Starting Chemo October 2014
Comments
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BookLady, YOU *ARE* KICKING CANCERS ASS. it's a pu**& and doesn't stand a chance against our team! Visualize, plan, conquer!
We've got this!
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Leto, I did sign up. Class is 11/17. I am hoping to connect with other women in my area. Thanks for talking me off the ceiling today.
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Leto -
I didn't see you get an answer on this - YES, I developed very low blood pressure during chemo, despite drinking water all the time! Oddly enough, it seems to have improved when they measured the last couple of times, but earlier I was seeing BP numbers as low as 83/62. More often in the low 90's/low 60's. Not sure why, but the onc & nurses mostly don't seem too worried. The really low one, though, they kept me there and gave me IV fluids.
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Trying not to freak out. I just got a call from my MO wanting me to come in today as my liver enzymes are high. I asked the nurse if I should be worried and she really didn't say. She said that it could be from the chemo and Neulasta or it could be a lab error. She said if it was still high when we get the results tomorrow that more blood work could be ordered or imaging (CT or MRI maybe).
Now I am freaked out that the cancer has spread to my liver. I haven't even gotten to my second chemo treatment yet.
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hugs to you ilovecoasters!
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KiLin Thank you for the response. I have been worrying about this all weekend because the readings were so low. I'm sure my little bp monitor is not as accurate, and I'm probably worrying for nothing. I finally got readings back in the 90s this morning after drinking a liter of Gatorade and some Pedialyte yesterday. Did you ever return to a normal BP level? I wonder too, if the headaches I get are caused by this.
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First full day back at work, I seem better in the morning than I am in the afternoon. I have a slight head ache, am achy all over and my stomach feels iffy. I remember something about the shot in my arm would cause my bones to be sore so to take the Claritin for five days, which I did. I didn't notice that till last night. I have been sipping gingerale on and off today. I notice this feeling tends to get worse if I get over heated or cold. Tomorrow should make for an interesting day since I have to spend the first half of the day on the firing range in full gear which can go either way as far as hot and cold. I suspect I will have a 'airplane bag' in my pocket just in case I feel I am starting to lose it.
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Leto- I normally have low blood pressure but after reading your post I am wondering is it too low and is that why I am having these head aches and mild dizziness. I remember they gave me a packet with the Neulasta information but I was kind of freaked out about the possible side effects and was still wrapping my mind around getting a port in the next few days to read with any comprehension. I will revisit my info when I get to the house. I am so overloaded with information, I look to the posts to help me weed through some of the stuff.
Keep posting, this is helping me so much more than reading clinical trial information.
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Ugh. I have a wonderful case of thrush. MO wants me to continue with baking soda rinses and has prescribed Diflucan.
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Leto - Even though I have one more chemo to go (last one tomorrow - woohoo!), my blood pressure has seemed to improve the last time or two. Might be coincidental, since I haven't been doing anything different. I wouldn't expect the low blood pressure to cause headaches, but dizziness would be a logical consequence.
See if your doctor is worried - mine isn't, and I've asked about my low BP. He says it's a side effect of the chemo. So you might not need to be worried even if it is low.
Oddly enough, my migraines have gone away during chemo, as have my more garden-variety headaches. It might be due to the anti-depressant the onc prescribed to help with my neuropathy, since those are often prescribed for migraine prevention. Anyway, it's nice to have a small silver lining!
I hope you can find a solution for your headaches!
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Hang in there Mandy! These chemo drugs can have an effect on liver function. Maybe it will just be a change to one of the drugs you're getting. My thoughts are with you.
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Mandy - do whatever works for you to get some good rest tonight! Scanxiety - I've read this is the term for what we will probably experience and we will get better at handling it. How frustrating for you to finally be getting your Treatment routine down and have this come up. Sounds like you chose good medical care as they are taking care of you. We got your back. Linda
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I'm wondering if the steroids cause my newfound puffy face? I didn't think only taking them a couple of days would cause that. I look like a chipmunk. Considering cutting back in them just a little. In total I take 12 pills in 3 days. Doesn't that sound like too much?
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Mandy try not to worry too too much, I know it's hard not to. I think chemo really messes with the normal functioning of everything, especially the liver. I hope you have answers soon.
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Holly ... I don't know about 'too much' ... I am taking 2 Dexamethason 4 mg. morning and evening, the day before and the day after chemo ... plus whatever they are giving me during the infusion. I haven't noticed a chipmunk look yet, although my face and chin was pretty round and pudgy before all this started.
