Welcome Carol

[Guest guest]

Hey I put a hold on that book at the library as I am to poor to buy anything LOL. Also put one on "Guide to Hepatitis C for Dummies" . Hmmm now I don't know if I want to pick up when they come in embarrased and ashamed even tho I shouldn't be. Got real angry at my honey for telling his family I had hep c when we were there for a reunion with his brothers and sisters. That was last month and SO STUPID of me as I had told one of his sisters whom I am tight with. We got close when I started going with her to all her chemo sessions for breast cancer and I knew she wouldn't say anything. Told my whole family tho didn't want to do it. Don't know why I react that way try not to do that but it really pissed me off when he did that, oh hush my mouth I am getting mad again hahahaha. He is so sweet and good to me and I am like a banshee sometimes and feel so bad as he doesn't deserve that treatment. Hoping the books will help him

so he doesn't get his feelings hurt as well as help me also. Thats one thing I worry about getting meaner [if thats possible ha] while on tx. Oh man got myself all worked up over nothing, my kids don't even kiss me on the lips anymore well except for youngest son who still does. cheek kissing is better than nothing but i miss the mouth contact with my kids and grandkids oh well such is life. sorry for making a big deal out of nothing..later pat Motley <dmotley@...> wrote: Welcome to the group, Carol. You’re a good friend and we’re glad to have you here. I’m aka De aka WWD in Georgia, 49, and have been undetectable for two years post-treatment. I, too, highly recommend asking your friend’s doc about anti-depressants if he/she isn’t already on them. You can sit quietly and read and learn stuff, or you can jump in and ask questions and let us get to know you so we can wrap our arms around you and support you. Your style, your choice. A good book for both of you is 1. Living with Hepatitis C: A Survivor's Guide, Fourth Edition (Living with) by T. Everson and Hedy Weinberg (Paperback - Jul 18, 2006) Buy new: $15.95 $11.96 43 Used & new from $8.99 (That’s from Amazon) Do not ask God to guide your footsteps if you are not willing to move your feet!

[Guest guest]

Pat,

HCV can only be transmitted by blood to blood contact – so kissing on the

mouth isn’t a danger unless both people have cuts on their lips.

Even if our blood got on someone’s skin, they wouldn’t get infected

unless they had an open wound also. They can’t get it by eating or

drinking after us, or touching us, or hugging or kissing us. Blood to

blood contact only.

Re:

Welcome Carol

Hey I put a hold on that book at the library as

I am to poor to buy anything LOL. Also put one on " Guide to Hepatitis C

for Dummies " . Hmmm now I don't know if I want to pick up when they

come in embarrased and ashamed even tho I shouldn't be. Got real angry at

my honey for telling his family I had hep c when we were there for a reunion

with his brothers and sisters. That was last month and SO STUPID of me as

I had told one of his sisters whom I am tight with. We got close when I

started going with her to all her chemo sessions for breast cancer and I knew

she wouldn't say anything. Told my whole family tho didn't want to do

it. Don't know why I react that way try not to do that but it really

pissed me off when he did that, oh hush my mouth I am getting mad again

hahahaha. He is so sweet and good to me and I am like a banshee sometimes

and feel so bad as he doesn't deserve that treatment. Hoping the books

will help him so he doesn't get his feelings hurt as well as help me

also. Thats one thing I worry about getting meaner [if thats possible ha]

while on tx. Oh man got myself all worked up over nothing, my kids don't even

kiss me on the lips anymore well except for youngest son who still does.

cheek kissing is better than nothing but i miss the mouth contact with my kids

and grandkids oh well such is life. sorry for making a big deal out of

nothing..later pat

[Guest guest]

Hi ..they say they know that but things have changed. Oh well life is to short to be sad all the time. pat Motley <dmotley@...> wrote: Pat, HCV can only be transmitted by blood to blood contact – so kissing on the mouth isn’t a danger unless both people have cuts on their lips. Even

if our blood got on someone’s skin, they wouldn’t get infected unless they had an open wound also. They can’t get it by eating or drinking after us, or touching us, or hugging or kissing us. Blood to blood contact only. -----Original Message-----From: Hepatitis CSupportGroupForDummies [mailto:Hepatitis CSupportGroupForDummies ] On Behalf Of patriciaSent: Monday, March 19, 2007 2:38 PMHepatitis CSupportGroupForDummies Subject: Re: Welcome Carol Hey I put a hold on that book at the library as I am to poor to buy anything LOL. Also put one on "Guide to Hepatitis C for Dummies" . Hmmm now I don't know if I want to pick up when they come in embarrased and ashamed even tho I shouldn't be. Got real angry at my honey for telling his family I had hep c when we were there for a reunion with his brothers and sisters. That was last month and SO STUPID of me as I had told one of his sisters whom I am tight

with. We got close when I started going with her to all her chemo sessions for breast cancer and I knew she wouldn't say anything. Told my whole family tho didn't want to do it. Don't know why I react that way try not to do that but it really pissed me off when he did that, oh hush my mouth I am getting mad again hahahaha. He is so sweet and good to me and I am like a banshee sometimes and feel so bad as he doesn't deserve that treatment. Hoping the books will help him so he doesn't get his feelings hurt as well as help me also. Thats one thing I worry about getting meaner [if thats possible ha] while on tx. Oh man got myself all worked up over nothing, my kids don't even kiss me on the lips anymore well except for youngest son who still does. cheek kissing is better than nothing but i miss the mouth contact with my kids and grandkids oh well such is life. sorry for making a big deal out of nothing..later

pat

[Guest guest]

Welcome Carol,

I don't run this list, but just sound like it.

Your body is trying to tell you something that your mind doesn't want

to hear.

This radiation from your Wi-Fi router is disrupting normal cell

function, causing cell stress/shock (the cell wall seals off and

starts to become toxic from reduced transfer in and out of the cell

wall).

Also, toxins are mobilized from deep muscle, bone and other tissues

into other systems and especially into sensitive areas like the ears,

eyes, heart, etc. brain because Wi-Fi and other microwave radiation

frequencies open up the blood brain barrier.

And you can guess why that is bad. When toxins get into these areas

like the brain, infections can set in as well as cause deterioration

of nerve function from exposure mercury, pesticides, fluoride, etc. on

and on... ad nauseam.

You first problem is how are going to get away from the router?

The second one is how are you going to deal with becoming a wack-job,

outcast, freak-show, conspiracy theory loving anti-socialite now that

you are " sensitive " to this man made poison that most everyone loves

to use (iPads, Crackberrys, ...)

Get rid of the router or find another job. Then get the plug-in hard

line connection for internet. It is faster, safer anyway.

You can read more at my website www.raleighes.info.

Good luck!

with love : )

McAfee

www.raleighes.info

andrewmcafee1@...

On Jun 10, 2011, at 4:20 AM, carol wrote:

> New to this group. Don't know where to start really. Does anybody

> any experience on wireless routers. There was one in my office at

> work (in a hospital) for a about a year. Other people said they

> could hear a squeal in my room. I couldn't. I rang our IT

> communications department and they said it could be faulty. They

> swapped it. Another 8 months and they new one is still there, with

> me working under it.

>

> I now have a sudden onset of constant tinnitus ( a week ago (sounds

> like a computer monitor (high pitched) and it is CONSTANT)). My GP

> has put me in for a hearing test which will take months.

>

> I need to know how to deal with it as I won't let it affect my

> life. Therefore I am starting to research tinnitus etc.

>

> All I need to know is does anyone think it could be related? I do

> not wish to blame but I find it highly suspicious.

>

> many many thanks folks.

>

>

> Carol

>

>

>

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

>

>