Re: Thinking of you all

[Guest guest]

Hmm, rest, what is that? As long as I can do something I will not

rest, life is too short to spend it all on resting

I am not really wise... I just pretend

I know, my little baby brother is the BEST, you all should be very

jealous! I mean it, he's the sweetest thing ever *proud sister*

Talk to you later

Loves and Hugs,

Jo

> Joanna, SOOOOOOO glad you are feeling better! You

> really scared us. Boy, you have one special brother.

> And a dr that makes house calls! Rest up now, and

> really take it easy- like I need to tell you- I wish

> there was something I could do to help. You are

> another one, " just a girl " , and so wise. Please hang

> in there, and share with us. My thoughts & prayers are

> with you.

[Guest guest]

,

you know we love you and will do whatever we can to help you through this.

((((((((((((((((((((LISA)))))))))))))))))))))))

L

& H,

-----Original

Message-----

From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ] On Behalf Of Davies

Sent: Saturday, February 25, 2006

6:03 AM

Hepatitis CSupportGroupForDummies

Subject:

Thinking of you all

Ok Gang, I have

some explaining to do - this I know. First of all I want to say that I

am sorry for shutting myself out and pulling away today, when I promised to

keep you all posted as to my results. I know Del wrote a very kind

letter to you all, and I am very grateful to him to do something so kind for

me.

However - there will never be enough words to explain my gratitude for

all you have done for me in the past - you all are the reason I made it

though treatment as long as I did. I could have never walked this road

alone, it was much more than I could of handled. You guys were the

greatest, and even when on treatment and I had those days, that seemed like

endless as the time, that I could not come on and talk about things - when I

did return, you never judged me, you accepted me back with open arms, and you

each gave of part of yourselves to help me pull through when all seemed

so hopeless.

As you know today I received the lovely new that I not only have

hep again, but my viral load is over 6 million. It never got over a1

mill before. It's pretty much set in stone for me that I must do

treatment again, I don't feel there is an option. I have 2 wonderful

and amazing grand daughters that I live for - they are so much a part of

myself and my soul.

And I want to watch them grow up, I want for them to know the love that

I had for them. I don't think I could bare it otherwise.

Along with the hep, I was also diagnosed with EVB - which is also known

as Mona. That is extremely taxing on my energy and fatigue, For

the last two weeks or more I have been off work at Doctor request, I have

been so week that there are days I can't make it down the stairs and to my car.

I didn't have any money saved as I was just recovering from taking care

of my ex when he got cancer and I become his only caretaker for over a year,

and them my Mother becomes seriously ill. So I take what funds I have

left, and move out here with the intention of over seeing her care, and

running her to from appointments, as there is no one else to do it and there

is no free service. Unfortunately she lives at 30 minutes from me,

somedays it can be quite the drive.

I remember that I had all the sides and them some, I am so worried I

will longer be able to help her onve I start the treatment. I

feel guilty and somehow responsible. And I have no other

siblings that are willing to help her. I am blessed and I have an

excellent insurance company, but I have to pay 285.00 a month

for cobra,not for sure how much longer I can afford this.

Everything has just become a complete mess, and I am feeling, angry,

scared, emotionally and phyiscally drained.

Well I guess I should get out my pity party.

And write more when I can be more supportive. And not do so much

whinning. I hope I haven't offended or hurt anyone here by not

writing right away - if so for this I am truly sorry for..

I will always love you guys, and have come to love and respect you all

as my true friends - someone I can depend on.

I am so very blessed and this I do know and realize.

Hope to hear from you all soon

Love, hugs, and prayers

Marie

[Guest guest]

- Sweetie, I know you will always be there for me, you were last time, and beyond the call of duty many times.

I love ya Kido

I have just got to get out of this mess somehow and pull my head up and stand strong - as right now I feel like I have had my ass kicked about 10 times over, if you know what I mean.. LOL but true..

