Re: More about me... and thanks

[Guest guest]

Bryce,

Have you been fitted with a lymphedema sleeve? Also physical therapy is good for lymphadema.

Hugs

nne

Breast Cancer Patients Soul Mates for Lifehttp://www.geocities.com/chucky5741/breastcancerpatients.htmlBreastCancerStories.comhttp://www.breastcancerstories.com/content/view/433/161/Angel Feather Loomerwww.angelfeatherloomer.blogspot.comCheck out my other ornaments atwww.geocities.com/chucky5741/bcornament.htmlLots of info and gifts at:www.cancerclub.com

More about me... and thanks

Hi,

Thank you all for such a warm welcome and for all the helpful information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time.

This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never finding out until they die.

I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood pressure and sleep anapa.

Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J

Bryce

No virus found in this incoming message.Checked by AVG Free Edition.Version: 7.1.405 / Virus Database: 268.12.2/441 - Release Date: 9/7/2006

[Guest guest]

Bryce, it doesn't matter to me about the intersex. I've seen shows about it on Discovery TV. You are very brave for going through all you have gone through! The Lymphoma, can it be treated? ShirleyBryce Satin wrote: Hi, Thank you all for such a warm welcome and for all the helpful

information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time. This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then

removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never finding out until they die. I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood

pressure and sleep anapa. Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J Bryce

[Guest guest]

Bryce, it doesn't matter to me about the intersex. I've seen shows about it on Discovery TV. You are very brave for going through all you have gone through! The Lymphoma, can it be treated? ShirleyBryce Satin wrote: Hi, Thank you all for such a warm welcome and for all the helpful

information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time. This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then

removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never finding out until they die. I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood

pressure and sleep anapa. Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J Bryce

[Guest guest]

Bryce, it doesn't matter to me about the intersex. I've seen shows about it on Discovery TV. You are very brave for going through all you have gone through! The Lymphoma, can it be treated? ShirleyBryce Satin wrote: Hi, Thank you all for such a warm welcome and for all the helpful

information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time. This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then

removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never finding out until they die. I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood

pressure and sleep anapa. Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J Bryce

[Guest guest]

Bryce, It took alot to write that but that is a birth defect just like any other. I know know they recommend for parents to wait and see which gender their child is going to become, not just look at the outside. There is also research that homosexuality is because there are three times during the three trimesters when the fetus receives the hormones that develope it into a male or a female and if they do not receive their hormones during this growth period they may be born as a male with female traits or a female with male traits. They need to do soo much more research on this to understand instead of condemn ' in TexasBryce Satin wrote: Hi, Thank you all for such a warm welcome and for all the helpful information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time. This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or

anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never

finding out until they die. I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood pressure and sleep anapa. Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J Bryce

[Guest guest]

Bryce, It took alot to write that but that is a birth defect just like any other. I know know they recommend for parents to wait and see which gender their child is going to become, not just look at the outside. There is also research that homosexuality is because there are three times during the three trimesters when the fetus receives the hormones that develope it into a male or a female and if they do not receive their hormones during this growth period they may be born as a male with female traits or a female with male traits. They need to do soo much more research on this to understand instead of condemn ' in TexasBryce Satin wrote: Hi, Thank you all for such a warm welcome and for all the helpful information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time. This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or

anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never

finding out until they die. I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood pressure and sleep anapa. Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J Bryce

[Guest guest]

Bryce, It took alot to write that but that is a birth defect just like any other. I know know they recommend for parents to wait and see which gender their child is going to become, not just look at the outside. There is also research that homosexuality is because there are three times during the three trimesters when the fetus receives the hormones that develope it into a male or a female and if they do not receive their hormones during this growth period they may be born as a male with female traits or a female with male traits. They need to do soo much more research on this to understand instead of condemn ' in TexasBryce Satin wrote: Hi, Thank you all for such a warm welcome and for all the helpful information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time. This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or

anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never

finding out until they die. I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood pressure and sleep anapa. Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J Bryce

[Guest guest]

I second what Shirley said. Welcome to the group. I hope you find it helpful.

E.

Colorado

"Insanity runs in my family. It practically gallops."

Cary Grant

Re: More about me... and thanks

Bryce, it doesn't matter to me about the

intersex. I've seen shows about it on Discovery TV.

You are very brave for going through all you have gone through!

The Lymphoma, can it be treated?

Shirley

Bryce Satin wrote:

Hi,

Thank

you all for such a warm welcome and for all the helpful information

that you have sent. I am not currently on any medication for MS as it

has really only been totally confirmed this week. My doctor is sending

me to a Neuro who I go and see on Monday for the first time.

