EMG With Dr Gordon, Toronto

PNMLT, EMG, SSEP, and other Nerve function testing.
The different techniques, results and opinions.
Chex
Posts: 58
Joined: Mon Aug 15, 2011 2:10 am

Re: EMG With Dr Gordon, Toronto

Post by Chex »

I go back to see Dr. Gordon on the 20th. I will get the results of the mri and I go to see dr. Peng for a consultation about the block. I had tried the diazapam suppositories Dr. gordon prescribed. They seemed to help a little but you are supposed to put them in at bedtime. I need something ofr the evenings so I can perhaps sit and watch some tv. I tried it but it was pretty leaky and messy. It did seem to help somewhat I think. Only thing is that thye gave me a yeast infection.

since having the yeast infection, I have stopped my daily physio homework. Stopping the physio seems to actully make things feel better but they keep telling me it could be worse before it gets better. Argh!! I hate the physio homework!!!! It hurts
DoubleEdgedSword
Posts: 201
Joined: Thu Oct 27, 2011 7:15 am
Location: Ontario, Canada

Re: EMG With Dr Gordon, Toronto

Post by DoubleEdgedSword »

I'd gone back to Dr Gordon in early March, and he went over my results. Seems the MRI tech didn't use the protocols he needed in order for Dr G to see what he wanted to. My EMG results showed normal reaction times on the right side, but slightly delayed reaction times on the left, so I suppose that's where my impairment comes from.

I'm going for an MRV next week to see if my problems are related to my pelvic veins. I really don't know what would be next after this. Dr G is also including me in a general PGAD study he got permission to re-open, and should he get enough participants, he wants to include me in a botox study in about 6-9 months' time.
On the road of discovery to see what is causing my PGAD.
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Violet M
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Re: EMG With Dr Gordon, Toronto

Post by Violet M »

DES, that's unfortunate about the MRI. Are they going to redo it?

Violet
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.
DoubleEdgedSword
Posts: 201
Joined: Thu Oct 27, 2011 7:15 am
Location: Ontario, Canada

Re: EMG With Dr Gordon, Toronto

Post by DoubleEdgedSword »

I really don't know if they will or not. I suppose I'll find out or ask once I've had the MRV on Wednesday. Guess it depends on what that shows them. It's so expensive to have an MRI, I don't know that they'll just offer up another one, but I'd like to know what's causing my problem.. :?
On the road of discovery to see what is causing my PGAD.
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Violet M
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Location: United States
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Re: EMG With Dr Gordon, Toronto

Post by Violet M »

Good luck with the MRV, DES. Hope it goes well for you and gives you some answers. ;)

Violet
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.
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