first chemo done
Comments
-
Hi there !
Dinner done, kitchen clean and now my son is making me nuts with his math homework. But, have a little time to reflect here.
Busy site tonight. It has been quiet for a couple weeks and then seems to be ramping up a bit.
Cindy - Nice, as usual, hearing from you. Sounds like you are doing about as well as can be expected, although sorry to hear about that rash. As if you needed that on top of everything else. I hope for your sake that the doc can limit your treatments. It looks like you have been through enough. The "depression" and being really mad about not being "normal" - I am afraid appears to be a common side effect that affects otherwise strong women. If you were to page back through this thread, you will see a common theme of coming to grips with our own vulnerability and not liking it very much. For some reason, these type of women seem to have found their way to this thread. To be honest, that is one of the reasons I kept coming back here. There was a group of really like minded women who were strong, did not care to have a victim mentality, but were willing to support when needed. And all of us at one point were struggling with the fact that we were vulnerable. So... welcome to the club on that front - even if it was one you did not want to join. One thing I will tell you that might surprise you though, that through this I found that I could be vulnerable and my family still loved me, my co-workers still respected me, and the world went on. And despite all the crap happening to you with this, the core of who you are still stays - it can't change who you are. You will be "normal" again - and maybe a little smarter for all your trouble. Now.. hang in there. You can do this.
As for me.. yes, my skin is terrible right now. My husband told me I looked "bruised" - and damn, if it doesn't feel that way. BUT.... I am done with the regular treatments. Today I had my first "boost" radiation. It was a lot quicker, but has a this scary looking contraption they put on the machine. It directs the beam right to the tumor bed site. This time next week, I will be done with radiation. You may hear a yell from Cincinnati that day ! And, I can get used to this braless thing. So far I have been getting by with wearing thick sweatshirts (OK... my boobs are not that big to begin with). I may go the cami route next week.
Comingtoterms - Hi. Nice screen name. Did I see somewhere that your given name was Tammy ? Anyway, welcome to our little clandestine thread. I always liked this thread for the reasons mentioned above, and also because it is in the wrong place on the board, started by someone who never came back, but seemed to attract a great group of ladies who just kept coming back to support each other as best we could. You have already picked up on the whole theme of us being the support system. You know, I have met a number of teachers going through this. All of them have said that the hardest part was not seeing their kids. But, I do understand that your doc doesn't want you being around them given the germ factor. I do know one lady who got her "fix" by going in once in a while to see her kids. Her doc seemed to allow that if there were "rules" about hugging and the like. My parents were both teachers (retired now), and very dedicated. So, I do understand your frustration with this. That said, you will be suprised at how fast the time can go. Now is the time to focus on you and getting better. You can't help them if you don't help yourself. Quite a conundrum, eh ? And yes, 48 is "young" by breast cancer standards - one rare benefit out of this ! Take care and let us know how you are doing.
mommy2dex - One advantage of being on a study is that they will watch her like a hawk. I do like her attitude. Also glad she is getting a port. I could not imagine going through this without mine.
Have a good evening ladies ! Welcome to all the new folks !
Jill
-
Hi Jill and hello to all the new ladies....
I understand the process and we will all get through this. They said it wasn't going to be easy. I just sucks what we women and some men have to go through the treatment.
Thanks as always for your support.
We just need to convince our family and friends to donate to research to end this terrible disease so our loved ones don't have to go through what we are experiencing.
I will anticipate hearing a YELL from you when you are through your treatment Jill....Can't wait to hear it!!!
As always...everyone stay positive and know we are all in this together....reaching out for hugs.
Cindy
-
cruise4life....research is certaintly the key. Relay for life is very big here in my small town. I have quite a few girlfriends who are very active with the cause who have been touched personally by this disease. Big fishing tournament coming up in a week actually with procedes going to relay. Hope you are well tonight and have a good weekend.
Miss Jill, I too am excited for you and am also looking forward to hearing that YELL next week.
You are all in my thoughts. Til next time Shannon(mommy2dex)
ps. I am going to set an appointment for my first mammogram. We have a strong family history and now mom....doc says 33 is a good time to start . Boobie smusher here i come
-
Hello, Ladies !
Cindy - Thanks for the kind words. I will be sure to yell extra loud. Doing relatively OK. While radiation is much easier than chemo (at least it is for me), it does have its own issues. My skin (particularly under my right arm) really hurts. Got that radiation fatigue too. Just a worn out feeling. Kind of like chemo fatigue but without the haze.
You have a great attitude (and forgot to tell you that I really liked the new picture). Hope you are doing well tonight.
