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and all,

I'm not doing very well, but at least I am off of the mtx and the arrava af=

ter that. Both had

me in constant nausea on top of the crushing fatigue and everything else. =

I just started

Humira which will take the place of the Remicade which I had developed anti=

bodies to.

Like I've always felt about this illness for me. It's one step forward and=

two steps back.

My case manager is trying to arrange a couple of days in hospital so I can =

catch up on all

of the specialist exams I never get around to because I barely sit up, let =

alone walk around

and stay in a waiting room. I had a urine catch which was supposed to be f=

or calcium but

instead they checked it for protien. Even though my specimen catch was a w=

hopping six

liters (I eat crushed ice all day to help with dry mouth and this odd heat =

without fever that

has moved deep inside of me). The protien level was two and one half times =

the cut off for

high. Also, my last MRI was inconclusive because of motion, but I warned t=

he techs and

they taped my forehead and chin down but good. if I have a tremor that stro=

ng, I want a

neurologist to look at it. My liver enzymes have been climbing, and my kid=

neys and liver

are usually very tender. I must see a GI, a urologist or renal specialist.=

If all that is not

enough, my cough is acting up and I am concerned about my central apnea ret=

urning. At

least those two docs (sarc and sleep apnea pulmonologists) already work wit=

h the IU sarc

clinic. I imagine I will here what's happening early this coming week.

I have missed everyone so much -- I know that's why my generally frugal hus=

band went all

out on this great laptop and the wireless networking. I can just lie here =

like a lady of

leisure and change to any position I need. Plus I was pulling my hair out =

just watching tv

every day, all day since December! Also, that sweetie totally redid the sc=

reened in patio

furniture -- redid the support ropes and bought new pads for everything, in=

cluding the

glider. My eyes aren't too great for reading books (morelike my hands are =

too weak to

hold the books open) and I can now just take this lovely machine with me.

So, sum it up, when I was on the arrava I was positive I was going to pass =

on any day, and

now I am feeling just normal yuk but still grateful for what I have and for=

my loving friends

and family. I am so glad to be back.

Reneness

>

> > Dear , et al:

> > I am returning from the missing, I hope. It's real late and I am

> > about to turn in, so more will come later. But I have some great news

> > to share with everyone . . .

> > I WON MY SOCIAL SECURITY DISABILITY AT LONG LAST THIS WEEK! This

> > is the best thing that has happened to me in a long time.

> > There are many details to share and I can't do it now. I would

> > have not have been away from here for this long except for chronic

> > computer problems and some damned Beagle virus, or some such thing. I

> > have finally defeated all these issues and I just had to say hello to

> > everyone. I see many new names here and I'm glad to see you all.

> > It is 4:49 a.m. and I must sleep now. I'll be back in touch very

> > soon, I promise. Until then everyone . . . please take extra good

> > care of yourselves tomorrow.

> >

> > In love and peace,

> >

> > ie Bear

> >

> >

> > ~~~~ *** ~~~ *** ~~~ *** ~~~~

> > The Neurosarcoidosis Community

> >

> > Live Group Chat:-

> > Mondays & Fridays 10pm EST USA

> > http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php

> >

> > Message Archives:-

> > http://groups.yahoo.com/group/Neurosarcoidosis/messages

> >

> > Members Database:-

> > Listings of locations, phone numbers, and instant messengers.

> > http://groups.yahoo.com/group/Neurosarcoidosis/database

> >

> >

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Oh Reneness, I was afraid something bad was going on with you since we hadn't heard from you in a while, sending you a big hug, and a wish for better days ahead. I appreciate the update even though it shows that you've not been very well, I'm certainly glad that you have a loving hubby that helps you and loves you so much, that has got to be a plus. We miss you and hope you can be with us more.

