Single, no kids, - how do you cope?

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This is basically a thread for that small minority of us that are single, never had kids, and are struggling to get through our treatments with little support. We are dependent on our own resources, careers, and insurance, or lack thereof. We may be dealing with our parents' health issues as well as our own.

What we do not have is a husband or long term SO that supports us through our trials. We do not have to contend with children or have them giving us a drive to live.  Unless you count our pets, perhaps. LOL  We are most likely living alone, having issues with not just mojo, but finances, having to do everything for ourselves and learning that we are not as independent or as strong as others think we are?!?!

I am 50. I never married; never had kids; buying my own home; had a successful career until BC; do not currently have a SO; have elderly parents that do not live close to me; struggling with Cobra and LTD; and worrying about my friends burning out with my constant reminder that we are all susceptible. I had no risk factors other than not having children. I have always been considered in good health and fit. I did develop asthma 15 yrs ago, after moving to a small town for my career.

Losing my breast was devastating. Becoming a hermit on LTD is frightening. 

I am afraid that I do not have a very religious side but all are welcome here. I just hope no one expects me to say that I am depending on prayers and faith.

Maybe we can find a niche here?

C

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Comments

  • LibraGirl
    LibraGirl Member Posts: 160
    edited November 2009

    Hi C

    Thanks for this thread.  I went through chemo last summer on my own (46 never had kids, no SO rigth now, family lives hundreds of miles away) and from the outset made a point of being very open about my diagnosis and recruiting friend, coworkers, and family to come to chemo with me and then stay a few days to a week afterwards to help me get through the worst of it.  Will you be/are you doing chemo or rads? I also had friends come to a lot of my onc appointments and take notes.  I'm actually finding it more difficult now that I'm done treatment (save for tamoxifen) and the sympathy train is over and there is no one to share the day to day reality of how my life has changed.  Luckily I met some other bc surivors during chemo, and I look forward to the rare times we can get together to listen, vent and share.  I envy the ones who are married with kids.  I had a double mastectomy and recon (still in progress) this time last year and am still "making friends" with my new body parts, and nowhere near even thinking about introducing them to someone else. ;-)

    Anyway, thanks for starting this.  You are not alone.  And reaching out for this support is good for you and for the rest of us.  

    Hugs

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Hi Libragirl,

    I had neoadjuvant chemo in June of 2007 and then surgery twice in the winter of 2007-08. I had chemo, rads, and Herceptin in 2008 until I developed Congestive Heart failure. Then all treatment stopped. I was 48 when dxed. I was also very open with friends and coworkers about my dx and recruited lots of them to help me get through it.

    You are ABSOLUTELY RIGHT!! It is now after the treatments are almost all over that the sympathy train has moved on to the next station. I am still trying to get thru recon as well. I had a unilateral mast and had a TE placed at the time of the surgery.  I thought I was going in 2 weeks ago for a DIEP pre-op appt and instead received another fill of 70ccs! I haven't had a fill since Feb 2008!!! Now who knows when I will get recon. I have been hoping for it to be before the end of the year, so that I don't have to worry about another deductible and because my Cobra ends in Feb 2010. I will officially go on Medicare at that time. 

    I am on disability due to the complications from my aggressive chemo and rads. Now, even if I felt like I could go back to work, my job has been terminated due to the economy.  I have to get reevaluated every few months for my disability. I am scared to death that my company disability will cancel me. Then I am left with only Soc Sec Dis.  

    I am hoping that this thread will help us all get through this. I am nowhere near introducing my new bod to anyone else either. Not to mention that my docs didn't tell me about some of the mojo SEs from the chemo. I have some capsular contracture with my TE and I am sooo iritated when the docs smirk and suggest massage will help.  As if I have a SO that would love to massage a brick! 

    Hugs to you as well! I am hoping this thread will bring out those like us that need a place to vent and get support. Since I live in a small town there are no support groups and few survivors willing to talk about their ordeal. 

    C

  • moonbuddy
    moonbuddy Member Posts: 64
    edited November 2009

    CM-

    I'm going to post my last post in other thread here as well.  In many ways i fit right in and you'll see why.  I do have kids, but they're sssssssssssoooooooooo busy and divorce at 42 landed me here with this group. BRB have to figure this out.  I have so many of same problems, glad you started this thread. 

    Marian

  • moonbuddy
    moonbuddy Member Posts: 64
    edited November 2009

    cmharris.

    .Question: Breast mound has complete feeling.......I don't understand i guess. I'm not having reconstruction, at least not right away after BMX.  You had spacers put in or something? Does that entail what for you? What's in there or out there that you can feel?  If that's not too intrusive a question.

    Nebraska, thanks.  I'm kinda embarrassed about always posting about Moon and Buddy, but they are my friends, my roomates, the largest part of my life really. Pretty shy, don't have much to do with anyone outside work, and mainly just stick with my folks (92,90) for socialization except people i meet on River Road walking the dogs.  It's the one constant I adhere to. I have to be really sick not to walk them.

