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 » myoclonus; eyelights glasses

 - UBBFriend: Email this page to someone!    
Author Topic: myoclonus; eyelights glasses
hiker53
Moderator
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
For those of you who have myoclonus, have any of you tried eyelights glasses. A chiropractor designed glasses in different colors and they have blinking lights on the inside. The idea is to stimulate one side of the brain if it is weak, so you only turn the lights on one side.

When I called the company, they said they had luck with the purple glasses and then putting sound into the opposite ear from the blinking lights.

Just curious if anyone has tried this and the results. www.eyelights.com Hiker

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 10174 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
dmc
Frequent Contributor (1K+ posts)
Member # 5102

Icon 1 posted      Profile for dmc     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've heard of this too but I was warned...have to be careful, can trigger seizures.
Posts: 2675 | From ct, usa | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
hiker53
Moderator
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
I tried a pair of green glasses and as soon as the lights flashed I had a seizure, but then left them on for 5 minutes and had no more. I wish there was a place who would lend them to you for a week to see if it worked, before you spend the money. Hiker

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 10174 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
GiGi
Frequent Contributor (5K+ posts)
Member # 259

Icon 1 posted      Profile for GiGi         Edit/Delete Post   Reply With Quote 
There are so many different forms/causes of Myoclonus, and I have not seen the colored glasses used for that specifically, the way you describe.

Dr. K. treats a number of conditions with colored eyeglasses. He has a set of all rainbow colors of eyeglasses in his office.

Upon determining the blockage of the autonomic nervous system with ART/muscle testing, the colors are tested as to which one will "unblock" the patient. That is all done in a couple of minutes.

The color is selected and the one that will keep the autonomics functional is the healing color. It is so simple - it is so painless and so swift.

He treats reading problems in children by selecting the proper color. He treats emotional upsets between partners. And emotional problems of one person.

He treated my being allergic and therefore deficient in phosphorus, briefly, for a few minutes) involving certain eye movements under
colored eye glasses.

Physiological problems caused by certain emotional events are solved that way. It is quick and wonderful.

He discovered that I had become allergic to phosphorus because I had too many bombs seen exploding during WW II burning my home and killing people. Allergies can have an emotional origin (there are several different forms of allergies!)

It took all of a few minutes with the glasses. I forgot which color. I had to follow it up with a little essay retelling my experience related to phosphor during the war.

That eliminated the problem once and for all. I have never ever been deficient in phosphor again and life depends on it.

An allergy toward a substance causes both: It cannot be absorbed and it cannot be properly eliminated by the body if it is in excess. That happens often with mercury. So before the body can release the excess, the allergy to the substance has to be broken. Colored glasses work well. (subconscious) memory of a certain conflict is brought to the surface by being asked "what do you remember about phosphorus"; then via the colored glasses this "bad memor" becomes separated physiologically from the nervous system; and is then followed up with the
strengthening of the belief system (my essay retelling it and emphasizing that the problem is long gone, not important any longer, a thing of the distant past.

I have seen him use it many times when teaching the subject at seminars and I am still amazed everytime I see the results.

That is healing on the emotional level, with the use of colored glasses.

Colored glasses are also used in combination with lasers for heavy metal detox by some doctors.

http://www.clevelandclinic.org/health/health-info/docs/1300/1310.asp?index=6061

Posts: 9834 | From Washington State | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Ms. Myoclonus
LymeNet Contributor
Member # 6750

Icon 1 posted      Profile for Ms. Myoclonus     Send New Private Message       Edit/Delete Post   Reply With Quote 
Haven't tried it, but flashing lights can definitely trigger my myoclonus.

Might be worth a try if you take it slowly and feel like you could handle an adverse reaction.

I wonder how they would know which side is the weaker side of the brain.

If you try it, let us know how it turns out.

Ms. Myo

--------------------
 -

Posts: 122 | From Texas | Registered: Jan 2005  |  IP: Logged | Report this post to a Moderator
hiker53
Moderator
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ms. Myoclonus:

For me the left side of the brain is weaker, because when the doctor moves a pen up to my nose the right eye will not track it. Hiker

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 10174 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
hiker53
Moderator
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
up

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 10174 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hubby has had several different chiropractors and doctors use different colored glasses on him during appointments, but honestly do not think they did anything. He has tremors/myoclonus/seizure-like episodes which come and go.

He did have what I would call a real seizure once when he walked into a room and saw one of those red lights flashing on a phone in a hotel.

I think he may have actually tried the flashing lights type of glasses once very early on when he only had the Parkinsonian tremor.

I do know that one chiropractic neurologist had him wear red glasses all the time for several weeks which may have helped slightly with photosensitivity.

This same doctor had him listen to music in one ear only which again did very little that we could tell.

A QEEG once (Quantitative EEG) showed that the left and right brain were not communicating correctly. This is a very expensive test and not usually covered by insurance.

At that time a chiropractic neurologist had hubby do what are called cross crawl exercises that stroke victims are often taught. I am pretty sure this has been discussed before.

While doing the exercises hubby's tremor would disappear, but it would come right back worse than ever as soon as he stopped exercising. This again was before any treatment when he only had a Parkinsonian tremor -- no myoclonus or seizure-like episodes then.

I think I would save your money for something else.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 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.