STEAM ROOM FOR ANGER
Comments
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Mara, that is such effing bullshiz what you're dealing with. Has your mom ever read the info sheets on ALL the side effects these drugs and procedures cause? Make her pull them up and read them!! Also the more cycles you're on, the worse it gets. I'm on cycle 9 of Xeloda, and some days I can barely move, let alone scrub a floor or clean a bathroom.
We're all doing the best we can. Rest assured much as you need to.
Lita
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Thank you Lita. I decided to request a social worker to talk to. I can't take the stress anymore. Mom will go out so it will be confidential. I am sure it will help. I actually managed a little more food today after deciding. I have adv mother that I will talk to others, ie doctors, online, but will not have family decide How I should be progressing.
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My rant. LONG, DEPRESSING, OPTIONAL READ. Please ignore if you choose. I've hit bottom.
I am an emotional BASKETCASE right now. I stayed in Denial for a few weeks, had about ten days of Anger, and now I have fallen into the depths of Depair.
My Dx looked like one of the easiest, most manageable at first. Two small IDC spots close together, detected early. Breast Surgeon said, quick lumpectomy, a few weeks of radiation, and I'm good as gold! I'm able to go about my life a bit shook up, but Denial was keeping me safe. I could joke about it. Given how much more serious other Dx are, I felt embarrassed making any kind of big deal out of it.
Except the BS booked the surgery BEFORE the MRI results came in. New spot, different location, presented differently. Could be different kind of cancer. Cancel surgery the day before (when everything had already been hastily arranged), and schedule MRI-guided biopsy. WHY DID BREAST SURGEON SCHEDULE SURGERY BEFORE ALL THE TESTS WERE IN? That's when everything started going downhill for me.
In the meantime, the only BC support group I've been able to find doesn't have its next MONTHLY meeting until the end of January. I called the Nurse Navigator early this week and told her I needed to talk to someone because I was losing my grip, and she said the Social Worker would call me. Days later, no SW call. I called the NN back, told her I wanted the Psychologist to call me instead of the SW who did NOT call me, VOILA, the SW leaves me a message later that day. I am now in the Anger state- FUCK YOU, SW, I DO NOT WANT TO TALK TO YOU, you did NOT CALL ME when asked to. My Anger stage is not cutting anyone any slack. I had to call NN and tell her i DO NOT WANT TO TALK TO SW NOW, I TOLD YOU SO, I WANT TO TALK TO PSYCHOLOGIST. Hope I get a call from a psychologist early next week.
THIS blessed forum has been the only place I have been able to go to rant, as well as gain from the wisdom of others. THANK YOU, folks.
The MRI-guided biopsy was awful. It took three people four+ tries to get an IV in me, and they were RUDE about it- I'm lying on the gurney, weeping- that's the moment when Anger cracked and Despair set it- and no one brought me a goddamn kleenex. I have usually had awesome experiences with nurses, so this was a shock. I was this annoying slab of meat on a gurney whose flesh was not cooperating. As I stared at the dusty ceiling crying, I started to wonder, "Who is this for, really? Is it for me, or am I now a pre-authorized goldmine for the Medical Machine? Are the treatments and drugs I'm being advised to undergo, really for ME, are they going to ruin my quality of life in exchange for a few more years lived in suffering?"
In the MRI machine, I could NOT lower myself fully relaxed (SURE) into position, as the plastic edge was painfully digging into my ribcage. After a few minutes of this irritated direction, someone located a firm piece of foam- which looked like it was MADE for this purpose- and the problem was solved. I guess everyone was pissed that the procedure was delayed because of how long it took for someone to get an IV line in. I felt like I had become a newly discovered Revenue Stream who could be wheeled in and out of expensive tests and procedures and BILLED BILLED BILLED. I kept thinking, "I DON'T WANT TO DO THIS." The only kindness I received during the whole procedure was from the biopsy surgeon, bless him, who would lay his hand on my shoulder or back and rub gently a bit to comfort me, and say, "Yes, I know, IT SUCKS."
