Starting Chemo in May 07

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  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    LeeAnne and Amy, image

    I'll be thinking of you both today!

    The way to post graphics (it's so much fun) is to set up a photobucket account at photobucket.com It's free. You just search for graphics and then choose the one you like. You need both websites open (photobucket and bc.org) Copy the second from the top link by your photo in photobucket. Click on it to highlight it then right click to copy. Then, when you're adding a post to this thread, be sure to click "preview my post" then click on the "Image" link under Instant UBB code. A little window will pop up, then right click in there and hit paste. Then hit okay and it will insert the graphic inot your message. That's it!

    Hope everyone has a good day today!
    Mandy
  • ocinny414
    ocinny414 Member Posts: 123
    edited August 2007
    Hi girls,
    Me again. I've been really busy since my last treatment, which was almost 2 weeks ago. I'm still week and my fingernail beds are still sore and discolored, but I didn't loose my nails.(I was taking taxotere/cytoxin). My eyes keep watering and my nose is running constantly, strange to develop new SE's when I'm done.
    I'm having a mild case of lymphodema in my left hand. It's swollen and has been for about 2 weeks. I have an appt with the physical therapist tomorrow so hopefully that will get better. There is no pain and its not red or anything so the Onc wasn't all that worried. Now I'm dealing with my ankles swelling and a little in the other hand. I think I'm just retaining water but I'm not sure. I go for bloodwork today and the lab is in the same office area as the onc so I will see if I can talk to him or the nurse and find out what to do. I was on my feet alot yesterday and by last night I didnt have ankles. Just fence posts connected to my feet. It looked really weird. I slept on my back with pillows under my feet and one under my arm. Not very comfortable but at least the swelling was down a little.
    I'm not sure why I'm having so many problems with my last treatment. Usually by now I'm back to normal (well as normal as can be expected) but this time its kicking my behind. I did move the treatment up from my usual Monday to having it the Friday before, but you wouldn't think 2 days early would be such a big deal. Oh well it will only get better.
    OK enough about me and my complaints.
    CONGRATULATIONS to all who are finished or just finishing up. And to those who still have a ways to go. Just remember that we are all still here for you and with each treatment the light at the end of the tunnel gets a little brighter.

    Have a great rest of the week,
    CindyKS
  • chemo072
    chemo072 Member Posts: 682
    edited August 2007
    CindyKS - I went to the ER back in the spring for shortness of breath following painkillers for post-biopsy pain, and the docs there poked at my legs looking for edema - the concern was heart issues. Also, it seems like maybe kidney function can be related to swelling? Especially if it's so uniform (on all limbs) doesn't sound like lymphedema - but, true lymphedema can be triggered by many things, and I'd hate for this to be the thing that triggers that for you.

    Ok, call me miss worrywart, I hope it's none of these things. But do let us know how it goes today!

    My guess is that they prescribe a diuretic of some sort...
  • NeoPat
    NeoPat Member Posts: 102
    edited August 2007
    Quote:

    Anybody else still having chemo?





    I have my last treatment (Taxol)on Wednesday, the 29th.

    Pat
  • cinrae123
    cinrae123 Member Posts: 419
    edited August 2007
    omg,,,,,,,,,,,,,i so love Jim Carrey and that video is cracking me up,,,,,,,,,,I needed a good laugh. lol A huuuuuuuuuge congrats to those of you ladies who are finished,,,,,,,,,,,soo good for you gals. And to those of you who have still more to go and surgeries,,,,,,,,,,hang in there gals,,,,,,,,I am thinking of you.
    Got the results of the nose culture back,,,,,,,,and yeah it was MRSA. Got on the right antibiotics so on the way to healing (after 2 trips to the urgent care that is) But its all good,,,,,,,,,swelling has gone done quite a bit, which is one huge relief,,,,,,,,,and (not meaning to get gross) but the draining from the nose and under the lip has stopped also. Besides looking weird with no hair,,,,,,,and having a face that looked like one of those Whoville people from the Grinch,,,,,,,omg I didnt even recognize myself. lol But am looking more like myself every day,,,,,,,ok, minus the hair loss. lol
    Weekend almost here,,,,,,,,,,,so probably wont post again for a few,,,,,,trying to rest as much as possible. My last treatment is supposted to be this Monday,,,,,,,,,,but have to talk to my onc tomorrow to see because of the staph infection, she may want to wait another week. Darn,,,,,,,am looking forward to finishing up soon. But,,,,,,if I have to wait for it to be better on my body, I will..........whats one week right? lol
    Have a great weekend,,,,,,,,,
    Cindy
  • PDXLeeAnne
    PDXLeeAnne Member Posts: 119
    edited August 2007
    Well here I am, sitting in chemo, waiting on my labs. It's going to be a long afternoon/evening. It's already 2:30, I haven't had my pre-meds yet, and the Taxol drip takes 3 hours...

