Is there a July 2011 group?
Comments
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bcisnofun: You are absolutely right! That is why I am still questioning it. The ER doctors last Monday thought that it was infection. Yesterday my oncologist told me that my long version of UTI test had come back negative. So they think all the pain that I had was from the Neulasta and Taxol. But, I have never heard of white counts that high, so I was putting it out there for you guys to see if anyone else's numbers had gotten that high without an infection.
I am still on for Taxol #2 on Friday along with ample quantity of Oxycodone and maybe a couple days off to suffer through.
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So happy for you Misswim! What do the WBC number signify? Are they in thousands? I'm confused. I was told last week I could not do the chemo with Abraxane because my count was 900. Would that be 9?
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Misswim --- so glad everything worked out. And Rabbit,let us know what's going on as soon as you find out. Do you have a port on that side? The line that runs from my chest port is under the skin but I can feel a bump where it goes over my collar bone and down in (vena cava?). Sending good thoughts.
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ellen-wbc I think are in the 1000's so you were low. Mine hover around 14.4 which would be 14400.
misswim-so happy for you, we all kept postive thoughts rabbit-thinking of you, stupid chemo! stupid SE's. only positive thoughts for you as well.
tomorrow is my day in the chair, Snoopy how about you? ready? set? go?
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dexxy - is this your last one?
rabbit - any word yet?
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Rabbit-thinking about you...hoping all is well.
Dexxy-good luck tomorrow and hoping for no SE's.
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Thanks for the info dexxy. That's kind of what I thought. My doc likes it to be above 10 to do the chemo so I'm just on the edge where he pulled the plug last week. Hopefully numbers will be better this week. Good luck in the chair tomorrow.
Rabbit, feel better.
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bcisnofun- Yeppers! the last I hope I ever have to do in my life!!
ellenquilt-do they have you on neulasta? you've had so much on you're plate this last week it does take its toll.
thanks ladies for all the well wishes, we are getting through this, just when you think its nevr gonna end, here it is! met with my RO yesterday and I will start radiation on October 3rd, 6 weeks
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Yea Dexxy!!! As a friend said to me to keep in mind - "one and done baby!"
so everybody - what do we do now when we're all done with chemo? Do we stay chemo sisters?
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Hello ladies, I am sorry i have been MIA:-( I was away on vacation last week with my kids & hubby, went to MD/DC to visit my sisters, cousins & friends, had a fab time, came back over the wkend, had tons of housework, grocery etc to do then back to work on tues and kids back to school, so did not ahve time to even sit on the comp! I have missed you gals:-) Hope that all of you ahd a great labor day weekend. Thank God, last week was my "normal" week and i still feel good:-)
Ellenquilt - Sorry about your house, atleast you son & adopted sons:-) are helping with the clean up. Hope all goes well wiht the insurance.
So tomorrow is my # 4 on the chair, then i will have 2 more to go, cnat wait!!!
Today i am not feeling so good emotionally, there is a girl i know who had BC about 4-5 yrs ago, she is ver very sick and in ICU as we speak. she had a masec then chemo, not sure if she had rads or any meds after coz she had a child after chemo, her youngest is 2 yrs her oldest is abt 7 yrs. anyway, i dont know her diagnosis very well, but i think the cnacer came back in her head then last week she had some sort of surgery to her lungs, then today she developed pnemonia and was taken to the ICU... i am feeling really down and scared, just praying so hard. Sorry to dampen you with this, i jsut had to let this out. Thanks for listening.
Sending you well wishes and positive vibes. Dexxy & Anna - All the best for tomorrow:-)
Hugs to you.
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hi all...sorry, was at the hospital for 7 hours!! What a way to spend my bday
oh well, could of been worse. Again, I have to copy and paste what I just posted on my caring bridge site, sorry to not be personal. I am absolutely beat, but here's the update:
Ok, where to start...woke up around 7am this morning feeling worse. Tenderness in the left side of my neck was worse, could barely lift my arm above my shoulder, when I turned my neck either way, but mostly to the right, it hurt BAD. So I phoned the oncologist office when they opened at 8am, they got Brooke, the PA, on the phone and she said to come right in. That she wanted to take a look at what was going on and that it sounded like it could be a clot.
I woke up mom "mom....you gotta drive me to the hospital" she almost jumped out of bed. We got there shortly after, saw Brooke and Dr. Hargis pretty quickly, they determined it was probably a clot in the jugular or thereabouts and sent me downstairs to get an ultra sound. My arm at this point is discolored, a tint of red (full of blood I guess) and my neck is more swollen on the left, the whole upper body on the left is swollen. And it feels tight...like it's being strangled.
