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Wow, Deb, you've had quite a life! Bull riding sounds.....jolting!

Sadly, I can relate to some of your symptoms, and have talked with many

other women who have had the same troubles.

The visual problems are common, although your description of them is worse

than any I have experienced! When I got sick, it seemed that everything

happened all at once, and the visual problems were one of the first signs.

I had a hard time just being comfortable with my eyes open at times, and I

remember the aggravation of driving the most. I would put on sunglasses and

have to take them off 5 minutes later, only to put them back on again soon

after that. On and on it went, on, off. My eyes just never felt

right--they ached, and were tired. I got into two car accidents in the

first year after explant. But an opthamologist declared that I had better

than perfect vision after an exam, and he looked at me very strange when I

told him I thought there was something wrong and that it had to do with my

saline implants. I'll never forget his look. It shouted " You must be a

stupid, crazy lady. "

I also can relate to the Bible episode, although mine had more to do with

comprehension and was very freaky. I went to read my Bible for comfort,

only to find out that I could not understand a single thing that I read! I

was reading, but it made no sense to me--it could have all been Greek, for

as much as I could comprehend it. I got so scared I went to watch TV with

my kids, only to find out I could not comprehend the TV show, either! That

was the day that my life changed, and I KNEW something was wrong.

The memory problems and lapses are all part of it....the aches, pains,

fatigue, frozen shoulder, dry eyes, thyroid problems....all common to women

with implant toxicity.

The exact mechanisms explaining the toxicity aren't fully understood yet,

but we do know that these symptoms are similar to what other chemically

toxic people have experienced. Therefore, the aim of healing is to detox

the body as fully as possible, and to support the immune system as it heals,

and help provide nutrients to rebuild healthy cells.

This means doing things that you wouldn't normally do, such as fasting,

colonics, enemas, cleanses, saunas or other sweating therapies, chelation

therapy, amalgam removal, changes in diet (this is vital), juicing, as well

as using supplements to help your body in the detoxification and rebuilding

process. It takes alot of effort at times.

There may be underlying viral or bacterial issues that should be addressed

as well. We have recently discussed the mycoplasma issue on the group.

There are also anti-viral foods and supplements that you can buy to reduce

your viral load.

I have to say the effort is time consuming, but all worth it. I have healed

tremendously in the last 3 years since explant. I have learned alot and am,

hopefully, a better person for it. They say everything happens for a

reason, and though I wouldn't wish anyone else to go through this, I have to

look at my experience in the light of what God wanted me to learn from it,

and I see where He wanted me to change direction.

I hope you will be encouraged in our group! Stay with us, ask questions,

and let us know how things go with your MRI and explant! Do you have a

doctor picked out yet? I do hope he helps you get your insurance to cover

it. Make sure you have a total capsulectomy done.

Take Care,

Patty

----- Original Message -----

From: " Deb " <wwjddeb_99@...>

< >

Sent: Saturday, July 14, 2001 9:59 AM

Subject: Has anyone had these symptoms?

> Hi,

> I just joined and I just woke up from 22 years of being sick and

> wondering why? It was not until a few weeks ago that I even

> connected that my saline implants could be the hidden cause of my

> troubles.

> I was implanted (and I still am.... yikes!) in 1979 with Heyer

> Schulte implants 1620 inflated with 175 cc of normal saline and 1630

> was filled with 250cc of NS with 20mg of SolUMedrol placed in each

> implant.

> A few years after this I started having problems with my left

> shoulder. I had a ton of pain and it would freeze up on me... I

> started with injections of cortisone and I have had them off and on

> through out the years when the soulder is too painful.

> In more recent years I have had a lot of visiual problems. I was

> reading my Bible at the kitchen table one day in 1996 all of a sudden

> the pages looked some what like this: " F od so l ved th w rld th

> H ga " the letters where gone! That freaked me out! But then what

> made this worse was the fact that the next thing that I remembered is

> that I was sitting on the floor in my bathroom with no clue as to how

> I got there... I wasn't sure if I could even talk at that time. The

> doctors told me I was having phantom migraine headaches this of

> course was better than the possible brain tumor they thought that I

> had at first.

> Now I am having double vision! " Every now and then " I my vision will

> become blurred or I will see a persons eyes on their cheeks!

> King couldn't come up with some of the freaky things that I've seen

> through my eyes lately! lol

> The doctor told me that I had " Atypcial MS " this was then ruled out

> by a specialist who only deals with MS patients after he reviewed my

> records... and this was also after I found out that I developed an

> allergy to Steroids... I had 1000 mg. of SolUMedrol given to me over

> 3 days it was continued with the use of Benedryl taken orally 1 hour

> before I got my 2nd and 3rd IV's because I started breaking out in

> hives before the first dose was finished. I cann't take the oral

> dose pack either it made me very very sick.

> Now I am left with the diagnosis of Chronic Fatigue, Chronic Pain,

> Fibromyalgia and periperal neuropathy.

>

> I have pain daily since the early 1980's. I am more stiff and

> painful in the AM's. I have always contributed this to the fact that

> I was a womens professional bull rider for about 3 years before I

> broke my back in 4 places in 1991. But looking back over my medical

> records from years ago I realized that I had a lot of these symptoms

> and problems before I took up the sport of bull riding...

>

> It's like the things that seem so " normal " to me today came on very

> slowly and I didn't realize that things were changing for me. When I

> started doing the visual things a few years ago I couldn't shun those

> symptoms off and make excuses for them... basically they freaked me

> out big time and I had to tell someone about them.

>

> I forget things all of the time, I don't have memory of a lot of the

> years gone by and no I don't take drugs or drink... I have difficulty

> with speach sometimes by slurring my speach or forgetting what I was

> saying in the middle of a sentence or by not using the correct

> word.

