Paralyzed Diaphragm
My name is John and I was diagnosed this past January with a paralyzed right diaphragm. Phrenic nerve damage has been ruled out because of the amount of time between my heart valve surgery and when this started. I still cannot figure how this happened, I have a couple of ideas but nothing conclusive. I have seen two pulmonary doctors and both say there is a surgical procedure that can be done but no guarantee that it will work. I would like to know if anyone out there has been diagnosed with a paralyzed diaphragm and if they had it fixed.
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"Diaphragm Plication" I believe is the name of the procedure....
Here is a case series from NIH on long term impacts of the procedure https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996377/
Hi John. I had a paralyzed left diaphragm. I suffered for many years. I was treated for COPD..asthma for a long time. Until a specialist finally found the problem. Although it being kind of rare the specialist did not perform that type of surgery to correct it. He did some searching & found a doctor for me. I had the surgery about a year & half ago. It has been great! Before the surgery I wasn't able to rush around, climb any sort of upgraded area, or even carry things without being very short of breath. When it got so bad I couldn't make it across a highway on the crosswalk before the light changes over or being able to get into my car & needed to catch my breath before locking my seatbelt I knew I needed to do something because it seemed to be getting worse over the years.
Anyways this amazing doctor did a surgery which now has my right side diaphragm help work my left side lung now. It's great now! I even did some hiking after my recovery.
Yes I have been tested for allergies. Dust, grass and certain drugs. I have covers on fabrics that can be washed, air purifier, no carpets. Don't do any outside work or around plants. Have a list of medicine that I can not take without going into antiphallic shock. Been there, done that.
Have done physical therapy for the back but not specifically for the breathing issues. They were treating me for COPD and asthma before they just found out the diaphragm problem. I see pulmonologist this month to talk about that. I am hoping to find out more on treatments at that time. And if I can cut out some of the meds I am on since it may be that I don't have COPD or asthma but were just mis-diagnosed. Any suggestions on questions I should ask him? Or treatments that I could try?
I live in small rural area. Have not heard of anyone that does MFR in this area. What type of doctor/facility offers this? I will have to do some research on this and if my insurance company will help.
I do use a cpap machine at night. They recently increased my pressure and it is helpful.
I will check those links. Thanks.
@labsmom5 It is usually physical or massage therapists who do myofascial release. You can search at this link. http://mfrtherapists.com/ You might ask the pulmonologist to explain the path of the nerve to the diaphragm so you know where it goes, and ask where it might be compressed that MFR and physical therapy may be able to release.
Hi
I was on high blood pressure meds, inhalers, nebulizer...i was also told i had COPD along with asthma. I had the surgery about 3 years ago. At the time of surgery while in the hospital my blood pressure was too low so they removed the meds. I told the doctor maybe i didn't need them any longer...his response was he never has met someone who has been on high blood medication & stop needing it. Well i am living proof! I no longer use inhalers, nebulizer for my breathing. It was so bad that couldn't even walk any upgraded area, carry groceries from the store to my car..even carry my grandchildren while walking. Now today...I do all that! It's like having a second chance. I'm so happy i did it. It was horrible living like that & at times wheezing..hard time catching my breath. It's all good now!
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@ethanmcconkey Thanks, Ethan! I'm glad you enjoyed the interview and my stories!
Brenda, It's John, I'm glad to hear the diaphragmatic plication worked for you. After reading about Brian I was a bit concerned. I have a couple of questions. Did your doctor get your phrenic nerve checked out? I'm thinking this would be the first thing to get checked. May I ask where you had the surgery done? As I mentioned to Brian in an earlier post the only place I could find was Cedars-Sinai Hospital in LA. As far as getting the phrenic nerve checked for me that would be the Mayo Clinic in Scottsdale AZ . Take care
@teresa. After my 23rd appointment, my lobes collapsed and I have been in ICU on a machine and just got moved to a chronic care unit. Good news is that I do not have a paralyzed diaphragm as testing indicated. Bad news, however, is that I am end stage chronic Atelectasis from advanced Bronchiectasis. I have been placed into a Monarch chest vest to help dislodge the mucous plugs along with an airway clearance system and lung expansion therapy using the MetaNeb CPEP/CHFO system by Hill-Rom. So far the treatments are helping and I am able to breathe more comfortably while being bedridden. Whether or not I will be able to breathe again out of bed or without assistance remains to be seen. Thank you, everyone, for your help with this issue.