October 2013 Chemotherapy
Comments
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Uds I am glad we are chemo buddies we can compare notes! Saw my MO yesterday for a follow up appointment post 1st chemo. I had a whole list of questions which he patiently answered, great guy!
Other than my hair falling out and this persistent sniffle---who knew nose hair were so important- I'm good. Going to return to the gym today. I have not been there since my surgery.
I use biotene daily and also a fluoride rinse (make sure it has no alcohol) for my teeth. I also bought the spray and the gel. I thought the gum was a bit overkill. :-).
Hope everyone has a good day! -
I got rx for magic mouth wash yesterday. It better be magic even with insurance it was $50 for the bottle! -
vintage gal- did u try it? I don't think I can do it again. Mine was only $5 with insurance?? -
anyone else sneeze a lot? Also, although my nose runs I feel like it is dry all time too -
I used prescription Caphosol, got a sample case from my onc, for mouth sores. It is two ampules that you mix together right before you use them, then swish and spit. Cleared the mouth sores within 48 hours. Unfortunately, I think it is $$$. -
lgkgde- I don't sneeze a lot, but I am constantly congested. So annoying! I tried Benadryl and Claritin, but they dried me out so much that I was having frequent nose bleeds. Now I'm just living with the congestion.
schoolcounselor- I'm impressed that you're working out! I haven't been back to the gym since the day before surgery. I had been doing boxing, which I loved, but it's probably the worst exercise to do after a mastectomy! -
Those of you going to the gym, did your Onc clear it? I asked and was told no, too many germs. I was told to exercise in open areas, like walking in a park. -
hey ladies! for those of you with congestion, have you tried a Nettie Pot? i know it's old school and some folks think it's gross but now that im used to it, it feels so good. i do it every few days. i had to get creative with allergy and congestion issues when i was pregnant and breastfeeding since i couldn't take any decongestants. the Nettie Pot really helped, as did hot water with organic cinnamon and LOCAL honey. oh man...are we allowed to have honey?
had my first AC yesterday. wasn't too bad...kinda shcoking to get that A push. sucked on ice like y'all told me and have been rinsing with salt/baking soda water today. had to take my first antinausea pill last night....not fun times for sure. no vomitting, just a general sense of "i don't feel good" My Rx pepcid actually helped, too. I also made my first infusion room friend (yay) and have been e-mailing her today. it was great to talk to someone with the same doctor and nurses and such. plus, she is almost done with her treatment, so she is a source of inspiration for me. i go for my Neulasta shot later and she recommended putting a dot of lidocaine cream on the injection area next time so it won't hurt. cool!
thanks for all the compliments on my hair! i feel pretty bad ass, although a bit chillyit's actually a relief. now i don't have to try and style my hair while getting furry hands - eww. for everyone hesitiating, my advice is to go for it. we put on some music (Eye of the Tiger) and i actually shaved a bunch myself. i felt kinda empowered! fiance cleaned it up for me and it's all good. we will see how i feel when it's shiny bald, but im just honestly glad to be off the Taxol and onto something that will work. And, NO MIGRAINES!!!!!!
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Headeast, I'll find out today if my hearts good and I can continue on the A. MO did tell me not to worry if I couldn't have the A because there were a number of other options. My appointment is in an hour. My nerves are really getting to me, both with anticipating chemo and worrying I won't be able to get it. -
I couldn\t have the A because my brother had a heart attack. Onc seems ok with me only doing the other two.
I love my nasal rinse but I find the squirt bottle much easier to use than the neti pot. What a difference it makes.
Glad everyone is doing ok in spite of SEs. -
anyone know if we can be around people that had vaccination with live virus?
My nephew had 4 month vaccinations today and they want to come and stay next week for a few days. I emailed onc but thought I would check here -
DebD, I worry about neuropathy too. I have it in my thigh thanks to positioning during surgery. It feels awful and I am hoping it goes away eventually. I think it was this that made me question whether to bother with chemo at all. I am really afraid of heart stuff. I have an anxiety disorder and I can imagine me calling 911 daily during chemo and especially if I was on a drug that had known cardiac issues.
