Member Since: April 24, 2008
Last Login: December 1, 2008
Location: CT United States
Occupation:
| Diagnosis: | Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
| Diagnosed: | February 22, 2008 |
| Type: | Invasive or Infiltrating Lobular Carcinoma |
| Recurrent? | No recurrence |
| Metastatic? | No |
| Stage: | Stage II |
| Lymph Nodes Removed: | 12 |
| Positive Lymph Nodes: | 0 |
| Tumor Size: | 4cm-4.9cm |
| Tumor Grade: | Grade 1 or low grade |
| Hormone Receptor Status: | Tumor has both estrogen and progesterone receptors |
| HER2/neu Status: | Tumor does not have an excess of HER2/neu receptors or genes |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Jun 16, 2008 05:34 pm
Starting Chemo May 2008Hi All, Counts were ok again, so I just returned from #3. No shot again this time, so I'm set until bw on next 2 Tuesdays. #4 (last!) will be July 8th. Family wedding Sat and reunion picnic Sunday this coming weekend. Should be past nausea by then (meds ready if not). Weekend will be my tired days, but I'll find shady lawn chair to chat with family and friends. Wig is ready, but I have scarf to match dress too. Either way will be fine. It'll be first time in 6yrs my folks and all 6 of us kids have been together. That's fun no matter what I wear or where I sit.
Still deciding about implants, but heavily leaning toward saline for both. I think I'd have better peace of mind with both saline, than the one/each type suggested by PS. I'll feel samples at PC visit 6/26 and have final discussion. But unless I see/feel something drastically different from the opinions I've heard and read here, I will still choose saline. Thanks for all opinions offered on both types. As usual, its great to have such info and support here. Especially from those who have been thru this already. Hope I can get past this and return that help to other newcomers. Hope everyone has good results and a smooth week. Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Breast Reconstruction, Created: Jun 16, 2008 05:10 pm
Saline vs. SiliconeHi, Thanks for your responses. I've heard various opinions on both sides here and on other threads. I know its truly my choice and I have to be internally happy and at peace with it. But it helps alot to have opinions from both sides. Thanks for all your help. Heard from one friend who had bilat and silicone last fall. Seems ripples are there but not visible in mirror, and no sloshing. They're a little softer than her real ones were, but not really flimsy. She says it's her new normal, they look great (don't look fake) and she's happy to be healthy again. That sounds like a good result to me, and one I could live with too. I plan to feel both samples in PS office 6/26, but so far I still expect to choose saline for both. I know I need to be happy inside and turn worry button off in my head. For me, I think that means saline. If I truly decide I don't like them later on, I can choose silicone next time. But from reading here, it sounds like that can be 5-15yrs away. In meantime, I too want to get healthy, get this over, find and see results of my own "new normal" and go on. Continued good luck to all whether saline or silicone. May we all have good results and get on to "life after bc." Will keep you posted. Thanks for all your help! Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Breast Reconstruction, Created: Jun 16, 2008 09:35 am
Saline vs. SiliconeHi All, I just found this thread and wonder if anyone chose saline implants? For mast side too? I had left mast and expanders 4/1. Will be having exchange late Sept. PS says if I choose saline on mast side (not covered by breast tissue), I will feel ripples on lower side of foob (external) . I will also (internally) feel the water sloshing around when I move. He says they no longer overfill saline implants (prior web research). It didn't fix ripples or sloshing and actually voided implant mfg warranty! PS suggests (and most patients chose) silicone for mast side and saline for booster. Saline booster is smaller size and covered by tissue. So no ripples felt, and less noticeable sloshing.
If anyone has had exchange with saline, I'm curious Do you feel ripples on outside lower side of foob? Are they noticeable enough to bother you? Can you see them in mirror too? In clothes? Through bra? Swimsuit? Do you feel internal sloshing? Did you soon "get used to it" and now not really notice it anymore? Are you Sorry you chose saline at all? If done over, would you have chosen silicone regardless of issues?
