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 » what to do for brain shaking/seizures

 - UBBFriend: Email this page to someone!    
Author Topic: what to do for brain shaking/seizures
lyme2health
Member
Member # 19981

Icon 5 posted      Profile for lyme2health     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm on lyme, babesia, bartonella protocol. As I went to bed the other night, my brain started shaking inside my skull and it seemed to last a while. It has done this before but never for so long. Now it feels swollen in one place and hurts some in that area. That hasn't happened before.

Is this something to worry about? Can you have damage?

Anything to take to heal the area?

Will talk with my doc soon about this but wanted your input, too. Thanks.

Posts: 62 | From U.S. | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
amodernjune
Member
Member # 32950

Icon 1 posted      Profile for amodernjune     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have that happen too! I have all sorts of tender spots on my head. Hurts to brush sometimes.
Posts: 31 | From texas | Registered: Jul 2011  |  IP: Logged | Report this post to a Moderator
lymeinhell
Frequent Contributor (1K+ posts)
Member # 4622

Icon 1 posted      Profile for lymeinhell     Send New Private Message       Edit/Delete Post   Reply With Quote 
You may likely have muscle spazms in your head area - typically on the back of the skull. When you lay down and relax, it may trigger the shaking sensation to make you think it's your brain.

I say this because you ended up with sore spots on your skull. This is called 'Referred Pain', which is pain that appears in an area different than the source.

For example, the muscle spazm(s) that is at the base of your skull, refers pain over the top of your head and behind your eye, or down through your ear to your jaw, or makes your hair 'hurt'.

Poke hard around with your knuckle and see if you find any spots that may feel like small lumps and hurt like heck. Find any?

We get these spazms from Magnesium deficiency, which is caused by Lyme.

You need to do 2 things - bust up the spazms, and properly address the magnesium deficiency so that this does not keep recurring in the future (because it will happen again if you don't).

I think at one point I had a half dozen spazms on my head and shoulders, causing me excruciating pain and nightime 'shuddering'.

Trigger point injections of lidocaine shot into the spazm(s) blissfully numbs the area causing the pain, while the needle itself helps disrupt the spazm and restore blood flow to the area. I had at least 4 series of shots (about every 10 days) to get rid of the ones covering the back of my skull and shoulders (that I had no idea that I had).

Taking oral magnesium, while necessary, will not effectively restore your magnesium levels. IV (which is easy, 20 minutes, tiny needle, and you're done) or IM shots are key.

--------------------
Julie
_ _ ___ _ _
lymeinhell

Blessed are those who expect nothing, for they shall not be disappointed.

Posts: 2258 | From a better place than I was 11 yrs ago | Registered: Sep 2003  |  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.