Has anyone started a forum for Chemo in Dec 2008?
Comments
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Firni, I know what you mean about anxious for the return of taste buds. I bought a few new healthy-eating cookbooks and have even made some of the recipes. I have to ask my husband how they taste because they could be school paste as far as I'm able to tell!
I finish chemo one month from today. I am so excited about the possibility of feeling good again! No more stomach ache, nose bleeds, dry mouth, missing taste buds or painful fingernails. I won't know how to act when I have energy again!!!!
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Simvog, Your family is also in my prayers! I wish we could do something to comfort you.
Sonia
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Texas357 - I can't wait for you to start feeling better soon too! I wish I could give you my taste buds. I am eating everything and it's starting to show. Ugh. I haven't had nose bleeds but when I blow my nose at least once a day there is blood. Does that count?
Simvog, I'm also praying for you and your family. When I pray each morning, I always say a prayer for everyone on these boards and anyone going through these trials. It's just so hard and it seems that all I ever hear these days is more bad news. I pray that one day soon there will be a cure for this!
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Hi Divas, we had to take the kids to the clinic this morning due to high fever last night, my oldest had 104F when we went to bed
Since I took them in, decided to get checked as well. Thank God I did, I have an ear infection topped with a bronchitis & pharyngitis! Phew.. kiddo #1 as ear infection and kiddo #2 has strep. Now we're wondering how come hubby is still healthy??? -
mimiwhite #4 1-Feb 4xTC

mmliv #4 3-Feb 4xTC

Brenny # 4 4 Feb 4xTC

isasayers #4 6Feb 4xTC

horsercn #1 9 Feb (TH) 4xAC
+12 Taxol+Herceptin ptjen #4 11 feb 4xTC

CindaD #4 12-Feb 4xTC

swest #4 13 Feb 4xTC

iktracey #4 17 Feb 4xTC
apfuentes #4 17 Feb 4xTC
bkokie #4 19 Feb 4xTC
Texas357 T#4 24 Feb 3xFEC
+9xTaxotere Catrenae T1-T12 26 Feb-14 May 4xAC
+12xTaxol Romiles #4 26 Feb

DrDecker #4 4 March 4xTC

Texas357 T#6 10 March 3xFEC
+9xTaxotereMandy1313 #6 10 March 8xCMF
Lainey64 #4T 12 March 4xAC
+4xTaxol
simvog T1-T12 13 March-29 May 4xFAC
+12xTaxol LindaBusEd #6 18 March 6xTAC
zuffa #6 18 March 6xTAC

cebula #6 23 March 6xTC
Majanumba1 #6 23 March 6xTCH
Bold #5 23 March 6xTCH
sdavis #6 23 March 6xTC
Texas357 T#7 24 March 3xFEC
+9xTaxotereberrypatch #6 24 March 6xTC
Firni #6 25 March 6xTC

Texas357 T#8 31 March 3xFEC
+9xTaxotere Texas357 T#9 4 April 3xFEC
+9xTaxotere
Bold #6 13 April 6xTCH

