COPD & Emphysema Support Group
COPD is a progressive disease characterized by airflow obstruction or limitation. Emphysema is characterized by loss of elasticity of the lung tissue, destruction of structures supporting the alveoli and of capillaries feeding the alveoli. Both have symptoms that include shortness of breath, among other respiratory troubles. If you are a COPD or Emphysema sufferer, join...
Its important for people newly diagnosed to understand that its ok to be breathless.
Helpful article, thanks Holly.
This is a post to all the others that are like me; get up and get out.
Getting out is extremely hard for me, as I was diagnosed with Agoraphobia, years ago. It is easier to stay alone than it is to be around people. Feel safer by myself than with any human. I get out and walk FOR Katie----is what I tell myself. This helps me force myself to shower and dress; otherwise I would just sleep,
and lie looking at the ceiling all day----feeling sad I am alone; and knowing that I am doing this to myself. Catch 22 situation for me.
Last night was quite cold, but I did put Katie in her coat and we went for a walk. I felt safe in the dark, as no one could see me.
Anyone reading this will think I am ridiculous. So be it. Until you have been phobic and filled with fear; you may not understand why I am a hermit? I tell myself that the more I do the more I can do-----the less I do the less I will be able to do. Your post explains this quite well. I hope everyone moves as much as they can. Best wishes to all.
I would ask your doc again about what sort of activity is ok for you to do. Being completely sedentry may not be at all helpful to your heart, lungs or health generally.
Glad you do get out for a walk occasionally tho and I'm sure your Katie appreciates it too.
Keep up the good work, Katie's health will be greatly improved too and I'm sure it brings you pleasure just to see how much Katie enjoys it.
Thanks for your good wishes to all Sally, good wishes right back at you. x x
I think, the bladder control issue can happen, especially if the bladder is full, I mostly make sure my bladder is empty before I go out for a walk or before exercise.
Also I think for some there is an oxygen related possibility too with this. Do you check your 02 sats when exercising?
You do good to keep the exercise going.
Bladder problems I don't think are because of COPD, but they could be because of low oxygen sats or it could be just an age thing.
The pelvic floor exercises can sometimes help if it is a weak bladder thing. I'm sure your doc can advise on this or anything else it might relate to.
Hope some of this helps.
Peta x
I have been told in Respiratory Rehab that this is very common among COPD patients. It could be because the muscles in the bladder are also regulated by the nervous system and we do understand how the nervous system reacts to our stress and other symptoms that come along with COPD.
I have my kidney function checked each year along with a physical and there has never been a problem with the results so I am inclined to believe what the RT told me.
Coughing usually bring a feeling of incontinence also
A while back, Holly had posted this article too...
Urinary incontinence might be a symptom of COPD
28 June, 2011
Assessment and management of urinary incontinence should be included in care plans for patients with chronic obstructive pulmonary disease (COPD), according to Swedish researchers.
The researchers surveyed 728 primary care patients with COPD in order to investigate the prevalence and characteristics of urinary incontinence.
They found that 49.6% of women and 30.3% of men with COPD reported some urinary incontinence, with the most common types being stress incontinence in women and postmicturition dribbling in men.
Also, those with urinary incontinence had a significantly higher BMI than those without.
The researchers said: The present results indicate that urinary incontinence content should be included in care plans for patients living with chronic obstructive pulmonary disease. In addition, the results imply that nurses and physicians working in primary health care should ask patients with chronic obstructive pulmonary disease about urinary incontinence and then offer appropriate assessment and management of it.
Hrisanfow E, et al. The prevalence of urinary incontinence among women and men with chronic obstructive pulmonary disease in Sweden. Journal of Clinical Nursing. 2011; 20: 18951905.
as to COPD and incontinence. There is a mite of information out there on it, but it is often buried in other texts...
Dennis
i can relate to what you are talking about when wanting to shun the world. but on a separate note....you might try a recumbant exercise bike. it can provide you with some cardio exercise while sitting and if you do get SOB, you will be sitting down already.....
http://www.dailystrength.org/c/COPD_Emphysema/forum/12371743-urinary-incontinence-might