Indeed I am very fortunate that there's an EP Foundation so close to me, let alone I was accepted!
Now, wonder what shall I eat this morning which has no MSGs.
Oh yeh! I used to own 2 Triumph Spitfires back in the 70s and their rival was the MG.
MG?
MSG?
So sconfusing..
--- In epilepsy@yahoogroup
>
> Pat,
>
> That is fantastic! I've never heard of a local EP
> group doing that before. I don't have a local group
> here. I think the closest one is in Indianapolis.
> About 150 miles away. I consider this group my local group.
>
> Thanks keeping on Craig. I would still like to know
> what he eats.
>
> Millie
>
>
>
>
>
> > I posted a few months back my Neuro suspected I may have TMJ
> > [temporomandibular joint disease]. The x-ray was normal and she wants a CT
> > scan as my symptoms still persist, even though my Prednisone has been
> > tripled for another illness. And I don't believe Prednisone [steroids]
> > really have any effect on TMJ, do they?
> > I am self pay and can't afford a CT scan and my jaws still pain me after
> > eating.
> >
> > I called our local Epilepsy Foundation and they took me on as a client and
> > I will receive free lab work, MRIs, x-rays and CT scans - whatever is
> > needed. I also get to visit one of their Neurologists for free and all
> > this is good for 1 year!
> > I am overwhelmed.
> > I see the new Neuro August 6th and already have all my medical records
> > with me.
> > I am enthusiastic about this 2nd Neuro as the EP Foundation will afford me
> > the opportunity to get tests done.
> > Now, I have NO clue if he will tackle the TMJ because maybe it doesn't
> > fall under EP guidelines for their services.
> > Whatever, it is free - THANK GOD - and at least maybe he can pinpoint more
> > accurately which types of seizures I am experiencing.
> >
> >
>
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