This

next part of my introduction is something I have been struggling with

for the last few days however before this Dx I was not ashamed and

still not ashamed of who I am. It is seem a little scarier to come out

about all this. However as I can now see that I am not going to be able

to hide this from Neuro doctors or anyone that I have to go to I might

as well be open here. Not to mention my yahoo profile and blog talk

about me. I was born with I call another birth defect I was born an

intersex person. At birth, I had both male and female body parts. Back

in the 50’s they would look at the child and say girl or boy. For me

they chose girl due to the fact I was born with one ovarie and uterus.

Then removed the male part from my body. Although I was able to have

children something I was suppose to have. (had to have a C-section) I

was a very sick person and in the hospital most of the 9 months. My

parents never told me and doctors would always blame me for having had

bad abortions. My parents never told me and I was in my early 30’s when

I found out. Since finding out I started to live my life as a male. One

thing I found out on my path that most may not know about intersex

people is that 1 in 2,000 babies born are born with some kind of

intersex and most can go their whole life never finding out until they

die.

I

tell you because one of the operations I had this past May, the removal

of my chest (breast) cause another illness that I am sure is the big

reason for this current new flare up. It is called Lymphedema; with

this, the lymp-nods stop working. I also have type 2 diabetics as well

as high blood pressure and sleep anapa.

Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J

Bryce

Check out the new AOL. Most comprehensive set of free safety and security tools, free access to millions of high-quality videos from across the web, free AOL Mail and more.

[Guest guest]

I second what Shirley said. Welcome to the group. I hope you find it helpful.

E.

Colorado

"Insanity runs in my family. It practically gallops."

Cary Grant

Re: More about me... and thanks

Bryce, it doesn't matter to me about the

intersex. I've seen shows about it on Discovery TV.

You are very brave for going through all you have gone through!

The Lymphoma, can it be treated?

Shirley

Bryce Satin wrote:

Hi,

Thank

you all for such a warm welcome and for all the helpful information

that you have sent. I am not currently on any medication for MS as it

has really only been totally confirmed this week. My doctor is sending

me to a Neuro who I go and see on Monday for the first time.

This

next part of my introduction is something I have been struggling with

for the last few days however before this Dx I was not ashamed and

still not ashamed of who I am. It is seem a little scarier to come out

about all this. However as I can now see that I am not going to be able

to hide this from Neuro doctors or anyone that I have to go to I might

as well be open here. Not to mention my yahoo profile and blog talk

about me. I was born with I call another birth defect I was born an

intersex person. At birth, I had both male and female body parts. Back

in the 50’s they would look at the child and say girl or boy. For me

they chose girl due to the fact I was born with one ovarie and uterus.

Then removed the male part from my body. Although I was able to have

children something I was suppose to have. (had to have a C-section) I

was a very sick person and in the hospital most of the 9 months. My

parents never told me and doctors would always blame me for having had

bad abortions. My parents never told me and I was in my early 30’s when

I found out. Since finding out I started to live my life as a male. One

thing I found out on my path that most may not know about intersex

people is that 1 in 2,000 babies born are born with some kind of

intersex and most can go their whole life never finding out until they

die.

I

tell you because one of the operations I had this past May, the removal

of my chest (breast) cause another illness that I am sure is the big

reason for this current new flare up. It is called Lymphedema; with

this, the lymp-nods stop working. I also have type 2 diabetics as well

as high blood pressure and sleep anapa.

Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J

Bryce

Check out the new AOL. Most comprehensive set of free safety and security tools, free access to millions of high-quality videos from across the web, free AOL Mail and more.

[Guest guest]

I second what Shirley said. Welcome to the group. I hope you find it helpful.

E.

Colorado

"Insanity runs in my family. It practically gallops."

Cary Grant

Re: More about me... and thanks

Bryce, it doesn't matter to me about the

intersex. I've seen shows about it on Discovery TV.

You are very brave for going through all you have gone through!

The Lymphoma, can it be treated?

Shirley

Bryce Satin wrote:

Hi,

Thank

you all for such a warm welcome and for all the helpful information

that you have sent. I am not currently on any medication for MS as it

has really only been totally confirmed this week. My doctor is sending

me to a Neuro who I go and see on Monday for the first time.

This

next part of my introduction is something I have been struggling with

for the last few days however before this Dx I was not ashamed and

still not ashamed of who I am. It is seem a little scarier to come out

about all this. However as I can now see that I am not going to be able

to hide this from Neuro doctors or anyone that I have to go to I might

as well be open here. Not to mention my yahoo profile and blog talk

about me. I was born with I call another birth defect I was born an

intersex person. At birth, I had both male and female body parts. Back

in the 50’s they would look at the child and say girl or boy. For me

they chose girl due to the fact I was born with one ovarie and uterus.

