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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