The Chemosabe March Cruise

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  • BettyeE
    BettyeE Member Posts: 267
    edited May 2007
    Put me on deck for Tues. May 22 for TAXOL #11 Whoppi!!!! I just may survive this journey.
    Bettye
  • GrammyNancy
    GrammyNancy Member Posts: 666
    edited May 2007
    Happy Saturday Everyone!

    3boys4me, so sorry to hear about your Mom...you and your entire family are in my prayers.

    MissShapen, 8 hours wow...I'm so sorry that your treatments take so long. How was the herceptin...I'm on to that next.

    Taurie...so sorry to hear about your arm and your doctor. Keep that arm elevated and take care of yourself and no jumping ship.

    Cynthia... hope that bone pain becomes just a memory real soon...I'm praying for you.

    Maxgirl...hooray for the peach fuzz....can't wait to see some of that.

    HollyHopes...so good to hear from you and I'm so sorry that you are having such a hard time. You are almost there so hang in there. I'm happy that you were able to make it to your son's graduation...I'm sure it meant alot to him. Sending you prayers and positive vibes.

    Hope everyone has a wonderful weekend!
    Nancy
  • dmknanny
    dmknanny Member Posts: 60
    edited May 2007
    Dawn
    I've been having the runny eyes/nose thing going on from time to time. I've been using Allegra D but I can't tell if it's helping or not. I think it may just be allergies - the pollen count has been very high here lately, and some days it's bad and other days I don't have problems.
    Holly
    Good to hear from you. I just finished Tx #5 (taxol #1) and have really been fighting off the depression. I've been so good up to this point, but the last week or so things really seem to be getting to me. And it takes almost nothing to make me cry.....Melinda getting the boot on American Idol almost did me in! Glad you could enjoy your son's graduation.
    Maxgirl
    I've been noticing that my remaining stubs on my head don't seem to be going anywhere - which is great because they help anchor my scarves in place.
    MissS and Lisa
    Don't know how you survive those long tx's..I went Tuesday at 8:15 and did not leave until 1:00 and thought I would crawl out of my skin! Had to pee 3 times during my infusion - just love pole dancing in the bathroom!
    3boys4me
    You and your family are in my prayers

    Keeping you ALL in my prayers with wishes for a peaceful, SE-free weekend
    Diana
  • Angelflight
    Angelflight Member Posts: 163
    edited May 2007
    Well my daughter will arrive tonight about 10-11pm. Can't wait to see her.

    I've been nursing a slight headache for 2 days but it seems to finally be subsiding now Thank God. Hubby's been a real charmer and he and my son's girlfriend cleaned the whole house from top to bottom yesterday and I can actually see my glass table tops without a film on them...lol My daughter is going to steam clean the carpets for me while she's here so I can stop worrying about that as well. It's going to be nice having some girls around who actually know what needs to be done. I'm actually looking a little forward to being pampered for a while.

    My daughter wants to take me for a massage this Tuesday and I made a reservation but hope it won't be in vain. That's about the time my se's of the big 'd' set in after chemo. Besides that I can only lay on my right side since the mast. and hope I'll even be able to accomplish anything. If not the credit card I stuck on file for the appt. will be charged one way or the other. Wish me luck.

    As far as stubles on the head. I still have what's left of mine and they're not going anywhere. Not growing or leaving. Funny about the hair on my legs though. I have about 1/4 of my hair still growing and nothing anywhere else on my legs....go figure.

    Glad to hear I'm not the only one noticing the stench of the chemo smell. Thought it was just me. Funny thing is I just never noticed it before with the first 3 tx's.

    Someone mentioned the bone pain. I got my first bone pain after tx #2 and it lasted in my knees for about 7-10 days. Started on week 2. Got it again after tx #3 only in the left knee that time and lasted about 3 days. Maybe it's a good sign it only lasted that long. Mine was from the Taxotere though and not the Neulasta or Neuprogen.

    I've been suffering terribly from the runny nose/eyes syndrom for a couple of months now. Bad allergies. Saw the Dr. She asked if Claritin etc worked and of course I told her it didn't. She finally prescribed Allegra for me as I wanted (seems to be the only thing to work for me). Went to get it filled. It needed a Tarr sent off so they called the Dr. office for the diagnosis. They changed it to Claritin instead of just giving the diagnosis. So needless to say I now have another appt. to see the Dr. the end of June only to go through what I've already been there for before. Why do these people not listen to what we have to say. It's so damn irritating.

