Sign in

or Register now

MultipleSclerosisCentral.com

See all of our health sites at www.HealthCentral.com
Monday, November, 23, 2009
  • Font size
Receive a FREE Osteoarthritis of the knee pamphlet. Start here.

Can anyone one help me find information on MS and how it effects your lungs and breathing?

theresag79
theresag79
Close
theresag79 is Blessed :)

I am a young woman living with MS.  I have a husband...

12/20/08
theresag79
Topics:MS SymptomsMS Hug

Hello everyone.

I believe I have been having these symptoms since the beginning of the year, but I can't remember accuratly when it started.  I have been having problems with my lungs. My chest feels tight, like it's constantly congested. I'm short of breath at times. I think I feel like how I believe an asthmatic would feel.  I have been searching on the internet trying to find info about how MS effects your lungs, I believe it is an MS symptom.  I haven't been to the doctor because of no insurance and I haven't been to the hospital because it's not an emergency. Help anyone?

Answer This
Answers (3)
Lisa Emrich
Lisa Emrich
Close
Musician, Patient Advocate, and Founder - Carnival of MS Bloggers

Lisa Emrich is a professional musician. She happens to live with...

Sunday, December 21, 2008

Hi Theresa,

 

Sorry to hear that you've been having persistent symptoms.  In looking for answers to give you, I found some good information at the Multiple Sclerosis Resource Centre website.

 

The description of a tight chest, being short of breath, and feeling asthmatic sounds like the MS Hug or MS Girdle.  What can happen is that the tiny muscles which hold the ribs together go into spasm and/or get really tight and breathing becomes much more difficult. Here is how one person described it -

 

"I find myself holding my arm folded across my abdomen in order to ease the discomfort and find I can't breathe deeply enough to get my breath. I tried taking my asthma inhalers thinking these would help but because it's a skeleto-muscular thing, they gave no relief."

 

In addition, a description of possible breathing difficulties in people with MS can be found here.  In addition to potential damage to the autonomic nervous system (which controls vital bodily functions such as breathing), there may be other causes of difficulties.

 

I hope that this helps in your search for possible answers.  Although you do not have insurance coverage right now, it really would be a good idea to be seen by a medical professional.

 

Thank you for your question,

Lisa

 

 

KatieS
Thursday, December 25, 2008

I have to agree with the post above mine.  I have similar symptoms that can last for just minutes or for weeks at a time (just like my other symptoms).  I went to the doctor and did my own research and the MS Hug or MS Girdle is the only thing I could find that would explain the symptoms.  If you type in "MS Girdle" into Google you'll get various kinds of information on it as well as tips on how to manage it.

 

Hang in there!

Merry Christmas.

JohnCE
JohnCE
Close
JohnCE is Professional Biomedical Engineering Director
Professional Biomedical Engineering Director

DXD in the late 1990's, was misdignosed, went to many neurologist,...

Thursday, December 25, 2008

There are a number of factors that can lead to the shortness of breath. Allergies, asthma, the MS not allowing you to have a proper workout (physically) fitique, CHF. When you breath you are using musles to bring in the air to your system and garvity causes you to exhale. If you have inflammation a broncodialator might help of the alvoli are not working up to speed. However only a good work-up will indicate your level of lung function or lack of it. A body box plesthysmograph (PFT) is used to measure changes in volume to a organ or whole body. Mst of the time they will give you the test and then retest you after you have had a broncodialaror administratored to you and see if their is a difference. However only your doctors can decide what is best for you and your condition.

Answer This

Ask a Question

Get answers from our experts and community members.

View all questions (1018) >

Important:
We hope you find this general health information helpful. Please note however, that this Q&A is meant to support not replace the professional medical advice you receive from your doctor. No information in the Answers above is intended to diagnose or treat any condition. The views expressed in the Answers above belong to the individuals who posted them and do not necessarily reflect the views of The HealthCentral Network. The HealthCentral Network does not review or edit content posted by our community members, but reserves the right to remove any material it deems inappropriate.

  • Font size
  • Bookmark
  • Save