The tech that did the ultra sound said she wanted the radiologist to come in the room to look at it himself,she had found something. Mom was in the room with me thankfully, not a good feeling when they are scanning your jugular vein and seeing clots!
The radiologist was very informative, he explained there was definite clotting, in the external jugular, not the internal or main jugular vein. I had no clue there was an internal and external jugular???
He said I would probably go on blood thinners..if it was too blocked there would be "other avenues" but thankfully my oncologist decided I just needed to go on lovenox injections daily until I am done with chemo, end of November.So today I learned how to give myself the shots..not too bad, tiny needle, did it in the gut. This med will prevent more clotting and hopefully dissolve the clotting that is there now. I was told it would be weeks or months before it dissolves. I hope the arm swelling goes down soon, that is annoying, now I have an idea how it feels to have lymphedema, it hurt to just pick up a glass with my left hand. I can't do any upper body exercising and nothing but walking really, can't take a chance that any vigorous exercise or straining dislodges the clot and I stroke out!
Well, I finally got home after almost 7 hours at the hospital...took a 30 minute rest, elevating my left arm, then had a few people over for my bday dinner. Blue, Nikki, Karen, Lynne, Dad and of course mom, Lauren and Kyle
it was fun, and I got some great presents. Mom made some awesome meatloaf and redskin mash potatoes..Nikki and Blue did an incredible zucchini dish with garlic YUMMMM, Dad bought me a peanut butter/dark chocolate bday cake that is so rich I could only eat a few bites, Lynne brought some blue chips and salsa, we had a great time, took my mind of everything today!
Love you all, will catch up tomorrow I hope
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Blessed Birthday Rabbit. I love your positive attitude!
Snoopy so sorry to hear about your friend. Cancer sucks big time. I had my #5 on Monday and it's worst than ever. Felt like a truck ran me over many times. Dare not think of my #6 side effects but at least it will be the last in my lifetime! -
Thanks for letting us know rabbit and so sorry to hear that news. Clots and blood thinners are serious business. My daughter was on blood thinners when she was a baby and I was terrified watching her learn how to walk with Coumadin in her system. But it sounds like you have things under control and I am sure you know how to walk without falling over by now. : )
Happy birthday and rest well!
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FrancesC: I am sorry to hear that treatment knocked you down so hard. That countdown is what is motivating me too! I have three more dd Taxol and as much as the last one knocked me down, I am ready for Friday and getting another over with. I hope you feel better soon.
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Thanks J-bug. All the best for Friday and I pray this time round it's easier on you.
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Today was Taxol #2 of 14. Longish day, but I got to see an old neighbor on the Metro. The first Taxol ran me over like a Semi. All I can think this time is Back Off Evil Truck. You shall not pass! I found that a couple of alleve worked for me. And sleep. Lots of sleep. Can't feel the pain when you're passed out. I have noticed that when I started drinking coffee again my blood pressure has gone DOWN. Weird, eh? Right now I'm still high from the steroids. Feels like I'm channeling Ellen. Wish I knew how to knit. I could make a shawl. Took a melatonin and hopefully that will help me go to sleep. Kinda feel like it won't. I can't clean because I live with 5 other people and I don't want to wake them. Argh! So much energy at the wrong time of day. sheesh.
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I have been away for a couple of days cause my chemo number 3 was very bad for me, not with the side effects but mentally.Im getting tired of all of this treatment specially cause a friend of mine from Chile is dying from this stupid thing.She had BC 3years ago and now in May she had mets in her lungs , did chemo didnt work and now is everywhere and she is sufering so much, she is only 38 like me , has a 6 years old gilr and all of this is breaking my heart and my hopes.
Today I had chemo number 4, not so bad like always and now to wait for the SEs, I hope they stay nice with me like until now.Finally my onco gave me sleeping pills so i can fight those stupid steroids that dont let me sleep.
Rabbit I hope you are doing better, too bad that you have to spend your birthday like that, but at the endwasnt so bad at all..you are a very positive women.
Frances C I hope those SEs go away pretty soon and you feel better.
good night and i hope we all have betters days.
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Paulamati hang in there- take care of yourself to fight this cruel illness. You must remain positive and strong. My heart goes out to your friend in Chile and I wish her all the best.
