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Hi Davena,

> Does anyone ever have muscle spasams?

Yes! That's what was my worst problem and made me

so desperate to find help but not quite anything like yours.

> <snip> I have yet

> to see my GP but was interested to know if anyone else has had these?

Keep us posted on what your GP tells you.

Patty B in the Pineywoods of East Texas

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Re: muscles spasms, early on Wayne had muscles spasms in his feet and ankles, he takes flexeril 10 mg at bedtime and that has taken care of it. Sharon

Re: [ ] muscle spasms

Hi Davena,> Does anyone ever have muscle spasams?Yes! That's what was my worst problem and made meso desperate to find help but not quite anything like yours.> <snip> I have yet> to see my GP but was interested to know if anyone else has had these?Keep us posted on what your GP tells you.Patty B in the Pineywoods of East TexasPlease visit our new web page at:http://www.wpunj.edu/icip/paWe are currently discussing new chat times. moderates a chat on arthritis atwww.about.com on Thursday evenings, so check thatout in the meantime! E mail at RA@... for details.

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  • 1 year later...
Guest guest

> B,

>

> I don't have restless leg syndrome but I do have muscle spasms in

my hands. This all occurred after I was diagnosed with carpal tunnel

syndrome. I had surgery in my right hand and it is feelng better

(the arthritis is still bugging though) but I am stll havng the

muscle spasms in both hands. Makes it hard to type, grasp things,

etc. It seems like things are always slipping through my fingers.

Anyway I have PA and fibromyalgia too. I am taking Enbrel, methodone

for pain, ambien to sleep, flexeril when needed for muscle spasms and

neurontin every night (it is supposed to be for pain but I really

notice no difference). You might want to ask your doctor about

putting you on neurontin. It is supposed to work well for restless

leg syndrome and help with sleep too. I should probably be on a

higher dose but it makes me feel too loopy.

>

>

Thanks for your response. I haven't had muscle spasms in my

hands, although I do experience a lot of pain in my fingers. I tried

Neurontin and didn't notice any improvement. I take Baclofen for

muscle spasms, but I'm going to ask my Rheumy on my next visit to try

something else. The spasms are in my back, arms and shoulders...I

might ask her to let me try Flexeril. Thanks for sharing...

B

>

>

>

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  • 2 years later...
Guest guest

muscle spasms? what do they feel like?

> Has anyone gotten a good answer to WHY we get muscle

> spasms?

>

> I just had another MRI of my neck, and the short

> answer is that " it looks normal " .

>

> So the question remains.... what's triggering the

> muscle spasms in my back, neck, and head, and why are

> they constant despite round-the-clock muscle

> relaxants? (And NSAIDs, and Remicade, and

> methotrexate....)

>

> Any clues?

>

> --

>

> =====================================================

> Stein

> http://www.noblefusion.com/astein

> http://www.livejournal.com/users/astein142/

> http://darkart42.deviantart.com/

> -----------------------------------------------------

> " Do or do not. There is no try. " - Yoda

> -----------------------------------------------------

> " If you're tired of fighting battles with yourself

> If you want to be somebody else, change your mind... "

> -- Sister Hazel

> =====================================================

>

>

>

> ____________________________________________________

> Start your day with - make it your home page

> http://www./r/hs

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Guest guest

Hi , re: muscle spasms -- I used to get

them ALL THE TIME (in my 20s and early to mid

30s). I even lost a job over the issue. I've

gotten them less frequently as I've aged, and one

reason is that I tend to move much more CAREFULLY

now. Almost subconsciously, I've trained myself

NEVER to make sudden movements, and to stretch a

lot and warm up before getting out of bed. That

being said, one thing that's known for sure to

help prevent them is exercise (I do light

swimming 4 times a week), and one thing that will

for sure trigger them for me is taking muscle

relaxants, such as flexeril. Yes, in the past

I've used them to get out of an acute spasm, but

the rebound effect frequently seems to occur when

I do. One alternative to the relaxants is

Cal-Mag (the calcium magnesium powder that you

mix with boiling water, and sweeten with apple

juice because it's really tart). I've actually

gotten out of an acute spasm by taking some

cal-mag, which those of us with PA should all be

taking anyway, drinking A TON OF WATER

(dehydration alone can trigger a spasm, and I

think my " drink tons of water " policy of the last

few years has actually staved off a number of

acute episodes!) and hopping (well, carefully

stepping, actually) into a hot bath, WATER BOTTLE

IN HAND! Good luck, -sheila

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  • 2 weeks later...
Guest guest

I actually just received a new diagnosis on Monday - Firbromyalgia. My Rheum

said that the spasms are not caused by the arthritis, but were classic fibro

symptoms. I don't know much about Fibro yet, so I can't really provide anything

but my personal experience. I have constant pain in the back of my head, neck

and shoulder blades (more intense at the insertions) which are very tender at

times. It feels like I have a metal spike in the base of my skull and it

radiates pain forward to my forehead. I also get fluid-like " bubbles near my

cervical vertebrae. For the past month, the joint pain has taken a back-seat to

these muscle spasms. My PA is relatively mild right now, but I'm sure it would

make the Fibro more complicated if it wasn't.

