Muscle spasms

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Muscle spasms

Postby Emmaxx » Fri Mar 07, 2014 7:31 pm

Hello does any1 suffer from muscle spasms it's so annoying don't no if its a symptom of FB xxx


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Re: Muscle spasms

Postby johanna symons » Fri Mar 07, 2014 7:46 pm

Hi yes i get them in my neck, very embarrasing especially when my head shakes with it. It's so painfull too, diazapam does help though
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Re: Muscle spasms

Postby humphreys » Fri Mar 07, 2014 7:47 pm

Hi Emma. Yes I suffer badly, especially in my feet, drives me mad when I'm trying to get to sleep, and also my thighs. I try to relax and it seems to go away after a while.
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Re: Muscle spasms

Postby Emmaxx » Fri Mar 07, 2014 7:59 pm

Thank you for yr reply I have only been diagnosed of fri with FB and HMS and really don't no much bout it but its a relief 2 see I'm not the only person xx


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Re: Muscle spasms

Postby fibrogirl90 » Fri Mar 07, 2014 8:08 pm

Hi emma is your fm and hms fibromyalgia and hypermobility syndrome
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Re: Muscle spasms

Postby Emmaxx » Fri Mar 07, 2014 8:15 pm

Hi ya yes it is sorry I'm a newbie on here xx


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Re: Muscle spasms

Postby Emmaxx » Fri Mar 07, 2014 8:23 pm

Don't no much about both just no I'm in alot of pain most days I'm 26 and have two children age 5 and 6 and working part time but i am really struggling at the mo xx


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Re: Muscle spasms

Postby Billsmum » Fri Mar 07, 2014 8:39 pm

Yes definitely a symptoms of good old fibro, get them a lot in hands, feet, legs. Actually everywhere I suppose :yikes: still trying a new strategy, a 100 days of being happy, so come on fibro, I'm going to get the better of you, would anybody like to join me? xXx
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Re: Muscle spasms

Postby Emmaxx » Fri Mar 07, 2014 8:53 pm

I'm with you on that one billsmum newly diagnosed soon as I get the right medication I will get the better of it and not let it ruin my life anymore xx


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Re: Muscle spasms

Postby SandraCRH » Fri Mar 07, 2014 9:31 pm

Hi. Yes muscle spasms are associated with FM however, never heard of anyone having FM with hyper mobility. Perhaps you need to check out EDS syndrome (Endlos-Danlos) as my friend has this & this too is associated with pain in joints & muscles. I don't take drugs at all as the side effects outweigh the benefits. All I can say is exercise in some form, low oxalate diet & pure water to keep hydrated. Good luck!
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