Constantly Sad
Comments
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I had my BMX w/ immed recon in May. I developed an infection and had to have the left TE removed in August. I am currently doing chemo and will be done on October 28th. I still have three more surgeries with this reconstruction process. I was a medical assistant and a full time nursing student before the bc dx. I feel like I am losing my mind sitting home. I am still doing alot as far as housework goes, but I feel so useless right now. I know my family is sick of hearing me whine and who knows maybe the people on this site are sick of hearing it too. I am sorry I come here and vent, but I don't know what else to do. I asked my PS today if it was reasonable to think I could start school again next Fall and he said no. I never dreamed this would take so long. I didn't have the highest self-esteem before all of this and now I feel so freakin ugly. I am bald, overweight and boobless. I feel like my husband hates me. My son just rolls his eyes if I say I feel crappy and my MIL expects me to come over every other day because "well you don't have a job or anything now" I want to say, well I don't have a job because I have had two surgeries and chemo in the last five months. The irony of the whole situation is I spend most days scared to death I will develop mets and die before my son graduates high school or gets married, yet I feel like I want to die. The thought of it just makes me cry. I was talking to my dad tonight and I told him I would be 40 by the time I gradute college and he said, "you probably won't make it to 40." I know he was just kidding and once I started crying he retracted and said he was sorry, but I just wish people could understand how their lack of compassion hurts. I just want to be happy again and quit being so jealous and driving my husband away. I almost think this would be easier if I were alone. At least when you're alone, no one is there to make you feel like a cry-baby or like you are somehow disappointing them. I am just so depressed and scared everyday and I need to feel better soon. I don't think I can handle feeling this sad forever. I would never do anything, so I don't mean to make it sound like I would, I just want to be happy. Does this misery ever end? Sorry for rambling and thanks for listening. Take Care. Allison
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Allison, I was where you are a few weeks ago. What helped me was a therapist and sleep. I was not sleeping more than 4 hours a night since June. I started SAM-E and melatonin and I can now sleep 6-7 hours for about 5 nights a week. That is way better. My body doesn't metabolize anti-depressants well and they knock me into la la land so SAM-E is a natural alternative. It takes several days to kick in but so do anti depressants.
Taks a deep breath and call and make the appointment. You have PTSD/depression. Who wouldn't?
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Thanks Barbara. You are right my sleeping is so screwed up right now. I am up almost all night and sleep most of the day. It is definitely screwing me up emotionally. I actually have melatonin, but I have never taken it. I wasn't sure how it would be with chemo. I will ask my oncologist about it when I go in Thursday. I was also going to ask him if he knew someone I could talk to about being so depressed all of the time. Thanks again. Allison
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Allison - first of all big hugs ((hugs)). As unbelievable as it seems things do get better - I don't mean life living with a cancer diagnosis, but learning to live with it. Everything changes. And as much as the people who love us really do love us, no one REALLY understands. We do here, we really do. No one really understands what it means to have cancer until you are the one being told. Life goes on for everyone else, and as much as that freaks us out, that is the way it is.
Does this misery ever end? No, probably not, but it changes into something else along the way. I feel your pain Allison and I am reaching my cyber hugs from over here in Australia to say that I understand totally what your post is about and I hope your agony and pain subsides over the coming days. Please PM me if you need a direct response.
big hugs
Helena
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Allison, I'm sorry to hear what you are going through. I have no words of wisdom or advise to offer except for the obvious (keep posting here for support, seek an in-person support group and go ahead with your idea and ask your onc. for advise re: coping with the side effects - have you asked for a referral to a psychiatrist or psychologist who sees people with a history of cancer?).
Sleep, or lack thereof can be a side effect of depression or of your treatment, so it should be tackled in the broader context of everything else. It's only one of many symptoms.
If it's any comfort, you should realize that you are not alone in the department of people appearing insensitive or weary of your complaints. I think almost all of us can attest to that. After a while, one just has to be stoic realize that maybe you don't complain as much as you think - otherwise your family would better realize what you were going through. I have been trying to convey for ages to some members of my family that I am having to choose between death and insanity, as the Tamoxifen and the principal med I take for my other illness (see profile) do not like each other. Do you think some of them even flinch? Nah. I think it's all too exotic for them, that death and insanity think. They don't live that reality, so they ignore it.
People simply do not understand serious illness, and that is a sad fact of life. They equate staying home with the good life, somehow, even if it is because you are getting poison injected in you are treatment.
Good luck to you.