    Queenlurker,

    I already thought about that.  How cool, though.  I now am getting to know an entire group of incredible people who are going to be ageing with me.  With upcoming surgery and recovery i don't see me leaving the forum for at least a year. 

    One reason i stick to this forum (nice to say forum, not thread) is i'm making friends, who i'm even starting to remember names and some people i remember where they live, if not, most of us have that posted, really like that.  Like to look where people live and wish i was there.

    A dream of mine: I so badly want to move to Alb./Sante Fe area of New Mexico.  Have dreamed of it for years.  Even since divorce somethings always held me back.  Now I would never leave while folks are alive.  But then i think about my grandkids.  Then, and this has to be common for all of us, I think, at what point can i move where i want?  When i'm too old to enjoy it?  First, it was your husband and kids, then kids, now grandkids, But damn, i don't even know how i'd accomplish it, but i really know, if i don't do it soon, i won't.  Input, do you guys get to see your grandkids?  i'm two hours away now.  But the expense of driving down there for everything is rather cost prohibitive. I could move closer and work in Lawrence, but there's few places more expensive.  Believe it or not, New Mexico is less expensive than Lawrence, KS.  Besides, if i moved, there's no saying both my kids won't eventually move.  55, divorced many years, no dates, damn that's not my choice, must be the small home town thing and i don't drink.  Actually don't really socialize, but in New Mexico there's everything to do and it doesn't cost. (Can you tell i've been there? :)  I have MS also.  I will say, change in drs. scare me, but that's just natural. Oh gosh, you guys, we're all within the same age range, I'm always going to be working,on limited income.  Own my house here, but if something happens i can't afford to fix it.  Sell after my parents are gone and go?  Rent, so i don't have to worry about upkeep. Can't manage it on my own.  What are your thoughts?  I can't follow my kids around, they'd be annoyed for sure.  I don't know they'll stay down there.  HELP? 

    Marian

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Marian,

    I replied to you on the other thread, but you are definitely welcome here.  It is difficult to go through this alone. I think one of the main differences for those of us without kids is that we do not have children or grandchildren that provide us with that "reason to live".  Not that we want to die, but we do have some separate issues.  I know that nieces and nephews would miss us or want to help us some, but it isn't really the same, is it?  I know when I think about a will there is really no one that stands out other than my parents. Since they are elderly it is hard to expect them to really be here for me either.

    I know for me, some days the only thing that keeps me going is the knowledge that my cats could not be cared for or loved as much as I do. No one else would consider spending $2000 on any one of them while they were going through chemo. I did. Because I know during my darkest hours of this struggle against cancer, my cats kept me from going over the edge. Unfortunately, the stress of my illness is already contributing to fatal outcomes for my cats. I lost one during my first round of chemo. I am losing another now, 2 yrs after my mastectomy.  The only reason that the vet can give me is stress. I have another that is pulling his own hair out because of the stress. Why so much stress? Because of the disabilities from the chemo tx, I am unable to work and often cry from the pain and despair. I guess my "early retirement"is proving to be "familiarity breeds stress and illness".  When "meommy" is on 3 different anti-anxiety drugs and Methadone amd Vicodin, the babies get stressed.  

    Frankly, I think it is more than that, but I have even taken my cats to the University Vet Hospital 90 miles from here (hence the $2000 on one cat) and no one can tell me why they are suddenly having problems. The first one that died was only 4 yrs old, the rest of the kitties are about 12 y/o. So maybe in some respects age is the issue.

    But I digress.... perhaps only a furbaby's meowmmy can understand.  But I run into mothers that cannot understand how I can feel as strongly about my pets as they do their children. I will go the extra mile for them. They are ALL that I have and ALL that I probably EVER will have.  When I think of my legacy, all that comes to mind is generations from now, a distant relative will say... "I think this belonged to a great aunt or something, don't know much about her". No beloved mom and grandmother...

    However, this is not the only issue that we singles have at this stage.  We also have as I said financial, insurance, etc...  

    I never thought that my decision not to marry or have kids before this was a bad idea. But right now... I wish that I had a husband or kids to cry on their shoulders.... sigh... I am tired of being alone.. OK it is almost dawn and I have been up all night so I am raving... LOL

    C

  • pitanga
    pitanga Member Posts: 596
    edited November 2009

    Girls,

    For so long I have been reading posts about ladies whose kids are what give them the strength to go on, feeling like I was the only one who not only didnt have kids but also no SO. It is a relief to know I am not the only oddball.

    I live abroad. When I got my first dx in 1999 I went back to the states for treatment. Like you CM I had no risk factors except for not having kids. 39 years old, active, thin, nonsmoker etc. I was in the middle of working on my PhD and after tx was over I came back to Brazil to finish. Also because I was in a relationship here at the time. But that fell apart because of the mojo side effects of tamoxifen. Still hurts to think of it.

    I defended in 2005 and since then have been scrambling to get myself a permanent job, very competetive in academia. So having kids was still not a viable option. I kept thinking I would eventually meet my soulmate and when that had stabilized, adopt. Until strike 2 came earlier this year-- Iocal recurrence and mets. Now even adoption is a pipe dream. As for the soulmate--as LibraGirl said, I am still getting making friends with the foob myself, introducing it to someone else is a big step.