    Talked to my onc about my pain and he prescribed me Darvocet, which I can take with Ibuprofen. Hopefully that will help my bone and joint pain. I have an appt. with radiation for a sim on Sept. 7 and he says I HAVE to start rads within a month so I will have to do some tricky negotiating to be out of town for 2 days for a breast cancer retreat in October. Hopefully I can be accomodated somehow, but they really don't like you to miss even one day.

    Also, I can't have my port out until a month after radiation ends. That's a bummer, but I understand why, because I am not in a good place to heal right now, and the scarring would be worse. Also there would be an increased chance of infection. So although I wish I could have it out next week, I can't. Onc said I could have good drugs for the removal though, like memory erasing ones!

    He also said I've done well, that I've maintained some muscle (although I have certainly lost some) and I'm overall in good shape. He thinks I'll do really well with radiation and will recover quite quickly once I get over this tx. All good to know... I should be thrilled this is my last one, and I am, but I know what an abyss I am going to have to dig myself out of to get to the other side!!

    LeeAnne
  • lizzzy
    lizzzy Member Posts: 285
    edited August 2007
    Hang in there LeeAnne! You'll get to the other side no problem. It's been a month since my last a/c and I feel darn good, but 4 rounds is probably easier to deal with than 8. So it may take a little longer but you'll do it.

    I am finished with all my pre-op tests and now I just have my surgery to look forward to. I'm getting the nesting instinct big time now. Don't want to leave anything undone while I'm recovering.

    Tonight I'm going with my husband and our mothers to the Hollywood Bowl to see the L.A. Phil "French masters" concert! We haven't really been out for anything except dinner since I started this whole thing so I'm excited.
  • Traci-----TripNeg
    Traci-----TripNeg Member Posts: 2,298
    edited August 2007
    LeeAnne!!
    Guess what? Did you know that you can go to ABC.com and view any episode of at least 2 dozen shows????
    I never watched Lost and my friend made me go online one time in the chemo room and it was awesome! I'm on season three now!!
    I don't normally go for blondes but, the guy Sawyer on that show is HOT!
    Don't worry girl....you'll get through. Wish I was there with a second set of head phones!

    Liz, have fun at your concert! You deserve it!

    Has anybody talked to Cynthia??
    Take care y'all.
    Traci
  • lizzzy
    lizzzy Member Posts: 285
    edited August 2007
    Ten things to do before going under the knife next Wednesday

    1. Sign advanced directive (in case of coma, etc.)
    2. Clean the house (visitors may be coming)
    3. Decide what to wear for the big day (button down shirts are all the rage for breast surgery patients)
    4. Put sheets on the bed in the spare bedroom (need arm strength to get into my bed)
    5. Go shopping for easily prepared foods (in case I get hungry and don't want to rely on hubby's cooking, wonderful and inventive though it may be)
    6. Go running (won't be doing that for a while) and do chest press machine at the gym (won't be doing that again EVER)
    7. Throw out all my underwire bras
    8. Have fun
    9. Make sure everything I need is below shoulder height (won't be lifting my arms for a while)
    10. Drink a champagne cocktail (or two)
  • Traci-----TripNeg
    Traci-----TripNeg Member Posts: 2,298
    edited August 2007
    Liz, You are funny.

