January 2013 surgery
Comments
-
Hello Everyone
Tubes out last Monday...along with wound vac. I have home health coming daily to change dressing where PS reopened me to clear the staff....Yeah! Iv antibiotics (picc line) out Thursday. I am taking oral antibiotics for two more weeks.I see plastic surgeon next week..surgeon after that to schedule lymph node dissection and get port for herceptin. I will be on this for a year. 2013....here we go!
I hope all is well with everyone....fighting.
I have had parents of students bringing dinner since Jan. I have been overwhelmed with support, although my mom returned home today and I willmiss her
I hope all is well with everyone....keep fighting!
Laurie -
Oh Laurie, what a rough time you have had, but you always sound so positive! I love that about you!
You've still got a ways to go, but you will do well because of your great attitude.
Isn't it wonderful how great people can be. I was amazed at the people who rallied around me, and I was new here. Had only lived here for about four months when this all happened.
Take care, and I wish you all the very best for a speedy recovery from the rest of your surgery!
-
Hi Laurie,
Glad your doing better and got your tubes out. What a nice feeling it is. It so nice to hear so many people are taking care of you! Keep on fighting. -
Thank you Ariom! I look at my little kiddos.. 4 and 6 and have no choice but to be positive. They are my heart and are my cheerleaders
. I am fighting through this for myself but for them as well
Laurie
P.S.
If it wasnt for the staff infection, my recovery would be right on track! -
Laurie~ Wow! Glad things seem to be turning around for you now! Those babies of yours are the best medicine! I'm trying a new antibiotic as of today...trying to clear the last bit of this cellulitis. It was definitely not as severe as yours but is proving very stubborn. Keep up the good fight!
-
Jen (jmotk) and Peanutsgal,
I will also be a surgery "sister" on April 15 for my exchange for my "squishies"....Woo hoo.
I had my last fill today, and maybe a "top off" in two weeks....then the waiting really begins....I am so ready to get these hard things OUT of my my body!
Hopex3, another WA resident here, been to your your city a lot of times, and Portland OR when I was showing my dogs, and my daughter was going to Portland state for her Masters.
Laura....bless your heart you been through a lot....here's to a full recovery now (and lots of hugs & kisses from you kids)
Tamiami,
kick that infection in the butt now! (I once had a post op infection 3 wks after a major surgery years ago, and ended up in the hospital)
Even though I had my BMX on Dec. 21 and my drains out on Dec 31. it was a tough time as far as support with, the holiday festivities were in full swing....I was not festive.
I had my tissue expander surgery on Jan 21
Di
-
For those of you who had nodes out, as you may know you're now at an increased risk for developing lymphedema. Many of us want to start exercising once our surgeons clear us, but we're rarely given any guidelines on how to exercise safely. Now there's a new set of Exercise guidelines on the Step Up Speak Out Lymphedema site that can help you start or resume your exercise program in a safe manner. It was researched and written by several women who post regularly here on the LE threads in BCO.
Here's a link to the guidelines:
http://stepup-speakout.org/Handout%20doc%20for%20SUSO-030113.pdf
Also, if you plan to work with a personal trainer, a physical therapist who is not familiar with LE, or plan on taking an exercise or fitness class like yoga, pilates or weight training, here's a document you can give to the trainer or instructor to familiarize them with LE so they know your risks and can give you alternate moves or otherwise help you exercise safely.
http://stepup-speakout.org/Trainer%20doc%20for%20SUSO-030113.pdf
Studies have shown over and over that getting 30 minutes of exercise most days greatly helps reduce the risk of recurrence. Once you've been cleared by your surgeon to resume exercise, it's important to get going. Even 10 minutes of walking a day is better than nothing. These guidelines will help you come up with a safe effective exercise program.
-
NatsFan....your awesome. Thank you for the info! It's just what I needed!
-
Me too NatsFan...me too! Thank you!
-
Lbwagner69,
I agree we have to stay positive for our kids! I have 3 daughters 16, 15, and 11. I have tried to show them strength and positive attitude during my whole journey but have to admit I have had a few "meltdowns" along the way also. Probably the best compliment I could have gotten was when my 16 year old told me a song on the radio made her think of me whenever she heard it. The song was Stronger by Kelly Clarkson. When I asked why she thought of me....she said because you have been so strong through all that has happened. I wanted to cry. I felt so happy that she could see what I was going through. Sometimes with teenagers that doesn't happen! Haha!! Stay strong but know it's normal to have bad days too. Best wishes to you. -
Happy St. Paddy's Day!! It's been awhile since anyone has posted...hope all is well and things are becoming more normal, or at least the new normal.