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Thanks everyone. As you see it is 6:45 am and I am still awake and depressed.....yippee!!! Athena - I love your Thank you to BC quote. I hope I can be that accepting of all of this once my recon. is complete. I think that will help me alot with everything.
Helena- Thank you for your reply as well. I can tell it is sincere and I may take you up on the PM if I need to sometime.
I think a big part of my problem with my husband anyway is I think maybe I am just being overly sensitive right now. Everytime he raises his voice or looks at me strange I think he is going to leave. I sometimes wish he would just tell me to leave, so I could quit stressing so much about what he thinks. That's what I was referring to when I said I think this might be easier alone. I feel him getting sick of me and my worrying more and more each day. I am embarrassed that I even care as much as I do. I used to be able to point out a pretty woman and say look at her and that would be the end of it and now if he looks longer than I think he should at someone or says something about some womans nice "chest" I am offended. I feel like it is a slap in the face. Sorry to be so vulgar, but if his "junk" was cut off, I certainly wouldn't be glaring at other men and telling him how nice it was. (not that I do that anyway
) Point being I am turning into a complete jealous lunatic and I hate myself and who I have become.
Anyway, I am going to attempt to go to bed now. Maybe, I will wake up tomorrow with a better attitude, but right now I am just not feeling so hot. Thanks again everyone. Allison
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Allison...sounds like your family is in need of a therapy, they have no idea of compassion that you need going through this....No pity needed just understanding and you are not getting that, even from your dad...Wow, it's not you, hopefully soon you will begin to heal and get your health back and the stronger you get, the more you will be able to handle this...I can't imagine going through this without my dh's support and I didn't even do chemo... Can you surround yourself with more positive people, maybe joining a support group or something..Once you start getting your self-confidence back, you may start to get your life back...I don't know a woman out there who would want a man with the lacking sense of judgement as the way your's is acting at a time of need to his own wife..Let him dream on as you work on getting your strength and self-worth back...
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Dear Sweet Allison,
First of all, you keep writing and talking and venting all you want. That is what we are here for. We get it and we are here to listen and help you in any way that you can! Tell you hubby that mentioning someting about some woman'schest is very offensive and that you want him to refrain from doing that EVER again. Sleep deprivation and not feeling like you can do what you want to do is contributing to the problem. Tell you mil just what you told us, you are recovering and in treatment and not having a vacation. Sweetie, if you have health insurance try to find a good therapist. Interview them. Find one that is understanding and that feels right for you. They are out there--it is usually not the psychiatrists that do therapy. Please take care of yourself, this shiz is so hard and we understand and we care and I want you to know that you are not alone!! xo
Ellie
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Thanks somanywomen and ellie. I am definitely gonna ask my onc for help today. I have chemo at 9:30, so I figured I'd see if he could recommend a good cancer psychologist or whatever. I think it would help alot. I am feeling somewhat better. I am still not sleeping. I was scared to take too much to sleep bc of the chemo, but I will ask the doctor about that as well. Thanks again for all your kind words and I will let you know what my onc says today about coping with all of this. Take Care and have a great day! Allison
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i recently went on an antidepressant.. what has helped me so much is the extra 30 minutes of sleep i get a day.
it has been marvelous.
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Allison, glad to hear you are feeling a bit better, but in your environment that will be challenging..You need fun, positive people around you now more than ever to help build your self-esteem..I know you said you stay home most of the time because of chemo and up-coming surgeries, but in your case, you might consider going back to school or work part-time..I think that you would have more support outside of your home..Even if you just did some volunteer work to help get you out of the rut that your family is keeping you in...If you find a good Cancer Psychologist I hope that your family also gets the counseling that they so need....Best to you.....
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Allison,
You are doing the right thing by being here with us ladies. We will hold you up when you are feeling down. Beauty is on the inside and you have to recognize that. I have been seeing a phychologist and it is very helpful. Between my shrink, this wonderful site and my friends, I have overcome quite a bit. Your husband was definately very insensitive to have said such things in front of you. He probably did not mean it. As the other gals will attest, know one can understand what we have been through. Hang out here and whenever you are down, just reach out and one of us will hold your hand.
Like you, I also had to have my left TE removed on 9/9 and I can't stand looking at myself in the mirror. I feel like a freak from a horror movie. I would recommend working with a phychologist as I found it extremely helpful in dealing with my emotions and keeping a positive outlook. Like you, I was torturing my family with complaining all of the time about the pain and discomfort and I get tired of hearing myself complain. My phycologist assisted me with addressing my family without screaming at them. You need to speak up wtih confidence in your voice and tell them how you feel. You have endured so much and deserve to vent. I also recommend that you find someone outside the home for support whether it be a friend, coworker or someone from school that makes you smile in their presence.