    Don't forget:

    11. Go shopping and spend some money on the softest....button up jammy tops you can find for your recovery. (Cut the bottoms off and make 'em into shorts.)
    12. Re-supply yourself with stool softeners.
    13. Put extra pillows on the spare bed cuz you are going to be sleeping practically sitting up for at least a couple of weeks.
    14. Put an extra end table on your side of the bed cuz the one that is there won't be big enough for all your stuff. (Pills, drinks, food, remotes, books, kleenex, phone, etc...)
    15. Make sure the cable and DVD player in the spare room is functioning.

    You can do it girl!!
    Hugs, Traci
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    LeeAnne, you must be done your chemo by now - yahoo!
    Amy - you must be too! Yahoo again!

    I am so happy for both of you - it's been such a hard road to travel - but you're done. I know you're not totally "done" and that there are side effects to follow but doesn't it feel good to know that this is the LAST time? I am far happier today than I was yesterday and I feel so much better at day 2 than I did with all the other treatments! I didn't even take any decadron! It's either in my head that I don't have to do this again or (more likely) that extra week because of my delay brought my body back to greater health and thus I am coping better...whatever - I am happy today. This could change at any time. I still have the body aches from coming off the decadron, the sinus pain from the cytoxan, the mouth sensitivity to deal with in the next few days, the wicked heartburn...but I'll get better!

    I'd raise a glass to you but booze would sit like krap in my body right now - and for a couple of weeks yet but let's have a virtual toast to your finishing chemo! (I prefer a shot of tequila myself)

    Liz - I will so be "with" you next week when you go for your surgery - I'm sure we all will. Just remember that we will be sending you positive thoughts, healing energy and well wishes. Also, as soon as you're well enough to post, please let us know how you're dong and that you're okay! You are STRONG and I'm sure - no, I KNOW will come through this just fine. I believe that being fit and active is such a benefit to recovery for you!

    I am a little disappointed in my family and friends. Yesterday was such a big day for me and I really hoped for some fan fare (cards, flowers, e-mails, etc.) but some people actually forgot that yesterday was my chemo day! I just can't believe that no one in my life (not even my hubby) recognized just how huge yesterday was to me!! After my surgery, I got so many cards, flowers, gifts, meals - it was amazing! Then after my first chemo, I got lots too, then each treatment, there was less and less until tx 5 - there was nothing - but I was leaving for holidays the next day so I attributed it to that. But my last one - that was cause to celebrate...but nothing. Oh well, I am celebrating in my heart and I know my friends and family are happy for me and love me. I guess that's what I get for not accepting any of their help all this time - I think they think this is not that big of a deal to me and therefore I don't need any of their support. That's okay too - if I asked them they'd be here for me in a heartbeat! I'm embarassed to even whine about this but it's been on my mind a little bit and you ladies are the only ones I can tell because if I share that with anyone in my life, they'll feel like krap and that's not what I want. So, here is a gift to me, from me (and maybe a litle eye candy for any of you who like Viggo too (he's my boyfriend on Fridays and Curtis is my boyfriend on Saturdays)
    image
    image

    Have a great evening eveyone. Gentle hugs for LeeAnne and Amy and for every single one of you! (Liz, I'll send you a big old bear hug since you won't be able to take any of those for awhile after surgery!)
    image

    Mandy
  • ocinny414
    ocinny414 Member Posts: 123
    edited August 2007
    Yummy Curtis is so cute and funny. I wish I lived in a town where he would actually visit, but I dont think he will ever come to Manhattan, KS and if he did I would probably not be lucky enough to be shopping at the time. He would pick up some cutsie college chick with all her hair and big perky boobs. LOL I watched a rerun episode today and I thought the lady was gonna eat him up. she looked so disappointed when he left. She fixed a meal for her best friend so he had 2 women watching his every move.

