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Lyme Disease ForumsGeneral & SupportAnyone have simple seizures at night with lyme
11/07/2011 05:57 PM
kev15
 
Posts: 104
Member

Before I know that I had lyme - I had started to get this sleep paralysis - simple partial seizure thing at night. Does anyone else have these with their lyme?

It is where I am suddenly frozen in a fearful state, not able to talk or move, I feel like I am drowning.

As several seconds to minutes go by I start to feel pain throughout my body, along with nausea and stomach pain, ringing in my ears, and a severe headache.

Does anyone else have these horrible things that I go through almost every night, and sometimes several times a night?

Thanks

Reply

11/07/2011 06:58 PM  Top
meakaye
meakaye
 
Posts: 44
Member

I experience this! It can be very scary. Sometimes my husband will be asleep next to me and I try to speak to wake him up but all I get out is little mumbles.

I will wake up in panic mode thinking someone is breaking in or I will hear voices or see shadows moving in the room.

It all seems so real at the time. It's usually accompanied by awful leg tremors and body sweats. Sometimes I even drool (gross I know)

It's like a body lock down. You're not alone.

-Malea


11/07/2011 07:00 PM  Top
AlostSoul
AlostSoulPosts: 124
Member

Oh your scaring me...

I had weird stuff tonight that i never had that Im gonna post to ask opinions on.

I had the numbness in rt side face and drooling.I almost went into full blown panic attack because I never had this before


11/07/2011 08:46 PM  Top
RavenLunatic
RavenLunatic
 
Posts: 2597
Group Leader

Alost -

It sounds like you suffered from a "Bell's Palsy" episode tonight.

I found that if you make a wash of water & ginger or cumin to your face, it will pull the toxins/build up out from under your skin & aleeve your symptoms.

"My Disabling, Chronic Illness Is More Real Than Your Imaginary, Medical Expertise!!!"

10/30/2012 11:59 PM  Top
sheep16
 
Posts: 19
Member

it could be sleep paralysis which is what it is called

Previous discussions I participated in:
armpits...
Multiple events
T* my story

10/31/2012 01:33 PM  Top
JasonMChicago
Posts: 307
Member

I get this too, but mostly in my face. My facial muscle move involuntarily... actually it is one of the last symptoms I'm having. It was the first one I had before I knew I had Lyme+.

I have rubbed bentontine clay on my face to pull out toxins. I also rubbed organic coconut oil. I tried colloidal silver the other day but it is SO STRONG and it kills the bugs along the cranial nerves. The the neurotoxins are stuck with no where to go.

I think getting Lyme out of the head/face is tough because it is far away from a circulation standpoint.

Don't know what can help but I take some sleep aids at night to stop the firing of nerves.

I am not in the medical field and anything I say is simply my opinion and should not replace the advice of your doctor.
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