Dear Ladies
Please join me in this forum if you are having reconstruction in June.
We can hold hands together and give each other support. I know I need all the support I can get. I have had breast cancer 3 times. Once in 1999, twice in 2007. It is now time to put me back together again.
After much research and much thought I am going to NOLA for delayed Bi-lateral reconstruction on June 4th. Since I am a candidate for both the Diep and the Gap they will decide at my pre-op appointment which end they want to use.
I know I won't be a 10 like some of the ladies who had immediate reconstruction. I will have a few more scars on my beauties. But I really am looking forward to having a prostheses burning party.
I went out and bought all these neat PJ's and robes for the hospital. Will I be able to wear them or should I save them for the hotel?
Sassie62
Xspectmiracles May 28th Exchange
Reni June 1st BM Diep NY
Sharkee99 June 2nd Exchange
Grace4me June 2nd Exchange
Frywoman June 2nd BM TE
TXBadboob June 2 Exchange/ Nip recon
Choward183 June 3rd Exchange
Stef58 June 3 Mastectomy/Expanders
KLE June 4th Exchange
Sassie 62 June 4th NOLA Diep/Gap
ci1326 June 4th Exchange
Emily2008 June 4th Exchange
Kimberley30 June 5th Surgery BC
cejjimom June 5th BM
SueUK June 9th LD
Ginamaria June 9th LD
2new1s June 11th TE
cookymkr June 11th TE
MonkeyD Kime 12th Exchange
YasminV1 June 15th TE
Alli62 June 15th Diep
Jan27 June 15th delayed recon mx 2004 mx2009
CaseyDoodle June 15th Exchange Silcone Implants
Sam1991 June 17th Revision implants
Jaimieh June 17th Exchange
Anglav70 June 17th TE
lene17 June 17th TE
cnemeth June 17th MX TE
Ally2 June 17th TE
Kam54 June 18th NOLA Diep or GAP
Momsdaughters June 18th NOLA Revision
Jondy Diep April 21 Will be in our cheering section loaded with info
Sammyjo June19th Implants healing issues with expander in Jan
Sandy's Friend June 19th NOLA Fix up Stage 1 Recon done elsewhere
Northstar June 19th Exchange to Silicone Gel Implants
pkb143 June 16th Mastectomy/Reconstruction/TE
Libby June 22nd TE Placed after bilateral mastectomy
Dottie123 June 22nd Revision Stage 2 Diep
Msdicken June 22nd Stage 2 Diep
JoniSeattle June 22nd mx2006 mx2008 Surgery for encapsulation
Nerak50 June 23rd BM
libby June 23rd TE
O2bhealthy June 23rd
Sailorgirl1 June 24 BM Skin sparing TE
Spinmaker June 24th MX + TE
Lene17 June 26th Revision Tram Flap
Casseddy June 26th Exchange + fat injections
Sorchaj June 26th right mx Tram Flap Recon
Mrsb45 June 26th BMX Diep Recon
Golfingle June 29 Exchange 410 Gummy Bears
JustSaying June 29th Exchange
Robyn33 June 29th Exchange + Lat Flap + implant
My560sel June 30th BM + Recon
lisahugs1 June 30th Expanders
Spdnyc June 30th Exchange
Southern Girl Date? Revis of Diep/ add implant on radiated side
02bhealthy Date? BM Reconstruction
Jellydonut July BM Delayed Implants
Trishia August Stage 2 Diep NOLA
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sueUK Joined: Jul 2008 Posts: 29 |
May 8, 2009 08:17 pm
sueUK wrote:
Hi Sassie! Im up for LD flap reconstruction on June 9th.....Im excited and scared all at the same time! Im in the UK so am very fortunate that I dont have the worries with insurance and all that...all reconstruction and any necessary follow up will be provided - I dont know how a lot of you ladies cope with the worry of the finances on top of everything else...you are amazing! I have bought my new pyjamas too...lovely cotton blue ones with cute little flowers - they will be so cosy! I have my robe which i bought for my mastectomy last year - white with big coloured spots - thats one cosy robe...I dont need another! Cosy is my buzz word....I imagine Im in for a good deal of discomfort so I need to surround myself with all things soft and cuddly! I am looking forward to the time off work I have to say....I have told them at least 6 weeks before I can drive....well, why not! I am a keen crafter so I call my time off 'crafting leave', and Im very much looking forward to it! I look forward to keeping in touch Sassy...we can compare experiences and hopefully our rapid recoveries. Good luck Sassy, I wish you all the best for as little pain as possible and a fabulous outcome!!! Sue x Dx 6/6/2008, IDC, 4cm, Stage I, Grade 1, 0/11 nodes, ER+ |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 8, 2009 09:41 pm
sassie62 wrote:
Dear SueX: So glad to have you aboard. Boy are you lucky that you don't have to worry about insurance. I am going to have to cash in my IRA to pay for my surgery. But the money will be worth it if everything goes well without complications. I will be traveling out of state for the surgery so I will be staying in a hotel. I haven't figured out how I am supposed to sleep at the hotel after surgery. Some doctors are adamant about you sleeping in a recliner so you won't roll on your side and your new breast. Some ladies say they just put a bunch of pillows around them. I think I will have to go out and buy a back rest that will keep me from going on my side. Otherwise I will be afraid to fall asleep. I have two sets of PJ's. One for cold and one for hot. I really don't have any idea how hot or cold they make the rooms in the hospital. Especially when it is 90 F degrees outside in Louisiana. When you have an LD flap do you have drains other than in your new breasts? Will they also put an implant under the flap? With the Diep or the Gap they say you need 2 -3 months before you can resume your normal activities. I am trying to figure out how I will wear a compression garment underneath shorts? It should be interesting. So glad you have joined us. Sassie62 |
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sueUK Joined: Jul 2008 Posts: 29 |
May 9, 2009 08:25 pm
sueUK wrote:
Hi Sassie, I hope you are having a great weekend! Ive had a very lazy day today...a little crafting, some prep for a craft room Im trying to create...but lots of watching tv and surfing the net! Of course, now its well gone bed time I am wide awake! Im not really sure what drains I will have Sassie - all I know is that they said they wont send me home before they are removed so I am looking at around a week in the hospital. I havent asked enough questions really - I dont know if I will have stitches or glue like last year...all sorts - Im just kind of going with the flow! I have opted not to have an implant under the flap Sassie....the doc said he may well get enough to work with to not need one, but if not and the result is a little small, I can either have lipofilling on the new breast or a small reduction in my good breast. As long as I end up NOT lopsided I really dont mind. With the recovery time, I dont know where I got the 6 weeks from....maybe I read it somewhere, but I gave that as an estimate to my workplace so they can work on the rotas for now! If I need longer so be it.....I was away for 4 months after my mastectomy, mostly with arm discomfort as a result of nerve damage...and experimenting with different meds until we found one that worked. Part of my job does involve a lot of reaching so I guess I might not be up to that for a good while, but if I can drive....then they will find me things I can do until I am fully fit again, even if its just answer the phone.....mmmm.....my least favourite task! Our summer weather here in the UK can be very unpredictable Sassie - it could be freezing or boiling, but the weathermen have said we are in for a very hot and dry summer....but when did they ever get things right lol! Last year, I was at home from July....in my view it was a beautiful summer with lots of sun, and definitely hot - I lived in front of the fan. But I think that was just me as everyone says how rubbish it was last year! I was permanently hot while others put sweaters on...and it was heaven to loiter in the chiller ailes at the supermarket! You are so right, I am very lucky to not have to worry about cost. We do pay heaps of tax and national insurance....but when it comes to needing such help, particularly in the area of cancer care, we get everything that we need and lots of support. Other areas of our health service are pants basically, and unless you earn an awful lot of money, you are not left with enough after taxes to pay privately for care. When I read on here about the astronomical amounts of money you have to find, I just dont know how you do it.....what if you cant do it....would you simply not get the care or treatment that you need? I do hope you can access everything you need Sassy, whatever it takes! Are you getting excited Sassie...or scared??? For me, nothing is as scary as that first diagnosis and going through surgery and waiting for results - not something I care to repeat, Im sad that you have faced this 3 times...and hopefully no more! The only thing that scares me really is the anaesthetic...I get afraid that I wont wake up! But I try to tell myself that that is so unlikely and i will be just fine...think positive, thats my motto! Sending you lots of sparkly vibes Sassie and hoping that you are having a nice relaxing weekend, and looking forward to our adventure ahead! Sue x Dx 6/6/2008, IDC, 4cm, Stage I, Grade 1, 0/11 nodes, ER+ |
