April & May 2015 Surgery Sisters
Comments
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downing thank you for your encouraging words. I will differently check out the other thread I never thought about.
Good luck to all this week😊
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Dtorrent, thank you for the inspirational post. You look amazing. I am now just two days out and find myself getting more and more nervous. I have been very impatient at work and know it's all the stress of this. The hard part is I don't feel sick, maybe a little tired but that's all. Ok... back to lurking lol.
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Hello ladies! I'm ten days away from my surgery. 4/23 I will have bilateral mastectomy and Diepflap reconstruction. Absolutely terrified!! This will be the first time I've ever been under anesthesia other than port installation. The thought of being under for eight hours is extremely scary for me! My fiancé thinks I'm being silly. That's easy for him to say!
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Stilstandi.....You can do this! Yes, it is scary, and, yes, it hurts like crazy, but I am almost done with day four and have gone on to using only Tylenol. I had a BMX, TE expanders and LNB. Be strong! We are here for you! Sending you peace and love
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Thanks mysunshine for the encouraging words!!! Will be so happy to be on the other side of surgery like you
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Hi all Im feeling a little down. I had a single mastectomy last Tuesday left side. They couldnt find my sentinel node because for whatever reason it wouldnt light up. Anyway, I have two drains in me now and I empty them. So gross! The way I look in front is gross (glad Im not a nurse).
How long are you suppose to feel tired after surgery? How long till I can take a descent shower? I hate juggling these drains and I want them out. He said he took out a lot of nodes but we wont know how many were affected till I go back to the surgeon this Wednesday morning. I have never looked more forward in going to the dr in hopes of these things being gone. I just want some normalcy. I do drive a short distance for good coffee and back home. At least I can do that.
I didnt fill the pain pills but Im sure numb some places under my arm. I think its starting to come around but not the whole area yet. Im going CRAZY
.
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Labhusky, I had my surgery last Tuesday also. I don't go back to the doctor until April 29th but I did get my pathology report last Friday. I had 20 lymph nodes out and I started taking my prescription pain Meds again today because my arm hurts. I have swelling under my arm and feel like I cannot put my arm down all the way. The flappy part of my arm is super sensitive and other parts are numb. I am really tired and have been sleeping a lot. I think it could be another week before we start feeling normal. :-(.
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hi lab husky. I had bmx and was tired for weeks! I napped off and on all day. The anesthesia lasts a long time in your body. Lots of healing happening. Just curl up with the remote and snooze. Your body and mind need it. Be good to yourself. This is hard on your body and mind. It's okay to take a pass on the next few weeks and do nothing. No heroes here and no medals for popping right back to your life. Feel what you feel and process it. Let others help you. Once I went back to work half days after taking 6 weeks off, I came home andslept for several hours. Just getting showered and dressed was enough! Take care and take it easy.
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stillstanding66: You're not being silly about the anesthesia. It was my only real concern too. I asked the Anesthesiologist if he guaranteed I would wake up. He had an awkward laugh and said there are no guarantees but did say he had never had someone not wake up. So I felt better. I did wake up and you will too. Drink plenty of water once you are able to clean out the anesthesia. Don't push your self, tell your fiance to pamper you. Good Luck, MJ
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Can I join this group? My surgery was supposed to be the end of April but now it was moved to May 4th. Right side MX with TE. I already had SNB and Neoadjuvant chemo. Glad to get a date but anxious about immobility and pain. So many are on the other side!!
PMR53
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I apologize for sounding so down but sometimes Im so slow to process in my mind b4 it really happens. After my biopsy the surgeon said it was stage 2-a. Because rudolphs nose didnt light up for him (my sentinel), he told me he had to take more out. I guess Im grieving in a way. Oh, and get this. Now I had my surgery like around 2 in the afternoon and I never felt so groggy in waking up. Then I kind of had a hard time sleeping in the hospital because my roomie had visitors. I fell asleep and the nurse said I was talking to her at 6:30 in the morning but then at 7 or 7:30, my lips turned a little purple and I was bubbling. They wheeled me in surgical ICU and I was scared because I didnt remember anything. I had a couple of scans plus an MRI later that night and nothing was conclusive.
It was funny because I guess theirs a part of the brain where you are allowed to have one spot for every decade you have lived. I should have had 5 but I had only one so we were joking around that that makes me 10. But back to what happened was I remember havibg to cough stuff up after that for awile and I sounded horse. They said I had no stroke, mini stroke, or pulmonery embolism. I have a habit of breathing shallow. I told my regular dr what happened when she called me b4 leaving her office on Thursday after I got sprung. She thought it could have been the anesthesia.
The last night I was in ICU, they made me sleep with a c-pap machine. Yuk I hated that.
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Wishing Outdoorswoman, Shelly and puppy4ever the best of luck and a speedy recovery.
Saw bs yesterday for pre op. I really like him so I feel very lucky. He answered all my questions and put me at ease.
