Chemo May 2011
Comments
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What a way to spend a holiday weekend - with chemo SEs! Oh well, at least I have the day off from work tomorrow!
A big THANK YOU to all of you that are or were military. I appreciate the service and sacrifice.
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Hi ladies. I see I have had alot of reading to do to catch up. Sorry for you having SE and glad for you feeling good. I will have #6 of 12 on Wed. of taxol/ herceptin. Not sure If I posted or not but for you ladies in need of a nice free wig. check out the website cricketts answe for cancer. Also a very enduring story there. It has been real hot here in Wva last 2 days and doesn't help with feet and leg pain. ha. Someday we can all hopefully be doing a cancer and chemo dance together. Better and healthier day ahead for all of us. I really would not have gotten as far as I have without all my sisters on here by my side. Once again Thank You for being here .
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Plils, DebRox and all of you--- I love you!!!' thank goodness we have each other.
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I like that start date and end date! My start was also May 24th - I don't have an end date scheduled but it will be that week so I will just say July 26th for now! One way to look at it is we all started around or before Memorial day and we will all be finished sometime around before or around Labor day. Is that right?
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Hi guys, hope everyone is well today...
Start day May26th end for Chemo July 28th and then 6-7 weeks of radiation so will be done sometime in Sept I think....hope and pray......
Good luck to all of you beautiful ladies...
Lot s of Hugs
Pam
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Cyborg,
Right back at youuuuuuu.. We are here for you.....
Lots of love
Pam
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I am taking my late father flowers today to the cemetery - he was my hero as well as my mothers and a veteran of the Korean conflict.
I didn't have it in me to participate in the golf outing with my DH and DD or the BBQ with the rest of the family. I have my next chemo tomorrow so the anxiety and dread has already started.
Plus... I don't want to see well meaning family members asking me questions. I am normally 5'2" 125 I have lost 15 lbs my size 4 jeans hang on me, my face is drawn I look grey, my hair is 1/4 inch and splotchy.
Ok, thank you sisters for listening to my vent. I get nutty the week of tx.</p>
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Thinking about you, Beaglesgirl! I have my next chemo tomorrow too. I agree, it's hard to face family members' and friends' well meaning questions. Is it your 2nd trt?
Sue
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Beaglesgirl. so this is your second treatment? You will do fine, I did have anxiety before my second but it was ok. I am kinda like you with the anxiety, I don;t want to venture to far from home or to far from my hubby, and when he is at work I basically stay home, although I am starting to work a few hours here and there, so I am trying to make work a safe place for me also, as they are all good friends. But still have to deal with stupid questions sometimes, like what is your prognosis. I hate that question. I lost alot of weight too, but with me I could stand to lose more.
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I would cry if someone asked what my prognosis is bkj! Yes this is my second tx. I'm doing dd a/c and the first one knocked me on my arse. My kids will be on summer vacation starting wednesday and I feel like I am going to miss out on their summer.
I do realize it partially in my mind, my SE might not be as bad the whole time... And then the taxol will be a whole different ball of wax. All I know is the first a/c was a bugger but we all live day to day through this journey. I am just down today. -
Ok I have not started treatments yet, but today and last night I was coughing up some yellow gunk. (looks alot like snot). Should I let the doctors know?
I really dont want to delay more.
Candice
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Yes, call your doctor, it's probably nothing a little anti-biotic won't fix but better safe than sorry!
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Which doctor should I call , the radalogist/oncologist that I will have radiation with OR the oncologist that I will have chemo with. or my family doctor?
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38 years old-I agree. Keep safe and tell your Dr.
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I would call my oncologist, he's the one that's going to be giving you chemo, let him know who your family dr is and your radiation guy is and he'll copy them.
That's my opinion because out of all of my new doctors, I love my oncologist the best. He was the only one who was pro-active on my wound issues, my BS looked at it, said don't do anything more it will heal on its own in 2-3 weeks and dismissed me. My oncologist was the one who got me on anitbiotics when it got infected and got the wound vac on me.
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Speaking of family doctors, I have a question for you all. Until my bc diagnosis, I have been very healthy. I have a gyn that I see for my annual exams, but no PCP. Every one of my bc docs (surgeon, oncologist, radiation onc) have asked for the name of my PCP. I don't have one. Never needed to see doctors (except annual gyn exam) until now. Do those of you with a PCP find it is helpful to have one as a central point of contact? Or do you work everything through your MO?
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I rarely see my PCP, I have only seen him 3 or 4 times in the last 4 years.
My primary contact was the surgern and is now my oncologist. They have a round table that they all talk together. There is the radiologist, oncologist, surgern, breast health nagivatior, pathologist, another oncologist.
I think it is all good.
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Neecee. I do have a longtime pcp. She was the one who gave me the diagnosis, but since then everything seems to go through my oncologist. My pcp call me every once in awhile to check up on me and think that is so nice of her.
