July 2015 Surgery Sisters
Comments
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mfana,
Another So Cal gal! Yes, BS ordered genetic testing. I should have it back in about 4 weeks. City of Hope is a great facility and I love my BS. I just wish I had thought to ask about further imaging during my appointment. I am not sure why it's not standard for them.
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Wonderful news, octogirl! !!
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i had to switch to the left side of the bed and its worked much better for me although it still feels weird. It's very hard to not use my right arm....sometimes I think I should just strap it to my side or put it in a sling to remind me!
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I agree that a sling or something as a reminder would help...it is very hard to remember not to use the right arm, especially being right handed...I reach for things without thinking, and then I feel it...
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I found the silky button up pjs great as well as a silky cami top and shorts for when I was too hot for the long sleeves and pants. The cami had spaghetti straps and I could step into it. I bought both at Target. They were polyester but they felt good to wear and did make it easier to slide in and out of bed. I'm a stomach or side sleeper, butbpost surgery I preferred to sleep slightly upright so I was already half way there, but to sit up, I'd bend my knees and dig my heels down to do the rest with my abdominal muscles. Like a sit up, and imagine someone holding your ankles down. Sometimes it was easier to slide to the edge of the bed, put one leg out from under the sheets, plant that foot down on the floor then sit up by pushing that foot down on the floor. You'll figure out how to shimmy yourself out!
I definitely felt worse days 3 and 4 than prior to that. I think the anti nausea I was given wore off before the anesthesia's side effects. And when I stopped wearing the surgical bra, the burning pains along the incisions and a little bruising under one of my arms from where the drain was pulled felt different (worse) than when it had been compressed. I was allowed to take Advil, it would help as did rest, e.g., lying down to rest my sore shoulders. 8 days out BMX no reconstruction I feel pretty good considering I just had major surgery but if I stand or walk around too long - 15 minutes - my arms feel like dead weights and hurt my shoulders and shoulder blades, so I end up crossing them and putting them across my stomach to rest! I love leaning back into soft chairs and do not like hard chairs with hard backs. Be careful sitting in too soft a couch too. It's hard to get up without using arms! You'll need someone to push you from your back or good quadriceps!
Gentle hugs to everyone! Welcome to the new ladies, and prayers for those dealing with new diagnosis or pathology reports.
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Excellent suggestions. Thank You all!
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Congratulations Octogirl! All those coming surgeries good luck and those recovering, I'm hoping it's a bit better each day!
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For some reason I have a lot of trouble typing a message on this site from my ipad. Words are mangled, it moves extremely slow, and it makes it almost impossible. I'm on the computer right now typing away with no issues.
I had stage 1 rectal cancer in 2013, exactly 1 year after my mom died. She was a very healthy 77 year old, and suddenly developed a blood disorder in October 2012 and died the next month just before Thanksgiving. She lived in Illinois and I'm in Florida, so I didn't get up there until she was on life support. Anyway, I truly believe that the stressors in my life along with her passing depressed my immune system to the point of my getting these 2 cancers. First rectal, which didn't require treatment beyond surgery, and now breast. No one in my entire family has had either. Only one aunt had cancer at all, and it was pancreatic.
I've been doing a lot of reading about the emotional causes of cancer and the big message is to find the things that make you the happiest and DO THEM. I've been in caretaker mode for so long that I'd lost my connection to the things I used to love. I'm a school nurse, and I love the kids, but I take it home with me. I call people in the evening because I'm worried about them. My 16 year old has CP, and he is the light of my life, but I don't let his father take care of him enough. I think that I do it best, and I can't give up the control. I plan to change that. In fact, I've been working hard to change it all summer.
This is a huge wake up call for me. I'm 53, very healthy otherwise, and cancer is a total surprise these past two years. We're nearly vegetarian, I don't smoke, drink a little and try to exercise as much as possible. For me, it's about stress levels and trying to control everything.
Just wanted to share this and see if anyone else can relate. Much love to all!
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Caroly62, I also am having trouble with writing relies on my iPad...interface doesn't seem to work well. I have no problem on my MacBook at all....maybe the Mods are listening for future upgrades/changes? All things being equal I'd rather use the IPad just because it is lighter and easier to pick up post surgery....
I am not sure about the whole stress thing but I will say that finding out what makes you happy and doing it always seems like the way to go.
Will be thinking good healing thoughts for all
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see, I can't even get your handle right...typing from my iPad...
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Carolyn62, I can definitely relate. I am a nurse also but do data abstraction for different registries in the hospital setting. Feel that stress has contributed to the development of breast cancer. Almost like it's one part of the equation that makes the "perfect storm" ....
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Carolyn62,
We are nearly the same age and similar life circumstances. I hope you have arranged for extra care for your sweet son while you recover this week. My prayers are with you.
I am 54. I have been through incredible stress for years but especially the last few years due to my special needs son getting very ill and being on hospice the last two years, my oldest sister dying of early onset Alzheimers, my mom having Alzheimers and my father passing away. If cancer is fed off stress than I am a candidate. I am incredibly healthy and this came as a complete surprise.
