posted
I have shortness of breath on a pretty consistent basis.
At the height of my illness, just when i was diagnosed, it was more of a:
I forget to breathe thing.
That is how I described it. I completely forget to breathe or the impulse to breathe is gone.
Over time, the impulse to breathe is better, getting better and so I think that's a plus on the brain recovery.
Yet, I still have this shortness of breath I never had when I was "healthy" (that means living with lyme and company's slow progression over the course of decades undiagnosed). But still, I ran 13 miles training for a half marathon and seemed to do okay.
It seems a combination of the impulse to breathe being forgotten and shortness of breath from
heart? Babesia?
When I take mepron, this gets worse, historically. I cannot vacum half a room without running out of breath when I am on the mepron.
Still, it is a constant problem I find that really needs to be addressed.
Has anyone had this shortness of breath resolved over time? And does it sound like a pure babesia problem? I supposed it could be a nerve problem related to the lyme. Or something else.
My sternum feels like its about to crack in half at this point, it has become weak over the duration of treating for over two years and the subesequent inactivity.
posted
Mine was cured with babs treatment. Mepron might make it worse before it makes it better. But, yes, I had just as you describe .... it was the babs.
-------------------- sixgoofykids.blogspot.com Posts: 13449 | From Ohio | Registered: Feb 2007
| IP: Logged |
AZURE WISH
Frequent Contributor (1K+ posts)
Member # 804
posted
I get the pressure/pain in my chest with the shotness of breath also... for me it is babs.
But i would make you dr aware of its severity... These tbds can effect the heart and ur dr may want to check ur heart just to make sure.
posted
At the peak of pain prior to abx, I had air hunger, shortness of breath, couldn't take in enough air even though I tried.
If I laid flat on my back to try and relieve pain or pressure, it felt like an elephant was sitting on top of me. I literally felt that I might die while doing so. That everything was going to stop working.
That said, I believe that it air hunger and other symptoms for me was babs. I think you are herxing and the air hunger "out of breath" symptoms will worsen.
I am so sorry you are dealing with this. It's very frightening.
Lisa
-------------------- Lymester Posts: 519 | From CT | Registered: Jun 2004
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/