Starting Chemo in JAN 2007

Options
1120121123125126326

Comments

  • IowaCindy
    IowaCindy Member Posts: 341
    edited May 2007
    I knew last year after my youngest was out of the house that I would open to a serious relationship. The BC journey derailed any attempts to start that up. So now I have these night time thoughts that I will be alone. I haven’t worried about that too much in the last ten years. But this month, after these last months, I’d sure like someone to hold me, to assure me that “Cindy” is still present and desirable.

    I look at this stumpy, worn, middle-aged, surgically mangled body that carries that frightening tag of ‘CANCER” and wonder – what man would be secure enough to walk into my world? It would take a pretty wonderful guy to do that.

    I hate having these thoughts and the emotions that come with them. I hate that as I look at life after BC, it – BC- will follow me like Pigpen’s dust cloud.

    Thanks for letting me put these words out there. I can’t share this part of my story with many people who would understand the BC portion of this.

    Damn cancer!

    Cindy
  • jonimb
    jonimb Member Posts: 900
    edited May 2007
    Hello everyone;

    Well I had a nice long weekend, my niece & her husband (Sarah & Doug) celebrated their 1st anniversary, and as I was still going thru chemo on our anniversary, the 4 of us went out for a really nice dinner on Saturday night. My sister and her husband (Sarah’s Mom & Dad) went to Great Falls, Montana for the weekend, so we were stand ins this weekend. Sarah & Doug also came over for dinner on Sunday, we had BBQ steaks, and everything was yummy. We had a blast playing TriBonds. Doug is learning how to fly fish, so I gave him my grandfather’s old Fly fishing tackle box, two fly fishing rods, and taught him how to make a wooly worm fly…lots of fun with the feathers trying to make wings.

    We had all kinds of weather this weekend, rain, sleet, hail, snow and even a bit of sunshine. It is unusually cold for this time of year, and tonite they are saying we may have a frost…there goes all my bedding plants. Life inAlberta!!

    MizSissy have a wonderful time camping!! Not only are you a fabulous artist, but it looks like you’re one heck of a seamstress too!! Wow to have so many talents!! Rebecca, congrats on your MRI, your children are beautiful!!. Viddie sounds like that doctor’s office is putting you thru the ringer. Skye like the name of your great niece, but not the spelling. RobbinJaye, I hope I have that much hair at Day 51!! I AM getting eyebrows though, so that is good. Mary, I have a very hard time rooting for the Wings, but whoever wins, just remember, I will be double cheering for the Ottawa Senators!! Mel I love the name of that dog…Muddy!! Shorti, sounds like you’re puttering around your garden like me, and I’m loving it. Jan, I had a tough time with Chemo #6, it took me almost three weeks to feel better, so big hugs to you. Caya, I bet you’ll love have your daughter around for the summer. Lynn, glad to hear you had a great holiday!! Melia, hope your son’s visit was nice. Amera, ignore those that shall not be named!! Nancy good luck on your trip to Georgia, oh…and good luck with the Immodium!! Tina I will have to put some colour on my hair too, as it is coming in all gray!!

    Cindy, just remember, that somebody that loves you doesn’t care what you look like, they care what is in your heart. You sound like the type of person that will meet a wonderful man and have a very good life with cancer in the background.

    Skye, should I read the books in any order? Beast of Bray Road or Hunting the American Werewolf?

    Well I’ve been on Tamoxifen for over a week now, with no side effects…in fact I think my hot flashes have slowed down a bit.

    Trust all are well…Big Hugs to everyone….

    Joni
    **********
  • luckymel
    luckymel Member Posts: 643
    edited May 2007
    Well, it's 3:00 and I'm still in my jammies - decided to have a do-nothing kind of day. Woke up feeling crummy and it was nearly 11:00 already, then my DH came home for lunch and wanted to know why the dog we're dog-sitting was, sitting on the front porch! Evidently he had dug out and fortunately didn't run away, but still, I felt guilty. I've been lying here on the bed listening to MySpace Music and Folk Alley, ordered a couple of cd's (of my old boyfriend, but don't tell) and visited with my mom, and if I accomplish anything more than that, it will be to go to the post office to mail a package. Very low goal setting in action here today.

    By the way, Tina, maybe DH does stand for damn husband! That was my laugh for yesterday, thanks!!

    Caya, Skye, Viddie - sign me up as a member of the Tight Pants Club also.

    Rebecca, I wish you could take video of Owen learning to ride his bike - although your description was so good I can see it in my mind already, especially after seeing the pics of him recently. At least get a snapshot or two - these are precious moments. And you don't HAVE to torture him with it when he's a teenager....but you could if you ever need to - depends on him. My nephew is almost 18 and just got out of high school, and thinks he is absolutely Mr. Cool, and all grown up. He's totally just acting his age.....but at the same time, he's just "begging" to be tortured. He's a great kid, but a couple more years will do wonders for him.

