September 2013 Chemo Group
Comments
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Thanks, BetterDay! I'm going to reactivate my FB profile this weekend. I hope all went well with your MRI.
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LighthouseLady,
I was surprised at how tired I was during rads too. It was kind of frustrating because I thought it would be a time where I would feel a lot more rejuvenated. The good news is that I'm three weeks post-rads and really starting to feel like my old self.
Going to help out at the Little League Concession stand today. Go Southern!! Then going to watch Tom's team play some baseball in Tacoma and do a little shopping. I might be exhausted by sunset, but I'm going to enjoy the euphoria in the mean time. ;-)
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if someone by the name of Talia friend requested me on Facebook, could you please PM me here at Breastcancer.org?
I am having trouble responding to your friend request because it will not let me message you.
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Hi Ladies. I wanted to find a group that started this BC journey at about the same time as me, and here you all are. I was dx in Aug 2013, with inflammatory BC. I had never heard of it. I like all women. am trained since little girl hood to check for suspicious lumps, but with IBC there often isn't one....the cancer forms in sheets or "nests", and mimics inflammation hence the name. I had a normal mammogram in Oct of 2012, and in June of 2013 I had odd symptoms of itchy breast, swelling and breast pain plus lymph node swelling and pain under my arm that sent me to my general doctor. I had read on line about IBC, and know it was extremely rare, so I suspected mastitis even though I was 52 at the time, and a long way from breastfeeding or any other breast issues that might start mastitis. My doc who I love suggested we try a round of antibiotics, see if I responded, and if not go for a sonogram as this is the better way to see IBC not mam. The crazy thing is I did respond, this seemed to improve, then came back with a vengeance. I have since learned that as IBC is rare, only 1 to 5 % of all BC, that you may be the only case your general doc has ever had in his practice or ever will. Yay me how did that happen?
My Oco set a positive tone from the start....he said to not pay attention to dire stats or survival rates, to expect a positive response with treatment and focus on a positive outcome. I have tried to do that and generally have succeeded in staying positive. I have been so blessed with great medical tx, great support, powerful prayer warriors on my behalf. I have been SO BLESSED.
I started chemo end of August 2013, last one Dec 10, Double mx Jan 2014, 33 rads starting in Feb. and ending last week April 7 2014. So thats me all over. I am so glad to be finished with tx. I have my first followup appt with my oncologist today. I have gone from being in treatment to being a survivor. I am NED. I am still getting used to that.
I have found this BCO website to be so great, I wish I had found it earlier, but did not, and just grateful that I did find it.
Thanks for reading my story if you have. Felt good to say it all at once. Now on to the day ahead!
Meadow
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hi Meadow,
Congratulations!! That is awesome!
I have IBC too. Very close timeline and experience to yours. Diagnosed in August, chemo from Sept-Dec, surgery in Jan, rads in Feb-March, and I have a scan on Friday to see if I am NED for sure. Still taking Herceptin (until end of August).
We just started a Facebook private group for folks who have posted in this group. Personal message me if you would like more information. There is also a Facebook private IBC group that I have found very helpful and supportive. Let me know if you would like more info.
Have a great day. :-)
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Hi Meadow. I wish you had found our little group earlier - we rock! LOL
I'm sorry you have to be here, but glad you finally stumbled upon us. I'm glad KJ chimed in - she's the only one of us with IBC I think. I was on a similar chemo/surgery schedule as you. I started AC on 8/29 and had my BMX on 1/3. I just now started rads, though... 5 of 33 done. Good luck at your follow-up today!
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Thanks KJ, I so appreciate this! Good to go through this not alone.
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Thank you Lady, Rads can be hard, my radiologist said he finds his patients to be more emotional at this stage of their journey, prob the cumulative effects of all the treatments and worry just get the best of them. I found this to be rather true, even though the treatments are brief compared to the chemo, I was tired afterward. Hang in there and thanks for the sweet welcome
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Meadow, welcome! I do hope you decide to join our Facebook group. I'm doing rads now (#11 of 33 today) and I agree with you about the emotional part. Although the rads are easy in the beginning, I find I am feeling a lot of ups and downs....just really wondering if my triple negative bc will come back. I see you are both TNBC and IBC. You won the double prize (just kidding). We are a great group of ladies and a great place for support. I think at least the core of us that have also signed up on the FB group will be hanging together for each other of the years to come.
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Hi Meadow!
Glad you found us. Well you know, I am sorry for the reason you had to find us....
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Welcome Meadow! You sound great! Positive is the key word I think! I strive for that every day!
OK, so you all didn't tell me you were still posting here AND facebook, how am I going to keep up now!!!!
I have just been reading that...duh...my children aren't all blonde for nothing..:)
Happy hair growing day!
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audra,
I've been extending invitations to the FB group to just about anyone who has posted here and has been 'seen' at the breastcancer.org site relatively recently. There are a lot of people who just posted once or twice but seem to lurke (read and not post much). I'm trying to make sure they feel welcome to join us over at FB too.