    Have fun ladies as this will prob. be my last post for a while.

    Angel
  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2007
    Day 3 after first Taxol/Herceptin - OW... serious bone pain. I smell like chemo, too. Ow, ow, ow. At least I'm not nauseated.

    Have a good weekend, sweet sisters.

    Miss S
  • pmarsh34
    pmarsh34 Member Posts: 108
    edited May 2007
    I am feeling so blessed today. First thing, I am having virtually no chemo issues right now. My sinus headache has even given me a few days relief. The other thing is, my church hosted a yardsale fundraiser to help me and my girls with the bills while I am going through treatment. (I haven't worked since I had surgery in February). It was a HUGE success and I know that I will not lose the house or have to go without electricity while I finish chemo and rads. I had given it up to God when I was first diagnosed. I knew that I couldn't do it without His help. This is just His confirmation of that faith. Thank you all for letting me post this wonderful blessing.

    I am praying for all of you who are having icky se's right now. I am pretty sure that the light at the end of the tunnel is not the train!

    Put me down for #4 on Weds.
  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2007
    I asked earlier if it's okay that I repost the "Erma Bombeck" letter on another thread and no one replied...I am assuming that it's okay to do so. I will credit this thread for it...

    Hugs
    Peggy
  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2007
    Sige, so sorry for not responding! Of course it's ok to repost.... we're glad you enjoyed it.

    Patti, that is so wonderful about the fundraiser. God is helping each of us in different ways and meeting our needs so graciously.... what a blessing.

    Angel, hope you get to take advantage of that massage and are enjoying your time while you're away from us.

    Diana, I've been battling some depression, too. Mine seems to be worse when I am running a fever or my counts are low. We are going through so much and it makes sense that it would get to us from time to time. Sending you a big hug! LOL at your pole dancing remark.... My stupid pole never wants to roll and I seem to tackle mine into the restroom when I have to go!

    3boys4me, please let us know how things are going...

    Max and Jacque, thanks for clearing up the difference between hand-foot syndrome and neuropathy for me. I guess so far what I have had is the neuropathy. One interesting thing I thought I might mention: I have some oogly feet, complete with several calluses. When the peeling started, my feet sloughed off the calluses. This after years of me filing, cutting, digging, etc.... poof. Gone.

    Holly, I am right behind you on the Taxol and I am hoping I don't have ten terrible days each time. Blech! I hope your se's level off some, too.

    Nancy, I have Herceptin weekly now, but don't know if you want to include that on the updates.. but 5-24 Herceptin #2. You'll be getting Herceptin, too, won't you?

    Also thinking about Jann, Terri, Marsha, Rosebud, Bettye (hooray for being almost done with Taxol!), Dawn, Keenie, Jillrush, Lisa..... and everyone else..

    I still feel pretty rough, but a little better!

    Love you gals!

    Miss S
  • dmknanny
    dmknanny Member Posts: 60
    edited May 2007
    Peggy
    Go ahead and repost the Erma Bombeck thing with my blessings! I don't mind, and I'm pretty sure Erma wouldn't either! Sorry I did not reply sooner.......
    Diana
  • Cynthia1962
    Cynthia1962 Member Posts: 1,424
    edited May 2007
    Put me down for my 4th AC tomorrow. I'm looking forward to getting it over with, but dreading it at the same time. My goal is going to be to not get a headache this time. It makes me feel so sick. Last time, I felt sicker the day of chemo than I'd felt before or since.

    My appetite came back today so I've tried to make the most of it. I have fewer and fewer good days now before my next tx.

    Good luck to everyone this week.

