Has anyone started a forum for Chemo in Dec 2008?
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Thinking and praying for you busqueen. Cebbie--good luck with that foot! xo
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Caroline, that is the kind of camping I could do.
It is weird about the pain subsiding with your cycle. Maybe discomfort somewhere else is distracting from your foot? Any way, good luck tomorrow. I hope you get some results tomorrow and not have to wait for days for someone to read the scan.
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Caroline: hope you got good news today.
Carrie: How are you doing?
Love and prayers to all,
Mandy
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Well, the good news is that I am getting surgery to remove whatever it is in my foot. Waiting to hear surgery date now. The bad news is that they still don't know what it is and I am REALLY FREAKED OUT & SCARED
I like my new dr, seems to be a bit more knowledgeable than the last guy. He gave me 3 possible options:
1. Osteoid Osteoma - But, my "spot" barely lite on the bone scan, and an osteoid osteoma usally gets REALLY bright. Also, it is typically more painful at night which I don't have any problems sleeping, the pain is usually best if my foot is not on the floor.
2. Giant Bone Island - Again, we're dealing with something that should light bright on the bone scan and it's not. At this point, he feels like it's neither.
3. Metastatic Cancer - While cancer rarely occurs below the knee, it IS possible and this is definately an open option at this point. And, I'm quite freaked out because he is the first dr to admit that at this point, it could be cancer. I don't think he strongly believes it, but I just shut down to be able to read his thinking and ask more questions.
So the plan is to go into surgery, remove the "thing" and do a biopsy. By then, hopefully they'll be able to pin point what it was, hopefully not cancer and I should be relieved of the pain (a few weeks later of course
Just waiting for a surgery date now...
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Got the call from the nurse, surgery is on Sept. 21st at 2:30PM, of course, I have to fast starting at midnight! Post-op where I'll find out about the biopsy result is not until Oct. 13th
But I'll be bugging them before that.. hehehe... At least it's finally moving and getting somewhere!
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Good news, scary news and frustrating news all at the same time. I'm glad the surgery date is soon. The 21st will be here before you know it. I can just imagine how you felt when he told you mets is possible. I don't think I would have been able to breathe much less think. Sooooo frustrating that you still have to wait over a month to get the results of the biopsy. Does it really take 3 weeks to get results back? I mean, how many specimens are laying around waiting to be tested? You are in my prayers, Caroline.
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Oh Caroline, I'm sorry you are freaked out and scared and still facing way too much time WAITING. Ugh. Do these people think we have nothing better to do than wait? I started freaking out as soon as my PET scan was done this morning, and spent the day overanalyzing everything the tech said and did when the scan was over to figure out if she 'knew' something. Sigh. My onc is out of town, so my results appt is Monday.
Breathe in, breathe out, breathe in, breathe out......
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Carie, you know you are in my prayers every day. Monday can't come soon enough!!!!!!!!
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I'm breathing right along with you Busqueen!
When I asked her why would it take that long for the biospy to come back, for my breast, same hospital, it took 2 days for me to find out. She said that the bone stuff isn't always as easy and sometimes they need to send it away to get second opinions. I figured, I'll give them a week, then call. The fact that my new dr really is a pediatric orthopedic surgeon doesn't help with all the waiting since he only does roughly 1-2hrs/week at the Cancer Center to see adults. But I like him, surgery might be slightly sooner if I was going to the first guy, but I didn't like him anyhow, so I'd rather wait a few more days and be comfortable that I'm in good hands. I'm feeling better tonight, we have friends visiting this weekend (the same one that visited us 2 days after my dx!!), they're close friends, so it will be nice to have them here.
Thanks for your prayers Firni, well appreciated right now.
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Caroline: what a bummer to need the surgery. But I am only going to think positive thoughts and to send you some positive thoughts. You are in my prayers. xoxoxo
Carrie: I think about you all the time and send up prayers for you too.xoxox
Cyber hugs,
Mandy
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More prayers from me Cebula! xo
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Thanks ladies. I'm just happy that surgery is soon and that the pain should go away after. I'll worry about the rest later.. haha, ok, so I'm lying. Seriously, I got to the point today that I realized that wether I worry about it or not, if God decided I am to have mets, well, there's not much I can do. So I have to have faith that God is in control and that he knows what is best for me, which is very comforting right now.
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Amen.
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Amen
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Amen.......always let go and let GOD!!!!! HE is always with us
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Besides your tumor markers would be elevated right? Most likely anyway. Its not cancer. I am just sure of it. I have not been wrong yet. hehe. Its soooo stressful. I'll send as many prayers as I can for you.
I am suffering from extreme fatigue it has come over me in the last 3 weeks and getting progressively worse. I have mad an appointment with my onc. I feel like I have a fever but I don't. The scary part is this is how I felt before I was diagnosed. gulp. What a ride this is huh? I'll keep ya posted. I joined a recovery group to take Tia chi and strength training and core building. I am trying to eat better. Maybe I'm just deconditioned. I hope thats all it is. but............
Hey queen thinking of you too and hoping that things are stabilizing.
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Well Bold, I hope I'm not the one to prove you wrong
My onc doesn't believe in tumor markers, so they have yet to be tested.
