Starting Chemo in July 2009
Comments
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Twinmom77 and Mnikityger...
I am also an Ohio girl....Cincinnati!
Tougherthan....Hang in there girlfriend.....hope this finds you feeling better. Day 8 was a turning point for me.....
Hugs and prayers to all,
Linda
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Tougher than - I wanted to make sure you had right info for asking doc - EMEND is a pill. They usually give you enough for 3 days. The patch which they added to my drugs for my 2nd chemo this upcoming week is called SANCUSO. Hope you feel some relief soon.
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Rad onco said no swimming b/c of chlorine and no hot tub b/c of bacteria..
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Pauldingmom~I did the exact same thing last night in my tub. I scrubbed for 30 minutes all the little nozzles with a toothbrush, then filled the tub with bleach/water and let it run for about 10 minutes with the jets on. I don't think we're paranoid...like you I love my baths.
I start chemo tomorrow so trying to get last minute cleaning and shopping done today. Will I really be there 5 hours???? Hope maybe I can get caught up on some thank you note writing.
Also having my wig styled on Tuesday, will I be up to it??
So great to have so much support on this thread, but sorry everyone has to be here. I've been out for a few days....so many posts and hard to keep everyone straight, but I know you all understand..don't say ya'll aren't having the same problem!!!
It's a beautiful day in the midwest...57 degrees this am on my walk!! Thank you Lord!
Joni(1)
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tougherthanithought-I don't know if this works for everyone, but in my case it wasn't that I was actually sick to my stomach, it was just the smell and thought of food that I couldn't stand. Try sticking to a bland diet and I've heard ginger really helps. I drink warm ginger/green tea in the morning now instead of coffee. Ginger ale is suppose to help too, only stir the bubbles out first.
Ya'all hang in there. Blessings sent to each of you.
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HI to all,
I have not felt up to reading. Today I have a lot more energy. My first AC (July 7) round ended up with extreme gas pressure in my stomach. I ended up in the ER that Sat for some relief. Then Monday morning same thing back to the ER. Needless to say I a have a gatro Dr. appt. This Tues. I followed a BRAT diet to the letter and no relief. Hopefully they can get to the bottom of the problem. If I did not have the gas problem I would of gotten along alright. Hugs to all...glad most of you are doing much better than I did the first round.
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Hi Girls....
Just joined this group~ I started my chemo on July 9th. Taxotere & Cytoxan every 21 days for 6 rounds. The first time went fine with just a few side effects. Like constipation and my mouth is sore. On day three I felt like I had the worst hangover of my life...but a nap cured that and so far I have had few problems.
My Question: I had a root canal done about 1 year ago .... and something is wrong with it...very tender..I also have a crown on that tooth. Before I started chemo and before I had my bilateral mast. They wanted to pull the tooth and put an inplant in...but my surgeon said no to that becuase of my upcoming bilat. but now I am into the chemo...and that tooth is really bothering me...any suggestions....has anyone else had this problem.
This site has been very helpful to me....thanks ladies!
Enjoy your day!
Balsie~
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Oh yeah here is a laugh at my expense ......I have a keen sense of smell. So for at least five days thats the worst smelling urine and bowel mvts so much so I was putting toilet paper up my nose so I could not smell it (all the gas pains I needed my hands free) He walks by on his way to the bedroom and says with a laugh what are you doing? then it hits him and he says "I don't blame you". I am going to buy nose plugs before my next round LOL LOL. Thank goodness that went away after a week.
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Balsie....
I work at a dental office, and your tooth may be infected. You should probably get on some antibiotics to get the infection under control, and get the tooth extracted as soon as you can. No dentist will do treatement while you are on chemo bc of the low white blood counts. But infection is bad for a normal person...and even more so when you are on chemo and your immune system is compromised. Call your onc and to see what they recommend and then call your dentist. Good Luck!
Linda
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Linda,
Thank you, I will call on Monday. I wish my dentist would have taken care of this when I went in last fall , he took an xray and said there really was nothing, but I knew it didn't feel right. I hope it all works out.
Thanks again
Balsie~
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Quarter405 I hear you on the smell thing...I can smell things..oh my I have to put vicks under my nose when we go out in public because I can smell things...and they are not good
The first couple of days after chemo...things really smell don't they!
My husband said I can smell farts that haven't yet been blown....oh he is a funny man.
