Clinical Trial E5103
Comments
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Good luck Swanny, they will monitor you more thoroughly since you'll be in the trial! That's good news!! hugs
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Just wanted to also send my best wishes to you Swanny! I don't think you will regret joining the trial. I only received 5 out of 8 possible Avastin treatments and had to be stopped on the drug due to side effects and I don't regret it for a minute. Like you said, attack it aggressively with every weapon available to you!! And like Kari said, the best part is how closely you will be monitored. That's always a good thing!!
Good luck to you!
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Like TexasRose I only got 4 out of 8 avastins. I had a reaction to taxol so they switched me to abraxane which is not allowed in the trial.
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Like TexasRose I only got 4 out of 8 avastins. I had a reaction to taxol so they switched me to abraxane which is not allowed in the trial.
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Thank you everyone. I am still waiting for scheduling to start chemo. Should be next week.
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Swanny- How are you doing? Have you started chemo yet? Been thinking about you and praying for you. I hope you are doing okay. It's a scary time, but we are here to hold your hand if you need us.
How is everybody else doing?
I'm enjoying my "break". Now that I am on the every 3-month schedule of Zometa, it's really nice to not have to go up to the hospital all the time!! The weather here is turning warm and our pool is ready to swim in. Unfortunately, we had a slight "cool" snap here today and couldn't swim this weekend for the first time this year. Hopefully soon!! I did see my first fawn today. We have a huge deer population and it's baby time!! We also had an email this weekend from our chief of police that a mountain lion had been spotted in an area just a few houses down from ours!
We've always had them, but I hate to hear they have been seen so close to houses although we are very wooded and secluded. Definitely keeping my eyes open for that!!
My hair is coming in nicely and I gave up the hat a few weeks ago. My hubby and I have volunteered to chair the golf tournament for a local organization that raises money for our local hospital's cancer research center. Very excited about that! I sometimes go several hours without thinking about cancer. I guess that is progress!
I hope you are all well and healthy and happy. I think of you often and pray for all of you.
Hugs, Mary
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Hi all! Swanny, thinking of you!!!!
Mary, your hair looks great! That was me a year ago, and now need haircuts/color!! Your pool sounds like heaven and the dear so sweet, but the mountain lion - eeks, be careful girl!! Awesome about the golf tourney. Good job!!
Hugs to all!!
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Sorry I have not posted. I had my first chemo session on Thursday. Been waiting for the ball to drop but for some reason I have not had any side affects yet. Lucky! I was so afraid of starting chemo that I had a couple of panic attacks. One on Monday before chemo at the doctor's office and one the morning before chemo at my office. Luckily my Dr. had given me a prescription for Atavan and that helps me from panicking. I got a new wig. I had one from the American Cancer Society but it did not fit too well (I have a big head). So I bought one locally and I really like it. I also bought a hallo (ring of hair) to wear with hats. I think I am ready for losing my hair. Should be within the next week. Hopefully I won't panic when the hair starts to shed. Hope everyone is doing fine. Oh and some bad news - I realized that I am triple negative - did not know what that meant until I looked it up. Very scary.
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Swanny, CONGRATS to chemo #1 Done! - check that off the list!!
I ended up shaving my head 2 weeks after chemo #1 as my hair started coming out - A LOT - and it freaked me out, so for me, I felt empowered cutting it all off before it all fell out! I took photos, before, during and after the haircut. My DH did the cutting/shaving and then warned everyone at work, which by the way, they were all so supportive of me throughout treatment. When I donned my new wig, I named her Ginger, and everyone in the office still has memories of Ginger, they liked 'her' look on me better than my own hair! UGH! haha
On the triple negative, I hear that the Herceptin is some good stuff! So what chemo regimen are you on??
Big big hugs sweetie, WE ARE WITH YOU!!!
kari
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Swanny,
Glad your started your treatment, important to stay on schedule, the panick attacks should decrease as you become adjusted to your routine of drugs. I didn't think that was possible, but knowing what to expect for me made me more comfortable. I am sure you will be as beautiful without hair as you are with, how many woman can say that??? I notice your markers are exactly as mine, I am doing pretty good health wise, small stuff compared to what you ladies are now going through. This journey changes our life, how is up to each woman. Herceptin is for triple positive; although one of my doctors told me he read that Tamoxifen could be used for all woman with BC. In my eyes that is scary, not in my eyes.
