I know this has been discussed before but could not bring it up using the search engines.
What I am looking for is an answer to give to the non lyme literate NP who comes once a week for the IV.
She has been bringing in the testing that you put your finger in to check your oxygen level.
Of course it is fine.
I try to tell her it is the lyme, but what is it about the lyme that causes this?
Is it because the diaphragm is too weak? Any ideas?
It happens with multi movement or activity. If I am just straight walking I am OK until I over do it...about 10 or 20 minutes and then the heavy breathing starts or shortness of breath.
Perhaps it is just the over all fatigue that goes along with lyme.
Just curious. I would like something to give to her to help her understand that goes beyond the oxygen testing that states I am fine when I am not.
It flares up...giving us false sensations, or slightly/temprarily paralyzing the diappragm.
Kent

Thanks
DLL
I don't know what is causing you to have this happen, but I do recall feeling this way many times when this first hit and I didn't know what was going on.
Three different times it got so scary that I considered going to the emergency room.
One time I finally did call a friend and she drove me in.
The other two times I called the number I had for the nurse line with the health care that I had at the time. They too said to go to the emergency room, but I didnt comply.
I really don't like docs and hospitals.
The one time I did go....just my vitals were taken and I laid there for several hours and then was sent home.
Now, I don't think it happens as often now because I am kind of learning to pace myself and not to over do it.
I also changed my diet and am on the abx.
Not sure which of these things helped...but not over doing it would be the first thing I try to keep at a minium.
I like to be able to breath! If I just lay still and concentrate on breathing in and breathing out and think good thoughts...it usually does go away.
I didn't listen to my body this am and tried to over ride it. I do this when people are here to help out. But, it is taking me a while to breath easily again.
I recalled one person mentioning it also feels like you are breathing through a sponge at times.
Not good...but there are people who deal with lack of oxygen all the time. At least we can breath normally most of the time.
It first happened to me when I was a youngster,in June, just after finishing the last dose of an antibiotic for a bad sinus infection. It felt as though I was trying to breathe with my mouth and nose squeezed shut! Seemed to go on for years after that. I stayed away from sports and exertion all through my teen years. Such a waste!
Sometimes I wonder if I've had lyme all this time. It would explain a lot.
From what I've read, the antibiotics should clear that up.
Best in health to you and yours!
Kathy
Ohhh.....I remember now. I went to an electropyhsiologist for my fast hearbeat when standing. He said he wouldn't want to cauterize the nerve affecting the heart because this is very near to the part that makes you breathe...and becasue I told him that many times my breathing stops as I'm falling asleep ( It's always ok after I fall asleep)that it was too dangerous and may affect my breathng. Anyone else have the probem of jerking awake every time you start to drift off to sleep? Sometimes I'm awake the whole night. Klonopin seems to help this
I have Babesia and used to get this symptom really badly and after treatment with Mepron/Azithromycin it has nearly gone...before when I was walking a short distance it was so bad I thought I was going to pass out as I felt like I couldn't breath.
Nowadays I only get breathlessness a bit if I am running up and down stairs!
BW
Emma
Tincup posted 'Cranial Nerves' which explains perfectly what's going on with us Lymies. I think it's in Medical.