We started out with having some fun with it - first I had a mullet and then a bit of a mohawk - then the clippers. I still cried but I try to keep telling myself that it is the cure doing this and not the disease. I could have skippted the cure and just let the disease and the cancer would have ended up killing me but instead I will let the chemo (aka - the cure) kill my hair for a little while if that means I beat this stupid thing! At least that is what I try to tell myself - it doesnt always work.
Kelly2 - I had my onc write a prescription for a cranial prosthesis which I found out is the medical term for a wig. Once I had that the insurance paid the bill for my wig.
I had my second chemo yesterday and the neulasta shot today - so far no SE except a little tired and a little nausea but either I don't remember last time but I think so far it is not as bad as round one. I am sure I would only be fooling myself if I thought I could make it the whole way thru this thing with only minimal SE but one can hope.
Since we are all going to stick together thru rads. does anyone know when they will start that - I am thinking that we get a month off between the last chemo and when rads begin. That would put me around the end of August.
As for the cruise - I am booking tomorrow - the one I picked deports out of Baltimore on Halloween. I picked this one because Baltimore is within driving distance of my house. Not a big airplaine fan so this worked for me - It is a five day to Bermuda - would love for any of you to join in
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Sukiann- No, definitely wasn't talking about football! That's funny. The weather in Dallas last night must have been awful. We are about 120 miles from there and we had a big storm come through also. Lost power just as I got in the bathtub! Looks like we might be in for another round tonight.
mom2twins- I'm looking forward to getting my boob. There isn't much I can wear right now with one boob. I can't wait to be even again! I haven't decided for sure about reconstruction, but my hospital won't do it until treatment is finished. Boy- some of those scarves are really elaborate. I have trouble just getting a bandana to look right! LOL I'll have to practice I guess.
Leslie- I wish I could knit! Those are so cute and look comfortable. My aunt has tried many times to teach me to knit, but I'm a knitting flunkie I'm afraid. I would ask her, but she had a heart attack and a stroke and she really can't do it anymore. I did love reading the instructions though. Funny stuff!
Kelly- I'm glad your second is going better than the first. Sorry about the bone pain though. And the nausea and the fatigue. I'm on day 3 of treatment #2 also, but I feel worse this time. I slept most of the afternoon. I do feel better after sleeping though. I shaved my legs and was hoping it was for the last time, but I have stubble popping up. Figures!
Deb- I haven't had any palpitations. Definitely ask your onc about that. Your hubby has a sense of humor like mine. Most of the time I laugh with him. Most of the time.
I know what you mean about the inspiration. I'm tired of people telling me how strong I am. Like you said, what choice do I have?
Lori- I haven't clipped yet. I need to buy a shaver and I wasn't comfortable going to Walmart or anywhere else today. I try to stay home for the first few days after treatment. Especially since kids are out of school now. I have to keep reminding myself that chemo is my friend. Chemo is not the enemy. Hard to remember that sometimes, but I try. I'm sure I'll do the shave this weekend.
I don't know about the rads because I'm not having them, but my chemo will go until October. I am looking at booking a cruise also, but I'm torn about how long to give myself after chemo ends. I'm also torn between repeating the Southern Caribbean out of San Juan or just taking one out of Galveston so I don't have to fly. So many unknowns and things to consider.
Does anybody get a sore throat? I have gotten one both times. I hate that. And my glands feel a little swollen this time.
Hope everybody is having a good day or as good as can be expected.
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TexasRose - So sorry - I am going to blame it on the chemo brain - I read back thru and realized it was mom2twins that was talking to you about shaving her head - soooo sorry. I do get a soar throat for 2-3 days after both times now.
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Have a bit of a sore throat now also with a couple of small mouth sores. I've been using salt water to try to keep it from getting any worse.
LoriR - I don't know about timing on the rads. It might be a little different for everyone. I will have surgery after the chemo and then the radiation so it might be later for me.
Hope everyone has a good night.
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HI May Marvels
I am sorry I haven't read all the posts yet, but wanted to pop in and say HI to everyone and leave you all a big huggles.
I am doing good still, have been busy working and then relaxing with my family in the evenings.
My throat has been sore also, but I have spent the last week coughing so much it probably raw, I have been having a lemon drink with paracetamol in it. Which has relieved it heaps. My bald head has started getting pimples on it and is very sensitive at the moment. That sensation when the hair starts falling out is still there. I have not worn my wig all week, been wearing my hat at work. I interact with many people in my work on a daily basis. I have not had one person ask me about my hair gone (with the hat it obvius there is none). I think it is one of those things that people notice but don't talk about it. and thankfully back to sleeping all night.
I am so grateful that I have my taste buds this time and not as tired as my first treatment.