    Eros....quite a strange name to give a kid. I'm sure that wasn't an easy one to grow up with, but at least it was easier to spell than Arrhiahna (pardon me if I misspelled it, but no matter how many times I look at it I can't seem to remember how it goes).

    Skye, hope you're up and running with the rad onc by now, or at least have something set up. Viddie, you gave it your best shot trying to get them to give you an appointment - I'm relaly surprised it didn't work, but oh well - you'll get there.

    Mizsissy, glad you decided to go camping - sounds like a great time. Wish we had a little camper or something. There was a time I wouldn't even entertain the idea of using a camper - we were totally tent campers, backpackers, campgrounds were even too civ ilized for me. I guess age and cancer changes things...now that is almost too much work. I'd like to do that, but a little more luxury calls to me too.

    OK....I'm the opposite of Cindy's situation. Not wanting to lose my post, I did it in word, then forgot to post it.

    Rebecca, GREAT news about your MRI. I know you're relieved, and we are also.

    Cindy, just read your post. Wish I were there to give you a big hug. I know you aren't asking for a solution to a problem. And I'm not going through this alone, so I can't even legitimately say I know how you feel. But I can say that I look at myself and am afraid, sometimes, that my husband, even though he is the sweetest, most loving guy in the world, will look at me some day, see me as I see myself and split. I'm not my most attractive right now for sure, and most of my energy is expended keeping myself going rather than attending to his needs, poor guy. I mean, he probably won't abandon me, but when I'm having those low days, I'm scared too. I don't think that breast cancer is necessarily always going to stand in the way of a relationship - you'll get past this, as we all will. We're getting older, but so are the guys, and they all have their own issues, medical and otherwise, as you well know. So, I acknowledge your feelings, but don't give up hope. There's more to you than BC.

    Joni, where are you? Hope all is well and you're enjoying life and feeling well.

    Melia, halfway through tomorrow - WOO HOO!!

    Love you all,
  • luckymel
    luckymel Member Posts: 643
    edited May 2007

    Joni, you posted while I was asking about you. So glad to hear you're fine! I'd trade you some of that cold weather for some of the summer weather we're having here already.

  • mer1957
    mer1957 Member Posts: 534
    edited May 2007

    Cindy, I second Mel's sentiments. I worry too if I am still attractive to my husband or if something happens will anyone want me. I thought of that when I pondered the reconstruction issue. Then I decided if a new husband (not that I'm looking for one) didn't accept me, body and soul, for what I am, what kind of person would that be? In fact, I think I am a "better person" for having gone through this bc. Yes sometimes I get cranky but I have found out how strong I really am. I have gone through chemo, surgery, fears, worries, and found new friends through it all. Although I regret this disease, I do not regret who I have become - a stronger, more faith-filled person through it all

  • TPPJ
    TPPJ Member Posts: 1,017
    edited May 2007
    Yeah, Nancy, I don't like the sounds of your chemo fog either....check it out. Sounds more like a chemo monsoon.

    Skye, I was partially kidding about my camping ability. I can camp if in a pop up trailer and it's a super nice, clean facility w/showers nearby. I have done that at Wells Beach, Maine with my friends several years in a row. They had a site for the entire summer but gave it up last year. They now do a pop up. I may go again this summer for a night or two, but I'll stay at either Misty Harbor Resort or a hotel. I hate to book in advance of knowing the weather there. If it's crummy, I'd just assume be down in the city (Boston, like an hour away). At least there, I can get together w/friends, go out to dinner, shop til I drop, etc.

    DH got home today. Ladies, you still haven't told me for sure what that is. I was glad he got home...he came to Pauly's 1st baseball game w/me. Kid pitch. 3 solid hours. Ouch. He loves it though and we sooooooo love watching him have such a good time. I've gotta say, watching our kids enjoy their lives so much is such the glue for us. Other than that, we get along well enough but def. do our own things... we aren't the attached at the hip types. My parents weren't either, so...not unusual for me... OK, I'm rambling.

    Trying to decide what, if anything, to do this weekend. We stayed at this luxurious, awesome cabin in the Smoky Mountains two years ago...priced reasonable and totally immaculate....only we don't care for Pigeon Forge or Gatlinburg so much. It's a five hour drive. Once we got there, we didn't care if we left the cabin the entire time, it was soooooooooo nice. Check it out if bored: www.edencrest.net We did Dollywood and although well maintained, once is enuf. They have Splash Country and it is supposed to be very hot so the kids would love that. I also last minute explored Mackinac Island in Michigan but it's like a 9 hour ride and Memorial Day Weekend prob. isn't the time to do the maiden voyage up there. Hell, in two more hours I could be home on my brothers boat in Boston Harbor. I can't get over how BIG Michigan is. Jeez. My other place I want to check out is Hershey Park, PA. It's only like six hours west of here and I want to stay at the Hotel Hershey. Looks elegant. That'd be the draw for me. I loooooooooooove nice hotels. But, of course, it's booked. I wonder how that park is....