I think I have basically been thinking of chemo as a crap shoot no matter what we get. My tumour has metaplastic sarcoma features and this has been shown to not respond to chemo at all.
I am going ahead with chemo plan just to say I did. :-) (having a down day....may have a different perspective tomorrow or an hour from now) -
I usually post in Sept, but read here, to check up on all of our August surgery gals, and also because I started at the end of Sept.
lg, I wanted to reply to your live virus question. I asked about this when getting flu shots for my kids. MO told me that if they had the live virus nasal spray, I could not be around them for a week. If it is a different type of vaccine, I am not sure. -
Thanks for the info about the beta blockers. I've been on beta blockers for 20 years. No one ever mentioned it could help with A cardiac issues. My obgyn was totally against me doing AC because of the cardiac issues. I opted for it anyway, i couldn't worry about something that might be a problem years from now. Nice to know that the beta blocker could be a weapon against the "rare" cardiac issues from A. Only time will tell.
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Yes nose runs, I blow it, I sneeze, people must think I have an awful cold. But just as quickly it all dries up & is uncomfortable. -
Well, I'm sitting in a recliner in the chemo suite, watching the red devil drip into my body. Crazy how I was so nervous that I would not be able to get it today and yet it's the thing that will make me feel hideous in a few hours.
Hope everyone who has visited the chemo bar this week is muddling through ok.
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Scoolcounselor - I haven't been to the gym since having my bilateral mastectomy. My oncologist said the gym is germ infested and the worst place to be. I've been walking around the track at the highschool. I also purchased T25 by Sean. I am missing the camaraderie at the gym though. I had the regular group of ladies that I worked out with, we saved spots in the zumba classes and spin bikes for each other. Can't wait to get back. I was going to ask my onco if I could start back during the TAXOL treatment phase. AC is tougher and takes a toll on the body.
Day 2 after 2nd AC treatment, SE's are pretty much the same as the first time around. Still nauseous, queasy no real appetite. I did eat a half bowl of Cheerios with coconut milk. My onco said drinking is much more important than eating but it just makes the queasiness worse for me. Not sure how to get around it...advice????? -
Good evening girls, I'm on day 8 of tx #3 and am still having stomach cramps. I was told to take Prilosec but it doesn't seem to be working too well. Any ideas? Thank God I only have 1 A/C left next Friday. Does anyone know if you get cramps with the Taxol? I'm hoping it's easier than the A/C. I can't wait to be done with all this crap and move on. I actually have 5 days in a row with no appointments, injections or tests scheduled!!! Nothing to next Thursday when I see my onc. Try and have a great weekend everyone! I'm waiting for my grandbabies to come over for a visit:) -
Gramof2boys, I take 40mg Prilosec (omeprazol) -
kbee - thanks yeah my MO office called back and said one week. Good thing I asked! Thanks -
lgk, it is good to know. We don't want to get sick and make the guests feel guilty! -
Gramof2boys, I had the really bad cramps, I take prescription Prilosec don't know if it is the same OTC, tylenol 3, and xanax. I really think the xanax helps relax the stomach muscles and helps with the cramps.
