April/May 2012 Chemo hang out
Comments
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Cher, welcome. I agree with Indigo; my original dx was supposed to be lumpectomy with tamox only. Of course, that was before they got into that boob and everything changed. And Indigo, I kind of "staged" myself at IIa and the my MO said no, Ib only because the lymph invovlement is so very minute. That's a good thing, I guess.
Fierro, enjoy the short hair while you can. Remind yourself that it's short during the summer, so you should be a bit cooler.
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I haven't even started chemo yet, but decided to cut my hair short anyway. I'm so glad I did!
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Hi Everyone!!! This is my first post, probably way overdue. Diagnosed on 15th Feb. Great 42nd birthday present. Lumpectomy 15th March. Chemo started 17th May. Got an infection in my bellybutton of all places and my neutrafils (WBC) dropped dramatically to 0.15, so have to be careful not to pick up anything else. Dont want to end up in hospital. At the beginning, i had alot of support. It was coming from everywhere and was great. Now, everybody has ditched me. I havent seen boyfriend for weeks (he has chest infection). Everybody else just got on with their lives cos they think they have done their support. when I try to ask for support, Im getting excuses and fobbed off to others but everyones doing it, so I am sitting in my house right now, staring at the walls and have been here since 17th May. I broke up with boyfriend yesterday as he has been to parties, bought a new motorbike, which Im sure he is enjoying right now. All I can do is sit here and ball my eyes out. Ive tried to tell everyone the situation. They just agree with me, say they will call in soon to catch up, then, nothing...Everything in my life has changed lately. Im a single mum with 3 kids. I have been off work since the op as all the appointments and juggling the kids got too much by myself. I now wish i never got tested to start with cos now my life sux, when before, I was happy in my deluded world where I thought everybody gave a crap. My boyfriend made me feel like i am needy nutcase but i just need something, i dont know what. I know I need to drag myself out of this rut and i have been trying but everytime I hit the wall and i end up in tears. I try to leave the house and only get as far as the car and back in i go. I dont know what to do. pls help me...
Kath
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I had my last AC treatment on weds & this time is totally different. The nausia has been minimal, I have energy & I have an appetite. The only thing different was the nurse gave me Ativan in my iv during infusion. I keep myself calm Becuz as good as this trip has been I know that I will probably crash, so just holding out til then. But in the meantime I am enjoying this new course. Best wishes to.everyone.
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kath99-Welcome to this thread along with the other newbies!!! Sorry to hear you are having such a rough time with everything. Take some deep calming breaths and know that you are not alone on this journey. If you are struggling with everything, you may want to check into getting some counseling where you live. The American Cancer Society may be able to help you. You may also want to talk to your doctors or the cancer center/hospital where you are getting your chemo treatments at or the church you attend. You may just want to round up your family and/or gal pals and let them know that you are in need of help--- help with the kids, meals, etc. Sometimes people don't know you are in need of help and assume you are doing fine. It just happens and it isn't on purpose. The fact that you recognize that you are struggling is half the battle; seems like you are looking for ways to move past this rough spot. Keep checking in here to let us know how you are doing..... this is a good place to let it out and release how you feel. (((HUGS)))
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Wow, Kath99, I'm sorry! This whole bc thing is so surreal and so crappy that it is hard to cope with any of it, in my opinion.
What has helped me so far is 1) accessorizing my bald head and 2) going for walks. I am not making light of what you are dealing with. But we have to power through for our kids. I have several people who really don't "get" it--rather, they don't want to. But this is the life I've got and I've got to put my head down and get through this treatment. Stay tough--you are clearly a strong person, you can do this. -
Thanks guys, at least we have eachother...I have an appointment with hairdresser/wig etc on Tuesday and the friend that was supposed to be coming with me bailed out the other day. I have hardly heard from her in the last 2 weeks as she is busy with college course, assignments etc... but i have gotten use to attending most of my appointments alone now anyway. The oncologist appointment prior to chemo was hard though, Im sure there is stuff i have just forgotten. I think that ur right that some people just dont want to know about it and thats just the way it is. I havent told my oncologist about the support thing cos to be honest, I find it all extremely embarrassing to admit to people that no-one is there.
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It reflects on them, not you!
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Hi all..guess I need to post here..get a port on the 4th of June..start chemo on the 6th..
kath99..wish i was closer to you..big hugs is all I can offer..Doris
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Yeah, I guess it does. Well, it worked!!! I feel better. Thanks so much anndh and melrosemelrose. I will make it a mission to try and get out of the house today xxx
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Thanks Doris,
I will take anything I can get right now and an airhug is just what the doctor ordered. Thank u and right back at u 2 and all our friends here. Hope ur treatment goes well.
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Kath99 Hello! I am so sorry you are feeling so alone. This can be an isolating illness. And some people don't know how to handle illness so they avoid it. And others may be right at your side who weren't that close to you before. I have a couple of family members who have not treated me well who I believe are really in denial as to the gravity of the situation. But I've had to ask for what I need a few times. Hope your support system gets better and I wholeheartedly agree with Melrose.