    I'm so disappointed to read this week that Kennywood has bought out Storyland in Glen, NH. I took my kids to Storyland in Ligonier, PA the week before my dx last year and it stunk compared to Storyland in NH. No comparison. I hope they don't ruin it. Amera, being a Nebraska girl, you may not know about it, but it's not far from you and your kids would loooooooooooove it... they have a website. I think I may take my kids back in Aug.

    OK... I'm rambling on even more now. I am a talker. As if you haven't noticed.
  • TPPJ
    TPPJ Member Posts: 1,017
    edited May 2007
    Mary, I've only slightly had those thoughts about "who'd want me" in this condition... if not my husband, who really has been more than I could ever ask for during this. He's been fantastic.

    But.... if for whatever odd reason, he wasn't around, I feel so much more confident, empowered, I don't know what, after going through this, I'd be disgusted w/a guy who didn't 100% respect me for what I've been through. It's kind of like after you have kids...you develop this whole new level of self confidence, won't take "crap" attitude...
  • skyedivine
    skyedivine Member Posts: 839
    edited May 2007
    Hey welcome back Lynn and congrats on going topless in that pool! I hope I have enough hair to do that by August when we take our cruise.

    Amera, the other night I told the dh I was sick of being "Cancer Woman" and I think I mean the same thing you are expressing. We may always be Cancer Woman but we don't have to let it be our main identity.

    Rebecca, super congrats on the clean MRI. And I will check out that series you ordered.

    Joni, read "The Beast" first, "Hunting" is the sequel. Thanks again for that! They should be a good distraction from everything else.

    Cindy, that was a very eloquent post. I think Joni has it right that the right guy is the one who sees what's in your heart. And in your case, that's a lot. I also think we all feel very insecure about our looks right now which is extremely understandable. But the hair WILL come back (that's my mantra right now) and we will be able to exercise again. The survivors I see a couple years out look pretty darn good. I also think it's normal to reassess our lives coming out of this big shock. With the dh and I it's been over what we want to live in and where...we want to simplify! I'm glad you felt you could open up to us about this. I think we will each have our turn.

    Mel, those jammy days can be very good. If I need one now and then I don't feel bad about it. Of course I had prior training with the fibro and chronic fatigue, which will probably come back now that chemo is over. And nope, still no word from the elusive rads onc.
    Hey is anyone else hooked on "Lost?" - Skye
  • luckymel
    luckymel Member Posts: 643
    edited May 2007

    Nearly forgot - for Jan, Lynn. and Viddie, the report on my friend Joyce - I went to see her at the hospital yesterday morning and ended up bringing her home, as they decided to discharge her! She looks fantastic. No major pain to speak of, just sore, of course, and taking the occasional Vicodin for that. Her breasts look fantastic!!! I was thrilled - made me very excited to get my own done. Even with the swelling, they were gorgeous, and she already has sensation. I couldn't ask for a better appearance or overall outcome for her, and hope mine is even half that good. Her tummy is also nice and flat. I just talked to her DH today, and he says she is up and around and doing well, but still resting a lot. So, girls, DIEP is the way to go! I'm ready any time.

  • Caya
    Caya Member Posts: 971
    edited May 2007
    But.... if for whatever odd reason, he wasn't around, I feel so much more confident, empowered, I don't know what, after going through this, I'd be disgusted w/a guy who didn't 100% respect me for what I've been through. It's kind of like after you have kids...you develop this whole new level of self confidence, won't take "crap" attitude...




    I agree with you Tina - In a strange kind of way I feel more empowered - I have always been the "nice, good girl" doing for others, letting myself be last on the list - not anymore...
    Mizsissy - I also have Ostopenia, my mother and her sisters all have osteoporosis - this may be one of the reasons my onc. wants me to leave my ovaries in, for now at least, so I can take the tamoxifen, which apparently is good for the bones. And enjoy your camping trip.
    shorti - I'm with you, wear mostly hats and caps now, it's getting too hot out for the wig, unless I really need to. good luck with rad, I hope the drive into T.O. isn't too bad for you...
    Nancy- are you feeling okay? what did your nurse say?
    Skye - did you get a rads appointment yet? it really is like Waiting for Godot.
    Amera - I hear you about people being overly interested, but they mean well - I think they may be questioning their own mortality, never mind ours...
    Rebecca - congrats on the good MRI report - we always like good news.
    Lynn - thanks for the blow-by-blow report re: the mastectomy swimsuit - all that adjusting. I am going to get one soon, as I want to start swimming in a few weeks when I have more strength. Also I am considering DIEP - want the reports from you and Vidde (anyone else having DIEP)...
    Joni- I saw on the Weather Channel about your crazy Alberta weather - did you really get sleet? Your weekend with your niece and her DH sounds great...
    Cindy - I agree with Mary and Mel's comments about your situation - there is a Jack for every Jill -