Big Hugs,

-- Re: Missing members

and all,I'm not doing very well, but at least I am off of the mtx and the arrava af= ter that. Both had me in constant nausea on top of the crushing fatigue and everything else. = I just started Humira which will take the place of the Remicade which I had developed anti= bodies to. Like I've always felt about this illness for me. It's one step forward and= two steps back.My case manager is trying to arrange a couple of days in hospital so I can = catch up on all of the specialist exams I never get around to because I barely sit up, let = alone walk around and stay in a waiting room. I had a urine catch which was supposed to be f= or calcium but instead they checked it for protien. Even though my specimen catch was a w= hopping six liters (I eat crushed ice all day to help with dry mouth and this odd heat = without fever that has moved deep inside of me). The protien level was two and one half times = the cut off for high. Also, my last MRI was inconclusive because of motion, but I warned t= he techs and they taped my forehead and chin down but good. if I have a tremor that stro= ng, I want a neurologist to look at it. My liver enzymes have been climbing, and my kid= neys and liver are usually very tender. I must see a GI, a urologist or renal specialist.= If all that is not enough, my cough is acting up and I am concerned about my central apnea ret= urning. At least those two docs (sarc and sleep apnea pulmonologists) already work wit= h the IU sarc clinic. I imagine I will here what's happening early this coming week.I have missed everyone so much -- I know that's why my generally frugal hus= band went all out on this great laptop and the wireless networking. I can just lie here = like a lady of leisure and change to any position I need. Plus I was pulling my hair out = just watching tv every day, all day since December! Also, that sweetie totally redid the sc= reened in patio furniture -- redid the support ropes and bought new pads for everything, in= cluding the glider. My eyes aren't too great for reading books (morelike my hands are = too weak to hold the books open) and I can now just take this lovely machine with me.So, sum it up, when I was on the arrava I was positive I was going to pass = on any day, and now I am feeling just normal yuk but still grateful for what I have and for= my loving friends and family. I am so glad to be back.Reneness> > > Dear , et al:> > I am returning from the missing, I hope. It's real late and I am> > about to turn in, so more will come later. But I have some great news> > to share with everyone . . .> > I WON MY SOCIAL SECURITY DISABILITY AT LONG LAST THIS WEEK! This> > is the best thing that has happened to me in a long time.> > There are many details to share and I can't do it now. I would> > have not have been away from here for this long except for chronic> > computer problems and some damned Beagle virus, or some such thing. I> > have finally defeated all these issues and I just had to say hello to> > everyone. I see many new names here and I'm glad to see you all.> > It is 4:49 a.m. and I must sleep now. I'll be back in touch very> > soon, I promise. Until then everyone . . . please take extra good> > care of yourselves tomorrow.> >> > In love and peace,> >> > ie Bear> > > >> > ~~~~ *** ~~~ *** ~~~ *** ~~~~> > The Neurosarcoidosis Community> >> > Live Group Chat:-> > Mondays & Fridays 10pm EST USA> > http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php> >> > Message Archives:-> > http://groups.yahoo.com/group/Neurosarcoidosis/messages> >> > Members Database:-> > Listings of locations, phone numbers, and instant messengers.> > http://groups.yahoo.com/group/Neurosarcoidosis/database> >> >

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Oh Reneness, I was afraid something bad was going on with you since we hadn't heard from you in a while, sending you a big hug, and a wish for better days ahead. I appreciate the update even though it shows that you've not been very well, I'm certainly glad that you have a loving hubby that helps you and loves you so much, that has got to be a plus. We miss you and hope you can be with us more.