    Cynthia
  • LisaSDCA
    LisaSDCA Member Posts: 2,230
    edited May 2007
    Diana - you cracked me up with you "pole-dancing in the bathroom" remark! You bet I have to waltz down the way with my pole a couple of times during my marathon infusions - not only do they give me a bag of saline, but I always take a full water bottle, then there is also the crushed ice for during the nasty stuff.
    Patti - I am so thrilled for you about the fundraiser and your relief of fears of financial 'doom'. I can relate all too well.
    Angel - enjoy having your daughter back at home - sounds like her idea of spoiling you with a massage is a good one. I do hope it all works out.
    MissS - wow - how cool about your calluses sloughing off! I am ready for that side-effect! I have had some thickening and peeling of skin on the backs of my hands and was bummed about it until I noticed that a couple of my brown "age" spots (yes, I garden in the sun without gloves) had left along with the scrufty parts. Cool!
    Holly - so good to hear you are still among us and making progress on into Taxol. I'm a neupogen gal, too - are you self-administering, too? I get bone pain bad only with the last few - it's weird. But boy, does it keep my neutrophil count waaaaay up there. I'm borderline for needing Procrit like you. I wish there were something (besides liver) that I could do myself. I did have fresh spinach with dinner!

    Several people have mentioned chemo smell lingering. Gee - I hope I am not reeking and simply not noticing it. I do enjoy nice long, hot soaks in my deep clawfoot tub with herbal bath salts, so maybe that is helping. Kinda leaching it out of me or something. I'm doing this more often because I don't have to worry about pinning all that long hair up and out of the way.

    Lisa
  • LisaSDCA
    LisaSDCA Member Posts: 2,230
    edited May 2007
    Cynthia - ask them to slow down the Cytoxan drip. Tell the onc. nurse that you get a horrific headache and she'll know that is it. Are you getting Emend with your pre-meds? I hope this ends up not being as bad as your last round.

    I wanted to tell you gals what my church did for me today. It wasn't a big fundraiser like Patti's benefit, but it touched my heart. There is a large group of women who participate in a Prayer Quilt Ministry. They gather weekly to prayerfully piece quilts for members in need of special comfort. My friend Bobbie (the 27 yr., est. neg. survivor I think I've mentioned before) had nominated me for one and today was the day it was presented to the congregation for tying. Each knot is tied with a prayer specific to the recipient. I was so moved to see members that I do not even know (it's a large congregation) take a moment to go up front to my quilt and tie me a knot of hope and strength. :::sniff::: This little blue quilt is quite a treasure to me already.

    Lisa
  • GrammyNancy
    GrammyNancy Member Posts: 666
    edited May 2007
    Bar Reservations week of May 21 - 25

    Monday: Jacque, Cynthia (#4)
    Tuesday: Rosebud (#4), Bettye (#11)
    Wednesday: Pmarsh (#4), Taurie (#3)
    Thursday: MissShapen (#2 Herceptin)
    Friday:

    Prayers for smooth sailing!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2007
    Cynthia, I am so sorry you're having such a hard time. I definitely second Lisa's advice on slowing the drip. It really does help. Congrats on making it to the last A/C. My thoughts are with you and Jacque today.

    Lisa, the story about your quilt is so touching. I know you'll treasure it always. Glad to hear you're losing age spots. It's only fair that we get some sort of benefits through all this, right?

    Nancy, thanks for posting the reservations... jhope you're feeling ok.

    Miss S
  • pmarsh34
    pmarsh34 Member Posts: 108
    edited May 2007
    Lisa, how wonderful that you have that quilt. The one thing you have to remember is, not only is it touching you but it is a blessing to everyone who tied one of those prayers in there! While I was at the yardsale (Thank God for the good days! ) I saw so many people who were being blessed. It may have started being about me and the girls but God used it to touch many, many people. Cherish the quilt and all the prayers in it.

    I am not lookin forward to tac#4 this week. I keep hearing about the se's lasting longer and getting worse as you go on. I am praying that doesn't happen for me. Of course, if it does, I will just deal with it! What choice do we have?