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Look at all those smiles by our names!
Firni - my taste buds are pretty much back, but salt is still "off" a bit for me..... maybe I just got used to no salt and now I am very sensitive to salt in my food; don't really like it. Can't say that I feel great yet, but radiation and a touch of the flu probably have something to do with that!
Simvog, cebula/caroline - prayers your way for strength and health.
I have only three more radiation treatments (am doing 16). Am to start Femara Apr 1st. Onc was going to start me Mar 1st but decided to wait until I was through with the side effects from radiation. Will be getting a mammogram in April as well.... so April will start the "monitoring" phase of this cancer demon.
Mary L
ps still not noticing any hair growing..... but my scalp is getting itchy.... hope that is a good sign!
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Mary, I'm glad you posted about your taste buds. I was wondering how soon they will return to normal. I've got 5 more weeks of chemo, and unfortunately my wedding anniversary falls 2 weeks before my last treatment. A nice dinner would be a total waste of money on me!
I'm getting a little discouraged and impatient. I'm so tired of feeling badly and so anxious to start reclaiming my vitality. I was up most of the night with a stomach ache and because my nails hurt so darned badly.
On a brighter note, I've started thinking of what I want to do for the doctors who have saved my life. I want to get the name of the radiologist who spotted the cancer on my original mammogram, and send him a handwritten thank you note. I also plan to give small gifts to my BS and Medical Oncologist.
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I have a question:
How many of you had prophilactic bi-matectomy and how do you feel about the decision? I have been thinking of having my right breast removed just for piece of mind but my doctor said it is not necessary to remove it. Even if i go that route i can still develop bc in other breast tissues that are located outside the breast ( chest wall, abdominal wall, collarbone) and those will be much harder to find in an early stage.
Any thoughts?
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Simvog I had my cancer free breast removed as I wanted the surgery all at once. Even though it was my "cancer free" side, I have had problems with that breast for ten years...every year having biopsies, etc. Which is why I was floored when they found the cancer in my left. For me, it was the right decision. After talking with my breast surgeon...I knew that is what I wanted to do.
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Simvog, I too had both breasts removed. Partly because ILC can jump to the other breast more readily than ductal cancers. And ILC is very hard to detect. I really didn't want the worry and my onc agreed with me. I did not have cancer in the "good" breast but there was a lot of suspicious junk in there. It was the right thing for me to do. Because my bc was caught early, and I'm having lots of chemo and anti hormones I'm feeling ok about not getting mets to the areas you mentioned. However, I do plan to be diligent on my annual tests and checkups.
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Good morning Divas. Wow, can you believe we were the December Divas? It's already March and almost Spring. As hard as this time has been, I have to say that it's passing pretty quickly for me. Of course, I can't wait until we can say it's Spring 2010 and we are all alive and healthy! And have hair again! I have let the hair thing bother me more than I thought it would. It's getting so warm here now and going out bald just hasn't been an option for me. I'm so self conscious. I always have been actually, with or without hair. But on Saturday I talked to God and said "heck with it" and threw on my ballcap and went out. No more wooly caps in 80 degree weather for this gal!
I am looking at my last TX this coming Thursday. I really can't believe it. I know I'll be faced with more pain and those wonderful muscle and bone aches but I can do it. Then it's on to rads. I'll still be here though.
Texas: I hope you're feeling a little better today. When my hands and fingers start to bother me I grab some ice cubes and hold on to them for a few seconds or so and that helps with the pain.
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Good for you Elaine
And yeah for the last treatment. And all went so quick for me as well, can't believe I'm almost there too. Love seeing all the smilies on the list. -
Hi my sisters: It has been a long time since I have posted here. I have been reading though and have kept you all in my prayers. I have 2 more to go. I can not wait till this fat lady sings. I have managed to gain 7 pounds. grrrrr. I will take care of it after rads. It looks like I am bringing up the rear on the TX chart. We are on our way to perfect health and balance in our lives.
Peace and prayers.
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Thanks for the tip Elaine. I may start keeping a bowl of ice, and a hand towel next to my keyboard on my desk.
I'm with you on the warm sunny weather and knit caps! I also went commando on Sunday, although admittedly no one else was home to enjoy the show. I figure once I get 1" of hair, I'll lose the hats. 2" and I'll lose the wig. We'll see how brave I really am when the time comes.
Bold, don't worry about bringing up the rear. I'm just a week ahead of you. We'll be drumming our fingers and marking off calendar days together!
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Good morning, Divas. It's been a week or so since I last posted, but I've been keeping up with posts and wishing you all well every single day. I'm finally starting to feel pretty decent again now that UTI is gone and my last Tx is nearly 3 weeks behind me. Next week I see the onc for bloodwork and to get the Rx for the anti-hormone drug. The following week it's off to the PS to get a surgery date for the exchange, which should happen the last week of March or the first week of April so I can start rads on or near April 20th. I'm a little nervous about the rads, but it is supposed to be easier than chemo so that's good news.
Elaine -- I'm self conscious too and never go out without covering my head with a hat, wig or scarf. The only time my head is bare is when I'm alone or asking my husband if my hair has grown. I do have a little hair now, but my head closely resembles a large, fuzzy billiard ball.
Simvog -- I had single mast, but would have had bilateral if I had known the seriousness of my Dx before surgery. Hind sight is 20-20, as they say. How is your MIL?