    My DH and younger daughter (Cassie) are going to Victoria,B.C. on Friday for a 4 day weekend at the University of Victoria - DD got accepted into their very prestigious and one of a kind B of Fine Arts in Creative Writing/Journalism- This is an orientation week end and she is very excited. I'm not so thrilled that she will be a 5 hour plane ride away, but I feel better after speaking with my onc. about my prognosis. I guess we have to let them go sometimes, and she will do fine, as she is very independent, but I will really miss her.

    hugs to all,
    caya
  • viddie
    viddie Member Posts: 547
    edited May 2007
    Hi all,
    Mizsissy,
    Sounds like you are going to have a great weekend. I have osteoporosis and they will probably put me on
    Tamoxifen. Is that your only choice? Did they suggest that you also take Fosamax? That could help prevent you from getting osteoporosis. Just curious: why don’t you need deodorant?
    Shorti,
    I am glad you are feeling better.
    Rebecca,
    That’s great news! You must be sooo relieved.
    Sounds like you are having a lot of fun with Owen. I did not have the patience
    to teach my kids how to ride their bikes. I left that to my dh.
    Skye,
    I hope you are feeling better. I can’t believe they haven’t called yet. Maybe you could call them tomorrow to light a match under them.
    Nancy,
    I also think you should call the nurse.
    Amera,
    It does get bothersome after a while. They mean well, but you want to move on. I find that friends or acquaintances are reassured when I smile and say I am doing just fine. I also have an old friend who lives in Ca who also found out about me and is calling quite frequently. So is my aunt who lives in Ca. I want to tell them to stop calling because I am okay, but I know they do care and I do not want to hurt their feelings. I sometimes do not want to answer the phone, but that will only mean that I will have to return their phone calls.
    Jan,
    I am glad you are feeling better. I think The Sopranos is going downhill- more violent- Tony is really losing it!
    Lynn,
    I am so glad you had a great time. Did your cold go away?
    Joni,
    I am so glad you had a fun weekend.
    Cindy,
    I know it is hard. This BC thing sucks! I know what you mean about not feeling desirable and I am sure most of us have had the same thoughts at one time or another.
    You are still present and desirable. We all are. We just do not feel like we are right now- actually we probably are not right now, but we will be again, after BC. Thoughts will follow us, but they will also pass, and it will get easier. We do not have “Cancer” written on us, although we think we do. Remember that everyone has their own set of problems and issues and there are wonderful guys out there who are looking for a wonderful warm loving soul mate.

    I guess I have worried about s/e, incompetent bureaucracy, my kids- all the stuff that is front of me, but I have not let myself think of the actual BC and what it means and what the future will be like. I am not even thinking about the actual surgery that lies ahead. I guess I am afraid to do all that. I do not want to break down, so I just plow ahead, worrying about the little things. Denial keeps me going. Denial can be a wonderful thing.

    Cindy, I am sending you a big hug. You are not alone and you are certainly not alone with your thoughts. We are always here for you and do understand your fears and feelings.
    Love,
    Viddie
  • Caya
    Caya Member Posts: 971
    edited May 2007
    Mel,

    You posted about Joyce and her DIEP while I was composing my post - I really think I should call my PS again and make another appointment to reasses my situation for the DIEP - when I originally saw her I had just had the breast reduction, with my original PS, the one who found the cancer - he does't do DIEP, only implants. So I went to Dr. Joan Lipa, a big name and very nice PS who said to come back when I felt ready, and she would reassess my body for DIEP - because at the time I was still healing from the reduction.
    Viddie, obviously you are getting this done while on Herceptin - how does your onc. feel about this? I am inclined to wait until after Herceptin in finished, but I will listen to what you, Lynn and Mel all have to report...
    Tina - that "friend" sounds like the old battalax (sp?) from hell - thank God for call display...
    caya
  • viddie
    viddie Member Posts: 547
    edited May 2007
    Caya,
    Is this your first child leaving for college? It is hard at first, and you will miss her, but you will quickly adapt. It becomes special when she comes home for the holidays. Even better, you get a place to visit and explore- and you get a travel guide. They grow up so fast.

