Starting Chemo in Nov 2016
Comments
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Amyemn - I think I remember form an earlier post that the American Cancer Society offers a first free wig! You could check the out.
Good luck!! :-)
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gmmiph, where are you located? I found the Biotene at CVS. I thought I'd need to order it on line but they had a whole array of products on the shelf.
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So many of you look truly cute with buzzed hair. I won't be posting a pix of myself but I'm enjoying all of yours.
Today I reread through most of this forum. I'm amazed at the wide variety of drugs that are being used for the side effects. Until this illness I'd only been on antibiotics once and no other meds except otc cold stuff. Now it seems I'm taking a life-time of pills over the course of a few months. It makes me think of Jefferson Airplane, "one pill makes you larger and one pill makes you small."
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well that nite I slept good.Next blood work THEN 2SD TREATMENT Dec.1st, So far so good
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they offer rembursment with your receipt up to $150.YOU MUST ALSO HAVE A DR.PERSCRIPTON.THEN I FOUND OUT EVERY AREA IS DIFFERENT.MY CANCER CENTER GAVE ME A LIST OF SOLONS THAT WILL GIVE U ONE FREE.IN ALL THE LITERURE THERE R PLACES THAT WILL DO SOME PERSONAL THINGS FOR FREE LIKE THIS,MAKEUP-MASSAGE.HOPE THIS WAS HELPFUL
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Here it is ... the last day of hair. See how excited I am?!? :-)
I know it will grow back.....but yes, there is the initial shock, even when you know it's coming.
I'll be a ball cap, beanie, hat wearing person and the first ball cap I'll wear Monday says, "My Oncologist Does My Hair". I think that should break the ice and possibly cut down on discomfort among coworkers. :-)
I hope everyone is doing well!!!
Have a great weekend!
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Hi aterry, thank you for your thoughtful post. I am from Manila, Philippines. I searched for Biotene in a popular drug store here but they dont have it. Gonna go to a mall today where they sell all sorts of imported medicines and hope they have it. Hugs.
Hi pmevans, thank you very much for the positive thought. I am including this November group in my prayers , that all will survive this terrible disease and have wonderful lives in the future. You are a sweet lady. Hugs.
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Pmevans,
I just sent my previous post and was surprised to see your posted pic just ahead. You have nice long hair. It really sucks to see it go to waste. Just early this morning, I ran my hand thru my hair and a few strands came off. Last night i was having this tingling sensation on my head too. Well, cancer may take away our hair temporarily but not our fighting spirits.
We can do this, we are WARRIORS!!!
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Pmevans: I'll be a ball cap, beanie, hat wearing person and the first ball cap I'll wear Monday says, "My Oncologist Does My Hair".
I always thought a good T-shirt would be "Chemo Hair, Don't Care,"
I am sure someone out there already thought of that ... might be a ready-made T-shirt out there.
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Hi gmmiph.
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My hair was the same length as yours. I love the hat you'll be wearing on Monday. Yes, it should break the ice nicely. (((hugs)))
I had a very good day. I teleworked, got a very good nap, ate and drank lots of water (like I always do). When my husband came home from work, I got another very good nap. We went to the store and to pick up some dinner to bring back home. He was surprised at my appetite, and I was a bit too lol. Now it's time for me to log off, and curl up on the loveseat and watch a movie.
I hope everyone has a great weekend. I'll be thinking of you all. (((hugs)))
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Well I went to the breast cancer fundraiser...it was fun for a little while but It was too much standing, loud and hot.....I drank lots of water (and one sprite) there wasn't enough food and stupid me didn't really eat before, so I felt a little dizzy...had to find a seat for a while, then my friend and I left early...my headache was still around, so maybe it is related to chemo? I started to feel twinges of nausea so I took a Zofran...
got home, tried to eat some crackers and cheerios and sipped on a ginger ale....I fell asleep pretty quick, but woke up a bunch, then again at 3, I felt like I was gonna be sick, started sweating, thought I was gonna pass out, stripped down splashed cold water on my body, went to lay in bed again and felt a little better....then back to the bathroom....the "d" word..ugh....but better then throwing up! now I'm watching cheesy movies on tv at 4am....