    The Onc prescribed Furosemide for my swollen ankles. I'm suppose to let them know how it works. I decided to start taking it in the morning so I could sleep tonight and not be up peeing all night long. Looks like another night of elevated legs and arms. I really hope this diuritic works cause I really liked my ankles and to have them be the same size and my calves is just not cool.
    I'll update and let you all know how I'm doing.
    congrats of finishing and I hpe the SE are not as bad this time.

    CindyKS
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    CindyKS - I hope your swelling goes down pronto! You've really had a round of SE's lately...

    Yes, in regards to Curtis - I have always said that if he picked me up in a supermarket (impossible since A) I live in Canada, B) I am 42 - no perky boobs here!) but IF it ever happened - you'd never hear from Curtis Stone again because he'd end up locked in my basement in a cage - let out only to cook me fabulous meals and be my love slave...ahhh - if that doesn't bring on a hot flash - I don't know what will!

    Feel better Cindy - try to sleep well in your elevated state!
    Mandy
  • lnmshoes
    lnmshoes Member Posts: 17
    edited August 2007
    Hi all,
    Had my last chemo today too.
    Leanne, I too was alittle disappointed that no one made it special for me. I don't thing they realize what a big day this is. My daughter and sister were there with me which I appreciate, they have been there all the way. My mom told my sister that she might stop by the hospital if she wasnt' too tired! give me a break!
    Oh well enough of my pity party. I am HAPPY!
    will till have herceptin but the nurses say that will be a breeze.
    Amya - Prior to the mastectomy I was leaning toward the reconstruction where they take from your back but since there was a chance I would need radiation the ps recommended the implant/expander. My intention is to end up a C cup so that I won't have to go our and buy all new bras. expansions are done now I wait for surgery on Oct 8.

    Hopefully just two more weeks of feeling like crap and then I will start feeling normal again. Hair will start growing back. I guess we have to create our own celebrations!

    Hugs to all,
    I plan on staying around here for awhile.
  • PDXLeeAnne
    PDXLeeAnne Member Posts: 119
    edited August 2007
    Yep I'm home and done and now just to get through the next few weeks.

    My sister (who lives in Amsterdam) got all her work friends to send me "congrats on your last chemo" emails, and what a lovely thing that was to wake up to this a.m. A guy I dated last year dropped off champagne while I was at chemo today, and last night I had 1/2 a glass of bubbly (it doesn't sit well) with 2 girlfriends who drank a whole bottle of wine and most of 1 1/2 bottles of champagne while they were here. LOL - it is interesting to always be the very sober one. I did get some other congrats emails as well, but noticeably no one from work has remembered except one gal.

    So here's a question for you all. What do you think of guys who want to go out with me while I'm in the midst of this? I'm not talking about guys that knew me before, these are men who have written to me on myspace (no worries, I know my way around the world of online dating, I've been doing that for years), KNOWING that I am going through cancer treatment. Isn't that a little weird? If you were going to pick out someone to pursue wouldn't you want them to be as healthy as possible? I have no energy to go out with anyone new (dating is a lot of work) and, in fact, can't even get up the energy to talk to anyone new on the PHONE, but I suppose that in a month I might be able to meet someone for coffee? I just think maybe the men a woman attracts during treatment might be the sort who like to play white knight to the rescue and then run when you're healthy.

    Anyone have any insight whatsoever?

    LeeAnne
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    Good Morning Ladies!

    Mary, LeeAnne and Amy - this is for you!
    image



    Mary - I did end up getting flowers last night and that made me feel much better! It's so weird - I don't want to be fussed over but then I am hurt when I'm not fussed over - how can my friends and family win?? You're right - we create our own celebrations because I for one am so damned happy!!! Next Friday I am having "Me" day! I'm taking the day off work, I have booked a massage, a reiki session and have a gift certificate to spend at Holt Renfrew (a store that I cannot afford to shop at but it's for $250 and that will likely allow me to buy oh, maybe a pair of pantyhose but I don't care - I am spending it on something silly if I feel like!! - GOSH! - I sound like Napolean!)) The whole day is all about me and my pleasure!

