Starting Chemo February 2013
Comments
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Hi Nancy!
We have a similar situation, and I'm about to start my first chemo treatment next Friday, May 3. Like you, I'll have four
treatments, 3 weeks apart. Wondered if you could tell me how it went for you ---- I think you may be finished by now!
Thanks,Julie
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Melody: congrats!!!! We all can't wait to be you!!!
Rdrunner: I have been thinking and praying for you. I hope they figure this out. Hang in there.
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julie0957 - I hope they have a thread like this for people starting Chemo in May 2013 - this particular board has been such a help to me as we all did our chemo together and shared various side effcts.. I made it through but not without many side effects..I wish you well and hope you do the best!!
Rdrunner - I hope all goes better for you..and everything works out for you.
the side effects this time have been brutal - today was the first day I could stay at work all day but not without pins and needles in my feet and fingertips..and the skin on my heel has peeled off and i can hardly keep a show on because of the pain.
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Rdrunner thinking of you and hope you are feeling better. Thanks for keeping us updated-we are all concerned and with you in spirit.
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Hi Everyone: Next Tuesday I go in for Chemo #5 (out of 6). Since Chemo #4 was tough to spring back from.......I'm worried about what chemo #5 will be like. I'm hoping for the best outcome. I have been so exhausted.
Congrats to those of you who have made it thru your chemo! I hope to join you in a few more weeks. Until then, I will keep you posted on what #5 has in store for me.
Until we have all reached our final chemo treatment, lets all stay positive and FIGHT THE FIGHT with all we've got!
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Yesterday was #4 for me. Usually the fatigue doesn't kick in until Saturday night. Today was rough...it was only 1 day. I kept dozing off in the waiting room while waiting for my Neulsta shot. I managed to finish my work day but soo wished I could just sleep on my desk instead of driving home. Not sure what to expect the next few days but from the looks of day 1 post chemo it's going to be a rough weekend.
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LW0919 - I think # 4 is the worst to recover from - I know how you feel - the side effects have been brutal and I am just hoping for them to end..
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Rdrunner - you have been in my thoughts. I hope everything turns out well.
My first taxol treatment was Friday. Yep, they used Taxol and not Abraxane. Then put me on a tapering off of steroids to avoid the sudden crash that sent me down the dark hole. No allergic reaction during infusion but I hated the way the benadryl made me feel. I couldnt stop shaking until I finally fell asleep. Thankfully they said they will half the dose next time. I did some very light garden work yesterday and ended up with some blood blisters on my hands. So the skin is thinner than I thought.
I know what you guys mean about losing lashes and brows. I have some latisse, but do i bother to put it on now or wait until treatment is over? I guess I could try it now and see what happens. One taxol down three to go. It is definitely easier than AC so far...no nausea but I am waiting for the muscle aches. Hopefully they wont show up.
Much love to all of you. -
I don't know if I posted this blog before but I thought since most of us are reaching that point of needing brows and lashes, I would post this blog. She has really great tips, especially regarding false lashes. Her videos are very well done and I enjoy listening to her. Hope you do too.
http://eyelineher.blogspot.com/ -
Hey ladies. Day 3 here after round 5 of TCH. Doing OK. Could do without the insomnia, though. Yesterday, I went for a 10 mile bike ride with my son. Prior to surgery, would have been no problem. While it felt awesome to be out and moving in the nice weather. It was also a bit disheartening to realize how much muscle tone I've lost and how just out of shape I've become with the decreased activity. Any hint of an incline, I had to use baby gear on my bike or my quads were absolutely screaming. I know everybody is different, I just wish I knew when I'll be back to where I was before all of this fun started. Something tells me it will take longer to regain than it did to lose it.
Bright side is, I only have one more round to go. And hopefully the side effects from rads will not be so severe and allow me to increase my activity level somewhat.
Hope you all are having a nice weekend. Take Care!
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DiZZyMom - congrats on a 10 mile bike ride! that is amazing - I'd be happy if I could do a 10 minute bike ride..
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Wildlyshel, that video is great, thank-you! Perfect timing for me as I only have a few eyelashes left and picked up some eyeliner, but I have never worn eyeliner before and wasnt sure the best way to apply. Now I can have some fun trying it out.
DIZZYMom, I'm so impressed. I can't even walk a block without getting out of breath. I just have to remind myself "this too shall pass"
Hope everyone is enjoying their weekend! -
Dont feel bad gals I cant even walk around the block! I have a VERY expensive bike that I look at everytime I am in the garage thinking oh how I wish I could go for a ride, but it will come. Might not be until the end of the summer, but I will ride again.......
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Wildy: Thanks for posting that link. I just watched it. Amazing. Going out and buying some liquid liner and black eye shadow. I hope I can make it look as good as hers!!!!