Enjoy your day ladies,
Balsie~
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oh to drink something that tastes normal, I can taste every grain of salt in plain water and it taste like tears, I did find that ruby red grapefruit juice taste kind of good, Today is day #4 and I am week alot of bloating discomfort, but no nausea. Did anyone else have strange feeling (like being disconected) with the steroids, I also am weak, I am overweight by 50 pounds and someone could knock me over with a little finger.
God Bless- Lori
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quarter405 - I hope you get some relief from the SE's soon.
On the keeping bacteria at bay front, a while ago someone suggested putting the toilet lid down before you flush is something we can do - thought I would remind us of that.(Not something I normally do) Another thing I have done is to replace toilet cleaning brushes in the bathrooms.
Chemo time - it seems some are there for a couple of hours, others up to five or more hours. Why the big difference?
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Lori,
I agree water does taste like salt. I suck on a lot of popsicles. I understand the disconected feeling....that is a good way of putting it. That feeling should pass , I am on day 10 and that has passed. Healing wishes to you!
Balsie~
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Hello all! Welcome newbies!
Today is day 17 and my very short hair is starting to say goodbye. If I put my hands through it, strands come out.....so I probably should think about just shaving the rest. We will see how I feel about that tomorrow. As far as SEs.....only had bad days on 4 and part of 5. Today I feel pretty good and have done all my laundry and housework.
Oh, to have a hot tub...that would be a wonderful thing!! I went in the pool three times, wonder why chlorine is bad for us?!?
Hugs to all!
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So is anyone else here doing TCH also? How is it going? And is anyone else juggling small children during all this? Any tips on helping them deal with mommy not being able to play? I have three year old twin boys and I'm so worried this is going to scar them for life! Thanks!
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Twinmom - is your "C" Carboplatin or Cytoxan? I am doing Taxotare/Carboplatin/Herceptin and so are a few others. Just had my first chemo on the 13th and only had a couple of bad days (3 & 4). Once you find your crummy days, maybe you could have some extra help with the kids for those days. The rest of the time you may find you feel pretty well. I shipped my 18 year old off to college yesterday and cleaned his room today. I wouldn't have tried that on Day 3 but here on Day 7 it's fine! I get tired easily, but I just slow down and take a break. I plan on going back to work next week.
gilly - I think it depends on what combo's and meds you are being given. I was six hours for treatment one, but my nurse said they like to go really slowly with the first tx to make sure there are no adverse reactions. She said next time will be 4 hours or less.
On the subject of drinks - the one thing that I have found that tastes REALLY good to me are Smoothies from Tropical Smoothie. My son brought me one that had strawberries, mango, and kiwi in it and it tasted great. I think I'm going to have my DH bring me one at chemo. I am having a lot of trouble drinking the required amount of water. I drank 4 20-ounce bottles of water during chemo #1 and got the frequent flier award for trips to the bathroom. Now water tastes awful to me.
And quarter here's a laugh for you about me: After no bowel movement by Day 5 after chemo I decided to be proactive. I wasn't feeling uncomfortable but after hearing all the constipation horror stories I figured a dose of milk of magnesia might be a good idea. WRONG!! I should have left things up to Mother Nature - things started moving immediately and I have now had diarrhea for 3 days. Lesson learned!
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Hi, I'm about to start 6 cycles of chemo on 30th July and my breast nurse has told me to expect hair loss after 2nd cyle. I will be having FEC-T. Now I've found you all, I promise I will be a regular visitor. Good luck ladies
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quarter405 and balsie - thanks for the laughs and I will be on the alert
Lori - I'm on day 4 too. So far, so good, Had trouble sleeping those first two days, then DH put on some instrumental music and made my room pitch black with no sound and out I was. I've been tired but am encouraging myself to get up off the sofa and out of bed. Even went to church this morning. Let's keep up with one another.
Paulding - I will keep you in my prayers for your first TX tomorrow. I hope that it goes smoothly.
Wanda
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Hi Triple J's - here is next weeks Chemo starters:
July 20: Carole01 = Adriamycin/Cytoxan DD x4/2 + Taxol x4/2
Jacee [Joni1] = Adriamycin/Cytoxan x4/3 + Taxol x12/1
July 21: Eliz46 = Taxotere/Cytoxan
Twimom77 = Taxotere/Cytoxan + Herceptin
July 23: Shaesaliah [Shae] = Taxotere/Cytoxan x 6/3
DeniseM808 [Denise] = Adriamycin/Cytoxan x4/2 + Taxol x4/2
I'll be thinking of you ladies as you start your treatments and sending out positive vibes for minimal/no SE's.