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Hi Nicole & friends, I was in ER last weekend after having fever over 100.4 from 11p Sat and through the night. My dh dropped me off Sun 7a (my 9yr old woke at at 6:30a without alarm, never happened on Sun, so we drove out together.....speaking of God's power!). There was no wait in ER, I was put in a private room. Did blood draw & everything. By 11a, my temp was down, blood counts were all good. I was released. After arrived home, temp back up over 100.....sigh....but since blood counts were good, I decided just rest. Since Mon morning, everything calmed down. Bone pain was minimal this round. Did take 2 tyrenol on the last Neupogen shot day. That eased me pretty fast. So fever battle was the highlight of this round. Hoping for 2 peaceful weeks until the eve of Thanksgiving - 3rd tx! Wishing everyone a joyful weekend. Jen -
Lonnie, that's imteresting. My MO said I could go to the gym. Just not work out next to any obviously sick people. He also said I could walk the mall. He said there is no reason to isolate yourself. I started to feel like I would go crazy, then it occurred to me, I have TC on Thursday so this is the week I feel most like myself. My gym is also 24 hours so I can go during the times that have less people. -
Headeast - thanks for the positive information on the lymphedema specialist. I was thinking about asking for a referral myself so this gives me more encouragement. I feel more heaviness in my underarm after my infusion and extra day of IIV fluid so I want to make sure I'm doing what I can to prevent anything long term.
Kbeee - welcome to the October Board :-)
After I get through the week following my infusion, I start to feel what I consider "normal". Yesterday I had the opportunity to do some Christmas shopping at a mall that was near where my husband was attending a conference. We live in a rural area so it was a treat plus there weren't very many people there first thing in the morning on a weekday - perfect for avoiding crowds and germs. But what I learned was my "normal" was behind the curve for mall shopping and I had to sit down and rest a few minutes hear and there. Guess I've got a new chemo treatment "normal". -
Pam - I wonder if we are around the same age? Fatigue has been a HUGE issue w/me; it lasted 5 days after chemo #1 and 9 days following chemo #2. I was warned: "fatigue will probably be an issue you have to deal with and likely will not be able to work as much as you think you are going to be able to" and they were right! (I will freely admit I am really worried about how bad the fatigue will be after #3 & #4!!!!!)
You know, when I heard "fatigue" I figured....ok, I'll be tired more often and will need naps. Well, was I wrong!!!! I now know fatigue is when every muscle in your body is so very weak that walking 50 feet can wipe you out. So I completely understand your need for rest periods while at the mall. Normal changes due to circumstances, doesn't it? I think we are all now experiencing our "new normal".
I'm 49 - how old are you, if you don't mind my asking.
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I was up very early. Of nowhere I found this thread. Must read. Great stories!
Something to enjoy while we battle through this journey...............
All Topics → Forum: Biographies and Inspiring Stories → Topic: Success Stories!Topic: Success Stories!
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thanks Jen!! -
Good morning "Chemo Sisters"- Day 9 after TX 2- beginning to feel more ``normal`` , more energized....will attempt to have a short walk! Will see how this goes...
JenSF- So sorry to hear about your visit at the ER last weekend. It must have been very scary for you. Hoping that you are feeling better. I have been fortunate so far not to get any fever (crossing fingers & toes) for this to last. My SEs on this 2e round have been constant heartburn. MO prescribed ``Pantoprazole`` which has helped to ease the symptom. Fortunately , I found that I didn`t experience as much bone pain with ``Neulasta`` as I did on my previous round with ``Neupogen``. I took Claritin as suggested and Advil, it made bone pain more doable this time.
LIli1964- Pam358- we aren`t on the same regimen however, extreme fatigue is a big factor for me as well. I was invited to a small birthday gathering yesterday. In less than 2 hours I was completely wipe out...feeling like I had run a marathon. It took the rest of the day to recover from this small expedition. On my next visit , I need to ask my MO what kind of supplements I can take to help boost my energy level.
Wishing a restful weekend to you all! -
Lisa, I'm actually a little older, just turned 52. I have the kind of fatigue you are describing for about 3 days after my chemo where I basically just sleep. Then I advance to tired - not doing much but no napping either for a couple of days before I return to a somewhat compromised new normal - where I still need to take it easy at times but can work in spurts (laundry, dishes, dinner). My in bed fatigued days changed from Tx #1 to Tx #2 but stayed the same after Tx #2 and Tx #3 so hopefully yours won't increase after #3.
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