I'm a single parent who has lived in a state whose climate i hate (WAY too cold), far away from the little family I have left, because of joint custody and a deep desire to give my child an emotional grounding and best possible launch into life. I've lived here 20 years, waiting for the time when MY life could start, and I could move back home. I've worked loooong hours at jobs I've hated so I could scrape up enough to live in this expensive part of the country for the sake being there for my child. Because of demanding work (read: exhaustion) and maintaining a house on my own, I haven't had the time or energy to pursue any kind of relationship. I always thought there would be a time to come when I could enjoy my body again, I was living for a time for ME once my child was out of the nest. I HAVE WASTED TIME WHEN I COULD HAVE GOTTEN SOME ENJOYMENT OUT OF MY BODY. I can't even remember how long it's been since I've had sex- six years? more? Now my body is going to be ruined.
Work was been reasonably understanding of my need to go to appointments and tests, although my work load hasn't diminished one bit, so some nights I stay until 8 pm to catch up. The RAH RAH corporate culture just seems like such utter BULLSHIT when you stand back and look at it in my current context, and it's hard to disguise my contempt for it.
I don't know if I even want to go through with any of this. I feel like I am DONE. My child graduates with an advanced degree this spring- I will have done my job, fulfilled my biological mission to launch my progeny successfully into the world, so I can slough off, not needed any more in the big picture of biological destiny. I don't want the rest of my life to be surgeries, paranoia, drugs that will sap the remaining life out of me, and age me 20 years in six months. I WANT MY ESTROGEN.
I'm not religious. My friends can't understand/can't handle/don't want to hear what I'm feeling today. So I'm just staying planted on the couch, crying, wondering what I'm going to do.
This is one hell of a mid-life crisis.
Carrie.
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Whoa, Carrie, that's some rant. I find myself upset along with you about the MRI biospy. You do deserve to be treated with compassion and respect. I get your frustration with waiting for a phone call when you desperately need help. I hope there is a good explanation for that. I understand the sacrifices you made for your child.
Now I know that maybe I shouldn't try to answer because sometimes what we really need is to just get it all out. But I can't help saying that I think it can still be your time now! Treatment will not necessarily ruin your life. Remember, there many bc survivors with no major problems who are not posting here on BCO because they are off living their normal lives. You likely don't even need to do any more surgery than the one to remove the tumors. Your child is now grown. Can you move to where you want and continue treatment there? This year will involve a lot of stupid cancer stuff, possibly with twists and turns, but then it should ease up. Life may be different from what you expected, but it can still be good.
Here is another place you might find in-person support:
http://gildasclubwestchester.org/about-us/mission-...
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My rant. LONG, DEPRESSING, OPTIONAL READ. Please ignore if you choose. I've hit bottom.
I am an emotional BASKETCASE right now. I stayed in Denial for a few weeks, had about ten days of Anger, and now I have fallen into the depths of Depair.
My Dx looked like one of the easiest, most manageable at first. Two small IDC spots close together, detected early. Breast Surgeon said, quick lumpectomy, a few weeks of radiation, and I'm good as gold! I'm able to go about my life a bit shook up, but Denial was keeping me safe. I could joke about it. Given how much more serious other Dx are, I felt embarrassed making any kind of big deal out of it.
Except the BS booked the surgery BEFORE the MRI results came in. New spot, different location, presented differently. Could be different kind of cancer. Cancel surgery the day before (when everything had already been hastily arranged), and schedule MRI-guided biopsy. WHY DID BREAST SURGEON SCHEDULE SURGERY BEFORE ALL THE TESTS WERE IN? That's when everything started going downhill for me.