Big Hugs,

-- Re: Missing members

and all,I'm not doing very well, but at least I am off of the mtx and the arrava af= ter that. Both had me in constant nausea on top of the crushing fatigue and everything else. = I just started Humira which will take the place of the Remicade which I had developed anti= bodies to. Like I've always felt about this illness for me. It's one step forward and= two steps back.My case manager is trying to arrange a couple of days in hospital so I can = catch up on all of the specialist exams I never get around to because I barely sit up, let = alone walk around and stay in a waiting room. I had a urine catch which was supposed to be f= or calcium but instead they checked it for protien. Even though my specimen catch was a w= hopping six liters (I eat crushed ice all day to help with dry mouth and this odd heat = without fever that has moved deep inside of me). The protien level was two and one half times = the cut off for high. Also, my last MRI was inconclusive because of motion, but I warned t= he techs and they taped my forehead and chin down but good. if I have a tremor that stro= ng, I want a neurologist to look at it. My liver enzymes have been climbing, and my kid= neys and liver are usually very tender. I must see a GI, a urologist or renal specialist.= If all that is not enough, my cough is acting up and I am concerned about my central apnea ret= urning. At least those two docs (sarc and sleep apnea pulmonologists) already work wit= h the IU sarc clinic. I imagine I will here what's happening early this coming week.I have missed everyone so much -- I know that's why my generally frugal hus= band went all out on this great laptop and the wireless networking. I can just lie here = like a lady of leisure and change to any position I need. Plus I was pulling my hair out = just watching tv every day, all day since December! Also, that sweetie totally redid the sc= reened in patio furniture -- redid the support ropes and bought new pads for everything, in= cluding the glider. My eyes aren't too great for reading books (morelike my hands are = too weak to hold the books open) and I can now just take this lovely machine with me.So, sum it up, when I was on the arrava I was positive I was going to pass = on any day, and now I am feeling just normal yuk but still grateful for what I have and for= my loving friends and family. I am so glad to be back.Reneness> > > Dear , et al:> > I am returning from the missing, I hope. It's real late and I am> > about to turn in, so more will come later. But I have some great news> > to share with everyone . . .> > I WON MY SOCIAL SECURITY DISABILITY AT LONG LAST THIS WEEK! This> > is the best thing that has happened to me in a long time.> > There are many details to share and I can't do it now. I would> > have not have been away from here for this long except for chronic> > computer problems and some damned Beagle virus, or some such thing. I> > have finally defeated all these issues and I just had to say hello to> > everyone. I see many new names here and I'm glad to see you all.> > It is 4:49 a.m. and I must sleep now. I'll be back in touch very> > soon, I promise. Until then everyone . . . please take extra good> > care of yourselves tomorrow.> >> > In love and peace,> >> > ie Bear> > > >> > ~~~~ *** ~~~ *** ~~~ *** ~~~~> > The Neurosarcoidosis Community> >> > Live Group Chat:-> > Mondays & Fridays 10pm EST USA> > http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php> >> > Message Archives:-> > http://groups.yahoo.com/group/Neurosarcoidosis/messages> >> > Members Database:-> > Listings of locations, phone numbers, and instant messengers.> > http://groups.yahoo.com/group/Neurosarcoidosis/database> >> >

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Welcome back , we missed you. Luv, DebbieReneness wrote:

and all,I'm not doing very well, but at least I am off of the mtx and the arrava af=ter that. Both had me in constant nausea on top of the crushing fatigue and everything else. =I just started Humira which will take the place of the Remicade which I had developed anti=bodies to. Like I've always felt about this illness for me. It's one step forward and=two steps back.My case manager is trying to arrange a couple of days in hospital so I can =catch up on all of the specialist exams I never get around to because I barely sit up, let =alone walk around and stay in a waiting room. I had a urine catch which was supposed to be f=or calcium but instead they checked it for protien. Even though my specimen catch was a w=hopping six liters (I eat crushed ice all day to help with dry mouth and this odd heat

=without fever that has moved deep inside of me). The protien level was two and one half times =the cut off for high. Also, my last MRI was inconclusive because of motion, but I warned t=he techs and they taped my forehead and chin down but good. if I have a tremor that stro=ng, I want a neurologist to look at it. My liver enzymes have been climbing, and my kid=neys and liver are usually very tender. I must see a GI, a urologist or renal specialist.=If all that is not enough, my cough is acting up and I am concerned about my central apnea ret=urning. At least those two docs (sarc and sleep apnea pulmonologists) already work wit=h the IU sarc clinic. I imagine I will here what's happening early this coming week.I have missed everyone so much -- I know that's why my generally frugal hus=band went all out on this great laptop and the wireless networking. I can just lie here =like a lady of leisure

and change to any position I need. Plus I was pulling my hair out =just watching tv every day, all day since December! Also, that sweetie totally redid the sc=reened in patio furniture -- redid the support ropes and bought new pads for everything, in=cluding the glider. My eyes aren't too great for reading books (morelike my hands are =too weak to hold the books open) and I can now just take this lovely machine with me.So, sum it up, when I was on the arrava I was positive I was going to pass =on any day, and now I am feeling just normal yuk but still grateful for what I have and for=my loving friends and family. I am so glad to be back.Reneness> > > Dear , et al:> > I am returning from the missing, I hope. It's real late and I am> > about to turn in, so more will come later. But I have some great news> > to share with everyone . . .> > I WON MY SOCIAL SECURITY DISABILITY AT LONG LAST THIS WEEK! This> > is the best thing that has happened to me in a long time.> > There are many details to share and I can't do it now. I would> > have not have been away from here for this long except for chronic> > computer problems and