Pretty excited it the weekend, and get a couple of days to rest, added bonus, my kids are going to there grandfathers tomorrow night, so I get a night with hubby. So I don't think I will be here tomorrow
Take care you all....... may tomorrow be marvellous
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Hi All
DEB: I did experience heart palpitation once. I took a couple of deep breaths and rested and they past. It certainly is something you should mention to your onc. on your next visit.
KELLY: I also have wigs that I am not totally happy with. It seems I can get a good cut, or a good color, but not both! I can't even believe I am so frustrated by HAIR!
I really admire your women who bought your wigs, accepted that it would be a different "look" and moved on!
LORIR: I like what you said about letting the cure for this disease kill your hair so that you can kill the disease! Good attitude - we need that here! Someone said to me this week, "It's a good thing your hair is falling out- it means the chemo is killing the cells it's suppose to kill." And, although I never thought about it like that, it was a perspective I was happy to hear. (still hate my wig though!)
LADBHAM: I am so sorry that you don't feel supported by your husband. Women are made to "talk" through our problems (hence the existence of these boards!) and men often tend to internalize. Do you have a local support group in your area? My local hospital, as well as my breast surgeon's practice has a group that meets once a month. Maybe you can look into that a a place to "vent" and be understood. Keep in mind, that he may likely just take more time processing this whole thing too, and will likely come around.
Love to all.
Janet
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Deb-I would like to take the Aleve but I am on Coumadin which is a blood thinner so no Aleve for me. I am not having the bone pain today so tylenol and Claritan must finally be working.
The wig store is working on finding the code number that my insurance is wanting and I will be getting a prescriptioon from my dr. so maybe I will get the wig I would like to have. The thing--do I go to church this Sunday or not--we'll see....wish I had the new wig first. lol.
I understand about the iinspiration bit...have had lots say that I inspire them. Well,,, I am glad but it is just doing what you have to do. No use just sitting around moping and feeling sorry for myself, after all...this will end and I am willling to fight this disease. It is a good perspective to see that when our hair is fallling out, the chemo is working.
I will be finishing chemo in Oct. then have rads in Nov-Dec. After that, just the Herceptin. Sounds fun to be planning a cruise. Have fun.....
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My husband went and bought the shaver today and shaved my hair tonight. It does feel pretty freeing to just be done with it. It was starting to hurt so much. My scalp was really sore and it feels better already. I'm not thrilled about it, but I'm glad it's behind me now.
Hope everybody is doing well. Hugs!
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Hugs to you TexasRose. I am glad your scalp feels better already.
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Hugs to all from hot, sunny Florida. Well, it's not sunny yet because it is 530 am. Just like always, up at the butt crack of dawn.....this part of the SE's is really annoying!! Had a great first day with my BF! We just hung around and got caught up a little and the boys went to the waterpark. Think we are just going to chill by the pool a little bit today. It is so friggin hot down here, I love the ocean sooooo much I have to go to the beach, but I just don't know how long I would last and that would be a pain in the ass for us to drive get all sandy to just come back. ya know? Oh well, probably the only post you will see from me while down here.................
Hang in there everyone! For some of us, this scarey roller coaster is half way done, for some just starting, but we are all in the same line..............ok that was stupid, it was supposed to be a cute little insprinig line but it is before 6 am......
HUGS!
Becky
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Hi All,
TEXASROSE: We certainly are on the exact same schedule! After my shower on Friday, my hair came out in clumps! Couldn't put it off anymore. It was almost a blessing the way things worked out, I called the girl who I bought my wig from so that she could style it and she actually ended up shaving my hair too. I was really hoping to make it to Monday as my daughte is singing Sunday night at church and I wasn't ready to be a wig yet. My head never hurt so I was crossing my fingers, but, it just wasn't to be. Oh well!
So, to those who have been through this hair thing already...especially those who live in the hot states...what's the best way to stay cool? My first day in a wig and/or cap with hair, and I'm HOT!
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Thanks for the hugs Titch. How are you doing?
Becky- Butt crack of dawn!! You crack me up girl!! We had a friend who used to say he had to kick the rooster in the ass when he got up very early. Glad you are having such a good time!! Enjoy the pool and if you hit the beach at all, curl your toes in the sand for me. I love the beach!!
Janet- Boy, we are on exactly the same schedule! It was a shock to wake up this morning and see myself in the mirror. I look like my oldest brother!! LOL I was hoping to make it a little longer too because my nephew is coming up today to celebrate his 21st birthday. I was hoping to still have hair, but it wasn't to be. I will be the wig lady. Dreading it because it is HOT, HOT, HOT here today. Should be nice and miserable! I'm only wearing wigs, hats or scarves when I leave the house.
Hugs to all!