(((((((((((((((()))))))))))))))))))) - My Friend...

Marie

-- RE: Thinking of you all

, you know we love you and will do whatever we can to help you through this.

((((((((((((((((((((LISA)))))))))))))))))))))))

L & H,

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ] On Behalf Of DaviesSent: Saturday, February 25, 2006 6:03 AMHepatitis CSupportGroupForDummies Subject: Thinking of you all

Ok Gang, I have some explaining to do - this I know. First of all I want to say that I am sorry for shutting myself out and pulling away today, when I promised to keep you all posted as to my results. I know Del wrote a very kind letter to you all, and I am very grateful to him to do something so kind for me.

However - there will never be enough words to explain my gratitude for all you have done for me in the past - you all are the reason I made it though treatment as long as I did. I could have never walked this road alone, it was much more than I could of handled. You guys were the greatest, and even when on treatment and I had those days, that seemed like endless as the time, that I could not come on and talk about things - when I did return, you never judged me, you accepted me back with open arms, and you each gave of part of yourselves to help me pull through when all seemed so hopeless.

As you know today I received the lovely new that I not only have hep again, but my viral load is over 6 million. It never got over a1 mill before. It's pretty much set in stone for me that I must do treatment again, I don't feel there is an option. I have 2 wonderful and amazing grand daughters that I live for - they are so much a part of myself and my soul.

And I want to watch them grow up, I want for them to know the love that I had for them. I don't think I could bare it otherwise.

Along with the hep, I was also diagnosed with EVB - which is also known as Mona. That is extremely taxing on my energy and fatigue, For the last two weeks or more I have been off work at Doctor request, I have been so week that there are days I can't make it down the stairs and to my car.

I didn't have any money saved as I was just recovering from taking care of my ex when he got cancer and I become his only caretaker for over a year, and them my Mother becomes seriously ill. So I take what funds I have left, and move out here with the intention of over seeing her care, and running her to from appointments, as there is no one else to do it and there is no free service. Unfortunately she lives at 30 minutes from me, somedays it can be quite the drive.

I remember that I had all the sides and them some, I am so worried I will longer be able to help her onve I start the treatment. I feel guilty and somehow responsible. And I have no other siblings that are willing to help her. I am blessed and I have an excellent insurance company, but I have to pay 285.00 a month for cobra,not for sure how much longer I can afford this.

Everything has just become a complete mess, and I am feeling, angry, scared, emotionally and phyiscally drained.

Well I guess I should get out my pity party.

And write more when I can be more supportive. And not do so much whinning. I hope I haven't offended or hurt anyone here by not writing right away - if so for this I am truly sorry for..

I will always love you guys, and have come to love and respect you all as my true friends - someone I can depend on.

I am so very blessed and this I do know and realize.

Hope to hear from you all soon

Love, hugs, and prayers

Marie

Letter Created By Jeni

Font DC Lindsey

May 2004

[Guest guest]

Gail - thanks so much for the advice and for caring. However, my siblings haven't even called my Mother let alone come to see her since she has been so ill. My only brother hasn't seen her in 20 years. One sister lives 45 minutes from here, and won't come.

When I decided to come out and help her - it was a decision that I felt I could live with. And I did let the others know that Mother was seriously ill and that they may at least want to call or some see her, as the Doctors said she may not be around for another Christmas. I have heard from none of them and neither has my Mother.

I could call them and ask them for help, but I know what the answer would be ahead of time, and it would only be a confrontation that I can't deal with at this time.

I am quite sure that word has gotten around or will soon about my condition, and just as before, there will be no calls, not even to ask if I am ok.

I have always been the rock, the strong one, and now I am weak once again - my family loathes any signs of weakness, not really my siblings fault, just the way my father raised us. Never to ask anyone for anything - always do it yourself. If I were living on a street or alley, and my Father walked by and saw me, he would turn his head and keep walking. Kind of sad but very true.

