RE: Liz S

[Guest guest]

My dragons name is "It" like the monster from the King novel IT . It makes my life miserable so I am ready to rid my body of his ass connie mcclain <crochetlady1001@...> wrote:

eliz what did you name him so you can scream die_____ you ___ a__h____!!! evict his ass. connie

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

I wish I had contact with my chidhood friends ( two of them) But when I moved to Nevada I lost all contact ... So I live out of the state of my childhood and now depend on my online friends . But for the most part most of those I knew in my childhood were losers so it is no great loss .. I do miss being near my family and life in the desert gets lonely , but on treatment its the online friends that are the ones who get me through it . Friends and family all seem to dissapear when one is sick and in need of care . LOL I will find out my treatment start date on Thursday , and then it all begins again .hehe Davies <lisamarie64@...> wrote:

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

Alright hon you know what to expect the first night of the first shot. Severe chills,etc.I felt like someone dumped me in the fridge a few hours after the first shot.I needed tons of blankets and a hot water bottle.It only happens with the first shot.Has the doctor put you on antidepressents yet.I wasn't allowed them cause I was on a trial but most of the rest of the group had them and it made a real difference during treatment.You got lots of groceries in the hourse that is easy to prepare.Hope you have a blender so you can make milk shakes on the days your stomach is upset.Wish I could be there to help you and start drinking lots of water now so that you are used to it for treatment.Were here hon.

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of elizabeth savageSent: October 2, 2005 12:55 AMHepatitis CSupportGroupForDummies Subject: RE: Liz S

I wish I had contact with my chidhood friends ( two of them) But when I moved to Nevada I lost all contact ... So I live out of the state of my childhood and now depend on my online friends . But for the most part most of those I knew in my childhood were losers so it is no great loss .. I do miss being near my family and life in the desert gets lonely , but on treatment its the online friends that are the ones who get me through it . Friends and family all seem to dissapear when one is sick and in need of care . LOL I will find out my treatment start date on Thursday , and then it all begins again .hehe Davies <lisamarie64@...> wrote:

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

for GoodClick here to donate to the Hurricane Katrina relief effort.

[Guest guest]

I think we all pretty well feel the same way about our hep family.Everyone is unique and very special.My family here is the best family a person could ask for ,the very best

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of DaviesSent: October 1, 2005 7:40 PMHepatitis CSupportGroupForDummies Subject: RE: Liz S

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

elizabeth savage <elizabethnv1@...> wrote:

How very touching and kind your post to me is , thank you so much for thinking of me in your prayers . I have faith but I know that the future is going to be hard , I think that is why my husbands company sent me with him to Europe this time . More than likely I will only be on treatment for a short time , LOL I never can keep my white blood cells up or my weight for that matter . But this time I have gained 40lbs so I have the excess to lose and not get to sick . It is a pleasure to meet you and I look forward to more correspondances from you in the future , I can never have enough friends ... Liz S Davies <lisamarie64@...> wrote:

Liz,

I hope you don't mind if I call you by that name. My name is which also comes from . Anyway, although I am probably new to this group to you - I am an oldie, just a few months after Liz and Deb started it. I just haven't been around for almost a year now.

I have been reading all the post that I can over the last week or so -have been extremely busy taking care of ill Mother. Nonetheless, I couldn't help but want to say hello to you.

My heart is with you Dear - I am so touched by your strenght and courage. In fact, lately I have found myself going through trials that I sometimes feel I can't handle - then I think of your strenght and it gives me strenght and courage.

I just wanted to let you know that, and also to tell you that you are in my daily prayers. Keep the faith - and know that this time, could just be the "Miracle".

Anyway - I just wanted to say hello and let you know that I am here and if I can help you in anyway - I would be happy to do so...

May God Bless you and keep you safe on this journey..

Love, Hugs, and prayers...

Marie

for GoodClick here to donate to the Hurricane Katrina relief effort.

for GoodClick here to donate to the Hurricane Katrina relief effort.

[Guest guest]

Ditto.

De

RE:

Liz S

I think we all pretty

well feel the same way about our hep family.Everyone is unique and very

special.My family here is the best family a person could ask for ,the very best

Gail

[Guest guest]

yup

--- Hepatitis CSupportGroupForDummies

<dmotley@...> wrote:

> Ditto.

