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.
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
Luggage? GPS? Comic books?
Check out fitting gifts for grads at Yahoo! Search.
--- In adie_syndrome@yahoogroups.com, Trish <qcgirl63@...> 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
>
>
>
>
>
>
> ---------------------------------
> Luggage? GPS? Comic books?
> Check out fitting gifts for grads at Yahoo! Search.
>
I suffer from headaches but will not take the major perscriptions because of side effects.
April <xapril77x@...> wrote:
--- In adie_syndrome@yahoogroups.com, Trish <qcgirl63@...> 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 > > > > > > > --------------------------------- > Luggage? GPS? Comic books? > Check out fitting gifts for grads at Yahoo! Search. >
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.com, Trish <qcgirl63@...> 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 > > > > > > > --------------------------------- > Luggage? GPS? Comic books? > Check out fitting gifts
for grads at Yahoo! Search. >
Don't let your dream ride pass you by. Make it a reality with Yahoo! Autos.
April, I don't have the sweating but doctors sometimes call Adies with sweating "Ross syndrome" so it's not unusual.
I have low reflexes instead of over-reactive ones. I didn't realize that I did until the chiropractor tested me and a tap on the right knee did not make the ankle jump up.
...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
--- In adie_syndrome@yahoogroups.com, linja@... wrote:
>Is Ross syndrome the same as Adies?
> The funny thing about my reflexes is when I accidentally drop my
arms close to my knee & my legs jump....it doesn't even have to be
very hard....I can barely touch around that area & it happens.
> April, I don't have the sweating but doctors sometimes call
Adies with
> sweating "Ross syndrome" so it's not unusual.
>
> I have low reflexes instead of over-reactive ones. I didn't
realize that I
> did until the chiropractor tested me and a tap on the right knee
did not make
> the ankle jump up.
>
> Reference: see the NIH page:
> _http://www.ninds.nih.gov/disorders/holmes_adie/holmes_adie.htm_
> (http://www.ninds.nih.gov/disorders/holmes_adie/holmes_adie.htm)
>
> Best wishes,
> Linda in Virginia
>
> April writes:
>
> ...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
>
>
>
>
> ************************************** See what's new at http://www.aol.com
>
I have absolutely no reflexes anywhere on my body.
linja@... wrote:
April, I don't have the sweating but doctors sometimes call Adies with sweating "Ross syndrome" so it's not unusual.
I have low reflexes instead of over-reactive ones. I didn't realize that I did until the chiropractor tested me and a tap on the right knee did not make the ankle jump up.
...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