April 2015 Chemo Crew... Starting in April? Please join us!
Comments
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Princess..yes. yes it can. our nose hairs could start growing like crazy!
Its 400 degrees in my office, which is nothing new since hot flashes started, and supposed to be 97 tomorrow. Yay, I get to hike! Actually super nervous about that. I HATE not being able to rely on my body!!!!!!!! Ok..off the ledge. Good body. Good cancer killing body. Good, strong, hairless,(except for nose hairs and stray pubes and fucking horse fetlock length ankle hair) body...
Gingeel, my wig is off to you! Remember, creepy little girls belong in horror movies, and super awesome bald ladies belong Everywhere!
Stacie, is it you who is already planning to get rads and deported??? You go girl! My MO wouldn't schedule me yet, he said its just an office visit and they will pop it out three weeks PFC. But Dammit! I want a date so I can count down the hours!
Well, go fitted for a lymphedema sleeve and glove today at PT, and learned some manual drainage techniques. That stuff seems like magic..I'm not used to any therapy working unless it hurts LOL. I don't have lymphedema and I want to keep it that way! On the plus side, my PT said that the cording and scar tissue has reduced even since Monday! Those freaky scar nodules that sent me to the MO are smoothing out, and I've started to regain range of motion in my shoulders.
Hope everyone is having a good day! Lynne, hiking is not mandatory
and you crack me up every damn time!
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anyone getting chemo Friday with me
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Why is it that I can only taste pie and gelato in my chemo yuck mouth! Not helping on holding the line on the chemo weight gain. Made Korean BBQ ribs and jalapeño slaw last night and could not taste the heat at all. Meat tasted like cardboard. Luckily, fruit works too. 7 days post TC #3 and my mouth is by far the worst it's been despite salt/baking soda and Biotene. Any other suggestions??
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I'm so glad I'm not the only one that can taste junk food lol. Healthy food just doesn't seem to have a flavor. Bananas taste like cardboard and I can't really taste milk or yogurt anymore. My taste is just extremely weak so when I cook dinner I have to ask my hubby to taste test it. I wish I had advice but you're doing everything in doing.
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Yep taste buds are gone. It is awful! Even worse as I want to eat and have gained some weight. What fun is that when I didn't get to enjoy the flavor?! Errrggghhh. Frozen fruit has been my go to munchie frozen grapes, etc. The cold tastes good. I also put fruit in all my water as plain water has that metallic taste. Hang in there.
Kbeee hope storms not bad by you in IA? We shall see what tonight brings. Lots of rain so far. Enough already. Quite the pattern that just doesn't want to break.
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Kbee - Your dreams just broke my heart. I do understand. The first time I was diagnosed my youngest was in junior high. I was so afraid I would not see her graduate. Thank God she is now 30 with 2 beautiful sons. You will be there too. My DH and I had a good laugh (which I needed) over the 12 rounds of chemo. Sad thing is it is so true!
Alibeths - I have treatment on Friday. I go in at 8:00 will have blood drawn, see MO and trial nurse, EKG, then at about 10:30 will start treatment. Will be done about 1:30.
Scarlett152 - I can taste lemon fruit popsicles, chili, hot links with bar-b-q sauce and believe it or not, fried corn.
Gingeel - Children are so honest. Bless them. They see something different and they stare and process it. Beats the heck out of people that try not to look at you like you are not there.
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rpayton, several tornadoes a few counties west headed our way. Hoping they die down. I am not planning on getting any sleep at work tonight at the fire station!!! Just hoping for no damage or injuries
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Hi All,I've been thinking of you often and hoping that each of you are doing the best that can be expected despite the treatments and crappy SE's. I am happy to report that at just about a month out of treatment-my taste buds have come returned (hair-not so much!).
I know it's been a while since I last posted but I wanted to share some of what I hope will be encouraging news to those of you who are having a rough time envisioning the "good stuff" again. With God's help-not to mention some major surgery and some kick ass chemo- I was able to watch both my daughter's 8th grade graduation and then my son's high school graduation! I can't begin to tell you how devastated I was back in November when they diagnosed my reoccurrence. I remember thinking over and over again that I wouldn't be able to see my kids graduate and crying and crying. Yet THERE I WAS beaming away and crying tears of joy (like so many other moms). We had a HUGE party in the back yard and despite the periods of rain (which any other time would have bummed me out)-I was just so happy and so thrilled to be a part of everything!!! I can't tell you that I don't have the "morbid thoughts" now and again but this weekend reminded me that I have to try to truly focus on the here and now and not miss the opportunities that are right here, right now! Wishing you all lots of those "right here, right now" moments this summer with your friends and families as well.
