Starting Chemo in JAN 2007

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  • Caya
    Caya Member Posts: 971
    edited August 2007
    Thanks so much everybody for the support while I wait it out. I spoke to a very good friend of mine who had a breast reduction years ago - she told me they call her back every time from her mammo because of the scar tissue and something call lucent? tissue from the reduction. I also posted on the Her2 website and several women responded that since this is my first post reduction mammo, this is more than likely what it is - residual scar tissue etc. So I feel better, but of course until I get the final word (hopefully tomorrow)...
    Debbie, sounds like you are holding up nicely with all your rads - the fatigue, the skin burning etc.
    Joni - I got to pick my oncologist. My GP recommended my onc., sent down a referral and I saw him the next week. Maybe it's different here in Ontario - also your pix are gorgeous.
    Tina and Jan - we have Costco here in Toronto too - I'll be looking for your "homemade" lasagna there. Glad school was great for your kiddies.
    Rebecca - sounds like you are more relaxed with your body - you will feel like "you", slowly but surely.
    Viddie - how are you doing? After this scare, I am seriously thinking about doing what you just did - the prophylactic mast. with DIEP -
    Mel, Mary, Robbin, Sharon (alias Janis Joplin) and everyone else - thanks again for fretting with me - I didn't have much time to think about it today because I took DD out for her dorm room shopping at Linens 'N Things and Walmart - burned a hole for about a grand on it all - just washing all the sheets and towels now, move-in day is this Sunday, and Cassie is working tonight, tomorrow and all day Saturday.
    xoxo
    caya
  • Rebecca
    Rebecca Member Posts: 971
    edited August 2007
    That is great news RobbinJaye!

    Debbie that stinks about your marks…I guess each marking method has its downside! I got tattoos…they do not wash off, but they will be there FOREVER. The marker marks are not permanent, but then…..you have to be careful not to wash them off! UGH. I am sure that your skin will heal quickly now that it is no longer being irradiated. It really sounds like you are experiencing a lot of discomfort….poor thing. It is almost over!

    Miz, that is an adorable cabin! Do not be so hard on yourself, I am sure your muse will return in time. Counseling is not such a bad thing, there is something to be said for a neutral person to talk to. I had a counselor to help me through treatment, and I think it made a big difference for me.

    Joni….
    Quote:

    Anyways...today I'm perky (Viddie are yours??)




    LOL

    Keep smiling honey… I know it is hard sometimes, but if you lose your smile then the beast has won. We can not have that now can we?

    I on the other (hypocritical) hand went off the deep end today and had a good sob fest….after all of my angst regarding my surgery, I finally (as Caya noticed) came to terms with it all, and was starting to feel a bit more comfortable over the last few days. This afternoon I brought in the mail and there was a slim envelope from my PS. I open it, and what do I find inside….a BILL for $22,000. Well ladies…I lost it. I do not have that kind of money…which is actually moot because this bill is BEFORE my insurance company has had a crack at it. I just can not believe that they SENT it to me….how insensitive is that? The last time I did not get a bill until after the insurance company had paid what it was going to, adjustments were made and then there was a residual balance. I think what bothered me is the “slap in the face” aspect of it….I was unhappy about it in the first place, and then to have someone imply that I might have to bankrupt my family to PAY for this procedure that I was unhappy about just really rubbed me wrong. I have peeled myself off the roof now, and I can deal with it….but it was rough going there for a bit today let me tell you!
  • Rebecca
    Rebecca Member Posts: 971
    edited August 2007

    Oh, and I also want to take a minute and thank all of you, my beautiful BC sisters for the lovely cards that you sent my way. I have them stashed on my dresser, and when I feel blue I read through them. They really helped through this tough time. I wish I could hug each one of you! {{{{{sisters}}}}}

  • Nancyab
    Nancyab Member Posts: 276
    edited August 2007
    Caya, we are here for you. I agree with Mel, it would be far kinder for them to wait and have all the details before they call. That seems so cruel. I also realize that no matter you are worried. I hate for you to go through this, again. Blasted disease!

