I take nothing for my pain. I just lay down and if they get to bad I'll wear my eye patch for awhile. You need to get dimmer switches for your lights and go from over head lighting to lamps. Adjust your computer settings and start wearing hats. They call me Gilligan now and never go outside without sun-glasses. I have noticed a slight jump in my BP so now I'm working on that. I'm sure it's all stress related.
Trish
April <xapril77x@...> wrote:
--- In adie_syndrome@yahoogroups. , Trish <qcgirl63@..com .> wrote:
How bad and often are your headaches? Mine are terrible! I take pain
pills & Stadol nose spray. If that doesn't work I have to go to the
hospital where sometimes they give me 2 or 3 shots of Stadol or
Demerol & if that doesn't work they admit me so they can deliver my
pain meds. through an IV......Headaches are the worst, not only for
me but for my family also. I wish they would go away.
>
> I suffer from headaches ... I can still see at night.
>
> Trish
>
> April <xapril77x@...> wrote:
> Hi, my name is April I am 29 years old & live in Texas.
I have had
> Adies for a little over 3 years now. It started when I was
pregnant
> with my 3rd son. My Dr. thought I might have had a stroke due to
my
> pre-eclampsia. I have had pre-eclampsia in all 3 of my pregnancies
and
> all were delivered early due to extremely high blood pressure. I
have
> had high blood pressure since the age of 15. I don't know if this
has
> anything to do with the Adies. I was tested for Lupus and it was
neg.
> Anyway, I have done lots of research and find that there are so
many
> people with different symptoms. I have excessive sweating, severe
> migranes, vision loss, cannot see at night, dialated pupil,
anxiety,
> over reactive reflexes, etc. Does anyone else ave similar
symptoms?
> I do not have alot of time to write but will try to post replies
> when I can. It's nice to be a member and know there are others
like me.
>
> April
>
>
>
>
>
>
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