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OMG Rabbit sorry you are having such a hard time Dam this diease Im sure glad you got infast to have alook @ what was going on.Hope you are feeling better,
Congrat's Dexxy on finishing up cant wait for that day
Jun bug I hope you are doing better and your results come back good.So Happy for you misswim Hope you are doing so much better,Im day 2 of 3rd Fec taxol and doing good I hope everyone else will be better real soon when this is all over we will have to have a big Reunion.
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thanks everyone for the kind thoughts and vibes! BC sucks, have I said that lately LOL
paulamati, I am so sorry about your friend. It's a horrible, nasty disease and sometimes it gets the best of us, it's such a shame. I will pray that she does not suffer.
FrancesC, hopefully your SEs have lessened by now, I know that feeling I had it with #3 and #4 worse than ever as well.
shinypop, how are you feeling today? I sure hope the SEs weren't as bad as the last go around. I know what you mean about the steroids, especially those first few days after chemo when on them, I am wide awake at the worst times. And I am up at like 6am every morning, even today, days after the steroids....they must linger for days, I have a love/hate relationship with them, are you channeling that too? LOL
J-Bug, I don't know about that, usually I can walk without falling over, but the chemo brain/fog, sure doesn't help. I catch myself losing balance every now and then, I do have to be much more careful for sure.
Sandy115, so glad your 3rd FEC wasn't terrible..that was my worst!
hugs and kisses to everyone!
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Rabbit.
So far this morning I feel great. Probably steroids talking. I woke at 7am, an hour too early. My pet rabbit was thrilled, he got lots of snuggles. Then the cat had a party in my room and there was no way I was going back to sleep. I'm at work right now. They're so awesome that if I start to feel bad I can always go home. I want to work though. I'm tired of sitting in my room watching tv.
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My x-ray came back negative as well. I am so thrilled. My onc thinks I was having SEVERE Neulasta reaction. As I am three weeks away from the Neulasta, I do feel a bit better. Having a bone scan did wonders for my head. I was freaking out ladies. The onc gave me a perscription for a massage, and a referral to a pschycologist to help with my anxiety. I know that I will have this fear for the rest of my life and I need to deal with it.
Rabbit- poor thing. Glad you will be ok, but so scary!
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Celexa is my friend right now! : )
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Oh honey, I have moved on from the Celexa. I have got klonpoin which is the best thing since sliced bread!
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Rabbit..belated happy birthday and so glad all is being treated..must have been terrifying.
PAulamati...so so sorry about your friend..this is such a terrible disease and when you hear what it can do, it is so hard not to live in fear
Frances I hope you are doing OK...you are almost there.
Sany115..hang in there
Snoopy 73... I have my last TC tomorrow and start rads on Oct 23rd too.
Jbug... you have amazing stregth..I hear it in your words.
shinypop...keeep popping those aleve...I get headaches a lot and find I am popping excedrin but being careful not to get too much tylenol...
Switching oncs once I am finshed with last chemo and SE's and switching rad onc too....was at a palce I loved but lost my confidence...everyone is great but I had to do way to much self advocacy and it has tired me out.
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Paulamati- I am so sorry about your friend.
Frances- Feel better! I had my first Taxol yesterday. Right now I am on the roid rush that Ellenquilt kept describing. Never had that on the A/C.
Painting- good for you. I am doing the same. Going to a consult at Dana Farber in October.
J-Bug- you are awesome.
Ana- thanks so much for your thoughts.
BCisno fun- my chemo buddy- your support has been amazing!
Even when chemo is over, we have to keep this thread going! You ladies are like sisters and I know I could not get through this without you!
Big, big cyber hugs to all!
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Hi ladies! Just popping in to see how everyone is. I started my 2012 Relay for Life team this week. Our team name is Across the Rainbow. You can check us out on Facebook. I am looking for some people to share their story on the page also. I want to put faces with stories. If anyone is interested please let me know. You can find me on FB also. My email is unc_boswells@yahoo.com. The ACS is doing the Strides for Breast Cancer here on October 1st so Raleigh will be full of pink! Since October is coming up, I have seen alot of contest to raise awareness for BC. Our local feed store is doing an animal contest. Animals should be dressed to promote awareness for BC. I am going to enter my doggie Callie and my SIL is entering my neices pony Nutty. I am a little stuck for ideas. I dont want to do the same thing as everyone else and put her in a pink skirt. ANy ideas? I really want to be out of the box, lol. Doing these things is getting my mind off my own diagnosis a bit. I had my last chemo and will start Tamoxifen on October 1st. I guess I am just nervous and I am in that kind of "now what" phase. My onc isnt going to do any bone scans or things like that. Just watch for anything that may pop up. Makes me a little nervous. Ready to move forward but scared to at the same time. I have an appointment to see my PS next week. He will be scheduling my exchange for mid October. Again, I am ready to get these boulders outta my chest and get some soft boobs but I am scared of another surgery. Just a lot of rambling going on with me now.