    This time around, for insurance reasons --as well as the fact that here I have a house and a temporary job -- I stayed in Brazil. My parents are both dead. My sibs and stepmother, for various reasons, couldn´t make it down here for my surgery. So, it has been a lonely battle. It is still.

    Nice to meet y' all.

    Lisa 

  • moonbuddy
    moonbuddy Member Posts: 64
    edited November 2009

    Ok,

    CM, I do have a little info to help you.  I also am on SSDI, And very proud that it's off my income and not my exhusband!

    There is a program that's called working healthy in Kansas.  In other states, you can find it under medicade buy-in.  If you can work at least enough to have FICA taken out of your check, it will allow you to buy medicaid to be your medigap insurer.  Basically, if you qualify because of finances, which i certainly do, you'll have your medicare part A and B and D paid for.  It will also pick up all buy a very very small amount for copays for all you have done until you're 64. (At this point, i'm not worried about after that).  You should have just gotten a booklet called medicare and you in the mail. Inside the front cover is numbers to call for the extra help. (PM me for #'s to call for info, etc)

    Also, you can work and make up to like 980 a month in 2009.  Maybe more in your state.  I work at SRS in KS, that's how i know this stuff.  Some of the southern states, have even looser rules about what they count for income and it's even easier to buy in.

    Hope that helps.

    The lack of a SO is something most married women don't get, unless, they are unlucky enough to be on this forum.  I think here they do realize, that they have the extra income, help, don't have to worry about missing work, losing job, insurance, and retirement being Oh god, i have no idea how bad retirement might be.  I used to have a company of my own, made plenty of money, spent too much on others, didn't worry and never really thought i could get struck with an illness. 

    I don't know about others, but i'm fairly good looking, my body is not as good as cmharris' picture for sure, but i work out, keep my weight down, had a rise in weight due to medicine a few months ago and again have to lose another 15# which on a short body is a lot. It's hard enough to find a SO in regular times.  I really do feel like i have to move somewhere else for that to happen.  it's just too small here, and the only free thing to do is walk the dogs on the River Road.  I need an area, where there is more free things to do, get involved, meet others who are maybe starting over.  I also think it would have to be one hell of a man before i would risk sharing my battlescars. 

    I can only work part time and keep my medical and SSDI and every time i've tried to work full time, i've crashed, gotten sick and been deeper in the whole.  Finally have accepted fact i work 15-17 hours a week, get good wage because of position and that's all i can work.  Period.  have tested it too many times to mess it up again.  I can pay my bills, buy my groceries, but if i miss work, look out, there's no leeway in my budget.  That's why i'm not getting reconstruction with my BMX in January because i can't take the time off.  Not sure what i'm going to do about the time i take off for surgery.  worry about that later.

    This may be a little naive a question, but will your CHF ever get better?  That's a horrible kick in the ass!  

    I kinda feel like i'm practicing at making friends here.  I'm hoping it will carry over a little into my real life.  I'm too shy.  People don't know it, assume i'm very confident, but in reality i am a hermit at home and without my animals, which seriously, i take their care so to heart that it gets me moving in the  worst of days.  Also i was wondering what do the rest of you do when you know you have to go to work to support yourself, you have to.  But sometimes you're so tired you just don't think you can make it?  I so struggle with that.  I go, but the exhaustion is horrible.  Any ideas from anyone?  I've seen the doctor, he tells me to slow down, shouldn't be working that much, he just doesn't have a clue.

    I exercise, eat right, am on the correct antidepressant Smilebut have to keep on keeping on.  Anyone else dealing with the exhaustion? (And the guilt that you haven't mowed the lawn yet for the last time before winter)?

    Enough.  I think i will be seeing answers to my questions, hearing that i'm so not alone and surely that itself will help. 

    I don't want to have to depend on a man to rescue me, you know.  I'm willing to do what i have to do.  But oh gosh, it would be nice to have someone to share the worry with.

    Thanks so much, CM for starting this thread, I really appreciate it.

    Marian

  • moonbuddy
    moonbuddy Member Posts: 64
    edited November 2009

    Oh Pitanga!

    My heart hurts for you.  And CM I do understand about the pets.  Not about not having the kids of course, but fortunately, unfortunately, I really stressed independence to them and refused to rule them with any kind of guilt, so.........................there are the reasons for 2 cats, 2 dogs.  I love them so much it hurts. 

    CM, i'm worried for you and i really think that info i gave you can help a little, actually a lot.  Your cats, i'm no vet, but i swear, i might as well have been i've had so many animals and of course, lost so many.  I swear if household stress could kill them, why didn't my year in a wheelchair when at home i was constantly crying into all four of their coats do it?  They looked at me and knew i'd feed them.  I never intend on getting another when i lose one, but i go to the shelter and there are so many many (especially cats) that need us.  I never replace, but I always seem to get another almost immediately so whoever's remaining won't go into a depression.  Then I fall in love with that one as well.  I have a house and a heart full of love for these animals.  I will probably always spend more on them than me.  Thankfully I have a small town vet that takes a hundred dollars a month from me from now until i die and doesn't bother billing me.  Hell, half the time, she has called me to take an animal when i've lost one. She says they just consider me an annuity.