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jondy Joined: May 2009 Posts: 40 |
May 9, 2009 10:02 pm
jondy wrote:
Hello everyone I just had diep flap bilateral on April 21. I will be starting my fourth week recovery starting this coming tuesday. I think the hardest part for me was the waiting between diagnosis and surgery. I had a small 5mm invasive ductal carcinoma left breast. I chose to do the bilateral diep flap because i had not yet gone through menopause and i live on the East coast so odds were it would return. Plus my mother had breast cancer. Im happy with the decision i made and i think you are all so brave! I was so happy to find out lymph nodes clear and i will not need any further treatment. Im frustrated a little at this point because i thought recovery would be quicker. As far as the hospital.i too picked out cute pajamas and slippers, and robe. Never used them once lol. I had 6 drains. Two under each armpit and one on each side of the abdomen incision. That made it very difficult for anything but the hospital gown. When i left the hospital ,one of the nurses gave me an extra gown and it was a God send for the following week out of the hospital. After 9 days all my drains were out (freedom!) but my incisions still sore. The most comfortable thing i still wear is an oversized T-shirt with a pair of my husband soft pajama pants. With the diep flap not only is your skin sore to the touch but the stomach incision and swelling makes everything feel tight. today was the first day for me to be able to put a pair of pants on but after a few hours they feel good to get them off. I also love to wear the big moo moos (like a house dress). My friend bought me a size 1x (i wear a size 8 in clothes) I have to say i love them because they dont rub against your skin and incisions. I also had a friend talk me into buying a cheap recliner and i am sooo glad i did..at four weeks i am just now able to get into a bed. i Wish you all well!!! I am so glad i had this surgery. Just listen to your body and rest, rest, rest God BLess! |
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Jaimieh Joined: Jan 2009 Posts: 950 |
May 9, 2009 10:24 pm
Jaimieh wrote:
Oh it's finally getting closer to June :) I am scheduled for an exchange of these wonderful TE (NOT) on June 17. I am lucky that I have only had my expanders since 1-8-09 and they look great but I have had a lot of nerve pain with them. I am nervous about the surgery BUT my PS said she is putting me in a surgical bra after the surgery to remind me that I had surgery so I am hoping she is correct. I would love to have to be reminded that I had surgery. She also told me that it should be a fairly short surgery so that was good. I meet with my PS last week and it really is helping me get thru my last treatment that I have everything planned for June. I am hoping that it makes my side effects from my last TC treatment a little easier.. Dx 12/24/2008, IDC, 1cm, Stage I, Grade 3, 0/2 nodes, ER-/PR-, HER2+ |
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sam1991 Joined: Jan 2009 Posts: 331 |
May 9, 2009 11:14 pm
sam1991 wrote:
Hi Sassie, Can I join your June ladies? I had my exchange in March but due to unforseen complications I'll be having pocket revisions and reinsertion of implants on June 17th. I had tissue expansion after a BMX 12/10/08. Just looking for a nice place to hang my bra and not deal with the multiple numbers regarding exchange. Unfortunately listened to others when I should have stuck to my gut. I too had and still have a lot of nerve pain that thankfully is well managed by Neurontin Thanks for starting this thread |
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Linda54 Joined: May 2008 Posts: 1,723 |
May 10, 2009 07:43 am
Linda54 wrote:
sam1991 I am so sorry you are having problems and that your nipples have been delayed.... glad you are managing the nerve pain.....Are you getting implants replaced? Don't deny the diagnosis, but defy the verdict.........