    Mel, I hope you feel better tomorrow. Thanks for the report on Joyce. I am glad she is doing so well. That is very encouraging. It looks like there are four of us that are having the Diep surgery: Jan, Lynn and Mel, and me and perhaps you also, Caya.
    Good night,
    Viddie
  • viddie
    viddie Member Posts: 547
    edited May 2007
    Caya,
    My oncologist had not heard of the Diep surgery. Cape Cod is behind the times. Nevetheless, she says it will be fine to have a bilateral mastectomy with any reconstruction surgery while I am on Herceptin. She wasn't the least bit concerned. My 2nd opinion oncologist from Dana Farber also told me that there would be no problem with me having surgery while I am on herceptin. My BS and PS feel the same way.
    I do have to be finished with the taxol for a month, but the herceptin will not be an issue. Also, when I have my taxol/herceptin tx, they give me herceptin first, then they take my blood counts, but only for the taxol. If my counts were low, they would not give me taxol for that week, but I would get the herceptin.
    As a matter of fact, the chemo nurse told me that they do not even consider herceptin a chemotherapy. It is a protein drug therapy that is administered intravenously, and has minimal s/e's as compared to chemotherapy.
  • Caya
    Caya Member Posts: 971
    edited May 2007
    Viddie,

    Cassie is my second child to go off to college. My elder daughter, Amanda, is in her third year at univeristy - but she is only a 2 hour drive away in London, Ontario - halfway between Toronto and Detroit. It was hard having Amanda go, but in the three years she's been away I've become much closer with Cassie - so we will be empty nesters this fall. But they do come home, and you're right, I will have somewhere new to visit. We will be taking her out on Labor Day weekend to move into residence, and I've never been to Victoria. It's supposed to be beautiful - very colonial, and it is the provincial capital.
    Let me know Viddie about you being on Herceptin and having the DIEP surgery
    thanks
    caya
  • Caya
    Caya Member Posts: 971
    edited May 2007

    thanks Viddie, I guess we were posting at the same time. I will speak to my onc. about this when I see him on June 7 for my loading dose of Herceptin.

  • TPPJ
    TPPJ Member Posts: 1,017
    edited May 2007

    I think you can pretty much do anything on Herceptin. A woman out here, married to an ex NFL player...she's kind of the like the local BC celeb..always on TV, guest speaker at every event... anyway, she discovered she was 4 mos. pregnant while on Herceptin. She said she may have been the first person to have a baby while on Herceptin. The girl is 4 now and appears to be doing fine.

  • TPPJ
    TPPJ Member Posts: 1,017
    edited May 2007

    I like my TRAM flap for the fact that I don't have to worry about it leaking, needing replacement. However, the recon'd breast is quite heavy because it's made of muscle. I have some areas of fatty necrosis in it..hard like a rock. I worry about recurrence in it because you can't feel inside all that well and it kind of hides the chest wall area, should it recur there. But an implant would do that as well. They don't MRI the recon'd breast. So many unanswered questions with this whole BC thing. But overall, I like what I did even though it needs some symmetry surgery, because it's permanent. Surgery was tough though. For sure. Surprised to hear Joyce came through so easily. Is DIEP the same as TRAM flap? Maybe not exactly. Viddie, scary to hear that a surgeon on the Cape hadn't heard of DIEP. It's not exactly new. When was the last time he/she picked up a medical book, took a continuing ed course or even read a Cancer magazine in the waiting room? (Not meaning to sound "smart" here....I just found that unnerving.)

  • TPPJ
    TPPJ Member Posts: 1,017
    edited May 2007

    Ha! Battle ax! Yes, that's her, Caya. But she thinks she's this NY sophisticate....reuses her Niemans bags so people think she's been there again... WHO CARES???!!! Who the hell do you think is looking at you so closely that they are saying "oh, gee, that woman shops at Niemans!" Get over yourself, I say. She wouldn't be caught dead at Target. Not my kinda person.

  • meliaanne
    meliaanne Member Posts: 682
    edited May 2007
    Good Morning all,
    Lots of interesting posts! Nancy, I hope you are feeling better. Did you call the nurse? Amera, I completely agree with you; I had said at the outset that the bc was NOT going to be the theme of the family, and I don't think it has. It has been all consumng for me, of course, and my oldest, who worries, asks all the time, but the middle girl, who is engaged, is concerned but immersed in her (our) fun planning. Our son is very restrained about it, was the most visibly upset at first, but is less focused now. I have found that extended fam rarely ask about it, which either hurts of is fine depending on my mood. And only a couple of other folks know. Am still unsure as to whether that is good or bad, just the only way I knew to handle it.

    Caya, empty nest threw me big time, though it was the same time frame as a career change which was wrenching, though turned out to be the best thing that could have happened. I wept for a couple of years. Oh yea, menopause at the same time. I was a mess. All three come home often, we see them frequently (not as much as I would like) and since they all live close to each other and seem settled, we will move near them in a few years when we retire. I want to be a hands on grandma, when that happens. Both girls say 2009 is the year.

