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Re: spasms-EMG

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I had two EMG's by the same guy, what a nightmare! Nothing short of

torture. Next time, I am following Laurie's advice and getting a ped neuro

to do it. I didn't think there was a less painful way, the tech (or

whatever he was) was with my neuro and was all I knew. I will never let

anyone torture me like that again. It felt like everyone else describes,

'shock, current, extremely painful. The tech (or whatever he was) who did

it acted like I was making a big deal out of nothing. Never again. :(

God bless,

Hazelpone

Re: spasms

I have sensation " memories " from my (extremely painful) EMG, in my

hands, they feel like either electric current or a shock, or plunging

my hands fingers first in a pot of boiling water. So I know what you

mean, unless we've both lost it!

Take care,

RH

> I have always had severe leg cramps and I have taken several types

of muscle relaxers over the years. I have very severe pains in the

right side of my head, ear, face and I have stabbing pains in my

right eye that feels like someone is sticking a needle in my eye, I

have been told that this is from trigeminial neuralgia. My

opthamologist spoke with my current neurologist and he increased the

dosage of neurotin from 300mg three times daily to 300mg four times

daily and it has helped the pain in the right side of my head, ear,

face and eye considerably. At least I do feel that it is livable

now. At times my feet feel like (please don't think I've lost it)

there is an electrical current going thru them. I do have peripheral

neuropathy in both legs, but with the antodyne thereapy and the

neurotin it isn't as bad as it was, for which I am very thankful.

I'm not sure if this is in any way helpful or if it just sounds like

the ramblings of an " old " lady (ha). Dolores johnson

>

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I think Laurie meant to have them use ped needles, not have a ped do the

EMG.

Hpone00 wrote:

>I had two EMG's by the same guy, what a nightmare! Nothing short of

>torture. Next time, I am following Laurie's advice and getting a ped neuro

>to do it. I didn't think there was a less painful way, the tech (or

>whatever he was) was with my neuro and was all I knew. I will never let

>anyone torture me like that again. It felt like everyone else describes,

>'shock, current, extremely painful. The tech (or whatever he was) who did

>it acted like I was making a big deal out of nothing. Never again. :(

>

>God bless,

>Hazelpone

>

>

> Re: spasms

>

>

>I have sensation " memories " from my (extremely painful) EMG, in my

>hands, they feel like either electric current or a shock, or plunging

>my hands fingers first in a pot of boiling water. So I know what you

>mean, unless we've both lost it!

>

>Take care,

>RH

>

>

>

>

>>I have always had severe leg cramps and I have taken several types

>>

>>

>of muscle relaxers over the years. I have very severe pains in the

>right side of my head, ear, face and I have stabbing pains in my

>right eye that feels like someone is sticking a needle in my eye, I

>have been told that this is from trigeminial neuralgia. My

>opthamologist spoke with my current neurologist and he increased the

>dosage of neurotin from 300mg three times daily to 300mg four times

>daily and it has helped the pain in the right side of my head, ear,

>face and eye considerably. At least I do feel that it is livable

>now. At times my feet feel like (please don't think I've lost it)

>there is an electrical current going thru them. I do have peripheral

>neuropathy in both legs, but with the antodyne thereapy and the

>neurotin it isn't as bad as it was, for which I am very thankful.

>I'm not sure if this is in any way helpful or if it just sounds like

>the ramblings of an " old " lady (ha). Dolores johnson

>

>

>

>

>

>

>Medical advice, information, opinions, data and statements contained herein are

not necessarily those of the list moderators. The author of this e mail is

entirely responsible for its content. List members are reminded of their

responsibility to evaluate the content of the postings and consult with their

physicians regarding changes in their own treatment.

>

>Personal attacks are not permitted on the list and anyone who sends one is

automatically moderated or removed depending on the severity of the attack.

>

>

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Guest guest

I think Laurie meant to have them use ped needles, not have a ped do the

EMG.

