MIDDLE-AGED WOMEN 40-60ish
Comments
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Elimar - Thanks for that explaintion, if rads sweep up the remain cancer and throw it in the trash ben it is well worth it.
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Isn't that the truth.
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Good idea, Meece. May we all be surviving 20 years from now.
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Lynn, OG and anyone I might have missed waiting on results and procedures...that pic of the two hands says it better than I can....we all care and love you all...none of us is alone in this journey...
3jays- you ain't going nowhere...age is a spirit indeed
And jo- your typo literally made me wet myself..I laughed that hard...I wish all the damn docs gave us the worst scenarios up front...scare the crap out of us and then we could find our own stages of reliefs throughout the processes-instead of what is often the reverse.
and I am with Meece on this thread's name change in a couple of decades...a bunch of us 70 80 and 90 and beyond somethings dancing like nobody is watching:)
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annette - If we can find humor in all this mess - the better off we will be. Sometimes my hands and brain don't make a good connection and I did not proofread like I usually do before hitting the submit button.
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oh jo- i loved it. I do that all the time and it is nuts because I also do it when TALKING:)
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Jo - can you pat your head and rub your stomach, or is it rub your head pat your stomach? I don't think I can do either.
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Annette - I have to confess, I do it while talking too.
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I can do it either way. Have always been talented like that...lol,lol,lol....
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Hi all! I got a weird call today and hope someone can help me. It was a nurse from the insurance company who is now my case manager. She seemed concerned about my recent stay at the hospital and asked me a few questions. My concern is this. Is this something I need to be leary about or is the heath insurance company really concerned about my health. I now if I stay well during my treatment its less of a cost to them. Or are they really concerned about my treatment. I mean come on Ive been treated one way or another for cancer since Oct 2010. But I land in the hospital this weekend and get a call. Any comments or tips would be helpful on how to handle her on the next call. She wasnt pushy I just have my back and be prepared for some slick insurance deal. Thanks
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I'd be very nervous about that as well ... especially in this economy!! You should be able to find information on their restrictions on the Web. Or, you could call and ask to speak to a representative to inquire about laws and policies at the insurance company.
You could also request the information to be sent to you about your rights.
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Paula, I have a division of United Health Care, and I have a nurse too who is there to make sure I am getting services needed etc. I have never really chosen to talk to her except yearly when I renew my premier cancer services through Sloan, it doesn't cost anything extra is just a way I think of keeping tabs. By going to one of their Cancer centers everything is paid for 100% no out of pocket or co-pays. Otherwise I don't know why she is calling...unless she is a specialist etc. I don't know how paranoid we need to be because they cannot cancel us anymore!
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ALL THOSE TEARS WAITING TO FIND OUT WANT THIS BLEEDING MEANS,AND SOMETIMES IT HAPPENS BECAUSE OF TAMOXFEN,I HAVE GOT TO SEE THE DR NEXT WEEK BUT IT LOOKS GOOD,THANKS FOR YOU KIND MESSAGES WHEN I WAS AT MY WORST.
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Thanks OG I forgot about that. Hmmmm.
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Thanks all I need all the hugs. I go to support group tonight. Than start Chemo tomorrow.
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Just found this site. I have been searching for side effects for herceptin. Found a few sites but are a couple of years old. I am 53 and was diagnosed last Jan./10. I have had the chemo and radiation and now on 17 herceptin cycles. I just had #13 last week. I am soooooo tired and have very sore joints. Nurses say this is not from the herceptin? Been to family doctor (who is awesome) was sent to specialist (Rheumatology). Had bone scan and found inflamation in areas that did not hurt?? Want to know if anyone here is in the same boat.
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Hi Paula; As part of our insurance plan, we have a nurse that is there to answer all questions needed concerning the plan and treatments. I think the insurance company is trying to make sure that we stay as healthy as possible.I have Aetna .
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ok...now i am zipping between madly excited and terrified about the unknown in regards to tomorrow's exchange surgery...11.5 hours (not that I am counting or anything)
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annette - Take a deep breath and relax. This is something you have been looking forward to. Don't overthink this thing it will just drive you crazy. You are going to do so well - I will be there with you holding your hand and giving you that gentle hug when you need it. You go girl! (That was my pep talk) LOL
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annette- good luck tomorrow. Breathe ....breathe....breathe...one step ahead of the other
Elimar- great explanation....I had such a visual as I was reading your explanaion...why can't the docs explain it like that????
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thanx, jo. i'll be 61 on the 24th, so thats' only a little "ish:" and there's too many dear friends here to leave! 3jays
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3jays - So glad you are going to stay - we would miss you.
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Good luck tomrrow, Annettek.
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annettek, Understandable to be excited and scared at the same time. Hope the exchange surgery goes well. We haven't had too many on this thread write about the whole expander/exchange option. I am kind of curious how the healing goes after the exchange, so tell us your tale when you are up to it.
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Good luck Annettek! I just started my fills.
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annette - Good luck today. Let us know how it goes.
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Annett breath and good luck with your exhange. Keep us posted on your recovery, we will be here for you.
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Any news, OG56?
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Annettek-good luck, I'll be thinking of you. All will turn out fine.
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chelemybelle - I was on Herceptin for a year. Didn't really have any side effects from it. I did however opt to do the weekly treatments instead of once every 3 weeks. Don't know if that made a difference or not. I just know it worked out best for me. Sorry I couldn't help you.
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