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 » Terrible Insomnia

 - UBBFriend: Email this page to someone!    
Author Topic: Terrible Insomnia
Lymewest
Member
Member # 52184

Icon 11 posted      Profile for Lymewest     Send New Private Message       Edit/Delete Post   Reply With Quote 
I’m new on LymeNet. Was just wondering what any of you have to share about sleep deprivation..

I’ve had Lyme and co-infections since 1993. Treated on and off with drugs and various supps. But it’s only been in the past year that my sleep has been severely disrupted. I’m lucky to get 1-3 hours a night, and if so, I usually have high anxiety dreams during that time.

People wonder how I make it through the day, but I don’t feel like sleeping in the day time either. It’s as if something ( Lyme? Bart? Babs? ) is blocking the mechanism in the brain that gives you that fatigued feeling, where you want to doze off. I don’t feel that anymore.

If I do doze off, I’m awake again pretty soon after. I don’t know how much longer I can go on like this. I’ve tried everything, and nothing works except one drug that kind of does, but I need to avoid it because of bad side affects. Trying to avoid regular drug use.

Which infection causes this symptom? I’ve had severe night sweats in the past that a Lyme doc gave me Malerone for, for just a month. And I haven’t had the severe drenching sweats since. But I do still get hot and cold shifts.

And I’ve also had a constant pressure and ringing in my head pretty much since I was first infected in 1993. I’ve been infected on two other occasions since then.

Would appreciate any feedback! This severe lack of sleep is gradually worsening my cognitive abilities, and can’t be good for the immune system.

Posts: 15 | From Southwest | Registered: Aug 2020  |  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 
Welcome!! I'm sorry you are suffering from insomnia. I have had trouble sleeping my whole life. (I've had Lyme for more than 60 years)

But ... about 6 years ago I found out I am sensitive to salicylates. They are really bad about causing insomnia....and guess what? They can cause ringing in the ears!!

I'll bring you a link for that so you can do some research.

Also consider the possibility of Mast Cell Activation Syndrome. Most MCAS patients have high levels of histamine in their bodies and that can also cause ringing in the ears.

Many Lyme patients have found that they have MCAS. (I was dxd 4 years ago but have had it "forever.")

Here is a link on MCAD (MCAS is a part of MCAD).

Also .. I still take Ambien, but can get away with not taking it sometimes.

Mast Cell Activation Syndrome:
https://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=036299;p=0

Salicylates:

https://www.fedup.com.au/factsheets/additive-and-natural-chemical-factsheets/salicylates

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Lymewest
Member
Member # 52184

Icon 1 posted      Profile for Lymewest     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you. I will look at this. My current Lyme doc thinks Babesia and possibly Bart is the cause of the head pressure and ringing. Insomnia too. But it could be a whole host of other things too. Very confusing.
Posts: 15 | From Southwest | Registered: Aug 2020  |  IP: Logged | Report this post to a Moderator
Lymewest
Member
Member # 52184

Icon 1 posted      Profile for Lymewest     Send New Private Message       Edit/Delete Post   Reply With Quote 
Also wondered if there are now Lyme Zoom meetings.
Posts: 15 | From Southwest | Registered: Aug 2020  |  IP: Logged | Report this post to a Moderator
daisys
LymeNet Contributor
Member # 11802

Icon 1 posted      Profile for daisys     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had terrible insomnia for many years. In the 1990's, I was stuck in a light sleep, so never was alert, and never got deep sleep or dream sleep. It was pretty awful.

I was diagnosed with fibromyalgia, which includes a sleep disorder, and also chronic fatigue syndrome. So, I'm sure what is behind my sleep disorder.

I see you're from the Southwest. I have found the best sleep specialist ever, and she's in Albuquerque. If you like, I'll PM her contact info.

I think I got about 8 hours last night, and woke up once. I've been cutting back on meds.

I'm getting better from Lyme disease, so that may account for the sleep improving.

Posts: 552 | From New Mexico, USA | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have only Lyme and that has caused me the same insomnia you're describing.

What worked for me for many years was knocking out successfully with benadryl 25mg. Then the effective dose upped to 50mg, then 75mg, and then I quit taking it. But I went years before that happened.

I guess any of us can experiment with herbs that are supposed to make us sleepy - I haven't had much luck with that, but there's a bunch of them - usually get them at the healthfood store, single or in combo form.

Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Lymewest
Member
Member # 52184

Icon 1 posted      Profile for Lymewest     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the replies and sharing your experiences. I was originally infected back east. I can literally feel something infecting my head / brain. And know the sleep problem is worse because of that. Just don’t know which of the infections is behind it.

Saw a lot of old posts on here talking about Babesia and describing my symptoms. Since I was diagnosed with that years back, Really just want to figure out what is best to attack the Babesia with. Preferably natural.

Had a bad herx from taking just one artemisinin capsule. So that tells me something. I wouldn’t mind getting the sleep specialists name in Albuquerque. Does she understand Lyme related diseases? Albuquerque is pretty bad with that.

Posts: 15 | From Southwest | Registered: Aug 2020  |  IP: Logged | Report this post to a Moderator
hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

Icon 1 posted      Profile for hopingandpraying     Send New Private Message       Edit/Delete Post   Reply With Quote 
Contact the New Mexico Lyme Support Groups - maybe they can help you. They would know better about NM.

http://whatislyme.com/new-mexico-lyme-support-group/

Posts: 8981 | From Illinois | Registered: May 2006  |  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 
Lymewest... I took arteminisin and zithromax for babesia. It worked very well.