Hpone00 wrote:

>I had two EMG's by the same guy, what a nightmare! Nothing short of

>torture. Next time, I am following Laurie's advice and getting a ped neuro

>to do it. I didn't think there was a less painful way, the tech (or

>whatever he was) was with my neuro and was all I knew. I will never let

>anyone torture me like that again. It felt like everyone else describes,

>'shock, current, extremely painful. The tech (or whatever he was) who did

>it acted like I was making a big deal out of nothing. Never again. :(

>

>God bless,

>Hazelpone

>

>

> Re: spasms

>

>

>I have sensation " memories " from my (extremely painful) EMG, in my

>hands, they feel like either electric current or a shock, or plunging

>my hands fingers first in a pot of boiling water. So I know what you

>mean, unless we've both lost it!

>

>Take care,

>RH

>

>

>

>

>>I have always had severe leg cramps and I have taken several types

>>

>>

>of muscle relaxers over the years. I have very severe pains in the

>right side of my head, ear, face and I have stabbing pains in my

>right eye that feels like someone is sticking a needle in my eye, I

>have been told that this is from trigeminial neuralgia. My

>opthamologist spoke with my current neurologist and he increased the

>dosage of neurotin from 300mg three times daily to 300mg four times

>daily and it has helped the pain in the right side of my head, ear,

>face and eye considerably. At least I do feel that it is livable

>now. At times my feet feel like (please don't think I've lost it)

>there is an electrical current going thru them. I do have peripheral

>neuropathy in both legs, but with the antodyne thereapy and the

>neurotin it isn't as bad as it was, for which I am very thankful.

>I'm not sure if this is in any way helpful or if it just sounds like

>the ramblings of an " old " lady (ha). Dolores johnson

>

>

>

>

>

>

>Medical advice, information, opinions, data and statements contained herein are

not necessarily those of the list moderators. The author of this e mail is

entirely responsible for its content. List members are reminded of their

responsibility to evaluate the content of the postings and consult with their

physicians regarding changes in their own treatment.

>

>Personal attacks are not permitted on the list and anyone who sends one is

automatically moderated or removed depending on the severity of the attack.

>

>

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Guest guest

Ok, thanks Laurie. Unfortunately, I got this message just after I sent the

one asking. Ignore that one.

God bless,

Hazelpone

Re: spasms

>> >

>> >

>> >I have sensation " memories " from my (extremely painful) EMG, in my

>> >hands, they feel like either electric current or a shock, or plunging

>> >my hands fingers first in a pot of boiling water. So I know what you

>> >mean, unless we've both lost it!

>> >

>> >Take care,

>> >RH

>> >

>> >

>> >

>> >

>> >>I have always had severe leg cramps and I have taken several types

>> >>

>> >>

>> >of muscle relaxers over the years. I have very severe pains in the

>> >right side of my head, ear, face and I have stabbing pains in my

>> >right eye that feels like someone is sticking a needle in my eye, I

>> >have been told that this is from trigeminial neuralgia. My

>> >opthamologist spoke with my current neurologist and he increased the

>> >dosage of neurotin from 300mg three times daily to 300mg four times

>> >daily and it has helped the pain in the right side of my head, ear,

>> >face and eye considerably. At least I do feel that it is livable

>> >now. At times my feet feel like (please don't think I've lost it)

>> >there is an electrical current going thru them. I do have peripheral

>> >neuropathy in both legs, but with the antodyne thereapy and the

>> >neurotin it isn't as bad as it was, for which I am very thankful.

>> >I'm not sure if this is in any way helpful or if it just sounds like

>> >the ramblings of an " old " lady (ha). Dolores johnson

>> >

>> >

>> >

>> >

>> >

>> >

>> >Medical advice, information, opinions, data and statements contained

>> >herein are not necessarily those of the list moderators. The author of

>> >this e mail is entirely responsible for its content. List members are

>> >reminded of their responsibility to evaluate the content of the postings

>> >and consult with their physicians regarding changes in their own

>> >treatment.

>> >

>> >Personal attacks are not permitted on the list and anyone who sends one

>> >is automatically moderated or removed depending on the severity of the

>> >attack.

>> >

>> >

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