Does saline foob feel "like half full ziploc" or water balloon? Or do you like how it feels? What made you choose saline? Especially on the mast side? Personal medical issues? Fears of silicone issues? My research suggests hi-profile for mast side (under muscle needs projection, and hi fits better on my slim body frame). Also suggests low or moderate for booster (above tissue only so less need for projection). I'm 5'5" and 125. Want more cleavage than my small B's but don't want to look like topheavy or too projected on my slim frame. Also don't want hi-profiles to look like permanent Madonna cones!! Any opinions here? Can you/did you get nipple on saline mast foob yet? What type? Did you have good results there too? I have issues about silicone. Some relating to my history (more reactions, skin rashes past 5yrs) and some re silicone (MRI required every 2yrs for leak detection and migration vs my dense tissue). I'm also about to get a new job. Would I be able to go back to work (desk job-10mi drive) 1wk after exchange? Surgery will probably be a Tues and hope to go back by Monday latest!! Mast surgery went smooth and healed well. Pain meds 4-5days then Advil/Tylenol. Hope to do same with exchange. Don't want to miss too much time from brand new (hopefully) job! Following my initial lumpectomy, I chose full mast to avoid needing 6mo f/u MRI's. Waiting 1wk for biopsy results drove me nuts. Didn't want to have to wait 6mos to see if I needed more lump surgery. If I choose silicone, I think I would be worrying the whole 2yrs if I may have bumped it or if it may be leaking!! But don't want to be disappointed every time I get dressed or look in mirror either. My already-low self image (prior bc and now) needs all help it can get to get back up again. If that would be silicone mast and saline booster, let me know. Didn't get to try/feel samples from PS office yet. Just going by his verbal opinions. Will try to go feel them this week. My next official PS visit is 6/26. Need to decide by then about saline/silicone. Size is going from B to C. Fill is at C and looks ok to me. Now just need to decide type, profile, and official surgery date. I'm also looking for any opinions from those with silicone. It may help alleviate some of my fears. It also always helps to hear from anyone who is past a journey you are still going on. Thanks for all responses. Good luck and/or continued smooth recovery to all. Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Jun 12, 2008 05:23 am
Starting Chemo May 2008Hi All Sorry I haven't been around lately, but its been a depressing week. My friends had been amazed at my positive outlook since dx March. I still have positive outlook about my prognosis. But I think all the stress of the hair along with the job hunt are taking away my shortterm positiveness. I have temp agency interview Fri. A friend (with working car a/c) is driving me. She plans to apply with agent herself too. I may wear wig to agent meeting. But once I say my Mar-Jun gap is from surgery, and that I have weekly followup visits Jun/Jul, I'm sure they will know something major is going on. If agent is ok with weekly time-off (I already have skills for job), I may not need to interview with company. They may just ask me to start asap. Counts were low last week, but I hope they are able to do #3 on Mon and shot Tues. If so, I could start new job Wedn. Even if I do Fri interview in wig, I'm sure I will be wearing scarf to job sometime soon. 80-90's are expected rest of summer and my car a/c is broken. I can't rock the bald, but I do feel better in scarf or hat. Would it be stupid of me to just wear scarf to agent interview Friday and see what reaction is?? Scarf should not interfere with job duties. Company is in medical field. And they should see that my past skills qualify me well for the position. Dh says to wear scarf--Between time off I need, Mar-Jun surgery, and possibility of wearing scarf thru summer he feels there's no real way I can hide my dx. Just go to interview, tell them about weekly time off I need and see what happens. If they give me job, take it. If not, go to next interview. I really need the job asap and this would be easy duties for me in between remaining Txs. By time I need week off for exchange (late Sept) I would have had 2mos to show them that I can do job. I would also be at end of my 3mo agency trial period. If they can't give me week off then (small office-no coverage available) , I would have to look elsewhere. I may also wear wig to Fri agent interview. Then if they don't give me job, I could feel it was because of my weekly time off (small office) and not a discriminitive reaction to my being a cancer patient. Which do you all feel is my best choice. I'd like to be honest day 1, but also need job. I've been up since 3:30am trying to figure this all out. I also have PS visit today to make final choices re exchange (good-side-booster and saline vs silicone) No wonder I can't sleep. Let me know your opinions re scarf vs wig for agent interview asap. Meeting is 10am Friday. Thanks to all and may you all have a smooth day. Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Jun 6, 2008 08:11 am