some damned Beagle virus, or some such thing. I> > have finally defeated all these issues and I just had to say hello to> > everyone. I see many new names here and I'm glad to see you all.> > It is 4:49 a.m. and I must sleep now. I'll be back in touch very> > soon, I promise. Until then everyone . . . please take extra good> > care of yourselves tomorrow.> >> > In love and peace,> >> > ie Bear> > > >> > ~~~~ *** ~~~ *** ~~~ *** ~~~~> > The Neurosarcoidosis Community> >> > Live Group Chat:-> > Mondays & Fridays 10pm EST USA> > http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php> >> > Message Archives:-> > http://groups.yahoo.com/group/Neurosarcoidosis/messages> >> > Members Database:-> > Listings of locations, phone numbers, and instant

messengers.> > http://groups.yahoo.com/group/Neurosarcoidosis/database> >> >

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Welcome back , we missed you. Luv, DebbieReneness wrote:

and all,I'm not doing very well, but at least I am off of the mtx and the arrava af=ter that. Both had me in constant nausea on top of the crushing fatigue and everything else. =I just started Humira which will take the place of the Remicade which I had developed anti=bodies to. Like I've always felt about this illness for me. It's one step forward and=two steps back.My case manager is trying to arrange a couple of days in hospital so I can =catch up on all of the specialist exams I never get around to because I barely sit up, let =alone walk around and stay in a waiting room. I had a urine catch which was supposed to be f=or calcium but instead they checked it for protien. Even though my specimen catch was a w=hopping six liters (I eat crushed ice all day to help with dry mouth and this odd heat

=without fever that has moved deep inside of me). The protien level was two and one half times =the cut off for high. Also, my last MRI was inconclusive because of motion, but I warned t=he techs and they taped my forehead and chin down but good. if I have a tremor that stro=ng, I want a neurologist to look at it. My liver enzymes have been climbing, and my kid=neys and liver are usually very tender. I must see a GI, a urologist or renal specialist.=If all that is not enough, my cough is acting up and I am concerned about my central apnea ret=urning. At least those two docs (sarc and sleep apnea pulmonologists) already work wit=h the IU sarc clinic. I imagine I will here what's happening early this coming week.I have missed everyone so much -- I know that's why my generally frugal hus=band went all out on this great laptop and the wireless networking. I can just lie here =like a lady of leisure

and change to any position I need. Plus I was pulling my hair out =just watching tv every day, all day since December! Also, that sweetie totally redid the sc=reened in patio furniture -- redid the support ropes and bought new pads for everything, in=cluding the glider. My eyes aren't too great for reading books (morelike my hands are =too weak to hold the books open) and I can now just take this lovely machine with me.So, sum it up, when I was on the arrava I was positive I was going to pass =on any day, and now I am feeling just normal yuk but still grateful for what I have and for=my loving friends and family. I am so glad to be back.Reneness> > > Dear , et al:> > I am returning from the missing, I hope. It's real late and I am> > about to turn in, so more will come later. But I have some great news> > to share with everyone . . .> > I WON MY SOCIAL SECURITY DISABILITY AT LONG LAST THIS WEEK! This> > is the best thing that has happened to me in a long time.> > There are many details to share and I can't do it now. I would> > have not have been away from here for this long except for chronic> > computer problems and

some damned Beagle virus, or some such thing. I> > have finally defeated all these issues and I just had to say hello to> > everyone. I see many new names here and I'm glad to see you all.> > It is 4:49 a.m. and I must sleep now. I'll be back in touch very> > soon, I promise. Until then everyone . . . please take extra good> > care of yourselves tomorrow.> >> > In love and peace,> >> > ie Bear> > > >> > ~~~~ *** ~~~ *** ~~~ *** ~~~~> > The Neurosarcoidosis Community> >> > Live Group Chat:-> > Mondays & Fridays 10pm EST USA> > http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php> >> > Message Archives:-> > http://groups.yahoo.com/group/Neurosarcoidosis/messages> >> > Members Database:-> > Listings of locations, phone numbers, and instant

messengers.> > http://groups.yahoo.com/group/Neurosarcoidosis/database> >> >

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> > Love, like the ocean reaching out to the horizon, like the sunset

> that

> > wraps around you in a gently hug of yellow, orange, pink, purple, and

> > red, like the air -- the fresh sea air which makes one want to

> swallow

> > rather than breathe... it is so soulful and filled with nourishment.