In the meantime, the only BC support group I've been able to find doesn't have it's next MONTHLY meeting until the end of January. I called the Nurse Navigator early this week and told her I needed to talk to someone because I was losing my grip, and she said the Social Worker would call me. Days later, no SW call. I called the NN back, told her I wanted the Psychologist to call me instead of the SW who did NOT call me, VOILA, the SW leaves me a message later that day. I am now in the Anger state- FUCK YOU, SW, I DO NOT WANT TO TALK TO YOU, you did NOT CALL ME when asked to. My Anger stage is not cutting anyone any slack. I had to call NN and tell her i DO NOT WANT TO TALK TO SW NOW, I TOLD YOU SO, I WANT TO TALK TO PSYCHOLOGIST. Hope I get a call from a psychologist early next week.
THIS blessed forum has been the only place I have been able to go to rant, as well as gain from the wisdom of others. THANK YOU, folks.
The MRI-guided biopsy was awful. It took three people four+ tries to get an IV in me, and they were RUDE about it- I'm lying on the gurney, weeping- that's the moment when Anger cracked and Despair set it- and no one brought me a goddamn kleenex. I have usually had awesome experiences with nurses, so this was a shock. I was this annoying slab of meat on a gurney whose flesh was not cooperating. As I stared at the dusty ceiling crying, I started to wonder, "Who is this for, really? Is it for me, or am I now a pre-authorized goldmine for the Medical Machine? Are the treatments and drugs I'm being advised to undergo, really for ME, are they going to ruin my quality of life in exchange for a few more years lived in suffering?"
In the MRI machine, I could NOT lower myself fully relaxed (SURE) into position, as the plastic edge was painfully digging into my ribcage. After a few minutes of this irritated direction, someone located a firm piece of foam- which looked like it was MADE for this purpose- and the problem was solved. I guess everyone was pissed that the procedure was delayed because of how long it took for someone to get an IV line in. I felt like I had become a newly discovered Revenue Stream who could be wheeled in and out of expensive tests and procedures and BILLED BILLED BILLED. I kept thinking, "I DON'T WANT TO DO THIS." The only kindness I received during the whole procedure was from the biopsy surgeon, bless him, who would lay his hand on my shoulder or back and rub gently a bit to comfort me, and say, "Yes, I know, IT SUCKS."
I'm a single parent who has lived in a state whose climate i hate (WAY too cold), far away from the little family I have left, because of joint custody and a deep desire to give my child an emotional grounding and best possible launch into life. I've lived here 20 years, waiting for the time when MY life could start, and I could move back home. I've worked loooong hours at jobs I've hated so I could scrape up enough to live in this expensive part of the country for the sake being there for my child. Because of demanding work (read: exhaustion) and maintaining a house on my own, I haven't had the time or energy to pursue any kind of relationship. I always thought there would be a time to come when I could enjoy my body again, I was living for a time for ME once my child was out of the nest. I HAVE WASTED TIME WHEN I COULD HAVE GOTTEN SOME ENJOYMENT OUT OF MY BODY. I can't even remember how long it's been since I've had sex- six years? more? Now my body is going to be ruined.
Work was been reasonably understanding of my need to go to appointments and tests, although my work load hasn't diminished one bit, so some nights I stay until 8 pm to catch up. The RAH RAH corporate culture just seems like such utter BULLSHIT when you stand back and look at it in my current context, and it's hard to disguise my contempt for it.
I don't know if I even want to go through with any of this. I feel like I am DONE. My child graduates with an advanced degree this spring- I will have done my job, fulfilled my biological mission to launch my progeny successfully into the world, so I can slough off, not needed any more in the big picture of biological destiny. I don't want the rest of my life to be surgeries, paranoia, drugs that will sap the remaining life out of me, and age me 20 years in six months. I WANT MY ESTROGEN.
I'm not religious. My friends can't understand/can't handle/don't want to hear what I'm feeling today. So I'm just staying planted on the couch, crying, wondering what I'm going to do.
The is one hell of a mid-life crisis.
Carrie.
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My boss left me a POST IT NOTE attached to some paperwork that said "You're my only employee who did this incorrectly." Well I'm sorry, assface, do you remember that I was out for over a month because I had a body part amputated?
