October 2013 Chemotherapy
For all those who will be continuing their chemo therapy treatment in October, have a start date for chemotherapy in October or anticipate a start date in October, are supporting those who are in treatment and for those who are on the other side and wish to impart their wisdom. All are welcome.
Comments
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I will be having an echocardiogram on Tuesday (9/17) to make sure my heart is healthy enough to start chemo and also this week on Thursday (9/19) I will meet with my BS to discuss when she will release me for chemo and an apptointment with my MO to discuss the start date of chemo that will be either the 1st or 2nd week of October. I will also get the results of a recent CAT scan on 9/19 which was done to see if I have any metastatsis from my breast cancer.
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Hi Pam, I hope all goes well with your electrocardiogram and that you get the all clear from your surgeon. The waiting game is hard isn't it?
I am starting on the 10th and was told that the drugs I am taking won't affect my heart. (I have two younger brothers who had heart attacks). I'm not sure if this means that they are less effective but i would rather gamble with recurrence than have to deal with heart disease in the future. I guess there are so many things to weigh.
Thanks for starting the thread. We can track each other here. :-)
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Hello. Thank you Pam for the thread. My start date is October 2nd. On Monday I am going for a follow up mri for a biopsy they did on my left breast before I have a port placed. I need all the support I can get. I feel like I'm on the worst rollercoaster ride right now.
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Wren I don't think it means the chemo is less effective, just a different side effect.
Jaybird - good luck with your MRI and your port placement. I have a port as well but because we knew before surgery I would need chemo I asked for mine to be placed during surgery and my BS agreed. -
Jaybird - I know what you mean about the roller coaster. I don't even like those on a good day. It seems to be lots of stuff all at once and then it settles for a couple days and you are off and running again. Hang in there!!
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Thx you for starting this, I start TCH on 9/30 and have been following the September group.
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Jaybird & Pam, Im with you and understand the roller coaster. It's been a whirlwind for me too. I had a whirlwind of doctor appointments, tests, 2 surgeries and more appointments since I was diagnosed. Right now everything has calmed down (as if its the calm before the storm). I will have my port installed on the 27th wish I had it done during my surgeries, didn't occur to me to ask about the port. I just wanted IT out of me.
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ML40 - I had an insider helping me. One of our cousins is a chemo nurse and she told me to ask about the port being done at the same time is surgery. Good Luck with your port placement.
And the rollercoaster started again - I got a call today and I have an ultrasound on Thursday to check out something suspicious they found on my right ovary in the CT Scan they did last week. They saw a small fibroid and some ovarian cysts but thought those were fine. I will see the MO, BS and have a pelvic ultrasound on Thursday.
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Hello Ladies,
ml40 I understand that calm before the storm feeling. I am actually feeling good and "normal" today after a very emotional weekend.
Pam I hope you receive good news about your ultrasound so the rollercoaster will slow down.
I had my mri today. I suppose I will here from the surgeon in 3 days and the person setting up my appointment for the port wasn't in today so I will be calling again tomorrow. I hope everyone has a peaceful evening. -
Good morning. I wanted to put out there that I came across a site that helps find you a mentor close to where you live and with the same diagnosis. If anyone is interested it is imermanangels.org. I hope everyone has a great day
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Thxs, for the website Jaybird- really need something like this hopefully they have something in Hawaii. I transferred to Hawaii with my military husband and two week later I was diagnosed.
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ML40 - I hope the website Jaybird mentioned works well for you. I bet someone would be willing to travel there to be supportive since it's so beautiful! I understand a little what it's like to be somewhere you don't know many people and yet have to deal with this big issue of cancer. When my husband retired from the military we moved and less than a year later I was diagnosed with cancer. Not breast cancer that time but it required surgery and 33 sessions of radiation. During that time my husband was working out of state 2 weeks a month. I was lucky that we were living with his parents while building our house. But I sure missed my friends and family 1/2 way cross the country. Still miss them this time too but have a little more support this time. Are there any support groups in the area? You've probably already checked with the FRG leader to see if s/he knows of anyone you could chat with - that network can be good support when it's an active group.
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Thxs Pam for sharing, I went to a support group that meets once a month, it was helpful. I haven't checked with the FRG leader but they don't appear to be a active group, but maybe I'm missing something since I've been a whirlwind since my diagnosis. My mom is coming to help out for my first treatment (she says she will stick around as long as I want) & my mother-in-law wants to come out too to help after my 1st treatment but honestly I don't feel comfortable with my mother in law. Thankful my kids are 21 & 18 and in college. I don't want to seem ungrateful and appreciate that my mother in law wants to come out to help but she has only come to visit us 5 times and I've been married 22yrs and when she has come out my husband acts as if the "queen" is coming and I don't want that stress. I've voiced my concerns to my husband but last night AGAIN my husband is asking me when can his mom come out. I wanted to scream.
