Newly diagnosed, starting chemo in 1 week, terrified
I'm new to this forum and new to the BC "club," of which none of us wants to be a member -- but here we are. I was diagnosed on 2/2/11 with Stage IIIC, infiltrating ductal carcinoma, with 24 of 25 lymph nodes positive. It has been one helluva roller coaster ride so far -- you all know what I mean. Had a bilateral mastectomy without reconstruction on 2/25. I start chemo a week from today -- AC plus T regimen, with radiation to be started along with the Taxotere. I had my port put in a week ago today, and the area is still quite sore. Is that normal? Has anybody used EMLA or any other numbing cream before chemo infusions? Is it worth it? Any other helpful hints for someone who is terrified to go down this road? I always swore that if I got cancer, I would never do chemo or radiation because I'm an "alternative medicine" person. But I guess it's easy to say that when you're not "wearing the shoes." Everything changes when they give you the worst news you've ever gotten. Thanks for any words of wisdom you might have.
Comments
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scc218,
Sorry you are joining our club, but you will find much support from the group of ladies. What a ride this is true, but you can and will do it. I am doing TAC ( I get them all at one time). I have a port, soreness gets better. I do not use the Emla cream, they just spray mine with cold spray, not bad at all. You will find the preparing for chemo info so helpful. Also look thru the recent months threads for advice and join the April chemo group. I found the 1st chemo the hardest, fear of the unknown. Never thought I would have BC or do chemo either, how fast life changes.
One day at a time, we are here for you,
christine
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You will be fine. I went through chemo and radiation and then had complete reconstruction in charleston and NOLA. If you ever need to talk, let me know and I will try and help you any way I can. If you ever decide to look at reconstruction: I highly recommend Dr. Massey adnd the NOLA doctors. I wish you all the best. chemo is really not too bad--it is doable. Drink plenty of water and take the meds they give you. Love, heather
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Sooooo sorry you have to be here. Just know that there's always someone here to offer support when you need it. You're at such an overwhelming juncture right now. It does get better. And the port pain does diminish. I never used a numbing cream before chemo and it wasn't a problem.
(((((hugs)))))
Adele
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I am receiving the same chemo except all together (and neoadjuvant) and have had two treatments so far with 5 more to go. They are out of adriamycin here so they have replaced it with epirubicin, though.
I am 50, and have been fairly sedentary in terms of regular exercise the last couple years - but before that, I stayed in good shape for many, many years. I honestly believe that has helped me.
So far I have a bad week following each treatment, with days 3-4 probably the hardest. The second treatment was easier because I knew what to expect. I guess it is fair to describe the symptoms as similar to the flu - I have a day or two where I am very weak and don't want to even stand up for more than a minute - then it begins to get better. By the 6th, 7th day I feel a little tired but pretty normal.
I am also trying to walk 4-5 times a week throughout this to keep my strength up-although I'm back to work this week and just have not made time. I also recommend drinking at least two quarts of water daily two days before chemo and during the week following. Take the nausea meds they give - the nausea for me lasts about 4 days or so. Both times I have gone back following chemo (once 3 days after, and once 2 days) and gotten supplemental fluids to help me bounce back. I am also receiving the neulasta shot which they give a day following chemo depending on the regimen. They check my cell counts weekly and so far the neulasta has worked very well and I haven't had low counts other than being slightly anemic.
Hang in there - it is doable - my sister also went through TAC chemotherapy 4 years ago and was fine. She was 57 at the time.
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Hi there!
The soreness will go away, but it can take a while. Mine took two weeks at least - I am very thin. When you go for AC, drink a TON of water DURING infusion. I aimed for 3 liters (two of those big Poland Spring bottles) during the infusion. I found it made a HUGE difference with nausea. I didn't drink as much water during my third AC and really regretted it. Try to walk every single day, but especially the few days after your chemo. You won't feel like it, but you want to get the stuff moving through your system. Don't let it "sit" anywhere. I ate a very healthy diet during chemo and felt this really, really helped me. PM me if you want. You are going to be fine!
Be well!
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So sorry you are joining us. I was also staged IIIc - and I am almost 2 years out from diagnosis. Your port will feel fine soon. I never put anything on the port area for the infusions. Hooking you up is just a pin prick - no big deal. I did dose dense AC followed by Taxol. You will get tired, but you can do it. Follow the advice of others - find a chemo thread and you will get lots of support and help from others going through the same thing. You can also hop over to the stage III forum - lots of great gals over there.
