Close to my ONLY symptom. Have an LLMD appt but not treating anything yet.
My body is just on a high sensory feeling, kind of like humming but also like almost when you feel dare I say and thank god no one knows me sexual charged like. Trust me I dont FEEL like
having sex but my sensory feeling is like that
It is mostly on one side on my body and makes me feel like I have to pee all the time.
Last night I felt like cutting off my leg just to get the feeling to go away.
PLEASE I need relief from this.
-------------------- Good friends are like stars... You don't always see them, but you know they are always there!!! Posts: 362 | From west chester, pa | Registered: Apr 2004
| IP: Logged |
posted
Amy, I get this a lot since being sick. I know you say you don't feel like having sex, but I can tell you that since I have been ill I haven't experienced a diminished sex drive at all. At times it has even increased and I think part of the reason is that sensory overdrive feeling you are speaking of has enhanced my sexual pleasure. It is indeed uncomfortable though to feel this way at times when you are otherwise not interested in sex. It is such an odd sensation, you are right.
Lyme can make our nerves extremely sensitive and that can result in a lot of these strong sensations. I think when you get on proper treatment that is effective, these strong sensations should diminish. When are you seeing the LLMD, is it soon? I wish you the best of luck. Jess.
Posts: 651 | From ct | Registered: Sep 2011
| IP: Logged |
posted
Thanks Jess....it is in two weeks...I cannot wait....
All the other times I was just tired and sore and headaches...
this nerve sensory is ahhhhhhhh
maybe heavy metals...parasites??
hormones???
-------------------- Good friends are like stars... You don't always see them, but you know they are always there!!! Posts: 362 | From west chester, pa | Registered: Apr 2004
| IP: Logged |
posted
Two weeks is fairly soon, so that's good. I think all of the issues you mentioned could be a factor. In my case, my dr seems to think its more from the Lyme making my nerves much more sensitive. Sometimes that causes intense pain, sometimes it causes intense pleasure. It's incredibly strange and frustrating too. And you're very welcome. I actually wanted to post about this for awhile but was afraid that people would laugh at it or think I was strange. So thanks for posting this. Jess.
Posts: 651 | From ct | Registered: Sep 2011
| IP: Logged |
posted
I was nervous too but then I thought if not here then where
Thanks- here's to hopping my husband gets home soon maybe relieve some of it
-------------------- Good friends are like stars... You don't always see them, but you know they are always there!!! Posts: 362 | From west chester, pa | Registered: Apr 2004
| IP: Logged |
posted
You are welcome again-and yes, husbands are good for some things I suppose haha. Jess.
Posts: 651 | From ct | Registered: Sep 2011
| IP: Logged |
It cannot be. I need some relief from this before LLMD appt.
-------------------- Good friends are like stars... You don't always see them, but you know they are always there!!! Posts: 362 | From west chester, pa | Registered: Apr 2004
| IP: Logged |
posted
I can only say I have the opposite problem. Lack of sensation. I have neuropathy, and a growing lack of sensation. I can barely feel whats going on during sex down there. I mainly just do it for hubbys sake anymore. I have no idea what to do about it. The neurologist has yet to figure out anything to help me AT ALL. I go to gyno in Oct. but I don't guess he will know what to do, and I've spoken some with my pain mgt. clinic about it, and they say it can't be my pain pills, but the neuropathy and to talk to neuro about it..
I think they will all pass the buck, and I will be stuck this way, as usual.
Sorry for your issues as well. Best of luck to you. Hope they can calm the nerves down, they can't seem to stimulate them at all.
-------------------- One day at a time Posts: 409 | From TX | Registered: Mar 2004
| IP: Logged |
posted
twicebitten~ SORRY, I hope they figure it out for all of us....
Maybe we can ask the Lyme gods if we can trade off everyother day
PLEASE
-------------------- Good friends are like stars... You don't always see them, but you know they are always there!!! Posts: 362 | From west chester, pa | Registered: Apr 2004
| IP: Logged |
AuntyLynn
Frequent Contributor (1K+ posts)
Member # 35938
posted
Have you tried taking magnesium? It can help to calm jangling nerves.
Posts: 1432 | From New Jersey | Registered: Jan 2012
| IP: Logged |
Are any brands better then others or all about the same?
-------------------- Good friends are like stars... You don't always see them, but you know they are always there!!! Posts: 362 | From west chester, pa | Registered: Apr 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/
UBBFriend: Email this page to someone!
![[bonk]](graemlins/bonk.gif)
![[Wink]](wink.gif)
![[Smile]](smile.gif)
![[cussing]](graemlins/cussing.gif)
![[bow]](graemlins/bow.gif)
Printer-friendly view of this topic