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I found out yesterday my chemo is scheduled to start October 9th. Everyone thinks it's awful because it's the week of my birthday but if what I've been reading about feeling better the second week comes true for me then I have a good shot at enjoying Thankgiving and Christmas. It's way easier to move a birthday dinner than it is to move Christmas!
I was excited to find out there were no other signs of cancer in my CT Scan. My MO said he wasn't concerned about the area in my ovary that the Radiologist was concerned about so I've let go of some of that anxiety too but will get rid of the rest of it after I hear the results of the pelvic ultrasound. That was a huge relief.
There were a few other things that showed up on the CTScan not related to the cancer (ie a small kidney stone, disc issues, etc) and typically they would be things to be concerned about but in light of breast cancer it seems like no big deal. Just things to keep an eye on - I'm not going to look for trouble.
BS thought everything looked good, released me for chemo, sent a referral to PT and I won't see her again until I get my port out in the spring.
ML40 - Glad to hear the support group was helpful. I wish FRG groups weren't so hit and miss. But maybe at least the leader might know of other resources or some others who have been in a similar situation. It will be nice to have your Mom there for your first treatment. As for a visit from "The Queen" - that is such a difficult situation. I don't know about you, but since my diagnosis I feel a bit more emotional and vulnerable than I usually do. That is not my preferred state of mind for a visit from a queen, I would want to be more on top of my game. Are you having a couple of different chemotherapy drugs - If a visit is inevitable maybe you can say you might not feel as well after several sessions and you might need her more later - the fireworks on New Years Eve on the Hale Koa beach are great. I think for me the beginning is most scary and more emotionally time consuming - and quite honestly difficult to focus on anything else. The bottom line is THIS time it's about YOU! The kids are old enough to take care of themselves on a day to day basis. You have probably coped with deployments, exercises, moves, events and last minute changes with grace and flexibility. (not to mention the kids stuff) This time is different, you come first! It's your turn!
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Wrenn - not sure which board you mention my hair but thought I could just respond here. Yes, I did get it cut short. Cut off two braids to send to Locks of Love - where they have wigs made for children with donated hair. I just thought I'd get started with "shorter" before I get to no hair. I'm actually enjoying it.
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Pam. Your hair looks great and what a nice thing to do. You start chemo the day before me so I will be following you closely. :-)
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Hi all, and thanks Pam for starting the October thread!
Just stopping in to provide some more helpful links, starting with the main Breastcancer.org site's section on Chemotherapy, including what to expect, types of chemo meds, and side effect management.
There are some really helpful key threads here in the Chemo forum too!
Great tips and practical advice on the following discussion board threads:
- Tips for getting through chemotherapy
- More Tips (and a Shopping List) for Getting Through Chemo
- PORT PLACEMENT: Detailed description of process
- Head Covering Options for Hair Loss
- wig advice
- Cold Cap Users Past and Present, to Save Hair
Also, Last Month's Chemo thread might be informative!
Hope you find this helpful!
--Your Mods
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Thxs Pam, you know my life. I have been the flexible graceful military wife, had to remind my husband that I am the ONE with cancer. I'm going to cut my hair short this week too.
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Hi ladies. I hope everyone has great plans for the weekend.
Pam: I will be starting a week before you ( oct 2). My birthday is also this month. I will be 40 on the 11th. I realized the schedule also in regards to the holidays but I am trying to keep my Disney trip with my son over the veterans day weekend. I am really hoping I fair well with the treatment.
ML40: how are you? I hope everything goes well with your mother in law visiting. I never felt close with mine. I am divorced now so I know she won't be visiting me. Did you look into the mentor? I received one but she doesn't live close to me.
Port this Tuesday coming and here I come chemotherapy the following Wednesday. I am nervous but ready to fight this head on! -
Hi ladies, I'm fighting a bad cold today, which sucks but trying to look on the bright side at least I haven't started chemo.
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Hi everyone! I think I will be starting on October as well. I have PET scan on Monday due to sarcoidosis in lungs. They want baseline before I start. It has been frustrating waiting but glad everyone is being cautious. I will be 40 in November so most likely will celebrate after this is all done. Great to meet everyone and be able to support each other here.
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lgkgde - Welcome, Sorry you have to join us, but so glad you found us. Good Luck with your PET Scan Monday. Yes, the waiting is frustrating and there seems to be a lot of it.