    LeeAnne - I am with you on the the guys who are persuing you during treatment. I'd feel a little uneasy too. I'd either suspect they are feeling sorry for me or have the Knight in Shining Armour thing going. Now perhaps I am being cynical - you ARE hot and that's probably what shines through in your messages - but it's one thing to meet someone face to face or get into a relationship with someone THEN find out they had cancer - it's another to know that up front before really connecting with them. I know if it were me who were single and I saw a man on line who was in our position - I wouldn't exclude him because of it but I would probably hesitate to get involved with them because I'd know (now anyways) how much they are really going through and I'd wonder how present they'd be able to be in a possible relationship with me. Then again - we are just talking about coffee and friendship to start with. Oh dear - I guess I should have thought this all out before I responded because I really haven't provided any insights whatsover! Hmmm... it's very interesting though - I am curious to hear other people's responses to this!

    Well, I hope you all have a great weekend planned. I think I may go to the Bluesfest we have gong on this weekend - Los Lobos is playing on Sunday night (LOVE them) so we may go if the weather is good!

    Talk to you all later,
    Mandy
  • lizzzy
    lizzzy Member Posts: 285
    edited August 2007
    Quote:

    So here's a question for you all. What do you think of guys who want to go out with me while I'm in the midst of this? I'm not talking about guys that knew me before, these are men who have written to me on myspace (no worries, I know my way around the world of online dating, I've been doing that for years), KNOWING that I am going through cancer treatment. Isn't that a little weird? If you were going to pick out someone to pursue wouldn't you want them to be as healthy as possible? I have no energy to go out with anyone new (dating is a lot of work) and, in fact, can't even get up the energy to talk to anyone new on the PHONE, but I suppose that in a month I might be able to meet someone for coffee? I just think maybe the men a woman attracts during treatment might be the sort who like to play white knight to the rescue and then run when you're healthy.

    Anyone have any insight whatsoever?




    First of all, CONGRATS on getting through the last treatment. I'm SO happy for you!

    I would have to say a guy has got to know you a bit first before he signs up to go through cancer with you. Especially someone you meet online. My first instinct was how great, these guys are willing to date someone with cancer, but I changed my mind. I really think they have to be emotionally invested before they decide to get into this with you. I am sure thinking about dating in the middle of this is nerve-wracking to say the least. But when you meet someone and they see what a beautiful person you are inside and out, then they will not hesitate to accept to join you on the cancer fight, I am sure.
  • lizzzy
    lizzzy Member Posts: 285
    edited August 2007
    Quote:

    give me a head with hair ...



    shining, gleaming, streaming, flaxen, waxen ...

    I do have hair envy. Especially when I see women with long hair like I used to have. BUT, there are definitely bennies to wigs. No morning styling. Get ready for anything in 20 minutes or less. Change hair color and style on a whim. Just go scarf or nothing at all! I like my new peach fuzz. It's still unsure what color it's going to be, but it's very soft and fun to rub.
  • Traci-----TripNeg
    Traci-----TripNeg Member Posts: 2,298
    edited August 2007
    Mandy,
    That cat was AWESOME!!!!! That made me laugh out loud! Girls, that should have done it for you! WOO HOO!! On your last treatment!!
    I gotta spend some time and add pictures. That is just to much fun.
    Have a great weekend girls.
    Hugs, Traci
    ps There is practically NO pain in my lower back today!
  • chumfry
    chumfry Member Posts: 642
    edited August 2007
    When my hair came back after my 2005 chemo, it started off as the softest white fluff. I loved to pet my head because it felt like a baby bunny.

    When it started coming in more, you could see it was this really weird battleship gray color--kind of like pencil lead. A lot of women get hair this color after chemo. But it's TEMPORARY, so don't freak out! LOL

    Some people colored their hair right away, but that sometimes caused weird hair colors, like orange or green. I think those wash-out color kits were OK. I just left mine gray and it eventually turned back into the medium-dark brown it was before.