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SCC- so sorry this is all happening to you (or to any of us, for that matter). The support you will find on this site is invaluable. I don't know how I would have made it through without it.
Please join the April 2011 chemo thread - those women will walk the walk with you day by day and you will become so close to them, you willl not believe it. My April 2009 chemo group is STILL close to this day!
I say YES to the Emla cream. Why not - even if it just helps a little? I put it on 90 min AT LEAST ahead of time - put a small piece of saran wrap over it, so it does not get on your clothes. You do not feel the stick AT ALL when you do it that way. A HUGE relief compared to getting stuck for IVs in your veins.
And, .... it took 2 weeks or so for me to get used to the port. I swore in the beginning I would never get used to it, but I did. Had to have it a whole year b/d of Herceptin, too. And after a while I just would forget about it for long periods. (Loved getting it out though - have to be honest!)I did a lot of alt supplements during chemo - saw an integrative physician who helped develop a regimen to support my immune system and deal with SEs. Send me a PM if you want more info on this.
And hang in there. Take it one day at a time. You can do this! (If I did it, anybody can.)
In sisterhood & support,
Amy
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SCC - it sucks to be here, but know that there's a lot of support here. You WILL make it through this!! I had a bilateral mastectomy, AC every 2 weeks for 4 treatments, and just finished 12 weekly Taxol infusions. Starting radiation in April and hope to have DIEP reconstruction in Oct/Nov timeframe.
First thing, take a deep breath and relax as best you can on your first treatment. I was distraught at my first chemo because it just seemed so unnatural to be doing what I was doing. Best advice I received was to drink tons of water (about 80 ounces) every day for 3-4 days leading up to chemo and 3-4 days afterward. Got to the point I was sick of water, so I switched to orange Kool-Aid.
I did use the EMLA cream - 60 minutes prior to my appointment, covered with Saran Wrap and plastic tape. Made the poke turn into pressure only. Also, take your nurse's advice. I was told to take Vit E, B supplement and D3. Took it religiously. When I started Taxol, they added 20-30g of glutamine to the mix, and I took that religiously. I had some neuropathy (slight tingling) in my toes and fingers with the Taxol, but that was it.
Definitely take your premeds before AC, and take Claratin with Neulasta (if you're getting the Neulasta shot).
Most importantly, if you end up with any kind of pains or other weird issues, tell your oncologist. There's a ton of things they can try to help you out.
I also agree with the "keep moving" advice. You're not going to want to, but it does help.
Deep breathe, and take one day at a time. If someone says they want to help, let them. And don't feel like you have to be the hero. Just focus on you when you need to.
Sandy
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scc218
I didn't find chemo to be nearly as bad as I thought. With all the newer drugs they really help to control alot of the side effects. I was able to work everyday...altho I know some people had it rougher.
I got the same drugs as you and then some.....
Mostly I just wanted to say hang in there.....i am in the "lots of nodes club"....and will be 7 years out in May. Best advice I can give you is ignore what you read....there are tons of us doing just fine many years out. So much of this is getting past the mental aspect of it.....the chemo will be okay.
If I can help at all let me know.
Jacqueline
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Hello from a fellow IIICer with a very similar dx.
Chemo is tough, but doable. The first chemo was the roughest for me, and after that many of the worst side effects were from the steroids. They can cause wild mood swings, strange energy bursts which can be very helpful for catching up on house cleaning and for some people, depression. Just be aware that added to the turmoil of a dx you may also have meds that mess with your emotions. I managed to taper down from the recommended dose which helped.
I needed the EMLA and used it 90 minutes to 2 hours ahead of the infusion. Exercise can be very helpful for keeping your strength.
Oh, and take the advice about checking your temperature seriously. When your white blood cells plummet you can become ill very quickly. I never ended up in the hospital during chemo, but father and sister both did.
Stage lll is a daunting dx but you'll find loads of support here and we'll pull you though the tough times.
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SCC,
When you start chemo, ask your chemo nurse for any tips regarding the sore port. I don't recall having that issue. Yes, this whole ordeal can be terrifying, but when I look back, at was all doable and none of my worst fears came to pass. I got through chemo and radiation and worked at the same time, and I'm thankful to be NED (no evid of disease) today. While this is an awful journey, in many ways I am a better person now...