The past few days have been good. Haven't been weepy and taking it one day at a time. Trying to stay busy and just live life as normal as possible.
Went to my bc support group last night and I met some very nice ladies. So that was nice.
I got in touch w an old friend who is also a sister and her young 25 year old daughter is having BMX tomorrow at Sloan Kettering because her braCAtest was positive. There are 7 generations of bc in her family. Unreal but true.
This disease is running ramid but we all have each other to lean on and I am so grateful for that.
As hard as it might seem to us at times, we will all get through this.
Hugs,
Lori
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Littletatas. My hospital was 2 hours from my home. My surgery ended up later in the day, so I spent the first night in the hospital. Next day hubby picked me up, we stopped off to grab a pillow (hadn't seen that recommendation!), then we drove 2 hours straight home. I did spend time flexing leg muscles and moving slightly in the car, but we didn't stop until we reached the house. I spent the first few days just walking around the house and negotiating the stairs and finally grabbed a shower 5 days post surgery. It's what felt right for me and I think that's the message from all the wonderful folks here. Read, listen to your body, and decide what works for you. This past weekend we took the train into the city and I did keep a teddy bear under my right arm. My current struggle is figuring out what bra will work. Best wishes to all.
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Hello from Kansas! I will have BMX + SNB on April 16. BRCA1+ and ER+. I think I am ready. I bought a pretty pink shirt which has pockets for the drains on the inside and buttons down the front. I think I will wear it every day for a while! Also I got a soft cotton bra which fastens in the front and has pockets for fiberfill. Got all my prescriptions filled.
Best wishes to all!
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best wishes for Outdoorswoman, Shelly and puppy4ever today, think of you
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Good luck to all having surgery soon. The past couple of days have not been so good. Make sure you have someone staying with you because you will not be able to get in or out of bed by yourself. And, you need help getting on and off the toilet and I could not pull my sweat pants down or up. Also, make sure they know how to strip the fluid from the drains. My pain meds are causing me to get sick, so I am just on Tylenol. Have stool softener ready because all this makes you constipated. I am just letting you know this information so you can be better prepared.
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mysunshine48 - sorry you are not feeling well. I actually got an anti-nausea med from my doctor before I came home. I used one that they had prescribed while I was on chemo that worked really well. You put it under your tongue to dissolve it. Also, they should give you stool softerner's before you leave the hospital, I was given 3 but I also started taking Mryalax (2 capfuls) in some tea every morning for the first 5 days until I started to have normal bowel movements. Remember with any surgery when you are put under your bowels fall asleep too so it takes a few days to come alive. I went 5 days without a movement but was not in pain because of the pain meds! Good luck and hopefully you start to feel better. -
What were the anti-nausea mess? I have to have chemo and cannot imagine starting that, but meet with the MO next week. This is terrible
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I feel you, mysunshine48. I felt great the day or two after surgery (it was last Wed). But my pain meds also make me sick, so I have Zofran to take along with them. But the combo makes me so lightheaded and loopy I decided to go with Tylenol only as of Saturday afternoon. Yesterday I was absolutely miserable, it's not so much pain but just incredible discomfort...and twinges of pain. Most of my pain is from underarm (2x SNB). So I am back on the Oxy/Zofran combo. I feel like it's one step forward/two steps back.
And yes, you have to have someone to strip the drains for you! There is NO WAY I could do it by myself.
Good luck to all!
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Welcome new April sisters StillStanding66, labhusky, PMR53 and Queen_Celeste.
StillStanding66, being terrified of the unknown makes you human. It is completely understandable that you are afraid of being put under for 8 hours. That's a lot of anaesthesia to recover from. Your fiancé should be supporting you and not trivializing your fears. Your chest, arms and stomach will be sore and you will be hunched over for a bit and you need him to be 100% supportive throughout your treatment, so I hope he is ready to step up and support you. Sometimes people say dumb things when they are a loss of what to say. Perhaps he is trying to scale it down for you so you will be less afraid. Tell him it's hurtful when he is dismissive of your fears. Your fear is real and stressful. Lots of women have had DIEP recon and find that that experience wasn't as bad as they feared. Focus on the fact that you are going to get through this, there will be some challenges, but you are going to be OK. You'll end up with nice feeling new breasts. Breathe deeply...it really helps calm you.
labhusky, I am sorry that you've experienced complications and had to spend the night in the ICU. It's easier said than done, but try and be patient and give yourself time to heal. Hopefully, you get good news at your Wed appointment.
Happy to have you join us, PMR53. You might want to do some stretching pre-surgery to facilitate your mobility and range of motion recovery. Most pain can be managed, so if by chance you are in pain, make sure you communicate this so your team can change your pain management meds to address it. No one should have to suffer in pain.
Queen_Celeste, you sound like you've got everything planned and ready in advance and are in a good place emotionally. There's a thread with suggestions for shopping/packing for surgery and recovery under the Surgery forum, if by chance you haven't seen it yet.