Here I go.......
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I'm sorry you ended up not feeling great BG. I do think all the standing and such takes its toll. I went to my daughter's musical and by the time we got home my port (installed Thursday) was killing me again. Too much trying to act like nothing is wrong I think and not being able to hold my arm or whatever the way I wanted to.
I hope you have an easy day today on your couch with those cheesy movies. Be kind to yourself today.
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Day 4 after my second infusion. My stomach has been acting up, but not as bad as the first time. My scalp is so sensitive! I am considering just cut it down with my brother's machine.
Anybody experiencing trouble sleeping?
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Latinmixy I haven't slept great since I was diagnosed...it sucks! the minute I wake up for anything (the kids, to pee) my head gets the best of me and I'm up for hours...
Hope your stomach feels better!
I'm only on day 1 of my first chemo and I'm in bed, my husband took the kids to a birthday party an hour away...I'm planning on doing nothing all day and keep taking my Zofran on time!
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I have tons of trouble sleeping. Days 1-4 after my first infusion I was up like clockwork from 2:30-5:30am. Determined that was the steroids. Since then, I pretty much can go to sleep fine, but I'm up, down, up down, up for a bit....if it's anywhere near 6:00am, I'm up for good, no matter how long I lay there.
Some I think is stress, my brain won't turn off on certain days. Some is pain, like rolling over onto my port last night. Others may be because I go to bed earlier than before so I'm getting enough sleep. I don't know. All I know is I really feel wide awake when I do get up, so I must be getting enough. I've felt like a nap a few afternoons, but I try not to lay down longer than 15-30 minutes because I don't want trouble at night again!
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it's day two for me. I was a bit nauseous. I was trying to go over tumor reports and noticed that nothing was marked final report. There were still portions labeled pending. It makes me feel uncomfortable.
Did anyone receive a finalized report that states it a final copy
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I find sleep difficult some nights. Because of the hydration I need to get up to visit the bathroom. If I get up after 4:30, or so, it's hard to go back to sleep. My brain goes over some of the bc questions and then problems in the news. My husband calls it cranium chatter when you can't turn your brain off.
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Aterry, I love that term!
Neulasta headaches and aches kicked in around 7pm last night. Ugh. Still battling with it a little today. Made myself get out with my husband for errands anyway though. Probably time for more Tylenol. Hoping to be out of the hangover portion of the chemo by tonight.
Hope everyone is doing well
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Day 2 after 2nd treatment and I'm feeling pretty good. My sister shaved my head today before it all fell out. I certainly don't like the look. I don't think I'll let anyone see me bald. I'm glad my grandson was there today. When I took my ponytail holder off so much hair came with it he got scared. He's 2 and a half years old. So as my sister started in with the clippers I just made it fun and laughed and said it tickled and that it felt like a massage and he definitely came around then. So glad I didn't scar him for life! Then we were off to the playground to play with monster trucks. All is well!!
Cranium Chatter! lol I love that!!
Fight on Warriors!!
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I really messed myself up. I had the 1st chemo Tuesday with the Emend, took my steroids and got the neulasta shot on Wednesday, and had the worst headache for 3 days and constantly queasy but never threw up. I never took the zofran or compasene because they said it could give me a headache and the hydrocodone could make me nauseous. I'm finally feeling human today but I really need my MO to tell me exactly what to do because I was way too confused with all the meds they gave me. No way I can do it like this again. I'm not feeling much like a warrior right now. :
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sleepless did you take Claritin? It seems to help with Nuelasta shot. If it doesn't work, you maybe able to go on Neupogin shot - it makehave less side effects for you.
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Sorry, Sleepless! I definitely take nausea meds for the first 5 days, then I'm normally good. I've been taking Tylenol for the Neulasta headaches and pressure. The Neulasta pain and aches areno joke. But I can attest after having a cold all 14 days of last cycle that it does work. My blood counts were good. So, at least it's working, to me, that makes it worth it.
Patti, doesn't it feel so much better off though? It's odd passing by a mirror and not recognizing myself.