Good luck to you as you begin, and we are all here for you!
Hugs
Bobbie
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SCC..Your port will be sore for a few weeks,I did use a lidocane cream on the port 1 hr.before,and covered it with saran wrap.I am sure you will do fine with chemo.I was so scared but they give some great premeds,I have to say I never felt sick.I even questioned my onco"are you sure your giving me chemo".I did know when my hair fell out.I also in the many nodes club,it will soon be 2 years for me.We are here for you.
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Thank you all so much for your replies! You're the greatest, and you make me feel so much better about everything. I also appreciate all the helpful advice about drinking LOTS of water, keep walking, and the use of EMLA cream. I will check out some of the other forums, too, as I know I will find lots of other good stuff on this site. Thanks, and hugs to you all! -- Suzy
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Scc...I was where you are at 5 years ago.....I had bilat followed by chemo then rads and ooph. It is a hard journey, but it is doable....I used Emla creme before chemo over my port....I would put in on, then put plastic wrap over it till I got to the clinic...it did help....when I forgot, they would use a numbing spray (and it was cold).....Take someone to eat with you to chemo....and to drink....I ate whatever I wanted to eat regardless if healthy or not....my preferences were apples, strawberries, watermelon, bread, potatoes, peanut butter on toast, chicken...I enjoyed strawberrie smoothies and DH would ususally go get me one when he went to get lunch.....Try to be as active as you can even if that means only taking a 5 minute walk....Do what you have the energy to do, but let others help.....Nap when you need to......I worked full-time throughout Tx....that gave me a sense of normalcy......5 years later, I only work 3 days/week!!. Be kind to yourself.....its one day at a time and sometimes one step at a time....whatever you are feeling is normal!!! Hugs to you....sorry that you had to join this club, but glad that you found the wonderful group of women.
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Hi suzy, Sorry you've joined us, but you'll be OK. I am almost " out" 6 years from a IIIC dx. It;s scary as he**. But it gets easier with time.
Come here often for support and reassurance, There are SOOO many os us stage III ers living Large!
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Hi Suzy,
Just want to welcome you the "club" and wish you good luck on your treatment. Take care.
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SCC,
So sorry your here, this was not in the plan was it? It's going to be OK!!!!!!!!!
I know right now you are feeling so many different emotions, its crazy, but like one of the other
sistah's said, just breath!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! I was dx in 2009, also a IIIcer, lots of nodes, My kids were 4 and 8 at the time. I got on my knee's prayed for Gods strength, and it came!!! You can do this! Here's some practical advice, I did use the cream with the plastic wrap, I just found it more comfortable, lots of water, although after, sometimes flavored waters will taste better to you.
Get those fluids in, that was great advice from all. walking, is good, you may not feel like it everyday listen to yiour body. Eat, eat, eat, I hope you have friends and family bringing meals
during your chemo week. You need to eat to keep your immune system strong, I would not worry to much
about what it is, I ate whatever tasted good, and I never needed a shot. Now I probebly ate to much, but it worked for me at the time. I am all organic now, and have lost all kinds of wieght, but that comes later, focus on keeping your body wieght healthy, I personally think it does really help. OK, here's somthing I want you to know about the chemo room, you will meet the most amazing people you have ever
met in your life!!! There are all kinds, you will meet sister's who will battle right along with you, your nurses will become your own personal angels. you will meet people that will inspire you in ways you never thought possible, it will become a very safe place for you. You will be kickin the
cancers butt, and feeling comfort where you could never think possible. I know it sounds crazy,
but I think most of the ladie's will agree with me. I have seen my son just turn 6 in Jan. I cried tears of joy, my daughter will be ten in 2 weeks! thats almost 2 years, Cancer free!! I am so thankful for all the options we have as bc patients, there are so many. you will see the other side of this journey!
THERE IS LIFE AFTER CANCER!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
AND DURING, THIS DOES NOT HAVE YOU, YOU HAVE IT!!!!!!!!!!!!!!!!!
