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 » Nighttime spasms causing poor sleep

 - UBBFriend: Email this page to someone!    
Author Topic: Nighttime spasms causing poor sleep
Pantsinsocks
Member
Member # 7440

Icon 1 posted      Profile for Pantsinsocks     Send New Private Message       Edit/Delete Post   Reply With Quote 
Can anyone offer any suggestions for helping my wife's nighttime spasms (mostly leg)? It starts as soon as she lays down. She has to take two soaking hot baths, one at midnight and one at 2am, to finally get it to quell...and then only sometimes.

We both have lyme. She is taking neurontin, magnesium, seriphos (herbal supplement) from LLMD to try to address this, with limited results.

Thanks

Posts: 67 | From Fredericksburg, VA USA | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Adding taurine to the magnesium may work. Taking magnesium up to 1,000 - 2,000 mg, just below bowel tolerance may help.

Be sure to add calcium in the proper ratio (but I'm never clear on what that is). Other minerals and electrolytes, too such as potassium (a banana) and zinc.

Restless legs can be a type of myoclonus - which can be a kind of seizure activity. Not to freak out about that, anytime the brain is overloaded with toxins, seizures can happen. Magnesium and FISH OIL are the two very best things.

Maybe a difference form of magnesium would be more effective. If she chooses shot, they can sting horribly but adding B-12 to the syringe takes the sting way down.

I wonder if the hot bath would be better as a WARM bath with some massage to follow.

=================

http://www.lymepa.org/Nutritional_Supplements.pdf

Nutritional Supplements in Disseminated Lyme Disease

===================

http://www.vrp.com/articles.aspx?ProdID=art1066&zTYPE=2

Seizures: A Nutritional Approach

Seizures can be attributed to a number of causes including metabolic abnormalities, infections, nutritional deficiencies, or trauma. . . .

============

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/77321

Topic: NATURAL SLEEP - Links to articles & supplements

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

Some Taurine choices (do not use in day time until you know how this will be for you. It makes me a bit sleepy.:

http://www.vitacost.com/productResults.aspx?ss=1&previousText=Taurimne&Ntk=products&x=0&y=0&Ntt=Taurine
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
[group hug] [kiss] sending you both moral support.

i too have restless leg syndrome; i'm all over the bed all night long; have to sleep alone due to this and my wierd hours of sleeping so hubby can get a good nights sleep.

prayers for you both. not on any med for that.

IP: Logged | Report this post to a Moderator
lymebytes
Frequent Contributor (1K+ posts)
Member # 11830

Icon 1 posted      Profile for lymebytes   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Magnesium deficiency can cause muscle spasms, heart palps and so much "muscle stuff", also helps w/sleep. Even if she is taking Magnesium it may not be absorbing or not big enough of a dose.

Magnesium Citrate pills did nothing for me, I bought powder form by NOW brand at Iherb.com and it has helped beyond words.

It won't be an overnight cure, but in time it will work. You may want to ask your LLMd for a muscle spasm reliver in the meantime.

Make sure to report this to your LLMd if you haven't already and you can even request tests magnesium. It is a water soluble vitamin so is in and out of the body quickly.

--------------------
www.truthaboutlymedisease.com

Posts: 2003 | From endemic area | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
DoctorLuddite
LymeNet Contributor
Member # 13853

Icon 1 posted      Profile for DoctorLuddite     Send New Private Message       Edit/Delete Post   Reply With Quote 
Mag Citrate absorbs way better than Mag Oxide. I had foot cramps last fall winter, stopped with the first dose of mag citrate. Now I take 100 mg 2X daily, then it was 400 2X daily.
Posts: 442 | From Biddeford, ME | Registered: Nov 2007  |  IP: Logged | Report this post to a Moderator
dsiebenh
LymeNet Contributor
Member # 5353

Icon 1 posted      Profile for dsiebenh     Send New Private Message       Edit/Delete Post   Reply With Quote 
Smoke marijuana before bed.

Take Baclofen or Zanaflex or Klonopin as rx by your doc.

Stay away from dopamine drugs like Sinemet, Mirapex or Requip; they work but have bad long term effects.

Good luck!

Posts: 252 | From NJ USA | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
MY3BOYS
LymeNet Contributor
Member # 17830

Icon 1 posted      Profile for MY3BOYS     Send New Private Message       Edit/Delete Post   Reply With Quote 
i have this too.. klonopin and the generic brand of unisom (which is just 50mg of benadrly)

when is real bad i have soma that can take 1/2 tab or whole tab.

also- i do take mag. lots of it. i found the one dr b recommends behind the pharm counter at walgreens. had to ask for it and they order it for me. is a slow release. i take it am, late afternoon, and eve.

