April 2015 Chemo Crew... Starting in April? Please join us!
Comments
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ugh. Dizz, can you just request that they excise it? Thinking of you!
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They probably will excise it if there is even the slightest chance that it's anything to worry about. I have 2 spots of scar tissue on the reconstruction site on my right (non-cancer) side. During the MX, the cautery tool burned the skin from the inside all the way through to the outside. The scars were pretty nasty in the beginning, but are now just small red/hard areas. Part of my next phase of reconstruction is to excise those areas of scar tissue and create much 'nicer', less noticeable scars. So, if they can do that, I don't see any reason why they wouldn't excise this other lump. I heard back from them this morning and the P.S. and S.O. are requesting the u/s images so they can evaluate the urgency and come up with a plan.
I am actually really puzzled by my ability to stay rather calm during this whole ordeal. I was a complete wreck between my repeat mammo, u/s and biopsy last year. All I could do was dwell on all the what if's and why's. This time, I've been keeping myself busy finishing up a room renovation we were supposed to work on last Spring before my DX. After DX, they whole project got ash canned. I wasn't about to let this little lump sabotage my DIY project again. I've also been focused on my Aunt. She had her 3rd brain tumor operated on Monday night. They think she'll be transferred closer to her home in order to get radiation. I don't know much about what the doctors are saying about her prognosis, but I do think it's a good sign that they are being very aggressive with her treatment. If there was no hope, I'm assuming that they wouldn't have put her through 2 separate brain surgeries in 1 week.
Anyway...If my surgical team reviews my u/s images and decides that it's okay for me to keep the surgery date the same, I think I am okay with that. My other option is to go to the surgeon I saw her after my original diagnosis. However, I doubt she could give me a surgery date much closer than my current one. When we saw her last year, she was scheduling 2-3 weeks out if we decided to have her do bmx. At the time, I was like "hell no!" I'm not waiting that long. That's how we ended up in Illinois.
Thanks for everyone's positive thoughts. I really appreciate them. I just hope that a few weeks from now, I can let you all know the good news...that this tiny, little trouble maker was nothing.
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Dizz, I'm glad you are feeling calm. Last time I had a lump I made my surgeon take it out even though he said he was 99% sure it was nothing. Yup. It was nothing. I am sure its the same for you!
So very sorry to hear about your aunt. I'm glad they are being aggressive and there is hope!
(Edited because I'm spazzing on roids for my disfunctional eustaceon tube issue)
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Jen, it's always a good time to write song lyrics!
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Thinking of you, Dizz...I am sure it's nothing but good to get these things checked out!
Jackbirdie, I love your dog! What a great thing he is doing, providing therapy for others as well as you!
I spent the last few days in Vancouver with my daughter and granddaughter - while my daughter was at a conference I was nanny. It was great, although little Kate gave me her cold. Third cold in a row...I guess my immune system is still not up to par. Oh well. I got in lots of cuddle time!
I have an ultrasound of my chest this morning. My GP noticed that my right axilla area is larger than my left but it's probably scar tissue. I am glad to have the ultrasound though, for peace of mind.
Andrea
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Hi Everyone,
Lovely dog! These pics lift my spirits.
Dizz - sorry about your aunt. You are in my thoughts.
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Hi, friends. The March 2016 chemo thread has been started, so April can't be far behind. As some of us have discussed, let's pay it forward to support these members with our year of experience!
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Andrea- arghhhh! Glad you are getting it checked out. Hope your cold gets better soon!
Steph- how did your nipples turn out? Have you seen them yet?
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Andrea, I hope you're feeling better soon. Keep us posted on the ultrasound.
Dizz, I am glad you are feeling calm. Your gut did not allow you to last time because it " knew". This time it probably "knows" it's ok...but you still do need to be 100% sure.
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dizz thinking of you there are going to be these scary moments through out the rest of our lives we just have to remain calm and strong..which you are!!
No nips yet jen Monday morning 715am bright and early
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Steph, what kind of nipple reconstruction are you having? I have my final reconstruction surgery and oophorectomy scheduled for March 3. Considering a nipple sharing graft (only on this site would you say "nipple sharing!). I had a nipple sparing mastectomy on the right side and immediate DIEP flap reconstruction but the nipple necrosed and had to be removed and replaced with a skin graft from my hip. Guess you could say I have "hip" areola! Anyway, new plastic surgeon is going to try to make the mess the old PS left.