ML 40 - sorry to hear about your cold, like you needed one more thing to deal with! You're right it is better now than during chemo! Hopefully it will disappear soon. I feel like we should all start wearing masks around other people and refuse to shake hands.
Jaybird - we actually share the same birthdate, the 11th, I'm just 12 years ahead of you. Your Disney trip is way more important than the other holidays. That will be a special time for you and your son. You can do it!! Good Luck with the port placement on Tuesday. Let us know how it goes.
I'm glad there are a group of 40 year olds gathering, I think you have some extra issues to deal with so I'm happy you have found each other. Wrenn and I will hold down the upper end
. I trust others of all ages will also join us as we get closer to October.
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I will be stating my chemo on September 27th. I will be having 6 cycles. I will post the names of chemo later. My port was placed on the 16th of September .
Right now, mentally I'm fine, but for the past month I was an emotional wreck, because this is my second time dealing with breast cancer. I survived the first time and gonna survive this time as well!!!!!! -
Is anyone else going to try Brian Joseph's Lash&Brow Conditioning Gel? I went to get a wig the other day and they gave me info about it and I wonder if it really works....it is $50 for 30 day supply
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Shorfi - welcome to the group, so sorry you had to come back. I'm glad to hear you are emotionally feeling better but I can certainly understand the devastating rocky start after diagnosis number 2. You are right though - you kicked it the first time and you can kick it again! I saw this funny sign on Facebook yesterday (hope it doesn't offend you) "If God doesn't give us more than we can handle, he must think I'm a bad ass" It just struck me funny.
lgkgde- I haven't heard of the conditioning gel. You have probably already thought of this but you might want to post in some earlier chemo groups (June, July) maybe someone there has tried it. If it works it's probably worth it, but I'd want to check it out too.
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I'm terrified debdylan. I bet many of us are but we don't have a choice but to carry through. It makes me feel out of control or like it is all out of my hands sometimes but coming to this forum helps immensely when you see the strong women who went before us. I'm glad you came to express your fears.
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DebDylan - I'm glad you found us! I think Wrenn is right, we are all scared, frightened, terrified and lots of combinations. From what I've read so far on these message boards is that the first chemo therapy infusion is the most scary because it's such an unknown as each of us reacts a little different and the rest get a little easier. I'm really hoping that is correct. I've also read several times "it's was easier than I thought it was going to be" - I'm just banking on those statements being accurate. I think for me I'm just at the tail end of dealing with finding out whether or not the cancer has spread anywhere else in my body (waiting for one more test result). So for me, although I've been worried about my chemo the idea of distant metestatic disease (not local metastatic disease like in my lymph nodes) has been way more scary than the thought of chemo because my chemo doesn't start until October. I had already gone from a stage IIa cancer pre-surgery to a stage IIIa after surgery and I have to say I'm terrified to jump again to a stage IV. Hopefully, that will all be behind me this week (which is how my Oncologist thinks it will go) and then I can focus just on my chemo which is my next big hurdle. So we are all scared/terrified/nervous in this together just at different stages. So please vent here!
As for ports - I think some people have them and some don't depending on what their veins are like, how much chemo they are having, whether or not they want them and if there are other issues, etc. For myself, my veins are OK for blood tests and not so great for IVs and since I am having 8 infusions plus the blood draws I didn't want to deal with the hassle of IVs. I also had 21 lymph nodes removed so I'm at a greater risk for lymphedema in my right arm so one way to decrease that risk a little is not to use that arm for treatment. For those reasons I wanted one so I asked for it. I was lucky enough to know some of my information before my surgery, like lymph node involvment and that I would need chemo, so I asked my BS to put it in during my breast cancer surgery and she was very willing.
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Hello!
I will be joining you ladies this month. I meet with my MO on Wednesday and RO on Friday. I just returned from a conference at Disney this past week which was a well needed escape from everthing since diagnosis. I bought me a few ears to wear to treatment and a coworker bought me a pair that she had embroidered with "Overcomer" on the back.
We can do this ladies!
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Yes, Deb....let's definitely all do this together!!!!
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Pam. good idea! I just posted in April and will let you know what they say.
DebDylan - I think I may be getting AC as well. Originally I was supposed to get TC for 4 rounds but prior to my surgery I was diagnosis with sarcoidosis in my lungs (lucky for me), MO is reluctanct b/c there could be some pulm toxicities. I am receiving chemo as I was high risk on Mammaprint. I am not sure about port but when we were talking about TC she told me I didn't need a port.
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