I am also having trouble sleeping which just started. I was initially sleeping all the time and now I am feeling as if I am speeding when trying to sleep. I think it is either the tamox or the effexor I have just started to take. i am grinding my teeth when I sleep too and wake up with not only a very uncomfortable chest area but my jaw hurts like hell too. Each time I wake up I am sad that this is not a dream and it is real.
Hang in there girl and keep smiling. As I like to say, fake it til ya feel it. You will again find happiness and be grateful to have lived through this. If you want to talk more, send me a personal message. I am not back to work and have all the time in the world, especially to support my sisters here. God Bless you and I hope you feel better, both physcially and mentally.
<<HUGS>>!!!
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Please, don't feel bad about venting and don't think that how you feel is wrong. You've been through major, major changes. And I know it's so frustrating to be limited in your activities when you're used to being a really active person. You just want it all to be over with so you can get back to something of a normal life.
But...maybe this all happened (the bc that is) as a way to tell you to slow down and start focusing on you and taking care of yourself. From what you wrote it seems like you need to slow way way down but you don't realize it. It seems like you're really focused on what's going on outside of you...you've mentioned worrying about what your husband, son, and mil think of you. You've mentioned worrying about how long it's going to take to finish school. You've mentioned keeping up with housework. It sounds like it's time to go inside yourself and focus only on you for awhile to heal your body AND mind. Meditation and yoga are great for calming your mind and reducing stress and yoga can be as gentle as you need it to be. Maybe find a workshop in one or both of those, or get a massage (some places offer free massages for people in cancer tx), something where your mind can just check out a while and you can slow down. Like I said, I know how hard it is to be someone who goes, goes, goes all the time and then have that suddenly change. It's so hard to sit in silence with yourself for just 5 minutes a day but it really, really sounds like your body and mind are telling you they need a break. And maybe you are already doing this and just didn't mention it. I'm just throwing things out there!
And I second finding a good counselor for you and your family. Your husband and son may be just as lost as the rest of us when it comes to how to deal with all this. But they need to learn the tools to help them cope and have more empathy for what you're dealing with. When regular counselors didn't work for me, I found a hypnotherapist and hypnotherapy has absolutely changed my life. Or maybe you have a support group in your area? If not, see if there's any interest and start one! You can't be the only cancer patient that needs to connect with others who know what they're going through. And it would look great on a resume when you do finish school!
Hang in there girl! I know it seems like this will never end, but this isn't forever!
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Allison,
I read your original post about an hour ago and can't stop thinking about you. Let's just say that you sound a lot like me a few years ago, after a devastating dx of MS and then BC. So here's what I learned...I'm not a therapist, but have climbed out of a deep, dark hole myself.
First of all, your family (especially dad) are practicing a simple survival technique...they are thinking of themselves and what they can handle. Obviously you look very different than what they are used to. Men, as we know, are very visual. They cannot reach out and comfort you because they are simply trying to stay afloat themselves. Don't start feeling paranoid about your husband. I learned that many women actually ask/force partners to leave, just to feel some relief from that overwhelming paranoia. Talking/whining to your DS and DH will probably frustrate them because they don't work that way... they are programmed to Solve Problems and they can't solve yours....find someone professional.
Depression, which I think is where you are, has LOTS of very physical side effects... a huge one being sleep issues. Combine that with the chemo, and it's no wonder you're sleep cycles are messed up. If you are offered sleep meds. use them carefully....very addictive.
Can you resume one or two classes, with an understanding prof. so that you can move forward? It's really important not to cut yourself off from what is your "normal" life. I think that just being around objective people (not emotionally involved with you) will give you a huge lift.
Lastly, plan small tasks for yourself and do them well. Keep a notebook of your day and what you've planned and accomplished. Make sure one of these tasks involves taking care of your physical self. Plan a diet lunch, do your nails, buy a great scarf/hat, take extra time with your make-up, take a long healthy walk, call a friend. It's the little things that matter now, so make them matter.
Just the fact that you're posting tells me that you've go something on the ball. Just look at the responses you've gotten immediately. We are all listening and caring.