    I guess i'm saying, i'm not completely sold that it's your fault they have gotten ill.  Just hard for me to buy.  They love to be cried on, I swear!

    Lisa, i only got my masters and thought the competitiveness was out of this world.  I hated it. After that i started my own company.  Was going for Doctorate when ex left after twenty years of marriage.  i was 42 and scared to death.   What are you looking at for future living? There or states?  a little lonely, bet that's an understatement.  please keep posting.

    Maybe we can all move to NM and rent a house together and fight, slam doors and hang ties when we have company??????

    I've thought about finding a roommate, but never even really thought about someone in the same position as me.  Hmmmmmmm need to think.  Really, seriously, have looked into the roommate situation possibility in NM.

    Maybe we all just need to start thinking out of the box??? Seriously.  Going to go to rest in chair for hour before work. 

    This is a very good, not exactly laughter yet, but maybe a problem solving, out of the box thinking thread?  It could turn out to be a very problem solving thread, seriously.  Oh lord, now i'm raving.........g'nite guys.  Much thanks, actually feel better, knowing youre out there.

    Marian

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Welcome Lisa!!

    Actually it was a post of yours that made me start this thread.  I really thought that I was alone on these boards. I figured that if there were other single, childless women with BC, either they had strong family support or were not using this site for support.  This is the only thread that I have started and it was thanks to you!

    Marian,

    Thanks for the compliment about my body!! My avatar was actually taken right after I started my first round of chemo. It was before the second infusion but after the first.  I have gained weight since then. It was necessary for the DIEP surgery. 

    I haven't received any info from Medicare yet, but did talk to a woman on the phone. Should get it within a couple of weeks. As for the CHF, it is improving but very very very sloooowly. I am out of breath frequently and cannot exert myself much.  I deal with exhaustion daily and then insomnia.  I feel very guilty that I am not working.  I feel like there are stage IV women that have more energy and motivation than I have.  I do not see how you doing and I can sympathize, but have no answers. 

    To all of you thank you for joining this thread. We are not alone!

    C

  • moonbuddy
    moonbuddy Member Posts: 64
    edited November 2009

    C

    Please please please do not feel guilty for not working. If you possibly can, enjoy it a little.  I did not go back to work after SSDI until my unemployment ran out. 

    Thats when i called Vocational Rehabilitation at SRS and asked if they could possibly help me with my COBRA.  They said no, but they had a part-time job and i could sign up for the medicaid buy-in.  It honestly took me from unbelievably high stress to medium stress.  My meds and dr and hosp bills are pd. for. 

    Whatever you are getting from your work for disability, figure out the highest paying part-time job you think you could get, have to be something that can be flexible, like if i'm sick on mon. i go in tues. wed. fri.  or mon. wed. fri. or tue. th. fri. whatever.Figure out how much you would have to work to replace it, knowing you don't have to pay COBRA.   Vocational Rehabilitation you automatically are eligible for because you're on disability.  They will help you find the right job.  They will help you with anything you need to remove barriers to working. (Like car repairs, any amt. of medical you owe after medicare and medicaid pay, more, just can't think). It's a great resource. The reason they couldn't help me at first, was i was asking for help w/o also wanting to work.  they are a work oriented program.  so when you're cobra runs out, you could only make like one hundred dollars a month and qualify and pay almost nothing for medicaid coverage.  Best program out there for people who want to work, and few people know about it. 

    You are dealing with an extra illness on top of BC.  Of course there are others who have more energy, even others with StageIV. 

    We'll get there together.

    Marian

  • moonbuddy
    moonbuddy Member Posts: 64
    edited November 2009

    C,

    By the way, are you getting the DIEP?  Why did they do the fill?  Will they have to remove that or keep it in or what?  Kinda confusing.  If and when i have reconstruction i want DIEP.  How long or you off work afterwards?  I thought it would be too long to add in with BMX. Figured i'd just do down the road.  Hope that's possible.  Know i have 15# they could have right off my stomach!

    Marian

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Marian,

    Thanks for all of the info! I will look into it. 

    I am getting a DIEP. MY PS called this am and scheduled me for 21 Dec 2009. Finally!!!

    I had a unilateral with delayed reconstruction. At the time of my mx, they inserted a TE behind the pectoral muscle. It failed and I had to have surgery to replace it but the second surgery was a breeze compared to the first.  They filled the second TE over a period of about 6 wks. How many fills depends on how big you want to be and how much you can stand each week. For me, the first one was put in completely expanded and it hurt. It is also the reason that it failed IMHO.The second TE was put in partially filled and I had fills of about 40-50 ccs each wk.  This last fill was 70 ccs. They said it was to allow for the sagging of the new breast in order to match my other breast. I think if they had done the DIEP earlier this year they would have found it sufficient LOL

    Having the TEs placed at the time of mx even if you are having a delayed recon ensures that the PS has skin to use. Otherwise you will end up with a patch job for new boobs. This is not aesthetically appealing in my opinion. So have a PS consult before and during your surgery. For a unilateral I had 2 breast surgeons and 2 plastic surgeons in attendance.  The TEs act as a place holder to keep the skin alive and plumped out like normal breasts. I can wear low cut blouses and no one knows I have had a mx. It looks like I had my nipple cut off and after the radiation it looked like a big softball under my skin. Very round very perky(?) 