> I remember being in the middle of an intersection a few years

> back and I couldn't figure out how to turn... horns started honking

> and I was in a fog just sitting in the intersection without a clue as

> to how I should get myself out of it. Lucky for me someone got angry

> and pulled around me and I followed that person through the

> intersection. (Thanks God! :))

>

> My eyes are so dry that I can hardly wear my contacts well I do wear

> them sometimes and I have to " peel " them off of my eyes... ouch! My

> throat hurts so much that it is difficult to even drink water

> sometimes. My mouth is dry and I drink water all of the time I'm

> talking over a gallon a day. Of course I'm in the bathroom about

> every 15 to 30 minutes a day and at least 3 to 5 times at night. I

> had a nerve in my arm transposed (moved over) a few years ago and I

> still drop things with my left hand. I had a total hysterectomy two

> years ago because of fibroids thus I had the periods from the pit of

> hell. I have had cystic breasts for years and since I got married

> two years ago (right before my hysterectomy) I have continue to gain

> weight. I have gained over 60 pounds without changing my diet or my

> activies. I was in a car accident two years ago 2 months right

> before I got married and the air bag hit my chest so hard that my

> right breast was the color of an eggplant for almost 3 months. It

> also hit my transposed nerve in my left forearm and that trufully

> hurt worse than the breast because I didn't know about the breast

> until I got undressed later that night. Since this accident that

> former eggplant colored breast seems to have sagged to my knees... do

> you think that it ruptured? Eeeewww!

>

> Since that time my spinal tap was pretty normal except for basic

> mylin protiens were elevated other wise it was normal. My evoked

> potential eye test was a bit prolonged too. My T-7 showed a very low

> T-3 uptake on the thyroid... who knows what that all means or if it

> is related to the implants?

>

> As I wait to see if my insurance will pay for an MRI of my breast and

> or send me to a plastic surgeon for explantation I sit in awe of how

> much I don't know about any of this.

> Please feel free to email me if you too have had any of these

> symptoms and let me know what you found out about them.

>

> Thanks to all of you for being here for others and me... it's nice to

> know I'm not crazy or alone and if I am nuts then it's nice to be

> nuts with the rest of you nice ladies... validation is a wonderful

> healing tool isn't it? God Bless and keep you all. Keep in touch!

> Deb

> wwjddeb_99@...

>

>

>

>

>

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Deb,

My name is e and I am a registered nurse who also

had saline implants and had them removed in Feb. Many

of my symptoms were similar to yours. In fact, many of

them were identical.

My first question to you is have you had a FLAIR MRI of

the brain? Many of your symptoms sound similar to a

stroke. I know that you don't want to hear that, but I

had several MRI's of my brain trying to rule out MS, and

nothing ever showed up until I had the FLAIR MRI. It

was then that I was diagnosed with a left cerebellar

stroke. I was also having forgetfulness and forgetting

where I was driving to, or where I'd parked my car, etc.

I also want to know if you've been tested for lupus.

The dry eyes is classic of Sjogren's Syndrome, which

usually goes hand in hand with lupus. It is a disease

characterized by dry eyes, mouth, and mucous membranes

and also by being very thirsty and drinking a lot, but

the dryness never goes away. I would insist on being

tested for lupus if you haven't already.

You're the first woman I've heard about that had

solumedrol placed in her implants. I had betadine

placed in mine. But your allergy to solumedrol can

probably be related to the fact that it was placed in

your implants, and your body has developed a sensitivity

to it.

Please write to me if you need any info on what lab

tests to request or if you have any further questions.

e

> Hi,

> I just joined and I just woke up from 22 years of being sick and

> wondering why? It was not until a few weeks ago that I even

> connected that my saline implants could be the hidden cause of my

> troubles.

> I was implanted (and I still am.... yikes!) in 1979 with Heyer

> Schulte implants 1620 inflated with 175 cc of normal saline and 1630

> was filled with 250cc of NS with 20mg of SolUMedrol placed in each

> implant.

> A few years after this I started having problems with my left

> shoulder. I had a ton of pain and it would freeze up on me... I

> started with injections of cortisone and I have had them off and on

> through out the years when the soulder is too painful.

> In more recent years I have had a lot of visiual problems. I was

> reading my Bible at the kitchen table one day in 1996 all of a sudden

> the pages looked some what like this: " F od so l ved th w rld th

> H ga " the letters where gone! That freaked me out! But then what

> made this worse was the fact that the next thing that I remembered is

> that I was sitting on the floor in my bathroom with no clue as to how

> I got there... I wasn't sure if I could even talk at that time. The

> doctors told me I was having phantom migraine headaches this of

> course was better than the possible brain tumor they thought that I

> had at first.

> Now I am having double vision! " Every now and then " I my vision will

> become blurred or I will see a persons eyes on their cheeks!

> King couldn't come up with some of the freaky things that I've seen

> through my eyes lately! lol

> The doctor told me that I had " Atypcial MS " this was then ruled out

> by a specialist who only deals with MS patients after he reviewed my

> records... and this was also after I found out that I developed an

> allergy to Steroids... I had 1000 mg. of SolUMedrol given to me over

> 3 days it was continued with the use of Benedryl taken orally 1 hour

> before I got my 2nd and 3rd IV's because I started breaking out in

> hives before the first dose was finished. I cann't take the oral

> dose pack either it made me very very sick.

> Now I am left with the diagnosis of Chronic Fatigue, Chronic Pain,

> Fibromyalgia and periperal neuropathy.

>

> I have pain daily since the early 1980's. I am more stiff and

> painful in the AM's. I have always contributed this to the fact that

> I was a womens professional bull rider for about 3 years before I

> broke my back in 4 places in 1991. But looking back over my medical

> records from years ago I realized that I had a lot of these symptoms

> and problems before I took up the sport of bull riding...

>

> It's like the things that seem so " normal " to me today came on very

> slowly and I didn't realize that things were changing for me. When I

> started doing the visual things a few years ago I couldn't shun those

> symptoms off and make excuses for them... basically they freaked me

> out big time and I had to tell someone about them.

>

> I forget things all of the time, I don't have memory of a lot of the

> years gone by and no I don't take drugs or drink... I have difficulty

> with speach sometimes by slurring my speach or forgetting what I was

> saying in the middle of a sentence or by not using the correct

> word.

