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Re: good news for all you scheduled for explant

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Lo,

Having women come back after being explanted to

encourage women to follow through with their instincts

to be explanted is what makes this group work! . . .

Thanks so much for letting everyone know that there is

life after explants . . . And that the body God gave

us is the best one after all!

Hugs,

Rogene

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Lo,

What a beautiful, inspirational and uplifting message. I am

thrilled that you are doing so well! Thank you for coming back to

share with us all that you have been through and how your healing

has progessed. I am also thankful that your doctor was so helpful

in validating what you were going through! If you want to share his

name so he can be available to help others, that would be awesome!

I understand the need to get away from this issue to clear your head

sometimes. There is nothing fun about it, (except for the new

friends you make!) and the depression and angst we feel can be

overwhelming. But, as you pointed out, there is surely hope here!

Women are getting better once they understand that the implants DO

INDEED cause illness, even when their doctors are telling them " it's

not the implants " . Explant is the only way to go.

Thanks again for sharing your remarkable story Lo!

Patty

--- In , " lolosky3 " <lolosky3@y...>

wrote:

>

> Hi Ladies!

> I know some of you remember me, my name's Lo, I'm 22 years old and

I

> have been a member for about a year but I haven't posted in a few

> months. I had saline under the muscle implants put in when I was

19

> and it was the biggest mistake of my life. I developed carpal

tunnel

> like symptoms within a month which persisted for about a year.

After

> a year I developed and then pain in all my limbs, shaking,

twitching,

> headaches, tingling, every weird symptom imaginable. I saw my

doctor

> and he had no explanation, I didnt have a high ANA therefore it

was

> rheumatory arthritis, and all other tests came out negative. My

> diagnosis was fibromyalgia, a pain and fatigue disorder that

doctors

> still don't know much about but they know can be brought on by

stress

> and a number of other things. It's the diagnosis they give people

who

> they usually don't know what the hell is wrong with them because

> there is no test to prove this disorder. I got explanted a few

months

> ago and I feel unbelievably better. I need to tell you all I'm

not

> so tired all the time and almost all my fibromyalgia symptoms are

> gone. Just this past month I noticed significant differences

since I

> still have slight pain in my wrists and breasts and sometimes am a

> little fatigued or get an occasional twitch when I'm stressed out

but

> gradually my symptoms have been regressing and I am totally

confident

> eventually I will be close to 100%. I just wanted to give you all

> hope who aren't sure if it is your implants, IT IS. I promise you

if

> you have fibromyalgia symptoms, it is 99% probable that it is your

> implants. I didn't want to lose mine so I kept my implants even

> after my instincts told me my pain was from them. I know you

spent a

> lot of money on them and they give you more confidence, but they

> ruined my whole life. I almost dropped out of college last year

> because I had a breakdown because I didn't know what the hell was

> wrong with me, I thought I had RA and MS and/or was just losing my

> mind. I'm getting over my depression finally and I have been

> depressed since getting them put in. Doctors told me they weren't

> the cause and I didn't want to tell my family health physician

> because he was a family friend and I didn't want him to know I had

> them, but I told him because he is a brilliant man and I really

> needed his medical opinion. Since he saw my progression of

symptoms

> and looked at the chart from the time I was implanted and when the

> progress of my symptoms took place he told me to get them out

> immedieatly before my symptoms got worse. He said he didn't know

if

> it was them but using the facts he had and previous experiences

from

> his patients who had improved after the explantation he urged me

to

> remove them. Because of his opinion my dad finally realized I

wasn't

> a hypochondriac and agreed to pay for then, but what was even more

> amazing is that my physican wrote a document saying how he

believed

> they were the cause of my fibromyalgia and my plastic surgeon also

> agreed to sign it so my insurance could pay for all of it. I am

> feeling so great now and I just wanted you all to know that you

have

> hope of feeling so much better. I believe a few months from now I

> will be 100% It takes time ladies, but you will only improve when

> you have them removed, in the meantime you may unfortunatly gain

more

> symptoms, like I did because I waited. I know how you feel, it is

a

> painful, lonely, depressing, hopeless, anxious feeling.

> Be healthy, don't lose hope, and I'm here for any questions about

my

> improvement progress, what symptoms I had/have, what prodcedure I

> had, anything! (write my name in the subject because I may miss

that

> a message is for me). Love you ladies, Rogene, Patty, Beth, I

> remember all of your help and I doubt anyone will ever take for

> granted the time and effort you put in helping us. I want you all

to

> know I consider these women who still persist checking this

website

> daily to help every stranded woman who needs answers out of their

own

> time are angels. I wish I had the time and the bravery to check

the

> website everyday but it has been too harsh a reminder and made me

too

> anxious until now because I am feeling better and want to help as

> well. I am so pleased with how my breasts look now, they feel

light

> and natural and look honestly beautiful (I'm not just saying this

to

> convince you, I really really like how they look now, I got bigger

> since my implantation slightly and it is such a nice natural

> difference from those " balls " as I called them). Please do what's

> right for your body, and not what looks right for your body. You

only

> have one, and you have to live how it works or doesn't work for

the

> rest of your life.