    Anyway for the surgery they will remove the TE and cut my stomach from hip to hip. They may have to move my belly button. They will harvest the fat from my stomach along with the blood vessels that feed the fat.  They will then stuff the fat into the pocket made by the TE and reattach the blood vessels from the fat to blood vessels in my breast. They will stitch it all closed. They will have to remove some skin from the belly so my belly button may have to be moved up to accomodate the skin being pulled down to the pelvic area minus fat.  It is compared to a tummy tuck.

    My understanding is that work is a no-no for at least 3 wks.  I think that there are several women that have had it all done at once. I could not due to the rads.  I was in pain for a full month after the mx I had. So I don't think the recovery time is much different. But I am not sure. I am livng proof that you can have a DIEP down the road. I do however STRONGLY advise that the PS doing the DIEP is on hand to handle the skin sparing mx. Otherwise your results will be disappointing to both of you. 

    If you have any more questions I will do my best to explain the procedure. I have a link somewhere to an actual DIEP surgery if you are interested in viewing that.

    C

  • moonbuddy
    moonbuddy Member Posts: 64
    edited November 2009

    C

    That is so amazing!!! If you ignore the fact that this is being done to you and just see how far they have come!  I just can't even imagine the skill involved.  I  just remember my aunt and what a mess that all was and how dangerous back then! I was only a kid, 9 or 10?  We were all put on alert she might die, blah blah blah.....not making fun, it was just such a daring, dangerous and very imperfect surgery way back when, if they even did it at all!!!  You did a great job explaining.

    By the way, in the other link when you were talking about "nerve" medicine, I'm on something, i'm trying to remember..lorazapam, it's generic for something, but it's similar to ativan.  Takes longer to kick in and lasts longer than valium.  Mine is for two reasons.  Two control involuntary muscle spasms and an anxiety suppressant.  When i first started taking it, i took it as prescribed.  now i take 1/3 of what's prescribed.  My dr. told me that i he thought (and he's a no pill dr.) i would probly need some small amt. of antianxiety just b/c of my personality.   It's not anything i can control.  i didn't go in asking for it or anything, he just felt for me.  He was so great.  He told me he could give me one to control anxiety along with the muscle spasms.  If my spasms get too bad in the day now and i have to take one, i have to go home, makes me too tired.  But when i took them regularly they didn't at least not after awhile.  I'm so glad he did. Really.  After my sister died I was on a constant disaster alert type mode.  Can't really explain it.  I remember it was awful,  just don't have it anymore, probably b/c of the medicine, but also i've learned coping methods and i have to take it or not or i'll flail myself out of bed with spasms :).  Kinda funny lookin'.  Anyway, i'm just saying, don't be ashamed or embarassed.  Our bodies and minds decide their own selves how they are going to react.  Some people have horrible, horrid panic attacks where they truly feel as if they are having a heart attack and dying.  Thank god there's no reason to have to feel like that anymore.  None of my business what you do, just giving support, ok?  Besides, i'm a therapist and i've seen too many people self medicate with drugs and alcohol when it wasn't necessary, they were just so miserable. 

    Hang in there kiddo.  And i think you should be some kind of scientific writer summarizing studies and stuff.  There are such jobs.  My sister in law had one, before she went back to work full time after kids.

    Dog walking time.....Marian

  • pitanga
    pitanga Member Posts: 596
    edited November 2009

    Girls,

    There is so much in your posts to respond to but my mind is a little fuzzy today. Not enough sleep. On top of everything else a few months ago I developed bursitis in my shoulder and the pain is worse when i am lying down. So sleep deprivation is becoming the norm for me. But it is really nice to connect with y' all so I wanted to touch base again.

    You were discussing insurance issues... One of the things that keeps me in Brazil is that I have insurance here. If I went back to the US I would have to try to get onto medicaid. I went that route during strike 1 and it was an extra source of stress. I know Obama is working on trying to improve that situation but I have not kept up with all the modifications that ended up getting made to the bill. Whatever watered-down version they end up passing, I hope it takes into account the special hell that the current system creates when people who have serious illnesses find themselves between jobs.

    As for reconstruction--Moon, you mention being concerned about extra recovery time. I was concerned about that too, also because my PS told me that for LAT flap and DIEP, they have to remove some muscle tissue as well, not just fat, otherwise there is not enough blood supply. Did your PS say anything about that, CM? But the longer recovery period is only for LAT flaps and DIEPs. For implants I think it amounts to the same thing. During my mastectomy surgery in March, I got a one-step thing called a Becker implant. It is a TE & permanent implant all rolled into one. I got it because the idea of no exchange surgery was appealing but I am not terribly happy with its tennis-ball consistency. So I am thinking of removing it to get a regular silicone gel implant. I could do that during the breast lift I am due to get on the non-mx side to correct the 4-inches difference in height between the "foob" and the "boob". On the other hand maybe the new implant will also have its problems, and if they mess with both sides I will be totally helpless for at least a week. A problem when you live alone.