> I remember being in the middle of an intersection a few years

> back and I couldn't figure out how to turn... horns started honking

> and I was in a fog just sitting in the intersection without a clue as

> to how I should get myself out of it. Lucky for me someone got angry

> and pulled around me and I followed that person through the

> intersection. (Thanks God! :))

>

> My eyes are so dry that I can hardly wear my contacts well I do wear

> them sometimes and I have to " peel " them off of my eyes... ouch! My

> throat hurts so much that it is difficult to even drink water

> sometimes. My mouth is dry and I drink water all of the time I'm

> talking over a gallon a day. Of course I'm in the bathroom about

> every 15 to 30 minutes a day and at least 3 to 5 times at night. I

> had a nerve in my arm transposed (moved over) a few years ago and I

> still drop things with my left hand. I had a total hysterectomy two

> years ago because of fibroids thus I had the periods from the pit of

> hell. I have had cystic breasts for years and since I got married

> two years ago (right before my hysterectomy) I have continue to gain

> weight. I have gained over 60 pounds without changing my diet or my

> activies. I was in a car accident two years ago 2 months right

> before I got married and the air bag hit my chest so hard that my

> right breast was the color of an eggplant for almost 3 months. It

> also hit my transposed nerve in my left forearm and that trufully

> hurt worse than the breast because I didn't know about the breast

> until I got undressed later that night. Since this accident that

> former eggplant colored breast seems to have sagged to my knees... do

> you think that it ruptured? Eeeewww!

>

> Since that time my spinal tap was pretty normal except for basic

> mylin protiens were elevated other wise it was normal. My evoked

> potential eye test was a bit prolonged too. My T-7 showed a very low

> T-3 uptake on the thyroid... who knows what that all means or if it

> is related to the implants?

>

> As I wait to see if my insurance will pay for an MRI of my breast and

> or send me to a plastic surgeon for explantation I sit in awe of how

> much I don't know about any of this.

> Please feel free to email me if you too have had any of these

> symptoms and let me know what you found out about them.

>

> Thanks to all of you for being here for others and me... it's nice to

> know I'm not crazy or alone and if I am nuts then it's nice to be

> nuts with the rest of you nice ladies... validation is a wonderful

> healing tool isn't it? God Bless and keep you all. Keep in touch!

> Deb

> wwjddeb_99@...

>

>

>

>

>

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HI Patty,

Thanks for the reply. I think that I would have a problem with some

of the sweating things... I live in Las Vegas Nevada and it's hot as

heck here, and I get sick as a dog if I get too hot! Are you the

Patty from Las Vegas? If so who is your doctor? If you are the Patty

from Las Vegas would you call me? My email is wwjddeb_99@...

send me an email and I will send you my phone number.

I will stay with the group and learn what I can thanks

Deb-

-- In @y..., " Patty " <faussettdp@m...> wrote:

> Wow, Deb, you've had quite a life! Bull riding sounds.....jolting!

>

> Sadly, I can relate to some of your symptoms, and have talked with

many

> other women who have had the same troubles.

>

> The visual problems are common, although your description of them

is worse

> than any I have experienced! When I got sick, it seemed that

everything

> happened all at once, and the visual problems were one of the first

signs.

> I had a hard time just being comfortable with my eyes open at

times, and I

> remember the aggravation of driving the most. I would put on

sunglasses and

> have to take them off 5 minutes later, only to put them back on

again soon

> after that. On and on it went, on, off. My eyes just never felt

> right--they ached, and were tired. I got into two car accidents in

the

> first year after explant. But an opthamologist declared that I had

better

> than perfect vision after an exam, and he looked at me very strange

when I

> told him I thought there was something wrong and that it had to do

with my

> saline implants. I'll never forget his look. It shouted " You must

be a

> stupid, crazy lady. "

>

> I also can relate to the Bible episode, although mine had more to

do with

> comprehension and was very freaky. I went to read my Bible for

comfort,

> only to find out that I could not understand a single thing that I

read! I

> was reading, but it made no sense to me--it could have all been

Greek, for

> as much as I could comprehend it. I got so scared I went to watch

TV with

> my kids, only to find out I could not comprehend the TV show,

either! That

> was the day that my life changed, and I KNEW something was wrong.

>

> The memory problems and lapses are all part of it....the aches,

pains,

> fatigue, frozen shoulder, dry eyes, thyroid problems....all common

to women

> with implant toxicity.

>

> The exact mechanisms explaining the toxicity aren't fully

understood yet,

> but we do know that these symptoms are similar to what other

chemically

> toxic people have experienced. Therefore, the aim of healing is to

detox

> the body as fully as possible, and to support the immune system as

it heals,

> and help provide nutrients to rebuild healthy cells.

>

> This means doing things that you wouldn't normally do, such as

fasting,

> colonics, enemas, cleanses, saunas or other sweating therapies,

chelation

> therapy, amalgam removal, changes in diet (this is vital), juicing,

as well

> as using supplements to help your body in the detoxification and

rebuilding

> process. It takes alot of effort at times.

>

> There may be underlying viral or bacterial issues that should be

addressed

> as well. We have recently discussed the mycoplasma issue on the

group.

> There are also anti-viral foods and supplements that you can buy to

reduce

> your viral load.

>

> I have to say the effort is time consuming, but all worth it. I

have healed

> tremendously in the last 3 years since explant. I have learned

alot and am,

> hopefully, a better person for it. They say everything happens

for a

> reason, and though I wouldn't wish anyone else to go through this,

I have to

> look at my experience in the light of what God wanted me to learn

from it,

> and I see where He wanted me to change direction.

>

> I hope you will be encouraged in our group! Stay with us, ask

questions,

> and let us know how things go with your MRI and explant! Do you

have a

> doctor picked out yet? I do hope he helps you get your insurance

to cover

> it. Make sure you have a total capsulectomy done.

> Take Care,

> Patty

> ----- Original Message -----

> From: " Deb " <wwjddeb_99@y...>

> < @y...>

> Sent: Saturday, July 14, 2001 9:59 AM

> Subject: Has anyone had these symptoms?

>

>

> > Hi,

> > I just joined and I just woke up from 22 years of being sick and

> > wondering why? It was not until a few weeks ago that I even

> > connected that my saline implants could be the hidden cause of my

> > troubles.

> > I was implanted (and I still am.... yikes!) in 1979 with Heyer

> > Schulte implants 1620 inflated with 175 cc of normal saline and

1630

> > was filled with 250cc of NS with 20mg of SolUMedrol placed in each

> > implant.

> > A few years after this I started having problems with my left

> > shoulder. I had a ton of pain and it would freeze up on me... I

> > started with injections of cortisone and I have had them off and

on

> > through out the years when the soulder is too painful.