Dx 3/7/2008, DCIS, <1cm, Stage 0, Grade 1, 0/0 nodes |
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sam1991 Joined: Jan 2009 Posts: 331 |
May 10, 2009 02:14 pm
sam1991 wrote:
Hi Linda, Yes, he is replacing my implants. I'm really bummed about my nipples being delayed. I'm also moving to Seattle in August so that complicates things even further. I'll have to fly back to MA if I want to have my nipples done by my current PS or find someone new in Seattle. Oh well....better that my implants are not under my arms!!! I meet with him again next week. Happy Mother's Day to you and thanks for the support. Kathie |
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Trishia Joined: Dec 2008 Posts: 234 |
May 10, 2009 02:28 pm
Trishia wrote:
Hi Ladies! I can't believe it is time to post June surgeries already! I am having Stage 2 of my DIEP done in NOLA on June 17th. How time flies!!! |
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cil326 Joined: Jan 2009 Posts: 58 |
May 10, 2009 07:33 pm
cil326 wrote:
Hi ladies, I'm too scheduled for 6/4 for exchange surgery. I want to get these hard turtle shells out. They've been hurting my girls whenever they come to hug me. I just finished my last TCH last Monday, less and less side effects as the week goes by. will keep you ladies posted about my surgery. Cil. BLM w/TE 11/24/08, TCHx6 1/15/09 BCRA neg
Dx 10/2/2008, IDC, 1cm, Stage I, Grade 3, 0/5 nodes, ER-/PR-, HER2+ |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 11, 2009 12:28 am, edited May 11, 2009 12:48 AM
by sassie62
sassie62 wrote:
Welcome to all that are scheduled for surgery in June. Thanks for joining us and sharing. I am sorry some of you ladies are having nerve pain. I just learned what a sciatic nerve was this year. Don't want to go there again. Nerve pain is the worst. I wish all of you the best and hope that we can support each other. I know I am getting the jitters as my time approaches - June 4th. If anyone can give me advise on how to get through these next 3 weeks I would appreciate it. I am concerned about fluid build up and abdominal bulges after the diep. I have read about others having this problem. Question for anyone that has gone to NOLA: Why doesn't Dr. D. order MRI or other types of Scans to locate the best veins to be harvested as a lot of other doctors are doing now for Dieps or Gaps? Even though I am having the Diep or Gap (what ever Dr. D. decides) I am very interested in all of the different types of surgeries. A very dear friend is having implants and she has so many questions. Like how do you know when enough is enough when they are doing the fills? And she wants the gummy bear implants and wants to know all about them. Also she was an A before she had a double mastectomy and she is wondering how does she determine what size is too big for her? She is 5'8'' and was a size 4 -6. Any answers to any of the above questions would be greatly appreciated. Sassie62 |
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Trishia Joined: Dec 2008 Posts: 234 |
May 11, 2009 12:50 am
Trishia wrote:
Sassie~ They do have you do a CT Scan the day before your surgery. No worries! |
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sueUK Joined: Jul 2008 Posts: 29 |
May 11, 2009 01:31 am
sueUK wrote:
Good morning from the UK girls! Thanks for adding me to your list Sassy....but Im LD flap...not DIEP....I hope lol!!!!! Do you know, its just really nice to belong to a group like this....obviously not at all nice that we are going through this, but if we have to be going through this...its nice to belong to a gang lol! Sassy, I kind of developed the skill of just putting 'the next appointment' out of my mind until it comes around - a useful talent if you can rustle it up! But then, when it all feels overwhelming, thats what we are here for....to have a natter and get things off our chests.....before we get things back on our chests!!! Sorry, as you can see....I am an early morning waffler - I need to go to work now so wishing you all a nice day. Hang on in there girls! Sue x Dx 6/6/2008, IDC, 4cm, Stage I, Grade 1, 0/11 nodes, ER+ |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 11, 2009 11:33 am, edited May 11, 2009 11:34 AM