Take care,
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Hi ladies,
Swanny, how's it going? My stats are very similar to yours and Brena's also. I'm another triple neg girl. Don't let all that stuff scare you too much! My onc and my BS neither one seemed to think it was any bigger deal than any other breast cancer. It's just different and comes with it's own set of challenges. But there are pluses about it too as it does respond very well to chemo. Hang in there girl!! We have walked the road you are on and we are right beside you now holding your hand.
Today is the one year anniversary of my first chemo. Like Kari, I shaved my head about two weeks later. It was coming out in huge clumps and I couldn't stand it anymore. My husband shaved it for me and it was so uncomfortable and prickly that I finally got some shaving cream and a razor and turned myself into Mr Clean. And now a year and many chemo treatments later, I have plenty of hair! Getting stronger everyday! Life is good!
Hugs to all, Mary
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Thank you everyone. Today will be my 2nd chemo treatment. Can't wait!
I have been very lucky so far. Side effects have been minimal (metal taste, tired, tired, & tired, and a kind of brain fog for day 4 & 5). Hope my good fortune continues. I still have hair but I am expecting to lose it any day now.
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Hello all, I am joining this discussion. I will be having my first chemo on Wednesday, June 2, 2010. Thanks for starting this thread!
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Jenni---We're starting pretty close together. I have my first treatment tomorrow, 5/28. Good luck to you!
Laura
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Good luck tomorrow Laura, I hope it all goes well and you have minimal to no side effects!!!! It may sound strange but I can't wait to get started already with my chemo, my surgery was six weeks ago tomorrow and I just want to battle this beast as much as possible!!!
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Swanny, glad you are doing well with the chemo. I hope that continues for you!!
Welcome Laura and Jenni!! I hope you both have an easy time of it also.
My clinical trial nurse called today. I have to have another ECHO and EKG for the trial. Oh well. Always nice to know they are following me closely and those tests are easy. I see my primary on June 7th and I know she will order a mammo on my remaining breast. I'm getting uneasy already just thinking about it. Guess that never goes away now. No test is "routine" anymore.
Good luck ladies! We are here for you if you need us!
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Had second chemo yesterday, Just metal taste right now and hungry (from the steroids). My hair started to come out yesterday also (two weeks to the day from my first chemo). Just maybe 5 strands at a time so I went to the beauty shop and had them "buzz" my head. It actually looks cute - believe it or not. So I wore a hat to work today. Everyone thought it looked great. The next few days should be challenging but I am off work till Tuesday so I should be fine by then. Good luck Larua and Jenni. Hope by me being a couple of sessions ahead of you will help you know what to expect. So far I have been very lucky.
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Laura and Jenni
How did your first chemo sessios go? I have my chemo on Thursday afternoons at 2 pm. Then I am tired and not feeling quite right until Tuesday at noon. After that, things seem to pick up for me. How has it been for you two? The metal taste is the worst. I love Pepsi and I have not been able to drink it since Friday. Last time, I gulped two bottles on the Weds and Thursday before chemo, it finally tasted good. I have some little black marks in my nail beds. Not sure what that is about but I remember reading one of the girls saying her nails turned black and I think they even fell off? Not sure about that.
Well - hope you are both doing well. Keep in touch.
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Hi Ladies,
I am going to join the thread. I am also going to partake in the trial. I start chemo next Tues 6/15. I have to admit I am anxious about starting but also getting more nervous as the days get closer. This thread had really helped me understand the possible SE's. My husband wasn't in favor of me doing the trial but after a lot of heart searching I decided it was right for me. Not only the advantage of possibly having the drug but the hope that I will help my (3) sisters if they get the "beast" behind me.
I hope Swanny and Jenweg make out ok on your treatments.
Take care All!
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Welcome grneyd5600
I have my 3rd treatment this Thursday. So far I have been very lucky and have minimal side effects. My buzz cut is finally starting to fall out. I can grab little sections and they come out. I still have hair everywhere else (arms, eyelashes, eyebrows). Maybe in another week I will be completely bald. As I have said before, I have chem from 2 - 5 pm every other Thursday and then I feel "yucky" but nothing bad until noon on Tuesday. Then all of a sudden I start feeling my same old self except for the taste part. I hope all goes well for you and keep in touch.
