posted
One of my symptoms I have not yet been able to have explained to me persists and is very concerning for those around me when it happens.
It used to hit me if I was walking, now that I can't walk far at all, it hits me just sitting.
I can start out walking next to someone, then I slow to the point where I am 20 steps behind, and then come to a point where I start going sideways, and I need assistance.
I need to be guided/dragged carried to a seat. I can't speak more than a mumble of a yes or no, sounds are multiplied, people walking toward me look like tunnel vision in a carnival. I stay slumped over, trapped in my own body for about an hour or so until it passes.
Now it happens sitting in a chair, all of a sudden I get quieter and quieter, and by the time I tell my husband it's time to go, it's too late. I need to be lifted up out of the chair, and need to be carried out.
Do any of you have this happen? The only thing I could find that was close to this was on the Under our skin documentary when Mandy was talking about swimming, and that if she swam a lap she would have to be dragged out like the catch of the day.
posted
I have something similar happen. My muscles just stop working. I have to sit immediately whereever I am. Comes on suddenly and then within 20 min it passes. It's so damn scary. My heart also races but that could be because it freaks me out and I panic. Hang in there.
Posts: 342 | From Philadelphia | Registered: Dec 2011
| IP: Logged |
posted
I agree hang in there. This is one of my symptoms that has greatly improved, I had really heavy legs and it felt like I was going to go down when walking. There's still hope for you
I feel like with these diseases things come and go, its something I have accepted.
My newest symptom is chest flutters - and I only get them at night when I lie down. It's scary. I think it might be from acid reflux though. Had my heart checked at the ER when this all started happening not that long ago.
-------------------- Diagnosed with Lyme 4/7/14
KB Posts: 87 | From Townsend, MA | Registered: May 2014
| IP: Logged |
Judie
Frequent Contributor (1K+ posts)
Member # 38323
posted
Before Lyme, what triggered it for me was toxic exposure which included car exhaust, fragranced items, cleaning products, new construction and anything with VOCs.
"This involves a brain response in which the person has seizures or seizure-like activity following exposure to chemicals. It has also been demonstrated that individuals who have toxic exposure can have reduced blood supply to the brain. When this is present, the individuals may have chronic difficulty with thinking, memory, concentrating, and other brain functions."
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/