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 » Spasms question

 - UBBFriend: Email this page to someone!    
Author Topic: Spasms question
6Hypnone
LymeNet Contributor
Member # 47629

Icon 1 posted      Profile for 6Hypnone   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
2 questions actually--

1) Is it normal to occasionally have body or appendage spasms/jolts?

2) In 2011, I had a 'shaking attack' that lasted an hour. Went to the ER and they didnt know what it was (big f*ing surprise [cussing] ). I thought it may have been due to a recent prozac med dose change... My psych at the time said no that's not the reason. My psych NOW, after I told him, said it could have been.

I had been going down in dose (from 600, gradually) and was at 200 mg...I went up to 400 and had the attack. So then I went to 300 and have been on that ever since as I'm scared to vary the dose at all now due to the attack.

Could it have been Lyme related? I was dx'ed in 2016 with it but they think I've had it 20+ years.

And for each of these questions, anything i can do?

Posts: 606 | From sw suburbs of chicago, Illinois | Registered: Mar 2016  |  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 
Hmmm... I'm with you. Keep the dosage the same for awhile and see how you do.

I have muscle spasms quite a bit. I think for me it's from MCAS and from the meds for that depleting my magnesium. I always try to up my mag when I get spasms. It seems to help.

There's a great product called ReMag you might want to look into. It gets mag right into the cells.

Feel better soon!

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
6Hypnone
LymeNet Contributor
Member # 47629

Icon 1 posted      Profile for 6Hypnone   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been at 300 since that time (2011).
I'm on I think 300 mg of mag glycinate. Maybe I should up it....

Posts: 606 | From sw suburbs of chicago, Illinois | Registered: Mar 2016  |  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 
-
. . . He found reports of tics and other neurological side effects . . . .

. . . the potential for brain damage . . . .

https://harvardmagazine.com/2000/05/the-downsides-of-prozac-html

The Downsides of Prozac

By Craig Lambert - Harvard Magazine - May 1, 2000

Excerpts:

Like many others, Elizabeth Wurtzel '89 and Lauren Slater, Ed. M. '89--the authors, respectively, of Prozac Nation (1994) and Prozac Diary (1998) -

- suffered "Prozac poop-out": the drug's mood-altering effects wore off and depression returned.

In fact, according to a 1995 study by associate professor of psychiatry Maurizio Fava, Prozac wears off within a year for about one-third of those who take it.

"This is tolerance," says clinical instructor in psychiatry and University Health Services physician Joseph Glenmullen, M.D. '84.

His new book, Prozac Backlash (Simon & Schuster), documents not only tolerance, withdrawal syndromes, and drug dependency,

but a panoply of dangers linked to "Prozac-like drugs"--selective serotonin reuptake inhibitors (SSRIs).

"We now have unequivocal evidence from a wide range of side effects that Prozac-type drugs

impair the normal functioning of the brain," Glenmullen says.

SSRIs include Prozac, Zoloft, Paxil, Luvox, Celexa--trade names that invariably include an x or z for drugs that are best known as antidepressants.

But "calling them that is misleading," says Glenmullen . . . .


. . . What is not washed out are the side effects, which include the potential for brain damage.

A few years ago one of Glenmullen's patients who was taking Prozac developed a tic--the tongue darting in and out of the mouth--that persisted for months after the drug was discontinued.

That sent Glenmullen to Countway Library. He found reports of tics and other neurological side effects, like drug-induced Parkinsonism, associated with SSRIs.

"The tics include lip smacking, lip puckering, fishlike kissing motions, and pelvic thrusting," Glenmullen says.

"They are involuntary, disfiguring, and can be very noticeable--and may persist long after the drug is stopped.

This is the dread side effect in psychiatry, and it can indicate brain damage. Such reactions are not rare. Neurologic agitation is estimated to occur in 10 to 25 percent of patients, and muscle spasms in 10 percent." . . . .

[Full article at link above]
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  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 
-
In a different thread, you report uro-genital pain deep inside (not outer tissue) . You say it's been intense pain that comes and goes.

the " pelvic thrusting" mentioned as a neurological "tic" side-effect &/or even nerve damage from prozac

might give a clue that, perhaps, prozac could be triggering the pain attacks in your pelvis just not to the point of thrusting, though it would be the same nerve pathway, likely.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  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 
-
Never just stop any SSRI / antidepressant. Very careful tapering off over time - - along with certain foods, specific nutrient & and anti-inflammatory supports are required.

Magnesium & the best quality Fish Oil, along with lots of green veggies (& maybe also B vitamins) top the list.

Turmeric also helps.

There are many organizations that help with this. Some doctors do. Both your LLMD & your Rx prescribing doctor - if experienced with this aspect of care could be a good help. Even if not, be sure they both know of any decisions you make to change your dosage.

If the Rx prescribing doctor is not open to this, find a doctor with this kind of experience. Your LLMD might know.


Some of the websites or YouTube videos by patients can be very helpful, too.

If you consider doing this, know there are ways to go about it safely but a plan must be in place. And there are other ways to offer relief from troublesome symptoms. Many other ways.

One that looks reasonable, at first glance, though keep in mind the personal accounts are not direct medical advice, just what helped others.

http://survivingantidepressants.org/

Surviving Antidepressants
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  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 
Magnesium glycinate is pretty high in oxalates. Oxalates rob us of minerals .. like mag.

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  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 
-
TuTu,

What is the best form of magnesium to take then, for someone wanting to be low oxalate? Is the the Re-Mag I've seen you suggest? Could you please post what ever form is best for 6Hypnone to consider - to save her time of sorting that out?
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  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 
I would say ReMag is the best. I think it's mag chloride. It goes right into the cells.

Some are able to tolerate mag malate .. but I'm not sure where it lands on the oxalate scale.

https://www.rnareset.com/products/remag-magnesium-solution?variant=13899661319

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
6Hypnone
LymeNet Contributor
Member # 47629

Icon 1 posted      Profile for 6Hypnone   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank u for the info. Seems like u don't think this has to do with Lyme.
And I'd love to come off but...
1) I'm afraid of the attack coming back
2) what if the initial depression I went on it for, comes back? I dunno what the initial cause was back in 1991. Seemed out of nowhere. Which leads me to believe w/out some 'help' it will hist return.
And I'm on glycinate bc its specific to nerve pain

Posts: 606 | From sw suburbs of chicago, Illinois | Registered: Mar 2016  |  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.