> > In more recent years I have had a lot of visiual problems. I was

> > reading my Bible at the kitchen table one day in 1996 all of a

sudden

> > the pages looked some what like this: " F od so l ved th w rld

th

> > H ga " the letters where gone! That freaked me out! But then

what

> > made this worse was the fact that the next thing that I

remembered is

> > that I was sitting on the floor in my bathroom with no clue as to

how

> > I got there... I wasn't sure if I could even talk at that time.

The

> > doctors told me I was having phantom migraine headaches this of

> > course was better than the possible brain tumor they thought that

I

> > had at first.

> > Now I am having double vision! " Every now and then " I my vision

will

> > become blurred or I will see a persons eyes on their cheeks!

> > King couldn't come up with some of the freaky things that I've

seen

> > through my eyes lately! lol

> > The doctor told me that I had " Atypcial MS " this was then ruled

out

> > by a specialist who only deals with MS patients after he reviewed

my

> > records... and this was also after I found out that I developed an

> > allergy to Steroids... I had 1000 mg. of SolUMedrol given to me

over

> > 3 days it was continued with the use of Benedryl taken orally 1

hour

> > before I got my 2nd and 3rd IV's because I started breaking out in

> > hives before the first dose was finished. I cann't take the oral

> > dose pack either it made me very very sick.

> > Now I am left with the diagnosis of Chronic Fatigue, Chronic Pain,

> > Fibromyalgia and periperal neuropathy.

> >

> > I have pain daily since the early 1980's. I am more stiff and

> > painful in the AM's. I have always contributed this to the fact

that

> > I was a womens professional bull rider for about 3 years before I

> > broke my back in 4 places in 1991. But looking back over my

medical

> > records from years ago I realized that I had a lot of these

symptoms

> > and problems before I took up the sport of bull riding...

> >

> > It's like the things that seem so " normal " to me today came on

very

> > slowly and I didn't realize that things were changing for me.

When I

> > started doing the visual things a few years ago I couldn't shun

those

> > symptoms off and make excuses for them... basically they freaked

me

> > out big time and I had to tell someone about them.

> >

> > I forget things all of the time, I don't have memory of a lot of

the

> > years gone by and no I don't take drugs or drink... I have

difficulty

> > with speach sometimes by slurring my speach or forgetting what I

was

> > saying in the middle of a sentence or by not using the correct

> > word.

> > I remember being in the middle of an intersection a few years

> > back and I couldn't figure out how to turn... horns started

honking

> > and I was in a fog just sitting in the intersection without a

clue as

> > to how I should get myself out of it. Lucky for me someone got

angry

> > and pulled around me and I followed that person through the

> > intersection. (Thanks God! :))

> >

> > My eyes are so dry that I can hardly wear my contacts well I do

wear

> > them sometimes and I have to " peel " them off of my eyes... ouch!

My

> > throat hurts so much that it is difficult to even drink water

> > sometimes. My mouth is dry and I drink water all of the time I'm

> > talking over a gallon a day. Of course I'm in the bathroom about

> > every 15 to 30 minutes a day and at least 3 to 5 times at night.

I

> > had a nerve in my arm transposed (moved over) a few years ago and

I

> > still drop things with my left hand. I had a total hysterectomy

two

> > years ago because of fibroids thus I had the periods from the pit

of

> > hell. I have had cystic breasts for years and since I got married

> > two years ago (right before my hysterectomy) I have continue to

gain

> > weight. I have gained over 60 pounds without changing my diet or

my

> > activies. I was in a car accident two years ago 2 months right

> > before I got married and the air bag hit my chest so hard that my

> > right breast was the color of an eggplant for almost 3 months. It

> > also hit my transposed nerve in my left forearm and that trufully

> > hurt worse than the breast because I didn't know about the breast

> > until I got undressed later that night. Since this accident that

> > former eggplant colored breast seems to have sagged to my

knees... do

> > you think that it ruptured? Eeeewww!

> >

> > Since that time my spinal tap was pretty normal except for basic

> > mylin protiens were elevated other wise it was normal. My evoked

> > potential eye test was a bit prolonged too. My T-7 showed a very

low

> > T-3 uptake on the thyroid... who knows what that all means or if

it

> > is related to the implants?

> >

> > As I wait to see if my insurance will pay for an MRI of my breast

and

> > or send me to a plastic surgeon for explantation I sit in awe of

how

> > much I don't know about any of this.

> > Please feel free to email me if you too have had any of these

> > symptoms and let me know what you found out about them.

> >

> > Thanks to all of you for being here for others and me... it's

nice to

> > know I'm not crazy or alone and if I am nuts then it's nice to be

> > nuts with the rest of you nice ladies... validation is a wonderful

> > healing tool isn't it? God Bless and keep you all. Keep in touch!

> > Deb

> > wwjddeb_99@y...

> >

> >

> >

> >

> >

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Guest guest

Another Las Vegan!!!

Yes, I am the Patty from Las Vegas. Sending an e-mail your way, so we can

chat.

There's quite a few Las Vegas ladies on our group!

Patty

----- Original Message -----

From: " Deb " <wwjddeb_99@...>

< >

Sent: Sunday, July 15, 2001 9:56 PM

Subject: Re: Has anyone had these symptoms?

> HI Patty,

> Thanks for the reply. I think that I would have a problem with some

> of the sweating things... I live in Las Vegas Nevada and it's hot as

> heck here, and I get sick as a dog if I get too hot! Are you the

> Patty from Las Vegas? If so who is your doctor? If you are the Patty

> from Las Vegas would you call me? My email is wwjddeb_99@...

> send me an email and I will send you my phone number.

> I will stay with the group and learn what I can thanks

> Deb-

>

> -- In @y..., " Patty " <faussettdp@m...> wrote:

> > Wow, Deb, you've had quite a life! Bull riding sounds.....jolting!

> >

> > Sadly, I can relate to some of your symptoms, and have talked with

> many

> > other women who have had the same troubles.

> >

> > The visual problems are common, although your description of them

> is worse

> > than any I have experienced! When I got sick, it seemed that

> everything

> > happened all at once, and the visual problems were one of the first

> signs.

