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 » NO FEELING IN LEGS / ARMS / SPINE

 - UBBFriend: Email this page to someone!    
Author Topic: NO FEELING IN LEGS / ARMS / SPINE
SacredHeart
LymeNet Contributor
Member # 44733

Icon 5 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Went to the neuro yesterday. I didn't realize I couldn't feel much of anything in the lower parts of my arms and legs until she did the scratch test.


Apparently I don't feel much of anything until mid point of my thighs, and the mid point of my arms. Also, a spot on my spine is blank of feeling.


She said she was worried because of the spine. So I have some MMR's scheduled, along with several other not so much fun tests. If I have any lesions, or white matter my LLMD is going to start IV.

Anyone else have this experience?

[ 01-13-2016, 01:54 PM: Message edited by: SacredHeart ]

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
Judie
Frequent Contributor (1K+ posts)
Member # 38323

Icon 1 posted      Profile for Judie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some meds can cause this like cipro, levaquin and tinidazole. The problems can occur after you stop taking the drugs.

Lyme causes a lot of nerve stuff too.

Posts: 2839 | From California | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Before I started antibiotics i knew I had lost some feeling from my LLMD's initial evaluation. I guess the MRI will tell the story if there is one,

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
WakeUp
LymeNet Contributor
Member # 9977

Icon 1 posted      Profile for WakeUp     Send New Private Message       Edit/Delete Post   Reply With Quote 
Your neruopathy ** might** be a reaction to Lyme neurotoxins and/or metals buildup in your body--first try detoxifiers such as Licorice root(helps me), sarsaparilla(helps me), burdock root(helps me), fenugreek, burbur, parsley, ginger, Horsetail tea(aluminum detox) cilantro+chlorella, and at least one liter of Silica-rich bottled water per day (best two brands are Volvic and Fiji.)

Silica rich water like Fji or Volvic--- will detoxify metals such as aluminum if you drink at least one litre per day over 5 weeks.

Personally, I have noticed a big difference with Burdock root tincture-- my tingling is pretty much gone after doing Burdock drops. I recently had a tingling reaction to a long term course of Olive Leaf extract. Previously, I had a several months tingling reaction (neuropathy) to a Tetanus booster--- it is filled with aluminum!! Burdock, Fiji water, Chlorella + Cilantro, and or Horsetail tea--- all take out aluminum..

Also, chemtrails have been proven to contain massive amounts of nano-aluminum chaff, which our best air filters cannot filter out because it is so tiny. It also gets in the rainwater. I don't even know if reverse osmosis can filter it out. You will never hear about this in the Mockingbird press! We are basically being poisoned with aluminum by a fifth column within our own taxpayer funded Air Force. Why? I have no ideal!!

Aluminum is most toxic when magnesium is low-- so the best we can do is take magnesium, and chelate aluminum and nano-aluminum.

A good overall mineral supplement can also detoxify--- since if you are deficient, then heavy metals will be taken up by your cells instead of the good minerals.

Posts: 696 | From New York | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for all of the information WakeUp!!!

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  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.