At the time I was going through this, I pictured myself in that deep hole. There were people I loved all standing at the top offering help, but no one threw me a ladder. The truth is that you have to build your own ladder! You will be so much stronger and have a ladder for life once this is over. Sorry for the crazy analogy, but it worked for me!
Caring.....Beth
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Dorothy, if you know you are grinding your teeth for sure, run don't walk to your dentist and have him make you a mouth guard...About 10 years ago, my nerve endings in my scalp went crazy, felt like I had worms in my head couldn't sleep, headaches etc....After seeing many docs and having many scans for about a year, even a brain MRI...I happen to be at my Dentist and mentioned my se's and he made me a mouth guard and low and behold, the first night I wore it that horrible year of aches, sensations and no sleep was gone..Just by wearing that mouth guard....Just a thought, hope it works for you too....
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Hey Somanywomen,
I have a mouthguard. I just had six of my front teeth crowned by a cosmetic dentist (at at cost of 12k) and finished the year long process right before my surgery. The dentist made me a mouth guard but it gags me so bad. Also I misplaced it. You are right though, I need to find it and get it in and try to get used to it or I will grind my new smile away. I had the same issue with retainers with braces on my teeth. I have an aweful gag reflex. I am glad you reminded me, there are times when I just fail to think! With everything else going on with the big C, I did forget about finding it. I had just gotten it a few days before my surgery. Once I had the surgery, I told myself that I will start trying to wear it again once I feel more comfy. Here I am 2.5 months later and did not think about it til you mentioned it. Yikes. Thanks again. I love it here, I can't say it enough.
Love and peace to all of my friends here!!!
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Dorothy, Glad to help, what I couldn't believe is that it took me a year of so many docs and tests and then by simply talking to my dentist about the se's that all the other docs were complexed about, that a simple guard to keep my teeth from grinding took away those horrible se's the first night I wore it..When our nerves are rattled (at that time, my dad had just passed away) and it started my grinding to major degree. to the point that I had to go on Paxil etc., and with this bc dx, I bet there might be a lot of us grinding away at night and not even realizing the extent of se's that this might be causing...If you can't find it, I believe Walmart sells one that you may get temporary relief with...Worth a try....Let us know if it works....Best of luck...
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((((Allison)))) I had many days where I felt like you do now, but I just have to tell you that yes, tx does eventually end, and your hair grows back, and the chemo weight (which is a lot of water weight) comes off, and you will see the light at the end of the tunnel.
I don't have any wisdom to make it all better at the point you're at now, but I do have two or three random thoughts about your situation. First, it sounds like you don't have a very supportive family -- especially if your son is rolling his eyes at you! Where is that coming from? It sounds to me like your DH & your son need to talk to a bc therapist as much as you do. What you are going through is tough, and if they can't have compassion for you, as well as be able to reassure you that it's temporary and you WILL get through it, they truly need an attitude adjustment.
I also know how disappointing it is to see the days go by and feel like you're not accomplishing anything, especially when you had specific goals for this time frame. So what I'm wondering is, if you're feeling up to it, could you possibly take a class or two on-line? Phoenix, Kaplan and others all have very credible on-line programs these days.
My other thought is, are you getting outdoors and getting any exercise? You need both fresh air and exercise to get your endorphins going to fight the bc blues, and I think you'll find that even walking around the block for 10 or 15 mins. to start will give you both time to sort through your feelings and the physical movement you need to start feeling like you have control of your body again. Trust me; it can make a big difference in how you view things.
I'm also going to PM you a poem someone shared with me early in my tx that kind of addresess what you're going through and helped me through those low points. But above all, remember -- you've had a rough time, but by this time next year, this will all be behind you and you will be reaching out to others who are you were you are now. Deanna
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Namaste!
Allison: You are going through a really rough time right now but trust that this will get better. Praying the serenity prayer "God grant me the serenity to accept the things I can not change, the courage to change the things I can, and the wisdom to know the difference" has helped me tremendously. You might try that.
I hope that you will have access to a counselor that works frequently with people going through cancer treatment. They will have insight to what your family is going through too. Your son and husband are certainly still reeling from your diagnosis and treatment and the urge for them to react how they are speaks to how overwhelming it is for them personally. But Allison, you have enough to do to just take care of yourself. It would be great if they could provide the nurturing and understanding that you need right now, but since they are not currently up to it you need to find the resources to take care of you. This group here is great. Also, it would be great if you could get into a face to face support group in your area. The baggage we carry is so much lighter when we share with each other. There is a sense of renewed strength after being with our sisters.