    Once my hair got long enough, it started to curl, which was way cool because I've been paying for perms for 30 years. But that, too, was temporary and the curls grew out about a year later. Ah well.
  • aimster1123
    aimster1123 Member Posts: 200
    edited August 2007
    Hey girls,

    THanks for all the well wishes!! I made it through my last infusion!! Now I just have to lay in bed for a week, more or less, and then I should be getting back to normal. All the nurses and my onc singed a special "Purple Heart Certificate" in honor of my finishing chemo today, so that was nice. My onc's inscription was "ALL DONE--WHEW!!" That pretty much sums it up.

    I have an appointment with my rads doctor on Tuesday--a consultation followed by a dry run in the radiation machine to see how they're going to do it. I also am supposed tohave th port out in about 2 weeks, rads will begin in about 3. No word yet on how many treatments.

    CindyMN, interesting about your hair. It's going to take a while to see what we TRULY will look like isn't it? I honestly think I'll just be happy to have hair of any kind. One of the nurses today said I'd probably have the short-short kind that I can wear alone by Christmas time.

    My onc had quite a few things he wanted to talk about, too. First, he said that as I transition out of active treatment, I should expect to feel paranoid about little aches and pains I might have from time to time. So he gave me the rule-of-thumb that I don't need to get concerned about them at all, until they've lasted more than 2 weeks. Then I should call him and we'll talk. So that was good to know.

    He also said that it will take about a year for me to feel "normal" again, physically. He said in about 6 months time I'll FEEL normal, but when I get to a year I'll look back and see how much better I feel than how I felt 6 months before. Also good to know. "Chemo is a BIG HIT--a REALLY big hit" he said, so we should all go easy on ourselves, right?

    Liz, we'll definitely be thinking of you next week--let us know as soon as you're typing, OK?

    LeeAnne, I think I'm inclined to agree with what others have said about the guy thing. Once you're feeling up to it, though, it probably wouldn't hurt to have coffee or somehting and get a better feel for them. Who knows, they could be perfectly fine. So my advice? Proceed with caution! And trust your instincts.
  • lizzzy
    lizzzy Member Posts: 285
    edited August 2007
    image

    Mandy, If you can do THIS, you can post your picture!
  • PDXLeeAnne
    PDXLeeAnne Member Posts: 119
    edited August 2007
    LOL, speaking of posting pictures and graphics, I spent at LEAST an hour at chemo yesterday trying to find JUST the right picture of Jon Bon Jovi to post for y'all. He makes ME happy anyway. It was too hard to choose one though, so I didn't. Obviously.

    Oh my gosh you guys, the Dexamethazone has made me SO irritable this time around. I'm so glad this is the last I'll have to take it. I have a girlfriend visiting from out of town and she really noticed how stimulated I was last night and today she told me I needed to lighten up on my mom. Apparently I wasn't as nice as I should/could have been. Makes me feel bad because I hadn't even noticed.

    LeeAnne... chemo beeeotch
  • chemo072
    chemo072 Member Posts: 682
    edited August 2007
    CindyMN - Many thanks for the, ahem, heads up on the hair color growing in....I looked at my 4 mm of peach fuzz this morning and it looked really gray - and i know that it wasn't pre-chemo. Had me a little worried.

    Amy- Congrats!!! I am so happy for you!!!

    Lee Anne - Well....in a week the steroids will be out of your system! And all will be forgiven, I'm sure. I know that I drove at least one friend nuts while I was on steroids...she kept saying, let's just calm everything down but I was amped on steroids and just wanted to get stuff done before I collapsed....it was definite "go" energy.

    Also, re rads - I was told 6 weeks after chemo...but in any case it's optional for me, and I'm leaning towards not doing it.

    Everyone - this is going to sound silly, but I got to drive All By Myself on the freeway yesterday. Going more than 40 mph was SO MUCH FUN. I didn't realize how much I missed driving over the past 4 months, when there were what, 3 days every two weeks that I felt comfortable driving.....

