chris_uk
Distinguished member
- Joined
- Aug 30, 2008
- Messages
- 111
- Reason
- Other
- Diagnosis
- 00/0000
- Country
- UK
- State
- CL
- City
- Stockton-On-Tees
Hi all
After 3 months of really bad twitching in my calfs, i had an EMG in december and was told i am ok, (i have later found out that the minor abnormalities were the slow nerve test they do at first)
I am due to see my Neuro on Monday and was going there with the hope of getting this fear of my back, i still twitch ALL the time in my calfs etc but after EMG being normal i thought to myself for the sake of my marriage and moving on again i have to let this go.
The thing that bothers me is the amount of people who seem to get clear EMG's then as as little as a few months later get other ones and there is changes on them. I know if i go and ask for another EMG on monday i will be causing a whole lot of heart ache for not not only myself but my wife, so i guess i am just asking for a bit of advice here.
I got a letter this week from my Neuro saying he wants to reassure me "as firmly as he can" that i do not have this disease and there is no evidence of it at all and he will talk more in depth on monday to me about it.
So when i go in on Monday what do you all think i should do? is it common for an EMG to change? i mean do i really want to go down this road again? my wife has been very supportive but i have had this fear for 4 months now (i know some of you have this horrible disease and me worrying for 4 months compared to what you go through is so tiny so please don't think i don't understand that because i truly do)
I have read and read on here and even just lately about getting an EMG to soon, mine was after 3 months and my twitches were really strong and violent. After all that Wright has said and others, an EMG would have picked anything up wouldnt it?
I am seeking your final advice here and contrary to what Wright has said to me in private i do and will listen.
Chris
After 3 months of really bad twitching in my calfs, i had an EMG in december and was told i am ok, (i have later found out that the minor abnormalities were the slow nerve test they do at first)
I am due to see my Neuro on Monday and was going there with the hope of getting this fear of my back, i still twitch ALL the time in my calfs etc but after EMG being normal i thought to myself for the sake of my marriage and moving on again i have to let this go.
The thing that bothers me is the amount of people who seem to get clear EMG's then as as little as a few months later get other ones and there is changes on them. I know if i go and ask for another EMG on monday i will be causing a whole lot of heart ache for not not only myself but my wife, so i guess i am just asking for a bit of advice here.
I got a letter this week from my Neuro saying he wants to reassure me "as firmly as he can" that i do not have this disease and there is no evidence of it at all and he will talk more in depth on monday to me about it.
So when i go in on Monday what do you all think i should do? is it common for an EMG to change? i mean do i really want to go down this road again? my wife has been very supportive but i have had this fear for 4 months now (i know some of you have this horrible disease and me worrying for 4 months compared to what you go through is so tiny so please don't think i don't understand that because i truly do)
I have read and read on here and even just lately about getting an EMG to soon, mine was after 3 months and my twitches were really strong and violent. After all that Wright has said and others, an EMG would have picked anything up wouldnt it?
I am seeking your final advice here and contrary to what Wright has said to me in private i do and will listen.
Chris