>

>

>

> De

>

> RE: Liz

S

>

>

>

> I think we all pretty well feel the same way about

our hep family.Everyone

> is unique and very special.My family here is the

best family a person could

> ask for ,the very best

>

> Gail

>

>

> _____

>

>

__________________________________

- PC Magazine Editors' Choice 2005

http://mail.

[Guest guest]

yup

--- Hepatitis CSupportGroupForDummies

<dmotley@...> wrote:

> Ditto.

>

>

>

> De

>

> RE: Liz

S

>

>

>

> I think we all pretty well feel the same way about

our hep family.Everyone

> is unique and very special.My family here is the

best family a person could

> ask for ,the very best

>

> Gail

>

>

> _____

>

>

__________________________________

- PC Magazine Editors' Choice 2005

http://mail.

[Guest guest]

I remember being cold all the time , and I mean cold !! My husband and children just about make the house run without me . There is not much I can eat while on treatment , I get taste perversion really badly but my husband will stockup on the bubblegum flavored popsickels and gatorade . I tend to get sick every shot like it was the first and my white blood cells by the end of the first week are under 2.0 . Which means I get to have injections of neupogen and all the long bone pain that goes with it , LOL Oh joy oh joy , I just cant wait ...rofl I have a script for Zophran because I still suffer from alot of nausea , but as far as a antidepressant ..........not needed , I usually get lonesome and not sad so I get online and chat . But I know that each time I treat it may be different so I will probably have a script for andi'd just in case I start walking around the house crying ,hehe . Your the best , take care .........if ya'll dont hear from me in the morning its cause i

didnt have a chance before we head home .gail <gaila@...> wrote

Alright hon you know what to expect the first night of the first shot. Severe chills,etc.I felt like someone dumped me in the fridge a few hours after the first shot.I needed tons of blankets and a hot water bottle.It only happens with the first shot.Has the doctor put you on antidepressents yet.I wasn't allowed them cause I was on a trial but most of the rest of the group had them and it made a real difference during treatment.You got lots of groceries in the hourse that is easy to prepare.Hope you have a blender so you can make milk shakes on the days your stomach is upset.Wish I could be there to help you and start drinking lots of water now so that you are used to it for treatment.Were here hon.

Gail

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

I remember being cold all the time , and I mean cold !! My husband and children just about make the house run without me . There is not much I can eat while on treatment , I get taste perversion really badly but my husband will stockup on the bubblegum flavored popsickels and gatorade . I tend to get sick every shot like it was the first and my white blood cells by the end of the first week are under 2.0 . Which means I get to have injections of neupogen and all the long bone pain that goes with it , LOL Oh joy oh joy , I just cant wait ...rofl I have a script for Zophran because I still suffer from alot of nausea , but as far as a antidepressant ..........not needed , I usually get lonesome and not sad so I get online and chat . But I know that each time I treat it may be different so I will probably have a script for andi'd just in case I start walking around the house crying ,hehe . Your the best , take care .........if ya'll dont hear from me in the morning its cause i

didnt have a chance before we head home .gail <gaila@...> wrote

Alright hon you know what to expect the first night of the first shot. Severe chills,etc.I felt like someone dumped me in the fridge a few hours after the first shot.I needed tons of blankets and a hot water bottle.It only happens with the first shot.Has the doctor put you on antidepressents yet.I wasn't allowed them cause I was on a trial but most of the rest of the group had them and it made a real difference during treatment.You got lots of groceries in the hourse that is easy to prepare.Hope you have a blender so you can make milk shakes on the days your stomach is upset.Wish I could be there to help you and start drinking lots of water now so that you are used to it for treatment.Were here hon.

Gail

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

oops my bad, you already mentioned that. connieelizabeth savage <elizabethnv1@...> wrote:

My dragons name is "It" like the monster from the King novel IT . It makes my life miserable so I am ready to rid my body of his ass connie mcclain <crochetlady1001@...> wrote:

eliz what did you name him so you can scream die_____ you ___ a__h____!!! evict his ass. connie

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

oops my bad, you already mentioned that. connieelizabeth savage <elizabethnv1@...> wrote:

My dragons name is "It" like the monster from the King novel IT . It makes my life miserable so I am ready to rid my body of his ass connie mcclain <crochetlady1001@...> wrote:

eliz what did you name him so you can scream die_____ you ___ a__h____!!! evict his ass. connie