    Jan, they do use a builders model that is cheaper and 5 years seems like the life of them. Frustrating. Tina, I am concerned about your issue. was it the compressor or the condensor that was bad? 900.00 for a warranty item is...how do I say in civil terms...just not right. I would love to see your invoice.
    I am going to fly to Phoenix Sept 28th to spend a week with my DD's. Just us 3 girls and no men!! Yes, looking forward to that.
    BE good everyone, I'll check in later.
  • viddie
    viddie Member Posts: 547
    edited August 2007
    Hi all,

    Caya,
    I am so glad you heard first hand from women on the her2 site who have been there and could give you some encouraging news. I really believe that doctors have to “tell all” for fear of being sued if they don’t. I had surgery last Monday and on Tuesday night around 7PM while I was still in PACU ( post anesthesia care unit), six fellows and residents were leaning over me and telling me they couldn’t hear a pulse on my new right breast flap. They told me they had to wait for Dr. Lee, my PS to get out of surgery so he can try to find my pulse on my new diep breast. When Dr. Lee finally arrived at 11PM, he couldn’t locate a pulse for 45 minutes- the longest minutes I have ever experienced, While waiting for him to find a pulse, I asked him what would be the worst case scenerio. He told me I would have to go back to have more surgery------ Then he told me my heart rate was real high----no wonder!!! I then asked for an ativan- really!!! LOL. The point being- they have to reveal everything. By the way, it was a false alarm. He finally found the pulse and all was fine after that.
    I am so glad I did the Diep surgery. I now feel I have done everything possible, considering I had DCIS, IDC and LCIS- all in the same breast- LCIS carries a cumulative 1% a year rate of occurrance in either breast. It was a huge decision though- only one you can make.
    Good luck this weekend dropping off Cassie. That is hard- just as hard as first day of school. I think harder because they do not come home in the afternoon.

    Mizsissy,
    The cottage is so cute. The scenery is I am sure, breathtaking. You’ll get your groove back.
    Lynn,
    How is work going? If you have any questions about BI or Dr. Lee, feel free to ask away. You too Mel and Jan. Now Ellie and I are a veterans of the Diep surgery. Whew!!
    Jan,
    Your dd and you made it through the first day of first grade with flying colors. Congrats. That’s a hard one.
    Rebecca,
    I am glad your appointment is behind you. Congrats on sleeping through the night. That is another milestone. I hope you start feeling better tomorrow. What a slap in the face- how rude and crude of the hospital!! Hopefully you are feeling better now. Hugs!!!
    Sharon, I hope your dd recovers from mono soon. At least she has the rest of the summer to rest---if she will!! Teens are funny- they do not feel sick on nights they have plans.
    Tina,
    You go girl!! Good for you for speaking up to your BS!!
    Mel,
    I just got it- Ati-man!! Took me a while- all these meds-LOL.
    Joni,
    Waiting is the hardest part. I can’t believe it is almost September. I know this is so cliché-ish, but Sept 7 will be here before you know it. We all have those days-and we are all here for you – and of course if all else fails- A job for Ati-Man!!
    Thanks for sharing all your beautiful pictures.
    I think I am, I think I am ( perky that is ). A little swollen and bruised, but that is expected for now.
    Ellie,
    How about you? Are you perky? Are your new boobs still swollen? Are they hard or soft? Mine are still a bit hard, but the PS says that that is temporary. My visiting nurse is very impressed with them- and she thinks they look perky and lovely - and she is my first knowledgeable outside source.
    Robbin,
    Congrats on your great report.
    Viddie
  • TPPJ
    TPPJ Member Posts: 1,017
    edited August 2007
    Debbie, good for you for doing water aerobics. I need to do something. I feel very out of shape after all of this. Got some unflattering pictures back from my Boston trip too, which has kind of spurred me into action.

    Robbin, I have a bit of swelling on the outer edge of my recon'd area...towards my underarm, but on the breast. I don't think it's lymphedema, but more like scar tissue too. The radiologist pointed out something to me that I hadn't thought of: if I get that area "tweaked" during the elective symmetry surgery, that could cause lymphedema. Anyone else heard of that? That's good reason to leave well enough alone, I'm thinking.