> -Lo

>

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Lo

Thanks for sharing! We really need ladies such as you to check back

in and let us know how great you are doing. I am glad to hear that

you doing so well.

Hugs, kathy

--- In , " lolosky3 " <lolosky3@y...>

wrote:

>

> Hi Ladies!

> I know some of you remember me, my name's Lo, I'm 22 years old and

I

> have been a member for about a year but I haven't posted in a few

> months. I had saline under the muscle implants put in when I was

19

> and it was the biggest mistake of my life. I developed carpal

tunnel

> like symptoms within a month which persisted for about a year.

After

> a year I developed and then pain in all my limbs, shaking,

twitching,

> headaches, tingling, every weird symptom imaginable. I saw my

doctor

> and he had no explanation, I didnt have a high ANA therefore it

was

> rheumatory arthritis, and all other tests came out negative. My

> diagnosis was fibromyalgia, a pain and fatigue disorder that

doctors

> still don't know much about but they know can be brought on by

stress

> and a number of other things. It's the diagnosis they give people

who

> they usually don't know what the hell is wrong with them because

> there is no test to prove this disorder. I got explanted a few

months

> ago and I feel unbelievably better. I need to tell you all I'm

not

> so tired all the time and almost all my fibromyalgia symptoms are

> gone. Just this past month I noticed significant differences

since I

> still have slight pain in my wrists and breasts and sometimes am a

> little fatigued or get an occasional twitch when I'm stressed out

but

> gradually my symptoms have been regressing and I am totally

confident

> eventually I will be close to 100%. I just wanted to give you all

> hope who aren't sure if it is your implants, IT IS. I promise you

if

> you have fibromyalgia symptoms, it is 99% probable that it is your

> implants. I didn't want to lose mine so I kept my implants even

> after my instincts told me my pain was from them. I know you

spent a

> lot of money on them and they give you more confidence, but they

> ruined my whole life. I almost dropped out of college last year

> because I had a breakdown because I didn't know what the hell was

> wrong with me, I thought I had RA and MS and/or was just losing my

> mind. I'm getting over my depression finally and I have been

> depressed since getting them put in. Doctors told me they weren't

> the cause and I didn't want to tell my family health physician

> because he was a family friend and I didn't want him to know I had

> them, but I told him because he is a brilliant man and I really

> needed his medical opinion. Since he saw my progression of

symptoms

> and looked at the chart from the time I was implanted and when the

> progress of my symptoms took place he told me to get them out

> immedieatly before my symptoms got worse. He said he didn't know

if

> it was them but using the facts he had and previous experiences

from

> his patients who had improved after the explantation he urged me

to

> remove them. Because of his opinion my dad finally realized I

wasn't

> a hypochondriac and agreed to pay for then, but what was even more

> amazing is that my physican wrote a document saying how he

believed

> they were the cause of my fibromyalgia and my plastic surgeon also

> agreed to sign it so my insurance could pay for all of it. I am

> feeling so great now and I just wanted you all to know that you

have

> hope of feeling so much better. I believe a few months from now I

> will be 100% It takes time ladies, but you will only improve when

> you have them removed, in the meantime you may unfortunatly gain

more

> symptoms, like I did because I waited. I know how you feel, it is

a

> painful, lonely, depressing, hopeless, anxious feeling.

> Be healthy, don't lose hope, and I'm here for any questions about

my

> improvement progress, what symptoms I had/have, what prodcedure I

> had, anything! (write my name in the subject because I may miss

that

> a message is for me). Love you ladies, Rogene, Patty, Beth, I

> remember all of your help and I doubt anyone will ever take for

> granted the time and effort you put in helping us. I want you all

to

> know I consider these women who still persist checking this

website

> daily to help every stranded woman who needs answers out of their

own

> time are angels. I wish I had the time and the bravery to check

the

> website everyday but it has been too harsh a reminder and made me

too

> anxious until now because I am feeling better and want to help as

> well. I am so pleased with how my breasts look now, they feel

light

> and natural and look honestly beautiful (I'm not just saying this

to

> convince you, I really really like how they look now, I got bigger

> since my implantation slightly and it is such a nice natural

> difference from those " balls " as I called them). Please do what's

> right for your body, and not what looks right for your body. You

only

> have one, and you have to live how it works or doesn't work for

the

> rest of your life.