> > This is the love I have for you and all who have suffered the

> > indiscribable and endured with grace to this day.

> > I love you, I am proud of you, and I am so humbled by all that you do

> > and all that you are.

> > 

> > WELLER, WELLER, WELLER, OY, OY, OY

> > RENENESS, GODDESS OF THE MEMORY OF ALL WE HAVE DONE AND ALL WE WILL

> DO.

> > 

> > 

> > 

> > 

> > ~~~~ *** ~~~ *** ~~~ *** ~~~~

> > The Neurosarcoidosis Community

> > 

> > Live Group Chat:-

> > Mondays & Fridays 10pm EST USA

> > http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php

> > 

> > Message Archives:-

> > http://groups.yahoo.com/group/Neurosarcoidosis/messages

> > 

> > Members Database:-

> > Listings of locations, phone numbers, and instant messengers.

> > http://groups.yahoo.com/group/Neurosarcoidosis/database

> > 

> >

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Guest guest

> > Love, like the ocean reaching out to the horizon, like the sunset

> that

> > wraps around you in a gently hug of yellow, orange, pink, purple, and

> > red, like the air -- the fresh sea air which makes one want to

> swallow

> > rather than breathe... it is so soulful and filled with nourishment.

> > This is the love I have for you and all who have suffered the

> > indiscribable and endured with grace to this day.

> > I love you, I am proud of you, and I am so humbled by all that you do

> > and all that you are.

> > 

> > WELLER, WELLER, WELLER, OY, OY, OY

> > RENENESS, GODDESS OF THE MEMORY OF ALL WE HAVE DONE AND ALL WE WILL

> DO.

> > 

> > 

> > 

> > 

> > ~~~~ *** ~~~ *** ~~~ *** ~~~~

> > The Neurosarcoidosis Community

> > 

> > Live Group Chat:-

> > Mondays & Fridays 10pm EST USA

> > http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php

> > 

> > Message Archives:-

> > http://groups.yahoo.com/group/Neurosarcoidosis/messages

> > 

> > Members Database:-

> > Listings of locations, phone numbers, and instant messengers.

> > http://groups.yahoo.com/group/Neurosarcoidosis/database

> > 

> >

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Reneness,

So glad to hear from you and so sorry you are having such a hard time with this old sarc monster, you are in my prayers sweetie and you have certainly been in my thoughts please take good care of yourself and keep us posted when you can.

Love ya and hugs,

Faith makes all things possible,Hope makes all things bright,Love makes all things easy.............

Jan.......

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Love, like the ocean reaching out to the horizon, like the sunset > that> > wraps around you in a gently hug of yellow, orange, pink, purple, and> > red, like the air -- the fresh sea air which makes one want to > swallow> > rather than breathe... it is so soulful and filled with nourishment.> > This is the love I have for you and all who have suffered the> > indiscribable and endured with grace to this day.> > I love you, I am proud of you, and I am so humbled by all that you do> > and all that you are.

How Lovely! thank you.

Jeri

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Guest guest

Love, like the ocean reaching out to the horizon, like the sunset > that> > wraps around you in a gently hug of yellow, orange, pink, purple, and> > red, like the air -- the fresh sea air which makes one want to > swallow> > rather than breathe... it is so soulful and filled with nourishment.> > This is the love I have for you and all who have suffered the> > indiscribable and endured with grace to this day.> > I love you, I am proud of you, and I am so humbled by all that you do> > and all that you are.

How Lovely! thank you.

Jeri

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Guest guest

Jan,

Really kind of you to write. In catching up with old posts I see

you've been through a lot as well. All I can add is the idea that we

can all be vessels of endless love no matter how sick we are.

Sending love your way,

REneness

> Reneness,

> So glad to hear from you and so sorry you are having such a hard time

> with this old sarc monster, you are in my prayers sweetie and you have

> certainly been in my thoughts please take good care of yourself and

> keep us posted when you can.