Shannon - Where exactly are you located ? I was just having another conversation with another woman on this thread (Debbie) about fishing. Also, given the strong family history you mentioned, has anyone in your family undergone BRCA testing ? It is a very expensive test and you or your family member will need to be referred by a genetic counselor for insurance to pay for it. But, if the link is there, might be worth considering going to see a genetic counselor to find out if the testing is warranted. Who else besides your Mom has breast cancer in your family ? Also prostate cancer (at younger than 68), ovarian cancer and pancreatic cancer have been shown to be potential indicators for passing of the gene mutation. Any of that in the family ?
I did have the test and was thankfully negative for BRCA 1&2 - which was great news for my daughter and sister as well. But, the genetic counselor told me that the rule of thumb is that a daughter should get her first mammogram at 40 or 10 years younger than the Mom's diagnosis - which ever comes first. In my daughter's case - that would be 33 (assuming all that research money has not eradicated this by the time she gets there !). Insurance also paid for my sister's mammogram no questions asked despite that she is under 40 - because of my situation. Good that your doc is on top of this ! Mammograms are not pleasant, but I did have one of my oncologists tell me that I should wear a T-shirt that said "Mammography saved my life". She was not being dramatic because digital mammography was able to detect a very small but nasty tumor for me - that is how I found mine. I continue to think that someone was looking out for me because of the timing for which I had the mammogram. Much later, and I would have been in a big mess - much bigger than I am now. So.. you are talking to the number 1 fan of mammograms.
Hope everyone is having a great Friday !
Jill
-
Jill, I have found myself checking this thread throughout the day to see if there are any new postings. I have become attached to you in a strange way and find your writings comforting and genuine. You really have a way about you. I hope you will continue to check in on the thread post treatment as you are an inspiration and i am sure all of these ladies have been to you as well.
My maternal grandmother was a breast cancer survivor two times over. The first was a radical mastectomy in the 80's before they really knew much about how to treat breast cancer. The 2nd came in the 90's, another mastectomy. I feel like such a jerk now for not knowing more about the particulars as far as type and the such, but I was a kid who just took for granted that grandma was alright and still with us. Grandmas was also amazing and always joked that she didnt mind the loss of her breasts because she could pick a different size every day of the week. She passed away about 5 years ago of another type of rare cancer that was in the billiary duct.
When mom got the dx, I tried to get my hands on everything I could to find out more about this disease. I belive that they are going to test mom for the BRCA gene sometime in the future and my sister and I will both be looking into it as well. There is a place in town to have this done. We live in Florida, about 45 minutes away fron UF in a small town called Dunnellon. A few of my girlfriends have made it a personal mission to raise the funds to find a cure for this in our lifetime. One is a 29 year old survivor who has 13 members of her family positive for the BRCA gene, 6 of whom have had a form of cancer.
I will close for the night and hope you ladies dont mind me taking up room on your thread with my stories. I really did just take a shine to you all. Like speaks to like. I will be setting my mom up with a screen name so hopefully you will meet her soon. She will be the beautiful bald lady. Take care til next time Shannon
also, has anyone heard of or had a thermogram in lieu of a mammogram?
-
Shannon,
I feel exactly the way you do - like you found a wonderful secret - a quiet cove where you can let it all hang out (tee-hee) and just say what you need to say without feeling like you need to worry about how everyone who doesn't have cancer will react! Jill is like the "club leader."
Sometimes I feel darned funny - like I could write a great monologue on this "thing" (something that Lilly Tomlin could have performed) - that's on a good day. Other times I feel so angry I swear I could hurt someone. I suppose no one else except another "member" can understand. I worry about saying the wrong things in front of my 8 and 17 year old sons, I worry about my 23 and 21 year old daughters, and how this affects their (previous) feelings of being indestructible, and, now, their terrifying realization that the person who has been the hub of the wheel is sick.
My functionally disfunctional husband/ex-husband situation will have both men (among others) waiting for me post-surgery. Crazy, I know. But each of them always does what is best for the kids. This is a blessing. All four know that both of the adult men in their lives are there for them.
Any words of wisdom anyone wants to pass on before Tues. the 3rd would be happily absorbed. I feel like I am falling apart, I am frightened, I never thought before how losing a breast means losing half of what fed your babies and bonded you to them and helped them to thrive and become the people they are today.
How could something so beautiful turn on you like that .....
-
Well.. you ladies are certainly good for my ego. And there would be some on this board that would say that is not necessarily a "good" thing because I have plenty of ego to spare.
Shannon - Thank you for your kind words. Over time, I have found that I have become very attached to some of the women on this board to the point I feel closer to them than I do to some people I see every day. There is something to be said for shared experience. Also, there is a certain freedom that comes from being able to be yourself without fear of ramifications or preconception. I have actually met two women on this board in person. Another one I talk to on the phone once in a while. Some others e-mail back and forth. I have learned a lot from the ladies I have met here and am grateful to them.
