Does anyone know if there is a connection between MS and lung/breathing difficulty. I have MS and was hospitalized three times in the last 6 mo. with pneumonia, dyspnea, and hypoxia. The docs are giving me a different diagnosis each time. First they said bronchitis, second asthma and now copd. I have done some research and found there is some breathing issues in about 20% of patients with MS and could really use some help in finding out if there is a relationship between the two and if so what kind. Thank you to anyone that has any information about this subject.
I have not had any breathing difficulties. I have swallowing difficulties.
Aspiration pneumonia is a concern when there is swallowing difficulties. I just did a search which brought up cases of breathing difficulty, but the cases are rare. Thus, you cannot dismiss it as not MS.
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MS diagnosed since October 3, 1982
MS onset circa 1977
Proud to be MED FREE!
Eternally blessed and eternally optimistic!<><
Aspiration Pneumonia is not a breathing issue. Its a swallowing issue- so its not related. Its not unusual for MSers to have difficulty in swallowing, however I havent seen or read anything which suggests that its MS related.
COPD or Asthma or even pneumonia are common to all people, with and without MS. Probably there is no connection to you having MS;however if you are susceptible to breathing issues, you might want to talk to them about the risks/ benefits of taking some sort of steroid inhaler to keep your bronchials and lungs clear.
Hi, I have read that the part of the brain that controls the lungs and breathing can have a lesion, which would make you feel like you cant breath. One girl said she felt like her breast was asleep and it was her lung. So it can def. be part of an MS attack.
I read about a girl with MS who had her breast feel like it was asleep, and it was her lung. Her lesion was on the part of the brain that effected her lung, so yes not be able to breath can be a part of an MS attack. Deprnding on where the lesions are. I would go have an MRI and ask MS Dr about it.
Thank you for your reply. My daughter is a nurse and has mentioned something about that happening, but I have never heard of it from anyone else. I am definitely mentioning this to my neurologist. Thank you again.
Thank you for your reply. My daughter is a nurse and has mentioned something about that happening, but I have never heard of it from anyone else. I am definitely mentioning this to my neurologist. Thank you again.
Good Morning,
Just read your post. As you, I have breathing problems. My Neuro has prescribed a Nebulizer to use when things get bad, plus I also use inhalers. Have you had your lungs checked to see if there is any Paralysis from MS? This may be part of the problem also. I know it's rare, but of late I have learned my L lung is 1/2 paralyzed from MS.
Currently, I am looking for information on lung paralysis from MS and have not found any.
Just take things day by day and try to keep your chin up!
Blessings to you.
The post you replied to is from 2010 and may not be answered.
Thank you for sharing about the breathing and lung issues with MS. I have breathing difficulties if I lie flat, but I never knew about lung complications as you shared. I will have more questions for my neuro on my next visit!
__________________
MS diagnosed since October 3, 1982
MS onset circa 1977
Proud to be MED FREE!
Eternally blessed and eternally optimistic!<><
Thank you for the reply. I would be very interested in the response your Neuro has. Yesterday, my Neuro told me Lung Paralysis is not very common, but he has seen it before.
I've spent considerable time on the Net today looking for information on Lung paralysis due to MS and found nothing. Great deal of information on Dyaphram Paralysis ..... I think this is a muscle that lays below the lung. I am not a DR. so am not sure.