Hockeygoddess, wishing you good luck tomorrow and quick healing.
Hugs to all April sisters recovering from their surgeries.
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mysunshine48 - I had several anti-nausea meds that I tried during chemo but the Zofran (Orndansetron) was the best and did the trick. I also am on Tramadol because I cannot take some of the stronger meds they like to prescribe first. Also during the night at the hospital they used alternate medicine and I was given a massage therapy with pressure points on my hands and knee area while breathing in Ginger Essential oils. I have Ginger tea and ginger candy that I used during chemo that also has helped keep the nausea at bay. If your cancer clinic offers a mentor take advantage of it because I have had a pink ribbon mentor since October and she was matched to me as far as the type of breast cancer and age. Plus it is great to have a survivor giving you tips on all the side effects because they know how you feel.
dtorrent - I agree it is just plain discomfort and when I do try to use that arm I just feel like it doesn't want to move! I read someone was using their husband's dress shirts so that is what I am wearing because the flabby part of my arm is so sensitive. I do notice the drain fluid is half of what it was last week and getting lighter colored every day. I could not do the stripping myself either. Today is change the dressing day around the tubes so that will wear me out! :-)
Each day brings us one day closer to feeling normal.
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Redporchlady, I get Zofran in my IV during surgery, but haven't needed it post-surgery before. My upcoming surgery will be a much longer surgery with more pain killers and a drug cocktail, so who knows what the SEs will be. Is it Zofran that you are taking sublingually? I can handle pain and discomfort (not that I want them), but I hate nausea, so I am going to ask for a script for whatever you are taking to have on hand, just in case. Interesting that your cancer center supports alternative medicine therapies - very progressive. My experience with the Western medicine practitioners I have encountered is that they look disdainfully and disparagingly upon alternative practices. I think there is a place for both. I would love a massage if I'm stuck with an overnight stay, but I know unless I import an RMT, it isn't going to happen.
dtorrent, I am a little disheartened to read of your setback, especially after your initial positive report. Stay focused on the goal, setbacks are inevitable and this will pass. Are you able to sleep?
mysunshine48, hope you are feeling better soon. Even if it's not good news that you are reporting, it's helpful to know what those following you have in store for us. It sounds like nausea is a common SE of the pain meds, so I want to be prepared.
My PS is unfortunately on the no shower bandwagon until drains are removed. I've just ordered some body wipes from amazon. I'm a shower person, but will definitely be taking some baths. I'm going to get my husband to wash my hair. Not sure how he will fair at styling. He's got a head of incredibly thick wavy hair that's wash and go, so he's never used a blow dryer ever. I'll have to take pics.
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Can anyone lay sort of flat at all? I have to be propped up to a sitting position with many pillows, and, a pillow behing my head. It is so uncomfortable and my back hurts! Let't fast forward to 2016!
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and, to think chemo comes in a month, or less. Ohhhhhhhhhhh
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where do you get shirts w pockets on the inside?
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That's what I'd like to know lmonelli!!
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Just bought pink pockets. 25.95 for 5 pockets. They stick on inside of your shirts easily removeable
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hey were a little pricy but the shirts were 60.00!!
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Thank you to all the April Surgery Sisters that have shared what your surgery and recovery has been like. It is important for us to hear the good and bad parts so that we can have a realistic expectation for our upcoming surgery. Hope I can return that help to others.
I saw my PS for the pre-surgery appointment today. I had a whole paper of typed questions ready for her. Glad I wrote them down as I would have forgotten half of them. I made sure to let her know about my motion sickness issue so that she could add something in my IV as well as an Rx for Zofran to take for the car ride home. She also gave me an Rx for the patch to put behind my ear the night before surgery. I was surprised to hear that I would be staying two nights in the hospital. Two more weeks before surgery!
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mysunshine48:
I too hate sleeping on my back. I'm using a reading bolster with a pillow, two pillows on my right (SNB side) for my arm, one on my left to keep me from rolling over, and two to prop my feet up on to ease the tension on my back. it is quite something to get in and out of bed. I'm also sleeping on a blow up mattress which is more comfortable at this time than my super expensive pillow top mattress. A little crazy but it works, although I only sleep about 2 hours at a time.
Also, your MO will give you a whole schedule of drugs to take for anti-nausea. If they don't work for you, don't suffer call them and they will adjust. You should never be nauseous on chemo. After my first treatment I was slightly nauseous the first night, went away in the AM. At my next treatment the MO added one more drip bag of anti-nausea at the end of my treatment and it worked like a charm. I was never again nauseous. Typical anti-nausea meds are decadron, compazine, and zofran.
StillStanding, lmonelli, look for athletic work out tops. I have a cotton zip up sweatshirt with pockets on the inside, although I just used an elastic drain belt. I had two one for the shower and one for post shower.
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