> > I had a hard time just being comfortable with my eyes open at

> times, and I

> > remember the aggravation of driving the most. I would put on

> sunglasses and

> > have to take them off 5 minutes later, only to put them back on

> again soon

> > after that. On and on it went, on, off. My eyes just never felt

> > right--they ached, and were tired. I got into two car accidents in

> the

> > first year after explant. But an opthamologist declared that I had

> better

> > than perfect vision after an exam, and he looked at me very strange

> when I

> > told him I thought there was something wrong and that it had to do

> with my

> > saline implants. I'll never forget his look. It shouted " You must

> be a

> > stupid, crazy lady. "

> >

> > I also can relate to the Bible episode, although mine had more to

> do with

> > comprehension and was very freaky. I went to read my Bible for

> comfort,

> > only to find out that I could not understand a single thing that I

> read! I

> > was reading, but it made no sense to me--it could have all been

> Greek, for

> > as much as I could comprehend it. I got so scared I went to watch

> TV with

> > my kids, only to find out I could not comprehend the TV show,

> either! That

> > was the day that my life changed, and I KNEW something was wrong.

> >

> > The memory problems and lapses are all part of it....the aches,

> pains,

> > fatigue, frozen shoulder, dry eyes, thyroid problems....all common

> to women

> > with implant toxicity.

> >

> > The exact mechanisms explaining the toxicity aren't fully

> understood yet,

> > but we do know that these symptoms are similar to what other

> chemically

> > toxic people have experienced. Therefore, the aim of healing is to

> detox

> > the body as fully as possible, and to support the immune system as

> it heals,

> > and help provide nutrients to rebuild healthy cells.

> >

> > This means doing things that you wouldn't normally do, such as

> fasting,

> > colonics, enemas, cleanses, saunas or other sweating therapies,

> chelation

> > therapy, amalgam removal, changes in diet (this is vital), juicing,

> as well

> > as using supplements to help your body in the detoxification and

> rebuilding

> > process. It takes alot of effort at times.

> >

> > There may be underlying viral or bacterial issues that should be

> addressed

> > as well. We have recently discussed the mycoplasma issue on the

> group.

> > There are also anti-viral foods and supplements that you can buy to

> reduce

> > your viral load.

> >

> > I have to say the effort is time consuming, but all worth it. I

> have healed

> > tremendously in the last 3 years since explant. I have learned

> alot and am,

> > hopefully, a better person for it. They say everything happens

> for a

> > reason, and though I wouldn't wish anyone else to go through this,

> I have to

> > look at my experience in the light of what God wanted me to learn

> from it,

> > and I see where He wanted me to change direction.

> >

> > I hope you will be encouraged in our group! Stay with us, ask

> questions,

> > and let us know how things go with your MRI and explant! Do you

> have a

> > doctor picked out yet? I do hope he helps you get your insurance

> to cover

> > it. Make sure you have a total capsulectomy done.

> > Take Care,

> > Patty

> > ----- Original Message -----

> > From: " Deb " <wwjddeb_99@y...>

> > < @y...>

> > Sent: Saturday, July 14, 2001 9:59 AM

> > Subject: Has anyone had these symptoms?

> >

> >

> > > Hi,

> > > I just joined and I just woke up from 22 years of being sick and

> > > wondering why? It was not until a few weeks ago that I even

> > > connected that my saline implants could be the hidden cause of my

> > > troubles.

> > > I was implanted (and I still am.... yikes!) in 1979 with Heyer

> > > Schulte implants 1620 inflated with 175 cc of normal saline and

> 1630

> > > was filled with 250cc of NS with 20mg of SolUMedrol placed in each

> > > implant.

> > > A few years after this I started having problems with my left

> > > shoulder. I had a ton of pain and it would freeze up on me... I

> > > started with injections of cortisone and I have had them off and

> on

> > > through out the years when the soulder is too painful.

> > > In more recent years I have had a lot of visiual problems. I was

> > > reading my Bible at the kitchen table one day in 1996 all of a

> sudden

> > > the pages looked some what like this: " F od so l ved th w rld

> th

> > > H ga " the letters where gone! That freaked me out! But then

> what

> > > made this worse was the fact that the next thing that I

> remembered is

> > > that I was sitting on the floor in my bathroom with no clue as to

> how

> > > I got there... I wasn't sure if I could even talk at that time.

> The

> > > doctors told me I was having phantom migraine headaches this of

> > > course was better than the possible brain tumor they thought that

> I

> > > had at first.

> > > Now I am having double vision! " Every now and then " I my vision

> will

> > > become blurred or I will see a persons eyes on their cheeks!

>

> > > King couldn't come up with some of the freaky things that I've

> seen

> > > through my eyes lately! lol

> > > The doctor told me that I had " Atypcial MS " this was then ruled

> out

> > > by a specialist who only deals with MS patients after he reviewed

> my

> > > records... and this was also after I found out that I developed an

> > > allergy to Steroids... I had 1000 mg. of SolUMedrol given to me

> over

> > > 3 days it was continued with the use of Benedryl taken orally 1

> hour

> > > before I got my 2nd and 3rd IV's because I started breaking out in

> > > hives before the first dose was finished. I cann't take the oral

> > > dose pack either it made me very very sick.

> > > Now I am left with the diagnosis of Chronic Fatigue, Chronic Pain,

> > > Fibromyalgia and periperal neuropathy.

> > >

> > > I have pain daily since the early 1980's. I am more stiff and

> > > painful in the AM's. I have always contributed this to the fact

> that

> > > I was a womens professional bull rider for about 3 years before I

> > > broke my back in 4 places in 1991. But looking back over my

> medical

> > > records from years ago I realized that I had a lot of these

> symptoms

> > > and problems before I took up the sport of bull riding...

> > >

> > > It's like the things that seem so " normal " to me today came on

> very

> > > slowly and I didn't realize that things were changing for me.

> When I

> > > started doing the visual things a few years ago I couldn't shun

> those

> > > symptoms off and make excuses for them... basically they freaked

> me

> > > out big time and I had to tell someone about them.

> > >

> > > I forget things all of the time, I don't have memory of a lot of

> the

> > > years gone by and no I don't take drugs or drink... I have

> difficulty

> > > with speach sometimes by slurring my speach or forgetting what I

> was

> > > saying in the middle of a sentence or by not using the correct

> > > word.

> > > I remember being in the middle of an intersection a few years

> > > back and I couldn't figure out how to turn... horns started

> honking

> > > and I was in a fog just sitting in the intersection without a

> clue as

> > > to how I should get myself out of it. Lucky for me someone got

> angry

> > > and pulled around me and I followed that person through the

> > > intersection. (Thanks God! :))

> > >

> > > My eyes are so dry that I can hardly wear my contacts well I do

> wear

> > > them sometimes and I have to " peel " them off of my eyes... ouch!