WE ARE ALL HERE FOR YOU, I AM A LOCAL AT THE STAGE 3 SITE, THE WOMEN HERE
ARE SOME OF THE STRONGEST MOST AMAZING WOMEN, YOU WILL EVER KNOW, YOU
ARE NOW ONE , NOT BY CHOICE I KNOW, BUT LOOK FOR THE SILVER LININGS,THEY ARE THERE I PROMISE!!!
On your really bad days, remmember that you treatment is temporary, that you will get through it
and you will see the other side of this, and life will go on.
You, SCC are in my prayers, I believe in the power of prayer, I pray for peace as you travel this road you do not deserve, I pray you will be surrounded by people that love you, and I pray that
you will never, never loose your HOPE, we have lots of HOPE. This journey has so many phases
Denial is usually the first, I remmember liking that one, the greatest phase is acceptence and complete surrender, I am still working on that one! What I am trying to say is take it one day and one phase at a time. Sometimes one hour at a time, and then theres the one minute at a time.
God bless YOU, I mean this with all my heart, I am sorry I went on for so long, your post just touched my heart.
Please check out the 2011 chemo site, and please join us over at the stage 3 site, you won't believe the support, they are so wonderful.
Please PM me any time!
HUGSSSSS
stephanie
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I didn't use anything to numb the skin around my port. When the nurse went to poke, I just looked away and thought about hiking in Scotland.
They may give you a steroid called decadron (dexamethasone). It's going to make you feel crazy...maybe very emotional, maybe irritable or aggressive. If you're having dark thoughts about your cancer, it's going to amplify them. Just know it's the drug and that you're not losing your sanity. I'm usually about as emotional as Mr. Spock, but decadron made me cry over TV commercials and CSI. So not me.
If you find that chemo makes you constipated, start taking something like Senocot and stool softeners the day of chemo. Don't wait until you're constipated to take something.
I had neupogen shots every day for a week following each chemo. They made my bones ache something fierce! Taking a half-hour walk at lunch helped a lot. Stay as active as you can. You'll find it will help physically and psychologically.
Everyone is different. I didn't have a hard time with chemo, and I had TAC. Maybe you won't either!
By the way, I swore I would never have chemo or radiation, too. Not only did I have both, but at the conclusion of treatment, I asked my onc, "What else ya got?"
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I was quite surprised at how everyone got me all hyped up about chemo. Once my first infusion was complete I remember saying, that wasn't bad at all. Don't get me wrong - a lot of the chemo is cumulative so it takes time to build up in your system and then a few side effects start creeping up on you. Overall I got through chemo just fine. Definately get the Emla cream. I put it on the port area about 1-2 hours before my infusion (cover it with saran wrap to keep it from getting on your clothing) and had no problems. I even forgot it a couple of times and it wasn't bad without it either. Just take time to rest when you need to. Take care -
~ Leslie
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Scc Chemo is very doable. I was on 6 cycles of Taxatere and Cytoxin- I was just as anxious and nervous about my first chemo treatment. However, when I went it was DOABLE. If I had a choice to do it I would not, but since I had to..is it not bad. I am sorry that you had to join this club but we are SURVIVORS and you will beat this and overcome this. Hang in there it will be over, before you know it...best of luck! Sending you lots of hugs.
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So much GREAT advice here...... gotta love the BCO gals! AWESOME!
I will just put this out there for ya.
I was NOT good with needles. SO... I put the numbing cream on ONE HOUR before the POKE.. like I was told.... I still felt a tiny poke.............
THEN:
I put the numbing cream on ONE HOUR AND 30 min before poke........... NOTHING., Cannot feel a thing.
I was like you..... sore from the port for three weeks.... so.... this can be totally normal.
Bottom line with the Emla.... in my case.
1 1/2 hours before the poke...... TOTALLY NUMB!
Ps..... YOU CAN DO CHEMO !!!!!!!!!!!!! just take all pain meds and nausea meds as PREVENTIVE... do not wait until you FEEL pain or nausea....
Prevent Prevent Prevent!
You CAN DO THIS!
(((( hugs)))))
PM me if you ever wanna talk.... Laura.
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Hello, you and I were diagnosed around the same time, the same week I think, but I went back for more testing (I'm sure you did also) and finally started the first stage of three stages of my treatment plan which was chemo. Surgery is the planned second stage in 6 months. This week I had my second dose--Taxol. I had the port put in five days before my first chemo and it felt like a bee sting. This time it didn't feel as bad. I didn't use the cream either time.
