June 2014 Surgery Sisters

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  • thinkpink4ever
    thinkpink4ever Member Posts: 205
    edited May 2014

    Well friends, The good news is that I did hear from NOLA today, so I'm feeling pretty pumped! I will keep y'all posted!

    gila, hope you're feeling better emotionally.  Hang in there! 

    jbdayton, I'm gonna push hard for autologous tissue surgery, and they can take it from anywhere they need to.  Lol!  I just don't want implants.  

    beths, I'm praying for a negative results on that path.  Stay encouraged!

    spooky, praying for you and the hubby.  It's okay to lose it.  You're going through alot and your emotions will be all over the place.  Things will get better - take it one day at a time...

    clynnoli, that part of the East Coast is really pretty.  Enjoy your vacay!  Hubby should be happy about that leg room.  It's the simple things that make us happy, right? ;-)

  • Wildflower50
    Wildflower50 Member Posts: 16
    edited May 2014

    Glad to find this group. I am having BMX on June 23rd with expanders. I will have the nipple sparing surgery on the right (where surgery is prophylactic) and will have additional surgery on the left to make a nipple 3 months after implants.  I am finishing up with chemo on May 29th (8 weeks of DD A/C and 12 weekly Taxol). My body is worn down from all the chemo so I'm worried about how long it will take to recover from surgery.  I pushed for an early surgery date following because I'm so ready to get this all behind me.  I'm totally at peace with my decision on the mastectomy (I have had 2 lumpectomies and did not get clean margins) but still kind of scared nonetheless. I was in great shape before my DX and am now easily fatigued.  I'm hoping it won't be as rough as I'm expecting. 

  • worryocd
    worryocd Member Posts: 41
    edited May 2014

    Hi!  I will be having a prophlacytic bilateral mastectomy June 26th.  I learned about a year-and-a-half ago that I carry the braca1 mutation.  Had a hysterectomy nine months ago now the PBM.  I am scared, but the surgery needs to be done.  I lost my mother to ovarian cancer at age 16, Two aunts(my moms sisters died of breast cancer.  I watched my mom battle cancer at age 10 for six years.   I am a mother of three small kids.  I don't want my kids to witness what I saw as a young child.  The docs told me the procedure is about 4 hours long.  I am going to have expanders.  I am scared of going under.  I hope and pray I wake up.  I had the same fear with the hysterecomy and remember waking up after and thanking God.  I am starting to purchase items for the surgery.  I can't believe how fast the time is going.  I passed my mammogram and MRI  I hope nothing is found in my pathology.  Can you pass those screening and still have breast cancer?   Thanks so much for starting the June surgery thread!  :)   

  • sandra4611
    sandra4611 Member Posts: 2,913
    edited May 2014

    Hi Wildflower50. The way we do it is when someone's surgery is getting close, we roll out the virtual pink bus...we hop aboard, go pick up whoever is having surgery that day, and party all the way to the hospital. One important thing...we bring snacks, so I'm glad to have another Texas girl 'cause we always do it up big. (I'm from San Antonio.)

    Recovery after a mastectomy isn't bad. The first couple of days are a blur, then little by little you feel better. Nearly everyone feels pretty good at the magic three week period. Some sooner...once in awhile it takes longer. Getting drains out is a big mark of progress and those are usually gone one or two at a time, with the last one out by two or three weeks. Having chemo before surgery does cause a slower recovery, but it shouldn't be bad.

    Welcome Worryocd. With a positive BRCA 1 report, you are doing the right things. Yes, it does take about 3-4 hours for the BMX (depends on how much breast tissue you have, whether lymph nodes are taken and how many, etc,) then the plastic surgeon takes over, creates the pocket and puts in the TE's. Tell your family not to be surprised if it goes past 4 hours. Mine expected the whole thing to be over in 4 hours and were panicked when another hour went by before a nurse came out to tell them what was happening. They didn't realize it would be two doctors and two procedures. I was very large breasted so part one was 4.5 hrs and part two to put in permanent implants, not TE's, was another 4 hrs. Long day. Since your preliminary tests have all been good, it should take less time. It is possible for breast cancer to be missed on mammograms and MRI's, but not likely in your case. You won't get pathology reports back for over a week so you'll meet with an oncologist at that point. They don't do much of an exam of the tissue in the OR.

