Pain & appetite after lung removal

Hi, 

I had my left lung removed 2 months ago. I have a lot of pain in my upper arms and shoulders. Has anyone else experienced this? I know I did a lot of lifting with my arms after surgery and expect some muscle pain. But this pain does not seem to be getting any better. 

I have read many messages and my stomach seems to be smaller also. Why is this, does anyone know?

Thank You,

CLW

clw1976 said:

Pain After Surgery

Hi, 

I had my left lung removed 2 months ago. I have a lot of pain in my upper arms and shoulders. Has anyone else experienced this? I know I did a lot of lifting with my arms after surgery and expect some muscle pain. But this pain does not seem to be getting any better. 

I have read many messages and my stomach seems to be smaller also. Why is this, does anyone know?

Thank You,

CLW

 

Hi CLW.. I'm new here I also had lobectomy 5 weeks ago doing well except the severe numbness pain from mid chest under ribs under arm and back side..hoping will subside but not yet. I' on GABAPENTIN 3x day, tramadol if needed as break through. Also oxycotin if need. I just don' like taking narcotics and sleeping unless unbearable.

CLW - I think I know what yours is:  you are breathing very shallowly, and the muscles of your shoulders and neck are doing the work that your diaphragm and lungs should be doing.  You need breathing exercises.  they tell me to do 'belly-breathing', relaxing my shoulders.  slower breaths, to reduce 'panic' feelings.  Can you get respiratory physio?  Or look up ACBT online.   BTW - I lost lots of weight after lobectomy, over a stone, and happily, it has not gone back on!  Wind, discomfort, cramps, raised paralysed left diaphragm, paralysed laryngeal nerve/left vocal cord, got it all.   Joan. 

BigRichFish said:

Right lung removed

Hello, my total right lung was removed on April of 2013. I have been dealing with constant pain. Sitting too long, or driving too long is the worst. When I walk, it's not as bad. I had special firm pillows made for me. I use them when sitting or driving. They keep a slight pressure on my ribs, where they went in. They give me pain relievers, but I'd rather not take them, unless I am really hurting bad, and have things to do. Also, they make me feel like the couch is my best friend, I don't like that. Do you have any info on getting relief, what do you do, thank you for any help you can give, respectfully, Rich Mullen

Hello Rich Mullen:

wish you doing well now.

Harvard professor David Sinclair's mom live over 20 years after removed one lung because of lung cancer. please check out the youtube video:

https://www.youtube.com/watch?v=AiCvqnUIe04&t=873s

He said Resveratrol might help. if you want to check out the more infor about reseveratrol, there are a lot of youtube video about resveratrol. my sister who had cancer benefit from it. that's why I involved in the health industry. check out my website if you want to.

https://www.jeunesse-opportunity.com

https://agracelily.jeunesseglobal.com

wish you be cured soon

Lily

Hilajoan said:

aches and pains after Lobectomy

Looking for stuff about arm pain brought me here, but am on the MMMT/uterine group, too.  Had upper left lobectomary 7 weeks ago, and now my diaphragm is raised right up under the remaining piece of lung (the lower lobe - which is now in the upper part of my chest) , and so is my stomach.  Of course I have pain, but keep it under control, more or less, with Paracetamol and the occasional Tramadol.  But I am SO breathless - I don't see that mentioned much - and I have trouble eating much at a time, and also have lots of 'wind' - will it improve, does anyone think?   and new aches in my left arm - I imagine it's nerve pain?  I have also more or less lost my voice, and have to see speech therapists to try and remedy it - left vocal cord is paralysed, apparently a fairly frequent result of this surgery - but I wasn't warned in advance, nor about the peculiar positioning of my diaphraphm and stomach.  As for fatigue, I find I cry if I overdo it - and currently overdoing it means spending a whole morning out and about, seeing medics, or whatever.........  I am normally stalwart - do others feel like me?   I also feel that anyway my cancer will recur AGAIN, it's always come back after 10 months or so, and it seems a bit futile keeping on cutting it out and poisoning it and burning it, just to get a few months off - though of course - I have had five years that maybe I wouldn't have had without the first treatments........   Sorry to drone on.  Joan (from London, UK).

Hello Joan:

I am sorry for you suffering. My uncle died of lung cancer and my sister has also. One day I happen to watch a video talk about a professor of Harvard Medical School treated his mom by Resveratrol and his mom lived overy 20 years with one lung while the doctor told her mom that she only had one year left. this is the link of the video

https://www.youtube.com/watch?v=AiCvqnUIe04&t=873s

if you want to know more infor about Resveratrol, You can google, youtube or check out the link below:

https://agracelily.jeunesseglobal.com

https://www.jeunesse-opportunity.com

All the best to you

Lily

floydb777 said:

newbe

 

I’m new to all of this. Today is 30 days postop from losing my right lung and I have only been home 5 days. I’m not on oxygen while resting, but am using 2lpm during light activity and sleeping. Not too bad for a guy who was told he probably wouldn’t survive a total lung removal. I welcome any advice that you have for me.

 

 Hello, i am a healthy 66 yr gal and Ialso had my right lung and lymphnode removed on July 18, 2018 at Brigham and womans hospital in Boston. I am going on 3 months soon in October.  I pray for all of us who go through this its no picnic.

I have noticed that i keep losing weight because of no appitite still..my back and under breast bone where they removed my right lung still gets sore. I still get short of breath at times but control my breathing for 1 lung.  No lifting is a must even if you feel better.  It will be 1 step forward 5 steps back if you do.  

Im also constipated at times because i am on a 3 1/2 bottle of fluid a day still total 1550 ml. I do not take or have taken any pain medicine or iborophin since August.  I also must sleep on a 45 Degree slant in bed head up most likely the rest of my days and the reason i was told the right cavity needs to fill with fluid then will gel to offset the other lung..i still need to rest a lot because of healing.  Im being patient through this as you and many of us are.  I am cancer free.. I have decided to try CBD drops.  To see if this might help pain its thc free no prescription needed .Zillus ultra cell i hear is the best .  i have seen others taking with with remarkable results.  I will let you know if you want to know how it works on me.  It surpresses pain and helps with energy.

I wish you well in your journey and pray you heal well.  Im here if you want questions answered.