This site has been very friendly and helpful in the short time I have been on here. I am wishing you the best and if I can be of any help or advice please do not hesitate to contact me, although I am really just starting the process of getting well it seems. Power of positive thinking! Christi
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Suzy,
You're gonna get through this just fine! So much wonderful advice from all the ladies here and of course, more support than you could ever imagine. Pretty amazing, that so many can come together and support one another without any other agenda, not caring about anything other than helping where we can. Complete strangers, but yet the feeling of being part of a big family is undeniable. Even for those who don't post and only read, these boards can be such comfort and solace...
As far as your port goes, my first one was in my chest, like most, and after about ten days, it had settled down nicely. I had my port put in on a Wednesday and had my first chemo infusion the next day. I never needed to put anything on the area when they accessed. Experienced nurses will access in a matter of a few seconds and it should be nothing more than a slight sting. I now have a port in my right arm and it's far less sensitive than the chest area, I barely feel a thing when it's accessed. The important thing to remember is that typically, an infusion port is a much better option instead of having to go through your vein for each treatment, that is definitely not ideal because the chemo drugs can cause damage to the veins and surrounding tissue, so the more direct route through the port is absolutely the best way to go.
Anyhow, you are going to do just fine and remember, chemo is a means to an end. With each treatment you receive, you will ultimately be one step closer to being healthy again.
Hang in there and above all, be kind to yourself, take good care of your body and be strong.
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scc218 , I'm sorry you are here in the club for 3's where nobody wants to be. But am very glad you were able to find us. All here are sensitive to each others needs and very caring and helpful. Yea we do get in little disagreeing tiffs once in a while, but it always ends up in group hugs. It's very scary anticipating your first cancer treatment with chemo. You mentioned AC an T. They always bring out the big guns for the stage III girls. Adriamycin, Cytoxin and Taxol. Hopefully your cancer center will educate you on what to expect with side efffects and give you meds to eliminate them. For instance, with my first infusion I was told that they would first infuse me with Emend (to prevent nausea) Benedryl (to prevent allergic reaction) and finally Ativan ( to relax me while the chemo was infusing). It was really fine. The onc nurses were very professional and made me very comfortable in a lounger with aTV and warmed blankets and tea while I sat there with DH. They sent me home with 3 more prescriptions to prevent breakthru nausea and vomiting. That's on SE in never really experienced due to the excellent care they gave me. The following day after Chemo you generally feel pretty good, but the third day and after you'll feel like you were hit by a truck and want to lay in bed and watch TV cuddled in a blanket. Try to take your over the counter pain meds for body and bone pain. I also kept Baking soda in the bathroom and brushed my teeth and rinsed with it as soon as I felt mouth sores starting. I found that if I stayed ahead of them the never develped into anything and disappeared the next day. Your hair will fall out in clumps by the 2nd chemo and you may want to have your hair designer buzz your head. I noticed that while on chemo, my skin looked really smooth and moist, actually healthy, I used my facial cream and eye make up and lipstick to make me feel still feminine. I bought a nice sythetic wig that matched my own blond shoulderlegnth hair, but hated wearing it , though it looked beautiful on me. It was to hot on my head, and i preferred going bald around the house with a little warming cap or scarf, Didn't really go anywhere much during that time. If you can check ou the chemo discussions about treatment on some fo the other forums :
Chemotherapy - Before, During and After
Regimens, side effects, and support from others going through chemo.
Barb
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scc, I've just quickly skimmed the great advice you've already gotten, and don't think I saw guided imagery CDs mentioned. Like you, I was always totally alternative in my approach to health, so wrapping my head around the idea of chemo was really tough for me. I fought it for many weeks, getting multiple opinions from several oncs. In the mean time, one of my SILs had given me a guided imagery CD that she'd used for surgery. That took away so much of my fears re. surgery, that I bought the one for chemo. You can find it here: www.healthjourneys.com It's the one by BellaRuth Naperstek, and I highly recommend it for calming your fears and helping you to visualize chemo in a more positive light.