Not sure how much I can about the nipple at this stage, but I'm going to be under anyway for the oophorectomy. Considering treating myself to a little chin lipo during the surgery. Age, estrogen suppression and tamoxifen seem to have left me with a few new chins! It is $3500 to add on the cosmetic procedure, so I probably won't do it, although I keep thinking I deserve some good surgery out of all this!
Has anyone else had an oophorectomy or thinking about it? I'm curious about recovery time.
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Hi all!
My ultrasound yesterday went well. Although the tech is not supposed to discuss findings, she told me that it looks like a simple seroma (accumulation of fluid). I did have an obvious seroma there postop, you could hear it sloshing away...so weird! So this is just the remnant of that, I guess. The tech said they can last up to two years. So nothing to worry about 😀
Scarlett, I had an oophrectomy and hysterectomy in November. The oophrectomy was done laparoscopically so just a few tiny stab wounds. Pain wise you will be uncomfortable for 2-3 days but it's not bad. You will have to take it easy for a while - ie, no heavy lifting or housework for 6 weeks. All in all though I was surprised at how quickly I recovered.
Andrea
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Great news, Andrea!
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Andrea I slso have a seroma! The radiologist suggested a petscan die it im like huh? My surgeon was like nope it's fine will eventually be absorbed
I don't know what my surgery is called just nipple recunstruction taking skin from my inner thigh and making it into a nipple I wasn't going to do it but I think it would make me feel more normal they are also going to fix my port scar it looks terrible since I had to let it heal open from the sepsis it's a huge nasty scar
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oh and yes I slso had an oopherectomy and to be honest for me it was a little more painful than I thought it would be but only for a week or so coughing hurt especially the left side I also had my 1 year old that still likes to be held one time I sneezed while holding Her ouch! Lol
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Happy Valentine's Day to my cronies in cancer...hope you are all having a happy day filled with love ❤️
My hunny and I are off to Vegas today's! Woohoo! 🎉🍹
Andrea
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Enjoy! We have a date for Thai food and backrubs. And I cleaned something nasty in the corner of the shower as my way to say "I love you!"
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Enjoy Vegas Andrea! Glad it looks to be a seroma and nothing more. I had one drained a long while back.
My recovery from oophorectomy was not too bad. It is painful for a few days to sneeze, etc. It hurts a lot up in the shoulder due to referred pain from them "inflating" you with air during the procedure. Thankfully I'd been forewarned of that. I was back to work in 3-4 weeks at the FD.
My nips were made with the skin that was already there. They tattooed an areola a few months later. I know tehre are lots of methods different PSs use.
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thanks for the feedback! I'll need a lot of support between now and March 3rd to get myself mentally ready to go back under the knife!
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Good luck Scarlett. It is hard getting your brain wraped around going back under the knife. My DIEP stage 2 is on March 3rd too. Good day for surgery I guess. I hope it isn't too bad and that your recovery is easy.
Hope you are having an awesome time in Vegas Andea. I am glad to hear about your good test results.
I've heard back from pcp about my hand x-rays. Results are: troubling signs of both osteoarthritis and osteopenia. She's putting in a rheumatology referral for after my surgery. From what I read online, however, osteoarthitis would be more likely if the pain came on during the day after activity. I am actually in most pain when I wake up in the morning. I can hardly get out of bed and when I do, it's the Frankenstein shuffle for the first 20-30 minutes or so. It's all coming on suddenly in my hands, wrists, elbows, shoulders and knees. 6 weeks ago, I treked all over Disneyland morning to night in chilly weather. I didn't have any of this joint pain. It was only after the first of the year that it started coming on bit by bit. Of course, Dr. Google has diagnosed me with everything...including: Gabapentin insensitivity, Estrogen depletion causing cartilage loss, celiac sensitivity, Fibromyalgia, and Rheumatoid Arthritis, Leukemia...just to name a few.
Between the trouble maker lump, my surgery, and this joint pain, it feels like I am being sucked back into the cancer bubble. I don't want to go back into the bubble. I was just getting used to being back in the real world. I have so many side effects stacking up, I can't even keep track.