> My

> > > throat hurts so much that it is difficult to even drink water

> > > sometimes. My mouth is dry and I drink water all of the time I'm

> > > talking over a gallon a day. Of course I'm in the bathroom about

> > > every 15 to 30 minutes a day and at least 3 to 5 times at night.

> I

> > > had a nerve in my arm transposed (moved over) a few years ago and

> I

> > > still drop things with my left hand. I had a total hysterectomy

> two

> > > years ago because of fibroids thus I had the periods from the pit

> of

> > > hell. I have had cystic breasts for years and since I got married

> > > two years ago (right before my hysterectomy) I have continue to

> gain

> > > weight. I have gained over 60 pounds without changing my diet or

> my

> > > activies. I was in a car accident two years ago 2 months right

> > > before I got married and the air bag hit my chest so hard that my

> > > right breast was the color of an eggplant for almost 3 months. It

> > > also hit my transposed nerve in my left forearm and that trufully

> > > hurt worse than the breast because I didn't know about the breast

> > > until I got undressed later that night. Since this accident that

> > > former eggplant colored breast seems to have sagged to my

> knees... do

> > > you think that it ruptured? Eeeewww!

> > >

> > > Since that time my spinal tap was pretty normal except for basic

> > > mylin protiens were elevated other wise it was normal. My evoked

> > > potential eye test was a bit prolonged too. My T-7 showed a very

> low

> > > T-3 uptake on the thyroid... who knows what that all means or if

> it

> > > is related to the implants?

> > >

> > > As I wait to see if my insurance will pay for an MRI of my breast

> and

> > > or send me to a plastic surgeon for explantation I sit in awe of

> how

> > > much I don't know about any of this.

> > > Please feel free to email me if you too have had any of these

> > > symptoms and let me know what you found out about them.

> > >

> > > Thanks to all of you for being here for others and me... it's

> nice to

> > > know I'm not crazy or alone and if I am nuts then it's nice to be

> > > nuts with the rest of you nice ladies... validation is a wonderful

> > > healing tool isn't it? God Bless and keep you all. Keep in touch!

> > > Deb

> > > wwjddeb_99@y...

> > >

> > >

> > >

> > >

> > >

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  • 9 years later...

Barb,

You wrote:

>

> I don't have any swollen glands in my neck that I can detect, but today

> I woke up with a puffy swelling above my collar bone at both sides of my

> neck. I've been having to clear my throat a lot, and having quite a bit

> of phlegm....

There are also lymph nodes there on your neck. This might be connected

to the thyroid, but infection is more likely. That also goes with

phlegm. Since I'm slow responding, you may already have other symptoms

by now.

I suspect your thyroid nodules are " active " in the sense that they are

producing thyroid hormones but not in a properly controlled way. That is

one of the things that the blood test and biopsy should determine.

Chuck

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Thank you Chuck! The side where my thyroid is the largest, has the biggest

swelling. It's about the size of a golf ball, but of course doesn't stick up

that far. It's barely raised, but easily visible. It's been very cold here in

FL and the house doesn't seem to ever get warm, but I suspect that might have

something to do with the irritated throat, and symptoms I mentioned. Those

symptoms seem somewhat better today, but the swelling hasn't gone down at all.

I googled swellings like that and found some people have had them for months or

years, and doctors don't seem to know what they are.

Today my endocrinologist called and said he could move my biopsy up to 12-23.

Since I have an appointment at the Mayo Clinic on the 27th for registration and

blood work, I called to ask what to do, because the results of a biopsy done on

the 23rd would be unavailable on the 27th. The doctor's office at the Mayo

Clinic said you don't want to have just anybody doing that test. At Mayo they

don't have endocrinologists doing the fine needle aspiration, they use surgeons

who do it all the time. She said it was important to have it done as soon as

possible, but it's only a difference of 5 days from the 23rd when it could be

done here, to the 28th when I see the edno at the clinic. So, I decided to wait

and have it done in ville, and am hoping I made the right decision. I

was back on 25 mcgs of Levothyroxin for 5 days and the doctor's office in

ville said to stop the meds again until I go there. Meanwhile, the TSH

is probably hovering somewhere between 7 & 8.

I remember reading here that undertreatment can cause goiters. The swellings

behind the collar bone and at the base of the neck on both sides, look like

pictures of goiters I've seen on the neck. They're soft and puffy like goiters.

It's not possible to have goiters where I have swelling is it?

Just to highlight the difference between what doctors here refuse to do, and

what they have planned at the Mayo Clinic, I am scheduled for blood tests on the

27th to check 16 different things. Here in Melbourne, they wouldn't even check

FT3, FT4, and Rt3.

I appreciate any and all feedback from everyone. Thanks again Chuck.

Barb

Re: Has anyone had these symptoms?

Barb,

You wrote:

>

> I don't have any swollen glands in my neck that I can detect, but today

> I woke up with a puffy swelling above my collar bone at both sides of my

> neck. I've been having to clear my throat a lot, and having quite a bit

> of phlegm....

There are also lymph nodes there on your neck. This might be connected

to the thyroid, but infection is more likely. That also goes with

phlegm. Since I'm slow responding, you may already have other symptoms

by now.

I suspect your thyroid nodules are " active " in the sense that they are

producing thyroid hormones but not in a properly controlled way. That is

one of the things that the blood test and biopsy should determine.

Chuck

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I think you did the right thing. As long as you are going to be there, it makes

sense to utilize their services to the fullest. Five days won't make any

significant difference. Good luck Barb at Mayo.

I hope they are able to figure all this out for you.

<>Roni

Immortality exists!

It's called knowledge!

 

Just because something isn't seen

doesn't mean it's not there<>

>

> I don't have any swollen glands in my neck that I can detect, but today

> I woke up with a puffy swelling above my collar bone at both sides of my

> neck. I've been having to clear my throat a lot, and having quite a bit

> of phlegm....

There are also lymph nodes there on your neck. This might be connected

to the thyroid, but infection is more likely. That also goes with

phlegm. Since I'm slow responding, you may already have other symptoms

by now.

I suspect your thyroid nodules are " active " in the sense that they are

producing thyroid hormones but not in a properly controlled way. That is

one of the things that the blood test and biopsy should determine.