Lyme links you may not have seen.

https://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=088555;p=0

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Lymewest
Member
Member # 52184

Icon 1 posted      Profile for Lymewest     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks everybody! Making a note of all these things. Think I’m going to try artemisinin again. Just slower. Seemed to herx real bad on it a couple weeks ago and stopped.

Glad you all are finding things that work for you. [spinning smile] :

Posts: 15 | From Southwest | Registered: Aug 2020  |  IP: Logged | Report this post to a Moderator
daisys
LymeNet Contributor
Member # 11802

Icon 1 posted      Profile for daisys     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just a thought--If someone has sleep apnea, they can suddenly wake up hyper alert because the body reacts to the drop in oxygen.

Measuring the oxygen one night will show if this is a problem. Then a sleep study will show which kind of apnea is to blame.

Posts: 552 | From New Mexico, USA | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
Brussels
Frequent Contributor (5K+ posts)
Member # 13480

Icon 1 posted      Profile for Brussels     Send New Private Message       Edit/Delete Post   Reply With Quote 
My vivid dreams / nightmares came basically during lyme.

I think when I got very toxic, they got worse. Like unbearable. I took chlorella in great amounts at that time, coupled with bear garlic tincture then.

I would suggest you to take some binders to pull the toxins off. Or high dose vit C? (I take liposomal Vit C that I prepare at home).

What you describe has to do with adrenal fatigue. Extreme adrenal fatigue. You cannot relax with it either....

For me, infections AND toxins cause me high anxiety. I know I'm well, deeply well, when I can sit, relax, doze, nap under the sun, have normal dreams and not wake up suddenly in fight and flight mode.

When infections stop to plague you, you'll get the feeling of relaxation back. But for that, I needed a lot of binders, many times a day, for years. Until lyme was finally gone.

I can get anxiety when I get some skin inflammation back, for example, or after coffee. That's pretty similar to the lyme + toxin anxiety.

Another thing that helped me was to keep grounded (earthed), but not without my binders....

Posts: 6199 | From Brussels | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
lymenotlite
LymeNet Contributor
Member # 33166

Icon 1 posted      Profile for lymenotlite     Send New Private Message       Edit/Delete Post   Reply With Quote 
For me, drenching sweats were babesia and especially with taking Mepron. I also suspect toxin overloads.

Hulda Clark recommended Ornithine for trouble sleeping and that did work once for me but I forget to take it. Tudca also helped once as well but I forget to take it. (Neuro lyme)

Posts: 705 | From WA state | Registered: Jul 2011  |  IP: Logged | Report this post to a Moderator
norcal
LymeNet Contributor
Member # 29829

Icon 1 posted      Profile for norcal     Send New Private Message       Edit/Delete Post   Reply With Quote 
trazadone and indica cannabis,wishing you success!
Posts: 342 | From northern california | Registered: Dec 2010  |  IP: Logged | Report this post to a Moderator
xoxoxox
LymeNet Contributor
Member # 18778

Icon 1 posted      Profile for xoxoxox     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sounds like Bart to me. I too have severe insomnia and ringing in my ears.
Nothing has helped the ringing. Generic form of controlled relief Ambien has been the only way for me to get sleep.
It's not for everyone, but there have been no problems for me.
If you do find a solution to either issue, please let me know [Smile]

--------------------
----------
Danni

Posts: 311 | From Glen Mills, PA | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
xoxoxox
LymeNet Contributor
Member # 18778

Icon 1 posted      Profile for xoxoxox     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sounds like Bart to me. I too have severe insomnia and ringing in my ears.
Nothing has helped the ringing. Generic form of controlled relief Ambien has been the only way for me to get sleep.
It's not for everyone, but there have been no problems for me.

--------------------
----------
Danni

Posts: 311 | From Glen Mills, PA | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
Lymewest
Member
Member # 52184

Icon 1 posted      Profile for Lymewest     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for all the great replies here. Can relate to a lot. Will look into these suggestions.

Brussels, I totally get the anxiety stuff. My infections do seem to key up my whole body, especially at night, kind of like caffeine.

Along with Chlorella and garlic, What are all the different binders? I realize I need to be doing these.

Right now I’m getting some sleep on Sonata. But only for maybe the first 3 to 4 hours. Don’t want addictive things though. Will look into some of these other things posted.

Posts: 15 | From Southwest | Registered: Aug 2020  |  IP: Logged | Report this post to a Moderator
LehighLyme
Member
Member # 41596

Icon 1 posted      Profile for LehighLyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
You have to take care of the Bart and the Babesia. Bart is notorius for causing insomnia. All tick born infections drain our bodies of essential vitamins and nutrients. Our family take Natural Vitality CALM (Get the one that says SLEEP on it). Try that for a week and may help before you go to bed. It zonked me out...

Also get Stephen Buhners book on Bartonella and he offers alot of herb solutions you can get through woodlandessence. com and it won't break the bank- best book to read on Bartonella though- will be amazed to read what it does in the body...

Posts: 13 | From Bethlehem PA | Registered: Aug 2013  |  IP: Logged | Report this post to a Moderator
Lymewest
Member
Member # 52184

Icon 1 posted      Profile for Lymewest     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks 😊
Posts: 15 | From Southwest | Registered: Aug 2020  |  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.