As for coming on this board "post treatment"... well.. I got a LONG time before I am done with treatment, even though I am finishing radiation. I will consider myself "done" when I get the port out, which will be about a year from now. I still have 15 herceptin treatments over the next nine months or so. So.. got a while. That said, I think I would stay on anyway because a) it is good to give back, and b) I am interested in the idea of "surviorship". How does one handle that ? What does it mean? It is still part of the journey.
A couple of clarifications of things for you. The BRCA test is a simple blood test that will be sent to Utah. There is only one place in the US that does this test right now (largely given patent issues) - one reason why it is so darned expensive. If your Mom tests positive, then you should likely get tested too. But, be aware that it is a myth that breast cancer can only be passed on Mom's side. In fact, less than 20% of breast cancers can be linked to a hereditary factor. In the case of the BRCA mutation, it is passed on the X chromosome. As women have two of these - one from Mom and one from Dad - it can be passed on either side. So, pay attention to Dad's side too.
As for a thermogram - most people still consider that an "add on" to mammograms (meaning it will supplement the sensitivity of your mammogram). A thermogram detects subtle changes in heat that could indicate the forming of a mass. A mammogram detects the mass itself. I saw somewhere that mammograms could detect 85% of masses, while coupled with thermograms, the detection goes up to 95%. Most folks like the idea of a thermogram because it does not require physical stuff like the "smushing" - rather it works by infrared imaging. But, given the advances in digital mammography, I don't think it is a substitute. That is my 2 cents on that.
comingtoterms - Hi again. You feel free to say what ever you want here. There will be no bad "reaction". Although, I will say, that there have been times that I have been called out on things when I needed to be (even as "club leader" - which is a title I did not know I had). Looking back on it now, I am grateful for those times when those ladies called me out because I needed to be. My friend Debbie, for example, called me out when I was over doing it and basically told me I had to slow down. She was right. But, I needed to hear it. Sometimes a gentle "hit over the head" is warranted.
Anyway, your home life sounds a little crazy. Now.. one thing I have found out is that for the older kids (particularly girls), they sometimes don't handle this so well. And what you need to remember is that it is really more about them then about you. They are scared. However, as your girls are a little older, perhaps they will be be better about it. Also, I am impressed about how both the hubby and the ex are there to take care of their kids. Nice guys and nice support system. There are not a lot of magic words when it comes to kids because households and kids are so different. But, for what it is worth, I have found that being open and honest with them has been a good thing. Kids know when you are BSing them. I let them know, for example, that Mom's prognosis is good, but I am going to have to do a lot of stuff to make sure it stays that way. Some of the stuff won't be too pleasant, but it was important. I also let them know they would need to pick up the slack.. and to my surprise, they did. So, just not trying to be wonder woman helps. Remember, it is OK to let folks help you for once (that is the HARDEST thing to learn). For the younger kids, it made a world of difference when they came into the treatment center one time when I was getting chemo. My son, in particular, got to see that it was chairs (not hospital beds) - and there was even snacks and TV (way cool). Turns out my daughter had a mental image of her Mom being tortured. So.. unveiling what is really happening made a big difference in my house.
You know, I have often thought about the whole nursing thing and then your boobs "turning on you". I nursed both of my kids (liked to have never gotten my son weaned - he would not wean). It does make you a little sad when something so wholesome becomes kind of sordid. But, I suppose it is like that for a lot of things. We get older - things come apart a bit. Unfortunately it happens.
Will be thinking about you on Tuesday. Just remember.. take it one day at a time. This journey is filled with milestones. Check them off as you get to them. And realize for every milestone passed, it is one step toward surviorship. That's where you need to keep your head.. in the end game. Got it ?
You ladies have a good night !
Jill
-
Hello Jill my Bud!
Sorry ain't been around, the taxol is kicking my rear end..not only mentally but physically..I think I cried most of the day yesterday, today I am fine, go figger....at first I thought it was my nerves or that I was gettin depressed, but today since I am in a great mood, I can only assume it's the taxol...
Hope things are going great for you!! I read where you have like 15 more herceptin...I have 4 more taxol to go, then onto surgery...then the dreaded 10 million trips to radiation....I'm not lookin forward to the next Taxol, seems like I just get to feeling better and BAM! I'ts time to go do it again....fingernails are horrid, they're all going to fall off I believe, both big toenails will come off...I could live with that, but man, I can't live with the time when I get down like that....And everyone was right, it's cumulative, each time I get more tired and more wore out....Worrying poor Rick to death....
Oh well wanted to touch base with ya hon!!! Nice to see ya in here...................