All I know is I tried to help someone I love out, as usual I am always the caretaker, sometimes so much I forget and neglect . And now I have failed, I have failed my Mother, my children, myself. The list probably could go on and on, but I won't bother.

All I know is I feel numb, I don't think I have let the whole having the "Hep-C" thing back, has really hit me, once again I have been to worried about my Mom and what will happen to her if I am not here for her.

Some how I will just have to get through all of this - it just feels so hopeless at this moment. I feel lonely, scared, tired of trying, this list is endless. I know I shouldn't say all these things, once again it is that pity party wanting to start up - but if I can't tell you all than who can I tell.

I love you guys....

Thanks for listening..

Marie

-- RE: Thinking of you all

Little lady you have a lot to be upset about.It is not fair that none of your other sibblings can help with your mother.You shouldn't be the only one especially with the problems you have right now.Can your mom move in with one of the other sibblings until you are finished treatment?I totally understand how you feel but I also feel everything should not be put on your shoulders.You have to have treatment cause you need a life with your family.Your sibblings should help with your mom so you can get your health back.Think about what your going to say to them and then go for it.

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of DaviesSent: February 25, 2006 3:03 AMHepatitis CSupportGroupForDummies Subject: Thinking of you all

Ok Gang, I have some explaining to do - this I know. First of all I want to say that I am sorry for shutting myself out and pulling away today, when I promised to keep you all posted as to my results. I know Del wrote a very kind letter to you all, and I am very grateful to him to do something so kind for me.

However - there will never be enough words to explain my gratitude for all you have done for me in the past - you all are the reason I made it though treatment as long as I did. I could have never walked this road alone, it was much more than I could of handled. You guys were the greatest, and even when on treatment and I had those days, that seemed like endless as the time, that I could not come on and talk about things - when I did return, you never judged me, you accepted me back with open arms, and you each gave of part of yourselves to help me pull through when all seemed so hopeless.

As you know today I received the lovely new that I not only have hep again, but my viral load is over 6 million. It never got over a1 mill before. It's pretty much set in stone for me that I must do treatment again, I don't feel there is an option. I have 2 wonderful and amazing grand daughters that I live for - they are so much a part of myself and my soul.

And I want to watch them grow up, I want for them to know the love that I had for them. I don't think I could bare it otherwise.

Along with the hep, I was also diagnosed with EVB - which is also known as Mona. That is extremely taxing on my energy and fatigue, For the last two weeks or more I have been off work at Doctor request, I have been so week that there are days I can't make it down the stairs and to my car.

I didn't have any money saved as I was just recovering from taking care of my ex when he got cancer and I become his only caretaker for over a year, and them my Mother becomes seriously ill. So I take what funds I have left, and move out here with the intention of over seeing her care, and running her to from appointments, as there is no one else to do it and there is no free service. Unfortunately she lives at 30 minutes from me, somedays it can be quite the drive.

I remember that I had all the sides and them some, I am so worried I will longer be able to help her onve I start the treatment. I feel guilty and somehow responsible. And I have no other siblings that are willing to help her. I am blessed and I have an excellent insurance company, but I have to pay 285.00 a month for cobra,not for sure how much longer I can afford this.

Everything has just become a complete mess, and I am feeling, angry, scared, emotionally and phyiscally drained.

Well I guess I should get out my pity party.

And write more when I can be more supportive. And not do so much whinning. I hope I haven't offended or hurt anyone here by not writing right away - if so for this I am truly sorry for..

I will always love you guys, and have come to love and respect you all as my true friends - someone I can depend on.

I am so very blessed and this I do know and realize.