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Yes, thanks Wildy. I hope to be able to master that when necessary. I hope you have a much better time this round with the change in meds!
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Ladies you are all do reallly good. Im able to walk again not very far but Im getting out. Still super tired even on 40mg of prednisone. Going for another CT scan this week, although there is some confusion as to if they are doing a CT guided biopsy to confirm Sarcoidosis. Super nervous about re starting chemo on the 3rd, worried it will make what ever is going on worse again.
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Good luck Rdrunner. You deserve a break from all the crap you've had to deal with! I wish you the best.
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You guys are certainly welcome in regards to the video. I liked the hints she gave in regards to fake lashes and how it was important to curl them. I would have never thought of that.
Dizz - congrats on the bike ride even though you are frustrated at the decline...you are ou there! And only one to go. Hurray!!!!
I was out doing some gardening yesterday. I was surprised. Never would have been out there this soon on AC. The shooting pains came to visit in the middle of the night last night like little gremlins. They aren't so bad now but not so fun either.
Rdrunner - good luck with this next round.
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Hi Friends,
My 5th chemo is coming up on Wednesday and I can't wait (now does that sound crazy or what???). I am ready to get this show finished.
I am really longing for my hair, which I know will be months away. But has anybody heard of using biotin for hair growth. And if so, when can you start taking it, does it work and how much to take?
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Kkmom we are on about the same schedule. my 5th is Friday. I cant wait either, The week can not go fast enough.Although I feel so good today it is a bummer thinking about how I will feel next week! Do you have ANY hair?? I have been using redken intrafource and nioxin. I'm just going to keep doing that.
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kkmom, I've been taking biotin for hair and nails. I take 1000 mcg, but I don't take it day before or until day 3 of chemo. My MO isn't really big on taking supplements on chemo, but doesn't care so long as I don't take it with the chemo. I've heard it doesn't really do any good while you're on chemo, but my nails started going funky, so I decided to give it a go. I'll definitely keep taking it after I finish and hopefully it helps with hair re-growth.
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Well its definate.. no more chemo for me. The way sarcoidosis effects the lungs its too dangerous with taxol and the risk of ending up on a ventilator is too high MO says. So starting on tamoxifen. It also could scratch radiation but rad onc wants to wait for biopsy and the other ct results to decide.
Just in case anyone is worrying.. this is not something chemo caused, it was something that was pre existing that we didnt know about and chemo brought it to the forefront. The next week or so is going to be rough as they have to take me off the steroids prednisone cold turkey to get the biopsy so they said my symptoms are going to return most likely.. heres to 104 fevers and rigors for hours on end (:
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Tangles - I have VERY thin hair on most of my scalp, it is about 1/4 inch long and looks like stubble. When I first had my hair shaved, it was shedding all over and continued to shed for about 2 weeks after. I figured the stubble would eventually fall out, but it has hung around.
DizzyMom - Thanks for the info on the biotin. I will definately try it when I finish chemo.
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Rdrunner so sorry. Please keep us all posted. Prayers to you!!
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Ladies, Today while I was getting ready go out for my pre chemo blood work and my fill appt with the ps this afternoon...I was drying off after a shower and noticed a small pin hole opening in my incision.
So I called my bs & went to see her immediately. She said the skin was very thin in that area from my surgery and that she has been watching it all along. Ended up getting the incision trimmed a lil & a few stitches along with an antibiotic. I was so bummed. She cancelled my ps fill and my chemo #5 this week. I will see her next week and if I get the "ok", Chemo #5 will be next Thursday instead of this week.
But I guess it is better to be safe and push things back a week. I was looking forward to being one treatment closer to being finished. Sooooooo bummed. Thanks for letting me vent!
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Rdrunner - so sorry you are going through all this..
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Gina I know how you feel. When I was in the hospital I had to be pushed back. If that wouldnt have happened I would be done here in 2 weeks! UGH! Oh well 2 more to go is better then saying 5 or 6 more to go. I pray everyday for no more set backs so I can get this done!!!! I got a fill yesterday and boy was I in pain last night. I can tell my skin cant take much more and I have two more to go. GOing to have to give in and start taking more pain meds even though I hate to!
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Rdrunner- what a crappy thing to have happen to you. I hope they get it settled down so you can feel decent again.
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I just had my 4th out 6 treatments TCH yesterday. I'm fine today it's the Nuelasta shot that always gets me.
I'm counting the days as we all are. 1 quick question for anyone.
Going to Florida in June after my last Chemo to visit my mom. What do I wear in the pool, ocean on my head?
Good luck everyone.
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Shasha, there are swim caps from 4women.com that look cute, I haven't tried them, but have several of their scarves and think they are well made. Just not sure if they would slip off your head (at least mine being so smooth!) I know their regular scarves are lined in a soft cotton that stays on.
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