Take care, Luv and hugs
Deb
-
Hi Everyone,
It has been a while but I am happy to be back. As some of you know I finished the last chemo. I never thought I would write those words and I can remember other people writing them and feeling jealous. So part of me is unbelievable thrilled to be done with it and another part aches for all of you. I pray, hope, wish, etc. etc. that none of had to go through this adventure. None of us know why we are chosen, it is just the unlucky card we were dealt. Through this however I can tell you that I have had an unbelievable amount of friends come to my aid (every chemo cycle I had 3 to 4 dinners delivered), my husband and our teenage daughter have become much closer, I have learned that it is OK to receive help from others, that I don't always have to be the "strong" one, and that other people really want and love to "give" to you.
Comingtoterms, I feel like I could have written exactly what you wrote, five months ago. I was also not suppose to get breast cancer. Also, premenopausal and only 50, in good shape, ate right etc. You will make it through this. This web site and others really will help you through the process, it has been a life saver for me. You are also allowed to feel sorry for yourself here because we really really understand. The teens that you mentor will be stronger because of you. Even if you can't work through chemo, visit with them and tell them what you are going through and that you are surviving and this could actually help them survive also.
I am going to see my plastic surgeon (PS) next week, I changed PS because I was able to get the pro! The nurses at my general surgeons office says he is the most handsome man she has ever seen. I think I better take my husband with me. Really weird having a really handsome man check my boobs out? Take care everyone. Kristi
-
Well... well...
Glad to see some "old timers" chime in. Nice hearing from you ladies.
Deb - I know all too well the cumulative effects of Taxol and how it can play with your emtions. You really don't have control of your emotions on that stuff. To make matters worse, you are very aware that you are behaving this way and that there is nothing you can do about it. Very frustrating. You know, you might want to talk to your doc about lowering the dosage for the last couple of treatments. I know Cristl was having some similar effects on the weekly Taxol thing and her doc lowered the dosage by about 25%. Another person I know on the weekly thing had her decadron dosage lowered because of the same thing. So, let your doc know what is happening. Maybe he can do something. Now hang in there. You can do this.
My friend Kristi - Well.. I know how you are doing as we have conversed, but nice to see your words of wisdom here. The new ladies can really benefit from your experience. Great news on the PS. And for the record, having a handsome man check out your boobs is a bonus ! A little "eye candy" is always a welcome thing. You can check him out while he checks you out. My husband always says "it does not matter where you get your appetite as long as you eat at home".
Have a good Sunday, ladies!
Jill
-
Geez I dont know if I can handle 4 more of these...I am soooooooooo freakin tired of it all...tired of my nose bleeding, hurting, tired of the eyes watering..tired of it all.....today I am ok, guess the majority of it finally left my body, if it weren't for the side effects I would feel normal...I plan on asking the onc, well the mid level assistant since that's all I see till the middle of the month about it.I'm probably just going to hear, yea that will go away, since that's her favorite saying. I told her last time, that's fine hon, but it's easy for you to say, you're not going through this. ..I hate being down like that....Oh and lost my baby toenail last nite, wonderful...
I apologize if I sound like a whining 2 yr old, I have just had every SE you can possibly get and it's getting old...
Hugs
Deb
-
Hi Ladies...
I wish that I would get an email when someone posts...I feel like an idiot not checking in to see how everyone is doing every day...I get lost in my own world and forget.
I am with you Deb from Ohio...Taxol kicked my a$$ and not liking the side effects... its been over a week and a half since my last session and I can now taste and feel a little like living again. I am on CT sessions going forward and not enjoying my next visit. WE WILL KICK IT....and it will get better.
Jill is an inspiration for all of us...thanks again Jill.
Kristi good luck at your PS visit...keep us posted.
Comingtogether...sorry I missed your Pre surgery and hope all turned out well for you. Sounds like you have an awesome family support system. Let us know.....we are anxious to hear.
Mommy2dex...you are a great support for your women friends...Keep them informed and join in anytime.
Bye for now...off to my weekly Onco doc visit and LAB.
Stay warm and well my friends....
Cindy
P.S. Thanks Jill for noticing my new pic...it was taken a few weeks ago on our dinner trip to San Francisco...we live about 40 minutes from the pier. We eat at Scoma's it is fabulous.....
-
Went today for #9, THREE MORE TO GO. Already achey.....yahoooo.................she did tell me she thought I was depressed told her how down I had been, so she prescribed Lexapro for me....so hopefully that will help a little...that's the worse part for me is being so down in the dumps, I'm normally a happy go lucky person and will do anything for a laugh, but I think the laugh has gone outta me. But I'm really counting on these pills. Took it when I got home, so far I don't feel sluggish or drowsey, guess time will tell...
And yes we will kick it Cindy along with the rest of the gals!!!!!!!!!!! And we will keep it gone. I'm trying to stay positive here. And I have met Jill, she's a doll, really smart and very inspirational...she's PM'd me several times cheering me up....