38 y/o I would talk to your oncologist first.
I work a 8 hour day tomorrow (my first 8 hours since diagnoses)and I am nervous I will get too tired to finish! I have clients booked so I would have to cancel them if I get too tired, but I guess I will do what I have to.
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Good luck tomorrow bjk66! Pace yourself, take breaks when you can. I am working through treatments, and have found that as long as I control my pace, I can generally manage to make it through the day.
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bkj66 - good luck tomorrow, i'm hoping that when my treatments start I'll only have to take a week off then can work the other two, but it's only a desk job. I used to be a hairdresser too, in my 20's.
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Hope it is an se free weekend for everyone.
I hope everyone is eating as healthy as they can right now. It is important to rebuild our bodies in between treatments. Protein is very, very important for muscle mass, hair growth and immune system. I've been eating cottage cheese and protein shakes with banana and fruit or scrambled eggs. I found a protein powder with added enzymes to make it easy to digest. Almond milk is nice addition to a smoothie. I also made instant pudding and added protein powder to give me the extra boost of protein.
Iron is important for the blood counts. Eat steamed or stir fried spinach. Red beets help boost your bodies rbc count. So does red meat, ugh, don't eat that often.
Watermelon is high in l glutamine and potassium and balances the electrolytes. Also adding freshly squeezed lemon to water helps detoxify your kidneys and liver.
Steeping some slices of fresh Ginger in hot water for 10 min makes a nice drink and alleviates nausea. If you need a little sweetener, add some agave.
Try to walk for at least 30 minutes daily. It keeps spirits up and keeps things moving.
Most of all, think positive, keep smiling. This is a hurdle we can all jump! -
Debrox - thanks for the pep talk! We can all get through this together!!!
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Happy Memorial Day, ladies.
You guys touched on a great topic; how to address friends' and family questions. So far, I haven't had anyone ask me anything really rude ; just inquiries about how I'm doing or offers of help. I did have two questions about what stage I was. But, I have limited whom I've told; only family, close friends and those that have a need to know (employer and co-workers). What do you suggest saying to those who ask retarded or otherwise inappropriate questions?
Tomorrow is treatment # 5 of taxol and the hair has thinned and began coming out heavily this morning. I have been dreading the idea of the wig. It's a beautiful wig but I don't want to HAVE to wear it for 5-6 months!
Hang in there everyone! -
Marybe, don't be silly. Of course, you should participate in this thread. No one is any more or less welcome because of their stage, which is just a number! We are all in this together. If anything, I think you are an inspiration. You look fabulous in your picture and your posts are very thoughtful and helpful.
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Yes, Marybe, comeback! I hope you are feeling ok, as we haven't heard from you in awhile.
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I agree with Patriotic, Everyone is welcome.
I started at the beginning of May (Actually the last day of April) at that time I thought I was a stage 2. I had many test done and now I am stage 4.
I tell everyone and any one. This Breast Cancer is not going to kill me!!
I also asked for a prognosis and was told that " we dont know for sure, I have see other with stage 4 have it go dormant for 10 years"
The number of stage is just that a number.
Tomarrow I will be having the setup for my raditation for my leg and arm; hopefully it will get rid of the pain and I will be able to move more again.
Daughters Kindergarten graduation is Wednesday.
I start chemo (I think) on Thursday.
Well I am going to try and get some sleep.
night night.
Candice
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Hey chemo pal, 38, Y/O, I am having chemo this thursday also because my doc is going out of town on my usual friday! We can cyber hold hands! I will be thinking of you!
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My second treatment will be tomorrow...trying not to get too nervous about it as I know that I have a long way to go until I finish these (doing 12 weeks of taxol and then 8 weeks of AC, followed by surgery and radition and ?). The first week was rougher than I expected, so I am trying not to feel overwhelmed. I'm missing my husband so much right now that it is hard to breathe (he died in November). I'm not sure why, but I feel more nervous about this second treatment than I did the first. I took a xanax before treatment last time, but I am worried that I will need something stronger. I guess I will play it by ear tomorrow.
Good luck to everyone else!
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Good luck Candice and Blondeelawyer for Thursday
A mass was found on the anterior of my vagina in March and gyno still doesn't know what it Is. I finally have authorization to get second opinion at UCLA on Thirsday. I hope I get to the bott of what it is. I hope I am not still bleeding by then too since the second opinion is a gyno. Yep. I know. -
Last Thursday was a great night, woke up Friday 3:00am with Nausea, vomiting and 103.5 fever -- spent last 4 days in ICU and Onc floor at my hospital.But looking at it another way, I had the opportunity to really be grateful to be alive and honor Memorial Day and really think about those who have given it all just for us.One day at a time. Ready for next round in my battle, the one we all share.Blessings to all.
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