    Lynn, your trip sounds like lots of fun. I hope your cold went away.

    Cindy,what everyone says is true, you are a lovely woman. I am sure the first conversation about surgery must be tough, but I also believe that if "he" is after you for just your body, he is the wrong guy. You have a lot to offer, esp the strength and courage of weathering this battle.

    Joni, lovely to have you back. How are you feeling? I see from another thread that you are planning a cruise?

    Mel, did you ever get the cleaning woman? Key to happiness, that is.

    I had a good visit with the onc yesterday. He is so reassuring. Taxol 6 today, will be done six weeks from tomorrow. I can do this. Viddie, how are you feeling on the taxol? And Nancy, aren't you doing it too?

    Have a good day all. You have no idea how you keep me going.

    Melia
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited May 2007
    Good morning ladies...

    Strength is coming back. I actually ran a little yesterday, not for the exercise, but because I needed to shake things up a bit (if you know what I mean)..well I didn't get instant success but the scale registered a bit lower this AM. Radiation fatigue is more difficult than chemo fatigue; it takes longer to recover.

    Got the camper packed up except for food, which will go in the car. We were pleasantly surprised to find out that all our towels, clothing, etc., fits in a storage area under one of the seats do we don't have to pack a suitcase.

    The camper idea came to me last summer after spending one (1) night in a tent at a local campground so we could canoe first thing in the AM. We had an inflatable bed, but it didn't inflate properly because the new pump broke almost immediately. It was *EXTREMELY HUMID* and we felt like we were sleeping in the bottom of a shower stall. I woke up exhausted, dirty, grumpy and looked around and saw the campers. So I just had in mind that we'd get one, a real light weight one, if it came our way, and one did. This is a very nice little compact thing and packs up into about the dimensions of a queen bed when we attach it to the car. My tent camping days are OVER!!!

    Deodorant? Viddie, no, I don't need it, anyway, not very often. I think it had something to do with going through menopause. BTW Jan, it is possible to get a very nice bath with just a sink and a bath scrub sponge. Fill the sink with water and put a fluffy towel down on the floor and watch and scrub away. You can actually get quite clean. This is also a great remedy for hot flashes; you can cool off quick!!

    Sewing..I've been doing it since I was about 12 because my mother thought clothes were nothing but vanity, and the only way I could get 'em was to make 'em. I've found that painting helped with the sewing, I felt more empowered. Also helps with color choices. The dress I made Mena was really a very simple easy one to sew. I really hope she likes as much as you gracious folks!!!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2007
    Lynn – I knew you would love Cirque – I am so glad you did! I’ll have to deal with a prothesis this summer in the pool since it looks like reconstruction won’t happen until late summer at the earliest. I’d love to hear anything you learned about dealing with it. We have a neighborhood pool that is a big social hub in the summer. Everyone knows everyone kind of a place, so I am very nervous about dealing with a bathing suit while in the pool with my kids. I hadn’t even thought about the scarf thing! Ugh! I don’t have a bit of hair yet.

    Cindy – I have a neighbor whose wife had a serious battle with leukemia before her met and married her. It’s not the same since she didn’t have the surgical scars, etc. But he did go into it knowing that there’s no guarantee how long she can stay in remission, etc. There are good guys out there who will appreciate you for who you are. I appreciate you sharing your fears, I know I share many of the same feelings about body image.

    DH does officially stand for “dear husband” or “darling husband” or even “domestic housemate,” may favorite online explanation read that beauty of the abbreviation is that it can change meaning depending on your mood. So maybe today it’s “dear husband” and tomorrow its “d**k head.”

    Skye – I am completely, helplessly hooked on LOST. I’ve never missed an episode even though the title is a good description of how I often feel after watching it – especially with chemo brain! My husband and I always watch it together – I am really looking forward to the season finale, although I’ll miss it over the summer. Who do you think the girls in the underwater hatch are – I didn’t see that one coming? Any what’s the deal with the report that their plane and bodies were found?!?

    TPPJ – sounds like a good call in avoiding the drama queen in OC. Who needs to deal with that! Kids make her “nervous” – WTF? You’ve got more fun things to do than deal with that! DIEP is similar to a TRAM flap. The big difference is that the DIEP does not take any muscle – instead they cut the blood supply and then reattach using microsurgery instead of moving the muscle to keep the blood supply attached. The microsurgery aspect seems to be the big reason why it’s not a more common surgery. There are relatively few doctors who are experienced with it. It’s also a longer surgery in terms of time.