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Welcome Laura, Jenni & Jackie,
I've been staying tuned this thread and checking on your progress. Hang in there girlies and Hugs Hugs Hugs to you all!
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Swanny, good to hear you are doing so well. I am hoping for the same! We are going to buzz cut my hair a few days ahead of the "fall out. My hair is down to the middle of my back and I am just not wanting to deal with the whole fall out in big clumps thing. So buzz cut will be first.
Kari - thanks for the welcome and the hugs! Both are great!
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Jackie, I did the same thing with my hair. Named my wig Ginger and tried to have fun with her...as much as I could at least. Only wore her to work and as soon as I got home whipped her off. My hair started coming back during the end of my Taxol's. I checked your chemo regimen, its the same as I got. I started chemo August 28, 2008 and finished January 15, 2009. I was in the Arm that continued on for the 10 remaining doses every 3 weeks. Finished that August 6, 2009. I missed one Avastin because of being exposed to Swine Flu.
I wish you all the best and sending you more HUGS!!
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Swanny thanks for the wishes, I am finally catching up today on the boards. Not liking this chemo thing but gotta do it. Had my first treatment last Wednesday and am feeling normal today finally. No throwing up, just horrible nauseau, dizziness and acid reflux. My voice still isn't back because of the acid. Well now I know to take more meds!!! Hopefully next time will go better. No mouth sores but my throat is swollen and hurts to swallow. But I am finally coming out of it, thank god. Next time I will def be popping more pills haha.
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Jenni
Hope it gets better next time. The nauseau isn't too bad for me. I take the meds they give me and then take maybe one extra pill a day for 3 or 4 days and then I am good till the next time. No dizziness but I did have one evening of acid reflux that was horrible. Never had it before. I do have little black marks at the top of my fingernail beds. The doc is going to check into it. She said that usually comes with Taxol. Doesn't bother me but not using nail polish so I can keep and eye on it. Now if I could just drink my Pepsi and have it taste good. But really, since I have been eating so much, not being able to drink the Pepsi is proabably the only reason I have not gained any weight. ha-ha. Take care - keep in touch.
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Kari - thanks for the note! I am glad to know you are done and made out ok. I am so ready to get started so I can get done! I actually put out my wig yesterday and put on one of the hats I bought. It was on the dresser when hubby came home and it made him laugh! I am like you will probably wear the hat to work but going "free" when I get home. I ride a harley so the doo rag is part of my normal attire anyway. I have a bunch ready to roll!
Jenni and Swanny - hang in there girls I am right behind you. I hope you both make out ok. Sending good thoughts your way!
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I am also triple neg, and had my first treatment on June 2nd, and will have the next one Monday June 14th. I'll have 4 AC and 12 T, followed by radiation. I'm in the 5103 trial also. The first few days after my first treatment were bad, but I've felt better every day since. I'm continuing to do Pilates and Spin classes, and just hope I can keep it up.
Good luck to you all.
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mitymuffin,
Sounds like our treatment plan is the same . . .I had my first AC on 5/28 and will be having my next on 6/18. I was EXHAUSTED and a bit nauseous the first several days after my first treatment, but I was good about taking the anti-nausea meds and that helped a lot. I've been feeling great since except for the sore on my tongue that appeared several days ago---sure makes it difficult to talk and eat (2 of my favorite activities!) I worry a bit that the next treatment could be a bit more difficult . . .trying to stay hopeful it might be the same. Will be halfway finished with the AC after next Friday regardless.
Good for you for keeping up with the exercise . . I'm thinking of getting back into my walking routine tomorrow.
Hugs!
Laura
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Laura, I had to use Magic Mouthwash (ask your onc for a prescription) all through chemo. I had the tongue thing the whole way through and it finally went away a month after completing Taxol. I bought Biotine mouth rinse and toothpaste, but I developed a gag reflex when using it...it was weird, I had all sorts of weird se's.
mitymuffin, welcome! Take it easy and listen to your body, each AC is cumulative and it can be an a**kicker!
Best of luck girls, you are doing it!!! steps closer to being done!! YAY
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Charliebird, Its good you are getting back into your walking routine. Walking is great medicine.
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