> Love ya and hugs,

>  

> Faith makes all things possible,

> Hope makes all things bright,

> Love makes all things easy.............

>  

> Jan.......

>

>

> ~~~~ *** ~~~ *** ~~~ *** ~~~~

> The Neurosarcoidosis Community

>

> Live Group Chat:-

> Mondays & Fridays 10pm EST USA

> http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php

>

> Message Archives:-

> http://groups.yahoo.com/group/Neurosarcoidosis/messages

>

> Members Database:-

> Listings of locations, phone numbers, and instant messengers.

> http://groups.yahoo.com/group/Neurosarcoidosis/database

>

>

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Guest guest

Jan,

Really kind of you to write. In catching up with old posts I see

you've been through a lot as well. All I can add is the idea that we

can all be vessels of endless love no matter how sick we are.

Sending love your way,

REneness

> Reneness,

> So glad to hear from you and so sorry you are having such a hard time

> with this old sarc monster, you are in my prayers sweetie and you have

> certainly been in my thoughts please take good care of yourself and

> keep us posted when you can.

> Love ya and hugs,

>  

> Faith makes all things possible,

> Hope makes all things bright,

> Love makes all things easy.............

>  

> Jan.......

>

>

> ~~~~ *** ~~~ *** ~~~ *** ~~~~

> The Neurosarcoidosis Community

>

> Live Group Chat:-

> Mondays & Fridays 10pm EST USA

> http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php

>

> Message Archives:-

> http://groups.yahoo.com/group/Neurosarcoidosis/messages

>

> Members Database:-

> Listings of locations, phone numbers, and instant messengers.

> http://groups.yahoo.com/group/Neurosarcoidosis/database

>

>

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Guest guest

thanks mucho. I mean all of it.

> In a message dated 6/28/04 1:46:30 PM Eastern Daylight Time,

> rkelty@... writes:

> Love, like the ocean reaching out to the horizon, like the sunset

> > that

> > > wraps around you in a gently hug of yellow, orange, pink, purple,

> and

> > > red, like the air -- the fresh sea air which makes one want to

> > swallow

> > > rather than breathe... it is so soulful and filled with

> nourishment.

> > > This is the love I have for you and all who have suffered the

> > > indiscribable and endured with grace to this day.

> > > I love you, I am proud of you, and I am so humbled by all that you

> do

> > > and all that you are.

> How Lovely!  thank you.

>  

> Jeri

>

>

> ~~~~ *** ~~~ *** ~~~ *** ~~~~

> The Neurosarcoidosis Community

>

> Live Group Chat:-

> Mondays & Fridays 10pm EST USA

> http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php

>

> Message Archives:-

> http://groups.yahoo.com/group/Neurosarcoidosis/messages

>

> Members Database:-

> Listings of locations, phone numbers, and instant messengers.

> http://groups.yahoo.com/group/Neurosarcoidosis/database

>

>

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Guest guest

thanks mucho. I mean all of it.

> In a message dated 6/28/04 1:46:30 PM Eastern Daylight Time,

> rkelty@... writes:

> Love, like the ocean reaching out to the horizon, like the sunset

> > that

> > > wraps around you in a gently hug of yellow, orange, pink, purple,

> and

> > > red, like the air -- the fresh sea air which makes one want to

> > swallow

> > > rather than breathe... it is so soulful and filled with

> nourishment.

> > > This is the love I have for you and all who have suffered the

> > > indiscribable and endured with grace to this day.

> > > I love you, I am proud of you, and I am so humbled by all that you

> do

> > > and all that you are.

> How Lovely!  thank you.

>  

> Jeri

>

>

> ~~~~ *** ~~~ *** ~~~ *** ~~~~

> The Neurosarcoidosis Community

>

> Live Group Chat:-

> Mondays & Fridays 10pm EST USA

> http://health.groups.yahoo.com/group/Neurosarcoidosis/chat.php

>

> Message Archives:-

> http://groups.yahoo.com/group/Neurosarcoidosis/messages

>

> Members Database:-

> Listings of locations, phone numbers, and instant messengers.

> http://groups.yahoo.com/group/Neurosarcoidosis/database

>

>

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