    Seems to me  like buying a foob is sort of like buying new shoes. They feel great in the store. It´s only after you get them home and start to wear them that you realize they give you blisters. By that time you cant return them anymore. I have so many pairs of shoes that I only wore one or two times. Now I´m working on a foob collection, LOL.

    Lisa 

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2009

    Let me jump in here...though I am married, my DH has 3 brain tumours and is sometimes like a child. He has no emtions anymore, no libido either. It's like he died 3 years ago...sigh. My kids are married and living their own lives and I see them a couple times a year. That's it. My step kids even less. I feel like I am living alone emotionally and financially as I am the bread winner. I HAVE to work. I didn't do recon as I can't afford the time off work. I am lucky that I have medical covereage, being in Canada. But I know I'll have to work until the day I die.

    My sibs live far away and no one asks how I am. They have swept it under the carpet with other bad things. I have no close friends as I come home from work, get up go to work, etc, etc.

    So I am alone even though theoretically I am not.....sigh.

  • NativeMainer
    NativeMainer Member Posts: 10,462
    edited November 2009

    C--thank you so much for starting this thread.  I, too, am 50, single-never married,no kids, no SO, my mother is nearing 80 and (thank God) doing well but doesn't really understand. If it weren't for the 2 dogs I had duirng rads (only one now) I would have been totally alone.  I went through biopsies  & lumpectomy with almost no help or support, only told my mom when I needed a driver for the lumpectomy.  Went throught rads, with multiple complications, with no support from friends or the rads "team".  Had to admit to needing help when I ended up in the hospital for 8 days in 2008 due to complications from rads, and a  mastectomy in Aug. 2008. 

    I did discover I can't do it without help, and that my mom isn't the best help for me.  I did  the typical Downeast Mainer thing-independant and private until I wound up in the hospital and couldn't hide what was happening anymore.  Since then I have been blessed with a number of friends who are more than willing to help--even to the extent of going to Boston with me when I have appointments,  But I feel like I'm interrupting their lives when I ask for something from them. 

    So many times I wished I had a husband or at least a roommate to fix a meal when I'm exhausted, to talk to in the middle of the night, for a shoulder to cry on, to know exactly what's going on and help me with all the paperwork and phone calls and faxing that goes into coordinating cancer care and reconstruction.  I even have to take responsibility for making sure mammogram and lab reports get to all the various doctors' offices.  It gets overwhelming sometimes. 

    I lost my job during radiaiton (FMLA ran out) and now work at a job that I absolutely love, but pays a little more than half what I was making.  I had to borrow a large amount of money from my mother to pay off credit cards and such.  A year later I'm still living paycheck to paycheck and terrified of a complication or recurrence taking me out of work for any length of time.  And this is WITH  good health insurance.  I'd have been better off if I hadn't had any insurance. 

    Sorry to go on so long, but it feels so good to be able to "say" this stuff where I know other women will understand.  Thank you so much for starting this thread, C.

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Hi All,

    Thanks for joining me on this thread. Feel free to vent and ramble as much as you like.  

    Barbe,

    You are definitely welcome here. It sounds as though you do fit right in here with us. I know how you must feel. I had a job that was male dominated and I, too, would go to work, come home, and go back to work again. Hard to make friends in that environment.

     Pitanga,

    I have discussed with my PS about the Diep and cutting muscle. He tells me that he will only cut muscle if absolutely necessary. At that point it is no longer considered a DIEP. He has said that if he does cut muscle, it will be very little. I am still very nervous about that.

    Mainer,

    My sister lives in Downeast Maine. I can fully relate to what you are saying. 

    Sorry I haven't posted and that thsi is so short. I lost a furbaby this week and my nerves are shot. Also, I felt that I had to make an appearance on some other threads and now I am tired. 

    Do come back, and let's see how we get through this mess. It looks like I may be spending Christmas and New Year's in the hospital for the DIEP.  The long stay is due to my being alone. My PS has suggested that I stay in a rehab hospital until I am well enough to go home and care for myself..

    C

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2009

    I am SO sorry about your furbaby! I do know how tough that is. My heart goes out to you. I am waiting to see if one of mine pulls through right now....

    The DIEP sounds like a marvelous way to spend Christmas! You will be taken care of and can't do housework or have to "perform". 

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Thanks Barbe!

    I have 4 cats and 3 of them are related to the one that passed.  She was 11-1/2 yrs old. She is also the second cat that I have lost since I was dxed. She had been struggling with inflammatory bowel syndrome for the last 2 yrs.  I knew that her chances were not good but I hoped and spent lots of money on her care in that hope.  Her condition had me very worried about having my surgery. Who could care for her while I was in the hospital? I guess fate has intervened and I am free to have my surgery now.