Plumster, Carolyn and the rest of you having surgery this week I am praying for you.
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Hello Ladies,
I was off the boards for several days so have been reading all the posts and getting caught up. Wow! What an amazing strong group of women!!! Hugs (gentle, of course) and prayers to all. 🙏💖🎀💐
Tam-iam: So sorry sweetie to hear about the positive nodes. Sending prayers and positive thoughts your way.
Queenmomcat: Regarding the post op swelling: I found out this week that I was given Decadron in the operating room to help with the pressure/swelling on my brain from the meningioma. That, along with the fluids and general anesthesia, is why I puffed up so much. I'm back to normal, thank goodness, and prepared for my next round which will be given to me at the end of the month when I have stereotactic radiosurgery for the meningioma. Sheesh! What a month.
Bunnybumps: I had my pre-op for the meningioma this week and picked up a brochure on Memingioma Momma! I'll definitely log on and join that group. Thank you so much for the info. You have 6 of them? Oh my!!! I read somewhere that women with ER/PR+ breast cancers also have a higher incidence of meningiomas.
Overall I feel pretty well. My right side is still very swollen, both my BS and PS said it could be swollen up to 3 months. I went for a walk this morning, 2.5 miles, trying to increase the distance a little more each day. I received my final path report from my BS. It confirmed that my nodes were negative and that no residual cancer was found in the tissue removed. Next step, meet with my MO to begin Tamoxifen and Gamma Knife radiosurgery for the meningioma on 7/30.
Prayers and positive thoughts to all those having surgery this week!
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For everyone having trouble typing on your iPad, click the "Use plain text editor" link next to the Submit button and it will work just fine.
Sweat Pea, it's good to read you again! Glad you're doing so well and have good news for nodes! Walking 2.5 miles after surgery??? I can't manage that now! Strangely, my bc is triple negative, so there doesn't seem to be a link for me.
Going in tomorrow for the bmx and diep. Still doesn't seem real. All this preparation makes it seem like we're having guests or packing for vacation. DH is taking me out for a nice dinner tonight; last meal and all... :-)
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we will be thinking about you bunnybumps.... check in when you can!
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Sweet Pea, I'm so glad to hear you have negative nodes! Good luck to everyone having surgery this week!
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Carolyn and all. . .I've been stressed for years with two autistic/ADHD children who have both had multiple surgeries. My mother, a doctor, has Alzheimers, both Dh and I work full time. I have given up trying to figure out why and focus my concern on keeping it from coming back. Cancer sux and for those with added stress my heart goes out to you.
I have spent the last 8 months trying to figure out what I can do better. Already vegetarian for 18 years, trying to limit caffeine (jury's out on that one as it may be good), trying to eat tons of antioxidants etc. Even if it's not helping physically it helps psychologically. I'm pushing myself at the gym and hiking and I'm trying not to cry about the 6 weeks of downtime starting next Monday.
One suggestion, DH bought me a "boyfriend" pillow after BMx only $49. Wraps around your whole body for support. I still sleep with it each night and travel with it despite the stares. It allows me to at least partially sleep on my side. Now to get on amazon and buy some button up camies.
http://www.amazon.com/Comfort-Total-Body-Support-Pillow/dp/B0010BBN7M/ref=sr_1_1?s=home-garden&ie=UTF8&qid=1437343880&sr=1-1&keywords=whole+body+pillow&pebp=1437344364632&perid=04M3EDR3FSE5E13JZ77YHugs to all.
Scottie
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Bunnybumps Thank you so much (absolutely love your user name)! You'll be in my thoughts and prayers tomorrow. 🙏 Enjoy going out to dinner tonight and rest well knowing that this time tomorrow surgery will be behind you and you'll be on the road to recovery. By the way, as for walking, my usual walk was 7-8 miles 2x during the week then 9-10 miles once or twice on weekends. It's how I decompress and de-stress. Little by little I'll get back there again. 😉
Tam-iam: Awww...thank you doll. When are you going to see your MO? Are you able to email and/or text him/her any questions? My BS, PS and MO have been wonderful and so accessible 24/7 via email or cell. It's been a huge help. I hope your team is as accessible to you to answer any questions or concerns sweetie.
Prayers to all having surgery this week. 💖
123justme and -
I'll be thinking of you tomorrow, Bunnybumps! Hope all goes well and you're up and around quickly!
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thinking of you Bunnybumps &; Greendolphin. I have to be at the hospital at 5:30am tomorrow so I had my sentinel node injection tonight. I got worked up about it but it wasn't too bad. Slight sting, then a burn but it was quick. Thinking about my mom who was diagnosed at age 38 and lost the battle at age 46 almost 31 years ago. I take comfort that much progress has been made since the 80s. Stay strong ladies.
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Bunnybumps, Greendolphin and Mavski80 prayers and hugs for tomorrow.
