COPD end stage: Anyone else?
Sorry havent been spending much time writing lately.Been going to hospital few times for breathing lately..Had a few discussions with pulmonologist,fev was 16 ,going to needa wheel chair.Right now cant even walk out to the car.Even room toroom getting hard..I realize copd doesnt get better but im only 63 not that old.
Interested in more discussions like this? Go to the COPD: Chronic obstructive pulmonary disease Support Group.
Ppeschke,im lucky my wife and children understand,ive been on a ventilator at hospital 5 times and have had grand mall epilepsy since i was 5 so i hope they be?ieve me.Ido feel like im a burden sometimes, b ut idont have much choice.
thankyou so much.
Waterboy,i can handle small breakfast,or lunch thats it.
bobp if you and doctors agree on transplant thats great.I was set to take coarse for lung transplant until cancer found,that stopped me from lung transplant.my age and condition ofcopd ruined my chance.
The biggest problem to get over is understanding the difference between life and living. Being alive is just mechanically advancing the calendar from one day to the next. We, as humans, need a reason to living... to watch our offspring grow and welcome new ones into this world, ECT. I have found a new one, volunteering for clinical trials concerning COPD. Maybe some of my data can be used to help some other COPD victim. I volunteer at Mayo clinic Rochester.. what a great group of people in a wonderful setting. In the first study it was about exercise at home.. tai chi style. Learned you don't have to sweat to get benefits. Give yourself a reason to live is the best medicine... and the cheapest.
Great words of encouragement! Trying to get to Mayo Rochester Pulmonology but the are not accepting any new referrals 🙁 > We moved from TN to MN in Dec 2015 and are now heading back and I was hoping to see a doc(s) in the best hospital in the world but I may not get the opportunity. I agree waterboy it is all outlook. I too will be looking at in home exercise i have to believe strengthening muscles will make breathing a little easier have a lower need for o2. Have breath easy day!
If you have challenges before you depart MN. I encourage you to stop by St Mary’s Hospital ER, in Rochester where they have a great pulmonary team who could look at you in ER! They can further diagnosis and they may make an appointment for you at Mayo. They are all connected aren’t they?
Best
Boy you have that right! In short 50% of living is attitude and determination! After my lung cancer surgery I woke up and had great difficulty finding my next breath... with most of my left lung removed.
The stigma and blame was a shock that just made me fighting mad! Doctors and staff understand that there is a lot of lung disease that any body can get.
Awareness Education & Research are critical to saving lungs and quality of life.
Exercise does certainly help along with diets and mindfulness. Dr Amit Sood Paced Breathing (began as a research study ) has helped my become Resilient.
I have learned to pace my breathing, and run. Even 10k races! And speak up/out
to help support the work of amazing and dedicated doctors and staff to help save more lungs and lives and give victims of lung disease. Because we must be one voice to give families and communities a better quality of life! Lung disease disease is Expensive and we must help change the face of lung disease together!’
I love your neVer give up attitude!
We actually live in Minnesota. St. Cloud Hospital is where my husband is. I believe they would suggest Mayo if they thought it would help. But, I do appreciate you input and will keep this suggest in mind and talk to doctors.
My husband was diagnosed with COP (BooP) having a biopsy of the lung. Cryptogenic Organizing Pneumonia. This is different the COPD. Antibiotics will not work, only steroids. My husban was on Finasteride and Tamsulosin for prostate problems.