    I hope everyone has a wonderful week with minimal problems.
  • jacqniel
    jacqniel Member Posts: 720
    edited May 2007
    Had my tx this morning. The nurse gave me my pre-chemo drugs and then decided to give me the Aredia (bone strengthener) while waiting for the chemo to come up from pharmacy. Right before they hung the chemo bags my heart went into Atrial Fib. Sigh. At least we know that it wasn't the chemo! It lasted about five hours and then calmed down. My onc went ahead and gave me my chemo - which I am glad as I have made plans through July based on my chemo schedule! I am hoping I won't have a repeat anytime soon, cause if I do, I will have to have a heart monitor - which is rather a pain.
    Otherwise, I am just tired. Will hit the hay early.
    Patti and Lisa - what touching tributes to your struggles. Both stories are wonderful.
    Cynthia, I hope your tx went well today!
    Hugs to everyone else! Jacque
  • LisaSDCA
    LisaSDCA Member Posts: 2,230
    edited May 2007
    Holy Schmoly, Jacque! Atrial Fib.!?!!?!!!! Oh my - you just don't hold back in the reaction dept., now do you? I am glad that you are stable and that your chemo went on as scheduled, but I also am hoping that those plans of which you speak don't involve any cliff-diving or para-sailing or anything to make your sweet heart be stressed. Whoa, I'll just bet you are tired. You poor thing :::pat pat pat::: Get a good night's sleep, hon.
    Cynthia - hope your treatment went okay today. Let us know when you come back up for air if they were able to moderate the administration of it for you.
    Patti - you are right that this quilt has blessed more than just me. But I declare, as I stood there after the service and watched all of that giving, I felt very blessed. Last night as I was reading before I got under the covers, I wrapped myself up in it and felt overwhelming gratitude.
    More gratitude today, as I opened a card from my brother (lives in VA) and out dropped a C-note! That $100 will go a long way, as I've been living on a very meager disability check for months, now.
    I saw my Rheumatologist this morning for our quarterly visit (I have 2 auto-immune diseases treated in Rheumatology). She last saw me soon after my diagnosis. She was pleasantly surprised to evaluate me as doing remarkably well - well, of course, I had on my wig and make-up and looked nearly normal. She said to take it easy on myself wrt the weight gain that upsets me so. On the positive side, she confirmed that I have no evidence of any systemic vasculitis = which the Kaiser plastic surgeon sometimes tries to use as an excuse why the microsurgery of a DIEP cannot be done. So I'm one step ahead, there!

    Gotta go do my #%!$& neupogen shot!
    Lisa
  • GrammyNancy
    GrammyNancy Member Posts: 666
    edited May 2007
    Good Morning!

    dmknanny, i relate to what you are feeling....it just seems so long. I know this chapter will be over but .....

    Angel...wishes that you have a wonderful time with your daughter and friends.

    MissShapen....so sorry to hear about your bone pain...how are you feeling? Hang in there.

    PMarsh, the yard sale sounds wonderful....I'm sure that it blessed many. Isn't it wonderful how we can see God working in so many ways in our lives even as we struggle.

    Lisa, I love your quilt story....how very special! Know that you have received much strenghth and support from this.

    Jacque, so sorry to hear about the Atrial Fib...that must be so scary. Happy that it got into control.....prayers for no repeats!

    Playwriter....how you doing?

    Nancy
  • taurie
    taurie Member Posts: 84
    edited May 2007
    I am heading to the bar again tomorrow, and of course didnt get my Emend again. After calling the company, the pharmacy and being on hold forever they are priority overnight shipping it again. But thankfully this time the hospital called and said chemo isnt until noon, so I should have it. Pharmacy said this time they are sending me 2 packages of it so it shouldnt happen again.
    Good luck to everyone this week, hope the SEs dont get everyone too bad.
    Thinking of you all.
    Dawn
  • Keenie
    Keenie Member Posts: 258
    edited May 2007
    Hi all,
    I paid my first visit to Radiation Island today. Aside from all the black felt pen all over my bra, it was okay! I only had my arm over my head for 25 minutes and I got 4 little pin-prick tatoos. The technician said, sorry about the pin prick. I said, are you kidding me? Compared to the chemo, this was a breeze. I have my first tx on June 1, and then 15 more over the following 3 weeks.

    I have to use unscented Dove soap on the area and pat myself dry and no deodorant or shaving. Not that I have any hair yet to shave. I keep checking to see if there's any "action", but nothing yet. It's only been 3 weeks since the last chemo, so I'm not sure why I keep looking!!

    Taurie, I hope your drugs arrive on time. You must be frustrated.