Once again, thanks for listening. Venting to someone who understands my fears and frustration is helpful.
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I hobble around when I first get up, but I was blaming Letrozole. I think these treatments all take their toll. I hope you get answers soon
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I hobble when I get up and if I've been seated for awhile. Tamoxifen is my culprit.
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i have nothing to blame it on but chemo and chemo pause, but I hobble too. And I have days long flares of whole body pain, which is everywhere and non specific. Its fun!
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I have two strategies: 1) Sitz baths with Epsom salt; 2) Zumba like it's going out of style so I feel like I've earned the aches and stiffness.
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looks like our common factor in the hobbling is Taxanes. I took a 2 week break from Tamixifen a while back and there was no improvement in foot pain or joint pain in hands. Maybe the good news is that it will eventually wear off as time goes by and the chemo gets fully out of our system?? One can hope!
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Re: hobbling - I've been dealing with this for months now. My PT finally started working on my feet about a month ago, now she does "therapy" on them every visit (2x a week). She uses these tools - I call them the implements of torture - to dig into the soles of my feet and my calves. I also got an orthotic evaluation, and now I have orthotics and I've been wearing my sneakers 99% of the time. PT thinks I have plantar fasciitis - I didn't think it was PF because I thought PF was a constant pain. My feet get better as I walk along (but then pain starts again about 1 mile in).
I wish I had better news to report - honestly I don't think that my feet have gotten any better. But, I also think that it will probably take a long while.
My cousin has PF, and she highly recommends OOFOs - I'm going to try a pair and see if they are as great as she (and other reviewers) says. I'm not a fan of clogs, but if they help, I may even buy a pair.
Lynne
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Hello all! I have gotten so busy preparing for new job, studying for upcoming exam and sometimes forget we are still "chatting" here too. I am more responsive on our Facebook group, sorry. Just caught up reading pages here. And reading interesting articles. This site has so much I keep finding and learning.
Dizz, WOW I would have demanded a supervisor or spoken to an administrator immediately. Please do write so that no one is subjected to that horrible care. Actually is scary that someone is working and untrained in that position. Poor quality patient care and unprofessional to say the least.
Andrea great news!!! Post pics of your travels!!! And safe travels with no weather problems! And I had a seroma after surgery too. I still think it is there off and on. It is a weird feeling, hard to describe. My surgeon said to massage the area and that does seem to help keep it looser.
Yes, that darn chemo brain is too real. I find names of people slip from my memory and they shouldn't. Embarrassing! And multi-tasking, I was always a pro at, has slowed down as I find myself double and triple checking myself. But in reality I'm probably more normal paced as I always seemed to run circles in accomplishing more than anyone else. But the self doubt is always in the back of my mind more now about did I remember that and do that right....eeerrrghhh I hope this gets better for all of us.
Lynne, I still have no feeling and pain numbness bottom of right foot. Taking so long to get better, isn't it?! Sometimes I think they lied and I'm just stuck with it. But then I remind myself that some of these symptoms are going to be around for a couple years and I need to be patient. It could be worse and I'm walking. Let me know if therapy is working for your feet.
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Hi all -
Back from Vegas, had a great trip although I wasn't feeling 100% because of my cold. I always seem to have a cold. But it was so nice to be walking around in the sunshine with short sleeves! It has been mild here on the west coast but certainly not like Vegas! I will post a pic Renee, when I get one from my hubby's camera...I didn't do any selfies!
I am glad I am not the only one with aches and pains. It is awful, I am sore all the time. I have had my hands x-rayed too Dizz, but have heard nothing back from my doctor. I also have muscle and joint pain pretty much everywhere, particularly when I first get up in the morning. I am on Tamoxifen too, I went off it for three weeks before I had my hysterectomy and oophrectomy in November and the pain did seem to be less.
I'm going to start swimming, I think exercise will help...
Andrea
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A couple of pics from Sin City. We ate at the Heart Attack Grill one night...I know, it's terrible for you...but that is the explanation for the hospital gown. All customers have to wear them! The syringe is actually a Jell-O shot. 😀
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Andrea, you look like you are having so much fun!!!! That syringe looks like adriamycin...... But way more fun than the red devil!!!!
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