> -Lo

>

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i am so happy you are feeling so well....it is nice to hear! do you

happen to live in AZ? i am trying to find medical people to be on my

side so my insurance will pay.......continued blessings!

kathie

> >

> > Hi Ladies!

> > I know some of you remember me, my name's Lo, I'm 22 years old

and

> I

> > have been a member for about a year but I haven't posted in a few

> > months. I had saline under the muscle implants put in when I was

> 19

> > and it was the biggest mistake of my life. I developed carpal

> tunnel

> > like symptoms within a month which persisted for about a year.

> After

> > a year I developed and then pain in all my limbs, shaking,

> twitching,

> > headaches, tingling, every weird symptom imaginable. I saw my

> doctor

> > and he had no explanation, I didnt have a high ANA therefore it

> was

> > rheumatory arthritis, and all other tests came out negative. My

> > diagnosis was fibromyalgia, a pain and fatigue disorder that

> doctors

> > still don't know much about but they know can be brought on by

> stress

> > and a number of other things. It's the diagnosis they give people

> who

> > they usually don't know what the hell is wrong with them because

> > there is no test to prove this disorder. I got explanted a few

> months

> > ago and I feel unbelievably better. I need to tell you all I'm

> not

> > so tired all the time and almost all my fibromyalgia symptoms are

> > gone. Just this past month I noticed significant differences

> since I

> > still have slight pain in my wrists and breasts and sometimes am

a

> > little fatigued or get an occasional twitch when I'm stressed out

> but

> > gradually my symptoms have been regressing and I am totally

> confident

> > eventually I will be close to 100%. I just wanted to give you

all

> > hope who aren't sure if it is your implants, IT IS. I promise

you

> if

> > you have fibromyalgia symptoms, it is 99% probable that it is

your

> > implants. I didn't want to lose mine so I kept my implants even

> > after my instincts told me my pain was from them. I know you

> spent a

> > lot of money on them and they give you more confidence, but they

> > ruined my whole life. I almost dropped out of college last year

> > because I had a breakdown because I didn't know what the hell was

> > wrong with me, I thought I had RA and MS and/or was just losing

my

> > mind. I'm getting over my depression finally and I have been

> > depressed since getting them put in. Doctors told me they

weren't

> > the cause and I didn't want to tell my family health physician

> > because he was a family friend and I didn't want him to know I

had

> > them, but I told him because he is a brilliant man and I really

> > needed his medical opinion. Since he saw my progression of

> symptoms

> > and looked at the chart from the time I was implanted and when

the

> > progress of my symptoms took place he told me to get them out

> > immedieatly before my symptoms got worse. He said he didn't know

> if

> > it was them but using the facts he had and previous experiences

> from

> > his patients who had improved after the explantation he urged me

> to

> > remove them. Because of his opinion my dad finally realized I

> wasn't

> > a hypochondriac and agreed to pay for then, but what was even

more

> > amazing is that my physican wrote a document saying how he

> believed

> > they were the cause of my fibromyalgia and my plastic surgeon

also

> > agreed to sign it so my insurance could pay for all of it. I am

> > feeling so great now and I just wanted you all to know that you

> have

> > hope of feeling so much better. I believe a few months from now

I

> > will be 100% It takes time ladies, but you will only improve

when

> > you have them removed, in the meantime you may unfortunatly gain

> more

> > symptoms, like I did because I waited. I know how you feel, it

is

> a

> > painful, lonely, depressing, hopeless, anxious feeling.

> > Be healthy, don't lose hope, and I'm here for any questions about

> my

> > improvement progress, what symptoms I had/have, what prodcedure I

> > had, anything! (write my name in the subject because I may miss

> that

> > a message is for me). Love you ladies, Rogene, Patty, Beth, I

> > remember all of your help and I doubt anyone will ever take for

> > granted the time and effort you put in helping us. I want you

all

> to

> > know I consider these women who still persist checking this

> website

> > daily to help every stranded woman who needs answers out of their

> own

> > time are angels. I wish I had the time and the bravery to check

> the

> > website everyday but it has been too harsh a reminder and made me

> too

> > anxious until now because I am feeling better and want to help as

> > well. I am so pleased with how my breasts look now, they feel

> light

> > and natural and look honestly beautiful (I'm not just saying this

> to

> > convince you, I really really like how they look now, I got

bigger

> > since my implantation slightly and it is such a nice natural

> > difference from those " balls " as I called them). Please do what's

> > right for your body, and not what looks right for your body. You

> only

> > have one, and you have to live how it works or doesn't work for

> the

> > rest of your life.

> > -Lo

> >

>

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