Take care babe
Hugs and Prayers
Deb
-
Hello Ladies !
Thanks again for the kind words. One of these days I hope to figure out why you think I am "inspirational", because I have to admit I don't feel that way most of the time. If I could figure it out, I would do it more often (and maybe get my teenager to pay attention!). But, I thank you again for the kind words. I have learned from everyone I have met here on this board, and to that extent, we are all inspirational.
Cindy - I have been to Scoma's and you are right, it is FABULOUS. It is where I found a liking for Dungeness crab (yum). I am jealous if you get to frequent it. As you might expect, living in the midwest, I only seem to get there when I travel west on business. But, every time I am in San Francisco, I make sure I get to go there.
And BTW, I agree that Taxol and its cousin, Taxotere, is a royal pain in the ass. It is a sneaky drug that plays with your emotions and makes you feel like hell. Let's just hope it is giving the cancer as much hell.
As for checking "every day" and feeling like an "idiot" - you check in when ever you feel like it. There is no prescriptive measure for that. You can set this thread up as one of your favorites and have it send you an e-mail. But, there will be days you won't feel like thinking about anyone else. That is perfectly fine. In fact, I got caught up in work and missed checking in for like 2 weeks and got called out by Deb at one point who wondered where I was (and threatened to come after me). But, that was because it was a little off my normal pattern. So, you post when you feel like it. It was nice that you thought to check on folks. Now... good luck with that next treatment. Will be thinking about you here.
Deb - Wow. I am happy for you. Only three more, and the damn doc finally figured out this was messing up with your emotions. Now... a word of advice... don't expect "miracles" on an anti-depressant. It will take a little time for these little buggers to work. There will be nothing instantaneous about it. At one point you will feel more "evened out". So.. stick with it.
That said, I did some research into this a while back and was astonished to find out that more than 50% of women undergoing chemo find themselves on anti-depressants at some point in treatment. I found that number astounding. But, clinical depression is all about chemical imbalance, mostly driven by how fast the body can "uptake" seratonin. Now, think about it - they are chemically imbalancing us all over the place right now on this stuff. So, it makes perfect sense we might be out of whack. So, do what you need to in order to get through treatment. I am glad they finally recognized it.
As for me - ONE more radiation treatment to go. Yee-haw ! My skin is actually peeling in some areas and I am unbeliveably sore. I have so much inflammation that I can be just sitting and feel pain in my boob. It even hurts to move my arm. Doc told me today that the effects of radiation are "cumulative" and that I probably would not hit "rock bottom" until about a week from now (oh joy). Also said it would take about 3-4 weeks until my skin returned to normal. Great.. get to be the braless wonder for a couple more weeks. Good thing I am not a busty woman (never thought I would be thankful for that). The upside is that my work folks kindly planned a happy hour on Friday for me to celebrate the end of radiation! I am really looking forward to that. On the other hand, the folks at work don't need much of an excuse to plan a happy hour. They would plan one if the weather was expected to change. But, more than happy to be the excuse this time !
Take care ladies ! Hope to hear from you soon.
Jill
-
Good Evening, Ladies !
Well... made it through the LAST radiation. Yeah !!!!! I am tired, sore as hell and happy to have another milestone out of the way ! (Cindy - Did you hear the yell in all the way over there in Vacaville?).
After the treatment, they gave me a "certificate" signed by the tech crew, congratulating me for finishing my course of radiaton therapy with "courage and determination". I thought that was a nice touch.
Doc says I will be sore and red for about another three weeks. But.. I can let these darn marks go away now, use deodorant under that arm, take a bath, and eventually wear a bra again, etc, etc. etc. Amazing what we take for granted.
Anyway, hope everyone is having a good night.
Jill
-
Congratulations Jill!!
-
Hi!
I have got to share this with all....
I haven't posted much as I finished my Chemo on January 7th. And I have been coming here and reading every now and then, but I have been reading and posting in the Rads section as I am going through my 30 treatments of Radiation (half ways through now)
Anyways tonight I discovered that I can now slide my reading glasses up on top of my head and they won't slide back down...Ya-hoo! Reason?!.....Because my hair is growing! I am so excited about this....for months my glasses have fallen back down if I tilted my head forward just a little...no hair to hold them up there. It was only two weeks ago my reading glasses would slide back down. But tonight nope.....I am finally getting enough hair to hold them in place.
I wanted to share this with the women who are still going through Chemo and have experienced hair loss....see there are things to look forward too....may be simple things....but these things are important
Take Care and as all of those have said before "hang in there the time will pass quickly"....it is true.
Remember..."healing begins with the mind". So be strong!
Denise/Onehalf
-
Jill...YES.....I heard the scream all the way from Cincinnati...CONGRATULATIONS......I am now really jealous...and hope to be where you are in a few months.....Now the healing begins for you and you can start your new life. Way to gooooo!!!!!