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I have to echo wendee, the key to coping IS focusing on the moment. My 17 year-old son, my youngest child, was killed in a car accident 3 years ago and I NEVER thought I'd get through that dark, deep and overwhelming despair. The ONLY way I found to cope was not to look ahead, it was too sad, too scary to think about the rest of my life without my boy. So my goal was just to get thru the next 5 minutes, that was all I could handle for the longest of time. I have emerged on the other side, I can smile again, I can sing along with the radio again, I can find joy in living, All things I was sure I'd never want again.
ilovecoasters, you CAN do this, you can! I remind myself of the droves who have gone before me. If they can survive this treatment, so can I! Start small, don't set yourself up to fail. If you are feeling physically well today (it's so hard to be positive when you feel miserable), start with telling yourself I can and I will do this. Reaffirm it frequently throughout the day, say it to others. Each time you successfully navigate a small hurdle give yourself a pat on the back. Do nice things for yourself, take a bubble bath, get a manicure or pedicure or a facial. Buy that book or see the movie you've been eyeing. Just treat yourself. Get out of the house and into that Florida sunshine, even if for a few minutes. I only dream about living in FL, in small doses the sun is so healing, rejuvenating. You CAN do this but it's your call on which mindset you'll do it with. You ARE in control of that! ((((HUGS))))
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Mandy, yep, I can only imagine it's very scary to get that call. Sending you big warm hugs to help you through the wait. Please let us know how you are. I'll be thinking of you.
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Becca, thank you. I know I need to get out of the house, it's part of the problem. Yesterday was a very dark day but I made it. You're right. I'm so focused on what's next instead of what's right now.
I am so sorry to hear that you lost your son. My heart breaks for you. I have a good friend who lost her youngest when he was 16. I just can't imagine..,.
As far as living in Florida, it was always my dream. I had lived in NJ until I was 21. I packed my car the day after I graduated college in 1991 and drove. I knew nobody. Fresh start. I couldn't imagine living anywhere else. We are 20 mins from Daytona Beach and 45 from the theme parks. Other than the bugs, snakes, tornadoes, hurricanes and oppressive heat during the summer - it's wonderful. Lol.
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Ilovecoasters, and everyone else. A friend who's gone through chemo gave me a tip about preventing thrush and mouth sores. She recommended starting the mouth was right away, same day as infusion. First round she had the sores, second round she started rinsing her mouth with salt and baking soda mouthwash right away and she never got the sores again. I took her advice and haven't had any troubles.
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though this is a small study, it does show actual physiological changes from meditation. You can meditate regardless of religion! I had a yoga teacher once that was furious that someone insinuated that she was a Buddhist, not Christian. I gently reminded her that they are not mutually exclusive.
There are also studies that show that stress can change your DNA. Would make sense then that meditation could too (for the better )
http://www.hindustantimes.com/lifestyle/wellness/w...
Wishing y'all a fantastic day. Ive caught my kids cold...trying to kick it's booty.
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The fun continues, I have a urinary tract infection. Probably as a result of the diarrhea from last week. I wasn't sure, but I went in anyway. Last UTI that I had resulted in a kidney infection. That was over 20 years ago but I remember that I wanted to die between the fever and chills and the pain. Don't want to go there again.
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Sjacobs - So sorry to hear you have a UTI, but glad you got it diagnosed and taken care of. Hoping that you won't get a kidney infection.
I got the second blood work results back and liver enzymes were good. Second chemo can go ahead as planned on Friday. My MO said that sometimes the blood sits too long at the lab and results get skewed.
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Sjacobs, definitely an unwanted problem, get better quickly so you have one less to deal with.
Mandy! Great news, so glad to hear!
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ok ladies, my hair officially started falling out. I'm trying to decide when to cut it and go with the wig. How long before the loss becomes noticeable? I should mention that I have short hair, and it is blond and fine.
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Sjacobs,
I have an appt for 4 today to have my head shaved. I am dreading, but it's important to me to make the decision of when it comes out. I figure it's inevitable.
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Hugs to Sjacobs an Ilovecoasters!
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s Jacobs, my hair was a chin length bob and also very fine but dark brown. day 14 it started coming out pretty good 15 16 and 17 it was really pickrd ip and by day 17 I did not personally do going out without some sort of head covering but prior to that I have been fine .when it goes. It really goes
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Sjacobs146, I have it on my calendar when it should be coming out. November 15th is the day, so far my oncologist has been target on for everything else so I am going with that he is probably right. I have it on my calendar and I planned to have it shaved down and start wearing my short and sassy wig the 17th at work so it appears seamless, but since nothing has gone the way I would have planned it I suspect it will start before then. I washed it last night and blew it out on a low setting but even my co-worker who helped me get it into some type of order this morning agreed with me it feels strange, like a synthetic wig and it won't curl at all and has no body. I know its just hair but I guess I want just a little control of something and with my husband being bald I never thought we both would be. Has anyone starting losing eye brows? I was told that it shouldn't happen but now I am thinking if you lose it in other places wouldn't the eyebrows and eyelashes go too. I have no idea how to draw on eyebrows so I would be at a total lost!
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She-Angel, my eyebrows started thinning about Day 18, the left far more than the right. Almost the entire outer half of my left is gone. I dread losing the eyebrows and eyelashes way more than that on my head. I signed up for the class offered by the American Cancer Society, Look Good Feel Better to learn how to camouflage the loss.
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Becca, My eyebrows and eyelashes only thinned and I never did lose them total. I also went to a LGFB class and learned how to draw the eyebrows on, put makeup on and lipstick. That was a turning point for me in my journey. It made me feel so much better that I didn't look sick anymore. Every morning I put on my face, girls and wig and confidently go to work.
She-angel, definitely go to a LGFB class.
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