Lisa -- I hope you are feeling well and enjoying life now that your treatment is over.
-Bonnie
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Simvog - I also had both breasts removed (delayed reconstruction). My BS said that I had a 38% chance of having BC eventually in the right breast (non-cancer breast). It was a good thing I had double mx. The right breast pathology had DCIS which was not caught on the Mammogram or the MRI. The thought of doing mx, chemo and etc all over in the future terrified me. I just wanted to get as much of this over with. I am very glad I made that decision. I don't know that I could emotionally take this again. (I say that because with my mx and chemo my % of occurrence I believe goes down to 6%. I feel like those are good odds.
Elaine - FANTASTIC! The light at the end of the tunnel!!! I am so happy for you and everyone who is seeing the end of chemo!
Caroline - Yeah! Your final date is coming up real soon! I know you have to be excited!
Bold - I think I can hear the fat lady! That's a great sound!!!
Lisa - I think I saw a post from you on the reconstruction thread that you have your exchange coming up. That is terrific! Please let me know when this is and how things go. I am just meeting with PS on 3/19 to discuss placing TE's. I am nervous but excited for the process to begin.
Everyone have a wonderful week. I hope you all who are still taking treatments are feeling well and in good spirits! I think about you all often!
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Hi everyone. It does seem odd that we've started this journey together almost 4 months ago. Some of us have been on different threads thru our diagnosis and surgeries. For me it's been 7 months since my diagnosis. Now I'm looking at the end of this horrendous experience toward the end of this month. I thought I'd sail thru chemo just like I did the surgery. No so. Like many of you, it's been quite difficult. But all my cyber sister Divas here have helped me thru it all, even when I have been absent from the boards. I thank you all so much!! Any way. This is my bad week. I feel like a steamroller ran me down. Next week will be a bit better and then my LAST Tx on 3-25. I can't wait.
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Has any of our December Divas completely lost their eyelashes or eyebrows. Mine have thinned out A LOT! Right eyebrow is 1/2 as long as it used to be. Having to pencil it in. Eyelashes are starting to get bald spots. I am not looking forward to this look!
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Swest - I am 5 weeks along from chemo and my eyebrows have thinned to about half their thickness and the eyelashes are bald in spots. I STILL do not see any hair growing on my head.... though I think that I am finally getting hair on my legs; still no need to shave.
Bonnie - I am doing the dose dense in rads (16 sessions instead of 33 or so). I just finished #14 today and no problems; just a slight tenderness, still wearing normal bras and not feeling increased fatigue. In fact now that chemo is losing its hold on me I am feeling better all the time.
Biggest problem with radiation is the daily schedule, hope your center is close. Mine is about an hour away - for a 10 to 15 minute radiation session!
Mary L.
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Wow Mary! You are almost done with Rads. That is terrific! Cheers to you on Wednesday!
I am so jealous. I had to shave my legs and arms during this whole journey. It is so unfair...hair where I don't want it but no hair where I want it...... I did check my head and it looks like through the remaining attached hairs there are black spouts starting. I can't really tell to much but I like believing it's growing.
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SWEST: I lost all but 5 eyelashes (I'm babying the brave survivors) and about 1/2 the hair in my eyebrows. To me, that's worse than losing the hair on my head, but I sure want all of it back soon!
Firni and Simvog: I also was diagnosed with ILC and I fully expected my BS to recommend prophylactic removal of the healthy breast. My husband and I were pretty shocked when he didn't. I didn't push it. Guess time will tell if I made the right decision or not. It would have given me more peace of mind. Judging from the way my insurance company has been acting, I might have wound up paying 1/2 the surgical bills which I could not afford.
I go for Taxotere treatment #6 today (chemo #9 so far). Then I get a week off before starting my final three. Three weeks after that, I start 33 rounds of radiation. Then my husband gets his knee replaced and I become the caregiver.
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Hi Divas! I still have most of my lashes and my brows are thinning out quite a bit. I am using eyeshadow to fill them in. I decided to wear a cute derby cap with a scarf to work today. No more wigs! I ordered another hat online. It's a Betmar cap. Betmar has some of the cutest hats I've ever seen. They are pricey though. I got mine from Hats.com. If you order one, use the discount code "fiveoff" and you get $5 off your order! I hunted online for the code. I hate to buy fullprice... lol
I feel fantastic today. No SE's at all. Of course, I got for TX in 2 days. But hey, it's the last one so I'll be ready for whatever it wants to throw at me! I went to Curves last night to workout and stopped at the store on my way. I was wearing only a pink ballcap. So there I was with my bald head and ears sticking out. I wasn't self conscious at all but proud! When I was checking out a woman approached me and patted me on the shoulder and told me she was a survivor. She just wanted to say hello and wish me luck. What an awesome experience. I have found that since I started to "embrace my bald" and not hide it so much, I have received so many kind words and compassion from people. It's amazing. I feel like I've only been "half living" through this experience.
Texas: Good luck with your TX today!!
Have a great day ladies.
I love you all, Elaine
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Swest my exchange surgery is March 20th...and I'm nervous, but so looking forward to getting rid of these turtle shells! LOL
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Texas357 - I know what you mean about babying your eyelashes. I am doing everything I can to try to hang on to them. Gently washing my eyes when removing my makeup. Good luck on your treatment today! I will be with you in spirit!