Then removed the male part from my body. Although I was able to have

children something I was suppose to have. (had to have a C-section) I

was a very sick person and in the hospital most of the 9 months. My

parents never told me and doctors would always blame me for having had

bad abortions. My parents never told me and I was in my early 30’s when

I found out. Since finding out I started to live my life as a male. One

thing I found out on my path that most may not know about intersex

people is that 1 in 2,000 babies born are born with some kind of

intersex and most can go their whole life never finding out until they

die.

I

tell you because one of the operations I had this past May, the removal

of my chest (breast) cause another illness that I am sure is the big

reason for this current new flare up. It is called Lymphedema; with

this, the lymp-nods stop working. I also have type 2 diabetics as well

as high blood pressure and sleep anapa.

Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J

Bryce

Check out the new AOL. Most comprehensive set of free safety and security tools, free access to millions of high-quality videos from across the web, free AOL Mail and more.

[Guest guest]

Thank you all for being so warm and welcoming.

To answer your question about Lymphoma no it can not be cured. I have what they call Secondary lymphedema, caused by having 3 lymph nodes removed. For information about it this is a good link. http://www.emedicine.com/med/topic2722.htm

Someone ask in another email if I have been fixed for compression sleeves, yes I have as well as socks and a compression vest. I do not have the socks of the sleeves yet but I do have the vest and I have to wear it at night while I sleep to keep the fluid from building up in my chest. I have to keep close eye on the skin to any cuts or skin changes and report them right away. I have to take precaution and wear rubber gloves when working in the yard or doing cleaning. Just one more thing to keep an eye on.

Well I am off to bed.. Thanks again...

Bryce

Re: More about me... and thanks

Bryce, it doesn't matter to me about the intersex. I've seen shows about it on Discovery TV. You are very brave for going through all you have gone through!

The Lymphoma, can it be treated?

ShirleyBryce Satin <basatincomcast (DOT) net> wrote:

Hi,

Thank you all for such a warm welcome and for all the helpful information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time.

This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never finding out until they die.

I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood pressure and sleep anapa.

Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J

Bryce

[Guest guest]

Bryce,

I have been lucky so far with just very minor lymphedema if I use that arm too much to do lifting etc. Somewhere I have a list of thngs you have to be careful about on the affected side. I know wearing gloves for gardening like you mentioned, using thimbles if you sew, don't carry anything heavy on that side, be careful of cuts etc.No b/p readings on that side, no IV's. Women don't carry purses on that side can't remember the rest but if you are interested let me know and I will try to hunt it up. You may already have these.

Hugs

nne

Breast Cancer Patients Soul Mates for Lifehttp://www.geocities.com/chucky5741/breastcancerpatients.htmlBreastCancerStories.comhttp://www.breastcancerstories.com/content/view/433/161/Angel Feather Loomerwww.angelfeatherloomer.blogspot.comCheck out my other ornaments atwww.geocities.com/chucky5741/bcornament.htmlLots of info and gifts at:www.cancerclub.com

Re: More about me... and thanks

Bryce, it doesn't matter to me about the intersex. I've seen shows about it on Discovery TV. You are very brave for going through all you have gone through!

The Lymphoma, can it be treated?

ShirleyBryce Satin <basatincomcast (DOT) net> wrote:

Hi,

Thank you all for such a warm welcome and for all the helpful information that you have sent. I am not currently on any medication for MS as it has really only been totally confirmed this week. My doctor is sending me to a Neuro who I go and see on Monday for the first time.

This next part of my introduction is something I have been struggling with for the last few days however before this Dx I was not ashamed and still not ashamed of who I am. It is seem a little scarier to come out about all this. However as I can now see that I am not going to be able to hide this from Neuro doctors or anyone that I have to go to I might as well be open here. Not to mention my yahoo profile and blog talk about me. I was born with I call another birth defect I was born an intersex person. At birth, I had both male and female body parts. Back in the 50’s they would look at the child and say girl or boy. For me they chose girl due to the fact I was born with one ovarie and uterus. Then removed the male part from my body. Although I was able to have children something I was suppose to have. (had to have a C-section) I was a very sick person and in the hospital most of the 9 months. My parents never told me and doctors would always blame me for having had bad abortions. My parents never told me and I was in my early 30’s when I found out. Since finding out I started to live my life as a male. One thing I found out on my path that most may not know about intersex people is that 1 in 2,000 babies born are born with some kind of intersex and most can go their whole life never finding out until they die.

I tell you because one of the operations I had this past May, the removal of my chest (breast) cause another illness that I am sure is the big reason for this current new flare up. It is called Lymphedema; with this, the lymp-nods stop working. I also have type 2 diabetics as well as high blood pressure and sleep anapa.

Again, I want to thank everyone for such a warm welcome. I will be calling all the place everyone recommend. Thanks… J

Bryce

No virus found in this incoming message.Checked by AVG Free Edition.Version: 7.1.405 / Virus Database: 268.12.2/442 - Release Date: 9/8/2006