    Mel – THANK YOU for that report! Whew – its hard to find happy reconstruction stories online. DH and I had a huge conversation (yet again) about reconstruction last night. He doesn’t see why on earth I’d want to put myself through DIEP and I can’t imagine getting implants. He’s fine with whatever I want to do, but totally doesn’t “get” it at all. I ended up having dreams about surgical problems all night!

    Viddie – I agree that denial is a wonderful thing – I just wish I could muster up some of it! I’d rather be in denial at the moment. I would be a lot more relaxed.
  • meliaanne
    meliaanne Member Posts: 682
    edited May 2007
    Where is Robertin?

    Nancy, how are you feeling? Did you call the nurse?

    Viddie, anything new with your surgery?
  • skyedivine
    skyedivine Member Posts: 839
    edited May 2007
    Hi Ladies,
    Melia I was wondering where Robertin went too. Robertin we miss you here!

    Tina, I also say ax the battleaxe. Almost every book I've read on dealing with cancer says to cut ties with anyone toxic if possible because you don't need the stress and antagonism. I've had to do that with a few people and now wonder why I didn't do it sooner.

    Jan, the underwater girls were a real shocker. They had better explain it tonight. And that thing about the plane and bodies being found is completely puzzling. The show is too weird for dh who has given up watching it with me but luckily my son has now become interested. It's just such an interesting blend of personalities and has so many twists it's never boring.

    Nancy hoping you will report in on your strange symptoms.

    As for me, it's beginning to feel like my own "spaced" opera regarding rads oncs. Turns out the one from Ft. Atkinson really was Godot, he doesn't work there anymore and was not replaced. So NOW I have to go to Oconomowoc which is a little farther than Fort but not as far as Kenosha. Fortunately this one appears to be confirmed and they have promised to call me tomorrow morning with an appointment. Ai-ai-ai, as my dear dad used to say. I get the feeling my insurance would prefer me NOT to have rads.

    Viddie, yes denial can be very useful, even in short doses. I practice it often.
    Good day, everyone,
    Skye
  • luckymel
    luckymel Member Posts: 643
    edited May 2007
    Good morning everyone. Well, I guess it's early afternoon, actually. Not dressed yet but got up and put on makeup and made dh some lunch. I'll dress later. Feeling better today - still tired, but much better than yesterday.

    Wanted to confess that I'm a "Lost" watcher also. I keep getting aggravated and saying I'm NOT going to watch it anymore, but so far I'm continuing on a week by week basis. I said this season they had better get their act together or I was going to stop watching, and I think a lot of other people felt the same way. I think they're trying. I still get confused, but watch it with dh and let him explain things - he has a better memory for details right now.
  • luckymel
    luckymel Member Posts: 643
    edited May 2007
    Jan........"d**k head* is even better! Thanks. My smile for the day.

    For you DIEP girls, I also have another friend here who has had Diep, and I've seen and felt her reconstructed breast, and it's awesome. I really think this is the way to go. There are lots of reconstruction horror stories out there, but if you'll notice, very few are DIEP related.
  • robertin
    robertin Member Posts: 78
    edited May 2007
    Robertin is still alive and kicking. I've been reading most of the posts, but have been kind of busy trying to squeeze in a full day at work. I finished chemo 2 weeks ago, and it is nice to get that energy back, realizing that it's here to stay. I went to a workshop in Iowa (Iowa City) last week. We drove, because it's only 5 hours away and for the first time I was wearing scarves all day, because most scientists had seen me in December with all my hair, and I thought it might be a shock for some of them. I am so used to the bald look that I kept scratching my head. One neat thing: this Nasa official from JPL (Jet Propulsion Lab) came up to me and asked me if I had cancer. I told her I had just finished chemo and she gave me a big hug, and told me that she had just recently finished radiation (she too had BC). As a matter of fact, when I saw her last November, she was still wearing a wig. She told me that radiation was easy. By the way, she did chemo and still would fly to Washington DC to discuss budgets. I think she practically lives on an airplane. She was so positive and happy. Great to see that.
    Last Monday I got my CT scan and markings. I felt like I was in a sci-fi movie, laying perfectly still on this narrow table with the lights dimmed and the x-ray machines rotating around me. Cool! I like the two techicians and the doctor too, although he was taken back when I asked him if I could have a copy of my treatment plan, so my friend can go over it. My friend got his Ph.D. same time I did, but he went on to become a medical physicist. He's a research scientist and intern in Philadelphia. Actually his research is on how to make the radiation less harmful for the heart and lungs. The oncologist didn't seem to like the request, but consented in the end. Hey, it's my body and if I'm offered a free second opinion, I will take it.
    I now have a peach fuzz on my head, but my eyelashes are still falling out. My nails seem to be floating on their nailbeds (I tried to each some pistachios the other day), and it looks like I will lose the nails on my big toes. I think radiation is going to be a breeze, because the hospital is only 10 minutes away. I will go during my lunch break each day. I am already putting the 100% aloe vera jel on my breast, and am looking for the non-metalic deodorant. I think our healthfood store has one. I guess I have to say goodbye to the Bath and Body Works body wash for a while. Ivory soap it will be.
    I've been reading about your trials and victories. Life sure is that way, so I keep thinking of my dear friend, who wakes up each morning and thinks "oh good, I have another day." Tomorrow I will find out if my liver is okay. The Hepatitis C flared up during taxol and I really don't want the treatment. It's equivalent to 18 months of chemo (although no hair loss, but the side effects are equally nasty), and the success rate is pitiful. I'm seriously considering no treatment at all. I've lived with the virus for 29 years now. It's always been dormant, but it took a bout with cancer for the thing to wake up. Oh well, this too will pass. Enjoy the day, and hopefully the sun. I'll pop up more often.
  • Dar1
    Dar1 Member Posts: 146
    edited May 2007
    Cindy, when I was diagnosed a good friend told me about her aunt - she had just started dating my friend's uncle when she was diagnosed with BC. She stopped taking his calls, thinking that he would not be up for that. He pursued and was with her through treatment. 16 years later they are married and going strong -he has more health problems than her! That story makes me cry - there are good guys out there and lots of people have health issues at mid-life.
    I'm back at work and it's going well. Today they started to notice I was there - or maybe they're just reviving from the post tax season crash!
    My dh and kids have planned a 50th birthday party for me on Sunday. I still feel pretty shaky and weepy, but I guess it's a bit of a statement - we're still here and let's celebrate!
  • goldnmom
    goldnmom Member Posts: 189
    edited May 2007
    Quote:


    Mel, I hope you feel better tomorrow. Thanks for the report on Joyce. I am glad she is doing so well. That is very encouraging. It looks like there are four of us that are having the Diep surgery: Jan, Lynn and Mel, and me and perhaps you also, Caya.
    Good night,
    Viddie




    I'm trying to catch up on posts. This is my first week of reduced hours (16/week now!), so have some time.

    Mel, I read in another post that you are some better with the swelling down now. That's great! I really have appreciated your reports on Joyce. Don't know her, but love that she is doing so well with her DIEP.

    Viddie, add my name to your DIEP list. The date is July 23rd and I can't wait. I look forward to getting it over with and having my new shape. Also in the back of my mind, I'm thinking I might retire then. I'm just not sure yet though. Someone mentioned DH meaning darling husband.....mine is retired and DH means something different every day! it really would be nice to have lazy days forever...I think.?
  • Lynn12
    Lynn12 Member Posts: 1,008
    edited May 2007
    Hey Ladies,

    Jan, I think if I had a situation as yours where I would be in the pool all the time with other people, I would think about some way to sew a prosthesis in the suit so it didn't move around. I'm not really sure how you would go about it though. Would foam work if sewn in? It seemed like the silicone prosthesis I have would kind of float inside the pocket, and move around. It just didn't feel secure at all and I was always fixing it. I hadn't thought about the hair/scarf thing either until I was there. Once I made the decision to just 'go for it', I was much more confident and all was fine.

    Mel, how long after your last chemo did you swell up? I look like I have elephant feet. I couldn't put on regular shoes this morning and ended up wearing flip flops to my meetings today. I'm not really sure if I'm swelling up anywhere else.

    I still have my cold and I am really tired of it. I'm sure it's because I'm only 2 weeks out from my last chemo and my wbc is probably still a bit low. I had some pretty bad ear pain on the airplane when we started to descend. Chewing gum yesterday helped a bit.

    Robertin, thanks for checking in and for the play by play on the CT scan for radiation. I have mine next Tuesday.

    So I'm at breakfast this morning with my boss and another co-worker. They asked me about Florida and how I'm feeling and so on. Wendy (my boss) then asked if my trip was for 'finishing chemo'. I responded that it was exactly for that reason. She then reaches in her bag and hands me a nice card with Red Sox tickets in it and said 'congratulations'! Wow! Now I'm not sure if any of you non New Enlanders know, but you just can't buy Red Sox tickets. Every game all year is ALWAYS sold out. These are box seats about 8 rows behind 3rd base! She got them for September to make sure I'm all done with treatment. I'm so excited, these are by far the best seats I've ever had. She has been so supportive of me throughout this ordeal. She also asked that whenever I decide to do any of the cancer walks (Susan Komen, Avon, ACS) to let her know because she and her mom want to do it with me. I am so touched.

    Tonight we're going into Charlston to have dinner, should be fun (this is my first time in Charleston). Looking foward to going home tomorrow night and sleep in my own bed.

    Have a great evening!

Categories