    Boy, next week's gonna stink: pelvic ultrasound and possible uterine biopsy for tamoxifen staining. Thurs. is MRI of the left breast.
  • Caya
    Caya Member Posts: 971
    edited August 2007
    Rebecca - OY!! 22 grand? sure hope your insurance co. takes care of this. Isn't there a law in the States that women must be covered for reconstruction? I know there is in Canada. Hope you are feeling calmer today.
    Nancy - that trip to Phoenix with your DDs in Sept. is something nice to look forward to.
    Viddie - thanks for your encouraging words. I plan to phone the plastic surgeon I saw last fall who is the DIEP specialist here in Toronto to make an appointment to discuss this with her again.
    Tina - how long have you been on Tamox? I think just a few months, highly unlikely for uterine cancer so soon. But obviously it has to be checked out. Man, it never ends does it ladies?
    I am going to call my BS's secretary to remind her about having my films read today, also to pass onto the radiologist that this is my first mammo since my breast reduction surgery (Oct.16, 2006). I really feel that whatever it is he saw is related to scar tissue, lucent microcalcifications etc. from that surgery. However...
    Have a good day ladies, as soon as I know anything I will let you know.
    caya
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited August 2007
    Real spotty connections here...so my posting is a minimum, but let me tell you...I've needed this forum even on vacation!!!

    I posted this yestereday in the WC so Puppy could see it...she's having a real bad time now:
    Quote:



    From Monhegan Island

    God works in mysterious ways. I was so low a few days ago, so depressed, but today I am having a great day.

    Was so tired I didn't want to go anywhere this AM. Just stayed in bed. DH went for a walk. The little old lady from the Sierra Club came back with another lady friend and they worked on the weeds again. After a couple of hours I went outside to meet them. One of them was a very, very nice person who had learned of my problems painting, and had some very soothing words. She said in just two months out of treatment I am still recovering. She wants me to come to a painting workshop next June that she's going to take, and she EVEN showed me a nice place where I can stay that her son owns.

    It is soooooooooo cute and so much nicer even than our cottage and has a nice view of the ocean. It is too nice to rent through the local realty, so they only want to rent privately.

    I found a pretty little birthday card in an empty drawer that someone left behind to a wife this morning. It said on the front "An angel came to me one day.." and on the inside it said, "...so I married her!" I took it out of the drawer and felt sad that it had been forgotten, and thought, we'll take it, and maybe someday DH will give it to me after I've forgotten about it.

    Just when I was thinking that I had been visited by an Angel today, DH came in with the with the card all signed, and he said, "I was planning to give this to you one day this week, but I guess you already found it, so here it is!"

    Mizsissy


  • Rebecca
    Rebecca Member Posts: 971
    edited August 2007
    Well, I am a bit calmer this morning regarding that humongous bill that I got yesterday. Yes, Caya, there is a federal mandate that guarantees all US women the right to have two reasonably symmetrical breasts (strange, you would not think that legislation would be required for that ) My insurance company is therefore legally obligated to pay for my surgery, but since my PS is not in-network I am still liable for some charges. I have no clue how much, nor do I have any idea of how I am going to pay for it. I went out of network because there was not another PS who operates at my hospital and who does breast work. When I got my Mastectomy, I showed my Breast Surgeon (who is chair of the dept of surgery at the hospital) the list of participating surgeons, and he did not know ANY of them….so I was not comfortable picking someone at random. Better to have no reconstruction at all than bad reconstruction.

    It does not appear that the PS office has submitted a claim yet…it is not in the system, and other claims from the surgery date ARE in (and already paid) so I think I need to call the Drs office to take care of it. I have been trying since yesterday to get them on the phone, but there is nobody in the billing office and they do not even have an answering service. Go figure. I really like my Dr, but this billing thing is the pits. What makes the whole thing even worse is that before he operated on me the FIRST time, DH tried to talk to him about how much this might possibly cost us so we could make an informed and responsible decision (I was not going to even consider reconstruction if it would bankrupt my family!) and the Dr told him “Not to worry about it”. GRRRRRRRRRR

    I will keep you all posted on how this turns out.

    Viddie it is so great to hear from you! I am glad you are feeling better.
  • Rebecca
    Rebecca Member Posts: 971
    edited August 2007
    Before I forget...I guess it is time for me to show off my new 'do....here is me yesterday.

    image
  • TPPJ
    TPPJ Member Posts: 1,017
    edited August 2007

    Rebecca, you look great! OMG, do you and your kids look exactly alike! Wow!

  • TPPJ
    TPPJ Member Posts: 1,017
    edited August 2007
    Oh, Nancy, ole chemo brain here doesn't even know where she PUT the invoice. And I paid cash! It's my only record of having paid. I have to find it. I know it's around here somewhere. The DH was flipping out that I misplaced it. I don't want to tip off the a/c company that I can't find it for fear they'll re-bill me.