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Yeah, I know Stacie. I do have 1 girlfriend that has been great but I worry that too much gets piled on her. She has had to deal with all of it and I dont want to overload her. Trying to take one day at a time atm, so todays mission is:
Go to the shops...lol
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Kath, I lurked here and read some posts every day for weeks before I finally signed up and started posting. There are some amazing, strong, been-there folks here, and it's been good for me. I have gotten a lot of empowerment here. I still cry several times per day. (I was set off by a coffee commercial earlier.) Still, I come here and borrow strength when I need a bit extra, and try to encourage others when I have some strength to spare. It's like the take a penny/leave a penny bowls at the gas station. (If that's only a weird American thing, let me know and I'll tell you what I mean.)
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Waiting for Oncotype results (will take two weeks dr said), then they decide my Chemo treatment and it all begins. I'm trying to wrap my mind around it. I know there is a lot they can do for side effects, and logically I know I will get through it, but emotionally I am trying to understand it all. How will I react when I lose my hair? How will I react with that first side effect that scares me? How will I react when I have my first dose of Chemo and know this stuff is in me? I know it's a day by day battle. I want to bring my IPAD to treatments and listen to music, will they let me? I want to be be-bopping to the music I logve, which I think will help me through the fear. What other things do you ladies do through treatments to help you deal with the emotions to relax and still enjoy what brings you pleasure? Please share...
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anybody that's scared right now about the possibility of chemo - please don't be afraid. I'm not saying it's a picnic but you can do it. I was so scared before my first round. It is doable. we've alll had a virus or the flu that made us feel icky for a few days. If you can handle that then you can handle this. for most of us the side effects can be managed. and all of us are here for you. I've learned more from these women then any doc has ever told me.
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Butterflylady, they let me bring pretty much any electronic toys I want to chemo. I just have a dumb phone but love my Nook Tablet, and when they told me they had WiFi, I told them, "Okay, I can do this!" DS#1 has been my buddy for my first two txs; he brought his laptop and we watched movies. Only littlr thing we've run into was access to an outlet, but the nurses have been great about letting us move stuff so we can reach it. You can ask where you are getting your infusions but I'll be surprised if you can't take your iPad.
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kath99- I didn't realize you were in Austrialia---- you may want to also join the Austrialian chemo thread since you may find that more help and support is also closer to you than you think!!!! But don't leave this thread----we would definitely miss you and need you to hang here with us, too!!! Hope you are feeling better--- nothing is easy about our journeys but we are stronger together. Yes, I love shopping therapy---- it's a great way to get out, get some exercise and feel how we felt before we began our journeys. (((HUGS))) and everyday be kind to yourself!!!!!
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Kath99, sent you a PM - hang in there!!!!!
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dancetrancer- I ended up getting diflucan (the prescription pill) for my thrush. Mine isn't bleeding, but it makes my mouth and throat burn when I eat or drink anything. It also gives me the WORST taste in my mouth all the dang time. Like the worst morning mouth, but all day long. I think I'm about over this round, maybe in a day or two.
butterflylady- I take my iPad with me to my treatments. I either read/surf the internet while listening to music, or watch a movie.
Welcome to all the newbies- this is a great group of ladies, and I've gotten so much support and information here.
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Just got home from a wedding. This one was better than last week. I didn't bawl my eyes out when the son danced with his mom. haha I got awful heartburn in the middle of it, and when I checked my bag, of course I had everything except Pepcid in there. Ugh.
Last night after my infusion, I got really really hot. I think my MO jinxed me! She asked me if I had night sweats. I said no. Sure enough, last night I was hanging out in front of the AC with a cold wash cloth on my bald head trying to cool down. No fever. I was just HOT! Damn steroids! But, again, I'm going to say, if this is as bad as it's going to get, then I should not be complaining. I just have to get throgh tomorrow. 1 shoot, then Im off til Tuesday. Monday should be my crash day. Sleep sounds awesome! I'll have to record my tv interview. I am not waking up for it. I probably look like a goof! haha
Welcome to all the newbies. You are in good company here! Just keep asking questions. We are all happy to help!
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Fierro6 - yes I have several moments of the day where I burst into tears, sometimes its the most rediculous things and I totally got that thing about the pennies...lol.
Melrose - No worries mate...sorry, forgot to put the aussie accent in...lol. Shopping was great therapy today and definately cheered me up. I have checked out the Australian threads but i preferred this one. I will keep reading them though.
Thanks to everyone for all your support, I will be regularly visiting and help where I can too.
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Hubby spent the day grocery shopping, cooking and preparing things for me to eat. He is such a caretaker. I worry about him running himself into the ground. Last nigh I fell asleep and woke up with pain throughout my chest. I couldn't tell whether it was heartburn, nausea, gas, constipation or difficulty breathing - maybe my gallstones acting up or pain in my sternum from the Neulasta? He convinced me to get up and walk around and I did get some relief and finally went to sleep. The best thing was that he just came in and talked with me - really talked and listened to all of my fears bubble up to the surface. It was cleansing to let it all out. I hope I turned some sort of corner and can be stronger today. My family needs me.