Elaine - Glad to hear you are feeling so well! Thank you for the hat website with the discount code. I definitely love discounts! I will definitely check this out. I love your story. I have only been wearing hats. I have a white hat with a pink rhinestone ribbon on it (gift from a dear friend). When I wear it I get a lot of people either telling me of their own journey with BC or even their wife's story. It is very touching. I have been amazed at how many people are touched in some way by BC.
Lisa - Wonderful! 10 days and counting! You will do great! You are so good to your body so I'm sure you will heal very quickly. Everyone I've met on these boards say they can't wait to get rid of their turtle shells but I'm kind of excited about having that look/feel. It has to be better than messing with prosthesis. They are heavy and I hate the Grandma looking bras (not very sexy). I can't wear many of my old tops because the bra show the straps or the cup shows in the scoop neckline. No matter what bra you buy the prosthesis pokes out of the top of the bra. Not a good look at all!
Enough of the griping!
Good day everyone!
Sonia
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Lisa -
I had my exchange surgery back in November - what a relief it is to get rid of those expanders. In my case, I healed very quickly and had no problems. You are so healthy and fit, I'm sure you will do fine. Good luck.
Regarding the lash thing - my lowers are very spotty and the tops are thinning rapidly even though I am done with chemo. I'm still putting mascara on what's left but careful when I remove. I don't even like to rub my eyes in the morning!! Still drawing on the brows - someone said the brows grow back fairly soon. I'll be waiting....
Simvog and others contemplating - I had both removed and glad I did because they found LCIS in the "good breast" and I would have been going through another year another time like this one..
Hang in there everyone - there is health at the end of the tunnel. Anyone having SE's from Arimidex - I am 6 days in with lots of joint pain?
Bobbi
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We have a wonderful natural market near us and they had a lot of out of season fruit on sale. So I went and bought a few things. I'm so disappointed that all of it just tastes like water to me. DH says the red grapes and plums are really good. It's sooooo frustrating. I have lost a couple of lbs tho. I just eat till I'm not hungry coz nothing tastes like anything. One good thing I guess.
Sonia, It is definitely worth having the expanders. Mine have not even been that uncomfortable. I'm over-expanded now and feel obnoxiously large. But I have been able to lay flat on my back and on my sides without discomfort. Even tho the expanders are turtle shell hard, it will be worth it in the end to have soft, squishy breasts. I hope your expander journey is easy.
I've not heard back from the PS office about moving my exchange date up from May 27th. It's been almost a week so I guess I'll call them today.
Lisa, I know you didn't have problems with your expanders either, but how wonderful to get the real deal in a little over a week. I'm really excited for you.
I'm so close to everything being done that I'm actually starting to get excited. Spring is coming, the weather is getting warm, I'm starting to feel alive again.
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By the way, my right eye has bald lash spots but not the left one. I'm not using any mascara because I don't want to have to rub to remove. I do use a wider line of liner along the lashes tho. My brows have thinned out to about where I would pluck them anyway. So far, no more has fallen out. What will we all do when we have to actually groom ourselves again?
My fingernails are hanging in there.
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Hi Divas. It sounds like thinning brows and lashes are pretty common with all of us. It's almost 3 weeks since my last chemo and my lashes are thinning and brows have practically disappeared so I'm using eyebrow pencil and powder, eyeliner and a little mascara. The hair on my head is filling in and beginning to grow but is still barely there. There is also stubble on my legs, but none under my arms. My fingernails aren't in the best of shape, but I keep using the Hard as Nails polish and they are at least staying put. I should get my exchange date on March 23 and it needs to be soon after that because the radiation onc wants to start my rads by April 20 and I need to heal from the surgery.
Wishing everyone a good day.
Mary L. -- Congrats on getting through rads so well! I hope to do the same.
Lisa -- You'll do great with your exchange and recovery! Keep us posted.
Bonnie
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My eyelashes have blad spot though out. Still wearing mascara but only if I get out of the house, makes me feel prettier
especially since it's warmer out and I completely ditched my scarves! Eyebrows are thinning as well, but since I have always had very thick brows most people aren't noticing. A couple weeks ago, I was out with my MIL and when I left, the first thing I did entering my car was to take off the scarf. She had until now refused to see me bald, I never pushed until it got warmer and told her she would have to get over it. So that night, I decided she would see it, I purposely didn't wait to remove the scarf and drove by her car. The next day when she talked to hubby, she told him that she saw me bald but I didn't know about it
LOL! She said it wasn't as bad as she thought, so I was night walk completely bald into her house, her first words were "you little brat" hahaha, but she did fine. -
Hi All I have not posted in a while but have been reading. It seems like a lot of you are finishing up your treatments, that is just GREAT NEWS!!! I met with the onc yesterday and she did a lot of blood work and then she went over all the vitamins she wanted me to take. I have to take 1000 Vitamin D, 1000 Calicum and 1 multi vitamin and 1 fish oil. Also I started taking the tamoxifen today. I feel ok just very moody today, I don't know if it is the drug or I am just moody. I meet with the PS tomorrow to sign the consent for my reconstrution surgery which is scheduled for 3/26. I will also go for the pretesting tomorrow so more tests!!! Is anyone having a reduction on their good breast? I may have to have one on the left side. They told me after my last fill on the rt. side that they were pretty sure the muscle was strectched has far as it can go. And the nurse said that if they tried to fill any more that I would be to tight and very uncomfortable. So I will have more recuperating then I orginally thought.
I am so happy to hear that so many of us are finishing up and for those of you who still have a few txs left, just remember that you will get through it.
Hugs to all,
Colleen
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