Twinmom: check out page 7 for a list of our July Triple J's, including start dates and what cocktail they are on...there are quite a few on TCH (depending on what C you are on).
Hugs to all
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Is anyone experiencing headaches? I continually have them - but just enough to know there is an ache? What do you take?
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Twinmom77, check out the thread "taxotere, carboplatin, and herceptin." It started in July 07 and there are many, many women who have done and are doing TCH.
Becky
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Michelle-You Rock!
Joni2
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Hi to All-
All the great advice is wonderful! As for my hair well, I went to my BFF house yesterday and somewhere during the middle of the pool party she asked if I would let het cut it. Now remember she is not a professional hairdresser so I was at risk for what ever she did. I have always known I wanted to cut it real short before the chemo so I let her her have at it. And I have to say it is Short! But it is short on my Terms not the cancer or the chemo doring it. It kinda looks like a high and tight Marine haircut (my daughter says). Of course during the cutting process I did have a couple mixed drinks. There were other real close friends thre and we had a great laugh at my hair coming off, but I do not regret letting her cut it. Better to laugh than cry.
Next I need to trim back my fingernails, which are between quarter to half in long. They are mine, all natural. I plan on doing that Tuesdy or Wednesdy evening.
I am praying for all
Stay safe
Shae
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Great, thanks everybody! I my C is indeed carboplatin, so taxotere, carboplatin, herceptin. I'll check out that link.
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BlessedOne2,
I have also had terrible headaches every day, they stopped at day 9 after my 1st chemo. Nothing really worked on them (Advil, Tylenol)....so I just dealt with them...but they were very annoying!!!!
Linda
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Wanda - I have had some wicked headaches - especially day 3 and 4. I do get migraines and I took my migraine medicine (relpax) day 4 and it helped a lot. Not sure if it is from the chemo or the neulasta.
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Hi Ladies, Im on day 12 and my hair is hanging on. I had it cut really short saturday and my stylist said she would have never known I was going thru therapy as it was not coming out whatsoever. I figure by day 20 I should be bald and Im armed. I got a new puppy! He is so sweet. I hope I can manage his care, his name is Charlie. ..watch him rip my scarves off in front of the neighborhood. ..should be interesting.
The emend is very expensive but works the best, I take th zophran as well and I find this is second best. Someone at my follow up mentioned that anytime she got nauseated, she would eat and it would curb it. I had only taken the drugs and they seemed to help. Nausea stopped day 10 and I haven't taken anti nausea since. I think the claritin (not the d) got me through week one starting the day of the neulasta shot so I highly recommend it along w/ alleave or tylenol. My supplements are calcium, vitamin b blend, D3 and magnesium - my nurse said these were ok to take and Ihave been feeling pretty good. Colace C works really well for the constipation. I take four every third night. Food tasted awful on day ten, I thought someone doused my fish in cod liver oil. I will never eat fish again. ..but this only lasted a day. ..watch drinking beer. I got a nasty thrush in my mouth because of five sips of a home brew and this took one week to cure. I heard the chlorine issue and not swimming but my friend went through the same regemin and swam all the time so Im not sure - is this for the skin? Ice chips during the kool aid (adria) portion helps keep mouth sores at bay for me and I intend to stick my hands and feet in ice water during the taxol ...just in case. My crash days are days 5/6 from the last round. Im really interested in hearing about everyones crash days. i wonder if there is any connection or if its entirely personal.
Does anybody know anything about staying out of the sun/beach and why. How about the ocean?
Good luck everyone, your stories are very encouraging. I hope my info is helpful to the newbies. I am encouraged to drink one gallon of beverage a day. I can't do this but Im trying. I go for round 2 of AC this wenesday and then only two more ACs.
Cheers!
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LindaSueH & BlessedOne2......I also had a headache everyday for the first treatment. Second time around on the day of treatment I added Gatorade to my fluid intake and/or electrolytes powder to my water and did not have one headache. With all the fluids flushing through our bodies, as well as the chemo drugs, we lose electrolytes which can cause headaches. There are also some bottled waters that contain electrolytes and are not sweet. So give one of these a try and see if that helps. Patti
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LindaSueH Hi to another Ohio girl wish we all could have meet under different circumstances but since we didn't I am glad all of us can be here for each other. Good luck & God Bless All
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