So glad you know Scoma's. There are many great restaurants in SF but we always go back to Scoma's for either lunch or dinner. The crab is the best...for sure. Check out their website as they share some great recipes.
I went back to my home page where you can click to get an email...should have seen that before..thanks Jill for telling me. I also changed my photo...my granddaughter took it this week of me and my new puppy Roxy who has kept me active....she's like a kid - gets into everything. LOL
Deb from Ohio...YEAH.....only 3 more.....me too...and looking forward to finishing and starting radiation. I maybe depressed but trying to handle it each day...and I am sure I will be really bad the next couple of sessions. I dread going to chemo now...knowing its going to give me those awful side effects...I am now just getting my taste buds back and not running to the bathroom every half hour. I can feel my toes and heels and my nails are turning black. I am sure it will be worse before it gets better. My doc thinks I am handling pretty good and will continue with the same regimen. Stay positive girl and keep those pills close at hand....I will ask my doc if I feel the need. Thanks for sharing....
Denise One/Half - Hi neighbor....good to hear from you again. You are halfway through your radiation...how is that going for you? Any input that you can share will be welcomed. Where do you go for treatment? Sac? Just being able to see hair again will be a joyous day for me....So it sounds like about 3 months after chemo the hair returns...awesome...can't wait.
I wear glasses too and mine feel really tight right now...and I know it is because of the weight gain...my gosh the last time I weighed this much I was pregnant with my son 40 years ago. I want to exercise and walk but I just don't have much energy. The weather hasn't helped either...maybe this is the depression that Deb from Ohio is experiencing....
Ladies...congrats on the milestones and keep posting your great thoughts and enthusiasm. We need to hear the encouragements.
Hugs...
Cindy
-
Yippppeeeee for the hair growth!!! Mine started coming back in a few wks ago, right after I started my Taxol rounds, so I know that feeling of finally...something is going right!!! Never mind that I have 5 eyelashes on each eye and next to no eyebrows...I am getting hair on my head!!(even if it is only 1/2"...) wooohoooo
I even lost the hair off of one of my big toes...now that is awesome!! When I first went in to my onco before starting chemo, I asked him if he could give me just enough chemo to kill the hair on my big toes...and he just busted up laughing....and told me chemo would not take the hair off my toes.....wait till I prove him wrong and show him my hairless big toe!!! Hey...you gotta celebrate the little things in life to appreciate the big things....RIGHT??
Also.. I am excited that I havent gained any weight...I have lost a total of 14 lbs..but it goes up and down.. ...but at least it's not weight gain!! Man..this steriod makes me hungry!! The day of chemo( which I had today) I want to eat and eat and eat......gessshhhhhhhh. I am still working so that helps me get some exercise. Also, I have basement steps that I go up and down for extra exercise.
Ok.. I will stop talking... that's another thing steriods makes me do...LOL
Love and Prayers to you all HUGS
~Belinda~
-
Ladies -
Hello from Cincinnati. The weather here is GREAT !!! Nice and warm. My flowers are coming up (gosh, I hope we don't get a freeze again). It is amazing how good weather can lift your spirits. I am even venturing out without a hat despite my limited hair. Too hot with the hat anyway, and the sun feels great on my head. Stares be damned.
Happy hour last night was outstanding. We laughed until we were almost sick. But, to my surprise, my group got me a framed poster about "Achievement" to celebrate the end of my radiation (and chemo) course. On the bottom it says "We acquire strength in what we overcome". I found it very touching. I am not one that gets easily choked up, but found myself a little choked up over that one. That one sentence summed up a lot of this journey for me.
This morning we had the infamous annual "Pancake Day" (yes, that is what it is called) for the school district Band and Orchestra boosters. Biggest event of the year for them and as I have one in the band and one in the orchestra (and both of them played this morning), I really needed be there - even if I did not indulge in pancakes. The reason I bring this up is that what struck me is there were two other ladies there - about my age - who were also in treatment for cancer. The funny part is that we found each other really quick (not hard when we are all in hats/scarfs or nearly bald), but there was this instantaneous bond even though we did not know each other. The other thing that struck me was "how sad". This school district is not huge, and to have three of us there who have kids in the band/orchestra (not the largest extra curricular by far) - says something about numbers. Kinda scary.
Cindy - You sould like you are doing a bit better these days. Nice picture. What kind of puppy is Roxy ? Kind of hard to tell from the pic. There are a number of animal lovers on this thread - yours truly included in that group. I think the pets run my house here.
Denise - Wonderful hearing from you ! And congrats on the hair and getting your glasses to stay up as a result. Amazing what we take for granted. But, doesn't it feel great to get to these milestones ? I hope radiation is treating you well. Congrats on your moving forward.