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

Yeah what Gail said about the water, its the number one most important thing to forceyourself to do. conniegail <gaila@...> wrote:

Alright hon you know what to expect the first night of the first shot. Severe chills,etc.I felt like someone dumped me in the fridge a few hours after the first shot.I needed tons of blankets and a hot water bottle.It only happens with the first shot.Has the doctor put you on antidepressents yet.I wasn't allowed them cause I was on a trial but most of the rest of the group had them and it made a real difference during treatment.You got lots of groceries in the hourse that is easy to prepare.Hope you have a blender so you can make milk shakes on the days your stomach is upset.Wish I could be there to help you and start drinking lots of water now so that you are used to it for treatment.Were here hon.

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of elizabeth savageSent: October 2, 2005 12:55 AMHepatitis CSupportGroupForDummies Subject: RE: Liz S

I wish I had contact with my chidhood friends ( two of them) But when I moved to Nevada I lost all contact ... So I live out of the state of my childhood and now depend on my online friends . But for the most part most of those I knew in my childhood were losers so it is no great loss .. I do miss being near my family and life in the desert gets lonely , but on treatment its the online friends that are the ones who get me through it . Friends and family all seem to dissapear when one is sick and in need of care . LOL I will find out my treatment start date on Thursday , and then it all begins again .hehe Davies <lisamarie64@...> wrote:

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

Yeah what Gail said about the water, its the number one most important thing to forceyourself to do. conniegail <gaila@...> wrote:

Alright hon you know what to expect the first night of the first shot. Severe chills,etc.I felt like someone dumped me in the fridge a few hours after the first shot.I needed tons of blankets and a hot water bottle.It only happens with the first shot.Has the doctor put you on antidepressents yet.I wasn't allowed them cause I was on a trial but most of the rest of the group had them and it made a real difference during treatment.You got lots of groceries in the hourse that is easy to prepare.Hope you have a blender so you can make milk shakes on the days your stomach is upset.Wish I could be there to help you and start drinking lots of water now so that you are used to it for treatment.Were here hon.

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of elizabeth savageSent: October 2, 2005 12:55 AMHepatitis CSupportGroupForDummies Subject: RE: Liz S

I wish I had contact with my chidhood friends ( two of them) But when I moved to Nevada I lost all contact ... So I live out of the state of my childhood and now depend on my online friends . But for the most part most of those I knew in my childhood were losers so it is no great loss .. I do miss being near my family and life in the desert gets lonely , but on treatment its the online friends that are the ones who get me through it . Friends and family all seem to dissapear when one is sick and in need of care . LOL I will find out my treatment start date on Thursday , and then it all begins again .hehe Davies <lisamarie64@...> wrote:

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

Yeah what Gail said about the water, its the number one most important thing to forceyourself to do. conniegail <gaila@...> wrote:

Alright hon you know what to expect the first night of the first shot. Severe chills,etc.I felt like someone dumped me in the fridge a few hours after the first shot.I needed tons of blankets and a hot water bottle.It only happens with the first shot.Has the doctor put you on antidepressents yet.I wasn't allowed them cause I was on a trial but most of the rest of the group had them and it made a real difference during treatment.You got lots of groceries in the hourse that is easy to prepare.Hope you have a blender so you can make milk shakes on the days your stomach is upset.Wish I could be there to help you and start drinking lots of water now so that you are used to it for treatment.Were here hon.

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of elizabeth savageSent: October 2, 2005 12:55 AMHepatitis CSupportGroupForDummies Subject: RE: Liz S

I wish I had contact with my chidhood friends ( two of them) But when I moved to Nevada I lost all contact ... So I live out of the state of my childhood and now depend on my online friends . But for the most part most of those I knew in my childhood were losers so it is no great loss .. I do miss being near my family and life in the desert gets lonely , but on treatment its the online friends that are the ones who get me through it . Friends and family all seem to dissapear when one is sick and in need of care . LOL I will find out my treatment start date on Thursday , and then it all begins again .hehe Davies <lisamarie64@...> wrote:

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

Beats the livin crap outa my blood family, thats for sure. conniegail <gaila@...> wrote:

I think we all pretty well feel the same way about our hep family.Everyone is unique and very special.My family here is the best family a person could ask for ,the very best