    It is important for all of you who have surgery coming up to research anesthesia and be prepared to talk to an anesthesiologist ahead of time. There are many different types and some have more side effects than others. The rule of thumb is that it takes about a week to get your head clear of anesthesia fog for every hour you were out. Some kinds are easier to metabolize.

    We are heading back to Texas tomorrow after a great vacation in Florida so I may not be back here for a couple of days. Depends on how far we get tomorrow and if the motel has Wi-Fi. It's an 18 hour drive without rest breaks, which we can't do anymore. Twenty years ago, yes. Now we need those breaks every three hours or so.

    Here's a picture of our imaginary Pink Party Bus of Support. I'll be calling, "All aboard" soon.

     

    image

     

  • trish01254
    trish01254 Member Posts: 128
    edited May 2014


    I'm having right mx with DIEP on June 11th.  I started this journey in Feb.  Knew I had a papilloma back in Oct and anticipated the lumpectomy this year.  Did not anticipate the DCIS they found after excision.  LCIS was confirmed after my previous papilloma excision.  So after DCIS found,  had MRI, then MRI biopsy where more DCIS was confirmed.  Multifocal eliminated my choice of mx or lump.  It has taken a long time to finally have a game plan.  After meeting with the PS this week I actually felt like dancing out of the office.  I had been torn between the bi or uni mx and whether or not to do immediate recon.  My left side has been very well behaved but LCIS increases risk.  I didnt have enough belly to do both so decided just to do the one.  I will be followed closely after anyways and i am praying that left continues to behave.  I wasnt feeling that optimistic that they wouldn't find invasive in pathology.  Was worried i would need rads after mx.  I decided to stop being pessimistic and start having more positive thoughts beginning with decision for the uni mx and immediate recon.  So many decisions and so hard to make them.  Best wishes to all of you.

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited May 2014

    hi June ladies! welcome and know you are supported here. Read the May, April and other surgery threads for stories of women who are going thru the same thing and their recoveries. The anticipation and worry is worse than the procedures!  For those getting TE- be sure to read the TE for Beginners thread...and try not to read or take with a grain of salt, the TE Troubles thread.  Many many more women do just fine with their TE tho there are some that have more difficulty, and that a supportive thread for them.  I got super scared before my surgery having read that one. Tho was glad I did for just education myself. But sailed thru and know you all will also!

  • shycat
    shycat Member Posts: 76
    edited May 2014

    I'm scheduled for a bilateral mastectomy on June 2nd, with no reconstruction.  I'll be rocking a bald Buddha look.  Happy

    Today I'm having a PETscan to determine how effective the chemo was, which will determine how many lymph nodes will be removed on the left side.  While the standard for IBC treatment is to remove all lymph nodes, I was so unhappy about the high risk of lymphadema that it was agreed among the medical team that I could have fewer removed if the chemo response was as good as they suspected.  I'm grateful that no one thought I was silly to be so concerned about my arm while fighting to beat such a grim cancer. 

  • sandra4611
    sandra4611 Member Posts: 2,913
    edited May 2014


    Welcome Trish and Shycat. Also delighted that Aviva popped in. She's got some good insight to share. I'm going to encourage a few of my other BCO friends to post here as well. It's always helpful to have different viewpoints.

    Trish, I can just feel how relieved you were to finally make a decision and have a plan. Those beginning weeks are torture, aren't they? Having a path laid out ahead of you is comforting.

    Shycat, so sorry about your IBC. It is a nasty one and I hope chemo did it's job so you can have a less involved surgery. Sounds like you have a good medical team. Not everyone is so lucky so you can be thankful they are supporting your so well.