Also, I would suggest developing a part of your life that has nothing to do with cancer. It doesn't seem like you have that right now. It is very possible that you could take a class or two to move towards your nursing degree. Talk with an advisor at the school you were at. You are going to be around a long time and you need to be thinking about this future. I am a nurse and I work with many other nurses who didn't start school until their kids were out of high school. Many of them did much of school part time and still have decades to practice their profession. You will too. The PS is probably only partially right. With your reconstruction surgeries their may be "short intervals" where you won't be able to do "clinical" student nursing but you certainly will have very little limitation on classroom or online classes. We need more nurses! If your current school won't work with you find another that will.
Hugs to you.
Karla
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Allison, we haven't heard from you today. Please report in, as I'm sure I'm not the only one wondering about you! Did you talk to your onc. today about a referral for a psychologist/therapist?
Hoping you're well....Beth
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Yes, Allison, please let us know that all is well. Your friends are here and thinking about cha! Hugs to you girl!
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Allison
So sorry for how you are feeling. We all have days like that and you definitely should reach out when you feel sad. When I got diagnosed my friends father had just got the all clear from 18 mos of treatment for Lymphoma. He visited me one night and gave me this tile that simply said "One Day at a Time". He said a bc survivor had given it to him and he was in remission and passing it on to me. He reminded me that I would have many sacrifices in my battle and one would be time. I needed to gear up and get ready for the fight and that meant that for a year or so I would have to just fully focus on getting better going through treatment...I needed to take this journey One Day at a Time. It sucks and its the hardest thing any of us will ever have to do...but we must. There are days that I feel so sad and lonely, fat and ugly..but then I remind myself of the endgame. I want to be here for my family and for my friends and we all have too much life to live. It is hard but you can do it. I wish too that someone told me in the beginning how long it would really take for reconstruction and chemo and just getting your body back. I had my reconstruction a few weeks ago and when the PS told me it would take 4-6 months for the swelling to go down and really see the results I broke down in his office. I felt tired of feeling ugly and lopsided.. a week after that I had my first MRI since dx. It was all clear!! That helped me put it all into perspective and really washed away some fears and I felt so happy for the first time in so long. You are still so early in your diagnosis and you just have to remind yourself YOU WILL GET THROUGH THIS. Sounds like maybe you need a night out or in with girlfriends...maybe some pampering or retail therapy!
Remember that everyone is here for you and you can PM me anytime...I never sleep.
Stay Strong!!
Di
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Allison..hey...I'm sorry you are having a hard time.... It's ok to have these feelings.. Will it get better .. Oh for sure .... But it will never be the sane ... the old life is now the new you ...You learn to take that first step and fight this 'c' one day at a time.... As the days go on you come to think less and less of " I have cancer' ...
I'm going on 7 years since my first dx... mine is mets to the Abdomen now..I wasn't ready for the page to turn in the chapter of my life.. But I guess a higher power was ...
Stay strong and get some help....I'll be thinking positive thought for you .. ((HUG)) goody :-)
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Allison - I think we all go through some of the same things you are going through now. Everyone's experiece is different, but as others have said, things will get better. I agree with others that you should try and find something to do so you can not be 100% focused on cancer.
I did 6 months of CMF chemo and, though it's considered a lite chemo, the last three months were miserable. I was depressed, tired, and had side effects, which, to me, were very difficult to deal with. I worried that I complained to my family too much and that they were tired of me taking naps and being irritable and irrational. I think it's true that we become a little paranoid about those we love.
What I want to say is that this will pass--at least the worst of it. I am already feeling better and looking forward to my exchange surgery in November. I'm tired of being lopsided and having a baseball for a breast! I think I was lucky in a way because my breast surgeon told me early on that it would likely be a year of surgery and treatment. The first time I met him he told me that "2010 would be my breast cancer year."
Hang in there and I hope you find some support to help you through your treatment. Use the women on these boards--they know what you're going through.
I'll be thinking positive thoughts for you.