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of DaviesSent: October 1, 2005 7:40 PMHepatitis CSupportGroupForDummies Subject: RE: Liz S

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

elizabeth savage <elizabethnv1@...> wrote:

How very touching and kind your post to me is , thank you so much for thinking of me in your prayers . I have faith but I know that the future is going to be hard , I think that is why my husbands company sent me with him to Europe this time . More than likely I will only be on treatment for a short time , LOL I never can keep my white blood cells up or my weight for that matter . But this time I have gained 40lbs so I have the excess to lose and not get to sick . It is a pleasure to meet you and I look forward to more correspondances from you in the future , I can never have enough friends ... Liz S Davies <lisamarie64@...> wrote:

Liz,

I hope you don't mind if I call you by that name. My name is which also comes from . Anyway, although I am probably new to this group to you - I am an oldie, just a few months after Liz and Deb started it. I just haven't been around for almost a year now.

I have been reading all the post that I can over the last week or so -have been extremely busy taking care of ill Mother. Nonetheless, I couldn't help but want to say hello to you.

My heart is with you Dear - I am so touched by your strenght and courage. In fact, lately I have found myself going through trials that I sometimes feel I can't handle - then I think of your strenght and it gives me strenght and courage.

I just wanted to let you know that, and also to tell you that you are in my daily prayers. Keep the faith - and know that this time, could just be the "Miracle".

Anyway - I just wanted to say hello and let you know that I am here and if I can help you in anyway - I would be happy to do so...

May God Bless you and keep you safe on this journey..

Love, Hugs, and prayers...

Marie

for GoodClick here to donate to the Hurricane Katrina relief effort.

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

Beats the livin crap outa my blood family, thats for sure. conniegail <gaila@...> wrote:

I think we all pretty well feel the same way about our hep family.Everyone is unique and very special.My family here is the best family a person could ask for ,the very best

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of DaviesSent: October 1, 2005 7:40 PMHepatitis CSupportGroupForDummies Subject: RE: Liz S

Liz,

I have to agree with you - we can never have too many friends. I am one of those people that use to surround myself with people constantly. I have always loved people in general, through the years I have learned that true friends aren't that easy to come by. I have one good friend that I have had since I was 15 and now 41 - we still to this day remain as close as ever, although miles have kept us apart. However, I must say that through My having Hep C - I have gotten to know some of the best people I have ever come accross in my life.

I have always said, even when I was as sick as a dog, and couldn't even make it to the bathroom without help - that even if I could turn back the hands of the clock and never have Hep - I wouldn't do it! I made too many wonderful friends, and have learned so much about myself, others, and life it'self - this diesease has humbled me in ways that I didn't ever imagine.

And I am like in you - God forbid but if for some reason my hep becomes active again - I will keep trying, I will never give up or give in....

And I already know you are doing the same.

Your courage is one I will never forget.

I look forward to knowing you also....

Take care of you and I will keep in touch

May God Bless and keep you and yours

Love, Hugs, a nd Prayers to all

Marie

elizabeth savage <elizabethnv1@...> wrote:

How very touching and kind your post to me is , thank you so much for thinking of me in your prayers . I have faith but I know that the future is going to be hard , I think that is why my husbands company sent me with him to Europe this time . More than likely I will only be on treatment for a short time , LOL I never can keep my white blood cells up or my weight for that matter . But this time I have gained 40lbs so I have the excess to lose and not get to sick . It is a pleasure to meet you and I look forward to more correspondances from you in the future , I can never have enough friends ... Liz S Davies <lisamarie64@...> wrote:

Liz,

I hope you don't mind if I call you by that name. My name is which also comes from . Anyway, although I am probably new to this group to you - I am an oldie, just a few months after Liz and Deb started it. I just haven't been around for almost a year now.

I have been reading all the post that I can over the last week or so -have been extremely busy taking care of ill Mother. Nonetheless, I couldn't help but want to say hello to you.

My heart is with you Dear - I am so touched by your strenght and courage. In fact, lately I have found myself going through trials that I sometimes feel I can't handle - then I think of your strenght and it gives me strenght and courage.

I just wanted to let you know that, and also to tell you that you are in my daily prayers. Keep the faith - and know that this time, could just be the "Miracle".

Anyway - I just wanted to say hello and let you know that I am here and if I can help you in anyway - I would be happy to do so...

May God Bless you and keep you safe on this journey..