I've been taking Skelakin (muscle relaxer) 3x a day for 1 month and have been

skipping the relafen so I can take excederin or I take 3 tylenol w/ the relafen

for the headaches, depending on how bad they are. The skelakin helps symptoms,

but they are still there just less severe. Massage helps immensely, but finding

the time/money can be hard. I find myself digging my own knuckle into the back

of my head constantly to try to get the " spike " to go away, but it never seems

to. I also do an ice compress, then heat compress and this helps too.

My doctor said that since I'm responding to exercise (yoga at least every other

day) and massage therapy, that there is no nerve damage. He stated a regular

exercise routine would make symptoms disappear, but the catch is, I went to the

gym 4 days a week before I had my first PA flare, and had to stop because it was

too painful. He suggested water exercise, but I have no idea how to fit that

into my schedule, so I'm going to stick with yoga every other day and cardio 4

days a week.

Hope this helps!

Jenn in Baltimore, MD

Stein <darkart42@...> wrote:

Has anyone gotten a good answer to WHY we get muscle

spasms?

I just had another MRI of my neck, and the short

answer is that " it looks normal " .

So the question remains.... what's triggering the

muscle spasms in my back, neck, and head, and why are

they constant despite round-the-clock muscle

relaxants? (And NSAIDs, and Remicade, and

methotrexate....)

Any clues?

--

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  • 6 months later...

Yes, but could be something simple like potassium shortage in system.

Standing barefoot on cold marble with stop cramping. Calicum is a nerve calmer.

You could try to either take supplements for a while or eat more bananas and

drink more milk to see if it helps. It could be the CMT which warm massage or

warmth would help.

Donna B.

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So, quinine helps? My mother has taken this and I was

considering it as well. Any side-effects?

I was told by a doctor that the non-painful spasms (called fasciculations?) are

the result of nerve damage. It may also indicate that a muscle is atrophying --

at least that's been my experience. The fasciculations will come in cycles and

I notice that my muscles are weaker afterwards.

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I have a demylenating form. I have really paid attention to it today

and when ever I relax my legs they are " jumping " all over. Little

spasms everywhere but mostly in my calfs. It is kinda scary for me.

Do you know of any research/articles on muscle spasms and CMT?

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  • 2 years later...
Guest guest

>

> If anyone needs a med that will help your muscle spasms then have

your doctor prescribe tegretol. I was having muscle spasms constantly

and was put on tegretol. If I am under a lot of stress then I will

still feel some minor spasms but normally they are under control. I

have been on tegretol since 1987.

> Good Luck

> Marie

>

I tried tegretol once, but it made my libido disappear. In the interest

of marital harmony I had to get off of it.

Fran

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  • 2 years later...
Guest guest

Yes. That's one of the funnier ones. It also happens with toes. I am not on

gleevec anymore. For some periods (weeks) I had nightly cramps in weird places

like on my ankles or the sides of my knees. They would go away with a

combination of my husband massaging the cramp and walking it out. On sprycel

now. No cramps or digestive problems. So far, so good.

Sent from my iPhone

On Aug 5, 2010, at 10:35 PM, " Karine " <karinevallier@...> wrote:

Has anyone had weird muscles spasms causing involuntary movement of one finger

going under another one while taking gleevec.

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Guest guest

YES!!! It was the little finger of my right hand. That went on for a few

months, then suddenly I started getting the same thing with my right foot.

It was so persistent I started worrying whether it was an early precursor of

Parkinson's, which my mom had. I saw a neurologist and he confirmed I did

not have Parkison's. He prescribed Neurontin, which ended up making a rather

horrible match with Gleevec. After a few months, I quit taking the

Neurontin, and the spasms never came back. I moved onto Sprycel then

Tasigna, but never had a recurrence of anything like that.

I'd forgotten about that. It was really quite creepy.

On Thu, Aug 5, 2010 at 7:35 PM, Karine <karinevallier@...> wrote:

>

>

> Has anyone had weird muscles spasms causing involuntary movement of one

> finger going under another one while taking gleevec.

>

>

>

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Guest guest

Yes, my fingers get all twisted up and they bend different directions.  The

pain is unreal when I get them, and it goes up  my arm sometimes.  Same thing

happens to my toes, and I was driving the other day and got it in both feet.  I

was close to home, otherwise I would have to pull over and walk it out.  I have

had to do that already.

From: Karine <karinevallier@...>

Subject: [ ] muscle spasms

Date: Thursday, August 5, 2010, 10:35 PM

 

Has anyone had weird muscles spasms causing involuntary movement of one finger

going under another one while taking gleevec.

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Guest guest

I have had these for years. sometimes they are so bad that I just want to cry.

I find that if I don't drink enough plaink water, they get worse.

On Aug 6, 2010, at 3:12 PM, Armour wrote:

>

>

>

> Has anyone had weird muscles spasms causing involuntary movement of one finger

going under another one while taking gleevec.

>

>

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