Belinda - Nice to hear from you too. Not long now until you too will be done. Interesting what you doc said about the hair on the toes. I lost hair EVERYWHERE but my arms (and even that thinned). Oh well.. goes to show how different we are. I am celebrating that despite getting my hair back on my head, I still have not managed to grow any on my legs and pits. No shaving ! Hey, I will take the positives where I can get them.
Take care ladies. Hope things are going well where you are.
Jill
P.S. Deb - I will answer your PM. Hope you are hanging in there.
-
Hi Girls...
Happy Saturday....the sun is shining and can't wait for SPRING.....move clocks ahead tomorrow night...Spring Ahead - Fall Back...LOL
Jill - Roxy is a Yorkshire Terrier....and she is so adorable. I have always wanted one...and my DH who was so against having animals since we cruise and travel so much...he broke down and let me get her. She has helped me through my rough days for sure.
Congrats on your celebration....sounds like there was so much love and admiration spread in your family.
Belinda...I have hair on my toes too....and it would be nice to get rid of them for sure. I have no underarm or leg hair and some sparce eye lashes and brows and very little in the v jay jay area...lol My DH says I have a black patch on the back of my head....so how can that be when the rest is all gray....????
BTW...How many more rounds of Taxol do you have?
Well this week is feeling good week until Thursday when I get the POISON again....and it starts all over again....
Keep celebrating girls and we will all be celebrating the elimination of "C" very soon!!!!!
Cindy
-
Cindy I also have a dark patch in the back of my head that never fell out....LOL And I would love it if hair never grew back anywhere but my head...oh and my eyebrows and eyelashes also.....but with summer coming up no hair on the "jay-jay" area would be sooooo nice...LOL
I have 8 more rounds of Taxol to go plus my radiation...if I opt for rads that is. I am wondering if they took the lump out, margins are clean, nodes are clean..after chemo what is left to radiate??
Jill nice to hear from you also.. and I am so glad you are having fun and living life to the fullest!! You are an inspiration to us all and I for one, appreciate it! Hugs
Hugs all around
~Snappy~
-
Hey Snappy...
I thought the same thing...if they got it out and then chemo is done...why radiation on the site where they took it all....But I am sure they know what they are doing...and all we can hope for is that the "C" doesn't pop back up ANYWHERE....
How is everyone else doing???? We want to hear...
-
Snappy, I think the way I understood it, is it's to catch any sneaky cancerous cells that might be left hiding...........at least thats the way I took what the doc told me about radiation..
On the good side, I went and had my mole looked at and he said it was NOT cancerous...course he took it off anyway...bout all that hurt was the numbing shot, but was so glad to hear NOT cancerous! I thought for sure with the way my luck was running, it would be...and it was so black...
Oh well, chemo tomorrow, and after that, 2 more to go! woooooooooohooooooooooooo
Hugs
Deb
-
Thanks for the replies:)
Cruise--I understand what you are saying...just at the point where I don't want one more thing to have to go through.. of course, I probably will..."just to be sure".
Deb--good news about the mole!! And good luck on your last treatments. Yiiiippppppiiieeeeeeeeee
The emotional side of the chemo has really gotten to me this last treatment(I take them on Fridays now) that and my financial status is really getting to me... I can't ever recall being this weepy...that's just not me at all. I think that's what I hate most about chemo.. it makes you something you aren't and so out of control... ECK!!!!!!!!! I have 8 more to go....this should prove interesting...LOL
Best of luck to you all.. whatever stage of treatment you are in. HUGS
~Belinda~
-
Cruise4life-
I do live in Davis, but my medical insurance is Kaiser so to do Chemo I had to go to Sacramento, and now for Radiation I drive to Rancho Cordova. Really when I look at waht all Kaiser covers ($$$$"s) I don't mind the little drives.
Radiation has not been bad at all.....I was told the same as mentioned above....If you have a lumpectomy then, the best follow up treatment is to do Radiation, because it willl get any hidden or missed placed cancer cells.
Radiation vs Chemo....Radiation is easier, except your side effects are now surface side effects.I have had 17 Radiation treatments (I will need 30 in all) and right now I am experiencing my skin in the arm pit area and the top of my breast feels like a rug burn.....this is not too bad as they have a "skin specialist" that keeps an eye on you and who is there to offer advice.
Too all the women on this forum who post pictures of yourself being bald.....I think you gals are awesome! Seeing these photos just made me feel stronger! I now know and can see I am not the only one!
Thank You for your strength.
Denise/Onehalf
-
Hello Ladies !
Have not posted in a bit because things have been a bit busy around here - but it is a good busy. Rather have it that way than not.