Some will prefer to stay here. That is ok. I'm going to check in here from time to time, but not as often. The FB group is much easier to follow the conversations on.
For anyone who is a lurker here, feel free to personal message me that you would like to join the FB group. Your only qualification requirement is that you have/had cancer. The only exception I can think of is Art123. I invited Art and/or his wife to join us too. :-)
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Thank you all for the warm welcome. Simplelife, Kj, Audra, Vintagegal, thank you so much, I am happy to be here with you all, it feels really good.
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Meadow, I hope you join us on the FB group if you haven't already.
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She did! ;-)
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SpecialK, how are you? Hope you are doing well. I am starting to get nervouse about surgery next Tuesday, mastectomy with axillary lymph node dis. So now that my energy is up, I am going around cleaning like crazy, etc. trying to keep my mind off everything. Hubby is taking next week off So thats good.
Take care
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Mercedes - thanks for thinking of me! I had another surgery on 4/2, still have at least 30 stitches on and under the left breast, those will be removed next week. The skin is repaired and I now have a smaller implant on the left so the skin is not so stressed. I am doing ok but seem to tire easily. Too much of doing nothing so my stamina is low, but I have been cleared to return to walking and the gym for lower body only. I am actually sitting in the hospital waiting room right now waiting as one of my best friends has a BMX with TE. She also had neo chemo but had to stop after 3 AC - her port and SNB incisions became infected even though her WBC was maintained with Neulasta. She will return for 12 weekly taxol when she is healed from this surgery. She had an excellent response to the AC and went into chemo node neg. You will do just fine with your surgery, try not to worry. I understand the "nesting" though - I do it every time!
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Hi just checking in., had my surgery on tuesday mastectomy with alnd All went well i will have pathology repirt in 3 weeks, i guess i'm officially in the uni-boobie club lol. Pain is minimal across the chest, but i am having these wicked sharp pains under my arm that are spontaneous and really take my breath away, i guess its from the nerves being cut. I know that some of the gals on FB saiid it was normal i hope
I dont have rads start date yet i meet with my BS next tuesday to remove drains.
SpecialK how are you?
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Hi Mercedes
oh yeah those sharp pains, the zings & pings, all those not so pleasant sensations are normal. Lots going on, lots trying to find its way back to heal.
My BMX was last month & just about a week ago I realized most discomfort had finally subsided. But now I just finished my first week of rads & am getting the picky feeling, some pains from that.
Hope all goes well for you!
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Mercedes, glad to hear you are doing ok. I found that light massage under my arm helped with the zings, plus stimulated blood flow helping prevent lymphoma. You know, just rub lightly to stimulate. I also found that when I was able to start the easy post op range of motion exercises that really helped too. Adjusting to the new body takes time, just love yourself, you are getting healthy again. Sounds like you are doing great.
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Yes SpecialK, hope you are healing and doing well.
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Hello VintageGal!
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Nope - not healing well. If my open area does not close by next week I will be losing my implant on the left for the summer.
Mercedes - glad the surgery is behind you - take it easy, important to go slow right now!
vintage - hang in there with rads, take good care of your skin.
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SpecialK,
Sorry to hear that. :-(
My right side isn't healing very well. It was the non-cancer side too. Go figure. CT showed seromas that I am hoping the surgeon will needle drain more from on Monday. Stark contrast to the left side that had the cancer, got the tougher part of the surgery, and was crispied with radiation. It is actually looking great. Wish the right side looked just like it. :-( -
Oh no SpecialK, what a bummer. Chit, you've been through sooo much. I was hoping all was going well and this was the end of all the surgeries for you!
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Kathryn, I'm sorry to hear that. My non cancer side was the one that got all the clots & I needed the reincision & evacuation so the scar is a bit thicker. And that is the side that had a bit of a wave effect when touched but it doesn't appear it developed into a seroma. Go figure...
I hope this gets taken care of for you easily!
Lyn
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Sadly, things are not looking any more promising so I am resigned to this happening. So another surgery to take the implant out, then down the line one more to put it back in. All of this started with the re-meshing and it has spawned three additional surgeries. So crazy!
My DH has a theory about the non-cancer side having issues - he says it is pissed because it didn't have cancer and was removed anyway - payback. He is silly.
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Sorry to hear that SpecialK and hope you heal quickly.
Holidays are over and back to work tomorrow.
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SpecialK, your husband is funny. I'm sorry to hear you are having all these issues too. (((hugs)))
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specialK , I am not a religious person, however, I am praying that you recover quickly from all this crap. Thinking of you
Vintage and Meadow thanks for the consult, I will try the massage, lightly that is, its no wonder that we're not a little nuts after all this, the funny part is that everytime i get zinged, i scream oooouch! And swear too, everyone here is getting used to it now even my dogs
Have a good Sunday
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