Love to all,
Fran
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Finally! I got my path report today during an appointment with my oncologist PA. Clear margins, no node involvement!!! Yea me!!! My MO had not seen my report yet, since they had to request a copy from the lab! Such inefficiency! Anyway, he still needs to determine what my remaining tx will be. PA thinks I should go ahead and have my last two chemos and have rads and then complete my year of herceptin and perjeta, but MO has final word on it. I'm hoping I'll hear from him tomorrow. Could you please draw this out a bit more for me!?! NOT!!!
Kbeee, I got goose bumps when I read your dream! I know that must have been so stressful! I'm glad you've put it behind you and are feeling better about stuff.
Thanks to all of you for your care and support. Love you guys! 😘
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Yay!
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Sheshe! Awsome! Big sigh of relief!
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Fran: so awesome, seeing your kids' graduations! Congratulations to them...and to you!
Sheshe: great news!
Re taste - I wish I had that issue but food still tastes good to me. Dammit! No losing weight here. I do get mouth sores but they are mild and more annoying than painful. The miracle mouthwash my MO prescribed seems to do the trick.
Re little kids and baldness...my grandson is 2 1/2 and is now quite used to the fact that Grandma has no hair. He is very matter-of-fact about it. He is very bright and talkative and says it's because Grandma is on chemo (though I am sure he doesn't know what that means). We have a spare room in our house where I keep my wigs...Peter calls it "the room where Grandma keeps her pink hair". So cute!
To him it doesn't matter if I'm wearing a wig or a hat or scarf, or am bald...I'm still Grandma!
Andrea
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Aw, Andrea, what a great story, it made me smile!
Sheila - great news!!! Now you can celebrate.
Fran, thanks for the pep talk, we all need it.
Renee, after T#1, started on day 2, my mouth felt like I had burned the inside, but it was a couple days into healing (if that makes sense). Food was not as tasty, but not totally cardboard either. Then it went away. I've been eating and tasting everything. I've been especially into ice coffee. My coffee maker makes coffee so hot, I can't drink it at first (I drink it black). The ice coffee feels so good on my mouth and throat.
Scarlett, hope your tastebuds come back too.
My food aversions are for stuff I stocked up on for snacks while I'm doing chemo. I had bought some cheese crackers, nuts, and some other single serving snacks. I had also brought frozen grapes to first infusion. Now, just the thought of those things makes me nauseated. I also had this home-made soup after my 1st infusion. I still have a bunch of it in the freezer, but can't bring myself to eat it again. I hope that goes away.
Still packing, doing laundry, and organizing. As I was trying to get all DD2's clothes together, I ended up filling 4 garbage bags full of clothes that no longer fit her, and 1 bag of donation/rags. It feels good to get stuff done, even though it's just a dent into the chaos that is my home. I almost wish I wasn't going on vacation so I could keep going with the purge.
Lynne
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just popping in to say hi... Looks like i have a lot of catching up to do.
Waiting for my blood draw, then upstairs to see mo and then if all good... Off to chemo #5!!!
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Hi everyone,
I went to a neurologist yesterday because I started having tingling/vibration in both feet and legs after 4th dose AC. He was not helpful and said it would be unusual to get this after AC. I am suppose to start Taxol tomorrow and am so scared of allergic reaction and that I am already having a nerve problem in my feet and legs my MO doesn't know what is causing it. I am so tired from not sleeping well due to leg tingling. So worried about taxol. I feel so stressed. Also do your doctors recommend L Glutamine before Taxol? My MO does not but my friend who is a NP told me to take it. Sorry to complain so much. I don't know why my feet/legs are tingling/vibrating after AC? So scared to start Taxol
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Ankledolphin, Hope all goes well today!
Lynne, Have a great vacation!!!