    Speaking of bills, Rebecca, I get these "This Is Not A Bill" statements from OSU all the time...they range from $12K to $22K for chemo, herceptin tx's. Such a waste of paper and postage if it isn't really a bill... means nothing to me until the bottom line. They oughta knock that crap off and use that money for treating cancer.

    Weird experience yesterday afternoon after school. I found a local 16 yr. old boy in my back yard, trying to peer around to the front of my house/the street. My neighbors daughter broke up w/him well over 6 mos. ago and he will just not let go. He's been spoken to by the police, etc. He was stalking her, trying to see down her street from my house as he's been warned to stay off her st. As a result, he cruises by my house ten times a day with his head turned down her st. instead of where he's going. Totally ticks me off because it's only a matter of time before he hits something, or God forbid, some of the young kids around here... I approached him and asked him what he was doing. he said nothing. I'm like "Jordan, you're out here, in the woods, running back and forth behind my fence, peeking out into the street for nothing? Come on! We both know what you are doing. You need to get some self respect. This is embarrassing...". Tried to shame him into acting human. He had hidden his car up in the neighborhood behind me and cut through 3 private yards to get to mine, a good vantage point to Maria's house. My friend Wendy spoke to him last week as he was parked in front of my house staring down Maria's street. It's really gotten out of control. He drives this late model royal blue Mustang w/plates that say J Cruz...very obvious. J Cruz is gonna be cruising straight to the slammer if he doesn't get a grip.
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    Rebecca - you look wonderful. My hair is almost exactly the same length. On the surgery bill - once you figure out what your insurance will pay let your doctor know what part of the bill you are left with. Not his nurse or billing office, but actually mention it to him during an appointment. He might be willing to reduce the bill for you. We've had some luck in the past with things like that - the billing office is heartless and I think doctor's are sometimes clueless as to what bills patients receive. When face to face with the reality they can sometimes be helpful. My husband had to have a EKG one time that was not covered by insurance at all and the cardiologist completely waived the bill for him.

    Tina - too weird about the teenager stalking your neighbor. Good grief I wish kids could realize that break ups aren't the end of the world. I had a boyfriend in college that stalked me for awhile. If he hadn't eventually moved far away I'm not sure how I would have gotten rid of him. It's very creepy. At least there are stalker laws now.
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited August 2007
    Pix from Monhegan...

    Cnection i sspotty...but here are some pix.

    http://picasaweb.google.com/mizsissy/Monhegan

    Mizsissy
  • luckymel
    luckymel Member Posts: 643
    edited August 2007
    First of all, Rebecca, you look beautiful!!! We all kind of have the same hairdo right now, but you wear it well - and you are gorgeous. Hope you get your PS bill straightened out - maybe they are expecting you to submit it since they're not in network? I have run into that once or twice.

    Caya, I was hoping you had gotten the all-clear by now and could stop worrying. My jaw dropped when you said you spent a grand on dorm room supplies...until I thought how many different things you need when you start from scratch. I guess it's not so amazing after all, but it IS a lot of money. I hope Cassie has a wonderful year - it is such a special time of life.

    Tina, I agree wtih you - all those "this is not a bill" bills they send out are a huge waste of money. My insurance company finally stopped sending out those EOB's since we can see them online - I liked them for that. I think you ought to call the cops on your little neighborhood stalker. He has no right to be carrying his stalking on in your yard, even if he does have no self respect. He's going to be in big trouble if he doesn't get a grip - maybe a big policeman talking to him would wake him up.

    Viddie, great to hear from you, and glad your new boobs are "perky and lovely." What more could you ask? They'll soften up in time. Are you enjoying your time at the cottage?

    Mizsissy, you little angel you, glad you're having a better time now. I can only imagine how wonderful it must be up there. Enjoyed your pictures. And speaking of pictures, Robbin, Joni and Sharon, thanks for sharing yours, too ! They are all so beautiful. Joni, sorry you're going to have to wait so long to find out you're ok - that just sucks. I'm sure that's contributing to your "down days," although I think we all have those now from time to time. Sharon, loved the Janis Joplin pic of you. I really do see it - you've got the attitude!