Mary
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Hi May Marvels.....
It is winter here in NZ and my head gets so hot with the wig. I have actually started wearing hats out in public, cause they are more comfortable.... So I could only imagine those of you in the US with your summer. I went out last night, went clubbing with my hubby and the sweat was pouring of my head cause of the heat. I actually felt like taking the wig off, but being in a club with lots of much younger people, I didn't.
TexasRose, I am all good.
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Titch--you are so funny. I just have to laugh. I can just imagine the looks from the people in the club if you take off your wig--lol. It was 106 degrees today where I live in Texas. I don't normally go bald but there are times when I 'm alone that I just take off whatever it is I'm wearing then one of my kids will come in and look at me strangely but they are getting used to it. lol. I have teens. I went grocery shopping for the first time in a while and I felt so self conscious in my wig, mainly because I don't like it but hope to get a new one soon. I feel that everyone knows it's a wig but I'm sure they don't . Probably just think I look funny!!! lol.
TexasRose--I understand the feeling of being free now that the hair is gone. You will get used to it. My sister took one look at me bald and said I look like my younger brother.lol. Just what I wanted to hear......
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I had my dh buzz off the rest of my hair tonight, it wasnt as bad as i thought because he was so stressed out worring about me or hurting me that i put my attention on him, i cut my hair short last week and it helped to kind of get used to it, when hair started falling out i used a net around the house but it would stick to my hair and made it fall out more, so i put on a shower curtain, and it was better than the net, yesterday was my birthday and i wanted one last night with hair, i was mostly bald on top, so i put on a pink cap, went out to our favorite bar and a friend i hadnt seen in a while came in and said, oh debbie you cut your hair it looks cute and she ran her fingers thru it, and she had a big clump of hair in her hand, oh the horror on her face was priceless lol! even after explaining to her what was goin on with me she looked like she wanted to run out of there i felt sorry for her, but it was funny, so anyyyy way,, i got tired of having hair all over the place so i got in the bath tub on a step stool and dh just buzzed off the rest, i feel releaved that i finally got it over with, and dont feel so bad, my head was cold but i put a lightweight turbin on, not so bad, dont like the stubbies but put lotion on and made it feel better
angel hugs debbie
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Hi all,
I to have joined the clan of the shaved head. When I got home from my 2nd A/C on Thursday I found that my hair was coming out - not a lot at a time but enough to know it was time to get out the clippers. It started with the whole family in the bathroom watching but before the first pass my daughter left the room. I did most of the clipping but my 9 y/o son got to do quite a bit and he thought it was pretty cool. I have 2 wigs and many hats so I think I'll be OK.
Janet, there is a breast cancer group that meets in the town I live in and I am going to check it out next week - if I can remember from the Chemo Brain. Anyone else feel like they can't find the right word or remember what they did earlier in the day? Very strange.
I've had the sore throat that Titch and NYmom60 have described as well as some big headaches. Tylenol seems to work but what a bother.
One quick word of advice, don't eat asparagus if you have become sensitive to smells.
Take care everyone - I hope we all have a great week.
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Hi all
Still doing the hair drama. I washed it this morning and it matted. Took ages to comb out and a lot came out. Lots of tears but could not stand to go to a strange hairdresser, was in Auckland for the weekend. Came home and got into bed. Want to hide my head under the pillow and wake up in November when it is all over. Rang a friend and she is organising a buzz for tomorrow nite, Yikes it is beginning to really hit home.
Susie
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Hi all
I've been following you from bed-- bone pain in legs is unreal but I had my last of 5 neupogen shots last night so I hope it will get better when the effects wear off. I cannot walk around for more than a couple of minutes without my legs truning to this weird lead-like, pins and needles feeling, with shooting pains below my hip joints and above my knee joints. It feels better to be lying down under heating pad. Boo. Whining done--thanks for listening:)
I am so sorry for all of the hair issues that you've all been having-- it sucks. I had purchased an electric razor after surgery as my surgeon said no more regular razors on surgical arm pit. My stubble was really sore and my hat would fall off at night and I would wake up from the discomfort-- so I askd my hubby to try the electric razor on my head to get rid of the stubble (the duck tape works a treat but takes for ever:). It worked and I cannot tell you how much better it feels to have no stubble-- it is not a pretty look as my head is white and my face to me at least seems yellow at the moment, but who cares if it feels good.. I bought a satin pillow case online and sleeping on that with a smooth head is wonderful. For those of you with stubble, give it a shot. It takes a while and you have to go slow (and wait for the razor to recharge!!!) but it feels so much better. I do have some bad acne on my head. Anyone else? None on my face this time which I guess is good:)
Hope you all have a great day--
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Hi May Marvels,
I started chemo May 6th and seem to be on the same cycle as many of you. Doing Cytoxan and Taxotere. All this time I've just sat back reading along and observing all the similarities as we go thru with this. Unfortunately I've wound up in the emergency room on day 2 of each cycle with A-fib. I posted the question on another thread to see if anyone else was having the same issues and if it was a common side effect.....no replies.....then my ONC says it only happens in less that 1% of patients, ugh.