    Love and prayers to all of you ladies!
    Christine
  • rosebud1962
    rosebud1962 Member Posts: 196
    edited May 2007
    Well, it must be a day of first cause I had my first Taxotere tx and it went well. No allergic reaction to it but they did dope me up on denadril. I didn't know where I was most of the time so that was pretty good..lol I got there at 8:45 had my blood drawn and then the Doc visit. He was running late the told me..an over statement. He was an hour late and then they told me they would start my chemo, that was an other hour wait and then she started the drip of the 25 min pre-meds but didn't check to see if it was dripping. I waited that hole time with nothing running. The nurse told me shed hated when she does that, like I didn't! What should have been a 2 hour deal took until 1 in the afternoon. Guess they don't think my time is important.
    I hate being there, there's so much sickness and despair, it hurts to see those people cause I can't do much to help them. They keep telling me I'm sick too but I tell them this is my day spa as long as I get my warm blanket and my "health" treatment..LOL
    One good thing did come of today, I'm going to start my rads during the last part of this. Next week I'm, going to get mapped out and then start. I wanted to get everything done before I returned to work in a couple of months. My std runs out before the rads but this way it's all done while I'm off. It's going to be harder but the Doc said it can be done but they may have to give me less chemo more often then the one time every three weeks. Guess my skin might react to the chemo and rads more then just to the rads alone. Anywho..I hope everyone had a better time at the bar then me but at least I'm not hung over like before. Here's looking at you kids...Huga all around..Rosebud
  • jacqniel
    jacqniel Member Posts: 720
    edited May 2007
    Hello ladies - we must all be busy or not feeling our best. I think this is the first time we went a whole day with no one posting!

    I had my tx last Monday and the side effects started raising their ugly heads yesterday afternoon. However, I do have to say I think, so far, they are milder than last time. I hope this continues!

    Prayers that all that stepped up to the bar this week have an easy time of it - and that you all enjoy this holiday weekend.

    Hugs, Jacque
  • pmarsh34
    pmarsh34 Member Posts: 108
    edited May 2007
    I made it through #4. I don't feel like I have licked any truck tires yet but the day is young! My anemia has gotten worse so I got a shot of Aranesp along with the Neulasta today. Not sure if there are going to be any side effects for that or not. So far, I feel pretty good. But then again, I did sleep the entire day!
    I hope all is well with everyone. Another lady in our church was diagnosed with breast cancer this week. (Our church is not that big, either!) I swear it is everywhere. Or am I just seeing it all the time because I have it? Something to ponder. Well, 2/3 done with the chemo for me.
  • Cynthia1962
    Cynthia1962 Member Posts: 1,424
    edited May 2007
    I also made it through #4. I'm so relieved. I told my nurses how awful the day of chemo was last time, so they made sure the drip was slow. Unfortunately, it wasn't slow enough as I started to get a headache, so they slowed it down more and I took some advil. Then, I started to feel nauseaus (a first during chemo) so I took an Ativan. After the meds were done, the nurses gave me another bag of fluids and I started to feel better. I think the xtra fluids helped a lot. It was the best I'd ever felt on chemo day.

    I asked my onc about my heart and he feels that since the palpitations come and go that it's nothing to worry about. He'd better be right. It so annoying, though, when it keeps me up half the night sometimes. Damn, Neupogen.

    I am so glad to be half way done. The nurses assure me that the Taxotere won't be nearly as difficult. I sure hope they're right.

    Thinking of everyone having their cocktails today and tomorrow, plus those recovering from theirs.

    Cynthia
  • rosebud1962
    rosebud1962 Member Posts: 196
    edited May 2007

    Cynthia..I'm doing Taxotere right now. I have 2 more to go and so far it hasn't been bad. I have had nausea, just tired. The nuelasta shot is what does me in. Makes my skin hurt to the touch and makes me feel like crap. I'm watching my hands and feet now but so far no major se to talk about. I hope all goes well for you..Hugs all around..rosebud

  • Cynthia1962
    Cynthia1962 Member Posts: 1,424
    edited May 2007
    Thanks, Rosebud. I'm sorry about the tiredness, I've heard it's a problem with Taxotere. I'm so tired now it's hard to imagine being even more so. The neulasta and neupogen shots are awful, aren't they? I was still having bone pain and palpitations a week after my last injection last time. Glad to hear that your feet and hands are okay. Every se we can avoid, the better. Congratulations on being half way through the Taxotere.

