There are no wrong turnings, only paths we did not know we were meant to take - Guy Gavriel Kay
Love & biggggggggggggggg hugggggggggggggsssssssssss!
Laure'
The finger of God touches your life when you make a friend.
----Mary Dawson Hughes---
I'm so sorry that you have had to go throuh all of this, and in such a small amount of time. I feel sor all that you are going through, but you are strong and will remain strong for that little cuttie of yours. She needs you to be there for all of the important things in life. That is what I think of when I get down, I think of my kids and the grandkids I will have some day.
We love you and will be here for you through everthing. Please keep your chin up and NEVER quit fighting.
Hugs:)
Thank you Bernadette also for sharing your chemo journey with me and Kattbird. It was such a help having both of you around. I have 3 more taxols to do, and will be done (hopefully) on Feb 15. After that I'm not sure what I will be doing - rads or mastectomy - it depends on how my genetic testing comes back as. I hope your last chemo goes well, and that you go out and celebrate after!
Very Happy New Year,
Love,
chantry
There are no wrong turnings, only paths we did not know we were meant to take - Guy Gavriel Kay
You have just 3 more Taxol? How many did you have all together? I will be done (hopefully) this week unless my Dr has some other plans for me. I know I will have a little time between Taxol and rads but not sure how much. You said that you might have a mast? I have not had the genetic testing but would like to. If I were positive I would opt for a mast too.
happy new year
Hugs:)
L & H,
Bernadette - I had 4 AC and then will have 4 taxols in total. I think that we are a little bit behind the US up here in terms of personalizing regiments. Basically, every woman who is early stage gets either 6 CEF, or 4 AC and 4 Taxol. Thats why this site has been such a help to me - I can get info on treatments that are standard in the states, but that may not be up here in canada.
Again, big big BIG thanks to everyone here for the help you've given me throughout this past year.
Lots of Love and hugs,
Chantry
There are no wrong turnings, only paths we did not know we were meant to take - Guy Gavriel Kay
Chantry0
((((((HUGS)))))
I spent a lot of time trying to stop the "what-ifs" and had set a goal for myself to go one whole day without even thinking about breast cancer. Since I log into here each day, that goal was not a realistic one, and I reframed it. Instead of trying to stifle the thoughts or "not think about it", I changed how I thought and what I did with the thoughts.
You have been treated for breast cancer and there is no way to deny it. It is a part of you now, but it does not have to be a bad part and it does not have to take over your life for one second. When I was willing to let it be a part of me, my anxiety lessened and the fear was less, as I was back in control.
I can't tell you how I did it, but I can tell you it took a long time, and that life after cancer treatment is different...it takes a new adjustment and an understanding that there will be some good times and some hard times along the way. For me, the key was to stop fighting the thoughts....but to let them happen and let them be with me, not taking over me.
Hugs,
Lori
Chantry: I agree what what everyone else has said. Having bc is the pits. We can't help, esp right after diagnosis, thinking about the "what-if's". That is only human nature. But, once you are finished w/ your treatments, and you begin to get your strength back, your attitude will be completely different. My youngest dd graduated from college 3 days after my mastectomy. I was unable to attend her graduation but she knew that I was there and how proud of her I was. Then 4 weeks later she got married to her hs sweetheart. Now talk about feeling like you were being stared at. It was to soon to wear a prothesis as I had not completely healed. Thank goodness I had delayed my chemo for the week following wedding. But I still felt that everyone was looking to see the "one boobed mother of the bride"! I also worried about my granddaughter. I had raised her since she was an infant. That was 5 yrs ago and I am still here. I have seen 2 granddaughters being born and one grandson. I have seen my dd and sil build a new home. So, hang in there. Don't let the cancer control you. Make jokes when you can and laugh as much as possible. You are a SURVIVOR!
Hugs...Deb
PS..if you dd gets really congested again. Close your bathroom door and turn the shower on hot. Let the steam buildup and then go in and sit w/ her for a little while. It works!
Thanks Lori for your words of wisdom too. I keep thinking that the worst is behind me (well, almost - 2 more taxol to go), and so when I hit that wall of emotion, it always takes me by surprise. I've read that once you've finished treatment, there are new emotional adjustments to go through - like those that Kattbird is dealing with. I just want it to be over, but it never,ever will. And I find that very depressing. Always keeping one eye out for anything that may be wrong. Yuck. But then I bounce back, and try to go about things normally.
Deb - i'm sure you looked stunning at your daughters wedding!Thank you too. Everyone here is an amazing help to me. thank you all for sharing your stories and personal experiences. This site is a life line to me.
And we've been doing th eshower thing for the past couple of nights and it is working. We also jacked up her matress to help her breathe. Hopefully by this weekend she'll be back to her old self!
Thanks everyone,
Love and hugs
Chantry
There are no wrong turnings, only paths we did not know we were meant to take - Guy Gavriel Kay
L & H
Candy
Two are better than one, because they have a good return for their work: if one falls down, his friend can help him up. Ecclesiastes 4:9-10
I'm so happy to have this knowledge now and can't wait for your further details.
Lori
I am NOT adverse to alternative meds/treatments. But, I have a problem w/ the above mentioned website. After visiting it and reading about it's author, I don't see where he has any medical background or training. I was surprised to see that he is from the town where I live. But, remember, anyone can make a website and post any and all info. That doesn't mean that it is valid. I would caution any of you to do thorough research before taking any of the alternative meds/treatments. As Lori said, this is not making headlines or radically changing the face of oncology.
Deb
http://www.healingwell.com/community/default.aspx?f=46&m=106997
I think you will find several reasons for not "discussing alternative methods". You have come here as a stranger giving more or less medical advice which also causes "discussions which are very upsetting" to those who are virtually fighting for their lives with breast cancer. We have well over a hundred members, we have lost 30 very dear friends who have courageously fought this disease with every treatment you can imagine. If the door was open to anyone anywhere who wanted to discuss alternative methods it would mean anyone with some snake oil would be allowed to post.
Why did you post here? To discuss breast cancer? Or to pass along information that can be found googling or so you say.
MK
Mageezy: I have to agree 1000% w/ what MK has said. This board is made up of members, all different ages, that are fighting breast cancer. Some are newly diagnosed and others have been fighting it for years. It is upsetting to have someone that has not personally had to fight this disease to come and imply that we aren't smart enough to decide what type of treatment we feel will help us stay alive. Each of us has done research to find the best treatment. We have asked the other members for their feedback and help and support. Each of us prays daily that there will be a cure found, not only for bc but for all types of cancer. I am delighted that those individuals you listed are alive and well today. But I am sure that you are aware that there are probably 10x more that chose that type of treatment that it did not help and are not alive.
I am sure that Peter, the administrator of this site, would be glad to email you the rules. MK moderates this site and makes sure that the rules that were set in place are kept. So please don't take a personal affront against her or any of the rest of us that reply to your post.
Deb