by sassie62
sassie62 wrote:
Dear Trishia & SueUK Thank you for the info and encouragement. Sorry SueUKI changed your Surgery to a LD Flap. I am glad they are going to do the scan Trishia it makes me feel better. I wonder which end they are going to scan? HA HA Since I won't know until Pre-op (after the hospital visit) which end they are going to take. What other tests can I expect when I go to the hospital the day before Pre-op? Question for Ci1236 & Sam 1991 what type of implants are you getting? Hugs to all Sassie62 |
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Emily2008 Joined: May 2008 Posts: 401 |
May 11, 2009 06:28 pm
Emily2008 wrote:
I'm joining the ranks, girls! Just found out today my exchange surgery is scheduled for June 4. I'm having my rt-sided TE exchanged, and my left-sided TRAM reduced. Cut me open, take stuff out, put other stuff in, slap on a couple of drains (again!) and send me home! Why does this all sound so stinkin' familiar? Oh, yeah! Cuz I've done it 2 other times! Sheesh! Considering all the procedures I've had, I would've been under general anesthesia 5 times in one year. That just can't be good for brain cells! Let's do it, ladies!!!! BRCA 2 pos.
Dx 5/14/2008, IDC, , Stage I, Grade 1, 0/5 nodes, ER+/PR+, HER2- |
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sam1991 Joined: Jan 2009 Posts: 331 |
May 11, 2009 07:27 pm
sam1991 wrote:
Hi Sassie, I'm not sure yet. I have my appointment with my PS on Thursday. I'll have more information after that. LOL. I noticed June 17th is a busy day so far. SueUK, My friend is going to see her son in the UK in June. I think it's an area called "Q"....I know that's probably not how it's spelled! Is anyone having a hard time sleeping? I'm so tired of Ambien as it doesn't really work for me. I tried sleepy time tea, which is mildly helpful (makes me have to get up in the middle of the night to pee tho) but I was wondering if anyone listens to relaxation tapes? I'm going to listen to a series called Graceful Passages tonight to see if that helps but if anyone else out there uses them I'd love some suggestions. Thanks! |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 11, 2009 08:17 pm
sassie62 wrote:
Dear Sam 1991 I have been so lucky to have found Gale Evo in Alternative Medicine connected with Beaumont Hospitals in Michigan. The first consultation (19 months ago) I had with her I told her what I was going through, what was bothering me physically and mentally and where I want to see my self in 5 years. She asked me a lot of questions and then made a relaxation/meditation/visualization tape for me. I have been back to her 3 times and have 3 tapes. The last one I am taking with me to surgery. I rarely make it through the entire 1/2 hour tape before falling asleep. She has a voice that is soothing. And it helps because she is talking directly to me. Believe me it has been my salvation when my mind won't turn off and I can't sleep. If you can find someone in your area that deals with cancer patients and visualization don't walk -run to them and make a tape. Unfortunately, with anything out of mainstream my insurance did not cover it. It is all out of pocket but sooooooooooooo worth it. Sassie |
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Jaimieh Joined: Jan 2009 Posts: 950 |
May 11, 2009 08:43 pm
Jaimieh wrote:
I have been on Lunesta since about 1 month after my mastectomy. It works most of the time. After chemo. I am going to change to melatonin (sp) but my psychiatrist wants me to wait until after I am finished with treatment. I am excited for my exchange but nervous about the anesthesia and the fact that they will be sending me home quickly afterwards. My surgery is at 10:15 and I should be home by 3pm and that makes me nervous. I'm not sure why but it does. I also kept asking my PS which profile would she be using and she said "oh I'll make sure I use the right one". WTH does that mean ?? I know I should just trust her because she really has done a great job with the reconstruction so far. She made sure that my TE looked natural to make sure I was happy so I guess I will just let this little issue go. She came highly recommended and this was by multiple women. Dx 12/24/2008, IDC, 1cm, Stage I, Grade 3, 0/2 nodes, ER-/PR-, HER2+ |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 11, 2009 09:01 pm