    Also, today, the day after the day-that-I-usually-have-chemo but don't because I'm DONE, well, today was a good day. End of the week but my energy level picked up. And there's more - I'm seeing more, not sure how to explain it - the world feels new, like I haven't "seen" it for a long time - I'm noticing more details - the color of the different bricks on my building, the fact that there are hills in the distance, etc. It's a strange experience, but I'll take it...kind of a consciousness expanding.... maybe I've just had tunnel vision for months.
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    Amy - nice to see you posting - how are you doing? You seemd really....coherent (not your usual post chemo self - I hope that means this tx is MUCH better than the others - and I hope I haven't offended you by suggesting that your usual post chemo self is incoherent...I just know from some of your other posts that you have really gone through a rough time)

    AmyA - It is so nice to hear about your post chemo experiences and your new perspective on life. You maybe have had tunnel vision with all the krap you've (we've all) been going through lately...so great to hear you're doing so very well!

    Liz, I was wondering when someone would notice that I STILL haven't uploaded my avatar...and there is a good reason for that! As you may remember, I had some computer troubles in July. I spent $300 on getting rid of viruses and krap from my computer. Of course, EVERYTHING got cleaned out including the viruses/trojans. Prior to the repair, my hubby had installed an E drive so we could have extra memory - to free up space on our hard drive, he transferred ALL of our photos to the new E drive storage vault. Well, somewhere between the computer geek guy cleaning up my system and my husband transferring everything - I now have NO PHOTOS!!! I have always refused to "erase" the memory card that goes into the camera - when they get full, I just keep them (like a negative I have always said). Well, if my photos ARE gone for good - then it's a damned good thing I have saved those memory cards!!!! So, now you're maybe thinking well, plug in the camera and then just upload the photos again - right? Ahhhh...well, our camera broke on holidays and was in the shop getting fixed - however, we have just learned that it's going to cost as much to fix it as it would be to buy a new one. SOOOO, I sit here with memory cards and no reader for them and an E drive with (supposedly all my photos on it) but no way to retrieve them on the computer. Am I frustrated????? You bet!

    So, until this all gets sorted out here is another silly dancing creature:
    image

    Mandy
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    Oh LeeAnne - forgot you in my previous post...I know how you feel about those wretched steroids! I didn't even realize how wired up I got on them until my 5th tx. We left for vacation the next day and I was feeling sooo good -mentally. I was driving down the highway, listening to my tunes, singing my guts out and then my daughter (13yrs. old) asked me to turn down the music because it had given her a headache! I thought to myself what a wimp - for a teenager - she sure can't stand music that is only slightly loud! Well, a few days later I turned up the volume to what it was when we were driving and holy moley - was it ever loud! How could I have not noticed that? My poor family - subjected to that noise - yikes!

    Then there is the let down in the following day/s. I too am short tempered and intolerant. I never noticed this much before - maybe we're simply less tolerant at this point in treatment? I'm sure our loved ones understand and won't hold it against us...I hope - I sure hate being a cow to the people I love!!

    Mandy
  • aimster1123
    aimster1123 Member Posts: 200
    edited August 2007
    Hey girls,

    Well, it's 5:11am and I haven't slept yet--don't ya just love those steroids!!?? I can't wait til they're GONE!

    Thanks for noticing that I wasn't slurring my words all over the keyboard this time! I only took 2 Marinol this time, so I've been more nauseated but also more coherent. I think I like this way better.

    It's still sinking in that this was my last tx! Amya, I liked what you said about "what would have been the day after a tx, but it wasn't cause you're done". That day will come in about 3 weeks for and I hope it's really cool!

    I get my anti-nausea pump off on Tuesday, and then I'll really start to feel better and better.

    NOt too much else to tell right now--just thought I'd say howdy since I"m UP!!!