    Joni, I'm not sure that I am changing oncologists for sure - I don't see my first onc. again until November, so no real need to decide until then. However, if I do, it would be because of the advantages of being in the M. D. Anderson system. M. D. Anderson is the top cancer hospital in the US, running neck and neck with Sloan-Kettering in New York. People come there from all over the world to be treated for cancer. It is a big, big complex hospital, which offers lots of services to patients, as well as being on top of all the latest technology and research. So why would I not want to be part of that? The only reason I didn't go there initially is because it is quite a drive through hellacious traffic to get there. Now, they have a branch 7 minutes from my home. I did like the oncologist I saw there very much, and she was easier to talk to than my first oncologist, although I managed quite well with him also, and he took good care of me. I'm conflicted, but if and when I have a recurrence I might want to be at M. D. Anderson, so...

    Well, I sat home all afternoon waiting for the new sofa to be delivered. When it got here, not only was it the wrong color, it was the wrong size and model - they just totally brought the wrong thing! Now it has turned into a big upset, because what they did was leave the wrong one here until they can bring the right one out, whenever that is. I'm sure this has to do with the fact that they had lots of deliveries and didn't want to put that sofa back on the truck, but what they said was that they would leave that one with us as a loaner until the right one comes. They just had me sign for delivery and write that the sofa is the wrong one - seemed reasonable to me at the time. Well, DH just got home and is very displeased with me for accepting the sofa in case we might end up liable for damages if it gets cat hair on it or something - talked to me like I didn't have any common sense at all. Then he threw a big old brown tarp over the thing, which looks like hell. I am not happy with him right now, so am trying to get the store on the phone to come and get it. I may let them take me with it.

    Well, I'll check later to see if anyone is in chat. Love you all.
  • TPPJ
    TPPJ Member Posts: 1,017
    edited August 2007
    See I missed you guys on Chatzy. Caya, was checking in on you to see how you made out. I'm guessing no news is good news... will check manana.

    Bummer about the sofa, Mel.
  • Lynn12
    Lynn12 Member Posts: 1,008
    edited August 2007
    Hi ladies,

    Viddie, wow, that must have been scary when they couldn't find the pulse. I think Dr. Lee told me they check quite often the first night. I'm so happy for you that all was well. Why were you still in the PACU the following night? I thought he told me I'd spend the first night there but then go to the floor the following morning. How are you feeling otherwise? are you still on pain meds?

    Caya, I'm glad you're feeling better and that you spoke with other women who have had similar. Please let us know when you hear something.

    Rebecca, you look fabulous! thanks for posting the pic. I would have been just as upset getting the bill like you did...geesh!

    Mel, sorry about your sofa woes, if I were you I'd be on the phone insisting on getting my couch tomorrow...they can 'make it work'.

    Joni, have a wonderful time at the wedding! I'll be sending positive thoughts your way when you get your scans!

    Debbie, hang in there with the rads, you're almost done!

    Mizsissy, what a wondeful story about the card...so sweet!

    Tina, OMG I'd be freaked about some 16 year old hanging in my backyard..I think you should call the police..you just never know.

    I missed chat tonight too, got there too late. I can't do Tuesday's anymore because I stay overnight in Cambridge for work...I just need to remember at the right time on Thursdays.

    I'll try to get DH to take a picture of my hair growth this weekend. It's so nice that we are all getting our hair back...think where we were 6 months ago.

    Tomorrow's Friday...YAY!

    love and hugs,
    Lynn
  • dkmaustx
    dkmaustx Member Posts: 363
    edited August 2007
    I completely forgot about chatting tonight. Oh well, there will be other chats.

    Every day puts me one day closer to being finished with rads. Today I looked at the machine before they moved me away from it. Boy, that thing is close for the boosts! I'm glad they stop before it punches me in the tummy.

    Now that I'm 7½ weeks out from Chemo, my hair is starting to get more noticeable and my eyebrows and eyelashes are really filling in. I'm not quite as far as some you, but I have hopes to be there soon.
  • TPPJ
    TPPJ Member Posts: 1,017
    edited August 2007
    Regarding the teen stalker, I let Maria's mom know what I caught him doing. She/her dh planned to let the local police know. I guess the police have already talked to this kid/his parents. I forgot that he had been suicidal at one point too, which is awful. But I hope not homicidal. I just worry about anyone getting in his path. We have about 15 kids under age 15 in immediate area. No sidewalks either, which stinks.

