Jump to content
The MS PEOPLE UK Forum
Support, help, advice and information for Multiple Sclerosis. Ask questions and share experiences with people affected by MS.
Larisa

Magnesium for muscle spasms

11 posts in this topic Last Reply

Recommended Posts

Larisa

I suffer from muscle spasms in my legs and I've heard magnesium supplements could be a way to help. Does anyone do this and anyone found if it works.

Share this post


Link to post
derby42

hi there. yes I take it. don't know if it helps or not cos this damned illness confuses the hell outta me! sometimes I think its helping then other times I wonder why I bother. I take it as a multi with calcium and vitamin d3.


derby x

Share this post


Link to post
Larisa

Hi derby, how much mag do you take per day. Are you on any other meds for your leg spasms X

Share this post


Link to post
derby42

not sure of the dose but if you Google magnesium calcium and vitamin d3 capsules it will bring it up. I think its made by natures health or natures aid. I can't look cos I'm in bed now and I'm on the 3rd floor up.

I take nothing else whatsoever apart from 2 paracetamol every morning to ease back and leg pain. I was offered baclofen by my neuro but was warned that it could make my legs weaker and I can't risk that happening.


Edited by derby42

derby x

Share this post


Link to post
BowLocks

I find 375mg of magnesium helps a great deal with spasm& cramp.

 

Share this post


Link to post
Lilbill

Hi, I can't take any of the drugs for spasm but I find drinking tonic water seems to help sometimes, but only if it s the one with quinine in it. It might be worth a try.

Lilbill x

Share this post


Link to post
Lilbill

I drink tonic water (with quinine in) and find is usually takes the edge off cramps as I cannot take the usual meds.

Might be worth a try.

 

Share this post


Link to post
Lilbill

Oops, first post disappeared, but it obviously didn't after all!!

Share this post


Link to post
Hezza

Hi Lilbill,

There's a bit of a bug on the forum at the moment which may be why you thought your post had disappeared. There's more info here: http://ms-people.com/forum/topic/16163-database-error/

 

I've come across the error when posting replys but find that when I refresh the screen my post is there ok.

 

Back to the topic - I've too drink tonic water having heard that it can help with muscle spasms.

 

:heartraining:


Life is short. Eat dessert first. Jacques Torres

Share this post


Link to post
cazza

Hiya Larisa,

Yes i take Magnesium 375mg daily along with super strength Vitamin D3; Omega 3,6&9 complex and a Vitamin B complex.

Personally i swear by them, no instant change, but over time i can really tell the difference, and yes they all help me.My GP is aware i take all these and has no problem with it (i even converted her to Magnesium which she now takes)

 

It's all a case of trial and error,what, and if, something helps and works for you,what have you got to lose.

 

I get mine from Healthspan www.healthspan.co.uk look it up and send for their free brochure to see what you think.

 

Good luck.

 

Cazza :wavebunny: x


*A Christmas Carole*

Share this post


Link to post
pigeon64

I have not tried anything at all, thought it best to wait until I find out what the cause is. But my neurologist did mention me taking Quinine Sulphate for cramps :hearts_circle:

Share this post


Link to post

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Similar Topics

    • Muscle twitching

      Hi all I have been diagnosed with MS for 18 months (remitting relapsing) and the last five weeks I have had muscle twitching! This has me really worried about motor neurone disease!! Seeing neurologist in 3 weeks!! Seen 4 different drs and they have tried to reassure me but it hasn't!! They all said it would be highly rare. Spoke to ms nurse and also said it would be extremely rare. Does anyone else have twitches. Grateful for any replies

      in General Discussion about MS

    • Spasms getting worse

      Hi All, I have had SPMS for some 15 years, with the main problem being mobility, with occasional (usually) night-time spasms (big toes bending upwards, nearly always right foot) whilst this used to be more annoying than anything else, it has got worse over the last few weeks and can last for over 3 hours at a time. It is now having a devastating impact on my routine, and I would love to hear any tips or advice from members on coping techniques.   I currently take up to 8 Baclofen daily, which I do think are effective any more, and am currently on a trial for Sativex- but this does not seem to touch an aggressive episode like last night, even a Diazepam on top didn't help   I have tried Gabapentin but had a bad reaction, and although usually effective, I don't want to become reliant on Diazepam.   Any help massively appreciated. Regards Mark

      in General Discussion about MS

    • Does Baclofen help with muscle aches? If not, what does?

      Good afternoon everyone. I started on my copaxone last August and have felt so well since I wished I had done it earlier. At my previous rate I should have had two relapses since then but I am relapse free and life feels good But, I am getting increasing pain in both legs and, sometimes my arms. The muscles feel weak and without strength - for example when I was doing my daughter's hair the other day I had to keep lowering my arms due to pain. My walking is now affected and the muscles hurt at rest. They are particularly bad when I first wake up. They feel stuff and achy but not really "spastic" if you know what I mean. The MS nurse suggested baclofen and my GP has prescribed it but I wondered if anyone had had similar symptoms to these and if the baclofen (or anything else) worked. Any words of wisdom would he gratefully received. Thanks, Sam

      in General Discussion about MS

    • Funny toes? Spasms?

      Hello guys, quick question. I keep getting foot pain in my left foot (arch of foot and down sides). It comes on periodically and after activity (decorating and Xmas shopping to date). My toes are also weird in just my left foot. The toes no longer match my right foot and and higgly-de-piggle-de all the time. Am I experiencing spasms? I don't necessarily have the foot pain all the time, but my toes are always weird. The pain can cause me to limp a little, but nothing major. I don't believe I've injured my foot and it's not tender to touch. Any ideas much appreciated! Thanks :-)

      in General Discussion about MS

    • Spasms

      I keep getting spasms in my legs, which is often accompanied by a strong burning sensation in my feet. I don't see my neuro for another month. Is there anything I can buy or ask my gp to prescribe me to help with these symptoms? Has anyone else got experience dealing with these things? After 10 or so spasms one after the other it starts to get painful :( feeling rather fed up of this :(

      in General Discussion about MS

About Us

Founded in 2004, MS People UK is a community website and discussion forum by and for people with Multiple Sclerosis as well as for friends, families, supporters and those interested in this disabling condition.

If you’re newly diagnosed or want to ask about possible first symptoms, or if you’ve had Relapse Remit, Secondary or Primary Progressive MS for some time, a welcoming group of fellow MS sufferers is here to chat with you about MS symptoms, diagnosis and treatments.

The atmosphere is friendly whilst being compassionate, supportive and caring. Members also post about a variety of subjects not related to MS, as well as share jokes, talk about their hobbies, have fun, and more.


The MS People Forum is not responsible for advice or information supplied by members. We suggest you seek medical advice before trying anything.
×