While I'm on here, I just want to say that I feel so rotten. I should be grateful, relieved, dancing in the streets because I got off easy with a DCIS dx, zero lymph node involvement, no radiation or chemo required. But I'm so depressed I can barely function, and then I feel GUILTY for being depressed, which makes me more depressed. I'm filled with anxiety too, because all I can think about is where in my body there might be more little cancers hiding. I can't sleep and I can't enjoy anything anymore. My reconstruction surgery is in three days, and I'm terrified that once all of this is over, I'm just going to be left with the emotions but nothing to blame them on. Why am I so ungrateful?? #worstpersonever
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Fotheringay and Perdly: Just let it all out here. This is what we're here for.
One of the things I emphasize is that it doesn't matter if you're St I or St IV. Cancer is CANCER! It's still a shit deal if you only have tumors extracted or if you're facing the death sentence that is St IV metastatic cancer. Everyone's situation is different. Everything has to be factored in...ass hole bosses, f'ing ex-husbands, undesirable living situations, insensitive family members, etc. Whether you have St I or St IV, you will go thru a plethora of emotions, and that's just how it is.
No one gets off scot-free...ever.
I'm sorry you can't find support where you need it. Shetland makes some good points. I don't give personal advice on this thread unless it is specifically asked for. I try to keep it general. We are not here to judge each other, and we're not shrinks, either. We're just here to offer a compassionate 'virtual' ear for you to voice your frustrations and misery.
Anxiety about recurrence is no joke. It DOES happen, and all you can do is take one day at a time...sometimes one HOUR at a time. One of the hardest things about BC (or any cancer, for that matter), is the isolation one feels. There is NO ONE who can understand exactly what you're going thru in YOUR body and in YOUR mind. And it's not as easy as popping an Ativan or Xanax either. When the drug wears off, the feelings are still there. Each woman has to work thru them in her way and in her own time.
Try to find some solace in knowing that things WILL get better for you. You are both St I, so you should have many more years ahead. Another thing that a cancer Dx does is make you take a good, long look at your life as it currently stands. It's a wake up call. You've been given a second chance. Leave that crappy job; move somewhere else; take a trip; make an effort to bring more people into your life if you can.
As for finding a way to cope a little better, BCO has threads for spiritual people and also for atheists. As I said, everyone has to navigate the waters in their own way. I've gone to both secular support groups and spiritual support groups...I stopped going to one secular group b/c I wasn't getting anything out of it and found the spiritual one had a little more meat in it, even tho it only meets 2X/mo.
December is a crappy time to find groups b/c a lot of them don't meet during the holidays. Feel free to pop in here and rant as often as you need to. You can also PM the ladies here as well. There are a lot of women who've really been to hell and back and they can offer some personal support.
Hoping this helps a little bit,
Lita
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I would be so tempted to leave my boss a little post it note. You're the only manager I've ever had to be so insensitive perhaps you never had an employee who has dealt with cancer. Make it an extremely large note posted for everyone to see on their door.
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Perdly,
Your boss should indeed be crowned (ideally, with a bucket of molten gold a la Game of Thrones) ASSHOLE BOSS OF THE YEAR.
I understand you paranoia about recurrence. Can't say more than that. I just understand the fear.
I haven't had my surgery yet, but I can project that it is something that tales a long time to recover from, physically AND emotionally.
I will be back here, so rant all you want, and people will listen.
Carrie
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Thanks, Lita,
I was a mess all day, paralyzed, crying, alone, and being able to wail and shake my fist at the universe here helped. and your response helped.
My friends' responses have infuriated me, as they range from "keep a positive attitude!" to "put your combat boots on and power through it!" Easy, coming from people with supportive spouses with secure finances who could quit work and lay on their bed of pain until they were ready to go back to work. or not go back to work at all.
I'm not eligible for FMLA, so if I take too much time off for my (what will likely be a mastectomy), they can fire me,
There I go ranting again.
