I am new to this board and having long term side effects.
Hi. I've been reading and everyone seems so nice. I'm having problems with a long term side effect from radiation that was done 7 months ago. I developed "radiation Pneumonitis" in my right lung where radiation was done for breast cancer. I got it around Christmas and it is better but not gone. So I can't have the rest of my reconstruction done yet and I really don't feel great and I am afraid. Did any of you have this or any long-term effects from radiation?
And I am on Femara and having a lot of arthritis pain in my hands and shoulders. I guess I'm asking too much at one time and I'm sorry. I was really on the mend before the "pneumonitis" and want to get back there.
Comments
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Welcome to the CSN Discussion Board
Hi Cavelsalb,
I did not have any long term side effect from radiation of the kind you mention. Femara does cause bone and joint pain, it is one of the side effects of aromatase inhibitors. I had them very bad on Femara but not on Arimidex. I wish that I could be of more help. Hopefully some other lady had that condition and might be more helpful.
Wishing you the best,
Doris
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Hi Doris,SIROD said:Welcome to the CSN Discussion Board
Hi Cavelsalb,
I did not have any long term side effect from radiation of the kind you mention. Femara does cause bone and joint pain, it is one of the side effects of aromatase inhibitors. I had them very bad on Femara but not on Arimidex. I wish that I could be of more help. Hopefully some other lady had that condition and might be more helpful.
Wishing you the best,
Doris
Thank you so muchHi Doris,
Thank you so much for answering and you did help me. My doctor told me that maybe Arimidex would have less bone pain but I haven't asked for it because I didn't know if that was true. Are there any other side-effects with Arimidex that I should know about? The only other side effect I have is Hot Flashes.Thank you so much again.
And the best to you.
Connie (I guess I can sign my own name, right?)
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Hi Connie,
I'm sorry you haveHi Connie,
I'm sorry you have the need for us. But I don't think you could find a better group of people. And yes, it's ok to use your name. I use mine all the time, but only my first name. Whatever you post here can be read on the internet, so you do want to be careful about how nuch and what kind of information you give out. If you have something more private to send to someone, you can use CSN email in the brownish pinkish box on the left.
I had to look up your condition, it wasn't anything I've ever even heard of before. Are treatments helping at all? You have my sympathy, I've been dealing with long term effects from shingles in my left eye since sept last year.
Please keep us posted.
Hugs,
Linda
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Pneumonitis
Hi:
Checked through my test result file and found one PET scan report done approx. 6-1/2 months after the end of radiation, which said "post radiation pneumonitis in the left anterior upper lobe (of the lung). I never had any symptoms. I had 6 months chemo, followed by a lumpectomy, followed by radiation. 9 months later the report suggested the pneumonitis was healing. However, the last PET scan showed again Post radiataion scarring in the lingula, nonmetabolic and unchanged. Hope you will feel better soon and able to go on with reconstruction. This site has been a God-send to me, so much information and emotional support.
Take care, Margeaux
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Femara CAN cause paih for some -SIROD said:Welcome to the CSN Discussion Board
Hi Cavelsalb,
I did not have any long term side effect from radiation of the kind you mention. Femara does cause bone and joint pain, it is one of the side effects of aromatase inhibitors. I had them very bad on Femara but not on Arimidex. I wish that I could be of more help. Hopefully some other lady had that condition and might be more helpful.
Wishing you the best,
Doris
But not for all! I've been on Femara/letrozole with NO pian related to it. So yes for some it can cause issues but it can't be said that it does cause pain for all - IT DOES NOT.
It is always so sad when one will state that something will happen because it was what they 'experienced' - especially from one wh0 has been around long enough to know that there is NO "One Size Fits All".
Winyan - The Power Within
Susan
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If this (or any symptom
If this (or any symptom persists), please keep investigating. I had trouble with 2 bouts of pneumonia right before I was diagnosed with metastasis to the ribs. The pulmonologist said that I may have some mets to the right lung too as there is a small pleural effusion, scarring and the lung is smaller than it should be. I was told my right lung will never be normal. I honestly don't think this is from radiation because I had radiation on the left side.
Please know I share this not to scare you. My sistuation was not pneumonitis. But I do preach now that a persistent symptom needs to be watched closely. Praying that this will get better soon!
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Welcome...
DeniseWelcome...
Denise
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I had rads, but, I didn'tCypressCynthia said:If this (or any symptom
If this (or any symptom persists), please keep investigating. I had trouble with 2 bouts of pneumonia right before I was diagnosed with metastasis to the ribs. The pulmonologist said that I may have some mets to the right lung too as there is a small pleural effusion, scarring and the lung is smaller than it should be. I was told my right lung will never be normal. I honestly don't think this is from radiation because I had radiation on the left side.
Please know I share this not to scare you. My sistuation was not pneumonitis. But I do preach now that a persistent symptom needs to be watched closely. Praying that this will get better soon!
I had rads, but, I didn't have this happen. I am so sorry. Please keep us updated.
Hugs, Lex
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Arimidex vs FemaraCavelsalb22 said:Hi Doris,
Thank you so muchHi Doris,
Thank you so much for answering and you did help me. My doctor told me that maybe Arimidex would have less bone pain but I haven't asked for it because I didn't know if that was true. Are there any other side-effects with Arimidex that I should know about? The only other side effect I have is Hot Flashes.Thank you so much again.
And the best to you.
Connie (I guess I can sign my own name, right?)
Hi Connie,
I was lucky on Arimidex but it also has the side effect of all aromatase inhibitors (Aromasin, Arimidex and Femara) of bone and joint pain. It's the luck of the draw, or some such thing. I did have fractures on Arimidex only because it was new and they had not posted to be careful not to fall. Arimidex for me was easier and I had a longer time on it without to many problems. Vaginal dryness is a problem for some too as well as hot flashes. I had hot flashes but they were always in the do able range.
Best to you,
Doris
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I had the regular radiationdisneyfan2008 said:Welcome...
DeniseWelcome...
Denise
I had the regular radiation treatments and had boosters afterwords. My skin was affected during the treatments, but, I've not had any after effects. My skin cleared up a few weeks after being done.
I hope you will be alright.
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I just wanted to thank
I just wanted to thank everyone for answering. I've taken the liberty of looking at some of your stories and reading more posts and I feel like I'm complaining about something little, because all of you are so brave and holding up so well. I hope it wears off on me and my thoughts and prayers are with all of you. You are all inspirations.
Hugs
Connie
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First, you are notCavelsalb22 said:I just wanted to thank
I just wanted to thank everyone for answering. I've taken the liberty of looking at some of your stories and reading more posts and I feel like I'm complaining about something little, because all of you are so brave and holding up so well. I hope it wears off on me and my thoughts and prayers are with all of you. You are all inspirations.
Hugs
Connie
First, you are not complaining about something little..it is important and you are just as brave as anyone on this site.
I never had this and I had rads too.
Has your onco or rads oncologist offered any help or advice?
Hugs, Diane
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