     

  • sandra4611
    sandra4611 Member Posts: 2,913
    edited May 2014

    Here is a wonderful breast surgery rehab video that will help you all next month. http://breastcancerrehabilitation.com/Rehabilitation.html

     


     

  • shycat
    shycat Member Posts: 76
    edited May 2014

    Just received awesome news from my oncologist!  The tumor and lymph nodes have completely resolved and all three doctors agree I don't need to have any lymph nodes removed.  I couldn't be happier.  Celebrating tonight!

  • linda505
    linda505 Member Posts: 847
    edited May 2014

    Hey All,

    A March surgery sister here coming over to offer my assistance any way I can.  I had bilateral mastectomy with TE - had have two fills and am at 250cc - I am fairly comfortable 90% of the time.  I had healing issues that delayed my chemo and my fills but my PS took care of that and all fine now.  It is a scary time for you all right now and you have every right to be scared and sad.  People will tell you to be strong and stay positive and some of that is right - BUT sometimes you just need to cry and cry hard and allow that.  Try to explain to you family and friends that sometimes you are gonna cry and they can't fix it.  All they can do is give you a hug and tell you that they love you.  It is hard on your families right now - they want to help but don't know how.  I went through and still go through all kinds of emotions. 

    Worryocd - I don't trust Mammos cause they failed me for years on both breast but I do trust MRI's - so I say if you passed that then feel confident that your pathology should be good.  Anything is possible but I would think chances would be very small.  MRI's move often than not light up with false positives so not lighting up is a very good thing.

    Eat lots of protein before and after surgery - will help with the healing - get button up PJ's and shirts - and some front closing bras - cheap ones at walmart are fine.  Check with you plastic surgeon but genie bras are great cause you can pull them up over you bum to put them on.  They are now my best friend as I am getting expanded.  You will have lots of questions as you start this journey - I have added this to my favs so that I can check in and answer what I can.  Julie is a great hostess and a wealth of information!!

  • scubalady
    scubalady Member Posts: 109
    edited May 2014

    Hi everybody,

    I'm an April surgery sister stopping in to say hello.  I had a UMX on the right side with a reduction and lift on the left on April 16.  Some things I found helpful that I would like to add to those mentioned by linda505.  

    I did get the button front PJ's, but got satin ones.  They made it much easier sliding in and out of bed.  I actually splurged on these and bought them from Victoria's Secret (online) to pamper myself a bit.  If most of your wardrobe is pullover tops, make sure you have some loose, roomy, button or zip front tops as you won't be able to pull shirts over your head for a while.  Also, if you leave the hospital wrapped in an Ace bandage, you'll need something big and loose.  You may want to grab a bed wedge to elevate you're head when you get home.  Bed, Bath, and Beyond has them.  I can't sleep flat on my back without getting a backache, but with the wedge, I had no problem.  You won't be sleeping on your side or stomach for quite a while.  My bed is quite high and I'm short, so I put a little stool by the bed to make it easier to get in.  Yoga pants or loose workout pants are much easier to pull on and off initially than trying to get into tight jeans.  There's a lot of other suggestions on these boards if you do a seach.

    Dealing with all this is by no means easy, but you take a step at a time and make sure you're well informed about every step in your care, and that you're happy with "your team" of doctors.  And ask questions here.  These boards are a great resource and the people here understand and care about what you're going through.  You can get through this!! 

  • sandra4611
    sandra4611 Member Posts: 2,913
    edited May 2014

    Shycat, the BEST NEWS EVER!!

    image

    Linda505 and Scubalady, thanks so much for jumping in to give us the benefit of your experiences.

     

  • Frostecat
    Frostecat Member Posts: 447
    edited May 2014

    Hi Ladies!