I don't have the results back from the second round biopsy, so I'm in the "waiting for results hell", too.
Point is, I needed to blow, somewhere where someone would actually GET IT. I do feel like I got it here.
THANK YOU EVERYONE FOR HELPING ME NOT TOTALLY LOSE MY SHIT TODAY.
Carrie
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Perdly, you are NOT the #worstpersonever. You have been through a lot too, and it is very normal to fear recurrence. Take care of yourself. Here is some information on Managing breast cancer fears. Vent here all you need!
Fotheringay, hang tight. We're all here for you, and please keep us posted!
Hugs to all you amazing strong people!
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Like most people with a BC diagnosis, it has been a terrible rollercoaster these past few months. I just find myself having to reassure other people - oh, it's not so bad, oh, the prognosis is good yada, yada, yada to the point I want to scream - I just want to start saying no, it's terrible, but then I turn into a blubbering mess. Better to stay positive and then wake up crying at night... Anyway, the surgeries weren't too bad, but I went through a terrible couple weeks where we didn't know if I was going to do chemo or not. My onco first said I should, then tried to talk me out of it once I decided to do it, and then let me walk out of his office with no further treatment. But that didn't feel right, so I kept bugging the dr and got a second and third opinion, until my MO decided to have my second tumor tested - thank goodness he did! It's a different cancer and HER2+, so more chemo and Herceptin for 1 yr.
The Sunday before Thanksgiving, I drove 9 hrs to Salt Lake City with my parents to go to a fertility clinic to have eggs preserved before starting chemo. My husband did not go with me because we had already planned a trip to his home state to visit family and he didn't want to cut that trip short. So he and our (nearly) 4 yr old daughter left on their roadtrip on Saturday, we left on ours Sunday. Monday and Tuesday were ultrasounds, shots, blood-draws. (besides the 2/day shots I've been giving myself for the 10 days prior, and the numerous blood draws over the past 2 weeks - my right arm vein was bruised from so many pokes). Wednesday morning, I had the egg retrieval - went well and got 17 mature eggs to freeze - woo hoo! Then I flew to city where In-Laws live to be with my family for Thanksgiving. I'm tired and crampy and not feeling great, but it's so great to see everyone.
Thanksgiving day was pretty normal, uneventful, it was at my Husband's Sister's house where we were staying. My MIL brought a nice bottle of wine that she knows I like. I know I'm not supposed to go crazy with the wine, but I hadn't been able to drink for 2 weeks, so I had a couple glasses. After dinner, BIL wants to go around the table and say what we're thankful for. I say something like thankful for an uneventful plane ride so I could be here with everyone. Other people say family or whatever. Then SIL is next to last and is going on and on about how happy she is that I'm doing well. And while I want to interrupt and say appearances aren't everything, I just smile and nod and sip my wine. The last to go is my 8 yr old niece. She smiles coyly and says "I'm thankful for the baby in mommy's tummy."
Jaw meet floor.
I chugged the rest of my wine and excused myself from the table. I just couldn't.
My husband and I were trying for a baby when I found the lump. I know that they shouldn't put their life on hold for me and I'm truly happy for them, but dear lord, have a little compassion. SIL knows I wanted to have a baby this year and everything I went through just to freeze eggs so that some day MAYBE we can have another kid.
Love my SIL, love my husband's family, but dear lord, that is not something I was prepared for. It's like SIL knew it was a bad idea, but thought she was making it better by talking about how great I was doing and that they were praying for me.
Ugh, I just wanted to scream. I went to the bedroom and had a good cry and did eventually talk to Husband and SIL about it, but had a puffy face the rest of the night. I still can't talk about it without crying.