sassie62 wrote:
Welcome Emily2008 Big STAR for you for making it this far with a great attitude. What were the 5 surgeries you had in one year? Sassie |
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sam1991 Joined: Jan 2009 Posts: 331 |
May 11, 2009 09:34 pm
sam1991 wrote:
Jaimieh I've heard about melatonin. I've seen it at the health food stores. Any idea what is a good dose? I can probably ask the folks at the store too. They're really helpful. I love your avatar. You look beautiful. |
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sammyjo Joined: Nov 2008 Posts: 32 |
May 12, 2009 01:36 am
sammyjo wrote:
Sassie62, can you please add me to your list. Had tissue expanders removed beginning of Jan due to seroma and wound healing issues, it is all now healed nicely so will be having implants placed and breast lift. Thanks Sammyjo |
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Jaimieh Joined: Jan 2009 Posts: 950 |
May 12, 2009 11:46 am
Jaimieh wrote:
Thanks for the compliment Sam :) I sure don't feel beautiful these days, my head looks like uncle fester. I'm not sure about the amounts but I read a thread on it here in the natural section and I do know you have to work up or else you will be sleeping all the time. If you don't mind me asking what happened that you need to go back for an exchange ?? I hope it all goes well. Dx 12/24/2008, IDC, 1cm, Stage I, Grade 3, 0/2 nodes, ER-/PR-, HER2+ |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 12, 2009 02:46 pm, edited May 12, 2009 02:47 PM
by sassie62
sassie62 wrote:
Dear Sammyjo: Glad you joined us. Do you have a date in June? Sounds like you have had a long journey like some of us. I am glad that all is well now. Since they took the expanders out in Jan does the pocket stay open for the exchange? Does anyone have any ideas why some people have a lot of problems with seromas and some fly through unscathed. Is there anything one can do to avoid this problem? Sassie62 Dx 11/2007, IDC, <1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 12, 2009 02:51 pm, edited May 12, 2009 03:03 PM
by sassie62
sassie62 wrote:
If anyone feels like adding where they live in their postings it would be fun to see if any of us are close geographically. Jamieh - Talking about stress and sleeping. My doctor has me take a powder drink of Magnesium. It is called Peter Gilham's Natural Vitality Natural CALM The anti-stress drink out of California.Natural Raspberry-Lemon Flavor. Balances your calcium intake. It is also good for constipation. You put 1-2 teaspoons in hot water and drink it like a hot tea. She also advised Melatonin 20mg for its anti cancer effects. Sassie62 Dx 11/2007, IDC, <1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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Emily2008 Joined: May 2008 Posts: 401 |
May 12, 2009 04:19 pm
Emily2008 wrote:
Hi Sassie! Thanks for the welcome! I had a lumpectomy, 2 mastectomies at 2 different times, and several procedures for some stomach problems I was having. Counting my up-coming exchange, that'll be 5 altogether. Jamieh, I know what you mean about ps saying "I'll make sure I use the right one." My ps told me today that he takes 3 different implants into the OR with him and then based on what he's dealing with, makes the decision. I so badly want to *know* if I'll be waking up with a C-cup or what, but I'm having a hard time nailing him down. I don't think he's intentionally being evasive, and he's done a terrific job so far. I guess I just want some degree of control here, and that ain't the case!! BRCA 2 pos.
