Has anyone started a Dec 2011 group?
Comments
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Clap clap clap! Welcome to this side of the finish line! Feels good, huh?
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Congrats, Laura! You may have a crash vs. energy now that you crossed the finish line. A sense of accomplishment that you've never felt before.
I have 3 more full breast radiation treatments and then 8 boosts. I'm really sore underneath my breast and strangely emotional today I hate when it hits and you can't explain it. "What's wrong?" Umm. . . nothing I can describe! I'm hoping my hormones are waking up again.
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Laura - YAY!!!!! Congrats on finishing chemo!
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Kelloggs - That massage sounds great! Glad you were able to use it. My co-workers gave me a gift certificate after I was diagnosed. I figure I'll use it after my exchange. I hope the relaxation lasts all weekend for you!
Laura - Congrats! Welcome to this side of the finish line. It will still be a little tough over the next few weeks, but you've made it through. Wishing you a quick recovery from any lingering SEs.
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Laura, clap, clap, clap, hug. You are DONE! Sounds like a great group of volunteers and medical staff. Good for you. Rads isn't half of what chemo was although visiting everyday is a bit daunting. Rest up and whatever se's you may have will be for the last time!
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Thanks Rachel. I have a feeling the effects will be wearing off tonight. My DH is a heavy metal drummer and they have a "gig" tonight. Heavy Metal is not my favorite music but I've missed some gigs due to my tx and I will be in the front row cheering him on tonight! Hope my ears can take it!
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Laura, congrats! I knew u could do it, I'll be joining u soon, but not soon enough! Got delayed another week due to low counts.
It has been an emotional roller coaster, but we r all survivors and will prevail! -
Congratulations Laura!!!
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Most insurance will pay for massage theraphy if the therapist is in a chiropractic office. My massages have kept me moving ESP with my fibromyalgia
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Thank you so much my wonderful friends! I have to say that although I am so happy to be done with chemo, it still doesn't seem quite real to me and I've been more exhausted than ever. I even slept through the steroids. Very emotional too.
Now I find myself feeling so disconnected, from treatment and doctors and from my former life. I guess it will be a step by step process.
Naan I'm so sorry about the delay. You will be done very soon!
Ok, a good day to all,
Love,
Laura
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Laura - completely normal feelings of disconnect and emotions. You fight so hard to get through, and then when you do. . . emotions. Let them out. It's therapeutic. And be kind for yourself as you rebound from the last treatment. Rest as much as you can.
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Congrats to everyone that are crossing the finish line!!!!!!
I had the BEST weekend ever!!! A friend of mine contacted me a couple weeks ago for a family photo session at her house. Fast forward to Saturday....the date of the scheduled session...early morning was opening day for my little boy's baseball league. It was cold and damp out so I called her to make sure we were still on for the day. Yep...just going to move it inside. Cool....raced to the studio to pick up an extra light and raced to her house.
Guess what...there was no photo session....she gathered a group of my friends (with my husband's help) for a no more chemo party!!!! I was totally shocked and speechless!!!! I really had NO idea this was happening!!! They all brought little pampering gifts--like a GC to Victoria's Secret and VS's Pink lotion and body spray!! I felt so great!!!!
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Lori, that's awesome and u so deserve it!
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Aww...Lori what a fabulous surprise! You certainly deserve it after the hard time you've had! She is a good friend.
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Lori, I was thinking about what a cool job you had while reading your story. Great surprise ending with the party. It does sound like you may not have been blessed with se's you are certainly blessed with good friends and family. How is the hair coming along? I have like five eyebrows in total:(. The head hair coverage has growth around the sides but a pretty bare top.
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Aww. Love that!
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Lori - That's wonderful!
Yesterday I had a "Thank You" brunch and invited many of the women who helped me through all of this. It was a really nice day, and I also raised some money for the local breast cancer resource center.
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What a great suprise, Lori! So thoughtful of your family/friends.
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Lori that is so cool! Rachel that is awesome that you did that.
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That's great Rachel, to give back. I would like to find some ways to pay if forward also.