Scottie
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Hi, Sweet Pea. No, I haven't yet heard from the MO. The referral went out on Wednesday and I'm still waiting to hear from the office to set up the appointment. I have the appointment coming up with the RO, even though it looks like radiation will come after the chemo. I don't like that it is taking so long to get an appointment after the referral, but I've asked around and it sounds like this is the best MO in town. I'm feeling much better about it all. The waiting now is much easier than waiting for the diagnosis and staging. I know basically what the plan will be, just need the details.
Bunnybumps, Greendolphin and Mavski80, I'll be thinking of you tomorrow. Good luck!
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You sound a lot like me! I was also doubting whether I should post here. I just had a lumpectomy with lymph node removal on Friday, the 17th. I don't have all of the details like others here. I was told we will know all of that after the pathology report from surgery.
I had a routine mammogram mid June, was called back for follow up tests, referred to a surgeon, and had biopsies on two lumps in the right breast. I was diagnosed on July 9. The pathology report said one lump was normal and one was ductal carcinoma. The surgeon has a good rep and I trusted his guidance when he said he believed it was contained and we should go ahead with surgery. I chose lumpectomy. He expects to follow up with radiation unless the pathology report has surprises for us.
It was out patient surgery and it's has not been difficult. The day after surgery I slept most of the day. Yesterday I was out of the anesthesia fog and was more active. This morning I feel normal. The incisions have not been painful. The lymph node incision under my arm is the most sore. It only bothers me when I raise my arm but it's not terrible. I do have a lovely divot on the top surface of my breast where they removed the tissue. Guess it's my souvenir!
This is my second fight with cancer. I had an unusual type of thyroid cancer exactly 20 years ago. I plan to win this go around too. Now I just need the patience to wait for the pathology report to come back.
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Hello all,
I'm back. My UMX with T/Es was performed on 7/14. I also had a reduction on the other non-cancer breast at the same time. Today is 6 days out from surgery - I am amazed by how good I have felt to date. In the hospital I was on morphine which made me itchy and that sucked - and I was ridiculously hot (combo of meds and AC not working right in hospital room). Came home 48 hours after surgery. I haven't taken pain meds (Vicodin) since Saturday. I am still taking ibuprofen daily and a muscle relaxer here and there.
Drains are annoying but not as bad as I thought they might be. Expect to have one of them out by the end of the week based on the low drainage amounts. SNB was clear in surgery, seeing BS on Wednesday to get full path report, fingers crossed that is clear too.
Hope everyone is doing well!
Welcome to the newcomers and positive thoughts and prayers for all, especially this week's surgery sisters.
_proudauntie
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For those ladies who have already had surgery this month, specifically a BMX or UMX. How long did you need to be in button up shirts? I am having my surgery out of town and will be there for two weeks. I am trying to pack before we fly there.
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TFoxy, I'm 10 days out from a BMX without reconstruction, and I'm only today able to put on tighter T shirts. I'm still not permitted to raise my arms straight above my head, but I can sort of bend at the waist and get looser shirts on over my head while bent over. Stretchie tank tops have worked since day 4 or 5. It helps to have someone close to you pull them down to your waist or pull them off when necessary. If you're having a UMX you might have greater mobility.
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Tfoxy I had surgery on July 7th, and I do not want to try to put a shirt over my head. Plus, I am still dealing with drains, and it would be annoying to access them (pull the shirt up off your stomach, try strip the drains, try to pour out the drains, etc). Just figure you will need button up the whole time and then you won't be uncomfortable or out of town with no clothes.
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TFoxy20. . .not sure my case is typical but I was in button up shirts/pj's for 3+ weeks until i could pull a loose shirt up over my arms. I completely forgot this go round that I need summer button up shirts as my tank tops are not going to cut it for a couple of weeks. Guess I'm going shopping since my go to Amazon was a bust on this need.
On another note, the hospital told me today to stop any herbal teas (among the usual suspects). I'm a major herbal tea lady and really not a happy camper. Has anyone else been told this?
Scottie
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Scottiemom1 my amazon search was a bust too. I found one button up camisole on there but that's it. I have a few zip up shirts and one button up. I feel like they need something underneath but I can't find anything that I like. If I was home I wouldn't care but I don't want to be stuck in the motel room and it is hot and humid outside.
I wasn't told about stopping herbal teas. Did they say why? I am using some right now to dry up my milk supply.
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I'm 13 days post-BMX now. The BS said that I'm healing nicely, and I don't have to see her again until January! I have 300 mL in each TE, and I go see the PS on Wednesday for another fill. Yikes. The filling timeline sure is aggressive/painful due to pending rads, but it's nice to see progress.
I still have drains. They're draining up to 35-40mL/side/day again. I'm starting to wonder if I will ever get these things out. The BS said to remember to use T-Rex arms, because more friction leads to more fluid (similar to a blister). Any other suggestions? These are sore, and I miss showers
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