    It has been very hard since the cats are like children to me. I sincerely hope that your furbaby pulls through. I am not just a cat person; I love dogs, squirrels, birds.deer, etc.

    I was actually thinking the same about Christmas just this morning. I had been dreading it but now... I can relax and let the nurses care for me. It isn't like I haven't spent a Christmas alone in the past. The difference is this time I won't have to worry about dinner, housework, etc. I am hopin ghtat my cat sitter will take over the basics of housework while I am gone. She is usually pretty good about that. Before this morning, my main concern was how to put on a happy face for Christmas while recovering from the surgery if I had to have it in Nov. Then I realized that I don't have to if I am in the hispital for it.LOL

    I am glad to have you on board here. I have read many of your posts and have always found them refreshing. I have never said it, but my heart goes out to you and your marital situation. I cannot imagine what it must be like. The closest that I can relate is watching my dad suffer with Alzheimer's. 

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2009

    I had 4 cats too and had to put the oldest at 21 down last year. I was beside myself with grief! This one with the problem is the baby at 16, it seems to be in his mouth/teeth and I just don't have the extra cash to take him to a pet dentist so we're feeding him soft food and milk and he seems just as spunky. With the hard food he was bleeding all over the house on every single piece of upholstered furniture we have. Poor guy!

    Watching my husband is hard. His mom has severe Alzheimers and doesn't even know him and he hasn't gone to see her in about 4-5 years though she is only about 2 hours away. I'm afraid he'll become like that.....sigh. She is in great health at 86 or 87....and will probably live forever!

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Oh I do know how you feel! I miss my little girl terribly. She was born in my arms in my bed and died in my arms in my bed.  One of my cats has feline leukemia and he has to eat soft food for his dental problems as well. Obviously, you are a very good mommy to them for them to have lived so long. I really believed that mine would live at least 16-18 yrs. Unfortunately one died at just 4 yrs old and now this one at 11. I feel like I have failed them somehow.  I don't know how much more I could have done, but it doesn't help my guilt and grief.

    My dad is also in very good health and is in his 90's. He will also probably live forever. Longevity runs in my family. On my mother's side, my grandmother and great-grandmother lived to be over 100. My mother is in her late 80's and although legally blind is in great health also. It was definitely a shock to find out that i had cancer.  I really thought that I, too, would live forever. LOL

    I know that it has been very hard for my mom to watch my father's battle with Alzhemimer's.  I can only imagine that it must be the same for you.  To love someone and watch them slip from your grasp has got to be excruciating. I am so sorry and I wish that I could offer more words of comfort.

    Hopefully, if nothing else, this thread can provide you with some support for getting through all of this alone. 

    I fight daily with depression about my quality of life. I am on 3 different anti-anxiety and anti-depressant meds. I am now disabled from the cancer tx.  It can be depressing since I feel some days that I have little purpose in life. Luckily, I have a fairly good disability plan from my former employer so I do get a paycheck. It is less than what I was making and I am considering bankruptcy. I never would have thought that I would be where I am now. My retirement funds are not that great and I do not know specifically how my disability benefits will change when I reach retirement age. But I know they will change for the worse.

    Right now, I am fighting hard to hold onto my health insurance. In June, my insurance premiums jumped from $130/mth to $610/mth. Grrrrrrrrr...   I only have to pay that much until Feb 2010. As you can imagine, between now and then seems daunting most days. My disability barely covered my expenses before June.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2009

    Finances can add so much to the stress of disease! I was bankrupt about 5 years ago when my DH showed me a grocery store bag PACKED with bills (that's when I began to see his mental decline). He answered the phone during the day while I was at work and shielded me from the creditors. I had NO idea....honest! We lost everything except the tiny house we moved in to as the market value hadn't increased so there was no profit in it. I live paycheque to paycheque LITERALLY. I am not kidding! I have no RSPs or savings, no bonds or stocks. Nothing to fall back on. One of the reasons I didn't do recon due to the recovery time. I HAD to get back to work and up to speed as quickly as possible. I got my drains taken out from my double mast and went right to work the same day! I was off over Christmas and New Years last year. A good time for down time!

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    I hate that you have gone through that. It is distressing to find ourselves living paycheck to paycheck. I do the same. I have some retirement savings but I was told that I cannot access it for almost 20 yrs. I can believe that you were blindsided. My brother had the same issue when his wife was dxed with cancer 5 yrs ago. She had kidney and lung cancer with mets to the brain. By the time she died he was in financial ruin and is still trying to get out of it. He has had to resort to going to a local food pantry to get free food. With the current economy, I think that we all need help finding ways to cut corners.

    I worry about all of you BC sisters in the north with the winter months approaching.  Heating bills can take their toll. Do you have social services that help you with heating bills in Canada? Some states here have programs that can offer aid to low income households. Unfortunately, in my state, I make too much money to benefit from it! I am no high roller,but I make too much.

