LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Anxious Feeling and Need to Move

 - UBBFriend: Email this page to someone!    
Author Topic: Anxious Feeling and Need to Move
Aniek
Frequent Contributor (1K+ posts)
Member # 5374

Icon 1 posted      Profile for Aniek     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been getting this really anxious feeling that is accompanied by uncontrolled movements. A neurologist diagnosed the movements as motor tic disorder, induced by Lyme.

I'm wondering if other people get this very anxious feeling or not. It feels somewhat like what I remember adrenaline shots felt like. I used to get them years ago for asthma attacks.

The feeling can be really bad when I wake up. I'll often press snooze for an hour in hopes of the feeling going away.

--------------------
"When there is pain, there are no words." - Toni Morrison

Posts: 4711 | From Washington, DC | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
Carol B
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Really just wanted to say Hi. [hi]

The only way I can respond is that a seizure aura can give you an anxious feeling, followed by uncontrolled movements can be seizure activity ,too

I'm sure that's not the answer you wanted though. Sorry. [Frown]

I'm surprised a neurologist didn't pick up on that-unless I am not understanding you correctly. [confused]

I'm having too much fun playing with the smileys tonight-hope it doesn't get on your nerves for such a serious subject.

Carol

IP: Logged | Report this post to a Moderator
Thereminator
Member
Member # 8324

Icon 6 posted      Profile for Thereminator     Send New Private Message       Edit/Delete Post   Reply With Quote 
Didnt someone just mention morning symptoms like that related to hypoglycemia? Alan

--------------------
Charter member of the ~ Delux Toasting Club ~
Our Moto:
"Take No Prisoners"

Posts: 95 | From San Diego | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
Aniek
Frequent Contributor (1K+ posts)
Member # 5374

Icon 1 posted      Profile for Aniek     Send New Private Message       Edit/Delete Post   Reply With Quote 
Carol - Smileys are fine. I had an EEG and it was normal, no seizure activity.

Thereminator - hypoglycemia is interesting. I know I am slightly hypoglycemic.

--------------------
"When there is pain, there are no words." - Toni Morrison

Posts: 4711 | From Washington, DC | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
docjen
LymeNet Contributor
Member # 7510

Icon 1 posted      Profile for docjen     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sounds to me a lot like restless leg syndrome. The "leg" part is really a misnomer...it is more like restless body. It does make you feel like you just got a big dose of adrenaline (even if you feel perfectly calm) and you have an incredible urge (and need) just to move. You feel like if you had to sit still you would go out of your mind. It is really really unpleasant.

It seems that RLS is a fairly common side effect to neuro involvement and neurotoxicity. There are a couple of different drugs that can help "calm" that need to move until your body has a chance to clear the toxins, which you might want to ask your doc about.

Just my humble opinion! Good luck!

Posts: 393 | From Washington, DC | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
5dana8
Frequent Contributor (1K+ posts)
Member # 7935

Icon 1 posted      Profile for 5dana8   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
hey Aniek

I get this at night the most when I am trying to fall to sleep but without the uncontrolled body movements.

It gets much worse when I am herxing.

Been told it's restless legg syndrome. I get nervous and anxious. As long as I move something like my leggs

or re-position myself, I don't get as much anxious. Needless to say this is not the best thing to have when I am trying to get to sleep. A 1/4 to 1/2 valium on occasion helps. I have heard people say muscle relaxers like flexerial help too. But be careful with either for long term use.

I believe it is from neurolocial damage from the lyme. Never had pre-lyme. The last 3 years of treatment have helped. But like I said when I am herxing it can be hard to bear.

I hope you can find something that helps and find some inner peace

--------------------
5dana8

Posts: 4432 | From some where over the rainbow | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
Aniek
Frequent Contributor (1K+ posts)
Member # 5374

Icon 1 posted      Profile for Aniek     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm on Flexeril. Been on it for over 2 years because it's the only thing that keeps the muscle pain down.

I have an appointment with a new alternative doc in a few weeks. He's an environmental specialist who has worked with autistics. I'm hoping he can give some guidance. I think this is out of my LLMD's knowledge.

The weird thing is that most people say RLS happens when going to sleep. I'm fine going to sleep. It's when I wake up or in the middle of the day that it hits.

--------------------
"When there is pain, there are no words." - Toni Morrison

Posts: 4711 | From Washington, DC | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
elley0531
LymeNet Contributor
Member # 9434

Icon 1 posted      Profile for elley0531     Send New Private Message       Edit/Delete Post   Reply With Quote 
I get the body anxiety to. It doesn't matter if I move around, sit down or whatever...I will feel anxious for no reason. It will make me snappy and irritable too.

It sounds kind of ridiculous, but usually it means for me that my brain is on overload with stress and emotion, so to be honest I will sit down and cry...like sob...for a good 5 or 10 minutes.

Afterwards I'll thrown on an episode of a favorite show...and I'll be back to normal after its over.

Doing this has made it so I could start quitting the Buspar..I have been cutting down on my doses since this started. It feels like my brain can't handle everything, so it comes out via my body unless I let it out a different way.

Posts: 594 | From NJ/NY | Registered: Jun 2006  |  IP: Logged | Report this post to a Moderator
docjen
LymeNet Contributor
Member # 7510

Icon 1 posted      Profile for docjen     Send New Private Message       Edit/Delete Post   Reply With Quote 
AnieK:

I took muscle relaxants and got no relief from the RLS. The only things I have found that quiet the urge to move and anxious feeling are dopamine agonists, and clonazapam. After a year of lyme tx I am almost completely off of both of those drugs. Now I take some supportive supplements for adrenals and neuro support which seems to help.

Good luck! I hope you find some relief.

Posts: 393 | From Washington, DC | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
groovy2
Frequent Contributor (1K+ posts)
Member # 6304

Icon 1 posted      Profile for groovy2   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Aniek

Yep I get feeling like that sometimes--

Seem to come and go threw time--

I quit drinking caffine and it helped
a bunch too-- Jay--

Posts: 2999 | From Austin tx USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
Aniek
Frequent Contributor (1K+ posts)
Member # 5374

Icon 1 posted      Profile for Aniek     Send New Private Message       Edit/Delete Post   Reply With Quote 
elley,
yes, mine is worse with stress. And I do break down and cry often when I have it, but that's mostly because I can't stop my body from moving. I cried a good 10 minutes in a bathroom stall at work this morning because my hand wouldn't stop shaking.

docjen,
I'm on the Flexeril for muscle pain, not this issue. It literally gave me my life back. I've been on Lyme treatment for over 2 years now, but this came on during a period that I was on lower abx because of GI issues. I think it's so bad right now because it's my on cycle for Flagyl.

Jay,
Tried no caffeine. Doesn't seem to make a difference. I'm not a huge caffeine person anyway.

--------------------
"When there is pain, there are no words." - Toni Morrison

Posts: 4711 | From Washington, DC | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.