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I went to the oncologist today and chemo. I waited nearly two hours to see the doctor before chemo and was soooo tired. He said he was kind of in a hurry as he was running behind, so I had so many questions about bloodwork, side effects, etc. that I totally forgot to ask him about therapy. I go in today at 1 for my Neulasta injection, so I thought I might ask the nurse. There is also a breast cancer nurse at the hospital that checks in with me occasionally, so I thought maybe I could call her as well. In response to the length of time this takes, I knew it would be a while, but originally they said January I should have my exchange and since I developed the infection and had the TE removed on one side it will now be January of 2012!!!! I know it will come eventually, but the waiting is certainly no fun. I appreciate all of you ladies so much. It is therapeutic in itself just to have you all here supporting me. I will let you know as soon as I talk to someone tomorrow. Thanks again and take care everyone. Allison
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Hey Allison,
Thanks for checkiing in. I am sorry that you had such a long day and also that you have to wait so darn long for the exchange surgery. It is not easy being patient as our bodies go through so much and like you, I am very anxious to get the reconstruction complete. I also have one side that is concave due to the TE removal. But it is a process and we have no choice but to grin and bear it while waiting.
I want to tell you that yesterday, I got outdoors and pulled some weeds, only for 45 minutes but the little workout I did was so invigorating and I felt the best I had since pre-bmx. I did nothing for the first eight weeks our of fear of breaking myself open again and it was so nice to do something that took effort and was productive too.
Sending love and peaceful thoughts your way. Hang in there honey. We are here for you.
xoxo
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Allison,
So good to hear from you! Funny that you would mention the BC nurse who checks in with you...she's checking in FOR A REASON! So let her know what's going on, and absolutely talk to her about a psychologist. Better yet, CALL HER.
Don't we all HATE the docs who tell us that "they're behind." I once walked out of a bs office when two other people checked in with my appt. time for the same doc. Never went back... it was very enpowering.
I, too, am sorry that your reconst, will take so long, but be glad that you are able to get it done at all. You're skin will be all healthy and ready for the surgery.
On the bright side, I have to tell you all about my other posts/issues because it's a bright spot. I'm going through a recurrence scare (seeing a new bc surgeon on Mon.). Had an MRI that was misread (yes, you read that correctly) and the mistake was discovered by another radiologist who did an diag. US a week later. I got the bill from the MRI place, $780-my portion. I called them and said that NO WAY was I paying. I actually got a call from the exec. dir. of the corp. who owns them, with an apology! Offered to pay for the US that discovered the mistake, too!!! I'm sure they're afraid of litigation, but who cares? I can't believe how happy this makes me....am I nuts for getting my jollies from someone else's mistakes?
It's a beautiful fall day here in IL., and, like Dorothy, I'm going to garden, rake leaves, enjoy my daughters home from college and not think about the future right now. Hope you can get outside and feel the sun today, Allison. (We all need the vit. D, too!!!)
Beth
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Hi Allison,
I am just checking in to see how your weekend is going. I hope that it has been a good weekend for you and that you got to enjoy a little sunshine. I have been thinking of you and hope that you are progressing and feeling better.
Beth, I pray that your appointment tomorrow goes well and that you get nothing but good news. And I must say, "empowering" is a great word to descibe the feeling of firing your doc lol. I had that feeling when I switched plastic surgeons; I had my records redirected and now they are calling to ask why. I am pondering my response. If I say how I really feel, I may get locked up!
Take good care, my friends! I hope it is a good day for all....
<<HUGS>>
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Hi Allison,
I read your posts and all the responses, and it doesn't suprise me in the least that you feel sad. You are in the middle of a tough treatment. You should see if you can add an anti-depressant to help even you out, and are you taking steriods right now? They really mess up your sleep and mood, and when I am tired, watch out! Steriods are for side effects, so ask your onc if you can back them down. I took them only a few days after treatment and none after 3pm. It really helped me in the sleep dept.
There are cancer social workers and therapists who work with cancer patients and their families. Much of it is free and might give everyone a chance to work through their feelings. Even my father went to one and helped tremendously.
Allison, right now is such a rough time for you, but it will get better. What I did during treatment was break it up into little pieces so that it wasn't too overwhelming. Surgery I just focused on surgery. Chemo I did 4 AC 4 taxol, and in my mind I broke it up so only 2 rounds in I could say "halfway through ac". Just sounded better to me.
All my best.
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Allison, Well, it looks like we're not going to go away! It's Monday, and a great time to make a phone call or, better yet, an appt. to see a therapist/psychologist!!! Hope you had a good weekend, and did some things for yourself.
Funny story....My 16 yr.old DD wore her BC shirt to school on Fri. (a sanctioned BC awareness day at her school). The shirts says, "Save Second Base". So then she has to babysit right after school, at the last minute, with no time to change. Well, you can imagine the conversations she had with the 6 and 8 yr. old boys she babysat. They are baseball fanatics and were very concerned that second base NOT be eliminated!!!!!
Hope that made anyone smile!!!! Beth
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- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team