Hope to hear from you all soon

Love, hugs, and prayers

Marie

Letter Created By Jeni

Font DC Lindsey

May 2004

Font: CluffHmkBold

Graphic artist unknown

[Guest guest]

Little lady you have a lot to be upset about.It is not fair that none of your other sibblings can help with your mother.You shouldn't be the only one especially with the problems you have right now.Can your mom move in with one of the other sibblings until you are finished treatment?I totally understand how you feel but I also feel everything should not be put on your shoulders.You have to have treatment cause you need a life with your family.Your sibblings should help with your mom so you can get your health back.Think about what your going to say to them and then go for it.

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of DaviesSent: February 25, 2006 3:03 AMHepatitis CSupportGroupForDummies Subject: Thinking of you all

Ok Gang, I have some explaining to do - this I know. First of all I want to say that I am sorry for shutting myself out and pulling away today, when I promised to keep you all posted as to my results. I know Del wrote a very kind letter to you all, and I am very grateful to him to do something so kind for me.

However - there will never be enough words to explain my gratitude for all you have done for me in the past - you all are the reason I made it though treatment as long as I did. I could have never walked this road alone, it was much more than I could of handled. You guys were the greatest, and even when on treatment and I had those days, that seemed like endless as the time, that I could not come on and talk about things - when I did return, you never judged me, you accepted me back with open arms, and you each gave of part of yourselves to help me pull through when all seemed so hopeless.

As you know today I received the lovely new that I not only have hep again, but my viral load is over 6 million. It never got over a1 mill before. It's pretty much set in stone for me that I must do treatment again, I don't feel there is an option. I have 2 wonderful and amazing grand daughters that I live for - they are so much a part of myself and my soul.

And I want to watch them grow up, I want for them to know the love that I had for them. I don't think I could bare it otherwise.

Along with the hep, I was also diagnosed with EVB - which is also known as Mona. That is extremely taxing on my energy and fatigue, For the last two weeks or more I have been off work at Doctor request, I have been so week that there are days I can't make it down the stairs and to my car.

I didn't have any money saved as I was just recovering from taking care of my ex when he got cancer and I become his only caretaker for over a year, and them my Mother becomes seriously ill. So I take what funds I have left, and move out here with the intention of over seeing her care, and running her to from appointments, as there is no one else to do it and there is no free service. Unfortunately she lives at 30 minutes from me, somedays it can be quite the drive.

I remember that I had all the sides and them some, I am so worried I will longer be able to help her onve I start the treatment. I feel guilty and somehow responsible. And I have no other siblings that are willing to help her. I am blessed and I have an excellent insurance company, but I have to pay 285.00 a month for cobra,not for sure how much longer I can afford this.

Everything has just become a complete mess, and I am feeling, angry, scared, emotionally and phyiscally drained.

Well I guess I should get out my pity party.

And write more when I can be more supportive. And not do so much whinning. I hope I haven't offended or hurt anyone here by not writing right away - if so for this I am truly sorry for..

I will always love you guys, and have come to love and respect you all as my true friends - someone I can depend on.

I am so very blessed and this I do know and realize.

Hope to hear from you all soon

Love, hugs, and prayers

Marie

Letter Created By Jeni

Font DC Lindsey

May 2004

[Guest guest]

You haven't failed anyone except yourself because you put yourself last.Your children and grandchildren have to come first when it comes to your health.You are a kind person and also very strong and you have proven it many times.With the new treatments you might be able to work regarless of being on treatment.The treatments seem good to what they used to be.The only energy you might have will only be for the job but at least you will have a pay cheque coming in.They won't put you on the same treatment as before because the virus will have built up an immunity to the last treatment.What kind of damage did you have to your liver on your last biopsy?The last treatment would have put a hold on further damage for a while.Is it possible where your mother can go into a nursing home for now while you are on treatment.They can't refuse her that.Sounds like your father was hard to live with and perhaps that is why your mom left,but couldn't support you guys and had to leave you guys behind to be sure you would be fed and have a roof over your heads.To bad the other sibblings can't look at it the way you do cause later on they are going to have a lot of regrets.Take care hon,but I think the doctor will be delaying treatment until your mono has settled down a bit.You are not wining you are worried like any normal person would be under the circumstances.Something will come up to help you with an answer.