Andrea, Your grandson is very wise and absolutely correct.......Grandma is still Grandma.
Sheshe, Great news! So glad you finally got your results. How frustrating that your MO did not get them. You'd think these places use the pony express, but in the age of computers, there's really no excuse.
Fran, Glad you stopped back in. It is always so nice to be reminded that normal will return.
Addie, Everything I eat tastes like cardboard too. That is exactly how I describe it to my husband! It's like eating the pizza box instead of the pizza.
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Bitterroots blooming today..sorry for the crappy cell phone pic. I am thankful that Taxol is allowing me to do a limited amount of field work...
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Jen, you'll have to change your screen name to "bigpinkflowers".
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Ha! I should. Weird thing is, I was staring at a boquet my husband got me when I found this site and wanted to join. It had little blue flowers in it. Such a scary time in my life..it would be good to leave that handle behind...:)
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yuck getting worse
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Had my last blood draw through the port this morning. Only 1 of 3 docs had their orders in, so I asked infusion to use the on-call doc to confirm it at one place and to honor a paper copy on the in-house form but without a signature, which it appears they did. I was polite and very clear that I'm not having extra blood draws.
Not sleeping well, worried about getting the port out and the sim next week. I'll feel better after I've done my weekend teaching. I'll feel much better when the port is out!
Edited to add: Oh, Stacy! Are they painful? You poor thing.
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Headed to Sandiego with the family for the weekend. Hoping to get some real rest. Today is day 15 PFC and I am still dragging and having heart palpitations. I start Radiation on July 1st. Ksusan the sims and tattoo is not bad . I pushed and got all that done prior to TC 3 so that could start radiation on July 1st. I wanted to be done before I have to teach in August . Littleblue the hiking trip sounds awesome.. Lynn enjoy your vacation. Kbee you are a very strong woman. The leader and power behind this group. I just want to get done and move on. It that is possible. I try not to dwell too much. My focus is to get rads going and see if I am strong enough and not having heart palpitations, so I can get back to the gym. I am so weak now. I will probably have to start back at 8 lb weights. My gym is circuit training so it is a mix of cardio and strength. Both of which I no longer have the endurance for. I will basically be staring from scratch. Ironically my whole body is staring over. Have a great day and weekend. Remember like my tag says" Tis the season of life" This has been a hard season of life for all of us sisters! Lisa
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Anyone know how to stop a nosebleed?
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my nose constantly bleeds also!
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littleblue: sit with head upright and apply squeeze pressure to nose for at least 10mins. Also gauze under top lip in front of teeth helps greatly. Ice pack to cheeks too. I hope it stops fast for you.
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Thanks Rpayton! Ugh..still bleeding..
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oh gosh! I know in some cases an ER or urgent care might be needed to cauterize the bleed for you. The awful part of our thinned out blood. Let me know how it goes. Hugs
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Kbeee: how were those storms last night on yiyr shift any where near you?
Lynne enjoy the vacay! Rockerwife you too!
Andrea: enjoy the grandkids that is priceless. Can't wait for my 5yr old nephew and 1yr old niece to come from CA labor day.
All of you I'm praying for small peaceful moments this week and weekend.
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Thanks rpayton! It mostly has stopped now...tried your gauze trick
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Littleblue, did your nose stop bleeding? Thanks for the kind words, KBee and Woodburns. Littleblue, you crack me up...little children are creepy....hahah
Awe, Sheshe so happy you got good news!
Lynne, lucky you! Go on vacation and enjoy every minute of it. You deserve it!
Andrea, my 4 year old told someone yesterday, "my mommy has no hair because she got a shot". I thought it was cute. That's what he can understand from all of this.
Sunshine, I hope you get some relief soon from your legs and hands. Can you take an ativan? I wonder if that would help.
re food. I'm ridiculous. I lost weight with AC, which wasn't an unwelcomed SE, although I hated being sick and nauseous all the time, but now I feel the weight slowly creeping back on. ugh. I'm sure you are all experiencing this? I really don't want to have to watch what I eat right now. But, I also don't want to come out of this heavy. Ok, done venting.
Feeling good, been busy with my 3 kids. Did notice some residual aching in my legs today. Just thought I'd mention that.
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