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You poor girl, what a cruel irony...I am so sorry. I'm glad you were able to talk to your hubby and SIL about it. Negotiating the emotions surrounding her pregnancy and birth will be tricky, just don't beat yourself up for anything you feel. It is damn hard to celebrate others' joy when the bottom has dropped out of your life and dreams. It isn't petty or mean to feel that way...we aren't saints, just human, and it doesn't make you a bad person. In spite of your pain, I know you will be a great and loving aunt. I wish you all the best with your treatment and healing and don't give up hope. {{HUGS}}
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I'm struggling this week with alot of "feelings" and I don't appreciate it. I had a nice Thanksgiving in spite of some shitty family stuff and I wanted to just stay in that after glow for awhile, but doesn't look like that is going to happen.
My mom really really upset me over Thanksgiving and while I was ready to move on from it, she just has to dig into and get it all worked up. We had planned for her to come for Thanksgiving and stay for a few days, the kids would all be here and she would be meeting her granddaughter's husband for the first time. It was supposed to be a wonderful time, but it took a turn for bad because mom has issues with driving, she just doesn't get into the car. I had hoped she would be able to get thru it, but it didn't happen and it was hurtful to everyone. This was a big deal to me too..more than I realized until after. But, this Thanksgiving marked 3 years from my mastectomy, and spending the holiday in the hospital. It was a blessed day as I was going to be cooking and I really wanted her here.
It has hit me like a ton of bricks, but the realization that my mother has put herself and her feelings in front of me so many times for so many years. I've overlooked it, blamed myself for it, made excuses for it. But, this time I'm having a really hard time doing that and keeping my feelings in check. I don't know how to tell her how hurt I am without feeling like I'm going to make her feel bad.
This thing with the car is a phobia, but it has caused so many issues in her life. She doesn't participate in life in a normal way, and to the point that she expects everyone to work around her issue. Mom didn't come see me in the hospital ever during treatment, hell she didnt even come after the birth of my 7 year old. She guilted dh into having us stop by her apartment on our way home from the hospital.
There's so much more to this, but I'm just really angry and depressed.
Also, I found out one of my friends here passed away. She had been MIA for awhile and I'd been asking around for her, and no one knew. Finally I was able to send a card to a mutual friend who was going to forward it to her....I sent that out and then found out a few days later she had actually passed away on 10/12. It happened quickly she was dx'd with mets earlier this year....and just like that she is gone. She was older than me and in some ways felt a little like a mother figure when I was going thru early dx and tx she would encourage me, commiserate with me....just be there ya know?
bleh, I hate BC and what it does to lives. Thinking about her kids and husband.
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Yesterday the physical therapist said I have one more appointment and then I'm released. This is my second round with PT and I am not the way I was before surgery. The surgeon broke me and I think the medical group should fix me. Now, I'm not talking about the chest wall, I'm talking about full range of motion with my arm. I'm talking about being able to put on and take off clothes without wincing in pain. "Just do your exercises"....well I did that last time you released me and look what happened....I came back 6 months later in more pain. Here's a thought-fix it! Then release me!
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Not sure that I am angry. I think I am more sad.
I lost a very dear friend on Monday night. She was fine in early Sept. She started to walk funny and her hands would not work right at the end of the month. She seemed confused and forgetful. Doctors were unsure what was going on. By the end of October, she was hospitalized and doctors were frantically trying to figure out what in the world was wrong with her. In hindsight, her husband had been noticing things for several months prior to October (maybe beginning in late June he said) and now she is gone. She was only 64.
The disease they are attributing to her fast and horrible death is CJD aka
Creutzfeldt-Jakob disease http://www.medicalnewstoday.com/articles/185884.php
This disease is so rare, that one in one million people in the world are diagnosed yearly. It can be familial although no one in her family of 5 siblings knows of anyone who had it. It can be spontaneous or, rarely, it can be attributed to eating affected meat (think Mad-cow disease) but that is very, very rare. But, she did go on a cruise to Bermuda in June as well as back to the island in August for their anniversary (they love Bermuda) staying in a hotel for a week.
The reason I posted this here is one never knows what will happen. Day to day, month to month, year to year. Life is short ladies. Live it. Eat that dessert, enjoy that movie instead of cleaning the closets.