    Sandra asked some of the March Surgery Sisters to hop on over to this board to see if we can offer any assistance.  I will say I do not envy any of you right now, you actually are in the hardest part of this journey.  The anticipation of what will be is horrific.  If it does make you feel any better, after surgery you will feel like you are climbing a mountain, and then at some point, and you will know when you reach it, you're heading down the other side of the mountain.

    Wondering the results of lymph node biopsy right after surgery, then waiting for final path results is tough too, and then there's the oncotype score.  I proceeded with a UMX with TE's and implant with a lift and reduction at the final surgery.  I am in the TE phase right now.  And yes, I still second guess if I should have had a BMX (especially now since I am extremely lopsided), but both my BS, my MO and PS said there was no medical reason to do that, so I listened to their advice and am leaving it in the hands of my PS to make me as symmetrical as humanly possible.

    I feel extremely fortunate that it did not spread to my lymph nodes, and my oncotype score was a 7 so no chemo.  I felt like I could breathe again.  Fortunately you start friending people on these boards.  Test results for all come back varied, and unfortunately this can be difficult too because you sincerely feel for these people who have not received good news.

    My advice is of course the button down pajamas, button down shirt for Dr. visit, a lot of people wear the tighter fighting camisoles with a hoodie that zips up, the bras from Walmart that hook in the front, I think they are Fruit of the Loom brand are good.  I didn't realize this until almost too late, get a lanyard that wraps around your neck for taking showers.  I was hooking up my drain in the pain pump bag they gave me that had closeable straps to the shower curtain rod.  Made it difficult to move around.  Then I finally figured out the lanyard, just hook the drain to that when showering (or any other time a needed), easy, breezy.  

    I don't think anyone is a fan of the drains, mine was in for 3 weeks (1).  Like Sandra said, when you hit the 3 week mark, it gets a little better, and a lot of that does have to do with the drains being removed, and you feel like you can get out, drive and what not.

    I know 3 weeks sounds like a long time, but the first few days/week you will be sleeping most of the time and on heavy drugs, so you won't even realize time is passing. And, each week, after week, it keeps getting better.  As far as the surgery, I remember the mask over me, knowing that I was going to go out, then waking me up in the recovery room, then wheeling me into my room, and that is all I remember, and they told me before I went in, "you won't know a thing happening" which was a huge reminder and relief.

    Also, if this can make you feel any better, here it is May, and our March board is practically down to nothing.  Many have moved on with their lives and don't really go on it much, and others are now more interested in other topics that pertain to them whether it be implant sizing, or maybe even chemo :-(  but we have dwindled for sure, but all those ladies helped me through one of the roughest times of my life, and for that, I am grateful.

    Our March board got a little long, but it might help some of you to read from beginning to end the process, obviously all posts won't pertain to your circumstance, but we didn't get off subject too much, unlike some other boards.  

    I'll put this on my favorite topics too like Linda, and check back every once in awhile.  Sandra is an excellent hostess!

    Just remember, you will get through this.

    This too shall pass.

  • jbdayton
    jbdayton Member Posts: 700
    edited May 2014

    To my June sisters, I am all set for June 2.  Finished all my pre-op appointments and tests today.  

    I was also an August 2013 mastectomy board member and a DIEP reconstruction in the March surgery board.  I will be having another tissue flap reconstruction this time.  All my recoveries seemed to go smoothly even with minor hiccups.  

    My mastectomy was a fairly easy recovery.  I was late getting into surgery (scheduled for noon actual start time 4:30) and did not get to my room until near midnight.  I woke up raring to go early the next morning, walked the halls by noon and released to go home about 4:00 that afternoon.  I did get a minor infection in my left breast 5 days post op.  Saw PS on day 6 he opened it up; cleaned it out; stitched it back up with new drains and within 7 days removed drains with no further complications. 

    I admit I had my ups and downs especially in March but I do not regret any part of my journey.  

    We can do it,  HUGS to all. 