    Lynn, haven't been to Cambridge in forever (was born there). Used to hang out in Harvard Square sometimes in my early 20's after work in the Charlestown Navy Yard. Lots of weird clubs and restaurants...

    Guys, you'd laugh your butts off if you saw my hair. I know we are all so glad to be getting some, but boy oh boy, if you have coarse hair...just wait to see what you're in for. It literally stands up STRAIGHT! You have no choice but to wear a scarf/baseball hat. If I slick it down I now look like Eddie Munster. Will the indignities ever end....
  • skyedivine
    skyedivine Member Posts: 839
    edited August 2007
    image
    Hi Girlfriends!
    Got back from the cruise last night and I've only had time to read page 178 so far so I'm going to share a little about the trip then I'll get to all the posts. Caya I did read that manicure story! What a sweet lady you met, and I loved how you responded. And you look lovely in your crew-do! Also Jan, I think post-treatment is the worst time for dwelling on recurrence, I'm sure all of us find our thoughts turning that way...I'm hoping it's a stage that passes.
    But anyway, despite the fact that we almost drowned, our cruise rocked! They wisely scratched the excursions to Grand Cayman and the Yucatan and instead we went to Nassau and Freeport in the Bahamas. We didn't see a drop of rain anywhere! The food was superb; we began overeating when we got on the plane and didn't stop til yesterday, I've gained back all my weight and more. The very first day I won a $100 spa facial in a raffle and that was a total treat, they also gave me a huge discount on a scalp, neck and face massage so I did that too. I felt so pampered. The folks we ate dinner with were great, we all became good friends. The photo above was taken on formal dinner night. Lots of fun stuff to do all the time, but I did spend an hour or two resting in the cabin every day. It was a wonderful break.
    Now for the drowning. We still wanted to try snorkeling so we signed up for a reef excursion off Freeport. The sea was very rough but they thought it would be ok. The boat took us and about 30 others waaaay out from shore and gave very quick and poor instructions. Steve and I did not get our life vests adequately inflated but we didn't realize that. Barracudas were in the area so we had to remove all jewelry. There were deep swells moving away from the boat. I can't believe we jumped into the ocean but we did, and about the first swell ripped the mouthpiece out of my mouth. I realized my arms were way too weak yet to make it back to the boat so I waved my arms and the ebony, dread-locked Bahamian Adonis running the tour had to jump in and haul my sorry rear back to the boat. Once I got back I was weak but fine. Steve's mouthpiece was also ripped out and he swallowed a lot of sea water which made him sick although he got back to the boat by himself. Others then began returning to the boat in droves, weak and gasping from fighting the waves. But we were all fine, and I'm glad I at least tried. I had one good glimpse of the ocean bottom thru my mask before all went haywire.
    I went topless the whole time. I was the only one of 2500 passengers with a chemo do, but it was just too hot for a wig. One drunk 21-year old girl spent most of an evening in the piano bar rubbing my head every few minutes which eventually got irritating. I felt a little bad that I could not "do" my hair when I wanted to look nice but otherwise just was resigned to being buzz cut lady. At least it was totally carefree. And it was a perfect way to celebrate our 35th. Dh loved the trip too, except for the snorkeling.
    So now I have to read the rest of everyone's posts and then get back to business, house cleaning, etc. I missed you all! -- Skye
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007

    Skye - just admit it - you faked it so the cute tour guy could rescue you. But, seriously, I am glad that you are back safely and that no one sunk. Sounds like you had a well-deserved wonderful and relaxing time. Welcome back. We missed you.

  • Lynn12
    Lynn12 Member Posts: 1,008
    edited August 2007

    Skye, welcome back! Wow, that is really scary about the large waves and snorkling. Glad everyone made it back safely, whew! You and Steve look wonderful in the pic, I'm so happy you had a great time, you deserved it!

  • Rebecca
    Rebecca Member Posts: 971
    edited August 2007
    Yay Skye! Glad you are home safely. Did you try to rub the 21 year old drunk girl's head in return? I bet that would have made her stop
  • luckymel
    luckymel Member Posts: 643
    edited August 2007
    Skye, so glad you are back safely! I thought about you all week long. That's really sad about the snorkeling - it really is such a wonderful experience if you're not drowning. I guess you'll just have to wait and snorkel in Akumal (which was fortunately missed by the hurricane). Half Moon Bay in south Akumal is calm and the world's best place for snorkeling - and you can walk out 10 feet from shore and snorkel there. Anyway, glad you had a good time otherwise, but we missed you. I guess you should be glad your hair isn't at the stage that Tina's is. And Tina, we need a picture of that, please! I can't wait to see if mine does that...

