Radiation countdown
Three more sessions to go! I can't wait to be done with this. So far, no real problems at all. This is the first part of the treatment that my body has tolerated well. This sure is one heck of a year. I have almost totally missed summer! I sure have learned a lot about people this time around. My entire family and friends have been away at their summer homes and travels and I have gone through this alone. Every day I got dozens of text messages and emails. I stopped answering them about a month ago. It just felt so impersonal and cold to me. What a world this is!!!
Comments
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GET READY TO RING THE BELL MS HAPB
Congrads..you almost ready to "ring the bell" I felt so blessed when the bell was ringing a few months ago when I completed radiation.
it got a little worse before it go better with the skin peeling and some slight pain...put nothing you cant handle!
YEAH sometimes Family dont know how to react..but they should visit and check on you when they can...
YOU ARE NOT ALONE.....GOD BLESS AND CONTINUED SUCCESS WITH YOUR TREATMENTS...HUGS
BEEPOSITIVE
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sorry you did this alone-I am
sorry you did this alone-I am happy it is almost over for you. I had BC 2008 and the ONLY date I remember with all i had done was my LAST day of radiation-June 28, 2008.
I still quietly do the happy dance in my head-unless you went through it, you do not get the anniversary.
Denise
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My cancer center did not haveBeepositive said:GET READY TO RING THE BELL MS HAPB
Congrads..you almost ready to "ring the bell" I felt so blessed when the bell was ringing a few months ago when I completed radiation.
it got a little worse before it go better with the skin peeling and some slight pain...put nothing you cant handle!
YEAH sometimes Family dont know how to react..but they should visit and check on you when they can...
YOU ARE NOT ALONE.....GOD BLESS AND CONTINUED SUCCESS WITH YOUR TREATMENTS...HUGS
BEEPOSITIVE
My cancer center did not have the Bell, BUT I did get a mini diploma.
You are right, some family and friends are not sure whether to mention the "C" or just go along like anyother day.
Denise
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Hi HapB,
Congrats on finishing radiation!! Are you finished with all treatments?
I am sorry to hear about the family support...I think that sometimes people who really mean well, just don't get it!
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Most dont get it...
Hap, Congratulations. Yah! Your are a warrior.
People dont get it. They just dont and I hope they dont have to. I would not wish this on an enemy. I dont think I have any, but still would not.
You do have us. We are here for you always.
Keep being kind to yourself, keep celebrating the little things. It matters and you matter.
Hugs,
Annie
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Treatments
Thank you everyone. Two more radiations to go!! Can't wait to be done with this. Mesch, i am doing Herceptin infusions every 21 days for a year, and an AI for 5-10 years. Never ending!
Tonight I got a phone call from one of my brothers to tell me one of his friends has BC and how awful a time she is having. I felt like screaming, but I didn't. I asked him if he remembered that I was being treated for BC. He said, yes, but they got all your cancer with surgery and you are just having treatment to prevent more cancer. WTH. LIke I want to do this? I just don't know what to say anymore.
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That would be frustrating!
I am sure that your brother has no idea how difficult what your are going through is, but it would be nice if he asked you!! I agree with you that BC treatment is never ending! 5-10 years is a long time to wait to feel great again. Again, I do not think that people realize how tough it is!!
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Challenges
Mesch, yes it is very frustrating and one of my challenges going forward is trying to understand and not be angry with the people who were not there for me and who just didn't get it. I understand that it is summer in New England and everybody had plans, but the level of minimizing breast cancer is something I never expected. I think people have been desensitized and are under the mistaken belief that there is a cure for this cancer. I don't want the insensitivity of people to change who I am, but it is going to be a challenge.
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Challenges
Many people that I have talked to about breast cancer do believe that stage 1 is easy. It is easier than stage 4, but there is a range of treatments based on the specifics of a diagnosis, and every treatment comes with possible side effects. People also think that because BC patients have anti-hormonals that they have a pill to "cure cancer.' They don't realize that what it is , is a pill that creates nasty side effects for 5-10 years, and may or may not prevent a recurrance.
I agree with Annie that I wouldn't wish this on anybody, and I also agree that they cannot understand it if they haven't experienced it up close and personal!
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At least WE get it!
While I am not glad to hear that others have had the same experiences with those around them not seeing that post active treatment we are still in treatment, at least we can come here to see that we are not alone. Post active treatment people see hair and we go back to our jobs and responsibilities, but I agree that unless you have experienced the SE of continued treatment or late effects, do not talk to me about how lucky I am.
Every lump we feel and scan we have, every change in meds and new SE we experience brings home the reality of how our lives have changed. Yes, we are lucky to still be here, but each day is a challenge.
Kathy
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People are dumbHapB said:Treatments
Thank you everyone. Two more radiations to go!! Can't wait to be done with this. Mesch, i am doing Herceptin infusions every 21 days for a year, and an AI for 5-10 years. Never ending!
Tonight I got a phone call from one of my brothers to tell me one of his friends has BC and how awful a time she is having. I felt like screaming, but I didn't. I asked him if he remembered that I was being treated for BC. He said, yes, but they got all your cancer with surgery and you are just having treatment to prevent more cancer. WTH. LIke I want to do this? I just don't know what to say anymore.
People are just dumb. It makes you wonder how in the world they get up everyday and actually function.
HUGS<
Annie
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YepTeach76 said:At least WE get it!
While I am not glad to hear that others have had the same experiences with those around them not seeing that post active treatment we are still in treatment, at least we can come here to see that we are not alone. Post active treatment people see hair and we go back to our jobs and responsibilities, but I agree that unless you have experienced the SE of continued treatment or late effects, do not talk to me about how lucky I am.
Every lump we feel and scan we have, every change in meds and new SE we experience brings home the reality of how our lives have changed. Yes, we are lucky to still be here, but each day is a challenge.
Kathy
You wrote that so well.
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Meschmeschellejensen said:Challenges
Many people that I have talked to about breast cancer do believe that stage 1 is easy. It is easier than stage 4, but there is a range of treatments based on the specifics of a diagnosis, and every treatment comes with possible side effects. People also think that because BC patients have anti-hormonals that they have a pill to "cure cancer.' They don't realize that what it is , is a pill that creates nasty side effects for 5-10 years, and may or may not prevent a recurrance.
I agree with Annie that I wouldn't wish this on anybody, and I also agree that they cannot understand it if they haven't experienced it up close and personal!
Because I am triple positive, the recommended treatment for stage 1 is exactly the same as for more advanced stages, which is mind blowing! I am so disappointed in people from all of this and I realize that after a lifetime of being there for anyone who needed me, I am alone. I think it is just the stage of life that I am in.
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