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Caroline, have you seen a copy of your last blood work with Onc? My onc doesn't believe in tumor markers either. told me he never does them. but when I got a copy of my blood work, there was a tumor marker test done. It's a fairly new BC mets marker. He just never told me. By the way, my # was nice and low.
Bold, I hope your fatigue is just a result of being de-conditioned and doing all that training. A check up never hurts anything tho. Prayers with you as well.
So, my calendar is filled with Dr. appts. for the month of Sept. PS for the giant divot on my foob, PS for the face that is sliding off my head, PCP for a flu shot, med review and to refreeze a pre-cancer on my wrist, GI for colonoscopy, well, I guess that's all. I'm switching to a high deductible ins. in Oct. I figure one surgery and I'll meet my deductible. (That will be filling the divot on my foob) Then the rest of the year should be free. But, I can't go see any Dr. from Oct. thru Dec since I don't want to pay the high deductible twice. Guess I should figure out what my meds will cost too. Just can't afford the monthly premiums of the policy I have any more. It's going to double Oct. 1.
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Yikes! But I understand you waiting until January for surgery. I always thought that one of the bad thing about being dx with cancer in October, was just that, surgery & 2 chemo before the end of the year, then more chemo in January so the deductible started all over! I hope this new insurance works better for you.
As far as the tumor markers, my last blood test was my day before chemo lab on my last chemo! Yeah, that's how much he doesn't believe in that, as long as I look good and not complaining, then no need for labs. I have a copy of all my labs and he never did the marker tests.
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Cebula,
All the best and stay positive. My onc told me that in 35 years of work she never had any pacient with bone mets lower than the knees. Don't stress yourself too much. I will have a glass of wine for you tonight and sending you good thoughts ( an excellent 2006 Merlot from Pomerol).
I am very upset tonight. The beast has stricken again. One of my daughter's classmates had brain surgery 2 weeks ago to remove a tumor. He is 13! He will have rads and chemo and maybe he gets 2 more years, if he is lucky. I really hate this disease!
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Cebula: hang in there and try to stay positive. You have been one of my role models during chemo and I feel that this is just one of those things that the tests cannot identify but that it will not be mets. We are here for you!
Havehope: That is awful for the child, his parents, his family, and his friends. But oncs are not magicians and maybe they will be wrong and he will show them and go into an unexplained full remission. It really does happen and that is what I am hoping for.
Peace be with you.
Cyber hugs,
Mandy
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Havehope, you are so nice to have a glass of wine for Caroline! LOL
Terrible when any child gets cancer. How do they get thru it? It's so hard for us, how does a child deal with their fears?
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My oncologist doesn't believe in tumor markers either although he measures them every time anyway. He says false elevations are common. Guess he's covering himself either way.
Firni, your schedule sounds like mine. I have two more surgeries to finish up the reconstruction (again cuz it failed the first time!) plus I need to schedule a colonoscopy because I had a pre-cancerous polyp 3 years ago. It's time to do it again. Uggh.
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Before I had BC, I went to the Dr. once a year. Now while I'm not going a couple times a week for something or another, I'm still going at least twice a month. Part of the new normal???
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Caroline, I refuse to allow you to have mets. There shall be no stealing of my thunder.:-) You can tell your doctor I said that.
Today is results day. It's 6:52am, wondering if its too early to start drinking.:-)
I'll let y'all know later.......
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Havehope, so sweet of you, so I joined you with a glass of wine Saturday night (or 2...). I hate seeing cancer in children, I don't know why, it just seems more wrong than with us. When we did the Relay for life last year, there was a little bald peanut walking around as a survivor, just watching that little boy made me want to cry, so young
How is your daughter dealing with it?
Thanks Mandy, so sweet of you.
The new normal? Please not... LOL!
Busqueen, alright, alright, I won't steal your thunder
Did you start drinking yet? Time to open the champagne? Patiently waiting here.. bring us some good news
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Oh boy!!!! Its sometimes just too much huh? I can not believe we are still so draconian in how we deal with this deadly disease. I been reading about these new research therapy that eradicate cancer by using radio waves. No side effect just remission. COME ON SCIENCE!!
I am going in today to see onc. GULP!! Just getting my new symptoms checked out. My fatigue is just getting worse and worse. Hoping that it is just some vitamin, mineral, or enema problem. Is it to early for MORPHINE!!
Sending healing and hope
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So. The good news is my lungs and liver are still clean ~ yay!! All of the spots that showed up in May are either stable or diminished, which is also good news.:-) However, there was a new spot that showed up, at the top of my right femur, which didn't surprise me because in the last week I'd been experiencing a new pain in that general area. My onc wants to spend some more time looking at the scans and showing them to the radiologist as well. I may end up with an additional hormonal to take, or some chemo, and/or some radiation. So, more of the waiting game for me, to find out what my new treatment plan will be.
Bold, hoping you can find something out soon. Praying for you.:-)
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Urgh
I was waiting all day to find out about your test results, I want to say it's overall good right? But then again, more treatments stinks. Hope you find out what the new plan of action is soon.
Bold, how did the appt go today? What about the fatigue, could they say anything about that?
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prayers for all my bc sisters! xoxox
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