    Cynthia
  • GrammyNancy
    GrammyNancy Member Posts: 666
    edited May 2007
    Good Morning!

    Rosebud...sorry to hear about your extended stay at chemo. How are your purses doing on ebay?

    Jacque...good to hear that you are feeling better with this treatment....continued prayers for your heart to behave.

    Pmarsh....congrats on 2/3 done!!! Hope those truck tires stay away this time.

    Cynthia...happy to hear that with some adjustments that chemo went better. Guess that IV proves the point to force fluids. From other threads I've read that the Taxotere is much easier than the AC...good luck!

    Well thanks everyone for your prayers....I finally had my appointment yesterday with the BS yesterday about the lump I found under my arm....turns out it was a little pocket of fluid...he drained it and it's all gone. I can't tell you how releived I was.

    Hope everyone has some nice plans for the long weekend. Do something special for yourselves.
    Nancy
  • jacqniel
    jacqniel Member Posts: 720
    edited May 2007
    Oh, Nancy - I am so happy that it was just fluid! Now you can enjoy your long weekend without that worry!
    Rosebud - the neulasta shot makes my skin hurt, too. Extremely yucky!
    Pmarsh & Cynthia - glad your tx is over and hope you are feeling well. The same goes for all our sisters who stepped up to the bar this week.
    Have a fun weekend!
    Hugs, Jacque
  • LisaSDCA
    LisaSDCA Member Posts: 2,230
    edited May 2007
    Oh, Nancy - I am so happy to hear that your 'lump' was just some fluid to be rid of. WHEW! Great way to start the weekend!
    Rosebud - what a comedy of errors you had with your first Taxotere trmt! I can't believe you had a "dry drip" for nearly a half hour! It is cool that they are going to let you start your rads early. Oh - BTW - congrats on getting a great winning bid on that cute pink purse on ebay - I was watching that but it went beyond my budget.
    Keenie - thanks for the report from Radiation Island! Have you stocked up on Aloe Vera gel or what do your people recommend?
    Jacque - I'm glad that after that atrial fib thang that the SEs this time seem to be a bit milder. <knock wood> I think some of mine have been, too - go figure.
    Patti - doesn't it feel good to be 2/3rds done?!? We are really on the downhill slope now! How low does your hemoglobin or hematocrit have to be before your doc decides on the aranacept? I ask because mine has gone lower each time but not yet critical. Sure hope the shot gives you a boost of energy as it boosts the RBCs!
    Cynthia - I'm so glad that they worked with you during your infusion this time and that the ativan and the extra fluids made you more comfortable finally. And now you are finished with adriamycin and cytoxan forever, right!?! So many women find the taxol or taxotere portion much more tolerable - and even start to grow back some hair. Maybe you will, too. Are you going to be doing the L-glutamine during the taxotere? It has sure seemed to help me avoid some of the SEs - or something has helped me avoid the bad nail problems and neuropathy so far (please, please, please).
    _________________________

    I saw the head of Plastic Surgery at Kaiser San Diego yesterday. Her preferred reconstruction is a Latissimus Flap and she does a lot of them. She did agree that with my back ground and desire to resume weightlifting, that a DIEP is indicated for me. She has done them for around four years. Which sounds good - except
    1- sometimes she goes 2 months between DIEPs so is not exactly highly proficient
    2- it takes 8-11 hours
    3- BIG ONE: she has a 1 in 5 failure rate!!!!yikes!
    4- she thinks she can give me a B cup despite the fact that I have been gaining weight with each treatment and I think I have a big ol' gut! I am currently a full D cup. This is unacceptable. I wanted an avg. C cup. I am 5'10" and a B cup hasn't been part of my life since I was 11.
    None of these would be an issue if I had the procedure done in NOLA, so I am going to have a fight on my hands, to say the least. I'll be posting on the recon. board because I don't think anyone else in our Chemosabe thread is having a bilat. DIEP reconstruction. :::sigh:::

    love to you all
    Lisa
  • BettyeE
    BettyeE Member Posts: 267
    edited May 2007
    I'll be having TAXOL # 12 on Tues. May 28. YEH Ha!!!! THe last one. But then I start FEC X 4. I see a little light at the end of the tunnel. I hope it's not another train!!!
    Bettye

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