Starting Chemo May 2008Hi All, Thanks for tips on my job issues. Website is great and will help alot too. I hoped full disclosure wasn't required but it's nice to have proof. Surgery is good reason for gap and followup visits (unless I'm done by then?) No other details. Rox, sorry for your problems. Hope you conquer them on your terms soon. It's supposed to be 90's here so I'll try out my safari hat and sunblock. Too hot for a bike ride I guess. It's way too early for this heat. Hope it's not a sign of how summer will be?? Take care and enjoy! Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Jun 5, 2008 10:30 am
Starting Chemo May 2008Hi All, Congrats Otter on your graduation, and Best Wishes to Rock and Nancy. "Time to Celebrate"!! We've all helped each other with the hair issues and s/e's. I have another topic I'd like help with--Re-entering the job market after bc. This probably belongs on another thread, but I wanted to start with you all first. Am I required to advise interviewer of bc dx? Is it dishonest to keep dx secret until after they hire me? Some say tell interviewer of bc dx and remainings txs. It effects staffing and he needs to be aware. I think admitting to bc in interview is too much info. Simply "surgery" gives reason for mar-jun gap in resume, and also makes him aware that I will need remaining time off in next few months. Giving "BC" info in interview could be used as reason not to hire. Once they hire me, I would feel more required to give further details (surgery was bc). They would also still have 2mo notice of time off needed for Sept exchange. I want to be honest, but also want to protect myself. Unfortunately, some of you are already feeling workplace discrimination of cancer patients (from inside). I am still outside but want to find best way to navigate around the sharks. I applaud those who have worked during tx. At times, I felt fortunate not to be working. But I also felt depressed or guilty to not be helping with $$ or not to have "normal" routine. I would rather have been working than not. Now I just want to get hired, get back to that normal routine, and close this chapter. Once exchange is done, I expect (hope) to be able to give 15-20yrs to the right employer. Just need to be given the chance first. Thanks for any opinions. Have a smooth day and a great weekend! Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Jun 5, 2008 08:28 am
Cysts not complicated, Getting results areJaly, Glad you have appt and may get answers that day too. Try to relax and enjoy June. Be proud! You have taken a positive step. Waiting and wondering would have only brought you more stress. Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: May 29, 2008 08:52 am
Starting Chemo May 2008Hi to All, Tx#2 went fine Tues. Counts still ok so no Neulasta this time. Hair is nearly all gone, but scarves are fine. Wig ok too for few hours, then I get migraines. I blew brake lines on my car on way to Tx tuesday. Glad I was already at stopped at red light! No crashes! AAA towed it home and Dx is fixing it. Wasn't needing that extra stress, but feel lucky it wasn't much worse.
I was on Ensure and Viactive yogurt pre-surgery. As long as I was eating real food, Onc didn't want me on them during chemo. And I was told calcium only but No daily vitamins. Seems like docs all have different ideas. No wonder we get confused (besides chemo brain??) Should I ask again? I liked idea of having extra protein, and probiotics help with immunity too. Today should be my last fill. Depending on my PS's vacation plans, my exchange is set for Sept 9th. I don't feel in a fog, but still can't truly believe this has happened. Helps alot to have so many friends here. Welcome to the new friends and good luck to all for a mild day and restful night. Enjoy Maui. Maybe if its crowded, our travel agent could book us for Aruba?? (Never been there either but heard beaches are great!) Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: May 28, 2008 07:57 am
Appt. w/ surgeon tomorrowTDR, I had a "dense area" on mammos last 2yrs. This year mammo was done at a different test ctr and decided area "looked different" than last year. Had US, MRI, core biopsy. ILC was cone-shaped 4cm lump above and under nipple, so I had left mast 4/1. Could have done another lumpectomy, but didn't want the 6mo mammos that follow that. Wanted mast and lump entirely gone now. Smaller dense area on right also tested clear. I was shocked my density (similar to my many other cysts) had grown to 4cm, but was glad new test ctr found it and that it is gone. I've also heard most of us have bc 5-8yrs before it is "visible" or found. Even if they had found my lump last year, surgeon said he would still have suggested mast due to my age (46-premeno) and dense breast history. I've tried to hold on to idea that all things happen (or are found) when they are found for a reason. Best you can do is have docs and surgeons you trust and keep at them until you get tests YOU feel you should have. And fight insurance co to get those tests done. Then no matter what your dx, you can always feel that you're in good hands and have done whatever was needed to fix the problem.