Gail

RE: Thinking of you all

Little lady you have a lot to be upset about.It is not fair that none of your other sibblings can help with your mother.You shouldn't be the only one especially with the problems you have right now.Can your mom move in with one of the other sibblings until you are finished treatment?I totally understand how you feel but I also feel everything should not be put on your shoulders.You have to have treatment cause you need a life with your family.Your sibblings should help with your mom so you can get your health back.Think about what your going to say to them and then go for it.

Gail

-----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ]On Behalf Of DaviesSent: February 25, 2006 3:03 AMHepatitis CSupportGroupForDummies Subject: Thinking of you all

Ok Gang, I have some explaining to do - this I know. First of all I want to say that I am sorry for shutting myself out and pulling away today, when I promised to keep you all posted as to my results. I know Del wrote a very kind letter to you all, and I am very grateful to him to do something so kind for me.

However - there will never be enough words to explain my gratitude for all you have done for me in the past - you all are the reason I made it though treatment as long as I did. I could have never walked this road alone, it was much more than I could of handled. You guys were the greatest, and even when on treatment and I had those days, that seemed like endless as the time, that I could not come on and talk about things - when I did return, you never judged me, you accepted me back with open arms, and you each gave of part of yourselves to help me pull through when all seemed so hopeless.

As you know today I received the lovely new that I not only have hep again, but my viral load is over 6 million. It never got over a1 mill before. It's pretty much set in stone for me that I must do treatment again, I don't feel there is an option. I have 2 wonderful and amazing grand daughters that I live for - they are so much a part of myself and my soul.

And I want to watch them grow up, I want for them to know the love that I had for them. I don't think I could bare it otherwise.

Along with the hep, I was also diagnosed with EVB - which is also known as Mona. That is extremely taxing on my energy and fatigue, For the last two weeks or more I have been off work at Doctor request, I have been so week that there are days I can't make it down the stairs and to my car.

I didn't have any money saved as I was just recovering from taking care of my ex when he got cancer and I become his only caretaker for over a year, and them my Mother becomes seriously ill. So I take what funds I have left, and move out here with the intention of over seeing her care, and running her to from appointments, as there is no one else to do it and there is no free service. Unfortunately she lives at 30 minutes from me, somedays it can be quite the drive.

I remember that I had all the sides and them some, I am so worried I will longer be able to help her onve I start the treatment. I feel guilty and somehow responsible. And I have no other siblings that are willing to help her. I am blessed and I have an excellent insurance company, but I have to pay 285.00 a month for cobra,not for sure how much longer I can afford this.

Everything has just become a complete mess, and I am feeling, angry, scared, emotionally and phyiscally drained.

Well I guess I should get out my pity party.

And write more when I can be more supportive. And not do so much whinning. I hope I haven't offended or hurt anyone here by not writing right away - if so for this I am truly sorry for..

I will always love you guys, and have come to love and respect you all as my true friends - someone I can depend on.

I am so very blessed and this I do know and realize.

Hope to hear from you all soon

Love, hugs, and prayers

Marie

Letter Created By Jeni

Font DC Lindsey

May 2004

Font: CluffHmkBold

Graphic artist unknown

[Guest guest]

Hey Rose? I'm a chronic low grade. Have you ever noticed a pattern with the fever?

For instance mine has a tendency to show up right around early afternoon. It's the strangest thing. But you know everytime I go to the doctor. My fever never measures on their therm. Hmmmm. But my cheeks are red and there is usually another part on my body that's on fire too like my chest or upper arms.....