Chuck

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Here's some info on the subject.

 

http://www.mayoclinic.com/health/swollen-lymph-nodes/DS00880/DSECTION=symptoms

 

Roni

<>Roni

Immortality exists!

It's called knowledge!

 

Just because something isn't seen

doesn't mean it's not there<>

From: H <macbarb0503@...>

Subject: Re: Re: Has anyone had these symptoms?

hypothyroidism

Date: Thursday, December 16, 2010, 11:18 AM

Thanks you so much .  I've saved the link you sent, since I didn't know

where the lymph glads were.  I've had swollen lymph glands before, but they were

nothing like this.  It's round, soft, and about the size of a golf ball.  The

ones I've had in the bast were enlarged to about the size of a big kidney bean,

but not soft and puffy like this.  Weird!

Barb

Re: Has anyone had these symptoms?

Hi, Barb. Your case to me appears so unique that I'm almost afraid to

even venture a guess!

You do have a group of lymph glands above the collar bone called the

" supraclavicular lymph glands " . The page below shows them:

..

..

> http://www.patient.co.uk/health/Lymph-Glands-Swollen.htm

..

..

It also mentions the most common cause of swollen lymph glands: infection.

I live near Tampa and am just getting over a rather strange cold,

basically bronchitis I guess. No sore throat or headaches; just chest

congestion, coughing and hoarseness. There seems to be a heck of a lot

of people who have it locally. In my band I think all four of us have

had it; no practice for the past week.

Luck,

..

..

> Posted by: " H " macbarb0503@...

>

<mailto:macbarb0503@...?Subject=%20Re%3A%20Has%20anyone%20had%20these%20symp\

toms%3F>

> westieabbey <westieabbey>

>

>

> Wed Dec 15, 2010 7:51 am (PST)

>

>

>

>

> Just to recap:

>

> After being diagnosed with Hypothyroidism in August, I developed an

> enlarged thyroid in October, and found after an ultrasound that I have

> bi-lateral nodules, and what the report calls a multinodular goiter.

> That is what they are calling the enlarged thyroid. I'm the one who's

> TSH went from over 8 to around 1 in just a couple of months of taking

> 25 mcg of Levothyroxin. I have a biopsy scheduled for January.

>

> Since that was a big swing, for a small amount of medicine, I was

> taken off the Levothyroxin for five weeks so another blood test could

> be done. The TSH went back up to over seven, the doctor told me to go

> back on the pills, and I've only been back on them 4 days. I asked to

> have T4, T3, and RT3 tested, but the doctor didn't order those tests.

> The 25 mcg also elevated my resting pulse rate to around 100, and it

> was 145 when I was working out.

>

> I don't have any swollen glands in my neck that I can detect, but

> today I woke up with a puffy swelling above my collar bone at both

> sides of my neck. I've been having to clear my throat a lot, and

> having quite a bit of phlegm.

>

> I called the doctor the first thing this morning, but as usual

> couldn't get through to even his nurse, so I left a message. This is

> getting scary.

>

> Thanks,

> Barb

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Thank you Roni. I appreciate the kind words and good wishes. I'll keep you

posted.

Barb

Re: Has anyone had these symptoms?

I think you did the right thing. As long as you are going to be there, it makes

sense to utilize their services to the fullest. Five days won't make any

significant difference. Good luck Barb at Mayo.

I hope they are able to figure all this out for you.

<>Roni

Immortality exists!

It's called knowledge!

Just because something isn't seen

doesn't mean it's not there<>

>

> I don't have any swollen glands in my neck that I can detect, but today

> I woke up with a puffy swelling above my collar bone at both sides of my

> neck. I've been having to clear my throat a lot, and having quite a bit

> of phlegm....

There are also lymph nodes there on your neck. This might be connected

to the thyroid, but infection is more likely. That also goes with

phlegm. Since I'm slow responding, you may already have other symptoms

by now.

I suspect your thyroid nodules are " active " in the sense that they are

producing thyroid hormones but not in a properly controlled way. That is

one of the things that the blood test and biopsy should determine.

Chuck

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I also found this. Having information and being able to understand what the

doctors are saying I have found really helpful, since they tend to be less than

forthcoming with ALL

the information.

 

http://www.endocrineweb.com/conditions/thyroid/fine-needle-biopsy-thyroid-nodule\

s

<>Roni

Immortality exists!

It's called knowledge!

 

Just because something isn't seen

doesn't mean it's not there<>

From: H <macbarb0503@...>

Subject: Re: Re: Has anyone had these symptoms?

hypothyroidism

Date: Thursday, December 16, 2010, 11:18 AM

Thanks you so much .  I've saved the link you sent, since I didn't know

where the lymph glads were.  I've had swollen lymph glands before, but they were

nothing like this.  It's round, soft, and about the size of a golf ball.  The

ones I've had in the bast were enlarged to about the size of a big kidney bean,

but not soft and puffy like this.  Weird!

Barb

Re: Has anyone had these symptoms?

Hi, Barb. Your case to me appears so unique that I'm almost afraid to

even venture a guess!

You do have a group of lymph glands above the collar bone called the

" supraclavicular lymph glands " . The page below shows them:

..

..

> http://www.patient.co.uk/health/Lymph-Glands-Swollen.htm

..

..

It also mentions the most common cause of swollen lymph glands: infection.

I live near Tampa and am just getting over a rather strange cold,

basically bronchitis I guess. No sore throat or headaches; just chest

congestion, coughing and hoarseness. There seems to be a heck of a lot

of people who have it locally. In my band I think all four of us have

had it; no practice for the past week.

Luck,

..

..

> Posted by: " H " macbarb0503@...

>

<mailto:macbarb0503@...?Subject=%20Re%3A%20Has%20anyone%20had%20these%20symp\

toms%3F>

> westieabbey <westieabbey>

>

>

> Wed Dec 15, 2010 7:51 am (PST)

>

>

>

>

> Just to recap:

>

> After being diagnosed with Hypothyroidism in August, I developed an

> enlarged thyroid in October, and found after an ultrasound that I have

> bi-lateral nodules, and what the report calls a multinodular goiter.

> That is what they are calling the enlarged thyroid. I'm the one who's

> TSH went from over 8 to around 1 in just a couple of months of taking

> 25 mcg of Levothyroxin. I have a biopsy scheduled for January.