Saying a prayer for you guys tonight! 🙏🏼😘
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sleepless DEFINITELY take the Zofran! I started last night (day of my first chemo) right when I felt a twinge of queasiness...the nurse said if you wait too long its hard to come back from it. I take it exactly every 8 hours (sometimes a little earlier to head it off) I took Claritin today about an hour before my Neulasta patch went off, and will keep taking that daily, and Tylenol as needed for my dull headache...
it is a lot to keep track of....also remembering to rinse my mouth with salt water and drink tons of water...
I had a nice long nap today and I felt so much better after.
Becky
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Hi Everyone,
I haven't posted for a while, I started AC on 11/1. We're all having such similar experiences.
Cut my hair short last week, but hair started falling out in clumps today in the shower. I'm not dealing with that mess, so I had my husband shave it. It feels so much better.
What I experienced this week with regard to side effects was not acceptable. I will be doing all I can to avoid how I felt on Thursday, 2 days after treatment. I just can't tell if it's the chemo, the withdrawal from the steroid, or the Neulasta, but I had an incredible headache and couldn't get out of bed just slept on and off. Nausea too of course. Can anyone tell me if they are getting headaches after the Neulasta and anything to help?
And then Friday felt like a new lease on life! Like in the movies when a person gets punched, then gets up swinging at everything? That was me!
Will keep checking in on everyone
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Thank you for all your advice ladies. Next time I start zofran on day 1. I'm now on day 6 with stomach cramps and D. When will this end? I feel like they gave me too big a dose of chemo or something. Will talk to MO.
On a side note, for those with yucky taste in mouth after eating like me - I found Mentos peppermint mints very helpful. Biotene works too, but mints are sometimes more convenient.
Have a beautiful Sunday!
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Sleepless, I don't wait until I have symptoms to take the nausea meds they gave me. I take 2 of them before I even go for chemo, 1 again later that night and 2 each day following for 2 or three. The meds they gave me for nausea are to prevent it, not stop it when it starts. If I feel nauseous, they said take gravol AS SOON as I feel it, and try to eat something because sometimes nausea is because you are hungry. Not eating makes it worse until you can't eat, etc.
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Sleepless & Grannemama, I'm sorry that you had such tough times. So many on this forum have had bad headaches related to Neulasta but when I asked the infusion nurse about it she said that is not typical--seems to be from reading here.
I'm off to the book store to get a stack of good fiction and to buy some holiday presents. I'm finding that I don't want to deal with nonfiction at the present. For my first infusion I read Ann Patchett's "Commonwealth"; a wonderful book. Today I'm going to pick up another of hers, "State of Wonder". A friend recommended Trollope for times like this--she says his novels take you completely away from your own experience.
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Hey ladies!
I'm out of the fog!! Wahoo!! Seems my SEs are exactly the same as round 1. Day 5 and I'm back to normal. I'll take it! Hair is almost comical, but luckily I have a good sense of humor. You really do just have to laugh! I figure I'll be close to totally bald by Turkey day.
Aterry, without question, all of the headaches and body aches are Neulasta based for me. On the night of day 3and all day of day 4 random body parts and muscles just hurt. But my skull, teeth, and spine pulse for about 24 hours. I'll be talking to my MO about it too, since it was the same as round 1. Maybe a touch more intense this time. Still zero nausea though. I've been good on the dried fruits, nuts, and steel cut oats this time around, so the big C is nowhere in sight! Winning!!
My appetite and mouth are still in great shape too.
Feeling very blessed on this Sunday! Now for some online Christmas shopping and football.
Hugs to you all!! 🤗🤗
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I hope everyone is having a good weekend.
First chemotherapy was on November 15, so today is day 5. I'm doing ok. I feel like I get a little stronger each day (and I so appreciate it). I feel chemotherapy makes one have to have rest periods / naps each day (and I listen to my body). I wouldn't be able to go without it. I still stay well hydrated with lots of water, and I continue to eat well (much less than before but still well).
I've had a lot of twitching of my left eye lid. Anyone else experience such?
All in all, I feel like I'm doing ok.
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