So,deb6563, I have to say how thrilled I was to see your post about palpitations (sorry, I know how scary they can be) I'm just glad to know I'm not alone. In my case they think it's the taxotere. The first time it lasted for about 14 hours and I converted back to a normal heart rhythm on my own. The second time it lasted 36 hours. Now I have to take heart medications and we'll see if it happens again on round 3 this coming Wed. Just warm up that gurney in the ER boys!
Has anyone started getting a burning sensation in their esophagus sort of like acid-reflux yet? At this point I don't know if it's the part where we start having the "internal chemical peel" from the chemo, or just the effect from one more drug. My doc ordered Prilosec, but I'm not sure I want to start up one more drug.
Here's something I do have info on. If you are having trouble with scalp soreness and acne from hair loss, known as folliculitus, there is a topical gel called clindagel you can get to help. Those little hair follicles just don't like letting go anymore that the rest of us do! I can tell you from past experience of having to shave my head everyday for two months (actually my whole body) for a play I was in a couple of years ago, (ironically playing a dying cancer patient.....yes, this is too weird), that I never had a single bump from razor burn or ingrown hair the whole time. It is definitely different when the follicle is being poisoned.....they're going down kicking and screaming!
I am getting ready to go to the airport to meet my 87 year old mother that has been hankerin' to get out here to be with the "baby" of the family since I was first diagnosed back in March. I've been super emotional all week thinking about how hard this must be for her, to see a third daughter battle breast cancer while she and every other member of our family has been spared. I have visions of forgetting the luggage on the carousel because we won't be able to stop blubbering all over each other.
So to all of you it's been fun reading along, good luck with the next go round.
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Morning Ladies,
6 days out from my third chemo and I can't wait for this to all be done. One more to go. Fatigue has been my biggest complaint. I also had another reaction to taxotere and for the next round I have to take decadron the day before. I know I didn't drink enough water this week and that is why my bodily functions have been burning the heck out of me. I feel like I have a yeast infection (maybe I do?) from the itching and the burning. My skin is raw!
echosalvaje - so sorry to hear about the afib. A rare side effect and it has to happen to you!! I have vfib (yes, I said vfib, the deadly kind) and have a defibrillator to zap me back to rhythm. So I definitely know how scary it can be. I had an allergic reaction to the taxotere and I was so scared I was going to go into vtach, then vfib. I totally freaked out on them. The whole office was in the chemo room to see the 44 year old breast cancer woman in anaphylatic shock with the defibrillator. I cause a scene where ever I go. Hopefully your new meds will do the trick. Beta blocker? I'm on Toprol.
Zuzee, ladbham, debbie6122 - shaved head are sexy. Join the club! emotional but liberating at the same time.
Texasrose - I just said to my husband that I look exactly like my older brother!! I wear a baseball cap most of the time and I'm getting a little bit fatter. With the extra weight on me, baseball cap and no hair (he has hair, but short of course and he really isn't fat) I look just like him!!! It's a good thing he's so good looking or I would be upset!
Becky - butt crack of dawn cracked me up too!!! Thanks for the laugh!
Titch - whip off that wig!!! I only wear mine if I'm out with my husband or my teenage daughter is embarrased by me (or wait, she's always embarrased by me....)
I have to go and drive the kids around. Why does everyone think things are status quo when we're going through this? It amazes me how sometimes people think you can just go on with all the regular activities when you feel like (you know what), especially the immediate family.
xoxo sukiann
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Good afternoon everyone - Hope you are all doing well. It seems most of us have joined the Mr Clean club at this point. It is amazing what some people say. I was sitting outside with a couple of friends on Saturday. They were all enjoying a beer while I was chugging on my 10th glass of water for the day UGH! It was a beautiful hot day and out of the blue she says - you are so lucky to not have any hair. LUCKY are you serious. I love her to death but really do you think that is what I wanted to hear? I told her I would be glad to take her in the house and shave her head for her so she to could be as lucky as me. She didn't take me up on it - hmmm wonder why? Just wondering how everyone's eyelashes and brows are holding up. I am finally getting used to the bald head I really don't want to have to deal with losing the brows and lashes too.
For those of you on the taxotere and cytoxin - me too - I have not had the heart SE you are talking of - sounds very scary for you - my onc. has had be on the dexadron all along not sure if that is why but best of luck to you!
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