Dx 5/14/2008, IDC, , Stage I, Grade 1, 0/5 nodes, ER+/PR+, HER2- |
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Jaimieh Joined: Jan 2009 Posts: 950 |
May 13, 2009 10:26 am
Jaimieh wrote:
Wow Emily I am complaining about having another surgery and this will only be #2 I think I will shut up now :) I think you are right I want some control about what I am getting. I need some control over something these days. I tried but she really wouldn't say and she told me something about the pocket is what it is and no matter what expander you put in there it will only look as good as the pocket. I'm not sure whether I believe it or not BUT I have been telling my DH that my foobs look different and he couldn't see it but when I went to the appt. she asked which one I like and will match them. They are only a very little bit different and the fact that she could see it made me happy. I have decided that I am going to go back to have my nipples done afterwards. My DH just wants me to have 3d tatoos but if I have gone this far I will finish it off I would like to look as normal as possible. He thinks I am silly because I may have to wear a bra for somethings but I don't care I will wear the bra and be happy about it. Now I just gotta get thru my last chemo. and the crash that comes along with it. Dx 12/24/2008, IDC, 1cm, Stage I, Grade 3, 0/2 nodes, ER-/PR-, HER2+ |
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Kimberley30
Joined: May 2009 Posts: 20 |
May 13, 2009 11:04 am
Kimberley30 wrote:
UM wow, all you ladies are very through with the details .. is it bad that I am not that educated with what I am going through? ( I am hearing impaired, so that doesn't help it) I have surgery set up June 5th, for my tissue to be taken out and an implant put in, and a nipple will be made for me I think at a later date. I am scared and nervous that I was told I have bc. But my friends and this site has helped me keep back the tears. I Love u all ladies, we are all unique and God will see us through to the end of it! Kimberley30 Kimberley
Dx 5/6/2009, 2cm, Stage II, Grade 2 |
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sassie62 Joined: Jul 2008 Posts: 183 |
May 13, 2009 07:12 pm, edited May 13, 2009 07:18 PM
by sassie62
sassie62 wrote:
Welcome Kimberley30. Glad you joined us. Kimberley, some women find a doctor they trust and put their faith in him that he will make the right decisions for them. They don't want to know all the details. Other women (like myself) has to know everything I can about my illness and surgery. There isn't a wrong or right way. What ever you are most comfortable with. Make sure if you are hearing impaired that you take a tape recorder with you so that you can review what the doctor has said later. If you don't understand something he has said ask him to repeat or ask the nurse to take time to explain to you. Also it is helpful to go to your appointments with someone that can serve as your advocate. We were all scared when we were told. After eight years being cancer free I was told that the little nodule on my mastectomy scar was cancer. Then they found it in my right breast. To say I was scared was kind of an understatement. Now I am looking forward to reconstruction. This site is a great place to ask questions. Someone has the answer or can direct you to a site that will give you the information you need. We can reach out to each other because we have all been there and understand. Sassie Dx 11/2007, IDC, <1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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Kimberley30
Joined: May 2009 Posts: 20 |
May 13, 2009 11:16 pm
Kimberley30 wrote:
Thanks alot Sassie, My BFF of 20 years is going to be there every step of the way. She has cried more then me! Thanks for your kind words & encouragment. You seem very strong! Kimberley
Dx 5/6/2009 |
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sammyjo Joined: Nov 2008 Posts: 32 |
May 14, 2009 12:34 am
sammyjo wrote:
Hi saasie, thank you for including me on your list, sorry my surgery date is 19th June. I have wondered myself about the pocket and muscle but my surgeon assures me the pocket is still there i also wonder whether there will be more pain with the next surgery with everything resting for so long as he also has me down for a 2 night stay. I never went through the dreaded experience of fills because of wound healing caused through necrosis of the nipple, I had skin sparing nipple sparing bi lat. My surgeon said my seroma was caused by the mastectomy and reaction to the expanders, I had open wounds and seroma for the whole 3 months, once expanders were removed I healed completely within a few weeks. |
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