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 » I am really scared and I feel so alone.

 - UBBFriend: Email this page to someone!    
Author Topic: I am really scared and I feel so alone.
luvema
LymeNet Contributor
Member # 26650

Icon 1 posted      Profile for luvema     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was on IV meds for 9 months with little improvement. Now, I am off antibiotics and my doctor is doing this anti fungal protocol and she couldn't put me on any antibiotics.

Well, my symptoms are getting scarier and scarier by day. I have constant head movements and head pressure. And recently I developed this new symptoms where when I am standing my body starts moving on it's own from side to side… twisting all the way, and even when I am sitting it starts rocking back and forth.

I am really scared, I don't have the control over my body and it's scaring me to death.

--------------------
Ema

Posts: 394 | From Southern California | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
lpkayak
Honored Contributor (10K+ posts)
Member # 5230

Icon 1 posted      Profile for lpkayak     Send New Private Message       Edit/Delete Post   Reply With Quote 
I dont have that but im pretty sure the girl on under our skin did and she git better

Please hang in there

I hope others come along soon that have experience with what you are going thru

--------------------
Lyme? Its complicated. Educate yourself.

Posts: 13712 | From new england | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
Dogsandcats
Frequent Contributor (1K+ posts)
Member # 28544

Icon 1 posted      Profile for Dogsandcats     Send New Private Message       Edit/Delete Post   Reply With Quote 
What does your LLMD say about your symtoms?

How long have you been off the antibiotics?

Have you tried to detox: dry brushing, Epsom salt baths?

I am not a medical professional- take care.

--------------------
God will prepare everything for our perfect happiness in heaven, and if it takes my dog being there, I believe he'll be there.

Billy Graham

Posts: 1967 | From California | Registered: Oct 2010  |  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 
Maybe try a different antibiotic? It doesn't sound fungal to me, but I'm not a doctor.

Bicillin has helped a lot after having several other antibiotics fail me.

It does sound scary. Can you get another opinion from a different LLMD? Sometimes you just reach the end of suggestions from one doctor and need a fresh perspective.

Posts: 2839 | From California | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
glm1111
Frequent Contributor (5K+ posts)
Member # 16556

Icon 1 posted      Profile for glm1111     Send New Private Message       Edit/Delete Post   Reply With Quote 
luvema,

you need to find a practioner that treats parasites asap. Antifungals won't work for that. I have had the rocking movement and it was from the parasites moving around inside. I have suggested this to you before.

If you can't find a doc that will treat you for parasites, you might have to treat yourself as many here have had to do. Check out the PARASITE WARRIORS SUPPORT THREAD for more info.

Gael

--------------------
PARASITES/WORMS ARE NOW
RECOGNIZED AS THE NUMBER 1 CO-INFECTION IN LYME DISEASE BY ILADS*

Posts: 6418 | From philadelphia pa | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
Carol in PA
Frequent Contributor (5K+ posts)
Member # 5338

Icon 1 posted      Profile for Carol in PA     Send New Private Message       Edit/Delete Post   Reply With Quote 
Is the antifungal Diflucan?

Diflucan is part of the Schardt Protocol, and has been found effective in treating Lyme.

Posts: 6947 | From Lancaster, PA | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
Catgirl
Frequent Contributor (5K+ posts)
Member # 31149

Icon 1 posted      Profile for Catgirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by glm1111:
luvema,

you need to find a practioner that treats parasites asap. Antifungals won't work for that. I have had the rocking movement and it was from the parasites moving around inside. I have suggested this to you before.

If you can't find a doc that will treat you for parasites, you might have to treat yourself as many here have had to do. Check out the PARASITE WARRIORS SUPPORT THREAD for more info.

Gael

DITTO (parasites)!! Gael is right, if you can't find anyone to acknowledge them, then an option is to self treat. Many people wake up and realize this if their docs won't listen.

A big part of the problem is the tests are pitifully inaccurate, so the doc's don't think people have them.

Visit THE PARASITE WARRIOR'S SUPPORT THREAD (loaded with info).

--------------------
--Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together).

Posts: 5418 | From earth | Registered: Mar 2011  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Luvema-Have you contacted your LLMD to let him/her know of the way your body has been since quitting abx?

It is important your LL knows about this.

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
luvema
LymeNet Contributor
Member # 26650

Icon 1 posted      Profile for luvema     Send New Private Message       Edit/Delete Post   Reply With Quote 
My doc is out of town, but I have an appt coming up with her.

is anyone familiar with these type of symptoms?

--------------------
Ema

Posts: 394 | From Southern California | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
You have nothing to lose by treating for parasites.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
do you mean like twitching? My head will move to the side and it seems to come in threes... if it goes over once then it follows right away with a couple more.

Same for my arms. and shoulders.

Sometimes my head moves like it is saying "no".

I thought these were all neuro symptoms of lyme, but maybe yours are different?

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
mlg
LymeNet Contributor
Member # 35383

Icon 1 posted      Profile for mlg     Send New Private Message       Edit/Delete Post   Reply With Quote 
Treat parasites with colonics.
Anti-malarials with heparin and artemisinin rotating with crypto

Posts: 697 | From CA | Registered: Dec 2011  |  IP: Logged | Report this post to a Moderator
luvema
LymeNet Contributor
Member # 26650

Icon 1 posted      Profile for luvema     Send New Private Message       Edit/Delete Post   Reply With Quote 
Would drinking water with a little bit of pink salt in it help with parasites?

@Lisa, yes, I get movements like that also.

--------------------
Ema

Posts: 394 | From Southern California | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ema-when I quit abx including IV abx for a week, my body reverted back to this.

My body did this pre treatment.

It has went away since restarting abx.

For me it was neuro lyme.

I know lyme is supposed to be s slow grower but many sources say lyme spirochete will emerge from the cyst form after abx is removed.

Perhaps this is what happened with me.

It is important to tell your LL as soon as you can about this.

What form of cyst buster were you on when you were on IV abx? Tinidazole, flagyl etc?

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
luvema
LymeNet Contributor
Member # 26650

Icon 1 posted      Profile for luvema     Send New Private Message       Edit/Delete Post   Reply With Quote 
@Greta, thanks for the info.

I was on Flagyl.

--------------------
Ema

Posts: 394 | From Southern California | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
Ames777
Member
Member # 43190

Icon 1 posted      Profile for Ames777     Send New Private Message       Edit/Delete Post   Reply With Quote 
I started doing something very similar with migraines, shaking head movements, rocking back and forth and body swaying immediately after I started minocycline. I think it was the neuro Lyme getting blasted, but the doctor just said the minocycline was too strong for me.

I agree that it doesn't sound fungal and sounds like the girl from Under Our Skin. If you haven't seen it, you can watch it free on Viewster.

Definitely tell your doctor about this. It is no fun having a body that moves itself. I hope things get straightened out soon.

--------------------
Amy

Possible infection date 6/21/05 (no history of tick bite but went to hospital with "unexplained" high fever)
Tested positive for Lyme and RMSF in Feb 2014 / suspected Babesia as well

Posts: 65 | From Atlanta, GA | Registered: Feb 2014  |  IP: Logged | Report this post to a Moderator
ladycakes
LymeNet Contributor
Member # 12619

Icon 1 posted      Profile for ladycakes   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Mine turned out to be encepahlitis (brain swelling). I had the twitching, terrible pressure headaches, general confusion. It really feels like you're losing any kind of control over your body.

My LLMD switched me to a different antibiotic, and thankfully that did the trick.

Posts: 306 | From Brownsville, PA | Registered: Jul 2007  |  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.