Butterfly, I am a week ahead of you and had all the same worries. I packed a bag with all kinds of stuff and honestly used everything I brough with me. The hospital wifi was fine for normal surfing, but not for streaming stuff and a site I wanted to look at was blocked.
Kath, I'm sorry people have seemingly ditched you. Is it possible that they just don't know when and how you need them? How old are your kids? Can you reach out to their friend's parents? (For example, "Is it possible for you to take Jenny to soccer? I have a chemo treatment and I am still shaky driving...") I started a Facebook group on my progress and I am able to indicate what is helpful without having to ask outright. Do you know anyone locally who has gone through this? I have several friends who I call my beacons of light, because they have come through on the other side and offer such hope and encouragement. No matter what, please know that you are definitely not alone. You matter to us here and we will hold your hand every step of the way.
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Thank you Indigo, I am going to have my husband buzz it today, but like you, I am not buzzing it too long, already cut it short and donated it, now buzz down some, then I should be good, I am tired of feeling like a shedding dog. Thank for all the tips.
Krsity
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hanging out here... while im waiting for my final patho report. sooner or later, i have to schedule for chemotherapy.
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Vballmom - I also get the sternum pain, I think its the neulasta mainly, but this time, my 3rd DD A/C I have had way more heartburn....fun stuff
. Seems like I get different SE each time. I have one more then surgery, starting to freak out a little about it
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Kath99- (((hugs))) I am sorry you feel so alone. I hope you find comfort in this group. I am a newbie to this group, but it is a very welcoming place.
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welcome kath99 - we are here for you!
Welcome any other newbies I've missed, too!
Well, today is Day 4 post my 3rd TCH, and, knock on wood, I am doing SOOOOO much better than I did at this point after my 1st two rounds. I only felt like I had a bit of a flu yesterday, just kinda yucko with some episodes of fairly uncomfortable heartburn (of course)...but no constant fever, big C or big D, no debilitating stomach cramps, severe heartburn, severe fatigue where I was exhausted just walking to the bathroom and back. I even felt like straightening up the house a bit and doing bills, of all things, LOL! I sure do hope it continues like this and my 4th chemo is similar. The first two kicked my *ss. I now understand how some of you have been able to work a desk job while doing chemo! Maybe my dose was just a bit too strong the first two times??? Or maybe getting the Neupogen earlier made the big difference this time? Or maybe it's b/c I've finally found the right combo of drugs to prevent the severe heartburn? Or maybe my body is just learning how to defend itself against the chemo damage a bit faster? I have no clue, I am just SO thankful this round is much milder for me!!!!!!
Cottontail - glad your thrush seems to be almost over - YAY! Ick, if I had those symptoms like you did, I'd be taking the Diflucan for sure. Mine just looks yucko, but otherwise, if I didn't look, I wouldn't know I have it. You know, I think mine is starting to improve finally. I read a little bit and discovered that I probably was reinfecting myself constantly by using the same toothbrush! So, I had DH go out and buy a bunch of cheapo soft toothbrushes and I use a new one every 2 or 3 brushings (I brush carefully after each meal). I collect the brushes and then boil them in water for several minutes to sterilize them so I can use them again. Just thought I'd share in case it helps anyone. I don't know if it makes a difference, but I figured it was worth a try.
vballmom - loved reading your description of your interaction with hubby. He sounds like a keeper, for sure! Oh, and regarding the sternum pain...I get that a lot with my heartburn. It feels like pressure/tightness/a bubble behind my sternum - along with burning at the base of my throat...made me worry about a heart attack...but then after I burp it goes away (til it recurs, LOL). Doc says this is indigestion, not heart issue, but if any sx go into L arm/jaw - then you've got to get it checked out. It's a really uncomfortable sensation. I hate it.
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Vball, glad you have a great hubby. Mine is pretty great too! Makes a world of difference! Do you do the Clairitin with your shot? If walking around work, hopefully it was just heartburn. Pepcid works good for me.
Wildflowe, buzzing mine off was the best thing I did. It was worse for me having it all come out in my hands. I couldn't stop myself from running my fingers thru my hair and pulling it out.
Kath, I also made a group page on facebook. Ive had a lot of people volunteer, but they dont know what i need. Thurs. I needed a ride home from chemo. All I had to do was ask someone. -
Hi Kath99, sorry to hear what you’ve been going through but glad you were able to get out for some shopping therapy because it truly does help. It’s so easy/comfortable to sit at home but sometimes too much of a good thing isnt good for you. In my situation i would lay in bed for days at a time while i let my mind run wild and i would cry, cry and cry some more. Although, crying does cleanse the soul its the crazy thoughts that werent good for me. I pray it gets better for you and i hope this thread can help you through this difficult time. Its no walk in the park but together we’ll all get through it. *HUGE HUG*
@Vballmom, reading about your husband made me think about mine. They sound so much alike. I too was having chest pain late the other night and could not tell if it was gas, shortness of breath or a heart attack creeping up. I said a prayer but after laying there for a while (and letting my mind run wild) i was scared i would die in my sleep and woke my husband up to let him know what was wrong. We too had a heart to heart and I let all of my insecurities out on the table. Its so amazing how understanding and how good of a listener they are.
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