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Good morning ladies, I have been mostly sitting in the background reading all the posts and I want to say Thanks for the sharing. I am leaving for my last chemo treatment in 30 minutes and don't know which I feel more of relief or dread. I am so ready for this to be over as everyone here is but the SE have been worse everytime. It seems like Dec was so long ago and this has been going on forever. Sorry just having a little pity party. Have to keep thinking this is it! I will be finished! OK party is over, just needed to vent. I can and wlll do this with my hairless head held high. Wish me luck!
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Congrats on your LAST tx Tskaiser!!!!! YAY!!!! Just remember, the SE's this time will be the last time! Welcome to the other side.
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Tskaiser - congrats! You will start feeling better n no time. You will be joining my pity party which is focused on getting my hair back. It's not happening fast enough for me! The cruel joke is that I now have facial hair! Never had that before. The gift that keeps on giving. Hmmm. Sigh.
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Lori, what wonderful friends! I'm so happy for you.
Rachel that was also wonderful of you. And a donation on top of that.
I've been pretty seqeustered these last months. This Sunday is a combo birthday for my dad and celebratory end of chemo for me. Just a few family members coming.
Tskaiser, contrats! Last one. Hope the se's are mild for you and you gain strength and stamina back quickly.
Kelly how was the gig? Sounds like a fun time.
Mardi, the waiting for the hair is difficult. I think I may be shopping for a new wig. A shorter one that won't be such a shock once I stop wearing it. I wonder how realistic it would be to cut the shoulder length one I have.
My hair is growing in around my head, sparse on top. Of course on my neck where they usually buzz you when you have a haircut.
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Seacret, I wouldn't waste money on another wig. I had them thin mine out when I first got it so I am sure they can cut the one you have. Smart girl for thinking that it maybe be a surprise to people and this would be less shocking. I was thinking I would tell people I cut my hair for a friend that has cancer. Lol. I have only told a hand full of people personally. It is a small town though and word gets around too.
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Seacret - the gig was fun, but OMG I forgot how loud heavy metal was!!! My brains were rattling! I actually made it until about 1:15am. I just love that man so much I have to try to support him after all he's done for me lately. I settled on a short wig too. In the beginning I was having fun, wearing different colors and lengths (everyone knew and I had a hairdresser friend give me a couple wigs). Now that I am done with treatment and I'm playing the waiting game I am wearing one particular short one. I think it will make the transition to my own easier for me...not them!
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Free camp for kids ages 6-16 yrs old, if u r interested for summer, the UCLA sponsored one still has space other states and locations check online search camp kesem or for UCLA camp contact via email mailto:ucla@campkesem.org. I signed up my girls ages 6 and 9, it's a special camp for kids touched by cancer, they provide fun and counseling for kids to help them deal with their sick parents.
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Whata, we're your friends, so technically not a lie, hee hee
Had treatment 9/12 finally, 3 more to go then surgery rescheduled for 6/8, then radiation. -
whata - thank you so so much for your generosity. Buzzing your hair just for me? How sweet
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Tkaiser - I hope your last chemo went well. Congratulations! Mixed feelings are normal. But you're DONE! Even if the SEs hit you harder this time, each day you make it is one day farther away from your treatments.
Had my first post-chemo checkup with the MO and six-month follow-up with the BS today. Both think I'm doing very, very well. Still some edema in the ankles but she said it was at a normal level to be expected - she'll give me a water pill if it's still around next week. Bloodwork was great; rbc while 'low' was supposedly very good for someone this soon out of treatment. Guess I'm glad I've been taking my iron supplements every night. I'm usually low on a normal basis.
So from here on in, it's bloodwork/MO appt every three months. No markers, though. She said my situation - no nodes, etc - doesn't warrant it unless they start to suspect something. Otherwise, there are too many wild goose changes when proteins can fluctuate for other reasons. Wish there was something to keep an eye on, but I guess we're all working from the assumption that they got it all through surgery and chemo was the 'just in case' mop-up. As for the BS, I'll see him once a year. Once a month he wants me to look in a mirror, raise my arms up and look for anything different.
So, I guess I can start to say, "And now, back to our regularly scheduled life...."
If only!
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