Hope everyone is doing good. I see alot are halfway through!!!!
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Rabbit: So sorry you are having so much trouble but glad you were able to celebrate your birthday anyways. The party must go on! I have been on blood thinners since 2007 for A-fib, but recently switched from Warfarin (rat poison, really!) to Pradaxa. It was a nuisance before, but the new med is better and I can have my veggies back again without the weekly finger sticks. Hope you are feeling better. I do have to watch and remember that I need to apply pressure when they "unhook" me from the port to prevent a subcutaneous bleed. Those are a bitch because they look nasty and they make my port hurt from the pressure.
Snoopy: I'm so sorry to hear about your friend. Cancer does indeed suck bigtime.
Frances: Feel better and glad you are only one away from being done.
J-Bug, we will be in The Chair on the same day. I have #8 of 13 with the herceptin and abraxane. I hope my wbc is high enough to get back into the chemo game. The sooner I get through the better. I wish I could test it at home so I'd know before I get my head set to spend my five hours there. Good luck tomorrow!
Shinypop I also had bad muscle pain after the first Taxol, but that got better until I became allergic to the big T. Now it's a crap shoot every week. LOL Have fun channeling me! hehe. I'll be channeling me tomorrow too. You can learn how to knit on You Tube you know.
And when I start to come down from the steroid high i reintroduce my ass to it's spouse, my recliner seat. It's a happy marriage.
Paulamati: So sad to hear about your friend in Chile. Again, cancer really sucks. Take care of yourself and keep a positive attitude for yourself.
Misswim: So glad everything turned out well for you!
Painting: Glad you are switching. Hopefully you won't have to fight so hard at the next place for what you need. BC is tough enough without having to deal with the extra crap.
I also hope this thread continues. You are all such a great group, I'd like to keep in touch!
Jamie: GEt some pink tulle and make her a tutu. And get a doggie tiara too. You can embellish with pink flowers. She will be adorable. So happy you are finished with chemo and ready to move on to the next step. I figure I'll be starting radiation sometime late October or early November and the herceptin continues until next July. After that I'll join you in the Tamoxifen party.
My friend Kathleen is joining me tomorrow (which is good since my old van is back in the shop, on its last legs and I need a ride, LOL) I made the decision to start looking for a new (well, not new, but certified pre-owned) car this weekend. For the past three years every time the check engine light went on in the car it also went on on me. And raised my blood pressure. I drive all over NYC for my job and I can't take the stress of dealing with a flaky car anymore. So I'm juggling things around and got my dad to agree to co-sign a loan for me (don't ask, my older son and his issues have not helped my credit over the past five years) so I can get a car without being destroyed by the interest rates. I'm looking forward to a relialbe set of wheels hopefully in the next week or so.
Still waiting for the adjuster and the FEMA people to do an inspection. I'm living in a storage locker still with bicycles and storage bins all over the hallways and the dining room. My bedroom has things piled up all over the place. It ain't pretty but it's a place to live. LOL Eventually I have to believe things will get back to some kind of normal. Whatever that is.
If anyone in the chair wants to chat tomorrow afternoon EST, I'll be plugged in around 2 p.m. until some time after 6. You can Skype me at "ellenquilt". Good luck to all and minimal or no SE for everyone!
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Everyone, catching up on your lives. I have been taking a break from reading just to get the BC off my mind. Tx 4 of 6 next week. Each one has new or worsened SE so just digging in to work a bit to keep my mind off it. Definitely wishing you all the best.
Probably a little late to respond but my WBC went up to about 65,000 with Neulasta on my first tx. We switched to neupogen so we could control how high it went but requires multiple daily shots and multiple repeat blood counts. It did make me feel terrible after the neulasta. But on neupogen, it was down to 2,000 and I felt tired then. So nothing is perfect. My understanding is WBC counts go up naturally with infection and inflammation so in our cases, elevation (after neulasta or neupogen) is desirable except when we have fevers above 100.... Good thoughts out to those of you struggling and best wishes for few SE to those getting tx this week. -
Yeah woke up feeling better this morning. The body aches have subsided. Another shot of neupogen today and hopefully the body aches don't come back.
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