Christene

>> Hello to all,> I have missed talking with you all, but on March 15th, I was put in the hospital because of so much pain in my rib cage area and back, also running a low grade temp. I have been without my implants since March 2, 2006 at first I felt real good and was walking better, but it all went way south in less than 2 wks.> The doctors ran all kinds of test and they could not find out what was wrong with me except that I have to hot spots in my rib cage area from a bone density test.> I told them that all this pain started right after I had my saline breast implants. No one seems to care. Now they think that I might have cancer in my ribs, so I have an appointment at a bone specialist.> I will keep all of you in my prayers and I am so glad to have met you good people that are suffering through no fault of our own, the Doctors failed to explain to us what I have found out since finding this wonderful group.> > Much love,> > Rommie> > > ---------------------------------> How low will we go? Check out Messenger's low PC-to-Phone call rates.>

[Guest guest]

Hi Rommie,

Sometimes we feel really good after surgery and then suffer a

setback, kind of like a honeymoon period. That's what happened to

me. Now I'm close to 6 months post-op and am starting to see some

minor changes. I hope everything works out ok with the hot spots.

Sis

--- In , Rose Avant <rosezy54@...>

wrote:

>

> Hello to all,

> I have missed talking with you all, but on March 15th, I was

put in the hospital because of so much pain in my rib cage area and

back, also running a low grade temp. I have been without my implants

since March 2, 2006 at first I felt real good and was walking

better, but it all went way south in less than 2 wks.

> The doctors ran all kinds of test and they could not find out

what was wrong with me except that I have to hot spots in my rib

cage area from a bone density test.

> I told them that all this pain started right after I had my

saline breast implants. No one seems to care. Now they think that I

might have cancer in my ribs, so I have an appointment at a bone

specialist.

> I will keep all of you in my prayers and I am so glad to have

met you good people that are suffering through no fault of our own,

the Doctors failed to explain to us what I have found out since

finding this wonderful group.

>

> Much love,

>

> Rommie

>

>

> ---------------------------------

> How low will we go? Check out Messenger's low PC-to-Phone

call rates.

>

[Guest guest]

Christene . . .

Were you the one who was saying she took Neurontin?

That can cause a deficiency in Magnesium that results

in burning sensations.

As far as I know Neurontin doesn't treat anything. It

just blocks a particular pain channel so you don't

feel the pain!

Neurontin really did a number on me!

Hugs,

Rogene

[Guest guest]

Rommie,

I hope your " hot spots " are nothing serious - and

that, whatever they are can be addressed readily!

Did you have your implants removed en bloc, or have a

capsulectomy? Including drains?

I've just been through a round with cancer . . . I'm

still kicking! . . . Please keep us updated on what's

going on with you.

We really do care!

Hugs and prayers,

Rogene

[Guest guest]

Rommie

Sorry to hear about your continuing pain. I am praying that the

tests will show that you do not have cancer. Are you feeling any

less pain than you were? I am so glad that you let us know what is

happening with you...I was wondering how you were doing. Please

keep us posted with how your doctor visit turns out. When is your

appointment? We care about you and you will be in my thoughts and

prayers.

Love, Kathy

--- In , Rose Avant <rosezy54@...>

wrote:

>

> Hello to all,

> I have missed talking with you all, but on March 15th, I was

put in the hospital because of so much pain in my rib cage area and

back, also running a low grade temp. I have been without my implants

since March 2, 2006 at first I felt real good and was walking

better, but it all went way south in less than 2 wks.

> The doctors ran all kinds of test and they could not find out

what was wrong with me except that I have to hot spots in my rib

cage area from a bone density test.

> I told them that all this pain started right after I had my

saline breast implants. No one seems to care. Now they think that I

might have cancer in my ribs, so I have an appointment at a bone

specialist.

> I will keep all of you in my prayers and I am so glad to have

met you good people that are suffering through no fault of our own,

the Doctors failed to explain to us what I have found out since

finding this wonderful group.

>

> Much love,

>

> Rommie

>

>

> ---------------------------------

> How low will we go? Check out Messenger's low PC-to-Phone

call rates.