>

> Since that was a big swing, for a small amount of medicine, I was

> taken off the Levothyroxin for five weeks so another blood test could

> be done. The TSH went back up to over seven, the doctor told me to go

> back on the pills, and I've only been back on them 4 days. I asked to

> have T4, T3, and RT3 tested, but the doctor didn't order those tests.

> The 25 mcg also elevated my resting pulse rate to around 100, and it

> was 145 when I was working out.

>

> I don't have any swollen glands in my neck that I can detect, but

> today I woke up with a puffy swelling above my collar bone at both

> sides of my neck. I've been having to clear my throat a lot, and

> having quite a bit of phlegm.

>

> I called the doctor the first thing this morning, but as usual

> couldn't get through to even his nurse, so I left a message. This is

> getting scary.

>

> Thanks,

> Barb

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That is great information Roni! I read it, checked out the information at

different links, and saved it. The following is especially interesting, and

makes me glad I didn't have the radioactive uptake test and scan.

" In conclusion, FNA of the thyroid is a safe, inexpensive, and effective way to

distinguish a benign from a malignant nodule and usually should be the first

diagnostic test performed. "

Thanks again,

Barb

Re: Has anyone had these symptoms?

Hi, Barb. Your case to me appears so unique that I'm almost afraid to

even venture a guess!

You do have a group of lymph glands above the collar bone called the

" supraclavicular lymph glands " . The page below shows them:

..

..

> http://www.patient.co.uk/health/Lymph-Glands-Swollen.htm

..

..

It also mentions the most common cause of swollen lymph glands: infection.

I live near Tampa and am just getting over a rather strange cold,

basically bronchitis I guess. No sore throat or headaches; just chest

congestion, coughing and hoarseness. There seems to be a heck of a lot

of people who have it locally. In my band I think all four of us have

had it; no practice for the past week.

Luck,

..

..

> Posted by: " H " macbarb0503@...

>

<mailto:macbarb0503@...?Subject=%20Re%3A%20Has%20anyone%20had%20these%20symp\

toms%3F>

> westieabbey <westieabbey>

>

>

> Wed Dec 15, 2010 7:51 am (PST)

>

>

>

>

> Just to recap:

>

> After being diagnosed with Hypothyroidism in August, I developed an

> enlarged thyroid in October, and found after an ultrasound that I have

> bi-lateral nodules, and what the report calls a multinodular goiter.

> That is what they are calling the enlarged thyroid. I'm the one who's

> TSH went from over 8 to around 1 in just a couple of months of taking

> 25 mcg of Levothyroxin. I have a biopsy scheduled for January.

>

> Since that was a big swing, for a small amount of medicine, I was

> taken off the Levothyroxin for five weeks so another blood test could

> be done. The TSH went back up to over seven, the doctor told me to go

> back on the pills, and I've only been back on them 4 days. I asked to

> have T4, T3, and RT3 tested, but the doctor didn't order those tests.

> The 25 mcg also elevated my resting pulse rate to around 100, and it

> was 145 when I was working out.

>

> I don't have any swollen glands in my neck that I can detect, but

> today I woke up with a puffy swelling above my collar bone at both

> sides of my neck. I've been having to clear my throat a lot, and

> having quite a bit of phlegm.

>

> I called the doctor the first thing this morning, but as usual

> couldn't get through to even his nurse, so I left a message. This is

> getting scary.

>

> Thanks,

> Barb

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Share on other sites

Glad I could be of help.

<>Roni

Immortality exists!

It's called knowledge!

 

Just because something isn't seen

doesn't mean it's not there<>

From: H <macbarb0503@...>

Subject: Re: Re: Has anyone had these symptoms?

hypothyroidism

Date: Thursday, December 16, 2010, 11:18 AM

Thanks you so much .  I've saved the link you sent, since I didn't know

where the lymph glads were.  I've had swollen lymph glands before, but they were

nothing like this.  It's round, soft, and about the size of a golf ball.  The

ones I've had in the bast were enlarged to about the size of a big kidney bean,

but not soft and puffy like this.  Weird!

Barb

Re: Has anyone had these symptoms?

Hi, Barb. Your case to me appears so unique that I'm almost afraid to

even venture a guess!

You do have a group of lymph glands above the collar bone called the

" supraclavicular lymph glands " . The page below shows them:

..

..

> http://www.patient.co.uk/health/Lymph-Glands-Swollen.htm

..

..

It also mentions the most common cause of swollen lymph glands: infection.

I live near Tampa and am just getting over a rather strange cold,

basically bronchitis I guess. No sore throat or headaches; just chest

congestion, coughing and hoarseness. There seems to be a heck of a lot

of people who have it locally. In my band I think all four of us have

had it; no practice for the past week.

Luck,

..

..

> Posted by: " H " macbarb0503@...

>

<mailto:macbarb0503@...?Subject=%20Re%3A%20Has%20anyone%20had%20these%20symp\

toms%3F>

> westieabbey <westieabbey>

>

>

> Wed Dec 15, 2010 7:51 am (PST)

>

>

>

>

> Just to recap:

>

> After being diagnosed with Hypothyroidism in August, I developed an

> enlarged thyroid in October, and found after an ultrasound that I have

> bi-lateral nodules, and what the report calls a multinodular goiter.

> That is what they are calling the enlarged thyroid. I'm the one who's

> TSH went from over 8 to around 1 in just a couple of months of taking

> 25 mcg of Levothyroxin. I have a biopsy scheduled for January.

>

> Since that was a big swing, for a small amount of medicine, I was

> taken off the Levothyroxin for five weeks so another blood test could

> be done. The TSH went back up to over seven, the doctor told me to go

> back on the pills, and I've only been back on them 4 days. I asked to

> have T4, T3, and RT3 tested, but the doctor didn't order those tests.

> The 25 mcg also elevated my resting pulse rate to around 100, and it

> was 145 when I was working out.

>

> I don't have any swollen glands in my neck that I can detect, but

> today I woke up with a puffy swelling above my collar bone at both

> sides of my neck. I've been having to clear my throat a lot, and

> having quite a bit of phlegm.

>

> I called the doctor the first thing this morning, but as usual

> couldn't get through to even his nurse, so I left a message. This is

> getting scary.

>

> Thanks,

> Barb

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