  • Juliecc
    Juliecc Member Posts: 4,868
    edited May 2014

    Hello June sisters.  I'm popping in from the March thread to offer any help or advice you need.  For those of you newly diagnosed, this is one of the hardest times.  I remember walking around thinking, "I have breast cancer."  I could feel the lump, my breast was sore, and my bra was tight on that side.  It was very hard waiting for surgery and not knowing what would happen next.

    Everything has gone very smoothly for me.  I was very nervous about the surgery.  I had only one other surgery back in 2009, an excisional biopsy for calcifications and a radial scar.  The BMX was a 6 hour surgery.  I got really nervous 10 minutes before and that's when they gave me the happy juice.  I swear that's all I remember.  It felt like only 5 minutes had passed and they were waking me up.  I felt great, was making jokes, and went home maybe 3 hours later.  Most spend at least one night.  I have Kaiser and they want to get you out fast and away from hospital germs.  A couple more tips about surgery - if you are having something more than a lumpectomy, ask your surgeon if they use Exparel.  This is amazing stuff they inject at the end of surgery that provides 3 days of pain relief.  Also, ask you anesthesiologist to give you anything they can to prevent nausea.  I told mine that I get car sick easily and have vertigo at times.  I had NO nausea after surgery.

    Recovery went well and I returned to work 4 weeks later.  Pain was minimal but I don't think I could have gone back at 3 weeks because I would get sleepy and I needed my naps.  I had help the first 2 weeks but after that, I was driving and doing normal things.  The drains were my least favorite part.  I was fortunate that I didn't need chemo or radiation.  Finally, youtube has a lot of videos about all sorts of things such as mastectomy recovery, DIEP, jp drains, tissue expaders, and anything else you can think of.  Watching videos helped me understand everything better.  Things are almost normal now for me and you will get through this, too.  I've noticed that I don't think about breast cancer or reconstruction every 5 minutes like I did in the beginning.  It's so nice!  I went the tissue expander route and will be getting my exchange surgery on August 8th.  I wish you all the best and feel free to PM me if you have any particular questions.

  • Wynne50
    Wynne50 Member Posts: 67
    edited May 2014

    Hi June girls.  I had a bilateral mastectomy with DIEP reconstruction and haven't regretted it for a minute.  I am old and was very out of shape when I had the surgery and have had zero complications!  I wasn't even in a lot of pain right out of surgery, but did take the pain pills as directed so that helped.  The worst part as you have heard was the drains and they are mostly just a pain and get in the way.  I did follow every single thing my docs told me to do and was very careful not to overdo it.  I have never really had any trouble lifting my arms or range of motion issues.  In fact the first thing I did when I woke up was raise my arms over my head.  The nerves heading into surgery can get to you especially the few days before, but once you are done, the time seems to fly by.  

    You will all do great and will have a lot of us oldies help you out along the way.

  • Mulligan
    Mulligan Member Posts: 205
    edited May 2014

    Hello ladies, long time lurker, rare poster here. I got my membership notice on May 15th and have made the decision (I told my doc before my last lumpectomy if I had cancer even if it's DCIS I wanted to go the mastectomy route) to have a bilateral mastectomy with tissue expanders and sentinel node testing. I am scheduled tentatively for June 6th. Although a lot of the information isn't new to me due to long time lurking and research I feel like I'm walking in a haze right now. I'm struggling with even the thought of telling my family let alone my close friends. I'm sure people will soon notice that my breast will look "odd" with the expanders, but since I don't even know the stage I have I don't want to field the barrage of questions that I'm sure people will ask. (FYI, the 4cm lumpectomy was filled with DCIS and also contained IDC)Yet at the same time I want to talk/tell someone, my hubby can only sympathise so much and I know he wants to talk about it as little as possible. He wants to stay positive and strong for me. So as much as this is a bit out of my comfort zone(hate talking about myself) I'm coming to you ladies, if that's ok. Thanks.

  • jbdayton
    jbdayton Member Posts: 700
    edited May 2014

    Mulligan welcome.  Sorry you have to join us but know this is a great place for you.  