Good luck with your appt. and keep us posted. We're all here to help each other thru this journey. Janice
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: May 28, 2008 07:24 am
Cysts not complicated, Getting results areJaly, My added good thoughts and prayers are with you. Let us know if we can help anytime. Can they do another type of biopsy sooner but with a larger needle? Mine was a core needle biopsy and still seemed pretty tiny. Is the 4mos to allow healing from FNA or just some standard follow-up timeline? Keep that stiff upper lip. I have English/Scot heritage mixed with German stubbornness. I've dug it out many times in past months. Hope yours helps you too. Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: May 25, 2008 05:59 pm
Starting Chemo May 2008Otter and Rocket both nailed it. Hair is first thing we notice when we meet others (before smile, eyes). Its great we can cover the loss with hats and scarves. And cheers to those that can handle "commando." But simply needing the hat is the most outward display of the inward admission that we are indeed sick and recovering. My loss took 2-3days and came out in handfulls and pillowfulls. May leave few stragglers of bangs, but expect to cut the rest off by Tues. I like the style of my wig and others like it too. But I still "feel" like its fake. Its either too lose (blow away or slide off) or too tight (migraine within 4-5hrs). I'm sure alot has to do with my inner self not admitting defeat. I have a kerchief scarf. Its not pre-tied, but I just tie the tails in knot and go. Its very comfortable and no elastic to cause headaches. Haven't tried it is wind, but it seems that it would stay put. I will probably order a few other colors and maybe a turban style too. I also have a newsboy cap with a drawstring fit and a safari brim hat with chinstrap (for rides in Dh's hotrod later this summer!) These feel more like a fashion statement, than an admission of illness. I'm glad I've found a resolution to my hair battle. Good luck to others still fighting theirs. May you find a similar comfort zone. I never wore scarves before dx and was surprised to find I liked them better than the wig. May even keep a few for later on! Do they make scarves with built in SPF? Is there an SPF lotion safe for scalp during chemo? I was very sun sensitive before and have plenty of lotion for skin. What is best protection for scalp besides hats? Besides Sungrubbies, are there other companies that provide sun scarves? Add me to the Tuesday swimteam. After the hair trauma this weekend, I hope tx goes smoothly. Meds and goodies are ready! And 2nd (last) fill is Thursday. Good luck and smooth swimming to all my teammates. Is it Hawaii this week?? Or a peaceful lakeside retreat?? See you there. Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Breast Reconstruction, Created: May 24, 2008 07:49 am
May 08 reconstructions unite!Hi, Go back to PS 5/29. He may add a little more to foob. If I'm happy with match as is, he may not. If I don't do boost, then I'm done with fills. Decision now is just for planning purposes. Foob is softening again but still bigger than right side. Mostly I want idea of how it will look after expanders are gone. We'll see if he can give me better idea of that this week. Also need to decide soon silicone or saline. And then about the nipple? Tattoo?? Any opinions on that? Thanks. Have a great weekend! Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Breast Reconstruction, Created: May 23, 2008 11:53 am
May 08 reconstructions unite!Hi All, I had my first fill 5/15. PS advised that often implants (foobs?) don't have natural droop and are rounder than real ones. He offerred to add an implant (another surgery) to help mine match. I don't know if anyone truly has a matched set. There are probably some differences left to right. Mine were about 1/2cup-size off (due to scoliosis) but it never bothered me. It wasn't obvious to others and clothes and bras fit fine. Now, I don't think I want extra surgery, expense, and time to try for matched set. I think I'd rather have a close match and my health. I need to give my decision to ps on 5/29. Am I missing the benefit of this booster surgery, or is it truly a personal choice? Any opinions are welcome. ps-Hair fallout is happening. This will bother me more than unmatched boobs ever did. Wigs and hats are ready, just need to "get over it" in my mind now (and in the mirror). Have a good weekend. Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: May 22, 2008 09:56 am
Starting Chemo May 2008Tina, Sorry you couldn't sleep but here is a great place to come to. I did a 4am visit last week and it really helped. Our minds should have on/off switch installed during this process?? Guess not. Good luck to you and everyone else for a smooth tx and less s/e's. Enjoy the weekend! Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: May 22, 2008 09:46 am
complicated cysts appearances nonspecificJaly, My lump was solid and they did MRI-guided core biopsy. Took tissue samples (not liquid but looked almost like liquid) thru needle. Maybe your lump is both?? Maybe its swollen from the procedure and that's why it didn't deflate?? Try not to worry until results come in. Do you celebrate Memorial Day (honors veterans) in Australia?? Anyway, enjoy your weekend. Best wishes to you for good results. Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: May 21, 2008 04:59 pm
Starting Chemo May 2008Hi All, I was having a pretty good week and hardly any se's. Until the fallout began Tues morning (Day#16/Tx#1). Its right on time but still the pits. Pillow has more each day and it comes out like little paintbrushes in fingers or comb. No real bald spots yet, but soon I guess. I had wig styled yesterday and I liked it. It slides abit (on my hair underneath?) which "reminds" me that its there. Friend feels it won't slide once hair is gone. It seems to sit back further than I would like and shows alot of my already high forehead. Any tips to keep it in place? I've ordered a wig hugger. Will that do trick? If I can get it to sit still and in lower position, I'll like it and wear it more. If not, I'll be glad to get the hat/scarf I ordered from tlc this week. I have a picnic in VT Saturday. If tlc arrives in time, I may wear hat instead of wig. Its a casual picnic, but my first public event. I also see what you all mean about the fallout being nerve wracking. I'm sure once hat arrives (if not sooner) I will cut fringes and be done with this mess.