>

[Guest guest]

Rommie, This exacerbation of symptoms after explant is completely normal. Most of the women who go through explant have what I call a "honeymoon period" right after surgery where they feel alot better and some even see some major improvements that proves to them for sure it was the implants making them sick. But about 6 weeks after explant surgery, some of those symptoms can return in full force and even get worse for a period of time. That happened to me. I even have blood work that showed I got worse before I got better. That healing process took a very long time....upwards of 4 years. I am not saying that everyone takes the same healing path that I did, but I do think that this exacerbation you are experiencing is within the realm of normalcy. Don't panic just yet, and don't let the doctors start experimenting on you. Take a breather and have some peace about this time after

explant. Let your body settle down a bit. It probably has something to do with the immune system taking a few hits from the anesthetic and surgery, and then bouncing back to overreact like when the implants were there. And then what follows is that long healing process where the immune system is learning to re-program itself into a healthy mode. What has to happen is that your body needs to clear out all those toxins and junk that was allowed to accumulate while your body was fighting off implants. The liver perhaps was not doing its job as well, toxins were building up in fat cells or any of a number of other areas were affected in such a way that the organs need time to renew themselves and start functioning well again. That is where detoxing comes in, which prompts the body to purge itself of toxins, and where eating healthy will help

rebuild what has been torn down. Be careful of taking too many drugs to help with symptoms or conditions, as those drugs will ultimately get in the way of your body's attempts to heal itself. Of course, symptom relief is a consideration, but don't let symptom relief get in the way of real healing. Be very cautious in your approach to taking pharmaceutical drugs. I am sorry you were in the hospital. Try to have some peace that your body, if it was healthy before you got implants, has a very good chance of getting back to where it was before all this happened. You just have to give it some time. I wish you wellness. Hugs, PattyRose Avant <rosezy54@...> wrote: Hello to all, I have missed

talking with you all, but on March 15th, I was put in the hospital because of so much pain in my rib cage area and back, also running a low grade temp. I have been without my implants since March 2, 2006 at first I felt real good and was walking better, but it all went way south in less than 2 wks. The doctors ran all kinds of test and they could not find out what was wrong with me except that I have to hot spots in my rib cage area from a bone density test. I told them that all this pain started right after I had my saline breast implants. No one seems to care. Now they think that I might have cancer in my ribs, so I have an appointment at a bone specialist. I will keep all of you in my prayers and I am so glad to have met you good people that are suffering through no fault of our own, the Doctors failed to explain to us what I have found out since finding this wonderful group. Much

love, Rommie

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[Guest guest]

Hi Rommie,

I was worse for a while after explant, too. Just as Patty said, I

think it was a combination of the anesthesia and just putting my

already weak body through yet another surgery - but I don't regret

having the implants removed for one second. Even though my body is

struggling to get well, at least it's got a chance without that

poison in my body. My one year anniversary of getting implants is

coming up - and I'm sure it's going to bring on a few emotional

thoughts - if I knew then what I know now. However, things are

looking up for me and in time they will look up for you, too. Just

keep the faith.

Sis

> Hello to all,

> I have missed talking with you all, but on March 15th, I was

put in the hospital because of so much pain in my rib cage area and

back, also running a low grade temp. I have been without my implants

since March 2, 2006 at first I felt real good and was walking

better, but it all went way south in less than 2 wks.

> The doctors ran all kinds of test and they could not find out

what was wrong with me except that I have to hot spots in my rib

cage area from a bone density test.

> I told them that all this pain started right after I had my

saline breast implants. No one seems to care. Now they think that I

might have cancer in my ribs, so I have an appointment at a bone

specialist.

> I will keep all of you in my prayers and I am so glad to have

met you good people that are suffering through no fault of our own,

the Doctors failed to explain to us what I have found out since

finding this wonderful group.

>

> Much love,

>

> Rommie

>

>

>

> ---------------------------------

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Great rates starting at 1 & cent;/min.

>