Good luck. I'm sure you'll do just fine! (((Hugs))) Deanna
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I just can't even begin to thank you all. I really appreciate all your good advice, positive thoughts, and virtual hugs. I've been managing to keep a very positive attitude during this whole thing, but I know there will be some bad/dark days mixed in with the good ones. I'm a little worried about work. I'm self-employed and work from home, but the work still has to get done. And if I don't work, I don't make any money. I do have some girls helping me out now, so hopefully it will all work out okay. I also think that work will help me focus my mind somewhere else -- instead of on my troubles. Thanks again for all your words of encouragement!
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Suzy, just want to add my welcomes as well!
As for work, I have little kids, so I didn't work during treatment, but you will probably find you are OK on most of the days. You won't know until you start how you are going to react, but for most of the time I just felt "off" rather than out and out ill. And that was only for the first week after the infusion - I had plenty of good days too. So it is probable that you will find you manage with work OK.
I also made a point of getting up every day, getting dressed, trying to be as normal as I could. I tried to get out for a walk every day too, which I think helped a lot with the mental aspect of it.
Anyhow, I hope it goes well for you. It won't always be fun, but you will get through it. And come here often - you'll get the best support in the world!
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Suzy
Welcome to the club nobody wants to join. You will find comfort and support in these message boards
I didn't find the emla cream adequately reduced the pain for me. I had the infusion nurse use lidocaine to anesthetize the area prior to the big stick. I have them do this for blood draws as well. It makes it relatively pain free.
I am also self employed. I have seven employees who depend on every penny of their paycheck. My biggest concern when diagnosed with stage III breast cancer was (and still is) whether I will develop mets. My second biggest concern was how I was going to survive financially. I have a large overhead - if I didn't work I was going to owe a great deal of money.
I worked as much as I possible could. I was able to work one week on and one week off during the A/C portion of the treatment. I was able to work full time during the 12 weeks of taxol.
I also asked for thelp. My landlord was willing to wave my rent if I was unable to work and tack what I owed to the backend of the lease. Other physicians in the community were willing to work some in my office. My office manager contacted the insurance companies and worked it out so that if the doctor saw the patient in my office, the payment would go to my practice. I then paid the physician 1/3 of what we collected. They were willing to do it without getting paid, but I figured eventually they would feel resentful.
I know some people feel that chemo wasn't too bad. That makes me crazy. I though much of chemo was dreadful. Never the less, I completed chemo relatively unscathed and I am sure that you will too.
I am sending virtual hugs to you and keeping my fingers crossed that your journey will not be too difficult
Elizabeth
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scc218,
Adding my welcome! Sorry you had to join us, though. I worked during chemo. Had chemo on Thurs and took Friday off. Was somewhat back to work by Monday. Just don't ignore your body. If you are tired and need a nap- take a 15-20 min power nap. The pleasure of being your own boss is that you can do that and not get written up for it
I don't get to the boards as often as I used to (I'm back in college and overwhelmed with homework, hehe). The ladies here on the stage 3 forum are the best. I truly consider us to be sisters.
You can do this! (oh, a friend of mine used the cream and loved it; I didn't use it and the needle prick didn't bother me)
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Suzy,
There is an April 2011 chemo bunch just started, it's in the main forum list under "Chemo, Before, During, After," that's the group you will spend a lot of time with, they will all be doing their treatments the same time as you, and so you'll be able to share various difficulties and whatnot that come up and help you with tips of how to handle stuff.
Anytime you have a major problem during your chemo weeks, if the drugs they give you just don't do the trick, let's say you can't sleep well, let your clinic know and they will prescribe something new, often side effect drugs they give work fine, other times you need an adjustment. Drink extra water daily thruout the day, get in a walk or some form of exercise, sleep as much as you like, keep protein going daily. The good thing about chemo is, the effects begin to wear off a number of days before he next one, and that's when you'll feel more like yourself and can get some stuff done. As others said, you feel like you got a bad flu is the biggest thing, with body aches. If you find you need pain control, ask the clinic for it. You can call them midstream and they'll jump on it.
I'm glad I came here before, it has saved me so many times, I can't tell you. Enjoy your April 2011 chemo sisters, my month's girls are my friends, it has become a daily visit to socialize, give and receive support, and whine. Smile. GG
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- 9 The Political Corner
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- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
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- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
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- 775 Diagnosed and Waiting for Test Results
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- 50 Immunotherapy - Before, During, and After
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- 591 Pain
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- 109 Welcome to Breastcancer.org
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