Thanks for listening.
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I am so sorry, April. What a terrible loss. My heartfelt condolences to you and her grieving family.
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I'm sorry April....((hugs))
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April....condolences. We just never know, do we? Glad I renewed my life ins policy. It went up a lot this last year cuz the 20 year term was up. I still want to keep it because it has a clause where you can cash out 25% when you're certified in hospice. We'll probably do that. It will help with my final expenses.
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I'm so sorry, April, that you lost a dear friend to suddenly something so rare and terrible.
"Live it. Eat that dessert, enjoy that movie instead of cleaning the closets."
Very wise words. I'm trying to learn a little of that myself since I got diagnosed.
Carrie
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Thank you everyone. The autopsy will be today. At first her husband was not really thrilled about having one, but her kids talked him in to it as they have a right to know if it is the rare familial type or more likely the spontaneous type. Also, medical science needs to study this very rare disease as much as they can since only around 350 people per year are diagnosed with this.
Thanks again for your condolences and hugs. As we head into the Christmas season, I will make sure I imprint all the memories I can on my heart.
Lita and Katty, an extra special hug for both of you as I am sure that as Stage IV, your time is very precious to you both. Thank you for consoling ME when you have so much more on your plate. My prayers for a blessed Holiday Season for all. xoxo
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Thanks, April. So very sad about your friend tho. It sucks when it happens during the holidays.
I'm planning on donating my body to either Stanford Med Ctr or UCSF Med Ctr. They take out the parts they need, cremate you for free, and return the ashes to the family in about 6-8 weeks. However, if I develop ascites (where the liver blows up w/fluid), they will NOT take me - that's their rule.
There really is a need for bodies that have been ravaged by St IV. Medical students need to open up the bodies and see for themselves what this horrible disease does up close. I have mets everywhere, so they're sure to have a fun time with that. I heard they take very good care of the bodies and refer to them by name. They are very respectful with the cremation, etc., and I'm sure it's the same at any reputable med school that takes in bodies of the deceased for research.
In case anyone doesn't know: You CANNOT be an organ donor if you have cancer. Even in organs that supposedly show NED (no evidence of disease) there could be hidden, undetectable sleeper cells waiting to grow and proliferate. That's all an organ recipient needs...a new liver or kidney, and bingo, X months later s/he develops full blown cancer. Of course, this could happen with donors who die in motorcycle accidents, too - they simply didn't know they had cancer, and the drs didn't bother to shove their bodies thru a CT scanner b4 harvesting organs. But they obviously have to lay the law down when it comes to KNOWN cancer patients regarding organ donation. Geez, I feel like some sort of ghoul discussing all this now. Well, happy Thursday.
L
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Hi Lita
I to have made arrangements tor my remains to got to the medical school here, both my parents donated their remains to the school
and yes the bodies are treated with the upmost respect. Here they kept the remains for almost a year then cremate and they have a memorial service each year for the donors and then we had our choice of how we wanted the ashes ...they would return to us or spread them in the memorial gardens at the school. I had no idea that I no longer qualified as an organ donor but it does make sense.
Charlene
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Lita, I so agree with science needing more information on what diseases do to our bodies. They need this to help them find treatments and cures for the many types of things that kill us, many of you way too young.
As for the medical schools treating the people they study with respect, I have heard this first hand from a good friend of mine who works in research and they use donated bodies. She said that even the worst prisoners such as murderers who donate are respected as they had an incident once where the doctors were saying terrible things about that person and one of the pathologists flipped out and said that the body belonged to someone's son, brother etc. and that they must be treated as such. After that, everyone realized that these were human beings, even those who they did not agree with their lifestyle.
I did know that you can't donate organs if you had cancer and I have had it twice so they definitely don't want mine. (the first time was over 35 years ago and it did not involve my breasts)
Have a wonderful holiday ladies!