    I understand your wish for the BMX.  It is your decision and you sound happy with it.

    Does your cancer center have a support group (or phone list) with current patients or survivors?  You might ask as that is one way to find someone to talk to who understands.  These boards were all I needed besides my immediate family for a while; until I met other people at chemo or rads and developed some sweet relationships .

    No need to go through this alone.  You now have a large family.  Many HUGS.

  • waterdog
    waterdog Member Posts: 46
    edited May 2014

    Adding my name to the list.  I just finished four rounds of a/c followed by four rounds of THP on May 15 and am scheduled for surgery on June 18.  I meet with my PS of June 10.  What I believe so far is that I am having a lumpectomy with or without lymph node removal, depending on whether the chemo resolved the positive nodes.  Still in the throws of my chemo so no energy this week.  Starting to get my house ready for my mom to come down and help out at the time of surgery.  I will be soooooo glad when this part is done!

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited May 2014

    yeah- what they said!!  great suggestions from the March and April ladies!  Small comfort now, but I think a lot of ladies find the waiting and reading about things and anticipation to the surgeries much worse than they feel after...expect pain and anasthesia recovery time, but go in to it knowing itll be hard for at least a bit, and you will be surprised (I hope) at it being easier than you thought.

  • kpmacmill
    kpmacmill Member Posts: 85
    edited May 2014

    Hi Everyone,

    Please add me to the June surgery list - June 4th!
    I am very lucky to only need a lumpectomy (and SNB), which I was really
    hoping for. I'm really not afraid of the surgery as I have had a few
    elective surgeries in the past, just the results of the tests afterward.
    From the original biopsy, I am grade 2 &3, so Onc says I should
    just get chemo, BS says wait until all the results come back (though she
    thinks oncotype will likely be high). I can't stop crying about the
    thought of chemo. I know so many here have made it through with flying
    colors, but I'm so scared and sad. Good luck to everyone scheduled for
    June as well!

  • Frostecat
    Frostecat Member Posts: 447
    edited May 2014

    KP - I'm so sorry that your are joining this board, it is a place where no one wants to be, but you will find good friends and advice here.  Try not to get yourself too worked up, wait until you have all the results then put your plan in place. It is my belief that the Dr's try and prepare you for what you may have lying ahead of you but they are not always right.  The bright side is you are fortunate to be able to have a lumpectomy, that would have been my first choice, but due to the fact that I was multi-focal that wasn't possible.  So hang in there and breathe.

  • aff
    aff Member Posts: 279
    edited May 2014

    Hi everyone,

    I'm new to this group. I am scheduled for UMX with immediate DIEP on June 6. I completed AC and 12 weekly Taxol on May 2. YAY!!! Rads will follow surgery and I have not read many posts with the same treatment plan. Any info about rads following DIEP would be great. 

    I couldn't even think about surgery while I tried to find my "normal" during chemo. 20 weeks of chemo seemed like a lifetime back then. It's hard to believe it's over and that surgery is less than 3 weeks away.

  • linda505
    linda505 Member Posts: 847
    edited May 2014

    kpmacmill - what you are feeling is very normal. Chemo scared and still does scare the chit out of me - forgive my french - I was a sailor in another life I think.  I have had two treatments and really the side effects have been very manageable and the docs have lots of things they can prescribe and the nurses have all kinds of ideas and tricks. 

    The hardest part of this journey for me so far is the waiting and the not having all the answers.  Once you have a plan you can at least deal with it - until then I feel so lost and confused.  I am in a far better place mentally now than I was in March before my surgery - still worried - but dealing with each worry one at a time instead of 10 at a time.  

  • jbokland
    jbokland Member Posts: 890
    edited May 2014

    TIPS FOR GETTING READY FOR SURGERY:

    Remember, your drains and surgical incisions are open ports to your body and quite susceptible to infection. It’s very important to be extra vigilant your first post-op days.