First, I want to address the radiation question - for those of you with a lumpectomy - I have seen the stats. Radiation in this context is a no brainer in terms of reducing recurrence risk. In fact, I have seen some studies that show up to a 40% reduction with radiation ALONE (i.e. without all the other crap we did). The rationale is that it finds the stubborn cells that are lurking in and around the tumor site. Theoretically, we hope that the chemo would get them, but attacking them systemically and "topically" makes sure we come at them at two different angles. I can't say as much for those still having radiation who went the mastectomy route, but I suggest that you ask your docs about the rationales.
For me, radiation was "easier" than chemo, but it had its own issues. The fatigue and skin irritation cropped up. However, after being a week out, I am amazed at how fast my skin is rebounding - and the number of people at work that told me that the "color in my face has come back" is amazing. Makes me wonder if I looked like a ghost before. I am still going braless, but I can see my way back at this point. It is a great feeling.
As for hair... well... eyebrows/eyelashes back in full force. Hair on my head is coming on nicely. The folks at work tell me it is "silver" instead of gray (aren't they nice?). My husband told me my hair "looked like the dog's" (we have a schnauzer). The sad part is that he is right. Me and the dog have the same "do". The upside is that it is really soft. I told him for a small fee I would let him carress my head. I got a kick out of the "V jay jay" comments. That is starting to come in too, which does not bother me a whole lot. BUT... the upside is that I am still not growing on the legs or the armpits. Score ! I will take the positives where I can get them.
Cindy - Yorkies are so cute ! As from the conversation above, you can tell that I also have a terrier. Great because they don't shed. But, they are also great fun - very loyal and feisty. Good luck with your treatment this week. Will be thinking about you.
Deb - Great news on the mole! That is one less thing you have to worry about ! Get through these last two now. You can do this.
Belinda - Sorry to hear the Taxol is playing with you. I hate that drug. Damn sneaky thing. Plays hell with your emotions and seems to catch up with you. How is it doing on the home front ? I am sure going through the job thing is not helping through all this.
Denise - I am still wearing a hat at work because the hair is not coming in as strong as I would like on top. BUT, it is coming in strongly on the sides and back. I have had several people this week at work tell me to forgo the hats. They said I can get away with the little hair I have because "I have a nice shaped head". They are so kind. I am getting more and more bold every day on that front. Now that it is getting warmer here, I might take them up on that !
Hope everyone is doing well tonight !
Jill
-
Good evening ladies. I hope this message finds you all doing well. Moms first treatment is in the A.M. and there are a million thoughts running through my head. But, the most important thing is that SHE is feeling strong and ready to get this underway. I cant imagine being as strong as any of you ladies. I guess you find the strength when there is no other option but to be strong. I am thinking of you all. Please keep mom in your thoughts as she begins her course. I am sure there will be more to post soon. Congratulations again Jill sounds like you are making great progress! I am looking forward to hearing from you other ladies as your chemo and rads continue to draw to an end. Til next time, take care all. Shannon
-
Hi Jill.. nice to 'see' you again! At home is where I can truly be anything I want to be...hubby allows me those feelings without judging or lashing back. It's more frustration then anything and hubbys lack of work doesnt help any. His unemployment ran out and of course we are in the area with the highest unemployment rate in the country
so work is really scarce in these parts. Worries over bills adds to the stress and frustration...but we are hanging on.. what other option is there?
Shannon....your mom will be in my prayers.. we all know that feeling of the "first" time. She will do fine and so will you.. just give her the love, support and patience she needs and she will get through it all. Hugs
-
Hi girls...
Well I am off in a little bit to get my labs done before my treatment tomorrow. I am not looking forward to feeling like crap for a week just when I am feeling great.
My insurance carrier called my doc and wanted to know why I wasn't working as the lab reports showed good results. Well my doc commented to them that he sees me and sees how worn out I am and how fatigued I am..so he is fighting the disability situation for me. GOSH they should experience what we experience to know how aweful the poison is....gee whiz.
Shannon...let us know how mom is doing we can hopefully help in words.
Snappy...is there community help for you...I mean some sort of cancer resources that can help you financially??? I would check into that in your local community...there must be helpful resources for you...
Jill...yes, Roxy does not shed and I am so allergic to anything. She is getting spayed in a couple of weeks so we will both be comforting each other...LOL
Denise...I thought you had Kaiser...I tried them once and went back to my HMO. I really love Sutter Solano they are great...I work in Rancho Cordova off of White Rock Rd. Since I commute so far my doc really doesn't want me to work for now...maybe when I start radiation treatment I can go back to work. I really miss my employees and being around PEOPLE it gets lonely staying at home and you can only watch paint dry for so long.....
Deb from Ohio...you and me only 2 more to go!!!!!!!! YEAH!!!! the countdown begins...
Well I better get to the LAB...
Hang in there ladies and keep us up to date with your happenings....
Cindy
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team