    Amy
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    Amy

    You had an anti-nausea pump? I ve never heard of that. I had 3 RX for nausia on my first tx and 4 for #2. However I still spent almost 10 days nausiated and here it is day 15 and my stomach is still cramping. I'd love to hear about the pump as I am starting with a new onc Monday.

    My other one was the onc from Hell, I have seen her only 2 times since I started chemo 5 weeks ago. (Yes, that also means no blood test this cycles, not even WBC, as she felt checking WBC... not important... until I go for tx #3. Oh if I developed a fever then I should call her. She also refused to answer any questions, including why she changed my tx from 3 to 6, or why I am having severe chest pains...understand why I changed?
  • VirginiaNJ
    VirginiaNJ Member Posts: 634
    edited August 2007
    Hi Ladies!

    Congrats to all of you that are finishing!! Just wait until you feel human again... I had my last chemo on 6/21 and I feel so good it's make me truly realize how HORRIBLE, wretched, awful, grueling, ... the chemo was. Gosh, those sleepless nights on the steroid... UGH. I don't miss those feelings...

    I have been documenting my hair growth with pics. So funny. Month 1 (July 21) - NO hair... Month 2 (Aug 21) I have quite a bit of HAIR! (Compared to being completely bald). My hair is coming in the same color it went out...dark brown with gray at the temples... The hair dresser (and the wig guy) said it will come curly but will revert to poker straight (which is what I have) quickly...

    I laugh at the posts where you all say how you miss your hair. Every morning I wake up and rub my head...and say, "yep, still bald" I guess I just hope that I will wake up in the AM like Rapunzel!

    I had a Longaberger basket party at my house last night. (It's a home show where people buy baskets). Anyhow, they have a Horizon of Hope campaign where they donate proceeds to breast cancer research. I went to Dresden Ohio last month for a special breast cancer luncheon with the president of Longaberger... It was so inspiring to meet other survivors outside of a hospital or medical setting. It gave me hope that my hair would grow back....and that I would be "normal" again...

    Anyhow, back to my basket party last night...I had all my friends laughing b/c I was constantly rubbing my head... It's now sub-conscious... I rub my head all the time to make my hair grow! LOL Anyhow, it was so nice to have a house full of my girlfriends...made me feel soooooo good.

    Best to everyone!!!!!!!! It's been such a comfort to read all of these posts!!

    Take care everyone!

    Virginia
  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2007
    Amy - I hope as I write this you are enjoying a sound sleep! I don't know how you ladies on Taxol do the massive doses of steroids before hand - you are all so strong!

    Jean - Your old onc. sonds like a real cow! No wonder you switched. I really wonder why some people get into medicine - I can understand the science aspect of it and that's obviously where their interest lies - but surely they realilze that they have to deal with real live people too????

    Virginia - I know what you mean about rubbing your head! I even invite people I know to rub it too - my "hair" looks like an old man's beard all grizzled and grey/black but it feels so soft - everyone is so surprised! My hair was already very curly so I am hoping for poker straight! (I highly doubt it) but as I mentioned before I will take ANY kind of hair! Your longaberger basket party sounds wonderful!

    Well, I have a psycho cat that's trashing my house here because he wants out and I am ignoring him (can you believe my nerve to IGNORE my cat??) so I'd better deal with him. He's such a bad boy - we don't let our cats out loose in the neighbourhood because: it's dangerous for them (my psycho cat was already hit by a car in Jan 06 and I don't want to live through that again - we almost lost him, he went through months of treatment and it cost us $6000!), our neighbours probably don't appreciate a cat in their yard, pooping in their flower beds, chasing birds, etc. and also we have a rash of cat mutilations happening in our city! Can you believe that? My Mom's cat was found last year dismembered - police still don't have any leads but they are working on it as there have been so many cats killed. I hope they catch those wretched "people". As a solution, we have built a cat fence which keeps our younger cat in the yard just fine - but my crazy guy - he's had a taste of the wild life (we got him from an animal rescue society that I volunteered for - he was a stray) anyways, he keeps finding little places to escape so we have to watch him carefully!

    Happy Saturday!
    Mandy

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