    Getting ready for surgery:

    If you have drains, buy a newlanyard to wear around your neck to hold them while you shower.

    I bought front closure sports bras from Walmart instead of the heavy surgical-quality bras they gave me in the OR.I attached the drains with large safetypins.

    Be sure you have some oversized, button or zip up tops to wear.You will not be able to raise your arms for a week or so, so it’s easier to slide into these tops.(yes, get dressed!, you will feel better)

    Wash your chest and upper bodywith Hibaclense or a surgical soap for 3 days before surgery.

    Install a new shower head (megabacteria living in your current one), replace the shower curtain liner andbleach the crap out of the shower before your first shower.

    When your home:

    If possible, consider that bathroom "yours" and an off- limit area for others.  If's that’snot possible, keep some Clorox wipes in the bathroom and wipe down EVERYTHINGafter anyone uses the bathroom. Keep this as your little clinic fordressing changes and emptying your drains.

    It is IMPERATIVE that whoever empties,milks and changes the dressings on your drains and chest wash their hands thoroughlybefore and after.

    Use clean scissors to cut a slit in the 2x2 gauze pads that will go around the drains.It will create a neat little ‘V” to wrap around the drain.

    Showering: Use a liquidantibacterial soap (like Dial) to wash your chest area.Wash this area first.Wash cloths are not recommended, but if youmust, used one wash cloth on each breast and each drain.The idea is not to carry or transfer anybacteria from one area of your body to the wounds or drains.

    When you get out of the shower,pat your chest and incision area dry with a clean towel FIRST, before you touchthe rest of your body. Do not touch that area after.   Use aclean towel every day.

    Wear a clean bra and pajamas every day, change any linens daily.  My BS had me sleep in a recliner fora few weeks and it was really helpful. 

    Do your deep breathing and coughing exercises.

    I promise you, 3 difficult daysand then it gets better!

  • aviva5675
    aviva5675 Member Posts: 1,353
    edited May 2014

    not all surgeons will allow showers if you have drains. Check with yours. If not have on hand lots of the heavy duty baby wipe kinds of things, if you have help someone can do your hair in the sink. You can also buy wonderful shower cap like hair washing things, at the drug store. You put it on your dry hair, rub your scalp a few minutes, and voila, clean hair! Like a miracle. They did that for me day 2 in the hospital and it was a godsend for feeling better.

  • sweetjam
    sweetjam Member Posts: 27
    edited May 2014

    Gila the book I'm reading is Prepare for Surgery, Heal Faster.  It also has some meditation cd's that go along with it. 

    I had someone ask the other day if I'm getting nervous.  I am honestly so excited to get this all over with.  Here's to hoping that those lymph nodes are clear cause that will be a game changer.  I don't want radiation I want to be done.

  • worryocd
    worryocd Member Posts: 41
    edited May 2014

    Hi!  Thank you for all the advice  especially to the ladies from the month of March. The advice is very helpful. I started buying some shirts that button in the front.  I need to buy more supplies.  Also, I never realized that the shower head can harbor so much bacteria....I may buy a new one.  Thanks again

  • sweetjam
    sweetjam Member Posts: 27
    edited May 2014

    I actually just bought drain pockets that stick to the inside of your clothing.  http://www.pink-pockets.com/  I have major neuropathy  and can't imagine handling safety pins. I have butter fingers right now. 

    Hibiclense is a product I sell to hospitals.  It is a miracle product and will help with surgical site infections.  You can buy it at the drug store in a tiffany blue bottle.  I have been washing with it in the shower every day.  It kills all kinds of stuff including cold and flu bugs.  Wash with it whole body 1 week before surgery avoiding the head and the private area.  You also have to be careful with lotions.  Some lotions deactivate the Hibi  A couple of easy ones to find in the local market that are compatible: Aveeno, Cetaphil Lubriderm and Eucerin.  Use Hibi to wash your hands before dressing changes and drain changes.

    Hope this helps.  All good advice from jbokland

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