Love, Hugs, and prayers...

Marie

for GoodClick here to donate to the Hurricane Katrina relief effort.

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

ohh shoot when did I tell ya , rofl ?? I dont remember telling anyone ,geeze brain foggies here connie mcclain <crochetlady1001@...> wrote:

oops my bad, you already mentioned that. connie

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

ohh shoot when did I tell ya , rofl ?? I dont remember telling anyone ,geeze brain foggies here connie mcclain <crochetlady1001@...> wrote:

oops my bad, you already mentioned that. connie

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

dam i THINK you did, cuz i remember it. and the clouds preeeevail. connie elizabeth savage <elizabethnv1@...> wrote:

ohh shoot when did I tell ya , rofl ?? I dont remember telling anyone ,geeze brain foggies here connie mcclain <crochetlady1001@...> wrote:

oops my bad, you already mentioned that. connie

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

dam i THINK you did, cuz i remember it. and the clouds preeeevail. connie elizabeth savage <elizabethnv1@...> wrote:

ohh shoot when did I tell ya , rofl ?? I dont remember telling anyone ,geeze brain foggies here connie mcclain <crochetlady1001@...> wrote:

oops my bad, you already mentioned that. connie

for GoodClick here to donate to the Hurricane Katrina relief effort. The light at the end of the tunnel may be you

[Guest guest]

NO way ............I drink gatorade only to this day . And when I am on treatment I have to drink more of it especially since I just about stop eating food . It gives me back the electrolytes I lose from vomiting and dehydration . Plus the little bit of sugar keeps my blood sugar from getting to low ..I keep myself hydrated good , thats about the only thing I do well on treatment ,lolconnie mcclain <crochetlady1001@...> wrote:

Yeah what Gail said about the water, its the number one most important thing to forceyourself to do. connie

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

I think I should start writing stuff down again , I dont need treatment to give me the foggies . But I do need a notebook with everything written for me , hahahaconnie mcclain <crochetlady1001@...> wrote:

dam i THINK you did, cuz i remember it. and the clouds preeeevail. connie

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

I agree on the hydration......I do a gallon of water every

day. It might be the reason I have had an easy time on tx.

Dick

At 11:25 AM 10/2/05, you wrote:

NO way ............I drink

gatorade only to this day . And when I am on treatment I have to drink

more of it especially since I just about stop eating food . It gives me

back the electrolytes I lose from vomiting and dehydration . Plus the

little bit of sugar keeps my blood sugar from getting to low ..I keep

myself hydrated good , thats about the only thing I do well on treatment

,lol

connie mcclain <crochetlady1001@...>

wrote:

Yeah what Gail said about the water, its the number one most

important thing to forceyourself to do. connie

[Guest guest]

The second time I treated I drank alot of water and it didnt keep me from having severe muscle pain, but when I started drinking nothing but gatorade types of drinks the muscle aches stopped being as bad. I still drink only gatorade I gave up soda .But I think it helped me cause I wasnt eating , gatorade isnt for everyone .Water is sometimes just what the doctor ordered Dick Southern <southern@...> wrote:

I agree on the hydration......I do a gallon of water every day. It might be the reason I have had an easy time on tx.Dick

for Good Click here to donate to the Hurricane Katrina relief effort.

[Guest guest]

Gatorade is fine.

It has lots of potassium in it which combats muscle cramps.

It was developed by the Univ. of Miami for their football team ( hence the name gatorade) to use during summer practice when the players were getting too dehydrated from the heat and were getting alot of leg cramps.

Bananas also have alot of potassium.

If you are using any sort of diuretics ( potassium strippers) you have to replace it.

Pharm 101. U-Mass.

Go Sox,

dannyelizabeth savage <elizabethnv1@...> wrote:

The second time I treated I drank alot of water and it didnt keep me from having severe muscle pain, but when I started drinking nothing but gatorade types of drinks the muscle aches stopped being as bad. I still drink only gatorade I gave up soda .But I think it helped me cause I wasnt eating , gatorade isnt for everyone .Water is sometimes just what the doctor ordered Dick Southern <southern@...> wrote: I agree on the hydration......I do a gallon of water every day. It might be the reason I have had an easy time on tx.Dick

for GoodClick here to donate to the Hurricane Katrina relief effort.

for Good Click here to donate to the Hurricane Katrina relief effort.