After Radiation- Long term effects and remedies
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hi, I just found out I have mild fibrosis in the periphery of my right upper lobe probably due to post radiation changes. Found on CT scan done to rule out blood clot,having shortness of breath. Also showed finding suggesting airways disease and trapped air in both lungs. Guess,i'll be adding a new Dr. to the mix,just hope i get some answers. what I've read the fibrosis can occur about 1 yr after radiation. I have no idea if it will continue to worsen! I surely hope not! I know I have it in my breast and pain which onc said a lot of her pts experience! What??? I know they tell us about the risks about chemo and radiation but the reality is a lot different than what I expected! -
Well I'm guess I'm going to be joining this group. I too was led to believe that the radiation wouldn't be bad or have any effects. But now that over 2 months out, I'm starting with fluid, swelling, scar tissue issues! I'm seeing the OT for therapy and that is very painful, didn't realize how sore my breast was until she started "massaging" it! Hurt so bad (and I have high pain tolerance) that I almost passed out! Also having rib pain, under arm pain and pain into my back! Such fun times! Not to say how it plays with your mind, or at least mine, always thinking it's more cancer!
Anyway, it's good to know about the possible issues! But sorry we all have to endure!
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So far I am the exception to the rule. I had 33 RADS treatments that ended in July 2011 and other than mild fatigue I haven't had the first problem from the treatments. I have read that sometimes SEs from the treatments don't show up until years later. Hopefully that wont happen to me. My Rad ONC told me to expect burning and fatigue as did my Oncologist. I have an appt with my Oncologist next month - 3 years out from my DX. I am sorry you guys are suffering. diane
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I have an appointment with a pulmonoligist on Tues,Christmas eve. I will post what he says about the post radiation fibrosis in my lung and lung issues.
Nettie,look up radiation pneumonitis. Have your Dr. check to make sure you don't have it. The time frame is about right,if caught and treated,you are less likely to develop lung fibrosis,if your lung received radiation. I liked my radiation dr but I wish he had told me about radiation pneumonitis and the symptoms.
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Hi
Did all of you have whole breast radiation? I wonder if that is why there are so many SE to the lungs.
I had a lumpectomy two weeks ago. Because I had a lot of radiation to my neck for laryngeal cancer two and a half years ago (oh yes I have the scars and stretched skin on my neck to show for it) my RO suggested I may want to try the partial breast radiation to reduce the area that gets radiation. I am nervous about getting any more radiation to my body and want to find out my risk if I don't do it at all. Once you get irradiated you can't get it again to that area. If I skip radiation and it comes back I could have radiation done then or do a mastectomy. If I get radiation now and it comes back mastectomy is the only treatment. No good answers.
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Lizzie,I had 33 whole breast radiation sessions plus 5 boost to lump area.
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hi all,had my appointment with the pulmonoligist . He said with the fibrosis from radiation,only 1% spreads. Most times it stay localized,will repeat cat scan in 6 wks to see. He said the air-trapping can be taken care of if I quit smoking and exercise,didn't seem too concerned on that. He was amazed at my lung functioning test,I scored 107% esp since I've smoked for almost 40 yrs! I told him I don't inhale,regardless that's my New Years resolution. He is concerned about heart damage from chemo,so Friday I have an appt for EKG,ECHO,and heart blood work. Hope everyone has a great Christmas.
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I too have had breast cancer radiation. I have been cancer free for five years. But, since the radiation, I have had increased issues with shortness of breath (dyspnea). I'm fine when sitting there. But, to get up and walk five steps now, I am panting like a ran a marathon. I have been to cardiologists and pulmonary specialist with no heart or lung problems seen by testing they did. All I know is with every day, I'm getting shorter of breath and I don't know what to do. I am at a loss here. Any ideas? I'm 84 and until a year ago, I walked over 5 miles a day. I do know that radiation will cause shortness or a deterioration of breathing capacity. This last year, I have seen the most deterioration of my breathing. But, no one can find anything. Hoping someone has some idea what it could be.
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Lsmith, I don't know if this will help but have your Dr check your vitamin D level and vitamin B. I had mine checked D was low, it can cause a lot of issues fatigue, muscle weakness, muscle, bone, joint pain, hair loss/thinning, depression/anxiety, bone loss, affect cardio function, sugar levels etc. My Dr put me on prescription dose for 12 weeks, retested it improved but still low so doing another 12 weeks.
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LSSmith, I think you need to keep searching for a reason of your breathing issues. You dont go from 5 miles to 5 steps for no reason! Some times Docs drive me crazy with their one size fits all answers! Did they check for a blood clot? I had tightness in my chest for a long time post radiation which triggered major anxiety for me, felt like i couldnt breathe. Docs act like radiation has no side effects, such blatant lies/b./.s . I do deep breathing to strech my lungs, yoga and other work outs that feel comfortable to me. I use essential oils and herbal supplements on those really bad days. Im not sure why your breathing in so short, but you need to find out why, that is not anyway to live. I hope you find out soon and can get back to walking. I was thrilled to see you are 84! My dad turned 80 last year and he is a powerlifter, sets world records and still makes working out a priority despite A-fib. He does NOt let Doctors write him off because of his age, he grabs em by the collar and says hey bud, im not your average coach potatoe 80 year old!
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