My 2nd swim in pool is 10am Tues. Glad to hear the s/e's may be less as txs continue. Hope that's true for all of us. Other than my cold (which I don't expect to repeat) I had very mild #1. 2nd (last?) fill is Thurs, but I already have ride there if I need one. Good luck to all and hope we can enjoy the holiday weekend. Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: May 20, 2008 08:56 am
complicated cysts appearances nonspecificJalydiju, What a great lady your Mom is. She probably doesn't expect you to help her or repay her. Being a strong and caring person yourself is a great tribute to your Mom. But I'm sure you will never stop being there for her (or making her proud!). Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: May 19, 2008 08:49 am
complicated cysts appearances nonspecificHi to all my new friends, Thanks for your kind advice. We are all in a special sort of stressful situation. It takes special friends to listen and understand. Glad we have each other. jaly & duke-Sorry you missed your granddaughter's special day. Find some comfort in hope that she will share many other special times with you in future. I've dreamt of being lost but I also dream of happy family gatherings and picnics. I know its stress of my dx and of feeling "out of control" of dh's health status. Hope to be past this in few months and back to the picnic dreams. Wish same for all of us. My adjustment to Mother Theresa quote is "I know God doesn't give us what we can't handle. Just wish it would be someone else's turn sooner. " Sometimes sooner doesn't come soon enough for us though, right?? Slept better last night. Also have decided to start looking for part-time or flexible work (for next few months). I think this will help me feel like I'm progressing back toward normal life. Also helps me feel like I'm helping with household again. I won't take any position that is too stressful, or that will not allow me adequate rest time and time off for dr appts. Just want to look around and see what I find. I'm don't feel sorry for myself. I have many blessings of family and friends. This is just short detour from what I (any of us) expected. But the stress shines light on other weak spots in our lives too. I've always been a "fixer". Just hard to break habit of wanting to or trying to "fix" all the troubles in my life and those I care for. Guess that's another lesson I am supposed to learn from my dx. Have a good day and a restful night. Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: May 18, 2008 04:44 am
complicated cysts appearances nonspecificHi All, Just reading about all the weird dreams! Last week I dreamt about my Grandma (lost her last July at 94!) I assumed that had to do with the first "Mother's Day". Just woke from nightmare about losing my dh. He's overweight and its causing bp issues (bp runs in his family too). Doc says he's (like a smoker) who's not ready to "quit" his bad habits yet. Still tells himself it will be ok. (I used to say that too until few months ago) My bc dx came from nowhere. I was the healthier one, and always thought dh's health would fail first. Since my dx, I worry even more about dh. He has doc visit June, and I expect he will have worse heart/bp issues or will get dx of diabetes. We also got news this week that friend's Dad (75) had bad stroke. I immediately thought of my dh. Is that silly? I know I'm just having a bad week, and stress isn't helping. I'm sure the stress of txs and related issues adds to the bad dreams too. Sorry to ramble on, but glad to have this "ear" (at 4am!!). I have followup bw visit Monday and may ask for some sleep meds. Sounds like they are common for us in this tx journey. Will also try to re-visit summer health discussion with dh. We're going on our first bicycle ride of season today (if I get back to sleep soon). We're avid cyclists but haven't been on bikes since last July!! Maybe that will be a good start to the conversation (again). Any other suggestions (other than meds)? Thanks again for "listening" and hope we all get some rest and happy dreams soon. Janice
Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: May 15, 2008 07:13 am
Starting Chemo May 2008Nancy, Sorry you had to come here but welcome! Where are your txs? My t/c's are at Gray Ctr. Lots of friends here but neighbors are great too. Maybe we can celebrate together when our txs are done!! Good day to all. Janice Dx 2/22/2008, ILC, 4cm, Stage II, Grade 1, 0/12 nodes, ER+/PR+, HER2- |
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