Home Rehab Network (HRN) is interactive Cardiac and Pulmonary tele-rehabilitation from the comfort of home. Here on our RU-vid channel, Home Rehab Network seeks to build and empower the patient community around breathing and pulmonary education, and to provide resources to those who may benefit from cardiac and pulmonary rehabilitation.
Guided by practitioners and clinicians that are well known in their field of practice, no other program offered in the United States can compete with HRN’s success rates in Pulmonary or Cardiac Telerehabilitation. To learn more about our community and what we do, please visit the website below!
The Best in Telehealth Home Rehab Network Cardiac and Pulmonary Rehabilitation
I did rehab 2 years ago was on top of the world now 20 percent lung funtion with both emphasima and asthma sir i cant get out anymore or tie my shoes is my life ending
You are a very stressful person to listen to. You waste what you "know" on your intense arrogant attitude. You spoke so demeaning. You said okay like you were projecting your rage unto people. These are the types of people that revel in this. You are looking at such sad traits that should not be exhibited by anyone in the medical profession. You want to hear yourself talk, or you could have said all of that in one minute. I hope you get some help man.
I stopped smoking breathing got worse also I was put on a steriod inhaler too early now on stage 4 I can't do jack jeez ride a bike seriously u clearly know nothing
I have COPD. Recent CT shows lung fibrosis. I also have severe sleep apnea and been on CPAP for 15 years. I recently had an updated Sleep Study done and it showed I have 82 episodes of apnea/hypoxia per hour. My pressure on my CPAP was increased from 5 all the way up to 11. For the first few months, I felt this pressure was going to blow my lungs out and was painful but I continued. I am posting because I wonder how many people out there have past due Sleep Studies and not know how bad their lungs really are. Enjoyed your videos.
@@alexgrichuhin1188 how am I confuse when am the1 doctors almost killed in the emergency room by refusing to give me oxygen when I asked for oxygen because I knew I needed it!!! I ended up in the resus room fighting for my life,every time I go to the hospital now I take my oxygen concentrator with me so I don’t have to beg for oxygen from the machines that we the tax payers payed for,now because of my experience u r such a fool n u tone make me sick u don’t know what u saying I saved my own life that day by fighting that doctor that said no to me n making my way to the machine
I was diagnosed last month, I have lupus and Scleroderma since 2016, and they say it destroyed my lung causing the scaring so now I have IPF and I find it difficult to believe my life has. been cut short. I want to treasure moments and create moments with my family.
Hi mate after looking at ur videos I really need your help mate,I'm a Sevier COPD Patient on top I'm a retainer. I retain high carbondiecside at this moment I'm using NIV at home Sleep with VPAP ST-A Lumis100 Anyway after using the vpap I'm still gagging for every breath and feeling heavyness on my head and pain on the right side of my head and pain all over my neck that's because my crb is very high and after using the vpap, last night I was unable to breath so called emergency line the ambulance came took me to hospital the doctor said on chest tray she saw infection on my right side of my chest,so now it made sense why I was unable to tolerate the vpap machine. I got appointment with Figiotheraphy to check if it's the right setting or not if needs changing then they will change it for me.but in the mean time any advice how to cope when unable to breath and when having a panic attack.thankyou
Useing stairs was tge first thing i noticed i had start of COPD i looked after my sister till she died not long after i was diagnosed its 13 yrs now for me iam on oxygen now August 2024 🌾🐿️🍂
Dr you dont know what your talking about when you have an set back there is NO NO NO Warning it happends so sudenly not a chance of getting anywhere you need an amdulance straight away you cant walk you cant talk or breath so how will you get to your DR sillt man
He doesnt know what he is talking about it happends in a split secound there is no warning at all if you live alone get one of thors wrist bands to get ambulance they are quick to attend when the hear th noise you are making
With flare ups i can not do a thing excapt push button on a wrist band for AMBULANCE so i dont know why you say go to an chemist ir do this or do that have you seen anyone having a flare up i cant do anything i make a dredfull loud noise it feels like i dying i cant get anythimg on or out you make sound so easy it i hell really
The lack of energy and no emotional and physical support...feels like im dead already or would prefer God to come fetch me. South Africa have no support groups. In a matter of 6 months i went from not being able sit still to stuck alone in my room....that's no life...please forgive my negativity, but this hit me hard. No emphysema, they don't know the reason and together with that Lupus, Sjorgens, and RA all at once!!!
Can you get COPD even if you don't smoke? I have low oxygen below 93 usually when i lay down,and i get a crackling sound when I breathe in when i lay down as well
Did you have this checked out? I'm no doctor, but in trying to figure out why I was short of breath, I came across a few things that said a crackling sound while breathing could be due to heart issues. You might want to make a doctor's appointment ASAP.
part of the plan when not treating covid early.... there was NO excuse to not implement early treatment..I'm a nurse,and this was a no brainer. I also became a patient....now damaged.
Ride a bike are you kidding me im stage 4 im out of breathe walking to the toliet seriously id swap my lungs for someone given out this advice struggling to breathe ill go for a bike ride jeez
I was diagnosed with ipf on March 7th of this year. I researched treatment options and set up to get umbilical cord stem cell transplants over a 3-week period in Bangkok. I have completed the treatment and I no longer have symptoms of the disease. My oxygen has returned to 99%. I can walk again, sing again, play trumpet again add exercise again. The scarring has been reversed in my lungs and the tissue has been regenerated
Accomplished night time nostril breathing . Do u do little steps at a time when i go out.? Practice little at a tim..?.. HELP ANY HELP.....thank you you are very helpfu.l xx
People say "fight to the end". Why? I've seen too many try to do that only to make themselves more miserable. I don't want to do that. God has me in His hands. I'll go when He feels it's my time. I have had IPF for 3 years. I am not taking Ofev or Espriet & don't plan to. No thank you to the rough side effects.