--------------------
i am not a Dr. any info is only for education, suggestion or to think/research. please do not mis-intuprest as diagnostic or prescriptive, only trying to help. **

dx in 08:lyme, rmsf, bart, babs, and m.pneumonia.

Posts: 422 | From TX | Registered: Oct 2008  |  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 
Try baths with Transdermal Magnesium Chloride or footbaths (several in a week) with the Transdermal in it. Massage in.
http://www.omega3global.com/shop/images/pdfs/Principles_and_Practices_of_Transdermal_Medicine.pdf

I posted on the subject of "transfermal vs. oral". Will find and post.

Consider getting Sircus' book, as in above link.

I found best price so far at http://www.swansonvitamins.com/

You may need to do a bunch of footbaths or others to get your reserves back to where they should be.

Take care.

Posts: 9834 | From Washington State | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
LindaS
Member
Member # 20251

Icon 1 posted      Profile for LindaS     Send New Private Message       Edit/Delete Post   Reply With Quote 
E-mail your llmd. He/she needs to know your wife's symptoms and will alter her meds or add something.

--------------------
Linda

Posts: 39 | From Lexington, Virginia | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
Pinelady
Frequent Contributor (5K+ posts)
Member # 18524

Icon 1 posted      Profile for Pinelady     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had a lady put 4 drops of valor essential oil on my painful shoulder yesterday. I was amazed at the results. May be worth a try. I could not believe it and wished I had got some then, but I am going back for more.

--------------------
Suspected Lyme 07 Test neg One band migrating in IgG region
unable to identify.Igenex Jan.09IFA titer 1:40 IND
IgM neg pos
31 +++ 34 IND 39 IND 41 IND 83-93 +
DX:Neuroborreliosis

Posts: 5850 | From Kentucky | Registered: Dec 2008  |  IP: Logged | Report this post to a Moderator
Elizabeth S.
LymeNet Contributor
Member # 22405

Icon 1 posted      Profile for Elizabeth S.     Send New Private Message       Edit/Delete Post   Reply With Quote 
I second baclofen.

I have severe spasms in my back, and it stops them.

A family member has Periodic Leg Movement Disorder (this sounds like your wife?) and it helps that, too.

The drug has been around a long time and is safer than most new meds, and can be taken for an extended time (if needed) while still having the same benefits as when you first started taking it

Good luck =)

Posts: 161 | From Southern United States | Registered: Sep 2009  |  IP: Logged | Report this post to a Moderator
Cass A
Frequent Contributor (1K+ posts)
Member # 11134

Icon 1 posted      Profile for Cass A     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dear Friends,

Klonopin is not generic benedryl, according to Wikipedia. It is a much stronger anti-seizure drug.

I had severe leg cramps overnight for some time. Taurine (one gram each time) along with increased magnesium handled it. Taurine was recommended to me by my LLND. At one point, I was taking 5 grams a day!!

Recently, I switched to magnesium oil (trans-dermal). I don't need to take anywhere near as much, and I don't have any leg cramps, either! I just rub 3-6 drops into the calf of each leg just before bedtime.

I still take 2 gms of Taurine per day, but am looking to decrease this, as a test, to see if a lower dose will still work.

Since the data on oral magnesium "feeding" Lyme actually penetrated the lyme fog, I've been using the transdermal magnesium oil instead. Results have been fine, with no adverse effect from switching.

Hope this helps,

Cass A

Posts: 1245 | From Thousand Oaks, CA | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
paulieinct
LymeNet Contributor
Member # 17514

Icon 1 posted      Profile for paulieinct     Send New Private Message       Edit/Delete Post   Reply With Quote 
My leg cramping was so bad I had to sleep in a sitting position for months. It turns out that I had severe central spinal stenosis, confirmed by MRI and myelogram. The spinal cord was being squeezed because the central canal was narrowed, I believe because of borrelia infecting all the ligaments and cartilage of my spine for decades.

Had decompression surgery to open up the canal. Got alot of relief. Then got dx'd with Lyme, started treatment, and cramping would return somewhat during herxes. 2 1/2 years of abx, and cramps are mostly gone.

Anyone with Lyme arthritis and leg cramps should have an MRI of spine to look for central stenosis.

--------------------
Sick since at least age 6, now 67. Decades of misdiagnosis. Numerous arthritic, neuro, psych, vision, cardiac symptoms. Been treating for 7 years, incl 8 mos on IV. Bart was missed so now treating that.

Posts: 765 | From nw ct | Registered: Sep 2008  |  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.