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I read about lady asked about hat, made me smile. I went to bc event this year couldn't do walk as ankles had swollen and my feet were killing me just getting to start of event, so I walked over to shade it was unbelievably hot that day. I wear wigs so no ones knows unless I want them to what's going on with me and frankly for me to pretend I'm fine. Alas I'm sweating feet are size of tree trucks I can't stand felt woozy I'm trying to wait for people to get gone but they keep coming just ignoring me which was all good, but I'm dying so I just said f*** it and took my hair off so could wipe off sweat 💦. I all of a sudden start getting looks of pity and people stopping to ask if I'm ok. Things I don't normally have to answer and this reporter wants me to tell him how this event has affected bc. I can't talk for lump welling up in my pit and eyes so I shoe him away. I realize at that moment I hide to protect myself. You brave souls who walk with your truth amaze me and if I ever stare too long I am so sorry, but I am proud of you.
Pam
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Your post brought tears to my eyes, Pam.
Don't ever forget that you are brave and courageous, TOO! It's perfectly fine to live your life privately if you choose. It's nobody else's biz but yours, and if that helps you get thru the horror that is cancer, then so be it.
(((Hugs)))
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I wish I could "like" posts here the same way we can on Facebook. Thanks Pam...thanks Lita...just love the authentic words, feelings, and thoughts that are shared here. ((Hugs))
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I am so pissed off with both my mother and father. They have no idea but I am fuming. My parents were divorced when I was 15 and I always thought they were blaming each other. Never in a million F'ing years did I believe it had anything to do with me their only child. I always lived with my mother there was no choice. Their fights were scary when I was 13 years old. I felt I couldn't have my friends over too embarrassed. At age 15 my parents divorced I always felt my Dad divorced me too. But I gave him the benefit of a doubt, he wouldn't help at all with my college expenses but that was not in the divorce agreement. Apparently everyone thought I was a worthless dolt of a girl. Sure proved them wrong.
Now Mom and Dad's health are waining. I told my father for years to come and stay he and his wife always said he can't travel they are too old. So things going pretty good since I retired I travel to the east coast atleast twice a year. Dad telling how happy he is that I visit. I've been doing it for the past 25 years but recently more often since I'm retired. Well now he asking me to join them in Cabo san lucas. What I thought you couldn't travel? He confesses he has blamed me for all these years for not supporting him during the divorce. But guess what he realises he was wrong. It took all my strength not to hang up. You F'ing jerk you are blaming your teenage daughter in 1975 and just now realize you are wrong 2016. Mom is demanding all my time since she has had a stroke. Jesus H. Christ what the hell. I am beyond disgusted and you know what I have been dealing with a huge black cancer cloud over my head.
I am so angry. I am going to spend my TIME with my husband of 34 years and my grown children. You know it is unbelievable how selfish parents can be.
I will never discuss things with either one, but you can bet I am not going to Cabo.
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Oh, Meow....I feel so bad for you.
Your dad gets the "One of the Shittiest Fathers of All Time" award. He blamed YOU for not supporting HIM? What the bleep!!
Maybe paying for college "was not in the divorce agreement," but he's your DAD for criminy sakes, and he should have at least helped out (i.e. "supported" you) a little in that regard. Then he bald faced LIED to you about not being able to travel all these years. Heck no, I wouldn't go to Cabo either. He'd probably expect you to pay your own way to boot.
Yes, parents can definitely be selfish. After a certain age, they start to act like babies. You don't need that when you're battling cancer.
I'm with you...just do your own thing this Christmas and don't even think about them. They don't deserve it, and you don't need the stress/aggravation.
We're here to support you.
L
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oh Lita, I am beyond pissed. I am going to focus on my children and husband. My husband is down playing the telephone call but I can tell he is pissed too. I am thinking it it his wife who doesn't want to visit. But my mom lives by herself and not with us. So you know they can't use that excuse.
I am done. Just want to rant because I certainly am not going to talk to my parents about it.
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