MIDDLE-AGED WOMEN 40-60ish
Comments
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Well I spoke with the Insurance company from DR. office. They said it should get paid for. I have a family who said to go and do it and we will figure it out later. I have a brother who could pay for it if I had to ask him. I just don't want to prolong my treatment any longer. I feel helpless right now and not knowing what is going to happen.
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Jo - hang in there and pick out the bathing suit...you are going on the water!! It will all work out.
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Well, Lynniea, you are lucky you have options. You'll feel better mentally once you get the tx ball rolling.
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Sandee - Already planning what to take on the cruise. I need to get off my butt and get our shore excursions booked. I definitely am looking forward to snorkeling in Cozumel.
Lynn - So glad you have some options. You will feel much better once treatment is underway. Hang in there.
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Jo -Excellent news!!!! Are you going to Playa del Carmen too? Gorgeous boardwalk there! Will you have time to check out some of the ruins in the area? OooohHH fun!
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Jo- if you need me to drag your butt on that boat in Galveston I will be happy to drive down there and do it:) Go and have fun my friend....it will be the BEST medicine of all:)
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How many are going on the May cruise ? Is it fun? Have you been ... ditching my husband, and thinking about it !!!!
Vicki Sam
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Sandee - We will be going to Montego Bay, Jamaica, Caymen Islands and Cozumel. We have done this trip 3 times before. Have been to Jamaica 6 times. Love it there. When we book a cruise we usually go out of Galveston and we don't care where the ship goes. No one can find us and we don't have to be at work.
Annettek - Give me two hours and my luggage will be packed and my butt will be on the road to Galveston.
52 days - but who is counting?
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Sandee......... thank you so much for your sweet words........HUGS to you! and yes, I will
((((((((((((((Sherry)))))))))))))))) I know........I do too, it would be easier to be able to sleep them away...but even when I do go to sleep on the day of his death anniversary, I wake up.....have every year about the same time he left... anyway........We can pm each other if you would like. Just want you to know.
Jo............I am so sorry to hear that!!!!! and now, the question.....what is a seroma??
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sunangel - A seroma is clear fluid build up in the breast. It is common after lumpectomy since some of the tissue has been removed. Pressure builds up and they can be painful. Once they are aspirated (drained) it is instant relief. Most of the time, the fluid is reabsorbed into the breast tissue.
I had a very large one right after surgery that had to be aspirated. Have had 2 small ones since and working on another. My BS told me I could have these up to a year after surgery.
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jo - hope you are leaving cell phones and laptops behind too:)
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Lynn glad you have some options and sounds like it is working out for you. Good Luck.
Sunangle we can always PM if you need to talk.
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Wow I feel like a new woman today. My rump its draggin on the floor, just close to it,lol. I had a TX friday so clear up to yesterday energy was low. I was able to fix my family a nice supper and cleaned up afterwards. Plus I got to eat chocolate, yahoo!!!
I sometimes wonder WTH insurance is really doing. I found out that my copay for my Nuelasta shot was 750.00. This really frosts my cookies. Im like really. I have paid my dang insurance every week like a good girl for 10 years. Hardly used it. Then I get cancer and bam, look out. I know what ya mean Lynn about the insurance dealings, grrrr. Good luck and keep on truckn!
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I am sooo grateful I am in Canada when I hear insurance nightmares...the only thing I have paid is $4.50 per tri-monthly tami prescription and now $14. per chiro appointment...I have not seen a bill and have no idea how much any of this is costing the Canadian taxpayer..and since I am one, well. I figur eI hav ebeen paying since I started my first job!. Like you Paula, I have paid into my health insurance for decades....I would lose my mind if I got a bill like that. Sounds like a fight could be in the works....$80. therapuetic massage bills are high enough..toss 'em in the fire!
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Sandee - The laptop does stay at home. The cell phones get turned off when we board the ship and put in the safe in our cabin for the week. We do need the cells when we travel.
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I am interested but from India it is impossible.
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I kind of wish I had gone last year. That is an impossible month for me to take off work.
Plus I get scared if I fly my lyphadema will get worse. But it sounds like fun.
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jo....... ok. I have had fibrocystic cysts.....sounds the same. I have had to have aspirated three times over the last ten years, and it was the same breast as the lcis......
Everyone have a good day....or the best you can have. I will be thinking of all of you!
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morning all! I staye dhome yesterday since my latest fill just made me feel too much like a fairly sized house was sitting on my chest. I posted the latest pincs on pic forum...determined to capture each stage of this to help those who behind me and in gratitude for those in front of me...Much more managable today and now will start counting down to 3/16 and the exchange....i have been on such a roller coaster the past 10 days or so...thank goodness I think the final effects of that )(*D# AI is out of my systems. Time to pull up my big girl panties and get cracking with moving forward instead of being scared of every little *ping* going off in my body. The cruise with BC folks sounds fun and maybe I can join next year...sounds like a blast...
Big hugs to all of you wonderful folks:)
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Good Morning all. Pet scan today. I feel that we need all the best test done and some how God will take care of the rest. I believe he will take care of everything and see me through it. This is a very humbling experience. Yesterday I got a phone call from my bosses sister which we just talked and expressed her concern. You realize you have so many people in your coner just there to yet you know we are going to get through this. These people know when I worked their I would not work on church nights. Well hope everyone has a great day and God Bless.
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Lynn...will be there with you in spirit holding your hand....
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Thank you
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Lynniea, may your PET scan stay nice and dark today.
Eph, So how did that lottery thing work out for you?
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((LYNNIEA)) Good luck!
Morning Eli!!
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Lynniea - Good Luck today - we will be here waiting to hear the results. (((HUGS)))
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sunangel, cysts and seromas are different things. Similar in treatment, but one could be a complex or simple cyst, but a seroma is like a bruise, it's a result of trauma. Normally the body absorbs it back, but sometimes too much fluid has built up and it has to be drained.
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I know this question has come up before. (I probably asked it before myself.) How many women are following up with the BS for the full 5 years?
Are most of you just seeing your MedOnc and going for the mammos once active treatment is finished?
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A BC cruise would be fun, maybe next year for me. DH does not want to go on a cruise so maybe a cruise with a bunch of fun ladies would be fun!!!!!!!!!!!!!!!
JO I guess I got lucky with my seroma. When they did my CT for my rads boost mine had completely healed from when the did the CT for my initial planning. I hope it was all the extra exercising I was doing.
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Med Onc only.
I only saw the BS twice after surgery, once a week later, then sometime during chemo.
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eli--I saw my BS for follow-up after sugery and that was it (unless there is a problem). My MO is "in charge" of all my care. I'll have mammo and MRI once a year.
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