I started back to work this week, but limited it to no more than 6 hours per day with a few built in breaks. The first 2 days, I was exhausted but by yesterday I was feeling great! So happy and thankful to be back to work! It was so nice to see my coworkers and clients again...I can't tell you how many people hugged me and told me they had been praying for me!
I also got to start my LET (lymphedema PT), and have had my arm wrapped the whole week. I think the swelling is decreasing...at least it feels that way. Yesterday, I had a little scare in the shower when I felt a lump under my armpit. Upon furter inspection it was a "cord" which feels like a long, hard. proturuding vein. I have a feeling that's what has been causing my underarm tenderness/pain and the pain in my elbow. I think it's been there awhile, but I couldn't see it until the swelling started to subside. I guess they either resolve themselves, or the LET should be able to help.
I'm curious as to how the rest of you all are doing. BTW I saw a thread on here that some of the 2008 BC girls have been doing a Vegas trip every year to celebrate kicking cancer's ass, and they always invite new sisters as well. It really peaked my interest! There are about 50 or so that go and it sounds like a blast. I'm not sure I will be able to take the few days off work, but I'm thinking about it. Check it out and see what you think...it's in the Get Togethers Forum.
Tami
-
I developed cording... It is.painfu but my pt really works it good its a hurts feels.good sort of thing! My range of motion has def improved due to going and doing the recommended stretches at home..... But overall mornings suck and are the worst for tightness so hard to get moving!
-
Hi Tami, I went back to work last week as well. Did 6 hours Monday and 8 hours each Tuesday, Wednesday, and Thursday, and Friday was holiday. You are right, getting out has been good. My low ab does feel full and very tight later afternoons and evenings. They go away in the morning. Jennifer keeps a great updated list and I always read postings here to see how my January surgery sisters are doing. Hope you LET works wonders for you. Vegas trip sounds like fun, but like you, I may not have the time to do it this year. Hope everyone is healing well.
-
Amy, I am the opposite from you!
-
Mornings are definitely the hardest for me as far as tightness. Before surgery the first thing I would do when I woke up was arch my back, raise my arms over my head and take a really long stretch. Now, I sometimes forget and do the same thing.....can you say OUCH? It doesn't take long for my body to remind me that I need to do these things much more slowly and my TE's definitely bring me back to my new reality : ( Less than a month to go, though!
I would absolutely love to meet you lovely ladies in person someday. Maybe next year after everyone recovers more completely from treatments and surgeries! -
Amy~ How long have you been dealing with the cording? Any idea how long it will take for the PT to get rid of it?
Tammy~ Is that from the Diep? I had a tummy tuck in 2007 and know exactly the feeing you are talking about! I wore spanx for a long time at work to help with the swelling from being on my feet.
Peanutsgal~ When is your exchange surgery? I agree that next year will be better for Vegas!
-
Amy- I just read your post on cording and OMG I think that is what is wrong with me. I had a terrible infection under my arm(due to shaving it and cutting it) and was in the hospital for ten days last month. I had a biopsy, long story.....anyway I mentioned to my oncologist I was feeling pain all the way down my arm. She just felt it and said its not swollen and feels ok. She said just keep an eye on it. Well Im sure because it was NOT the breast cancer side she wasn't concerned. ( maybe she forgot about the infection under that arm) Anyway I can feel a cord like feeling under the armpit and it hurts all the way down my arm. Feels almost bruised inside and goes from the armpit down. I also keep comlaining that that side of my chest hurts More which I keep thinking that makes no sense as it isn't even the cancer side. I keep blaming it on my port. Now I think hmmm maybe I have this cording????? What should I do??
Tami thats great you are back to work. I think this chemo is hitting me harder then most. I get so so tired just going to the grocery store. I dont think I could work. I guess I will go back after all this chemo is done and Im sure I will have lost 50% of my clients. Who comes back comes back and who doesn't doesn't. I was really worried about it at first but now Im just not. It will all work out in the end. I do miss the social part of working but my TE are still so painful and energy level not good. I need to call the PT next week. I only went once then got sick and didnt end up going back. Maybe that would help
Mary
-
Hi Tami! Just wanted to chime in that I had cording as well. It hurt the most when it first developed and then only seemed to hurt when my arm was in certain positions, but felt 100% fine in other positions! I could see the cords pop out in my armpit and inner elbow. They reduced my flexibility because they were so tight and I couldn't stretch past them. I diligently did stretches and it seemed to resolve in about six weeks (about 10 days before my pt was finally approved!!) When I saw the pt I had full range of motion back and no visible cording. Unfortunately since starting radiation some of the armpit pain and reduced flexibility has come back. I've been told to continue lightly stretching but not to push through the pain as it could cause the cording to come back. Sorry you are having to deal with this. It caused me much distress because I was worried I wouldn't be able to get into position for radiation. I hope yours resolves itself soon!