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Oh Marian,

    I meant to recognize you here as well. I am sorry my brain has been shutting down in self defense - too much depression... sigh. I am very sorry to hear that you lost your sister. No matter how much time has passed we still have our moments. I lost my best friend of 30 yrs over 15 yrs ago. When I was dxed, it really hit me hard that I could not talk to her about it.

    I have started having massive "twitches", no that's not it.. spasms? jerks? It is like sometimeswhen you are almost asleep and your leg jerks. Except that since chemo, I have had much more than just a leg jerk. My body will sometimes lift off the bed. I wonder if it is the same thing that you are describing?

    My degree is in geology so maybe I should look into some scientific writing. I avoided looking into anything like that since with chemo brain, I do not think as clearly or as analytical as I did before. I am constantly rereading my posts and editing them. I have lost a lot of my math skills as well. I am also considering going back to school. I was wondering if a school loan would help me with finances? I don't know what that would do for my disability though?!?!

     Lisa,

    I love the  comment about the shoes and picking foobs! I was lmao. My TE feels like a huge softball strapped to my chest. It is painful now due to the fill.  My skin was not used to being stretched.

    I am afraid that I have not kept up with the last mods on the health reform bill either. I have a feeling that it bodes ill for those that are falling in the cracks. We really need something for those that are unemployed or underemployed that does not limit their assets to less than $3000. That limit is just ludicrous to me.  There are so many people whose assets could amount to 5X that amount or more and they still cannot afford insurance.  Our health care leaves much to be desired. But I don't want to bore you all with my soapbox on that hot topic.

    Well girls,

    Once again, I have been up all night and I need to either get some sleep or get up and work on the dishes. My house is a disaster area right now. Good thing the cats don't care.

    I hope that Libragirl comes back and that all of you find a home here to get solutions and support. The idea of living together in NM is actually not a bad idea.  A BC commune so to speak.... LOL

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2009

    As for winter heating, we haven't turned our furnace on for the last two winters! We do have a gas fireplace in our livingroom that we keep on low and then bundle up in bed. Though we get a lot of snow, and I mean a lot! the cold doesn't bother me as much as the heat does.

    Have a good sleep....

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    By the way, Barbe,

    I have been meaning to say that I had read under other threads about your recent  issues. Please know that you are in my thoughts and that I hope it is minor and can be resolved quickly. I am sorry if it is more serious than I remember. Right now, my brain is foggy on the details.

    I am trying to figure out what bills have been paid this month and which haven't. I am afraid that the latter is more likely the case for all of them. I am so messed up right now.  Taking care of the little kitty took so much of my energy that I am having a hard time getting back to any kind of routine.

    Does Canada have disability programs similar to our Social Security? I am just wondering if there is some program that can help you, since you are the sole breadwinner in your household.

    Lots of love to all,

    Connie

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited November 2009

    Connie, I haven't paid ANY bills this month as we are finally getting our kitchen put back together. Sounds like a dumb thing to do when money is tight, but our house is worth a lot less with a torn up kitchen! We started to rip it out THREE years ago...and then life happened....sigh.

    I have tests this week and may know more. Thanks for your thoughts.

    I will go on short term disability if I have to do rads and/or chemo just to cram it into as short a time as possible. From what I've heard, I don't think I'll be able to drive an hour to work and an hour back after working 8 hours....sigh.

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    Good luck on your tests Barbe!

    I know the feeling! I think I have paid my house pmt and my car insurance but thats it. UGH

  • Meli3313
    Meli3313 Member Posts: 1
    edited November 2009

    Hello All!
    It has been very interesting to read your posts.  I have just been diagnoised with DuctalCarcinoma Insitu and been given the choice of a Mastectomy or Lympectomy.  I was shcoked and dumb founded.  My life has taken a 96 degree turn.  I just finished my last course to finish my degree and WHAM!!  I got hit with this.    I too am single, have been for about 5 years.  Divorced 9 years ago  2 cats that I"m certain they know I am going through something.  My youngest one always wakes me up by coming up close to my affected breast and laying on it.  I wonder if she knows???  I have no children.  My mother passed away 7 years ago which put me through a major depression which is why I got my first cat.  SO I decided to stay busy by working and going to school for the last 4 years hoping to possibly meet someone to share my life with and now I'll be going through this alone.  I have a sister close by, 2 brothers and a sister that live far away and never talk to and a father who is 1 1/2 hrs away.  I keep in contact with him but not at all very close.  I am 52 years old.  It's been very difficult growing older, going through menopause and gaining weight and...then this!!  I too am acertain that I will probably loose my job and benefits.  But I'm certain I can live off of disability for at least a year and hopefully find another job

    Tomorrow is my first support group.  I'm looking forward to going and meeting other women.  I am going with a friend that has already been through it.  She has been very supportive.  I hope I too can do the same for another.  I just talked to a women who is studying to be a nurse.  I didn't know that breast cancer is the #1 cancer!!!  7 out of 10 women will get it!!  I hope I will be able to help others against the fight in breast cancer.

  • cmharris59
    cmharris59 Member Posts: 496
    edited November 2009

    7 out of 10???? Last I had heard it was 1 out of 7?

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