    Caya, any word yet? We're all waiting with you.
  • Caya
    Caya Member Posts: 971
    edited August 2007
    I called the BS's secretary this morning and she checked online - the radiologist has not yet posted the addendum to my original mammo report. So she said she would email him to ask about it, but she wasn't sure if he would respond today as she did not know which hospital he would be at.
    Then I called the onc. who said she would get back to me today (had to leave a message at the oncololgy dept.), but quite frankly if the report isn't ready, what is she going to tell me? Can you believe this? So I'm going to wait another hour to see if the onc. calls me back - if not, I will call the hospital's main switchboard and have her paged. I am so pissed off, as you all can imagine. If I were the BS's wife, I would have had a detailed report 2 days ago.
    Thanks so much for all your support guys.
    Skye, glad you're back - you and DH look great.
    xoxo caya
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007

    Caya that just sucks. I hope you get the report today.

  • Caya
    Caya Member Posts: 971
    edited August 2007
    okay so the update so far is that I spoke the Bs's secretary and she got the addendum from the radiologist, which she will fax to me. But briefly she read it to me over the phone and the dr. thinks he sees some cysts, but wants me to have a breast ultrasound to confirm it. Man, do they not get it - I had the mammo and breast ultrasound last June showing NADA - and then less than 4 months later my Plastic S. finds the frigging tumour. So I told Betty (the sec.) all this and that okay I will come down next week for the U/S - she's trying to book it for Monday or Tuesday - but to please speak to Dr. Leong - the BS - and repeat my story that I need an MRI. She said she would.
    I also called the onc. and had her paged - I mean business now - she just called me back to tell me she is in a meeting but would call me back in about an hour and a half and will look at the addendum.
    So that is where I am at - I really think it is probably just a cyst or some residual something from the reduction surgery, but naturally it all has to be checked out, and I have to worry about all this.
    I will keep you all posted.
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007

    Caya - how frustrating this must be. All that waiting and still no real new information. Just keep demanding that MRI, you'll get it.

  • Lynn12
    Lynn12 Member Posts: 1,008
    edited August 2007

    Caya, I agree with Jan, push push push!

  • Caya
    Caya Member Posts: 971
    edited August 2007
    Just got off the phone with the onc. on call - Dr. Enright -I went over the mammo report with her, and I am going to post some of it because I know Mel is a nurse and maybe somebody else out there will be able to decifer this:

    Post reduction heterogeneously dense breast parenchyma is noted and this may lower the sensitivity of the mammogram. Multiple nodularities are detected in the left breast outer quadrant, the largest one measures about 3.3 cm. x 4.3 cm. in size. No definite suspicious microcalcifications are noted in the left breast.
    Impression: Several nodular masses in the left breast upper outer quadrant, probably benign cysts.

    Addendum: (after reviewing the June 2006, pre-reduction mammo) The nodularity in the left breast in the upper lateral part in now more marked than on previous left mammogram. Again this finding suggests the presence of cysts but this can be confirmed with a left breast ultrasound.

    So I again told Betty the sec. that just an ultrasound will not do it for me. She seemed to agree and will discuss this with the BS. Dr. Enright the onc. was reassuring, told me again that after the chemo the odds of me having a new BC are highly unlikely, but that she believes I should have an MRI. If the breast U/S confirms just cysts, then the MRI would not be right away ( but I will still push for this). Of course if the U/S is inconclusive, I will get the MRI very quickly.
    I have the U/S booked for Monday at 8:30 a.m. I will try to hang around and see if I can at least get a verbal that morning. So I feel better, but man, this ride is worse than a roller coaster.
    I would also like to add that I had the mammo and will have the U/S at Princess Margaret Hospital - this is the #1 cancer hospital in Canada - right up there with Sloan and M.D. Anderson. So I have to think they have the best equipment and the best radiologists reading the images.
    The sec. just called back. She spoke to my BS and he advises I speak directly to the radiologist and ask for the MRI. And I will, believe me.
    So that's it for now girls. Thanks so much for being there and listening. I'm not telling anyone about this until I know - just DH and one close friend know.
    xoxo Caya

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