-
Mary~ Here is a link about cording. Maybe this will help you figure it out. Was your PT trained in lymphedema or do they work primarily with BC patients? If so, they may be able to help with the cording. I hope so!
http://www.stepup-speakout.org/Cording_and_Axillary_Web_Syndrome.htm
Also, I totally get what you mean about losing your clients. I finally came to terms with that as well. It's hard to see them in your coworkers chairs, but you will build back up quickly when you feel well enough to work! I never thought I'd say it, but I liked working 6 hour days! I hope the chemo gets better for you. How much longer?
Fight4two~ Thanks for the encouragment about the stretching...I have some I am supposed to do for the range of motion. I will know not to stretch to the point of pain. My LET is out of town until April 1st, so she doesn't know about the cording yet. Check out that link as well.
Tami
-
Tami,
My exchange is scheduled for April 15th and since I don't cout today or the day of surgery, I have 28 days left! (It's childish I know, but anything to convince myself that I don't have very long, right?)
Amy,
Sorry to hear about your cording issues. I have read about how painful that can be : (
I really hope you turn the corner with that soon!
Mary,
I would definitely go to PT. If you can find a lymph edema PT that would be really great. I go to a myofascial release PT and in just a few visits I have made great improvements in my ROM. Like Amy said, it's a hurts, feels good sort of thing, but definitely worth it! Sorry to hear about your infection ordeal. This disease is just the gift that keeps on giving! -
Pam~ You are 2 weeks in front of me! Please keep me posted if you are up to it!
-
The PT I saw is an occupational PT with rehabilitation, she works in the breast cancer unit and is a survivor herself. I will call tomorrow and see if I can get an apt.
-
That sounds like a good plan! Hope you can get it all figured out!
-
yes, Tami, I had BMX with DIEP.
-
Tangles... Yes go to a pt who specializes in lymphedema. I can tell you from my experience that my sides have been hurting like a burning pain that runs along my side next to my breast. I figured it was my body healing. My ps said it was my nerves coming back to life! I am not sure if you had reconstruction using alloderm but both my pt and ps Recommended I get a good cream or lotion I use palmers with coco butter and vitamin e. Anyway they said to massage the side... Start on your side and work toward your breast over it and in to the nipple in a horizontal motion then do the same.from the bottom of your breast up. I told my pt I was hurting here and she did a wonderful massage to my sides and it releived the pain for sure.
I see you also had an alnd in my opinion any woman who has nodes removed should see a pt my bs was the one who set up the appt.for me. And if you do have cording the pt will help you work it out and get your ROM back faster... Mine showed me all.sorts of home stretches to do also!.hope this helps! -
Tami,
I'm in Tennessee and on April 15th you will probably hear me shouting in Michigan once I get these things out. I really shouldn't complain. I haven't had it nearly as rough as some of you, but seriously, I will keep you posted. -
Tami,
I'm in Tennessee and on April 15th you will probably hear me shouting in Michigan once I get these things out. I really shouldn't complain. I haven't had it nearly as rough as some of you, but seriously, I will keep you posted. -
Pam~ I look forward to hearing those shouts of joy!!! Have you thought ahead to the final phase yet? I'm almost 100% committed to getting the 3d nipple tattoos from Vinnie and forgoing the whole nipple surgery. What about you?
-
I'm still on the fence about the nipple, but I am definitely going to Vinnie for tattoos. I'm getting a little tired of just the thought of surgeries, so the 3D tattoos are really appealing! I have a non-breast related surgery Wednesday, then three weeks later I'll have my exchange surgery. After that, I plan on taking an extended break from all things surgery!
-
I skipped surgical nips and did Vinnie tats and am very pleased with them. Spared myself an extra surgery, and no "headlights on" issue. The first time my doctors saw them, none of them could believe that they weren't surgical nips - he really is that good at doing a 3D effect. And he's a super nice guy also.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team